US2858251A - Indolo [2, 3-c] quinazo [3, 2-a] pyridine derivatives - Google Patents
Indolo [2, 3-c] quinazo [3, 2-a] pyridine derivatives Download PDFInfo
- Publication number
- US2858251A US2858251A US616632A US61663256A US2858251A US 2858251 A US2858251 A US 2858251A US 616632 A US616632 A US 616632A US 61663256 A US61663256 A US 61663256A US 2858251 A US2858251 A US 2858251A
- Authority
- US
- United States
- Prior art keywords
- oxo
- methyl
- quinazo
- tetrahydroindolo
- pyridine
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- VNHBYKHXBCYPBJ-UHFFFAOYSA-N 5-ethynylimidazo[1,2-a]pyridine Chemical class C#CC1=CC=CC2=NC=CN12 VNHBYKHXBCYPBJ-UHFFFAOYSA-N 0.000 title description 49
- 239000000203 mixture Substances 0.000 claims description 65
- 150000001875 compounds Chemical class 0.000 claims description 22
- 239000002253 acid Substances 0.000 claims description 13
- 239000012458 free base Substances 0.000 claims description 11
- MNDIARAMWBIKFW-UHFFFAOYSA-N 1-bromohexane Chemical compound CCCCCCBr MNDIARAMWBIKFW-UHFFFAOYSA-N 0.000 claims description 5
- KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 claims description 5
- 229940073608 benzyl chloride Drugs 0.000 claims description 5
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 claims description 5
- 230000003276 anti-hypertensive effect Effects 0.000 claims description 4
- 239000003937 drug carrier Substances 0.000 claims description 4
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 claims description 4
- KIWBPDUYBMNFTB-UHFFFAOYSA-N Ethyl hydrogen sulfate Chemical compound CCOS(O)(=O)=O KIWBPDUYBMNFTB-UHFFFAOYSA-N 0.000 claims description 3
- RDHPKYGYEGBMSE-UHFFFAOYSA-N bromoethane Chemical compound CCBr RDHPKYGYEGBMSE-UHFFFAOYSA-N 0.000 claims description 3
- VUQUOGPMUUJORT-UHFFFAOYSA-N methyl 4-methylbenzenesulfonate Chemical compound COS(=O)(=O)C1=CC=C(C)C=C1 VUQUOGPMUUJORT-UHFFFAOYSA-N 0.000 claims description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 92
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 69
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 68
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 68
- 238000010992 reflux Methods 0.000 description 63
- 239000000243 solution Substances 0.000 description 55
- 238000000034 method Methods 0.000 description 40
- 239000002585 base Substances 0.000 description 36
- 239000004615 ingredient Substances 0.000 description 34
- -1 methylenedioxy Chemical group 0.000 description 33
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical class C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 32
- 239000000725 suspension Substances 0.000 description 32
- GVOWHGSUZUUUDR-UHFFFAOYSA-N methyl N-methylanthranilate Chemical compound CNC1=CC=CC=C1C(=O)OC GVOWHGSUZUUUDR-UHFFFAOYSA-N 0.000 description 28
- 239000007903 gelatin capsule Substances 0.000 description 27
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 26
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 24
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- 238000003756 stirring Methods 0.000 description 22
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 22
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 21
- 125000000217 alkyl group Chemical group 0.000 description 21
- 239000008101 lactose Substances 0.000 description 21
- RERZNCLIYCABFS-UHFFFAOYSA-N harmaline Chemical compound C1CN=C(C)C2=C1C1=CC=C(OC)C=C1N2 RERZNCLIYCABFS-UHFFFAOYSA-N 0.000 description 18
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 17
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- 125000004432 carbon atom Chemical group C* 0.000 description 17
- 150000003839 salts Chemical class 0.000 description 17
- 229920002472 Starch Polymers 0.000 description 16
- 239000008107 starch Substances 0.000 description 16
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- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 15
- 125000003545 alkoxy group Chemical group 0.000 description 14
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 14
- 239000000047 product Substances 0.000 description 14
- 239000013078 crystal Substances 0.000 description 13
- 229910052739 hydrogen Inorganic materials 0.000 description 13
- 239000001257 hydrogen Substances 0.000 description 13
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Natural products OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 13
- 239000007787 solid Substances 0.000 description 13
- 230000008878 coupling Effects 0.000 description 12
- 238000010168 coupling process Methods 0.000 description 12
- 238000005859 coupling reaction Methods 0.000 description 12
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 12
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 11
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 10
- 108010010803 Gelatin Proteins 0.000 description 10
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- 229910000041 hydrogen chloride Inorganic materials 0.000 description 9
- 238000001953 recrystallisation Methods 0.000 description 9
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 8
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- 125000005843 halogen group Chemical group 0.000 description 8
- 239000000314 lubricant Substances 0.000 description 8
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 8
- VAMXMNNIEUEQDV-UHFFFAOYSA-N methyl anthranilate Chemical compound COC(=O)C1=CC=CC=C1N VAMXMNNIEUEQDV-UHFFFAOYSA-N 0.000 description 8
- RWZYAGGXGHYGMB-UHFFFAOYSA-N o-aminobenzenecarboxylic acid Natural products NC1=CC=CC=C1C(O)=O RWZYAGGXGHYGMB-UHFFFAOYSA-N 0.000 description 8
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- 239000000454 talc Substances 0.000 description 7
- 229910052623 talc Inorganic materials 0.000 description 7
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 7
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 6
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 6
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- 150000002148 esters Chemical class 0.000 description 6
- 235000019359 magnesium stearate Nutrition 0.000 description 6
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
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- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 5
- 235000019483 Peanut oil Nutrition 0.000 description 5
- 229930006000 Sucrose Natural products 0.000 description 5
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 5
- 238000009835 boiling Methods 0.000 description 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 5
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- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 4
- QCQCHGYLTSGIGX-GHXANHINSA-N 4-[[(3ar,5ar,5br,7ar,9s,11ar,11br,13as)-5a,5b,8,8,11a-pentamethyl-3a-[(5-methylpyridine-3-carbonyl)amino]-2-oxo-1-propan-2-yl-4,5,6,7,7a,9,10,11,11b,12,13,13a-dodecahydro-3h-cyclopenta[a]chrysen-9-yl]oxy]-2,2-dimethyl-4-oxobutanoic acid Chemical compound N([C@@]12CC[C@@]3(C)[C@]4(C)CC[C@H]5C(C)(C)[C@@H](OC(=O)CC(C)(C)C(O)=O)CC[C@]5(C)[C@H]4CC[C@@H]3C1=C(C(C2)=O)C(C)C)C(=O)C1=CN=CC(C)=C1 QCQCHGYLTSGIGX-GHXANHINSA-N 0.000 description 4
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- 150000004677 hydrates Chemical class 0.000 description 4
- 150000002475 indoles Chemical class 0.000 description 4
- 238000002955 isolation Methods 0.000 description 4
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- 229940102398 methyl anthranilate Drugs 0.000 description 4
- FAIAAWCVCHQXDN-UHFFFAOYSA-N phosphorus trichloride Chemical compound ClP(Cl)Cl FAIAAWCVCHQXDN-UHFFFAOYSA-N 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- YXZFFTJAHVMMLF-UHFFFAOYSA-N 1-bromo-3-methylbutane Chemical compound CC(C)CCBr YXZFFTJAHVMMLF-UHFFFAOYSA-N 0.000 description 3
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 3
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- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 3
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- IUVCFHHAEHNCFT-INIZCTEOSA-N 2-[(1s)-1-[4-amino-3-(3-fluoro-4-propan-2-yloxyphenyl)pyrazolo[3,4-d]pyrimidin-1-yl]ethyl]-6-fluoro-3-(3-fluorophenyl)chromen-4-one Chemical compound C1=C(F)C(OC(C)C)=CC=C1C(C1=C(N)N=CN=C11)=NN1[C@@H](C)C1=C(C=2C=C(F)C=CC=2)C(=O)C2=CC(F)=CC=C2O1 IUVCFHHAEHNCFT-INIZCTEOSA-N 0.000 description 1
- URXXVVWXSNKYOH-UHFFFAOYSA-N 2-amino-4-propan-2-ylbenzoic acid Chemical compound CC(C)C1=CC=C(C(O)=O)C(N)=C1 URXXVVWXSNKYOH-UHFFFAOYSA-N 0.000 description 1
- IQHSSYROJYPFDV-UHFFFAOYSA-N 2-bromo-1,3-dichloro-5-(trifluoromethyl)benzene Chemical group FC(F)(F)C1=CC(Cl)=C(Br)C(Cl)=C1 IQHSSYROJYPFDV-UHFFFAOYSA-N 0.000 description 1
- ONSYFGRVJCIZKU-UHFFFAOYSA-N 2-hydroxybenzoic acid;pyridine Chemical compound C1=CC=NC=C1.OC(=O)C1=CC=CC=C1O ONSYFGRVJCIZKU-UHFFFAOYSA-N 0.000 description 1
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- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
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- NDHJFACYRWUMHT-UHFFFAOYSA-N 4-(2-methylpropoxy)aniline Chemical compound CC(C)COC1=CC=C(N)C=C1 NDHJFACYRWUMHT-UHFFFAOYSA-N 0.000 description 1
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- 101100025412 Arabidopsis thaliana XI-A gene Proteins 0.000 description 1
- 244000105624 Arachis hypogaea Species 0.000 description 1
- 241000416162 Astragalus gummifer Species 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
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- 206010012735 Diarrhoea Diseases 0.000 description 1
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- NHTMVDHEPJAVLT-UHFFFAOYSA-N Isooctane Chemical compound CC(C)CC(C)(C)C NHTMVDHEPJAVLT-UHFFFAOYSA-N 0.000 description 1
- 238000006147 Japp-Klingemann synthesis reaction Methods 0.000 description 1
- 235000010643 Leucaena leucocephala Nutrition 0.000 description 1
- 240000007472 Leucaena leucocephala Species 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 238000007126 N-alkylation reaction Methods 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical class O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- YZCKVEUIGOORGS-IGMARMGPSA-N Protium Chemical compound [1H] YZCKVEUIGOORGS-IGMARMGPSA-N 0.000 description 1
- LCQMZZCPPSWADO-UHFFFAOYSA-N Reserpilin Natural products COC(=O)C1COCC2CN3CCc4c([nH]c5cc(OC)c(OC)cc45)C3CC12 LCQMZZCPPSWADO-UHFFFAOYSA-N 0.000 description 1
- QEVHRUUCFGRFIF-SFWBKIHZSA-N Reserpine Natural products O=C(OC)[C@@H]1[C@H](OC)[C@H](OC(=O)c2cc(OC)c(OC)c(OC)c2)C[C@H]2[C@@H]1C[C@H]1N(C2)CCc2c3c([nH]c12)cc(OC)cc3 QEVHRUUCFGRFIF-SFWBKIHZSA-N 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 229920001615 Tragacanth Polymers 0.000 description 1
- 159000000021 acetate salts Chemical class 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 description 1
- GZCGUPFRVQAUEE-SLPGGIOYSA-N aldehydo-D-glucose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O GZCGUPFRVQAUEE-SLPGGIOYSA-N 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000003849 aromatic solvent Substances 0.000 description 1
- 230000004872 arterial blood pressure Effects 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- ASGJEMPQQVNTGO-UHFFFAOYSA-N benzene chloroform Chemical compound C(Cl)(Cl)Cl.C1=CC=CC=C1.C1=CC=CC=C1 ASGJEMPQQVNTGO-UHFFFAOYSA-N 0.000 description 1
- WIRUZQNBHNAMAB-UHFFFAOYSA-N benzene;cyclohexane Chemical compound C1CCCCC1.C1=CC=CC=C1 WIRUZQNBHNAMAB-UHFFFAOYSA-N 0.000 description 1
- 125000001246 bromo group Chemical group Br* 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 238000010531 catalytic reduction reaction Methods 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- UXTMROKLAAOEQO-UHFFFAOYSA-N chloroform;ethanol Chemical compound CCO.ClC(Cl)Cl UXTMROKLAAOEQO-UHFFFAOYSA-N 0.000 description 1
- 150000001860 citric acid derivatives Chemical class 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 239000008120 corn starch Substances 0.000 description 1
- 229940099112 cornstarch Drugs 0.000 description 1
- WZHCOOQXZCIUNC-UHFFFAOYSA-N cyclandelate Chemical compound C1C(C)(C)CC(C)CC1OC(=O)C(O)C1=CC=CC=C1 WZHCOOQXZCIUNC-UHFFFAOYSA-N 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 150000008049 diazo compounds Chemical class 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 1
- JVSWJIKNEAIKJW-UHFFFAOYSA-N dimethyl-hexane Natural products CCCCCC(C)C JVSWJIKNEAIKJW-UHFFFAOYSA-N 0.000 description 1
- 230000003292 diminished effect Effects 0.000 description 1
- MKYNHKOAYQRSBD-UHFFFAOYSA-N dioxouranium;nitric acid Chemical compound O=[U]=O.O[N+]([O-])=O.O[N+]([O-])=O MKYNHKOAYQRSBD-UHFFFAOYSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- XCLWRWMGOGPGDS-UHFFFAOYSA-N ethyl 3-[(dimethylamino)methyl]-1h-indole-2-carboxylate Chemical compound C1=CC=C2C(CN(C)C)=C(C(=O)OCC)NC2=C1 XCLWRWMGOGPGDS-UHFFFAOYSA-N 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 238000001640 fractional crystallisation Methods 0.000 description 1
- 239000012362 glacial acetic acid Substances 0.000 description 1
- OCDGBSUVYYVKQZ-UHFFFAOYSA-N gramine Chemical compound C1=CC=C2C(CN(C)C)=CNC2=C1 OCDGBSUVYYVKQZ-UHFFFAOYSA-N 0.000 description 1
- GOERTRUXQHDLHC-UHFFFAOYSA-N gramine Natural products COC1=CC=C2NC=C(CN(C)C)C2=C1 GOERTRUXQHDLHC-UHFFFAOYSA-N 0.000 description 1
- 150000007857 hydrazones Chemical class 0.000 description 1
- 229910000042 hydrogen bromide Inorganic materials 0.000 description 1
- FUKUFMFMCZIRNT-UHFFFAOYSA-N hydron;methanol;chloride Chemical compound Cl.OC FUKUFMFMCZIRNT-UHFFFAOYSA-N 0.000 description 1
- TUJKJAMUKRIRHC-UHFFFAOYSA-N hydroxyl Chemical compound [OH] TUJKJAMUKRIRHC-UHFFFAOYSA-N 0.000 description 1
- 230000001631 hypertensive effect Effects 0.000 description 1
- 208000021822 hypotensive Diseases 0.000 description 1
- 230000001077 hypotensive effect Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 229910001867 inorganic solvent Inorganic materials 0.000 description 1
- 239000003049 inorganic solvent Substances 0.000 description 1
- HVTICUPFWKNHNG-UHFFFAOYSA-N iodoethane Chemical compound CCI HVTICUPFWKNHNG-UHFFFAOYSA-N 0.000 description 1
- 230000002475 laxative effect Effects 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 150000002688 maleic acid derivatives Chemical class 0.000 description 1
- PNCJBJQLNOUGJI-UHFFFAOYSA-N methyl 2-(benzylamino)benzoate Chemical compound COC(=O)C1=CC=CC=C1NCC1=CC=CC=C1 PNCJBJQLNOUGJI-UHFFFAOYSA-N 0.000 description 1
- PEFDATUXUCRRKT-UHFFFAOYSA-N methyl 2-(butylamino)benzoate Chemical compound CCCCNC1=CC=CC=C1C(=O)OC PEFDATUXUCRRKT-UHFFFAOYSA-N 0.000 description 1
- UPVUQELOASQBMY-UHFFFAOYSA-N methyl 2-amino-3,4,5-trimethoxybenzoate Chemical compound COC(=O)C1=CC(OC)=C(OC)C(OC)=C1N UPVUQELOASQBMY-UHFFFAOYSA-N 0.000 description 1
- VGRACNKLIBCDHG-UHFFFAOYSA-N methyl 2-hydroxy-6-nitrobenzoate Chemical compound COC(=O)C1=C(O)C=CC=C1[N+]([O-])=O VGRACNKLIBCDHG-UHFFFAOYSA-N 0.000 description 1
- DXWUYJUHIZEMFP-UHFFFAOYSA-N methyl 6-amino-1,3-benzodioxole-5-carboxylate Chemical compound C1=C(N)C(C(=O)OC)=CC2=C1OCO2 DXWUYJUHIZEMFP-UHFFFAOYSA-N 0.000 description 1
- 230000011987 methylation Effects 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 239000012044 organic layer Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- BHAAPTBBJKJZER-UHFFFAOYSA-N p-anisidine Chemical compound COC1=CC=C(N)C=C1 BHAAPTBBJKJZER-UHFFFAOYSA-N 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 230000003285 pharmacodynamic effect Effects 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- FRPUEBLBJZHNFU-UHFFFAOYSA-N propyl 2-(methylamino)benzoate Chemical compound CCCOC(=O)C1=CC=CC=C1NC FRPUEBLBJZHNFU-UHFFFAOYSA-N 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 239000008213 purified water Substances 0.000 description 1
- OENLEHTYJXMVBG-UHFFFAOYSA-N pyridine;hydrate Chemical compound [OH-].C1=CC=[NH+]C=C1 OENLEHTYJXMVBG-UHFFFAOYSA-N 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000006476 reductive cyclization reaction Methods 0.000 description 1
- BJOIZNZVOZKDIG-MDEJGZGSSA-N reserpine Chemical compound O([C@H]1[C@@H]([C@H]([C@H]2C[C@@H]3C4=C([C]5C=CC(OC)=CC5=N4)CCN3C[C@H]2C1)C(=O)OC)OC)C(=O)C1=CC(OC)=C(OC)C(OC)=C1 BJOIZNZVOZKDIG-MDEJGZGSSA-N 0.000 description 1
- 229960003147 reserpine Drugs 0.000 description 1
- MDMGHDFNKNZPAU-UHFFFAOYSA-N roserpine Natural products C1C2CN3CCC(C4=CC=C(OC)C=C4N4)=C4C3CC2C(OC(C)=O)C(OC)C1OC(=O)C1=CC(OC)=C(OC)C(OC)=C1 MDMGHDFNKNZPAU-UHFFFAOYSA-N 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- HELHAJAZNSDZJO-OLXYHTOASA-L sodium L-tartrate Chemical compound [Na+].[Na+].[O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O HELHAJAZNSDZJO-OLXYHTOASA-L 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
- 239000004299 sodium benzoate Substances 0.000 description 1
- 235000010234 sodium benzoate Nutrition 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000001433 sodium tartrate Substances 0.000 description 1
- 229960002167 sodium tartrate Drugs 0.000 description 1
- 235000011004 sodium tartrates Nutrition 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 229940095064 tartrate Drugs 0.000 description 1
- 239000000196 tragacanth Substances 0.000 description 1
- 235000010487 tragacanth Nutrition 0.000 description 1
- 229940116362 tragacanth Drugs 0.000 description 1
- 230000002792 vascular Effects 0.000 description 1
- 239000008215 water for injection Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains three hetero rings
- C07D471/14—Ortho-condensed systems
Definitions
- This invention relates to a medicinal composition having unusual pharmacodynamic properties and especially useful as an antihypertensive agent. relates to a novel method of producing antihypertensive activity in human beings.
