NO128110B - - Google Patents

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Publication number: NO128110B
Authority: NO; Norway
Prior art keywords: compound; general formula; formula; benzodiazepine; dihydro
Prior art date: 1969-02-14

Application number

NO00292/73A

Other languages

English (en)

Norwegian (no)

Inventor

J Hellerbach

A Walser

Original Assignee

Hoffmann La Roche

Priority date (The priority date 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 date listed.)

1969-02-14

Filing date

1973-01-24

Publication date

1973-10-01

1973-01-24 Application filed by Hoffmann La Roche filed Critical Hoffmann La Roche

1973-10-01 Publication of NO128110B publication Critical patent/NO128110B/no

Links

150000001875 compounds Chemical class 0.000 claims description 114
239000001257 hydrogen Substances 0.000 claims description 15
229910052739 hydrogen Inorganic materials 0.000 claims description 15
238000000034 method Methods 0.000 claims description 13
150000003839 salts Chemical class 0.000 claims description 11
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 10
125000002252 acyl group Chemical group 0.000 claims description 8
125000003545 alkoxy group Chemical group 0.000 claims description 8
229910052736 halogen Inorganic materials 0.000 claims description 8
150000002367 halogens Chemical class 0.000 claims description 8
125000000217 alkyl group Chemical group 0.000 claims description 7
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 7
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 6
125000004644 alkyl sulfinyl group Chemical group 0.000 claims description 6
239000000460 chlorine Substances 0.000 claims description 6
229910052801 chlorine Inorganic materials 0.000 claims description 6
125000005059 halophenyl group Chemical group 0.000 claims description 5
125000002088 tosyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1C([H])([H])[H])S(*)(=O)=O 0.000 claims description 5
238000012546 transfer Methods 0.000 claims description 5
125000004414 alkyl thio group Chemical group 0.000 claims description 4
125000004438 haloalkoxy group Chemical group 0.000 claims description 4
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
238000004519 manufacturing process Methods 0.000 claims description 4
125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims description 4
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 claims description 3
229940053197 benzodiazepine derivative antiepileptics Drugs 0.000 claims description 3
150000002431 hydrogen Chemical class 0.000 claims description 3
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 3
125000003310 benzodiazepinyl group Chemical class N1N=C(C=CC2=C1C=CC=C2)* 0.000 claims 1
238000002560 therapeutic procedure Methods 0.000 claims 1
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 114
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 72
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 55
WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 46
239000000243 solution Substances 0.000 description 46
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 42
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 33
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 33
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 33
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 30
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 24
239000003960 organic solvent Substances 0.000 description 24
229960000583 acetic acid Drugs 0.000 description 23
238000006243 chemical reaction Methods 0.000 description 22
-1 cyclopropanecarbonyl Chemical group 0.000 description 22
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 21
238000002844 melting Methods 0.000 description 19
230000008018 melting Effects 0.000 description 19
238000002425 crystallisation Methods 0.000 description 18
230000008025 crystallization Effects 0.000 description 18
239000011541 reaction mixture Substances 0.000 description 18
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 18
150000002430 hydrocarbons Chemical group 0.000 description 17
229930195733 hydrocarbon Natural products 0.000 description 16
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 15
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 15
150000002170 ethers Chemical class 0.000 description 14
239000012362 glacial acetic acid Substances 0.000 description 14
238000001953 recrystallisation Methods 0.000 description 14
XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 13
239000000499 gel Substances 0.000 description 13
239000000155 melt Substances 0.000 description 13
229910052710 silicon Inorganic materials 0.000 description 13
239000010703 silicon Substances 0.000 description 13
KFSLWBXXFJQRDL-UHFFFAOYSA-N Peracetic acid Chemical compound CC(=O)OO KFSLWBXXFJQRDL-UHFFFAOYSA-N 0.000 description 12