- the novel medicinal composition of this invention has outstanding activity as an antihypertensive agent with remarkably few side effects. Specifically, this composition lowers arterial blood pressure and slows the pulse rate. It is particularly useful in mild to moderate cases of essential hypertension and alone, or in combination with other agents, in the treatment of more severe hypertensive vascular conditions. Side effects, such as diarrhea, severe laxative action or general depression are often seen with like-acting medicinal agents. For instance the use of reserpine has been limited by the severe depression often encountered with relatively high dosage regimens. Such limiting side effects are much less pronounced with the composition of this invention.
- the medicinal composition of this invention comprises a pharmaceutical carrier and a medic ament which is a member of a series of compounds represented by the following general structural formula:
- R represents alkyl having from 1 to 18 carbon atoms; aralkyl, preferably phenylalkyl, having 1 to 6 carbon atoms in the alkyl portion; or -CH -alkenyl, the alkenyl portion having 2 to 17 carbon atoms;
- R represents hydrogen, lower alkoxyl, lower alkyl, CH -alkenyl, the alkenyl portion having 2 to carbon atoms, halo, hydroxyl and trifluoromethyl;
- R and R when individualradicals represent .hydrogen, lower alkoxyl, lower alkyl, CH -alkenyl, the alkenyl portion having 2 to 5 carbon atoms, hydroxyl, halo and trifluoromethyl and when taken together in adjacent positions, represent methylenedioxy;
- R represents hydrogen, lower alkoxyl, lower alkyl
- This invention also.
- R and R when individual radicals represent hydrogen, lower alkoxy, lower alkyl, -CH -alkenyl, the alkenyl portion having 2 to 5 carbon atoms, hydroxyl, halo, carbomethoxy and trifluoromethyl and when taken together in adjacent positions, represent methylenedioxy;
- R represents hydrogen, lower alkoxyl, lower alkyl and halo.
- lower alkyl or lower alkoxyl as used herein and in the claims, branched or straight aliphatic groups having not more than 6 carbon atoms and preferably not more than 4 carbon atoms are indicated.
- hydroxyl is intended to include moieties hydrolyzable thereto, for example, acyloxy having 2 to 6 carbon atoms.
- Preferred compounds in the composition of this invention are compounds of the above structural formula where R and R are members selected from the group consisting of hydrogen, lower alkoxyl and lower alkyl; R R R R and R are hydrogen; and R is lower alkyl.
- Exemplary of a particularly useful compound for inclusion in the composition ,of this invention is l0-methoxy- 14-methyl-5 -oxo-5 ,7 8,14-tetrahydroindolo[2,3-c] quinazo+ [3,2-alpyridine.
- non-toxic organic and inorganic acid addition salts and quaternary ammonium salts can be used.
- Exemplary of non-toxic acid addition salts are those formed with maleic, fumaric, benzoic, ascorbic, pamoic, succinic, bismethylenesalicylic, methylsulfonic, ethanedisulfonic, acetic, propionic, tartaric, salicylic, citric, gluconic, lactic, malic, mandelic, cinnamic, citraconic, stearic, palmitic, itaconic, glycolic, benzenesulfonic, hydrochloric, hydrobromic, sulfuric, sulfamic, phosphoric and nitric acids.
- These salts are prepared by several methods but preferably by heating a suspension of the base in a large volume of methyl or ethyl alcohol with one equivalent of acid. The volume is reduced and the solution cooled to separate the crystalline salt. Often an excess of acid is used with equally satisfactory results.
- salts can be prepared by double decomposition of suitable compounds.
- acetates of the polycyclic bases dissolved in water will react with aqueous solutions of sodium bromide or sodium tartrate to form the slightly soluble hypotensive bromide or tartrate salts which will separate from the reaction mixture directly.
- the quaternary salts are prepared by heating a suspension of the base in a suitable solvent, such as benzene or ethyl alcohol, with a reactive alkyl halide such as methyl iodide, ethyl bromide, n-hexyl bromide, benzyl chloride or another reactive ester such as methyl sulfate, ethyl sulfate or methyl p-toluene sulfonate.
- a suitable solvent such as benzene or ethyl alcohol
- a reactive alkyl halide such as methyl iodide, ethyl bromide, n-hexyl bromide, benzyl chloride or another reactive ester such as methyl sulfate, ethyl sulfate or methyl p-toluene sulfonate.
- the polycyclic compounds of this invention may exist as hydrates which contain variable amounts: of water.
- the tendency to form hydrates is particularly noticeable with solutions of the free base forms of the compounds of this invention. It is intended to include in the specifi cation and claims the hydrates as well as the non-hydrates of the free bases and the acid addition and quaternary ammonium salts of the free bases.
- the l oxo 1,2,3,4-tetrahydropyrid[3,4-blindoles are condensed with the N-alkyl or N-aralkyl anthranilic acid or ester preferably in approximately equimolar amounts.
- the amounts of reactants may be varied widely, however, with appreciable yields of polycyclic compounds resulting.
- the condensation is carried out by heating the reactants in the presence of phosphorus oxychloride as a condensing agent.
- the reaction may be carried out with widely varying amounts of condensing agent, such as with an excess of phosphorus oxychloride, which then serves as reaction medium as well, or with as little as 0.6 mole of phosphorus oxychloride in a suitable substantially inert solvent.
- a solvent in which at least one of the reactants is partially soluble such as an inert organic solvent, for example, benzene, toluene, xylene, chlorobenzene, chloroform, carbon tetrachloride, ethyl acetate, dioxane, dibutyl ether or cyclohexane.
- an inert organic solvent for example, benzene, toluene, xylene, chlorobenzene, chloroform, carbon tetrachloride, ethyl acetate, dioxane, dibutyl ether or cyclohexane.
- inorganic solvents which do not alter the-course of the condensation may be used, for instance, phosphorus trichloride or thionyl chloride.
- the preferred solvents are the aromatic solvents, such as toluene, xylene or benzene.
- the solvent will not contain any substance that will react with the POCl for example, a compound containing hydroxyl or amino groups, and, in any event, the amount of such substances, if present, should be insuflicient to cause substantial depletion of the POCl
- the reaction temperature is preferably maintained between about 30 C. and about 200 C. The rate of the reaction varies directly With the temperature. Advantageously temperatures of about 140 C. are used; It is convenient to run the reaction at the boiling point of the reaction medium; preferably, for instance, in boiling benzene, toluene or xylene.
- reaction time varies with the amount of condensing agent, solubility of the reagents and the reaction temperature. In the preferred range of temperature, from fifteen minutes to five hours is usually sufficient to complete the reaction. Preferably a period of from one to three hours is used.
- the 1-oxo-l,2,3,4-tetrahydropyrid[3,4-b]indoles may 'ylaminomethylindole 2 be prepared conveniently by the method which is outlined below:
- the ring C substituted pyrid[3,4-blindoles are advantageously prepared, for example, by alkylating 3-dimethcarboxylate, prepared by the method of Brehm and Lindwall, J. Org. Chem., 15, 685 (1950), with l-nitropropane under alkaline conditions in a typical gramine condensation.
- the resulting ethyl 3- (Z-nitrobutyl)-inclole-2-carboxylate is cyclized under reductive conditions with stannous chloride to give the desired starting material, 3-ethyl-l-oxo-l,2,3,4-tetrahydropyrid 3,4-b] indole.
- the substituted N-alkyl or aralkyl anthranilic acid derivatives are prepared by several methods which are in the literature. Many of the substituted anthranilic acids are specifically known. Simple esterification in an excess of an alcohol with gaseous hydrogen chloride followed by N-alkylation by an alkyl halide or alkyl sulfate or by N-aralkylation by an aralkyl halide or aralkyl' sulfate has proved satisfactory.
- the compounds in which. one or more of the substituents R through R are hydroxyls are prepared by first forming, by the above described method, the compound corresponding to the desired hydroxyl substituted compound but having an alkoxy radical, for example methoxy, in each position where a hydroxyl is desired.
- the alkoxy substituted compound is then hydrolysed to form the desired compound with hydroxyl radicals replacing the alkoxy radicals.
- the hydrolysing may be accomplished by refluxing with an aluminum halide, for example aluminum chloride in an inert solvent, for example, benzene or by heating under reflux with a concentrated hydrohalic acid, for example, hydrobromic acid.
- the hydroxy substituted compounds can readily be formed by first forming the corresponding acyloxy, for example, acetoxy, substituted compound and hydrolysing the acyloxy radical to a hydroxyl radical by heating under reflux in the presence of dilute hydrochloric acid.
- the acyloxy compound is formed by condensing a l-oxo-l,2,3,4-tetrahydropyrid[3,4-blindole with an N-alkyl or N-aralkylanthranilic acid or ester with either or both of the indole and the anthranilic acid or ester substituted with acyloxy radicals in the positions where hydroxyl radicals are desired.
- EXAMPLE I A solution of 20 g. of 3-carbethoxy-2-piperidone in 220 ml. of 5% potassium hydroxide solution is allowed to stand at room temperature for twenty-four hours. After neutralizing with glacial acetic acid and adding 46 g. of potassim acetate, the cooled solution is stirred while a previously prepared solution of the diazonium salt prepared using 14.4 g. of p-anisidine is added at C.
- the coupled diazo compound is separated by filtration and washed with isopropanol.
- a mixture of 9 g. of the coupled product in 80 ml. of 70% formic acid solution is heated at reflux for two hours and quenched with water.
- the resulting solid is recrystallized from ethanol to a pure sample of 6-methoxy-1-oxo-1,2,3,4-tetrahydropyrid[3,4-blindole, M. P. 276-278 C.
- a suspension of 1.2 g. of 6-methoxy-1-oxo-1,2,3,4- tetrahydropyrid[3,4-blindole in 20 g. of phosphorus trichloride with 0.6 g. of phosphorus oxychloride is heated at reflux for twenty minutes.
- the reflux period is interrupted while 1.8 g. of methyl N-methylanthranilate is added.
- the reflux period is continued for two hours.
- the volatiles are taken olf in vacuo.
- the residue is carefully diluted with ice water.
- the mixture is extracted by shaking with chloroform and ammonia water.
- the chloroform extracts are concentrated, diluted with benzene, filtered and reconcentrated to separate red needles of 10-methoxy-14-methyl-5-oxo-5,7,8,l4-tetrahydroindolo[2,3-c]quinazo[3,2-a]pyridine, M. P. 200 C (decomposes gradually).
- a suspension of 60 g. of the red free base (prepared as above) in 2 l. of ethanol is prepared and mixed with a solution of 40 g. of tartaric acid in 1 l. of ethanol.