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 12
238000003756 stirring Methods 0.000 description 11
239000002253 acid Substances 0.000 description 10
150000001298 alcohols Chemical class 0.000 description 10
239000003513 alkali Substances 0.000 description 10
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 10
239000012043 crude product Substances 0.000 description 10
WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 9
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 9
KJONHKAYOJNZEC-UHFFFAOYSA-N nitrazepam Chemical compound C12=CC([N+](=O)[O-])=CC=C2NC(=O)CN=C1C1=CC=CC=C1 KJONHKAYOJNZEC-UHFFFAOYSA-N 0.000 description 9
229910052938 sodium sulfate Inorganic materials 0.000 description 9
235000011152 sodium sulphate Nutrition 0.000 description 9
239000002585 base Substances 0.000 description 8
239000000047 product Substances 0.000 description 8
239000007858 starting material Substances 0.000 description 8
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 7
238000003776 cleavage reaction Methods 0.000 description 7
230000007017 scission Effects 0.000 description 7
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 6
KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 6
238000004587 chromatography analysis Methods 0.000 description 6
230000003647 oxidation Effects 0.000 description 6
238000007254 oxidation reaction Methods 0.000 description 6
238000010992 reflux Methods 0.000 description 6
239000012312 sodium hydride Substances 0.000 description 6
229910000104 sodium hydride Inorganic materials 0.000 description 6
VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 6
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 6
XJUZRXYOEPSWMB-UHFFFAOYSA-N Chloromethyl methyl ether Chemical compound COCCl XJUZRXYOEPSWMB-UHFFFAOYSA-N 0.000 description 5
239000001961 anticonvulsive agent Substances 0.000 description 5
238000001816 cooling Methods 0.000 description 5
NPOMSUOUAZCMBL-UHFFFAOYSA-N dichloromethane;ethoxyethane Chemical compound ClCCl.CCOCC NPOMSUOUAZCMBL-UHFFFAOYSA-N 0.000 description 5
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 5
239000000203 mixture Substances 0.000 description 5
235000011121 sodium hydroxide Nutrition 0.000 description 5
LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 5
RFVALKDVKAUSQV-UHFFFAOYSA-N 1-(2-chloroethoxymethyl)-7-nitro-5-phenyl-3H-1,4-benzodiazepin-2-one Chemical compound [N+](=O)([O-])C=1C=CC2=C(C(=NCC(N2COCCCl)=O)C2=CC=CC=C2)C1 RFVALKDVKAUSQV-UHFFFAOYSA-N 0.000 description 4
ZEKCCTITMKRCDA-UHFFFAOYSA-N 1-(ethoxymethyl)-7-nitro-5-phenyl-3H-1,4-benzodiazepin-2-one Chemical compound [N+](=O)([O-])C=1C=CC2=C(C(=NCC(N2COCC)=O)C2=CC=CC=C2)C1 ZEKCCTITMKRCDA-UHFFFAOYSA-N 0.000 description 4
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 4
DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 4
230000001773 anti-convulsant effect Effects 0.000 description 4
229960003965 antiepileptics Drugs 0.000 description 4
239000003795 chemical substances by application Substances 0.000 description 4
JWMLCCRPDOIBAV-UHFFFAOYSA-N chloro(methylsulfanyl)methane Chemical compound CSCCl JWMLCCRPDOIBAV-UHFFFAOYSA-N 0.000 description 4
239000013078 crystal Substances 0.000 description 4
230000007062 hydrolysis Effects 0.000 description 4
238000006460 hydrolysis reaction Methods 0.000 description 4
125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 description 4
239000012071 phase Substances 0.000 description 4
239000002904 solvent Substances 0.000 description 4
238000012360 testing method Methods 0.000 description 4
LUTWEKBTDWRTSE-UHFFFAOYSA-N 1-chloro-2-(chloromethoxy)ethane Chemical compound ClCCOCCl LUTWEKBTDWRTSE-UHFFFAOYSA-N 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 3
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 3
CWRVKFFCRWGWCS-UHFFFAOYSA-N Pentrazole Chemical compound C1CCCCC2=NN=NN21 CWRVKFFCRWGWCS-UHFFFAOYSA-N 0.000 description 3
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
150000008065 acid anhydrides Chemical class 0.000 description 3
229910001854 alkali hydroxide Inorganic materials 0.000 description 3
229910052783 alkali metal Inorganic materials 0.000 description 3
150000008044 alkali metal hydroxides Chemical class 0.000 description 3
150000004703 alkoxides Chemical class 0.000 description 3
150000001408 amides Chemical class 0.000 description 3
229940061627 chloromethyl methyl ether Drugs 0.000 description 3
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
230000000694 effects Effects 0.000 description 3
150000008282 halocarbons Chemical class 0.000 description 3
150000004678 hydrides Chemical class 0.000 description 3
238000002955 isolation Methods 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
239000007800 oxidant agent Substances 0.000 description 3
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 3