- the mixture is heated to boiling, diluted with l l. of hot distilled water.
- the clear solution is then cooled to C. with stirring. After one hour at this temperature a large crop of bright yellow tartrate salt was obtained as a hydrate, M. P. 220-221 C. (dec.).
- citric, maleic, nitric, phosphorus, glycolic', ethanedisulfonic and perchloric salts of the above formed base are each prepared by dissolving equivalent amounts of the red base and the appropriate acid in minimum quantities of acetone. The salt separates almost immediately.
- a suspension of 9.8 g. of finely-divided 6-chloro-l-oxo- 1,2,3,4-tetrahydropyrid[3,4-blindole in 200 ml. of xylene with 4 g. of phosphorus oxychloride is heated at reflux for fifteen minutes.
- a 15 g. portion of methyl N-methylanthranilate is added to the reaction mixture and the reflux period is extended for two hours with stirring.
- the solvent is removed in vacuo.
- the residue is carefully diluted with water, washed with ammonia water and extracted into chloroform.
- the dried organic extracts are concentrated, diluted with benzene and saturated with dry hydrogen chloride gas.
- the purified hydrochloride is shaken with chloroformammonia water.
- the chloroform layer is dried, concentrated and diluted with benzene to yield orange-red needles of free base, M. P. 210 C. (decomposes gradually).
- the base is then regenerated by the use of ammonia water-chloroform to yield deep red needles of 10,14 dimethyl 5 oxo 5,7,8,l4 tetrahydroindolo [2,3-c]quinazo[3,2-a]pyridine, M. P. 223-225 C. (dec.).
- . '7 prepared by adding ether to an acetic acid solution is dissolved in .water.
- a solution of 1.7 g. of sodium benzoate in '20 ml. of water is added dropwise to the swirled acetate to separate the desired 10,14-dimethyloxo 5,7,8,14 tetrahydroindolo[2,3 c]quinazo[3,2- alpyridine benzoate.
- EXAMPLE VI A suspension of 5.0 g. of 1-oxo-1,2,3,4-tetrahydropyrid[3,4-blindole, prepared using aniline in the coupling procedure of Example I and using polyphosphoric acid as the medium for the rearrangement, in 120 ml. of dry toluene with 3 g. of freshly distilled phosphorus oxychloride is heated at reflux for fifteen minutes. After the addition of 7.5 g. of methyl N-methylanthranilate, the reflux period is extended for three hours.
- the free base is recovered from the hydrochloride salt by shaking 3 g. of the salt in a mixture of ammonia water and chloroform.
- the dry chloroform extract is concentrated and diluted with benzene-cyclohexane to precipitate orange needles of the free base, M. P. about 198 C.
- EXAMPLE VII A suspension of 5 .0 g. of finely powdered 1-oxo-1,2,3,4- tetrahydropyrid[3,4-b1indole in 50 g. of freshly distilled phosphorus trichloride with 2 g. of phosphorus oxychloride is heated at reflux briefly with stirring. After the addition of 7.5 g. of methyl N-butylanthranilatc, prepared by monobutylation of anthranilic acid with nbutylbromide by the method of Gilman et al. E]. Am. Chem.
- EXAMPLE VIII A suspension of 4 g. of 7,8-dimethyl-l-oxo-1,2,3,4- tetrahydropyrid[3,4-blindole, M. P. 236-238 C., prepared by using 2,3-dimethylaniline hydrochloride in the coupling synthesis described in Example I, in 50 ml. of chlorobenzene with 2 g. of phosphorus oxychloride is heated at reflux for ten minutes. After the addition of 6 g. of methyl N-methylanthranilate and ml. of chloro- 8 benzene, the reaction mixture is heated at reflux for one hour.
- EXAMPLE X A suspension of 3.0 g. of 5-chloro-8-methoxy-1-oxo- 1,2,3,4-tetrahydropyrid[3,4-blindole, M. P., 214-215" 0., prepared by using 5-chloro-anisidine as starting material in the coupling synthesis described in Example I, in 40 g. of phosphorus trichloride witht 2.5 g. of phosphorus oxychloride is heated at reflux with stirring for twenty minutes. After addition of 4.5 g. of methyl N-methylanthranilate, the reaction mixture is heated at reflux for two hours. The solvent is evaporated and the residue quenched in ice water.
- the base is characterized by dissolving 3.3 g. of the red base in 75 ml. of ethanol along with 1.5 g. of salicylic acid in 50 ml. of ethanol.
- the solution is filtered hot and concentrated to a low volume. Cooling, following addition of petroleum ether, separates a yellow salt, 11- methoxy 14 methyl-5-oxo-5,7,8,l4-tetrahydroindolo- [2,3-a] pyridine salicylate.
- the dried chloroform extracts are concentrated and replaced with dry benzene.
- Gaseous hydrogen chloride separates the impure hydrochloride which is washed thoroughly with benzene and then converted to the orange base by shaking with sodium bicarbonate solution into benzene.
- The. colored base is characterized by forming the maleate salt by reacting 4.2 g. of the base with 1.2 g. of maleic acid in ethanol.
- EXAMPLE XIII A 15 g. sample of 3-carbethoxy-2-piperidone is hydrolyzedovernight by standing in a dilute potassium hydroxide solution containing 1.5 base equivalents. The hydrolysate is cooled, buffered and treated with a cold diazonium salt solution prepared from 18.4 g. of p-iodoaniline. After stirring at room temperature fortwo hours, the coupled hydrazone is separated by filtration and dried in vacuo. This material is then heated at reflux in 500 g. of 70% formic acid for one hour. After filtration, a
- a suspension of 3.0 g. of 6-iodo-l-oxo-l,2,3,4-tetrahydropyrid[3,4-b]indole in 100 ml. of toluene with 2.5 of phosphorus oxychloride is heated at reflux briefly, then 4.5 g. of methyl N-methylanthranilate is added and the reflux period continued for one hour.
- the volatiles are removed in vacuo.
- the residue is quenched in ice water.
- the aqueous mixture is then neutralized with ammonia water and extracted with chloroform which is dried and replaced with benzene. Gaseous hydrogen chloride is passed into the benzene solution to separate a yellow crystalline hydrochloride.
- the orange base is isolated following the procedure outlined in Example II, l4-ethyl-2-isopropyl-5- oxo 5,7,8,14 tetrahydroindo1o[2,3 cl quinazoi 3,2 a]- pyridine.
- This base is characterized by dissolving 3.6 g. in 75 ml. of ethanol. An excess of ethanolic hydrogen bromide is added to the base solution. The solution is filtered hot and allowed to concentrate on the steam bath. Cooling separates yellow crystals of 14-ethyl-5-oxo-2- isopropyl 5,7,8,14 tetrahydroindolo[2,3-c] quinazo- [3,2-alpyridine hydrobromide.
- EXAMPLE XV A suspension of 2.7 g. of a mixture of 5(7)-bromo-1- 0X0 1,2,3,4 tetrahydr0pyrid[3,4 blindole, prepared by using m-bromoaniline in the coupling synthesis,as described in Example XIII, in 50 m1. of toluene with 1 g. of phosphorus oxychloride is heated at reflux for ten minutes at which time 2.0 g. of methyl N-methylanthranilate is added.
- condensation product is isolated following the procedure in Example II, to give the crystalline base 10 hexoxy l4 methyl 5 ox-o 5,7,8,14 tetrahydroindolo [2,3-clquinazo [3 ,2-a] pyridine.
- Example II The solution is treated as in Example II, however, the final chloroform extract is concentrated to a low volume and triturated with aqueous ethanol to separate 3-ch1orol4 methyl 5 oxo 5,7,8,14 tetrahydroindolo [2,3-clquinazo[3,4-b]pyridine hydrate. Yellow plates of the hydrate are obtained by recrystallization from a large volume of aqueous ethanol, M. P. 186-188 C. (dec.).
- the chloroform solution is dried, diluted with benzene and evaporated to give a red. crystalline solid which is redissolved in chloroform and acidified with. hydrogen 1 1 chloride gas to give the hydrochloride salt.
- the red base is again regenerated as before, M. P. 270-275 C. (dec.), 14 methyl 2,3 methylenedioxy 0x0 5,7,8,14- tetrahydroindolo[2,3-clquinazo[3,2-alpyridine.
- a yellow solid hydrate separates from the ethereal layer and is filtered and recrystallized from hexane.
- the product consists of fine yellow prisms of the hydrate of 14-octadecyl-S-oxo 5,7,8,14 tetrahydroindolo[3,2-a]quinazo [2,3-'c]pyridine, M. P. 119 C.
- EXAMPLE XXII Ethyl 3-dimethylaminomethylindole-2-carboxylate is alkylated with l-nitropropane in the presence of sodium hydroxide to yield ethyl 3-(2-nitrobuty1)-indole-2-carboxylate, M. P. 154155 C. A reductive cyclization of this substituted indole by stannous chloride gives 3- ethyl-l-oxo-l,2,3,4-tetrahydropyrid[3,4-b]indole, M. P. 188l89 C.
- EXAMPLE XXIII EXAMPLE XXIV
- a suspension of 5.0 g. of l-oxo-l,2,3,4-tetrahydropyrid[3, 4-b]indole, 5.0 g. of phosphorus oxychloride, 7.25 g. of methyl N-benzyl-anthranilate, in 110 ml. of dry toluene is heated at reflux for three and one-half hours. After working up the reaction mixture essentially as in Example XIX, orange crystals are recovered, 14-benzyl-5-oxo-5,7,8, l4-tetrahydroind-olo [2,3 -c] quinazo- [3,2-a1pyridine.
- EXAMPLEXXV A suspension of 5.0 g. of 1-oxo-l,2,3,4-tetrahydropyrid[3,4-b]indole, 5.0 g. of phosphorus oxychloride, 10.2 g. of methyl N-(6-phenylhexy1)anthranilate, pre- 1'2 pared by the alkylation of methyl anthranilate with 6- phenyl-n-hexyl bromide and sodium acetate, in ml. of dry toluene is heated at reflux with stirring for three hours.
- Example XXI The mixture, after working up essentially as in Example XXI, gives yellow crystals of the hydrate of 5-oxo-14-(6"- phenylhexyl 5,7,8,14 tetrahydroindolo[3,2-a1quinazo [2,3-c] pyridine.
- methyl-10,1 l-methyleuedioxy-S-oxo-S ,7,-8, l4 tetrahydr0- indo1o[2,3-c]quinazo[3,2-a]pyridine is obtained first as the hydrochloride, and then as the red base.
- Example XII The mixture is worked up as in Example XII to give the desired base, 14-methyl-5-oxo-5,7,8,14-tetrahydro 1l-trifluoro-methylindolo[2,3-0]quinazo[3,2-a]pyridine.
- EXAMPLE XXXIII A suspension of 1.9 g. of 1-oxo-1,2,3,4-tetrahydropyrid- [3,4-blindole, 2.0 g. of phosphorus oxychloride and 2.0 g. of methyl N-allylanthranilate, prepared by alkylation of methylanthranilate with allyl chloride, in 75 ml. of dry toluene is heated at reflux with stirring for three hours. Following the isolation procedure of Example XXI, the desired base, 14-allyl 5 -oxo-5,7,8,l4-tetrahydroindolo- [3,2-alquinazo[2,3-c]pyridine, is recovered.
- EXAMPLE XXXV A suspension of 4.5 g. of 6-allyl-1-oxo-1,2,3,4-tetrahydro[3,4-b]indole, prepared by using p-allyl'aniline in the coupling procedure of Example I, 5.0 g. of phosphorus oxychloride and 3.5 g. of methyl N-methylanthranilate in 100 ml. of dry toluene is heated at reflux for two hours. After carrying the reaction through as in Example I, the base, 10-allyl-14-methyl-5-oxo-5,7,8,l4-tetrahydroindolo- [2,3-] quinazo[3,2-a]pyridine, is recovered.
- the pharmaceutical carrier may be a solid or a liquid.
- Exemplary solid carriers are cornstarch, lactose, talc,
- composition of this, invention may be in the form of a tablet or a hard gelatin capsule for oral use.
- the medicament may be in a suitable oily menstruum such as, for example, peanut or soybean oil and the admixture placed, if desired, in a soft gelatin capsule.
- a suitable oily menstruum such as, for example, peanut or soybean oil
- Water alone or in. admixture with other agents such as carboxymethylcellulose, polyoxyethylene monostearate, acacia, tragacanth or. methylcellulose is a satisfactory liquid carrier for oral use.
- thefollowing carriers are exemplary: saline water, aqueous propylene glycolor peanut oil.
- composition of this invention will preferably con tain from about 1 mg. to about 150 mg. and advantageously from about 10 mg. to about 75 mg. of "the medicament compound, preferably as the base.
- the carrier will preferably be present in an amount of from about 5 mg. to about 18 g. and advantageously in an amount of from about 25 mg. to about 5 g. Where. a solid carrier is employed, it will preferably be present in an amount of from about 5 mg. to about 750 mg. and advantageously in an amount of from about 25 mg. to about. 500 mg.
- Example A2 Composition: 1 1 Gm./capsule 10-hydroxy-14-methyl-5-oxo-5,7,8, 14 tetrahydroindolo- 2,3-c] quinazo 3,2-a] pyridine hydrobromide 0.010 Lactose 0.290
- Example A3 Composition Gm./ capsule IO-chloro-14-methyl-5-oxo 5,7,8,l4 tetrahyhydroindolo-[2,3-c] quinazo [3,2-a] pyridine Lactose Prcedure.--The ingredients are mixed and pulverized sufficiently to pass through 100 mesh sieve and then incorporated into size #2 hard gelatin capsules. 1
- Example A4 Composition: Gm./capsule Isoamyl bromide quaternary salt of Z-methoxy-l4-methyl-5-oxo-5,7,8,14 tetrahydroindolo[2,3-c]quinazo[3,2-alpyridine 0.100 Starch 0.150
- Example A5 Composition: Gm./capsule 10,14-dimethyl-5 oxo- 5 ,7,8,14 tetrahydroindolo[2,3-clquinazo-[3,2,-a] pyridine 0.050 Calcium carbonate 0.150
- Example A6 Composition: Gm./capsule 10,l4-dirnethyl-2-methoxy-S-oxo-5,7,8,l4-tet rahydroindolo-[2,3-clquinazo [3,2-a] pyridine Mannitol Pr0cedure.-The ingredients are mixed and pulverized sufliciently to pass through 100 mesh sieve and then incorporated intohard gelatin capsules.
- Example A7 0.025 gram of 14 methyl 5 oxo 5,7,8,14 tetrahydroindolo[2,3-c] quinazo[3,2-a]pyridine hydrochloride is mixed with soybean oil to produce a flowable mass. 7 The thus produced compositionis then encapsulated in a soft gelatin capsule.
- Example A8 0.015 gram of 14 butyl 5 oxo 5,7,8,14'- tetrahydroindolo[2,3-clquinazo[3,2-alpyridine hydrate is mixed with soybean oil to produce a flowable mass.