239000011347 resin Substances 0.000 description 3
229920005989 resin Polymers 0.000 description 3
ODZPKZBBUMBTMG-UHFFFAOYSA-N sodium amide Chemical compound [NH2-].[Na+] ODZPKZBBUMBTMG-UHFFFAOYSA-N 0.000 description 3
235000017550 sodium carbonate Nutrition 0.000 description 3
229910000029 sodium carbonate Inorganic materials 0.000 description 3
239000000126 substance Substances 0.000 description 3
125000001424 substituent group Chemical group 0.000 description 3
239000000725 suspension Substances 0.000 description 3
ANILELZNVKYUSS-UHFFFAOYSA-N 1-(methoxymethyl)-7-nitro-4-oxido-5-phenyl-3H-1,4-benzodiazepin-4-ium-2-one Chemical compound COCN1C(C[N+](=C(C2=C1C=CC(=C2)[N+](=O)[O-])C2=CC=CC=C2)[O-])=O ANILELZNVKYUSS-UHFFFAOYSA-N 0.000 description 2
QWELSYQNDFTISP-UHFFFAOYSA-N 1-chloro-1-methoxyethane Chemical compound COC(C)Cl QWELSYQNDFTISP-UHFFFAOYSA-N 0.000 description 2
125000006012 2-chloroethoxy group Chemical group 0.000 description 2
125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 description 2
125000004198 2-fluorophenyl group Chemical group [H]C1=C([H])C(F)=C(*)C([H])=C1[H] 0.000 description 2
BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 2
LARVUPCHJCRZIC-UHFFFAOYSA-N 7-chloro-1-(methoxymethyl)-4-oxido-5-phenyl-3H-1,4-benzodiazepin-4-ium-2-one Chemical compound ClC=1C=CC2=C(C(=[N+](CC(N2COC)=O)[O-])C2=CC=CC=C2)C1 LARVUPCHJCRZIC-UHFFFAOYSA-N 0.000 description 2
YDLYPIAFWWRAQA-UHFFFAOYSA-N 7-chloro-5-(2-fluorophenyl)-1-(methoxymethyl)-3H-1,4-benzodiazepin-2-one Chemical compound ClC=1C=CC2=C(C(=NCC(N2COC)=O)C2=C(C=CC=C2)F)C1 YDLYPIAFWWRAQA-UHFFFAOYSA-N 0.000 description 2
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
XRILEJTYVMLSKR-UHFFFAOYSA-N ClC=1C=CC2=C(C(=NC(C(N2COC)=O)O)C2=CC=CC=C2)C1 Chemical compound ClC=1C=CC2=C(C(=NC(C(N2COC)=O)O)C2=CC=CC=C2)C1 XRILEJTYVMLSKR-UHFFFAOYSA-N 0.000 description 2
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Chemical compound 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 2
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 2
238000005903 acid hydrolysis reaction Methods 0.000 description 2
230000010933 acylation Effects 0.000 description 2
238000005917 acylation reaction Methods 0.000 description 2
238000006136 alcoholysis reaction Methods 0.000 description 2
238000005904 alkaline hydrolysis reaction Methods 0.000 description 2
230000029936 alkylation Effects 0.000 description 2
238000005804 alkylation reaction Methods 0.000 description 2
239000007864 aqueous solution Substances 0.000 description 2
125000003435 aroyl group Chemical group 0.000 description 2
150000001557 benzodiazepines Chemical class 0.000 description 2
125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 2
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
229910052794 bromium Inorganic materials 0.000 description 2
229910052799 carbon Inorganic materials 0.000 description 2
238000009903 catalytic hydrogenation reaction Methods 0.000 description 2
CHIFCDOIPRCHCF-UHFFFAOYSA-N delorazepam Chemical compound C12=CC(Cl)=CC=C2NC(=O)CN=C1C1=CC=CC=C1Cl CHIFCDOIPRCHCF-UHFFFAOYSA-N 0.000 description 2
FJKIXWOMBXYWOQ-UHFFFAOYSA-N ethenoxyethane Chemical compound CCOC=C FJKIXWOMBXYWOQ-UHFFFAOYSA-N 0.000 description 2
SRCZQMGIVIYBBJ-UHFFFAOYSA-N ethoxyethane;ethyl acetate Chemical compound CCOCC.CCOC(C)=O SRCZQMGIVIYBBJ-UHFFFAOYSA-N 0.000 description 2
ZKQFHRVKCYFVCN-UHFFFAOYSA-N ethoxyethane;hexane Chemical compound CCOCC.CCCCCC ZKQFHRVKCYFVCN-UHFFFAOYSA-N 0.000 description 2
WBTKTOHWTWDQCC-UHFFFAOYSA-N ethyl 7-chloro-1-(methoxymethyl)-2-oxo-5-phenyl-3H-1,4-benzodiazepine-3-carboxylate Chemical compound CCOC(=O)C1N=C(C2=CC=CC=C2)C2=CC(Cl)=CC=C2N(COC)C1=O WBTKTOHWTWDQCC-UHFFFAOYSA-N 0.000 description 2
OAYLNYINCPYISS-UHFFFAOYSA-N ethyl acetate;hexane Chemical compound CCCCCC.CCOC(C)=O OAYLNYINCPYISS-UHFFFAOYSA-N 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
239000012467 final product Substances 0.000 description 2
150000004820 halides Chemical class 0.000 description 2
238000006317 isomerization reaction Methods 0.000 description 2
HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 description 2
239000002609 medium Substances 0.000 description 2
BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
239000002480 mineral oil Substances 0.000 description 2
235000010446 mineral oil Nutrition 0.000 description 2
230000004048 modification Effects 0.000 description 2
238000012986 modification Methods 0.000 description 2
239000012452 mother liquor Substances 0.000 description 2
AKPLHCDWDRPJGD-UHFFFAOYSA-N nordazepam Chemical compound C12=CC(Cl)=CC=C2NC(=O)CN=C1C1=CC=CC=C1 AKPLHCDWDRPJGD-UHFFFAOYSA-N 0.000 description 2
150000007524 organic acids Chemical class 0.000 description 2
150000004965 peroxy acids Chemical class 0.000 description 2
239000000825 pharmaceutical preparation Substances 0.000 description 2