- the thus produced composition is then encapsulated in a soft gelatin capsule.
- Example A9 0.030 gram of 5-oxo-5,7,8,14-tetrahydro-l1,12,14-trimethylindolo [2,3-c] quinazo 3 ,2-a] pyridine acetate are encapsulated in a soft gelatin capsule following the procedure of Example A8.
- Example A10 I 0.030 gram of 14-methyl-5 -oxo-l2-propyl-5 ,7 ,8, 14- tetrahydroindolo [2,3-c] quinazo [3 ,2-a] pyridine are encapsulated in a soft gelatin capsule following the procedure of Example A8.
- Example A11 0.050 gram of 9-chloro-12-methoxy-14-methyl-5-oxo- 5 ,7,8, 14 tetrahydroindolo [2,3-c] -quinazo 3 ,2-a] pyridine are mixed with peanut oil to produce a flowable mass which is then encapsulated in a soft gelatin capsule.
- Example A13 0.025 gram of 10-isobutoxy-l4-butyl-5-oxo-5,7,8,l1- tetrahydroindolo [2,3-c] quinazo[3,2-a]pyridine are mixed with peanut oil to produce a flowable mass which is then encapsulated in a soft gelatin capsule.
- Example A14 Composition: Gm./tablet 10 iodo 14 methyl 5 oxo 5,7,8,14-
- Pr0cedure The above ingredients were thoroughly mixed, granulated using a 10% gelatin solution and compressed into tablets using an admixture of 7% starch and 1% magnesium stearate based on tablet weight.
- Example A15 Composition: Gm./tablet 14 ethyl 2 isopropyl 5 oxo 5,7,8,11-
- Pr0cedure The above ingredients were thoroughly mixed, granulated using a 10% gelatin solution and compressed into tablets using talc as a lubricant.
- Example A16 Composition: Gm./tablet 5(7) bromo 14 methyl 1 oxo 5,7,8,11-
- Pr0cedure The above ingredients were thoroughly mixed, granulated using a 10% gelatin solution and compressed into tablets using talc-stearic acid as a lubricant.
- Example A17 Composition: Gm./tablet l0 fluoro 2 methoxy 14 methyl 1- 0x0 5,7,8,11 tetrahydroindolo [2,3 c] quinazo[3,2-a]pyridine 0.025 Lactose 0.275
- Pr0cedure The above ingredients were thoroughly mixed, granulated using a 50% sucrose solution and compressed into tablets using an admixture of 7% starch and 1% magnesium stearate based on tablet Weight.
- Example A18 Composition: Gm./tablet 10 hexoxy 14 methyl 5 oxo 5,7,8,14-
- Example A 19 1 7 I Example A20 Composition: Gm./ tablet 3 chloro- 14 methyl 1 oxo 5,7,8,14- tetrahydroindolo [2,3 c] quinazo[3,4 b]
- Prcedare The above ingredients were thoroughly mixed, granulated using a 50% sucrose solution and compressed into tablets using talc as a lubricant.
- Example A21 Composition Percent w./v.
- the above ingredients are mixed to make a solution and filtered.
- the filtrate is autoclaved at 120 C. at 18 pounds pressure for 25 minutes.
- the thus treated composition is suitable for injection.
- Purified water in an amount to bring the total volume to 5 cc.
- the 10 methoxy 14 methyl 5 oxo 5,7,8,l4- tetrahydroindolo[2,3-c]quinazo[3,2-a] pyridine is reduced to a fine powder so that all will pass a 325 mesh sieve. The remaining ingredients are mixed to make the vehicle.
- the 1 0 methoxy 14 methyl 5 oxo 5,7,8,14- tetrahydroindolo [2,3 c]quinazo[3,2 a]pyridine is incorporated in the thus formed vehicle and homogenized.
- Example A23 Composition: Gm./capsule 14 methyl 2,3 methylenedioxy 5 oxo- 5,7,8,14 tetrahydroindolo [2,3 c]quinazo[3,2-a]pyridine 0.010 Lactose 0.290
- Pr0cedare The ingredients are mixed and pulverized sufiiciently to pass through 100 mesh sieve and then incorporated into size #2 hard gelatin capsules.
- Example A26 Composition Gm./ capsule 7 ethyl 14 methyl 5 oxo 5,7,8,14- tetrahydroindolo[2,3 clquinazo [3,2 a]
- Example A27 Composition: Gin/capsule 2 carbomethoxy 14 ethyl 5 oxo- 5,7,8,14 tetrahydroindolo [2,3 clquinazo[3,2-a]pyridine 0.050
- Example A28 Composition: Gm./ capsule l4 benzyl-S-oxo 5,7,8,14 tetrahydroindolo [2,3-clquinazo[3,2-al-pyridine 0.001
- Example A29 Composition: Gm./ tablet 5 oxo-14 (6-phenylhexyl) 5,7,8,14-tetrahydroindolo[3,2 alquinazo [2,3 r clpyridine 0.050 Lactose 0.250
- Example A30 Composition: Gm./ tablet l4-methyl 5 oxo 5,7,8,l4-tetrahydro-l,2,3-
- Example A31 Composition: Gm./ tablet 5-oxo 5,7,8,14 tetrahydro 9,10,12,14-tetramethylindolo[2,3 cl quinazo[3,2-a]pyridine 0.075 Lactose 0.125 Starch 0.045
- Procedare The above ingredients were thoroughly gelatin solution and compressed into tablets using talc-stearic acid as a lubricant.
- Example A32 Composition: Gm./tablet 14 methyl 10,11 methylenedioxy 5 oxo- 5,7,8,14 tetrahydroindolo [2,3 clquinaZo[3,2-a] pyridine 0.025 Lactose 0.275
- Pr0cedare The above ingredients were thoroughly mixed, granulated using a 50% sucrose solution and com pressed into tablets using an admixture of 7% starch and 1% magnesium stearate based on tablet weight.
- Example A33 Composition: Gm./ tablet 14 methyl 5 oxo 5,7,8,14 tetrahydro-l 1- triflu0romethylindolo[2,3 c] quinazo [3,2-a] pyridine 0.100 Lactose 0.100 Starch 0.045
- Prcedure The above ingredients were thoroughly mixed, granulated using a 10% gelatin solution and compressed into tablets using an admixture of 1% magnesium stearate based on tablet weight.
- Example A35 Composition: Gm./ tablet 4 bromo 14 methyl oXo 5,7,8,14-tetrahydro 2 trifluoromethylindolo[2,3-c]
- Pr0cedare The above ingredients were thoroughly mixed, granulated using a 50% sucrose solution and compressed into tablets using talc as a lubricant.
- Example A36 Composition: Gm./capsule 3 isoamoxy -'14 methyl 5 oxo 5,7,8,14-
- Example A37 Composition: Gm./ capsule 14 allyl 5 -'oxo 5,7,8,14 tetrahydroindolo [3,2a] quinazo-[2,3-c]pyridine 0.010
- Example A38 Composition Gm. capsule 14-o1eyl 5 oxo 5,7,8,14 tetrahydroindolo [3,2-a]quinazo[2,3-c]pyridine hydrate 0.010
- the ingredients are mixed and pulverized sufliciently to pass through 100 mesh sieve and then incorporated into size- #Z'hard gelatin capsules.
- Example A39 Composition: Gm./ capsule allyl-14-methyl-5-oxo-5,7,8,14-tetrahydroindolo[2,3-c]quinabo[3,2-a]pyridine 0.050
- Example A40 Procedare The ingredients are mixed and pulverized sufiiciently to pass through 100 mesh sieve and then incorporated into hard gelatin capsules.
- Example A41 Composition: Gm./ capsule 10 hydroxy-14-methyl-5-oxo-5,7,8,14 tetrahydroindolo [2,3 c] quinazo 3 ,2-a] pyridine hydrobromide 0.050 Calcium carbonate 0.150
- Example A42 Composition: Gm./ capsule 2 hydroxy-14-methyl-5-oxo-5,7,8,14-tetrahydroindolo [2,3 -c] quinazo 3,2-a] pyridine hydrobromide -2 0.001 Mannitol 0.299
- Example A43 Composition: Gm./tablet 10 acetoxy 14 methyl-5-oxo-5,7,8,14-tetrahydroindolo [2,3 c] quinazo [3 ,2-a] pyridine hydrobromide 0.05 0 Lactose 0.250
- the method in accordance with this invention comprises administering internally the above described medicinal composition to a human being to produce antihypertensive activity. Oral administration is preferred.
- An. antihypertensive medicinal composition comprising a pharmaceutical carrier and a compound of the class consisting of a free base and its acid addition, methyl iodide, ethyl bromide, n-hexyl bromide, benzyl chloride, methyl sulfate, ethyl sulfate and methyl p-toluene sulfonate, salts, the free base having the formula:
- composition of claim 1 characterized in that R and R are members selected from the group consisting of hydrogen, lower alkoxy and lower alkyl; R R R R and R are hydrogen and R is lower alkyl.
- composition of claim 1 characterized in that the carrier is a solid.
- composition of claim 1 characterized in that the carried is a liquid.
- composition of claim 1 characterized in that the composition is in the form of a tablet.
- composition of claim 1 characterized in that the composition is in the form of a capsule.
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Description
United States Patent INDOLO [2,3-c] QUINAZU [3,2-11] PYRIDINE DERIVATIVES No Drawing. Application October 18, 1956 Serial No. 616,632
6 Claims. (Cl. 167-65) This invention relates to a medicinal composition having unusual pharmacodynamic properties and especially useful as an antihypertensive agent. relates to a novel method of producing antihypertensive activity in human beings.
The novel medicinal composition of this invention has outstanding activity as an antihypertensive agent with remarkably few side effects. Specifically, this composition lowers arterial blood pressure and slows the pulse rate. It is particularly useful in mild to moderate cases of essential hypertension and alone, or in combination with other agents, in the treatment of more severe hypertensive vascular conditions. Side effects, such as diarrhea, severe laxative action or general depression are often seen with like-acting medicinal agents. For instance the use of reserpine has been limited by the severe depression often encountered with relatively high dosage regimens. Such limiting side effects are much less pronounced with the composition of this invention.
More specifically, the medicinal composition of this invention comprises a pharmaceutical carrier and a medic ament which is a member of a series of compounds represented by the following general structural formula:
wherein:
R represents alkyl having from 1 to 18 carbon atoms; aralkyl, preferably phenylalkyl, having 1 to 6 carbon atoms in the alkyl portion; or -CH -alkenyl, the alkenyl portion having 2 to 17 carbon atoms;
R represents hydrogen, lower alkoxyl, lower alkyl, CH -alkenyl, the alkenyl portion having 2 to carbon atoms, halo, hydroxyl and trifluoromethyl;
R and R when individualradicals represent .hydrogen, lower alkoxyl, lower alkyl, CH -alkenyl, the alkenyl portion having 2 to 5 carbon atoms, hydroxyl, halo and trifluoromethyl and when taken together in adjacent positions, represent methylenedioxy;
R represents hydrogen, lower alkoxyl, lower alkyl,
This invention also.
-CH -alkenyl, the alkenyl portion having 2 to 5 carbon atoms, hydroxyl, halo and trifluoromethyl;
R and R when individual radicals represent hydrogen, lower alkoxy, lower alkyl, -CH -alkenyl, the alkenyl portion having 2 to 5 carbon atoms, hydroxyl, halo, carbomethoxy and trifluoromethyl and when taken together in adjacent positions, represent methylenedioxy;
R represents hydrogen, lower alkoxyl, lower alkyl and halo.
By the terms lower alkyl or lower alkoxyl as used herein and in the claims, branched or straight aliphatic groups having not more than 6 carbon atoms and preferably not more than 4 carbon atoms are indicated. Similarly the term hydroxyl is intended to include moieties hydrolyzable thereto, for example, acyloxy having 2 to 6 carbon atoms.
Preferred compounds in the composition of this invention are compounds of the above structural formula where R and R are members selected from the group consisting of hydrogen, lower alkoxyl and lower alkyl; R R R R and R are hydrogen; and R is lower alkyl.
Where hereinafter the symbols R, R R R R R R and R are mentioned in the description, they will indicate the substituents indicated for them above as appropriate except where otherwise specified.
Exemplary of a particularly useful compound for inclusion in the composition ,of this invention is l0-methoxy- 14-methyl-5 -oxo-5 ,7 8,14-tetrahydroindolo[2,3-c] quinazo+ [3,2-alpyridine.
Equivalently, non-toxic organic and inorganic acid addition salts and quaternary ammonium salts can be used. Exemplary of non-toxic acid addition salts are those formed with maleic, fumaric, benzoic, ascorbic, pamoic, succinic, bismethylenesalicylic, methylsulfonic, ethanedisulfonic, acetic, propionic, tartaric, salicylic, citric, gluconic, lactic, malic, mandelic, cinnamic, citraconic, stearic, palmitic, itaconic, glycolic, benzenesulfonic, hydrochloric, hydrobromic, sulfuric, sulfamic, phosphoric and nitric acids. These salts are prepared by several methods but preferably by heating a suspension of the base in a large volume of methyl or ethyl alcohol with one equivalent of acid. The volume is reduced and the solution cooled to separate the crystalline salt. Often an excess of acid is used with equally satisfactory results.
Many of the salts can be prepared by double decomposition of suitable compounds. For instance the acetates of the polycyclic bases dissolved in water will react with aqueous solutions of sodium bromide or sodium tartrate to form the slightly soluble hypotensive bromide or tartrate salts which will separate from the reaction mixture directly.
The quaternary salts are prepared by heating a suspension of the base in a suitable solvent, such as benzene or ethyl alcohol, with a reactive alkyl halide such as methyl iodide, ethyl bromide, n-hexyl bromide, benzyl chloride or another reactive ester such as methyl sulfate, ethyl sulfate or methyl p-toluene sulfonate.
The polycyclic compounds of this invention may exist as hydrates which contain variable amounts: of water. The tendency to form hydrates is particularly noticeable with solutions of the free base forms of the compounds of this invention. It is intended to include in the specifi cation and claims the hydrates as well as the non-hydrates of the free bases and the acid addition and quaternary ammonium salts of the free bases.
These compounds, except where one or more hydroxyl groups are present, are conveniently prepared by condensing substituted l-oxo-l,2,3,4-tetrahydropyrid[3,4-b]- indoles with substituted N-alkyl or N-aralkylanthranilic acids or esters according to the following reaction:
CO R R1 5 2 8 6 NHR POOla 7 R; 8 R5 in which R is H or alkyl and preferably alkyl having 1 to 6 carbon atoms.
The l oxo 1,2,3,4-tetrahydropyrid[3,4-blindoles are condensed with the N-alkyl or N-aralkyl anthranilic acid or ester preferably in approximately equimolar amounts. The amounts of reactants may be varied widely, however, with appreciable yields of polycyclic compounds resulting.