229910052698 phosphorus Inorganic materials 0.000 description 2
239000011574 phosphorus Substances 0.000 description 2
125000005543 phthalimide group Chemical group 0.000 description 2
238000012545 processing Methods 0.000 description 2
239000011877 solvent mixture Substances 0.000 description 2
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 2
238000010626 work up procedure Methods 0.000 description 2
RBIIKVXVYVANCQ-CUWPLCDZSA-N (2s,4s,5s)-5-amino-n-(3-amino-2,2-dimethyl-3-oxopropyl)-6-[4-(2-chlorophenyl)-2,2-dimethyl-5-oxopiperazin-1-yl]-4-hydroxy-2-propan-2-ylhexanamide Chemical compound C1C(C)(C)N(C[C@H](N)[C@@H](O)C[C@@H](C(C)C)C(=O)NCC(C)(C)C(N)=O)CC(=O)N1C1=CC=CC=C1Cl RBIIKVXVYVANCQ-CUWPLCDZSA-N 0.000 description 1
USVVENVKYJZFMW-ONEGZZNKSA-N (e)-carboxyiminocarbamic acid Chemical class OC(=O)\N=N\C(O)=O USVVENVKYJZFMW-ONEGZZNKSA-N 0.000 description 1
AQTWOCCPBLHBEY-UHFFFAOYSA-N 1,1,1,3-tetrachloro-2-(1,1,1,3-tetrachloropropan-2-yloxy)propane Chemical compound ClCC(C(Cl)(Cl)Cl)OC(CCl)C(Cl)(Cl)Cl AQTWOCCPBLHBEY-UHFFFAOYSA-N 0.000 description 1
VNCFXJZJWFZZGY-UHFFFAOYSA-N 1-(1-ethoxyethyl)-7-nitro-5-phenyl-3H-1,4-benzodiazepin-2-one Chemical compound C(C)OC(C)N1C(CN=C(C2=C1C=CC(=C2)[N+](=O)[O-])C2=CC=CC=C2)=O VNCFXJZJWFZZGY-UHFFFAOYSA-N 0.000 description 1
SMBJEZLHGIEKIR-UHFFFAOYSA-N 1-(1-methoxyethyl)-7-nitro-5-phenyl-3H-1,4-benzodiazepin-2-one Chemical compound COC(C)N1C(CN=C(C2=C1C=CC(=C2)[N+](=O)[O-])C2=CC=CC=C2)=O SMBJEZLHGIEKIR-UHFFFAOYSA-N 0.000 description 1
AGDIDCDJVCRQCJ-UHFFFAOYSA-N 1-(chloromethoxy)hexane Chemical compound CCCCCCOCCl AGDIDCDJVCRQCJ-UHFFFAOYSA-N 0.000 description 1
KSBCMTMWFZJSKL-UHFFFAOYSA-N 1-(methylsulfanylmethyl)-7-nitro-5-phenyl-3H-1,4-benzodiazepin-2-one Chemical compound CSCN1C2=CC=C(C=C2C(=NCC1=O)C1=CC=CC=C1)[N+]([O-])=O KSBCMTMWFZJSKL-UHFFFAOYSA-N 0.000 description 1
WJYXMFSAHFWRCA-UHFFFAOYSA-N 1-(methylsulfinylmethyl)-7-nitro-5-phenyl-3h-1,4-benzodiazepin-2-one Chemical compound N=1CC(=O)N(CS(=O)C)C2=CC=C([N+]([O-])=O)C=C2C=1C1=CC=CC=C1 WJYXMFSAHFWRCA-UHFFFAOYSA-N 0.000 description 1
IFMYFXJJIIGOIS-UHFFFAOYSA-N 1-(pyridin-3-ylmethyl)piperidin-4-amine;trihydrochloride Chemical compound Cl.Cl.Cl.C1CC(N)CCN1CC1=CC=CN=C1 IFMYFXJJIIGOIS-UHFFFAOYSA-N 0.000 description 1
URGLIMIKUNFFMT-UHFFFAOYSA-N 1-chloro-1-ethoxyethane Chemical compound CCOC(C)Cl URGLIMIKUNFFMT-UHFFFAOYSA-N 0.000 description 1
LBLYYCQCTBFVLH-UHFFFAOYSA-N 2-Methylbenzenesulfonic acid Chemical compound CC1=CC=CC=C1S(O)(=O)=O LBLYYCQCTBFVLH-UHFFFAOYSA-N 0.000 description 1
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 1
NXOPPEVVHROAKQ-UHFFFAOYSA-N 5-(2-chlorophenyl)-1-(methoxymethyl)-7-nitro-3h-1,4-benzodiazepin-2-one Chemical compound N=1CC(=O)N(COC)C2=CC=C([N+]([O-])=O)C=C2C=1C1=CC=CC=C1Cl NXOPPEVVHROAKQ-UHFFFAOYSA-N 0.000 description 1
LLSSRQADOWGWCE-UHFFFAOYSA-N 7-chloro-1-(1-methoxyethyl)-5-phenyl-3H-1,4-benzodiazepin-2-one Chemical compound COC(C)N1C2=CC=C(Cl)C=C2C(=NCC1=O)C1=CC=CC=C1 LLSSRQADOWGWCE-UHFFFAOYSA-N 0.000 description 1
QITBHQXQJULEIL-UHFFFAOYSA-N 7-chloro-1-(methylsulfanylmethyl)-5-phenyl-3h-1,4-benzodiazepin-2-one Chemical compound N=1CC(=O)N(CSC)C2=CC=C(Cl)C=C2C=1C1=CC=CC=C1 QITBHQXQJULEIL-UHFFFAOYSA-N 0.000 description 1
UYQKAAVANZLHCA-UHFFFAOYSA-N 7-chloro-1-(methylsulfinylmethyl)-5-phenyl-3h-1,4-benzodiazepin-2-one Chemical compound N=1CC(=O)N(CS(=O)C)C2=CC=C(Cl)C=C2C=1C1=CC=CC=C1 UYQKAAVANZLHCA-UHFFFAOYSA-N 0.000 description 1
NDJGAFQWMURJLX-UHFFFAOYSA-N 7-chloro-5-(2-chlorophenyl)-1-(methoxymethyl)-3h-1,4-benzodiazepin-2-one Chemical compound N=1CC(=O)N(COC)C2=CC=C(Cl)C=C2C=1C1=CC=CC=C1Cl NDJGAFQWMURJLX-UHFFFAOYSA-N 0.000 description 1
NJZQRLHMKHSIEX-UHFFFAOYSA-N 7-chloro-5-(2-chlorophenyl)-1-(methylsulfinylmethyl)-3h-1,4-benzodiazepin-2-one Chemical compound N=1CC(=O)N(CS(=O)C)C2=CC=C(Cl)C=C2C=1C1=CC=CC=C1Cl NJZQRLHMKHSIEX-UHFFFAOYSA-N 0.000 description 1
XGUUGSIHCHNCJY-UHFFFAOYSA-N 7-nitro-5-phenyl-1-(2,2,2-trichloroethoxymethyl)-3H-1,4-benzodiazepin-2-one Chemical compound [N+](=O)([O-])C=1C=CC2=C(C(=NCC(N2COCC(Cl)(Cl)Cl)=O)C2=CC=CC=C2)C1 XGUUGSIHCHNCJY-UHFFFAOYSA-N 0.000 description 1
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
DGHPGDOXTYFOLQ-UHFFFAOYSA-N C(CCCCC)OCN1C(CN=C(C2=C1C=CC(=C2)[N+](=O)[O-])C2=CC=CC=C2)=O Chemical compound C(CCCCC)OCN1C(CN=C(C2=C1C=CC(=C2)[N+](=O)[O-])C2=CC=CC=C2)=O DGHPGDOXTYFOLQ-UHFFFAOYSA-N 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
108010010803 Gelatin Proteins 0.000 description 1
AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
241000699670 Mus sp. Species 0.000 description 1
PCLIMKBDDGJMGD-UHFFFAOYSA-N N-bromosuccinimide Chemical compound BrN1C(=O)CCC1=O PCLIMKBDDGJMGD-UHFFFAOYSA-N 0.000 description 1
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
239000007868 Raney catalyst Substances 0.000 description 1
NPXOKRUENSOPAO-UHFFFAOYSA-N Raney nickel Chemical compound [Al].[Ni] NPXOKRUENSOPAO-UHFFFAOYSA-N 0.000 description 1
229910000564 Raney nickel Inorganic materials 0.000 description 1
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
229920002472 Starch Polymers 0.000 description 1
KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 1
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
229960001413 acetanilide Drugs 0.000 description 1
239000003377 acid catalyst Substances 0.000 description 1
238000010306 acid treatment Methods 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
125000005041 acyloxyalkyl group Chemical group 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
229910000102 alkali metal hydride Inorganic materials 0.000 description 1
150000008046 alkali metal hydrides Chemical class 0.000 description 1
125000004849 alkoxymethyl group Chemical group 0.000 description 1
229910000147 aluminium phosphate Inorganic materials 0.000 description 1
150000008064 anhydrides Chemical class 0.000 description 1
229940125681 anticonvulsant agent Drugs 0.000 description 1
239000002249 anxiolytic agent Substances 0.000 description 1
230000000949 anxiolytic effect Effects 0.000 description 1
229940005530 anxiolytics Drugs 0.000 description 1
239000012736 aqueous medium Substances 0.000 description 1
239000008346 aqueous phase Substances 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
239000012965 benzophenone Substances 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
238000009835 boiling Methods 0.000 description 1
239000000872 buffer Substances 0.000 description 1
KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
125000004063 butyryl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000002775 capsule Substances 0.000 description 1
125000001589 carboacyl group Chemical group 0.000 description 1
150000001718 carbodiimides Chemical class 0.000 description 1
150000001721 carbon Chemical group 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
239000012876 carrier material Substances 0.000 description 1
239000003638 chemical reducing agent Substances 0.000 description 1
VXIVSQZSERGHQP-UHFFFAOYSA-N chloroacetamide Chemical compound NC(=O)CCl VXIVSQZSERGHQP-UHFFFAOYSA-N 0.000 description 1
125000002668 chloroacetyl group Chemical group ClCC(=O)* 0.000 description 1
FCYRSDMGOLYDHL-UHFFFAOYSA-N chloromethoxyethane Chemical compound CCOCCl FCYRSDMGOLYDHL-UHFFFAOYSA-N 0.000 description 1
229940117975 chromium trioxide Drugs 0.000 description 1
WGLPBDUCMAPZCE-UHFFFAOYSA-N chromium trioxide Inorganic materials O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 1
GAMDZJFZMJECOS-UHFFFAOYSA-N chromium(6+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Cr+6] GAMDZJFZMJECOS-UHFFFAOYSA-N 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
238000006114 decarboxylation reaction Methods 0.000 description 1
230000018044 dehydration Effects 0.000 description 1
238000006297 dehydration reaction Methods 0.000 description 1
GGRWZBVSUZZMKS-UHFFFAOYSA-N demoxepam Chemical compound C12=CC(Cl)=CC=C2NC(=O)C[N+]([O-])=C1C1=CC=CC=C1 GGRWZBVSUZZMKS-UHFFFAOYSA-N 0.000 description 1
UVCOILFBWYKHHB-UHFFFAOYSA-N desalkylflurazepam Chemical compound FC1=CC=CC=C1C1=NCC(=O)NC2=CC=C(Cl)C=C12 UVCOILFBWYKHHB-UHFFFAOYSA-N 0.000 description 1
WBKFWQBXFREOFH-UHFFFAOYSA-N dichloromethane;ethyl acetate Chemical compound ClCCl.CCOC(C)=O WBKFWQBXFREOFH-UHFFFAOYSA-N 0.000 description 1
SPWVRYZQLGQKGK-UHFFFAOYSA-N dichloromethane;hexane Chemical compound ClCCl.CCCCCC SPWVRYZQLGQKGK-UHFFFAOYSA-N 0.000 description 1
239000008298 dragée Substances 0.000 description 1
239000003814 drug Substances 0.000 description 1
238000001035 drying Methods 0.000 description 1
230000008030 elimination Effects 0.000 description 1
238000003379 elimination reaction Methods 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
MDKXBBPLEGPIRI-UHFFFAOYSA-N ethoxyethane;methanol Chemical compound OC.CCOCC MDKXBBPLEGPIRI-UHFFFAOYSA-N 0.000 description 1
DTKOQJNQMOCKQU-UHFFFAOYSA-N ethyl 7-chloro-2-oxo-5-phenyl-1,3-dihydro-1,4-benzodiazepine-3-carboxylate Chemical compound C12=CC(Cl)=CC=C2NC(=O)C(C(=O)OCC)N=C1C1=CC=CC=C1 DTKOQJNQMOCKQU-UHFFFAOYSA-N 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
239000000284 extract Substances 0.000 description 1
229910052731 fluorine Inorganic materials 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
235000019253 formic acid Nutrition 0.000 description 1
125000000524 functional group Chemical group 0.000 description 1
239000008273 gelatin Substances 0.000 description 1
229920000159 gelatin Polymers 0.000 description 1
235000019322 gelatine Nutrition 0.000 description 1
235000011852 gelatine desserts Nutrition 0.000 description 1
229940093915 gynecological organic acid Drugs 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