The condensation is carried out by heating the reactants in the presence of phosphorus oxychloride as a condensing agent. The reaction may be carried out with widely varying amounts of condensing agent, such as with an excess of phosphorus oxychloride, which then serves as reaction medium as well, or with as little as 0.6 mole of phosphorus oxychloride in a suitable substantially inert solvent. Preferably from about 1 to 5 molar equivalents based on the l-oxo-l,2,3,4-tetrahydropyrid[3,4-b]- indole are used in a solvent in which at least one of the reactants is partially soluble, such as an inert organic solvent, for example, benzene, toluene, xylene, chlorobenzene, chloroform, carbon tetrachloride, ethyl acetate, dioxane, dibutyl ether or cyclohexane. Alternatively, inorganic solvents which do not alter the-course of the condensation may be used, for instance, phosphorus trichloride or thionyl chloride. The preferred solvents are the aromatic solvents, such as toluene, xylene or benzene.
Preferably the solvent will not contain any substance that will react with the POCl for example, a compound containing hydroxyl or amino groups, and, in any event, the amount of such substances, if present, should be insuflicient to cause substantial depletion of the POCl The reaction temperature is preferably maintained between about 30 C. and about 200 C. The rate of the reaction varies directly With the temperature. Advantageously temperatures of about 140 C. are used; It is convenient to run the reaction at the boiling point of the reaction medium; preferably, for instance, in boiling benzene, toluene or xylene.
It will be recognized that the length of reaction time varies with the amount of condensing agent, solubility of the reagents and the reaction temperature. In the preferred range of temperature, from fifteen minutes to five hours is usually sufficient to complete the reaction. Preferably a period of from one to three hours is used.
Many of the starting materials for this process are specifically known to the literature together with methods for their preparation. Where certain compounds desired for use as starting materials are not specifically described in the literature, they are prepared by like methods.
The 1-oxo-l,2,3,4-tetrahydropyrid[3,4-b]indoles may 'ylaminomethylindole 2 be prepared conveniently by the method which is outlined below:
M B2 O 0 Rs III N H it NH N R: ii H O 3-carboxypiperid-2-one is reacted with a suitably substituted benzenediazonium halide under Japp-Klingemann conditions to give a piperid2,3dione-3-R ,R ,R -phenylhydrazone which in turn is heated in formic acid or polyphosphoric acid solutions whereby an intramolecular rearrangement takes place to give the substituted l-oxol,2,3,4-tetrahydropyrid[3,4-b]indoles. Other methods of preparing these compounds are reported in the literature. However, this method is a simple preparation which has been found to be satisfactory on a broad scale.
The ring C substituted pyrid[3,4-blindoles are advantageously prepared, for example, by alkylating 3-dimethcarboxylate, prepared by the method of Brehm and Lindwall, J. Org. Chem., 15, 685 (1950), with l-nitropropane under alkaline conditions in a typical gramine condensation. The resulting ethyl 3- (Z-nitrobutyl)-inclole-2-carboxylate is cyclized under reductive conditions with stannous chloride to give the desired starting material, 3-ethyl-l-oxo-l,2,3,4-tetrahydropyrid 3,4-b] indole.
The substituted N-alkyl or aralkyl anthranilic acid derivatives are prepared by several methods which are in the literature. Many of the substituted anthranilic acids are specifically known. Simple esterification in an excess of an alcohol with gaseous hydrogen chloride followed by N-alkylation by an alkyl halide or alkyl sulfate or by N-aralkylation by an aralkyl halide or aralkyl' sulfate has proved satisfactory.
The compounds in which. one or more of the substituents R through R are hydroxyls are prepared by first forming, by the above described method, the compound corresponding to the desired hydroxyl substituted compound but having an alkoxy radical, for example methoxy, in each position where a hydroxyl is desired. The alkoxy substituted compound is then hydrolysed to form the desired compound with hydroxyl radicals replacing the alkoxy radicals. The hydrolysing may be accomplished by refluxing with an aluminum halide, for example aluminum chloride in an inert solvent, for example, benzene or by heating under reflux with a concentrated hydrohalic acid, for example, hydrobromic acid.
Alternatively the hydroxy substituted compounds can readily be formed by first forming the corresponding acyloxy, for example, acetoxy, substituted compound and hydrolysing the acyloxy radical to a hydroxyl radical by heating under reflux in the presence of dilute hydrochloric acid. The acyloxy compound is formed by condensing a l-oxo-l,2,3,4-tetrahydropyrid[3,4-blindole with an N-alkyl or N-aralkylanthranilic acid or ester with either or both of the indole and the anthranilic acid or ester substituted with acyloxy radicals in the positions where hydroxyl radicals are desired. The procedure outlined above for condensing substituted 1-oxo-l,2,3,4-tetrahydropyrid[3,4-b]indoles with substituted N alkyl or N-aralkylanthranilic acids or esters is followed here. This method is particularly advantageous where the desired compound contains both alkoxy and hydroxyl radicals since it permits the use of mild conditions to 5 hydrolyse the acyloxy radicals Without hydrolysing the alkoxy radicals.
Reference may be made to copending application Serial No. 616,631, filed October 18, 1956, which is directed to this process. The following examples will specifically illustrate compounds useful in the composition of this invention and the method of their preparation.
EXAMPLE I A solution of 20 g. of 3-carbethoxy-2-piperidone in 220 ml. of 5% potassium hydroxide solution is allowed to stand at room temperature for twenty-four hours. After neutralizing with glacial acetic acid and adding 46 g. of potassim acetate, the cooled solution is stirred while a previously prepared solution of the diazonium salt prepared using 14.4 g. of p-anisidine is added at C.
After stirring at room temperature, the coupled diazo compound is separated by filtration and washed with isopropanol. A mixture of 9 g. of the coupled product in 80 ml. of 70% formic acid solution is heated at reflux for two hours and quenched with water. The resulting solid is recrystallized from ethanol to a pure sample of 6-methoxy-1-oxo-1,2,3,4-tetrahydropyrid[3,4-blindole, M. P. 276-278 C.
A suspension of 1.2 g. of 6-methoxy-1-oxo-1,2,3,4- tetrahydropyrid[3,4-blindole in 20 g. of phosphorus trichloride with 0.6 g. of phosphorus oxychloride is heated at reflux for twenty minutes. The reflux period is interrupted while 1.8 g. of methyl N-methylanthranilate is added. The reflux period is continued for two hours. The volatiles are taken olf in vacuo. The residue is carefully diluted with ice water. The mixture is extracted by shaking with chloroform and ammonia water. Some unchanged pyrid[3,4-b]indole material is recovered. The chloroform extracts are concentrated, diluted with benzene, filtered and reconcentrated to separate red needles of 10-methoxy-14-methyl-5-oxo-5,7,8,l4-tetrahydroindolo[2,3-c]quinazo[3,2-a]pyridine, M. P. 200 C (decomposes gradually).
A solution of 5.0 g. or" the red free base (prepared as above) in 100 ml. of dry benzene is saturated with gaseous hydrogen chloride. The yellow microcrystalline solid which separates is recrystallized from ethanol to yield pure yellow crystals of lO-methoxy-14-methyl-5-oxo- 5,7,8,14-tetrahydroindolo[2,3 clquinazo[3,2 a]pyridine hydrochloride, M. P. 243 C. (dec.).
A suspension of 60 g. of the red free base (prepared as above) in 2 l. of ethanol is prepared and mixed with a solution of 40 g. of tartaric acid in 1 l. of ethanol. The mixture is heated to boiling, diluted with l l. of hot distilled water. The clear solution is then cooled to C. with stirring. After one hour at this temperature a large crop of bright yellow tartrate salt was obtained as a hydrate, M. P. 220-221 C. (dec.).
The citric, maleic, nitric, phosphorus, glycolic', ethanedisulfonic and perchloric salts of the above formed base are each prepared by dissolving equivalent amounts of the red base and the appropriate acid in minimum quantities of acetone. The salt separates almost immediately.
A solution of 3.3 g. of the red base (prepared as above) in 75 ml. of dry benzene is treated with 2.0 g. of benzyl chloride in 25 ml. of benzene. The mixture is heated under reflux for ten hours and the yellow solid separates. Filtration yields crystals of -methoxy-14-methyl-5-oxo- 5,7,8,l4-tetrahydroindolo [2,3 c]quinazo[3,2 alpyridine benzyl chloride quaternary salt.
EXAMPLE II A mixture of 5 g. of 3-carbethoxy-Z-piperidone in 1.5 equivalents of 10% potassium hydroxide solution is allowed to stand at room temperature overnight. The resulting hydrolysate is then buttered with 2.6 g. of acetic acid and 11.0 g. of potassium acetate. A previously prepared solution of diazonium salt using 3.72 g. of
6 p-chloroaniline is added to the buttered reaction mixture at ice bath temperature.
After two hours stirring at room temperature, the crude coupled product is separated by filtration, washed with ethanol and dried. A suspension of 4.8 g. of this chlorophenylhydrazone in ml. of 70% formic acid is heated at reflux for two hours. After quenching in an excess of water, long needles of 6-chloro-1-oxo-1,2,3,4-tetrahydropyrid[3,4-blindole are isolated by filtration and recrystallization from methanol, M. P. 225-226" C.
A suspension of 9.8 g. of finely-divided 6-chloro-l-oxo- 1,2,3,4-tetrahydropyrid[3,4-blindole in 200 ml. of xylene with 4 g. of phosphorus oxychloride is heated at reflux for fifteen minutes. A 15 g. portion of methyl N-methylanthranilate is added to the reaction mixture and the reflux period is extended for two hours with stirring. The solvent is removed in vacuo. The residue is carefully diluted with water, washed with ammonia water and extracted into chloroform. The dried organic extracts are concentrated, diluted with benzene and saturated with dry hydrogen chloride gas. Fractional crystallization of the gummy precipitate from ethanol results in 10-chloro-14-methyl 5 oxo 5,7,8,l4 tetrahydroindole- [2,3-c]quinazo[3,2-alpyridine hydrochloride, along with some starting material.
The purified hydrochloride is shaken with chloroformammonia water. The chloroform layer is dried, concentrated and diluted with benzene to yield orange-red needles of free base, M. P. 210 C. (decomposes gradually).
EXAMPLE III A solution of 5.2 g. of l-oxo-l,2,3,4-tetrahydropyrid [3,4-blindole, prepared from aniline according to the coupling procedure described in Example I, in ml. of toluene with 7.5 g. of phosphorus oxychloride is heated at reflux with stirring for ten minutes. After the addition of 6.5 g. of methyl 4-methoxy-N-methylanthranilate, prepared by esterifying 4-meth0xy-N-methylanthranilic acid in methanol with gaseous hydrogen chloride, the reaction mixture is heated at reflux with stirring for three hours. The toluene is removed in vacuo. The residue is treated with ammonia water, then taken into chloroform with vigorous shaking. The dry chloroform extracts are concentrated, diluted with benzeneethanol and cooled to yield a yellow crystalline hydrate. The crystalline 2-methoxy-14-methyl-5-oxo-5,7,8,14-tetrahydroindolo[2,3-c]quinazo[3,2-a]pyridine hydrate is purified by recrystallization from chloroform-ethanol, M. P. 195-l96 C. (Dee).
A mixture of 3.3 g. of the hydrate and 100 ml. of benzene is evaporated on the steam bath to remove water. A solution of 1.8 g. of isoamyl bromide in 25 ml. of benzene is added dropwise to the boiling reaction mixture. The solution is allowed to concentrate as crystals of the isoamyl bromide quaternary salt of 2-methoxy- 14 methyl 5 oxo 5,7,8,14 tetrahydroindolo[2,3 cl quinazo [3,2-alpyridine separate. The yellow crystals are separated by filtration and air dried.
' EXAMPLE IV A solution of 9.5 g. of 6-methyl-1-oxo-l.,2,3,4-tetrahydropyrid[3,4-b]indole, prepared from the p-methyle phenylhydrazone coupled product as in Example I, in ml. of toluene with 4 g. of phosphorus oxychloride is heated at reflux with stirring briefly. After the addition of 15 g. of methyl N-methylanthranilate, the reaction mixture is heated at reflux for one hour. The product of the condensation is isolated as in Example II. The hydrochloride salt is recrystallized from hot water to purification. The base is then regenerated by the use of ammonia water-chloroform to yield deep red needles of 10,14 dimethyl 5 oxo 5,7,8,l4 tetrahydroindolo [2,3-c]quinazo[3,2-a]pyridine, M. P. 223-225 C. (dec.).
A solution of 4.8 g. of the acetate salt of the base,
. '7 prepared by adding ether to an acetic acid solution is dissolved in .water. A solution of 1.7 g. of sodium benzoate in '20 ml. of water is added dropwise to the swirled acetate to separate the desired 10,14-dimethyloxo 5,7,8,14 tetrahydroindolo[2,3 c]quinazo[3,2- alpyridine benzoate.
EXAMPLE V A suspension of 2.0 g. of 6-methyl-1-oxo-1,2,3,4-tetrahydropyrid[3,4-blindole and 1.95 g. of methyl-4-methoxy- N-methylanthranilate in 50 ml. of dry dioxane with 0.5 g. of phosphorus oxychloride is heated at reflux for three hours. The product, 10,14-dimethyl-2-methoxy-5-oxo- 5,7,8,14 tetrahydroindolo[2,3 c] quinazo[3,2 alpyridine, is isolated as in Example II.
EXAMPLE VI A suspension of 5.0 g. of 1-oxo-1,2,3,4-tetrahydropyrid[3,4-blindole, prepared using aniline in the coupling procedure of Example I and using polyphosphoric acid as the medium for the rearrangement, in 120 ml. of dry toluene with 3 g. of freshly distilled phosphorus oxychloride is heated at reflux for fifteen minutes. After the addition of 7.5 g. of methyl N-methylanthranilate, the reflux period is extended for three hours. After distillation of the toluene under diminished pressure, the reaction product, 14-methyl-5-oxo-5,7,8,l4-tetrahydroindolo [2,3-c]quinazo[3,2-a]pyridine hydrochloride, is isolated following the procedure in Example II. Purification by recrystallization from either ethanol or water gives yellow crystals, M. P. 238 C. (dec.).
The free base is recovered from the hydrochloride salt by shaking 3 g. of the salt in a mixture of ammonia water and chloroform. The dry chloroform extract is concentrated and diluted with benzene-cyclohexane to precipitate orange needles of the free base, M. P. about 198 C.
A solution of 3 g. of 14-methyl-5-oxo-5,7,8,14-tetrahydroindolo [2,3-c] quinazo[3,2-alpyridine in 150 ml. of dry benzene is heated at reflux while 6 ml. of dry methyl iodide is added in three portions over a period of two hours. The product, 14-methyl-5-oxo-5,7,8,14-tetrahydroindolo[2,3-clquinazo[3,2-a]pyridine methiodide is obtained by cooling the reaction mixture, recovering the precipitate and recrystallizing the salt from 70% aqueous ethanol, M. P. 208-210 C. (d6C.).