238000006698 hydrazinolysis reaction Methods 0.000 description 1
125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
238000005984 hydrogenation reaction Methods 0.000 description 1
150000004679 hydroxides Chemical class 0.000 description 1
239000005457 ice water Substances 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
239000013067 intermediate product Substances 0.000 description 1
239000011630 iodine Substances 0.000 description 1
229910052740 iodine Inorganic materials 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
239000007788 liquid Substances 0.000 description 1
239000012280 lithium aluminium hydride Substances 0.000 description 1
235000019359 magnesium stearate Nutrition 0.000 description 1
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
239000011976 maleic acid Substances 0.000 description 1
239000000463 material Substances 0.000 description 1
239000011707 mineral Substances 0.000 description 1
235000010755 mineral Nutrition 0.000 description 1
150000007522 mineralic acids Chemical class 0.000 description 1
HZAXFHJVJLSVMW-UHFFFAOYSA-N monoethanolamine hydrochloride Natural products NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
229940035363 muscle relaxants Drugs 0.000 description 1
239000003158 myorelaxant agent Substances 0.000 description 1
PBMIETCUUSQZCG-UHFFFAOYSA-N n'-cyclohexylmethanediimine Chemical compound N=C=NC1CCCCC1 PBMIETCUUSQZCG-UHFFFAOYSA-N 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
239000012299 nitrogen atmosphere Substances 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
150000007530 organic bases Chemical class 0.000 description 1
230000003204 osmotic effect Effects 0.000 description 1
MUMZUERVLWJKNR-UHFFFAOYSA-N oxoplatinum Chemical compound [Pt]=O MUMZUERVLWJKNR-UHFFFAOYSA-N 0.000 description 1
125000004430 oxygen atom Chemical group O* 0.000 description 1
230000020477 pH reduction Effects 0.000 description 1
238000007911 parenteral administration Methods 0.000 description 1
DDBREPKUVSBGFI-UHFFFAOYSA-N phenobarbital Chemical compound C=1C=CC=CC=1C1(CC)C(=O)NC(=O)NC1=O DDBREPKUVSBGFI-UHFFFAOYSA-N 0.000 description 1
229960002695 phenobarbital Drugs 0.000 description 1
FAIAAWCVCHQXDN-UHFFFAOYSA-N phosphorus trichloride Chemical compound ClP(Cl)Cl FAIAAWCVCHQXDN-UHFFFAOYSA-N 0.000 description 1
229910003446 platinum oxide Inorganic materials 0.000 description 1
229920001515 polyalkylene glycol Polymers 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
239000003755 preservative agent Substances 0.000 description 1
125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
239000012429 reaction media Substances 0.000 description 1
238000007363 ring formation reaction Methods 0.000 description 1
239000005060 rubber Substances 0.000 description 1
229940125723 sedative agent Drugs 0.000 description 1
239000000932 sedative agent Substances 0.000 description 1
238000007086 side reaction Methods 0.000 description 1
239000000741 silica gel Substances 0.000 description 1
229910002027 silica gel Inorganic materials 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
239000008107 starch Substances 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
239000000829 suppository Substances 0.000 description 1
239000003826 tablet Substances 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
235000012222 talc Nutrition 0.000 description 1
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
229940099259 vaseline Drugs 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
239000008158 vegetable oil Substances 0.000 description 1
210000003462 vein Anatomy 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
239000011701 zinc Substances 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
- C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
- C07C271/10—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C271/22—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of hydrocarbon radicals substituted by carboxyl groups
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
- C07D209/12—Radicals substituted by oxygen atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K1/00—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
- C07K1/006—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length of peptides containing derivatised side chain amino acids
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Analytical Chemistry (AREA)
Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Biochemistry (AREA)
Biophysics (AREA)
General Health & Medical Sciences (AREA)
Genetics & Genomics (AREA)
Medicinal Chemistry (AREA)
Molecular Biology (AREA)
Proteomics, Peptides & Aminoacids (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Nitrogen Condensed Heterocyclic Rings (AREA)
Plural Heterocyclic Compounds (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Pyridine Compounds (AREA)