EXAMPLE VII A suspension of 5 .0 g. of finely powdered 1-oxo-1,2,3,4- tetrahydropyrid[3,4-b1indole in 50 g. of freshly distilled phosphorus trichloride with 2 g. of phosphorus oxychloride is heated at reflux briefly with stirring. After the addition of 7.5 g. of methyl N-butylanthranilatc, prepared by monobutylation of anthranilic acid with nbutylbromide by the method of Gilman et al. E]. Am. Chem. Soc., 62, 977 (1940)] and subsequent esterification with methanol and dry hydrogen chloride gas, the reaction mixture is refluxed for one and one-half hours. The excess solvent is removed in vacuo. The residue is made basic with ammonia water and extracted into chloroform. The dried chloroform extract is concentrated, diluted with benzene and acidified with gaseous hydrogen chloride. The resulting dark gum is extracted withboiling water. After cooling, the filtrate is neutralized with ammonia water to give 14-butyl-5 oxo- 5,7,8,14-tetrahydroindolo[2,3-c]quinazo[3,2 alpyridine hydrate as yellow plates from ethanol, M. P. 178179 C.
EXAMPLE VIII A suspension of 4 g. of 7,8-dimethyl-l-oxo-1,2,3,4- tetrahydropyrid[3,4-blindole, M. P. 236-238 C., prepared by using 2,3-dimethylaniline hydrochloride in the coupling synthesis described in Example I, in 50 ml. of chlorobenzene with 2 g. of phosphorus oxychloride is heated at reflux for ten minutes. After the addition of 6 g. of methyl N-methylanthranilate and ml. of chloro- 8 benzene, the reaction mixture is heated at reflux for one hour. The base, 5-oxo-5,7,8,14-tetrahydro-11,12,14-trimethylindolo[2,3-c]quinazo[3,2-a]pyridine, is isolated following the procedure of Example II, as orange-red needles from benzene-chloroform, M. P. 24Q-243 C.
A solution of 2.2 g. of the base in 50 ml. of acetone is mixed with 1 g. of acetic acid in 25 ml. of acetone. The solution is concentrated and cooled to give crystals of 5 oxo 5,7,8,14 tetrahydro-l1,12,14-trimethylindolo- [2,3-clquinazo[3,2-alpyridine acetate.
EXAMPLE IX aniline as starting material in the coupling synthesis described in Example I, in ml. of benzene with 4 g. of phosphorus oxychloride is heated at reflux briefly. After the addition of 9 g. of methyl N-methylanthranilate, the reaction mixture is heated at reflux for four hours. The product, 14-methyl-5-oxo-12-propyl5,7,8,l4-tetrahydroindolo[2,3c]quinazo[3,2-alpyridine, is isolated following the procedure in Example I.
A solution of 3.5 g. the orange base in 50 ml. of. ethanol is heated to boiling and added to a solution of 1.2 g. of maleic acid in 50 ml. of ethanol. The solution is filtered hot. The filtrate is concentrated somewhat and cooled. Addition of a small amount of isooctane causes crystallization of l4methyl-S-oxo-l2-propyl-5,7,8,14- tetrahydroindolo [2,3-c] quinazo 3,2-a] pyridine maleate.
EXAMPLE X A suspension of 3.0 g. of 5-chloro-8-methoxy-1-oxo- 1,2,3,4-tetrahydropyrid[3,4-blindole, M. P., 214-215" 0., prepared by using 5-chloro-anisidine as starting material in the coupling synthesis described in Example I, in 40 g. of phosphorus trichloride witht 2.5 g. of phosphorus oxychloride is heated at reflux with stirring for twenty minutes. After addition of 4.5 g. of methyl N-methylanthranilate, the reaction mixture is heated at reflux for two hours. The solvent is evaporated and the residue quenched in ice water. After neutralizing the aqueous mixture with dilute sodium hydroxide, the product is extracted with several portions of chloroform. The chloroform extracts are combined, dried and concentrated. Fine orange crystals of base, 9-chloro-12-methoxy-14- methyl 5 oxo-5,7,8,14-tetrahydroindolo[2,3,c]quinazo' EXAMPLE XI A suspension of 10.8 g. of 7-methoxyl-oxo-l,2,3,4- tetrahydropyrid[3,4-b]indole in 100 ml. of xylene with 6- g. of phosphorus oxychloride is heated briefly at reflux with stirring. After the addition of 8.3 g. of methyl N- methylanthranilate, the reaction mixture is heated at reflux for two hours with stirring. The desired base, 11- methoxy 14 methyl 5 oxo 5,7,8,14 tetrahydroindolo[2,3-clquinazo[3,2-a1pyridine, is isolated by the isolation procedure of Example II.
The base is characterized by dissolving 3.3 g. of the red base in 75 ml. of ethanol along with 1.5 g. of salicylic acid in 50 ml. of ethanol. The solution is filtered hot and concentrated to a low volume. Cooling, following addition of petroleum ether, separates a yellow salt, 11- methoxy 14 methyl-5-oxo-5,7,8,l4-tetrahydroindolo- [2,3-a] pyridine salicylate.
EXAMPLE XII A suspension of 6.7 g. of 6-isobutoxy-1-oxo-1,2,3,4- tetrahydropyrid[3,4-blindole, prepared by utilizing 4-isobutoxyaniline in the coupling synthesis in Example I, in 450 ml. of cyclohexane with 3 g. of phosphorus oxychloride is heated at reflux with stirring briefly. After the addition of 5.8 g. of methyl N-butylanthranilate, the reflux period is extended to four hours. The volatiles are removed in vacuo. The residue is then shaken vigorously in an ice slurry which is then neutralized with ammonia Water and extracted with several portions of chloroform. The dried chloroform extracts are concentrated and replaced with dry benzene. Gaseous hydrogen chloride separates the impure hydrochloride which is washed thoroughly with benzene and then converted to the orange base by shaking with sodium bicarbonate solution into benzene. The organic layer is concentrated in vacuo and the residue recrystallized from benzene to give the crystalline base, lO-isobutoxy-l4=butyl-5-oxo-5,7,8,l4- tetrahydroindolo [2,3 -c]quinazo [3 ,Z-a] pyridine.
The. colored base is characterized by forming the maleate salt by reacting 4.2 g. of the base with 1.2 g. of maleic acid in ethanol.
EXAMPLE XIII A 15 g. sample of 3-carbethoxy-2-piperidone is hydrolyzedovernight by standing in a dilute potassium hydroxide solution containing 1.5 base equivalents. The hydrolysate is cooled, buffered and treated with a cold diazonium salt solution prepared from 18.4 g. of p-iodoaniline. After stirring at room temperature fortwo hours, the coupled hydrazone is separated by filtration and dried in vacuo. This material is then heated at reflux in 500 g. of 70% formic acid for one hour. After filtration, a
crystalline product separates on cooling. Purification of the 6-iodo-1-oxo-l,2,3,4-tetrahydropyrid[3,4-blindole is accomplished by recrystallization from benzene, M. P. 229-231 C. (dec.).
A suspension of 3.0 g. of 6-iodo-l-oxo-l,2,3,4-tetrahydropyrid[3,4-b]indole in 100 ml. of toluene with 2.5 of phosphorus oxychloride is heated at reflux briefly, then 4.5 g. of methyl N-methylanthranilate is added and the reflux period continued for one hour. The volatiles are removed in vacuo. The residue is quenched in ice water. The aqueous mixture is then neutralized with ammonia water and extracted with chloroform which is dried and replaced with benzene. Gaseous hydrogen chloride is passed into the benzene solution to separate a yellow crystalline hydrochloride.
After recrystallization from hot water, the free base, 10 iodo 14 methyl oxo 5,7,8,14 tetrahydroindolo[2,3-clquinazo[3,2-alpyridine is regenerated from the hydrochloride salt by ammonia water, taken into benzene; orange-red needles, M. P. 224 C. (dec.).
EXAMPLE XIV A suspension of 9.3 g. of l-oxo-1,2,3,4-tetrahydropyrid[3,4-b]indole in 200 ml. of toluene with 6 g. of phosphorus oxychloride is heated at reflux with stirring for fifteen minutes. A 11.5 g. portion of methyl N-ethyl- 4-isopropylanthranilate, prepared by esterification of 4- isopropylanthranilic acid with methanol and dry hydrogen chloride gas, then monoalkylation with ethyl iodide, is added and the reaction mixture is heated at reflux for two hours. The orange base is isolated following the procedure outlined in Example II, l4-ethyl-2-isopropyl-5- oxo 5,7,8,14 tetrahydroindo1o[2,3 cl quinazoi 3,2 a]- pyridine.
This base is characterized by dissolving 3.6 g. in 75 ml. of ethanol. An excess of ethanolic hydrogen bromide is added to the base solution. The solution is filtered hot and allowed to concentrate on the steam bath. Cooling separates yellow crystals of 14-ethyl-5-oxo-2- isopropyl 5,7,8,14 tetrahydroindolo[2,3-c] quinazo- [3,2-alpyridine hydrobromide.
EXAMPLE XV A suspension of 2.7 g. of a mixture of 5(7)-bromo-1- 0X0 1,2,3,4 tetrahydr0pyrid[3,4 blindole, prepared by using m-bromoaniline in the coupling synthesis,as described in Example XIII, in 50 m1. of toluene with 1 g. of phosphorus oxychloride is heated at reflux for ten minutes at which time 2.0 g. of methyl N-methylanthranilate is added.
After a reflux period of three hours, the yellow crystalline hydrochloride of 9(11)-bromo-l4-methyl-5-oxo- 5,7,8,14 tetrahydroindolo[2,3.-c] quinazo[3,2-a]pyridine is isolated following the procedure of Example XIII.
EXAMPLE XVI A suspension of 4.1 g. of 6-fluoro-l-oxo-1,2,3,4-tetrahydropyrid[3,4-b]indole, prepared by using p-fluoroaniline, from the catalytic reduction of 1-fluoro-4-nitrobenzene, as starting material in the coupling synthesis of Example XIII, in ml. of chlorobenzene with 5 g. of phosphorus oxychloride is heated at reflux briefly with stirring. After addition of 4.3 g. of methyl 4-methoxy- N-methylanthranilate, the reaction mixture is heated at reflux for four hours.
Following the isolation procedure of Example II, the base, 10-fluoro-Z-methoxy-l4-methyl-5-oxo-5,7,8,14-tetrahydroindolo [2,3-c] quinazo 3,2-a] pyridine, separated as red-orange crystals.
EXAMPLE XVII A suspension of 4.8 g. of 6-n-hexoxy-1-oxo-1,2,3,4-tetrahydropyrid[3,4-blindole, prepared from 4-hexoxyaniline by the coupling procedure described in Example I in ml. of benzene with 7 g. of phosphorus oxychloride is heated at reflux with stirring for ten minutes at which time 3.5 g. of propyl N-methylanthranilate is added to the reaction mixture. The reflux period is extended to two hours. The condensation product is isolated following the procedure in Example II, to give the crystalline base 10 hexoxy l4 methyl 5 ox-o 5,7,8,14 tetrahydroindolo [2,3-clquinazo [3 ,2-a] pyridine.
A solution of 2 g. of the base in 100 ml. of dry benzene is heated at reflux while 1 g. of n-hexyl bromide is added. The condenser is removed and the solution is allowed to concentrate on the steam bath as: the crystalline hexyl bromide quaternary salt of l0-hexoxy-l4- methyl 5 oxo 5,7,8,l4 tetrahydroindolo [2,3-clquinazo[3,2-a]pyridine separates and is isolated by filtration.
EXAMPLE XVIII A solution of 3.4 g. of l-oxo-l,2,3,4-tetrahydropyrid [3,4-blindole in 120 ml. of dry toluene with 3.5 g. of phosphorus oxychloride is heated at reflux for ten minutes. After the additionof 4.0 g. of methyl N-methyl- S-chloroanthranilate, M. P. 63-64" C., prepared by N- methylation of S-chloroanthranilic acid with methyl sulfate followed by methanol-hydrogen chloride esterification, the reaction mixture is heated at reflux for two hours. The solution is treated as in Example II, however, the final chloroform extract is concentrated to a low volume and triturated with aqueous ethanol to separate 3-ch1orol4 methyl 5 oxo 5,7,8,14 tetrahydroindolo [2,3-clquinazo[3,4-b]pyridine hydrate. Yellow plates of the hydrate are obtained by recrystallization from a large volume of aqueous ethanol, M. P. 186-188 C. (dec.).
EXAMPLE XIX A suspension of 2.0 g. of l-oxo-1,2,3,4-tetrahydropyrid- [3,4-b1indole, 2.0 g. of phosphorus oxychloride in 55 ml. of dry toluene is heated at reflux for ten minutes. After the addition of 2.5 g. of methyl 6-methylaminopiperonylate, prepared by alkylating methyl 6-aminopiperonylate, with dimethyl sulfate in benzene, the reaction mixture is heated at reflux for three hours. The solid, which separates after standing for 12 hours, is separated and shaken with ammonia water-chloroform mixture. The chloroform solution is dried, diluted with benzene and evaporated to give a red. crystalline solid which is redissolved in chloroform and acidified with. hydrogen 1 1 chloride gas to give the hydrochloride salt. The red base is again regenerated as before, M. P. 270-275 C. (dec.), 14 methyl 2,3 methylenedioxy 0x0 5,7,8,14- tetrahydroindolo[2,3-clquinazo[3,2-alpyridine.
EXAMPLE XX EXAMPLE XXI A suspension of 5.0 g. of l-oxo-l,2,3,4-tetrahydropyrid[3,4-b]indole, 5.0 g. of phosphorus oxychloride, 12.1 g. of methyl N-octadecylanthranilate, prepared by the alkylation of methyl anthranilate with n-octadecyl bromide and potassium acetate, in 125 m1. of dry toluene is heated at reflux with stirring for 2 /2 hours. The filtered reaction mixture is diluted with hexane to separate a solid which is treated with ammonia water and ether. A yellow solid hydrate separates from the ethereal layer and is filtered and recrystallized from hexane. The product consists of fine yellow prisms of the hydrate of 14-octadecyl-S-oxo 5,7,8,14 tetrahydroindolo[3,2-a]quinazo [2,3-'c]pyridine, M. P. 119 C.
EXAMPLE XXII Ethyl 3-dimethylaminomethylindole-2-carboxylate is alkylated with l-nitropropane in the presence of sodium hydroxide to yield ethyl 3-(2-nitrobuty1)-indole-2-carboxylate, M. P. 154155 C. A reductive cyclization of this substituted indole by stannous chloride gives 3- ethyl-l-oxo-l,2,3,4-tetrahydropyrid[3,4-b]indole, M. P. 188l89 C.
A suspension of 0.45 g. of 3-ethyl-l-oxo-l,2,3,4-tetrahydropyrid[3,4-b]indole, 0.38 g. of methyl N-methyl anthranilate and 0.5 g. of phosphorus oxychloride in ml. of dry toluene is heated at reflux for two hours. A yellow hydrochloride is obtained by following the procedure of Example XIX. After recrystallization from water, the salt is neutralized, separated and recrystallized from ethanol, pale yellow crystals of 7-ethyl-l4-methyl-5- oxo-5,7,8,14-tetrahydroindolo[2,3-c]quinazo[3,2 a] pyridine, M. P. 162-l63 C. (dec.).
EXAMPLE XXIII EXAMPLE XXIV A suspension of 5.0 g. of l-oxo-l,2,3,4-tetrahydropyrid[3, 4-b]indole, 5.0 g. of phosphorus oxychloride, 7.25 g. of methyl N-benzyl-anthranilate, in 110 ml. of dry toluene is heated at reflux for three and one-half hours. After working up the reaction mixture essentially as in Example XIX, orange crystals are recovered, 14-benzyl-5-oxo-5,7,8, l4-tetrahydroind-olo [2,3 -c] quinazo- [3,2-a1pyridine.
EXAMPLEXXV A suspension of 5.0 g. of 1-oxo-l,2,3,4-tetrahydropyrid[3,4-b]indole, 5.0 g. of phosphorus oxychloride, 10.2 g. of methyl N-(6-phenylhexy1)anthranilate, pre- 1'2 pared by the alkylation of methyl anthranilate with 6- phenyl-n-hexyl bromide and sodium acetate, in ml. of dry toluene is heated at reflux with stirring for three hours. The mixture, after working up essentially as in Example XXI, gives yellow crystals of the hydrate of 5-oxo-14-(6"- phenylhexyl 5,7,8,14 tetrahydroindolo[3,2-a1quinazo [2,3-c] pyridine.
EXAMPLE XXVI A suspension of 6.0 g. of 1-oxo-1,2,3,4-tetrahydropyrid[3,4-b]indole in ml. of anisone with 5.0 g. of phosphorus oxychloride is heated at reflux briefly before 5.2 g. of methyl N-methyl-3,4,S-trimethoxyanthrauilate, prepared by N-methylation of methyl 3,4,5-trimethoxyanthranilate with methyl sulfate in benzene, is added. The reflux period is extended to one hour. The product is isolated following the procedure of Example XII-I to' give 14-methyl-5-oxo-5,7,8,l4-tetrahydro-l,2,3-trimethoxyindolo [2,3-c] quinazo[3,2-a] pyridine.
EXAMPLE XXVII acid in ethyl acetate to form crystals of the citrate salt.
EXAMPLE XXVI I I A suspension of 6.9 g. of 6,7-methylenedioxy-l,2,3,4- tetrahydropyrid[3,4-b1indole, prepared by using 3,4-. methylenedioxyaniline in the coupling synthesis of Example II, 5.0 g. of phosphorus oxychloride and 5.2 g. of methyl N-methylanthranilate in 50 ml. of toluene is heated at reflux with stirring for two hours. After working up the reaction mixture as in Example XIX, 14-..
methyl-10,1 l-methyleuedioxy-S-oxo-S ,7,-8, l4 tetrahydr0- indo1o[2,3-c]quinazo[3,2-a]pyridine is obtained first as the hydrochloride, and then as the red base.
EXAMPLE XX-IX A suspension of 5.1 g. of l-oxo-l,2,3,4-tetrahydro-7- trifluoromethylpyrid[3,4-b]indole, prepared by using 3- trifluoroaniline in the coupling synthesis of Example XIII and separating the resulting 5 and 7 isomers by fractional; crystallization and 4.0 g. of phosphorus oxychloride in 100 ml. of toluene is heated briefly at reflux. After the addition of 3.5 g. of methyl N-methylanthranilate, the reaction mixture is heated at reflux for two hours. The mixture is worked up as in Example XII to give the desired base, 14-methyl-5-oxo-5,7,8,14-tetrahydro 1l-trifluoro-methylindolo[2,3-0]quinazo[3,2-a]pyridine.
EXAMPLE XXX A suspension of 2.3 g. of 1-oxo-1,2,3,4-tetrahydro-5,-6,8- trimethylpyrid[3,4b]indole and 2.2 g. of methyl N- methyl-3,4,S-trimethoxyanthranilate in 75 ml. of toluene with 4.0 g. of phosphorus oxychloride is heated at reflux for five hours with stirring. The product, l4-methy1-5- oxo-5,7,8,l4-tetrahydro-l,2,3-trimethoxy 9,10,12 trimethylindolo[2,3-c] quinazo[3,2-a] pyridine, is isolated by the procedure of Example XIII.
EXAMPLE XXXI A suspension of 1.9 g. of l-oxo-1,2,3,4-tetrahydropyrid-l [3,4-blindole, 3.0 g. of phosphorus oxychloride and 3.2
EXAMPLE XXXII A suspension of 1.9 g. of 1-oxo-1,2,3,4-tetrahydropyrid- [3,4-blindole, 2.5 g. of phosphorus oxychloride, 2.5 g. of methyl 5-isoamoxy-N-methylanthranilate, prepared by standard procedures from methyl 2-hydroxy-6-nitrobenzoate in 75 ml. of benzene is heated at reflux for three hours. After proceeding with the isolation steps of Example I the desired base, 3-isoamoxy-14-methyl-5-oxo- 5,7,8,14-tetrahydroindolo [2,3 c] quinazo[3, 2-a]pyridine, is recovered as the hydrate.
EXAMPLE XXXIII A suspension of 1.9 g. of 1-oxo-1,2,3,4-tetrahydropyrid- [3,4-blindole, 2.0 g. of phosphorus oxychloride and 2.0 g. of methyl N-allylanthranilate, prepared by alkylation of methylanthranilate with allyl chloride, in 75 ml. of dry toluene is heated at reflux with stirring for three hours. Following the isolation procedure of Example XXI, the desired base, 14-allyl 5 -oxo-5,7,8,l4-tetrahydroindolo- [3,2-alquinazo[2,3-c]pyridine, is recovered.
EXAMPLE XXXIV A suspension of 5.0 g. of l-oxo-l,2,3,4-tetrahydropyrid[3,4-b]indole, 5.0 g. of phosphorus oxycbloride, 12.1 g; of methyl N-oleyl'anthranilate, prepared by the alkylation of methylanthranilate with oleyl bromide in the presence of potassium acetate, in 125 ml. of toluene is heated at reflux with stirring for four hours. The product is isolated as in Example XXI; 14oleyl-5-oxo-5,7,8,14- tetrahydroindolo[3,2-a] quinazo[2,3 cJpyridine hydrate.
EXAMPLE XXXV A suspension of 4.5 g. of 6-allyl-1-oxo-1,2,3,4-tetrahydro[3,4-b]indole, prepared by using p-allyl'aniline in the coupling procedure of Example I, 5.0 g. of phosphorus oxychloride and 3.5 g. of methyl N-methylanthranilate in 100 ml. of dry toluene is heated at reflux for two hours. After carrying the reaction through as in Example I, the base, 10-allyl-14-methyl-5-oxo-5,7,8,l4-tetrahydroindolo- [2,3-] quinazo[3,2-a]pyridine, is recovered.
EXAMPLE XXXVI EXAMPLE XXXVII A solution of 5.0 g. of 10-methoxy-l4-methyl-5-oxo- 5,7,8,14-tetrahydroindolo[2,3 c] quinazo[3,2 a] pyridine (prepared as in Example I) in 100 ml. of 48% hydro bromic acid is heated at reflux for eight hours. After cooling and diluting the reaction mixture with an equal volume of Water, a fine yellow solid separates. Recrystallization from aqueous ethanol gives yellow needles of IO-hydroxy 14 methyl--oxo 5,7,8,l4-tetrahydroindolo- [2,3 clquinazo[3,2 a] pyridine hydrobromide, M. P. 266267 C. (dec.). This material dissolves completely in dilute sodium hydroxide solution to give a magenta colored solution whose color rapidly fades to a pale yellow.
EXAMPLE XXXVIII A solution of 0.5 g. of Z-methoxy-14-methyl-5-oxo- 5 ,7,8,14-tetrahydroindolo [2,3 c] quinazo [3,2 a] pyridine hydrate (prepared as in Example III) in 14 ml. of 48% hydrobromic acid is heated at reflux for four hours. After Working up the reaction mixture as in Example 14 XXXVI, yellow prisms of Z-hydroxy-14-methyl-5-oxo- 5,7,8,14-tetrahydroindolo[2,3 c] quinazo[3,2.- a]pyridine. hydrobromide are obtained from aqueous ethanol, M. P. 346 C. (dec.).
5,7,8,14-tetrahydroindolo[2,3 clquinazo[3,2.- a]pyridine.
hydrobromide (prepared as in Example XXXVII), in 75. ml. of acetic anhydride is heated at reflux for three hours. The reaction mixture is concentrated in vacuo and the washed residue is purified by several recrystallizations from ethanol to give the desired product, 10-acetoxy-l4- methyl 5 oxo-5,7,8,l4-tetrahydroindolo1[2,3 -cl]quinazo- [3,2-alpyridine hydrobromide.
A small amount of the salt is triturated with concentrated ammonia to give a small return of the base of the 10'-hydroxy starting material. 1 t t Z The pharmaceutical carrier may be a solid or a liquid. Exemplary solid carriers are cornstarch, lactose, talc,
magnesium vstearate and starch. 'Where a solid carrier is employed, the composition of this, invention may be in the form of a tablet or a hard gelatin capsule for oral use.
Where a liquid carrier is desired, the medicamentmay be in a suitable oily menstruum such as, for example, peanut or soybean oil and the admixture placed, if desired, in a soft gelatin capsule. Water alone or in. admixture with other agents such as carboxymethylcellulose, polyoxyethylene monostearate, acacia, tragacanth or. methylcellulose is a satisfactory liquid carrier for oral use. For parenteral use thefollowing carriersare exemplary: saline water, aqueous propylene glycolor peanut oil.
In any of the pharmaceutical forms of this invention the foregoing is illustrative of the dosage units possible and it is recognized that variations within the skill of the art are feasible and often of advantage. For in stance the addition of flavor, preservatives, colors, etc., is often desirable to attain pharmaceutically elegant preparations. i i
The composition of this invention will preferably con tain from about 1 mg. to about 150 mg. and advantageously from about 10 mg. to about 75 mg. of "the medicament compound, preferably as the base. The carrier will preferably be present in an amount of from about 5 mg. to about 18 g. and advantageously in an amount of from about 25 mg. to about 5 g. Where. a solid carrier is employed, it will preferably be present in an amount of from about 5 mg. to about 750 mg. and advantageously in an amount of from about 25 mg. to about. 500 mg.
The following examples are illustrative:
Example A1 g Composition: Gm./capsule l0 methoxy-l4-rnethyl-S-oxo-5,7,8, l4-tetrahydroindolo[2,3-c]quinazo[3,2-alpyridine 0.010
Lactose 0.290
Procedure-The ingredients'are mixed and pulverized sufficiently to pass through mesh sieve and then incorporated into size #2 hard gelatin capsules.
Example A2 Composition: 1 1 Gm./capsule 10-hydroxy-14-methyl-5-oxo-5,7,8, 14 tetrahydroindolo- 2,3-c] quinazo 3,2-a] pyridine hydrobromide 0.010 Lactose 0.290
Procedure.The ingredients are mixed and pulverized suificiently to pass through 100 mesh sieve and then. incorporated into size #2 hard gelatin capsules.
15 Example A3 Composition: Gm./ capsule IO-chloro-14-methyl-5-oxo 5,7,8,l4 tetrahyhydroindolo-[2,3-c] quinazo [3,2-a] pyridine Lactose Prcedure.--The ingredients are mixed and pulverized sufficiently to pass through 100 mesh sieve and then incorporated into size #2 hard gelatin capsules. 1
Example A4 Composition: Gm./capsule Isoamyl bromide quaternary salt of Z-methoxy-l4-methyl-5-oxo-5,7,8,14 tetrahydroindolo[2,3-c]quinazo[3,2-alpyridine 0.100 Starch 0.150
Procedure.-The ingredients are mixed and pulverized sufficiently to pass through 100 mesh sieve and then incorporated into hard gelatin capsules.
. Example A5 Composition: Gm./capsule 10,14-dimethyl-5 oxo- 5 ,7,8,14 tetrahydroindolo[2,3-clquinazo-[3,2,-a] pyridine 0.050 Calcium carbonate 0.150
Procedure:-The ingredients are mixed and pulverized sufliciently. to pass through 100 mesh sieve and then incorporated into hard gelatin capsules.
Example A6 Composition: Gm./capsule 10,l4-dirnethyl-2-methoxy-S-oxo-5,7,8,l4-tet rahydroindolo-[2,3-clquinazo [3,2-a] pyridine Mannitol Pr0cedure.-The ingredients are mixed and pulverized sufliciently to pass through 100 mesh sieve and then incorporated intohard gelatin capsules.
' Example A7 0.025 gram of 14 methyl 5 oxo 5,7,8,14 tetrahydroindolo[2,3-c] quinazo[3,2-a]pyridine hydrochloride is mixed with soybean oil to produce a flowable mass. 7 The thus produced compositionis then encapsulated in a soft gelatin capsule.
Example A8 0.015 gram of 14 butyl 5 oxo 5,7,8,14'- tetrahydroindolo[2,3-clquinazo[3,2-alpyridine hydrate is mixed with soybean oil to produce a flowable mass. The thus produced composition is then encapsulated in a soft gelatin capsule.
Example A9 0.030 gram of 5-oxo-5,7,8,14-tetrahydro-l1,12,14-trimethylindolo [2,3-c] quinazo 3 ,2-a] pyridine acetate are encapsulated in a soft gelatin capsule following the procedure of Example A8.
Example A10 I 0.030 gram of 14-methyl-5 -oxo-l2-propyl-5 ,7 ,8, 14- tetrahydroindolo [2,3-c] quinazo [3 ,2-a] pyridine are encapsulated in a soft gelatin capsule following the procedure of Example A8.
Example A11 0.050 gram of 9-chloro-12-methoxy-14-methyl-5-oxo- 5 ,7,8, 14 tetrahydroindolo [2,3-c] -quinazo 3 ,2-a] pyridine are mixed with peanut oil to produce a flowable mass which is then encapsulated in a soft gelatin capsule.
; v H Example A12" 0.050 gram of 1l-methoxy-l4-methyl-5-oxo-5,7,8,14- tetrahydroindolo [2,3-c] quinazo[3,2-a]pyridine are mixed with peanut oil: to produce a flowable mass which is then encapsulated in a soft gelatin capsule.
16 1. Example A13 0.025 gram of 10-isobutoxy-l4-butyl-5-oxo-5,7,8,l1- tetrahydroindolo [2,3-c] quinazo[3,2-a]pyridine are mixed with peanut oil to produce a flowable mass which is then encapsulated in a soft gelatin capsule.
Example A14 Composition: Gm./tablet 10 iodo 14 methyl 5 oxo 5,7,8,14-
tetrahydroindolo [2,3 c] quinazo[3,2 a] pyridine 0.050 Lactose 0.250
Pr0cedure.The above ingredients were thoroughly mixed, granulated using a 10% gelatin solution and compressed into tablets using an admixture of 7% starch and 1% magnesium stearate based on tablet weight.