NO00292/73A 1969-02-14 1973-01-24 NO128110B (fr)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH225569A CH562220A5 (fr)	1969-02-14	1969-02-14

Publications (1)

Publication Number	Publication Date
NO128110B true NO128110B (fr)	1973-10-01

Family

ID=4229492

Family Applications (2)

Application Number	Title	Priority Date	Filing Date
NO00510/70A NO128328B (fr)	1969-02-14	1970-02-13
NO00292/73A NO128110B (fr)	1969-02-14	1973-01-24

Family Applications Before (1)

Application Number	Title	Priority Date	Filing Date
NO00510/70A NO128328B (fr)	1969-02-14	1970-02-13

Country Status (23)

Country	Link
AT (10)	AT302316B (fr)
BE (1)	BE745852A (fr)
BR (1)	BR6915093D0 (fr)
CA (1)	CA971960A (fr)
CH (1)	CH562220A5 (fr)
CS (1)	CS159260B2 (fr)
DE (1)	DE2005508A1 (fr)
DK (1)	DK137899B (fr)
DO (1)	DOP1970001703A (fr)
ES (1)	ES376528A1 (fr)
FI (1)	FI49965C (fr)
FR (1)	FR2034550B1 (fr)
GB (5)	GB1306455A (fr)
IE (2)	IE33988B1 (fr)
IL (2)	IL33821A (fr)
IS (1)	IS1906A7 (fr)
NL (1)	NL156401B (fr)
NO (2)	NO128328B (fr)
OA (1)	OA03435A (fr)
PL (1)	PL80826B1 (fr)
RO (5)	RO57160A (fr)
SE (1)	SE358393B (fr)
SU (12)	SU415880A3 (fr)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
BE787117A (fr) *	1971-08-04	1973-02-05	Hoffmann La Roche	Derives de benzodiazepine
JPS4867288A (fr) *	1971-12-14	1973-09-13
US3932637A (en) *	1974-07-22	1976-01-13	Sumitomo Chemical Company, Limited	Methods and compositions for improving the feed intake of meat producing animals
CA1163266A (fr) *	1980-07-31	1984-03-06	Albert E. Fischli	Derives de benzodiazepine

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3136815A (en) *	1959-12-10	1964-06-09	Hoffmann La Roche	Amino substituted benzophenone oximes and derivatives thereof

1969
- 1969-02-14 CH CH225569A patent/CH562220A5/xx not_active IP Right Cessation
- 1969-12-15 BR BR215093/69A patent/BR6915093D0/pt unknown
1970
- 1970-02-02 IL IL33821A patent/IL33821A/xx unknown
- 1970-02-04 CA CA073,934A patent/CA971960A/en not_active Expired
- 1970-02-05 OA OA53847A patent/OA03435A/fr unknown
- 1970-02-06 IE IE156/70A patent/IE33988B1/xx unknown
- 1970-02-06 IE IE618/73A patent/IE33991B1/xx unknown
- 1970-02-06 DE DE19702005508 patent/DE2005508A1/de not_active Ceased
- 1970-02-10 SU SU1691525A patent/SU415880A3/ru active
- 1970-02-10 SU SU1400104A patent/SU497774A3/ru active
- 1970-02-10 SU SU1665719A patent/SU431673A3/ru active
- 1970-02-10 SU SU1658463A patent/SU406359A3/ru active
- 1970-02-10 SU SU1691944A patent/SU402219A3/ru active
- 1970-02-10 SU SU1691526A patent/SU421195A3/ru active
- 1970-02-10 SU SU1691948A patent/SU453841A3/ru active
- 1970-02-10 SU SU1691947A patent/SU406360A3/ru active
- 1970-02-10 SU SU1666627A patent/SU428603A3/ru active
- 1970-02-10 SU SU1670155A patent/SU430552A3/ru active
- 1970-02-10 SU SU1691943A patent/SU404253A3/ru active
- 1970-02-11 GB GB4314272A patent/GB1306455A/en not_active Expired
- 1970-02-11 CS CS95470*#A patent/CS159260B2/cs unknown
- 1970-02-11 GB GB6675372A patent/GB1306454A/en not_active Expired
- 1970-02-11 GB GB645070A patent/GB1306451A/en not_active Expired
- 1970-02-11 GB GB3375172A patent/GB1306452A/en not_active Expired
- 1970-02-12 IS IS1906A patent/IS1906A7/is unknown
- 1970-02-12 BE BE745852D patent/BE745852A/fr unknown
- 1970-02-12 DO DO1970001703A patent/DOP1970001703A/es unknown
- 1970-02-13 DK DK72870AA patent/DK137899B/da not_active Application Discontinuation
- 1970-02-13 FI FI700400A patent/FI49965C/fi active
- 1970-02-13 NO NO00510/70A patent/NO128328B/no unknown
- 1970-02-13 NL NL7002084.A patent/NL156401B/xx not_active IP Right Cessation
- 1970-02-13 AT AT504971A patent/AT302316B/de not_active IP Right Cessation
- 1970-02-13 AT AT505171A patent/AT302317B/de not_active IP Right Cessation
- 1970-02-13 AT AT505671A patent/AT302322B/de not_active IP Right Cessation
- 1970-02-13 AT AT505371A patent/AT302319B/de not_active IP Right Cessation
- 1970-02-13 SE SE01893/70A patent/SE358393B/xx unknown
- 1970-02-13 AT AT505271A patent/AT302318B/de not_active IP Right Cessation
- 1970-02-13 AT AT131770A patent/AT299208B/de not_active IP Right Cessation
- 1970-02-13 AT AT505571A patent/AT302321B/de not_active IP Right Cessation
- 1970-02-13 ES ES376528A patent/ES376528A1/es not_active Expired
- 1970-02-13 AT AT505771A patent/AT302323B/de not_active IP Right Cessation
- 1970-02-13 PL PL1970138780A patent/PL80826B1/pl unknown
- 1970-02-13 AT AT505071A patent/AT301555B/de not_active Expired
- 1970-02-13 AT AT505471A patent/AT302320B/de not_active IP Right Cessation
- 1970-02-13 FR FR707005175A patent/FR2034550B1/fr not_active Expired
- 1970-02-14 RO RO68266A patent/RO57160A/ro unknown
- 1970-02-14 RO RO68269A patent/RO57161A/ro unknown
- 1970-02-14 RO RO62467A patent/RO58075A/ro unknown
- 1970-02-14 RO RO68268A patent/RO57030A/ro unknown
- 1970-02-14 RO RO68267A patent/RO57028A/ro unknown
- 1970-05-12 GB GB3385272A patent/GB1306453A/en not_active Expired
1971
- 1971-05-13 SU SU1657960A patent/SU517258A3/ru active
1973
- 1973-01-24 NO NO00292/73A patent/NO128110B/no unknown
- 1973-05-22 IL IL7342330A patent/IL42330A0/xx unknown