Example A15 Composition: Gm./tablet 14 ethyl 2 isopropyl 5 oxo 5,7,8,11-
tetrahydroindolo [2,3 c]quinazo[3,2 a]
pyridine 0.025 Lactose 0.175 Starch 0.045
Pr0cedure.-The above ingredients were thoroughly mixed, granulated using a 10% gelatin solution and compressed into tablets using talc as a lubricant.
Example A16 Composition: Gm./tablet 5(7) bromo 14 methyl 1 oxo 5,7,8,11-
tetrahydroindolo [2,3 c]quinazo[3,2 a]
pyridine 0.075 Lactose 0.125 Starch 0.045
Pr0cedure.The above ingredients were thoroughly mixed, granulated using a 10% gelatin solution and compressed into tablets using talc-stearic acid as a lubricant.
Example A17 Composition: Gm./tablet l0 fluoro 2 methoxy 14 methyl 1- 0x0 5,7,8,11 tetrahydroindolo [2,3 c] quinazo[3,2-a]pyridine 0.025 Lactose 0.275
Pr0cedure.The above ingredients were thoroughly mixed, granulated using a 50% sucrose solution and compressed into tablets using an admixture of 7% starch and 1% magnesium stearate based on tablet Weight.
Example A18 Composition: Gm./tablet 10 hexoxy 14 methyl 5 oxo 5,7,8,14-
tetrahydroindolo[2,3 c]quinazo [3,2 a]
pyridine 0.100 Lactose 0.100
'Starch 0.045
Procedure.--The above ingredients were thoroughly mixed, granulated using a 10% gelatin solution and compressed into tablets using talc as a lubricant.
Example A 19 1 7 I Example A20 Composition: Gm./ tablet 3 chloro- 14 methyl 1 oxo 5,7,8,14- tetrahydroindolo [2,3 c] quinazo[3,4 b]
pyridine hydrate 0.050 Lactose 0.150 Starch 0.045
Prcedare.The above ingredients were thoroughly mixed, granulated using a 50% sucrose solution and compressed into tablets using talc as a lubricant.
Example A21 Composition: Percent w./v.
l0 methoxy 14 methyl oxo 5,7,8, 14 tetrahydroind'olo[2,3 c] quinazo [3,2-a]pyridine tartrate 0.153 Dextrose, anhydrous 4.90 Water for injection q. s a- 100.00
The above ingredients are mixed to make a solution and filtered. The filtrate is autoclaved at 120 C. at 18 pounds pressure for 25 minutes. The thus treated composition is suitable for injection.
Example A22 Composition: Gm./ 5 cc.
methoxy 14 methyl 5 oxo 5,7,8,14- tetrahydroindolo [2,3 c]quinazo[3,2 a]
pyridine 0.010 Sucrose 2.500 Methyl cellulose 400 0.050
Purified water in an amount to bring the total volume to 5 cc.
The 10 methoxy 14 methyl 5 oxo 5,7,8,l4- tetrahydroindolo[2,3-c]quinazo[3,2-a] pyridine is reduced to a fine powder so that all will pass a 325 mesh sieve. The remaining ingredients are mixed to make the vehicle. The 1 0 methoxy 14 methyl 5 oxo 5,7,8,14- tetrahydroindolo [2,3 c]quinazo[3,2 a]pyridine is incorporated in the thus formed vehicle and homogenized.
Example A23 Composition: Gm./capsule 14 methyl 2,3 methylenedioxy 5 oxo- 5,7,8,14 tetrahydroindolo [2,3 c]quinazo[3,2-a]pyridine 0.010 Lactose 0.290
Pr0cedare.-The ingredients are mixed and pulverized sufiiciently to pass through 100 mesh sieve and then incorporated into size #2 hard gelatin capsules.
Procedure-The ingredients are mixed and pulverized sufficiently to pass through 100 mesh sieve and then incorporated into size #2 hard gelatin capsules.
Example A26 Composition Gm./ capsule 7 ethyl 14 methyl 5 oxo 5,7,8,14- tetrahydroindolo[2,3 clquinazo [3,2 a]
pyridine 0.100
Starch 0.150
' mixed, granulated using a 10% 18 Procedure-The ingredients are mixed] and pulverized sufiiciently to pass through mesh sieve and then incorporated into hard gelatin capsules.
Example A27 Composition: Gin/capsule 2 carbomethoxy 14 ethyl 5 oxo- 5,7,8,14 tetrahydroindolo [2,3 clquinazo[3,2-a]pyridine 0.050
Calcium carbonate 0.150
Procedure-The ingredients are mixed and pulverized sufliciently to pass through 100 mesh sieve and then incorporated into hard gelatin capsules.
Example A28 Composition: Gm./ capsule l4 benzyl-S-oxo 5,7,8,14 tetrahydroindolo [2,3-clquinazo[3,2-al-pyridine 0.001
Mannitol 0.299
Pr0cedlre.-The ingredients are mixed and pulverized sufiiciently to pass through 100 mesh sieve and then incorporated into hard gelatin capsules.
Example A29 Composition: Gm./ tablet 5 oxo-14 (6-phenylhexyl) 5,7,8,14-tetrahydroindolo[3,2 alquinazo [2,3 r clpyridine 0.050 Lactose 0.250
Pr0cedare.--The above ingredients Were thoroughly mixed, granulated using a 10% gelatin solution and compressed into tablets using an admixture of 7% starch and 1% magnesium stearate based on tablet weight.
Example A30 Composition: Gm./ tablet l4-methyl 5 oxo 5,7,8,l4-tetrahydro-l,2,3-
trimethoxyindolo[2,3 c]quinazo[3,2 a] pyridine 0.025 Lactose 0.175 Starch 0.045
Procedure-The above ingredients were thoroughly mixed, granulated using a 10% gelatin solution and compressed into tablets using talc as a lubricant.
Example A31 Composition: Gm./ tablet 5-oxo 5,7,8,14 tetrahydro 9,10,12,14-tetramethylindolo[2,3 cl quinazo[3,2-a]pyridine 0.075 Lactose 0.125 Starch 0.045
Procedare.-The above ingredients were thoroughly gelatin solution and compressed into tablets using talc-stearic acid as a lubricant.
Example A32 Composition: Gm./tablet 14 methyl 10,11 methylenedioxy 5 oxo- 5,7,8,14 tetrahydroindolo [2,3 clquinaZo[3,2-a] pyridine 0.025 Lactose 0.275
Pr0cedare.-The above ingredients were thoroughly mixed, granulated using a 50% sucrose solution and com pressed into tablets using an admixture of 7% starch and 1% magnesium stearate based on tablet weight.
Example A33 Composition: Gm./ tablet 14 methyl 5 oxo 5,7,8,14 tetrahydro-l 1- triflu0romethylindolo[2,3 c] quinazo [3,2-a] pyridine 0.100 Lactose 0.100 Starch 0.045
Pmcedure.The above ingredients were thoroughly mixed, granulated using a 10% gelatin solution and compressed into tablets using talc as a lubricant.
Prcedure.The above ingredients were thoroughly mixed, granulated using a 10% gelatin solution and compressed into tablets using an admixture of 1% magnesium stearate based on tablet weight.
Example A35 Composition: Gm./ tablet 4 bromo 14 methyl oXo 5,7,8,14-tetrahydro 2 trifluoromethylindolo[2,3-c]
quin-azo[3,2-a]pyridine 0.050 Lactose 0.150 Starch 0.045
Pr0cedare.-The above ingredients were thoroughly mixed, granulated using a 50% sucrose solution and compressed into tablets using talc as a lubricant.
Example A36 Composition: Gm./capsule 3 isoamoxy -'14 methyl 5 oxo 5,7,8,14-
tetrahydroindo1o[2,3 c] quinazo[3,2 a] pyridine 0.010 Lactose 0.290
Procedure.-The ingredients are mixed and pulverized sufliciently to pass through 100 mesh sieve and then incorporated into size #2 hard gelatin capsules.
Example A37 Composition: Gm./ capsule 14 allyl 5 -'oxo 5,7,8,14 tetrahydroindolo [3,2a] quinazo-[2,3-c]pyridine 0.010
Lactose 0.290
Procedure.-The ingredients are mixed and pulverized sufliciently to pass through 100 mesh sieve and then incorporated into size #2 hard gelatin capsules.
Example A38 Composition Gm. capsule 14-o1eyl 5 oxo 5,7,8,14 tetrahydroindolo [3,2-a]quinazo[2,3-c]pyridine hydrate 0.010
Lactose 0.290
Procedare.The ingredients are mixed and pulverized sufliciently to pass through 100 mesh sieve and then incorporated into size- #Z'hard gelatin capsules.
Example A39 Composition: Gm./ capsule allyl-14-methyl-5-oxo-5,7,8,14-tetrahydroindolo[2,3-c]quinabo[3,2-a]pyridine 0.050
Lactose 0.250
Procedure-The ingredients are mixed and pulverized sufiiciently to pass through 100 mesh sieve and then incorporated into size #2 hard gelatin capsules.
Example A40 Procedare.The ingredients are mixed and pulverized sufiiciently to pass through 100 mesh sieve and then incorporated into hard gelatin capsules.
20 Example A41 Composition: Gm./ capsule 10 hydroxy-14-methyl-5-oxo-5,7,8,14 tetrahydroindolo [2,3 c] quinazo 3 ,2-a] pyridine hydrobromide 0.050 Calcium carbonate 0.150
-' I Pr0cedure.-The ingredients are mixed and pulverized sufficiently to pass through mesh sieve and then incorporated into hard gelatin capsules.
Example A42 Composition: Gm./ capsule 2 hydroxy-14-methyl-5-oxo-5,7,8,14-tetrahydroindolo [2,3 -c] quinazo 3,2-a] pyridine hydrobromide -2 0.001 Mannitol 0.299
Procedure.-The ingredients are mixed and pulverized sufliciently to pass through 100 mesh sieve and then incorporated into hard gelatin capsules.
- 1 Example A43 Composition: Gm./tablet 10 acetoxy 14 methyl-5-oxo-5,7,8,14-tetrahydroindolo [2,3 c] quinazo [3 ,2-a] pyridine hydrobromide 0.05 0 Lactose 0.250
Procedure.-The above ingredients were thoroughly mixed, granulated using a 10% gelatin solution and compressed into tablets using an admixture of 7% starch and 1% magnesium stearate based on tablet weight.
The method in accordance with this invention comprises administering internally the above described medicinal composition to a human being to produce antihypertensive activity. Oral administration is preferred.
What is claimed is:
1. An. antihypertensive medicinal composition .comprising a pharmaceutical carrier and a compound of the class consisting of a free base and its acid addition, methyl iodide, ethyl bromide, n-hexyl bromide, benzyl chloride, methyl sulfate, ethyl sulfate and methyl p-toluene sulfonate, salts, the free base having the formula:
Rt9 8 R1 in which R is a member selected from the group consisting of alkyl having from 1 to 18 carbon atoms, phenylalkyl, having 1 to 6 carbon atoms in the alkyl portion and CH -a1kenyl, the alkenyl portion having 2 to 17 carbon atoms; R is a member selected from the group consisting of hydrogen, lower alkoxyl, lower alkyl, CH -alkenyl, the alkenyl portion having 2 to 5 carbon atoms, halo, hydroxyl and trifluoromethyl; R and R are members selected from the group consisting of hydrogen, lower alkoxyl, lower alkyl, CH -alkenyl, the alkenyl portion having 2 to 5 carbon atoms, hydroxyl, halo and trifluoromethyl; R is a member selected from the group consisting of hydrogen, lower alkoxyl, lower alkyl, CH -alkenyl, the alkenyl portion having 2 to 5 carbon atoms, hydroxyl, halo and trifluoromethyl; R and R are members selected from the group consisting of hydrogen, lower alkoxyl, lower alkyl, -CH -alkenyl,-
2. The composition of claim 1 characterized in that R and R are members selected from the group consisting of hydrogen, lower alkoxy and lower alkyl; R R R R and R are hydrogen and R is lower alkyl.
3. The composition of claim 1 characterized in that the carrier is a solid.
4. The composition of claim 1 characterized in that the carried is a liquid.
5. The composition of claim 1 characterized in that the composition is in the form of a tablet.
22 6. The composition of claim 1 characterized in that the composition is in the form of a capsule.
References Cited in the file of this patent
Claims (1)
1. AN ANTIHYPERTENSIVE MEDICINAL COMPOSITION COMPRISING A PHARMACEUTICAL CARRIER AND A COMPOUND OF THE CLASS CONSISTING OF A FREE BASE AND ITS ACID ADDITION METHYL IODIDE, ETHYL BROMIDE, N-HEXYL BROMIDE, BENZYL CHLORIDE, METHYL SULFATE, ETHYL SULFATE AND METHYL P-TOLUENE SULFONATE, SALTS, THE FREE BASE HAVING THE FORMULA:
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US616632A US2858251A (en) | 1956-10-18 | 1956-10-18 | Indolo [2, 3-c] quinazo [3, 2-a] pyridine derivatives |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US616632A US2858251A (en) | 1956-10-18 | 1956-10-18 | Indolo [2, 3-c] quinazo [3, 2-a] pyridine derivatives |
Publications (1)
Publication Number | Publication Date |
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US2858251A true US2858251A (en) | 1958-10-28 |
Family
ID=24470334
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US616632A Expired - Lifetime US2858251A (en) | 1956-10-18 | 1956-10-18 | Indolo [2, 3-c] quinazo [3, 2-a] pyridine derivatives |
Country Status (1)
Country | Link |
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US (1) | US2858251A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2485533A1 (en) * | 1980-06-24 | 1981-12-31 | Chinoin Gyogyszer Es Vegyeszet | INDOLO (2 ', 3', 3,4) PYRIDO (2,1-B) QUINAZOLIN-5-ONES AND PROCESS FOR THEIR PREPARATION |
US6787073B1 (en) | 1999-08-05 | 2004-09-07 | Invista North America S.A.R.L. | Waste polymer processing device and method |
-
1956
- 1956-10-18 US US616632A patent/US2858251A/en not_active Expired - Lifetime
Non-Patent Citations (1)
Title |
---|
None * |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2485533A1 (en) * | 1980-06-24 | 1981-12-31 | Chinoin Gyogyszer Es Vegyeszet | INDOLO (2 ', 3', 3,4) PYRIDO (2,1-B) QUINAZOLIN-5-ONES AND PROCESS FOR THEIR PREPARATION |
US4472399A (en) * | 1980-06-24 | 1984-09-18 | Chinoin Gyogyszer Es Vegyeszeti Termekek Gyara Rt. | Indolo[2',3';3,4]pyrido[2,1-b]quinazoline-5-ones, a process for the preparation thereof, and diuretic compositions and methods using them |
US6787073B1 (en) | 1999-08-05 | 2004-09-07 | Invista North America S.A.R.L. | Waste polymer processing device and method |
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