Also Published As

Publication number	Publication date
IE33988L (en)	1970-08-14
DK137899C (fr)	1978-10-30
SU497774A3 (ru)	1975-12-30
NL7002084A (fr)	1970-08-18
RO57160A (fr)	1974-12-11
SU406359A3 (fr)	1973-11-05
RO57030A (fr)	1975-01-15
SU404253A3 (fr)	1973-10-26
IL42330A0 (en)	1973-07-30
ES376528A1 (es)	1972-04-16
SU428603A3 (ru)	1974-05-15
AT302323B (de)	1972-10-10
AT302316B (de)	1972-10-10
AT302322B (de)	1972-10-10
CA971960A (en)	1975-07-29
IE33988B1 (en)	1974-12-30
NO128328B (fr)	1973-10-29
DK137899B (da)	1978-05-29
AT299208B (de)	1972-06-12
SU517258A3 (ru)	1976-06-05
FR2034550B1 (fr)	1974-02-22
SU431673A3 (fr)	1974-06-05
CH562220A5 (fr)	1975-05-30
AT302320B (de)	1972-10-10
AT302317B (de)	1972-10-10
IL33821A0 (en)	1970-04-20
FI49965B (fr)	1975-07-31
AT302321B (de)	1972-10-10
SE358393B (fr)	1973-07-30
BE745852A (fr)	1970-08-12
SU415880A3 (ru)	1974-02-15
IS1906A7 (is)	1970-08-15
OA03435A (fr)	1971-03-30
IE33991B1 (en)	1974-12-30
BR6915093D0 (pt)	1973-03-08
SU453841A3 (ru)	1974-12-15
RO58075A (fr)	1975-06-15
SU421195A3 (ru)	1974-03-25
CS159260B2 (fr)	1974-12-27
GB1306451A (en)	1973-02-14
DOP1970001703A (es)	1975-02-14
FI49965C (fi)	1975-11-10
SU430552A3 (ru)	1974-05-30
RO57161A (fr)	1974-12-11
GB1306453A (en)	1973-02-14
NL156401B (nl)	1978-04-17
AT301555B (de)	1972-09-11
AT302318B (de)	1972-10-10
IL33821A (en)	1974-05-16
SU402219A3 (fr)	1973-10-12
RO57028A (fr)	1974-12-11
GB1306454A (en)	1973-02-14
SU406360A3 (fr)	1973-11-05
DE2005508A1 (de)	1970-08-27
GB1306452A (en)	1973-02-14
PL80826B1 (en)	1975-08-30
GB1306455A (en)	1973-02-14
AT302319B (de)	1972-10-10
FR2034550A1 (fr)	1970-12-11

Publication	Publication Date	Title
US3275644A (en)	1966-09-27	Certain 1-azolylindol-3-ylaliphatic acids
NO153262B (no)	1985-11-04	Fremgangsmaate for fremstilling av en fettblanding.
NO135173B (fr)	1976-11-15
NO147914B (no)	1983-03-28	Mellomprodukt ved fremstilling av farmakologisk aktive imidazol (1,5-a)(1,4)diazepinforbindelser
NO118914B (fr)	1970-03-02
NO128110B (fr)	1973-10-01
US3784542A (en)	1974-01-08	Benzodiazepin-2-ones
US5420153A (en)	1995-05-30	Tetronic, thiotetronic and tetramic acid derivatives as phospholipase A.sub.
NO117366B (fr)	1969-08-04
US3470203A (en)	1969-09-30	Intermediates for preparing 1-aroylindole-3-alkanoic acids
US3201414A (en)	1965-08-17	New 1-heteroacyl-3-indolyl aliphatic acids
NO883339L (no)	1989-01-30	Fremgangsmaate for fremstilling av benzimidazol-2-yl-pyridiniumforbindelser.
US3886214A (en)	1975-05-27	Benzodiazepin-2-ones and processes for the preparation thereof
US3732211A (en)	1973-05-08	1-acyloxyether-1,4-benzodiazepin-2-ones and methods for their preparation
US3296251A (en)	1967-01-03	3-mercapto and 3-substituted mercapto-1, 3-dihydro-2h-1, 4-benzodiazepin-2-ones
US3242185A (en)	1966-03-22	Lower aliphatic acids, salts and derivatives thereof
US3148183A (en)	1964-09-08	Delta4 and delta4, 6-17alpha-acyloxy-20-oxo-steroid-[3, 2-c] pyrazoles of the pregnane series
US4464300A (en)	1984-08-07	Triazolo benzazepines
IL33961A (en)	1973-03-30	Benzodiazepine aminoalkyl carboxylates,their preparation and pharmaceutical compositions containing them
US3634419A (en)	1972-01-11	17-azasteroids
CH573926A5 (en)	1976-03-31	Benzodiazepines
CH573415A5 (en)	1976-03-15	Benzodiazepines
SU404253A1 (fr)
CH574423A5 (en)	1976-04-15	Benzodiazepines
CH574422A5 (en)	1976-04-15	Benzodiazepines