NO784039L - Substituerte 1,3-dihydrospiro(benzo(c)thiofener) - Google Patents

Substituerte 1,3-dihydrospiro(benzo(c)thiofener)

Info

Publication number: NO784039L
Authority: NO; Norway
Prior art keywords: ether; compound; benzo; thiophene; piperidine
Prior art date: 1977-12-02

Application number

NO784039A

Other languages

English (en)

Norwegian (no)

Inventor

Helen Hu Ong

Vernon Brian Anderson

James Arthur Profitt

Original Assignee

Hoechst Ag

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.)

1977-12-02

Filing date

1978-12-01

Publication date

1979-06-06

1978-12-01 Application filed by Hoechst Ag filed Critical Hoechst Ag

1979-06-06 Publication of NO784039L publication Critical patent/NO784039L/no

Links

RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 312
229910052739 hydrogen Inorganic materials 0.000 claims description 162
150000001875 compounds Chemical class 0.000 claims description 81
-1 hydroxy, benzoyloxy Chemical group 0.000 claims description 44
150000003839 salts Chemical class 0.000 claims description 41
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims description 36
238000000034 method Methods 0.000 claims description 35
229910052731 fluorine Inorganic materials 0.000 claims description 28
125000000217 alkyl group Chemical group 0.000 claims description 22
239000011541 reaction mixture Substances 0.000 claims description 21
239000002904 solvent Substances 0.000 claims description 21
239000001257 hydrogen Substances 0.000 claims description 18
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 16
125000004432 carbon atom Chemical group C* 0.000 claims description 16
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 14
238000002360 preparation method Methods 0.000 claims description 14
AHWALFGBDFAJAI-UHFFFAOYSA-N phenyl carbonochloridate Chemical compound ClC(=O)OC1=CC=CC=C1 AHWALFGBDFAJAI-UHFFFAOYSA-N 0.000 claims description 12
239000000460 chlorine Substances 0.000 claims description 8
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 8
125000003545 alkoxy group Chemical group 0.000 claims description 7
125000003884 phenylalkyl group Chemical group 0.000 claims description 7
125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 6
229910052801 chlorine Inorganic materials 0.000 claims description 6
125000006254 cycloalkyl carbonyl group Chemical group 0.000 claims description 6
239000003085 diluting agent Substances 0.000 claims description 6
125000001589 carboacyl group Chemical group 0.000 claims description 5
125000000753 cycloalkyl group Chemical group 0.000 claims description 5
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 5
IPWBFGUBXWMIPR-UHFFFAOYSA-N 1-bromo-2-fluorobenzene Chemical compound FC1=CC=CC=C1Br IPWBFGUBXWMIPR-UHFFFAOYSA-N 0.000 claims description 4
UENWRTRMUIOCKN-UHFFFAOYSA-N benzyl thiol Chemical compound SCC1=CC=CC=C1 UENWRTRMUIOCKN-UHFFFAOYSA-N 0.000 claims description 4
238000009835 boiling Methods 0.000 claims description 4
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
150000001350 alkyl halides Chemical class 0.000 claims description 3
230000003287 optical effect Effects 0.000 claims description 3
239000000825 pharmaceutical preparation Substances 0.000 claims description 3
239000000932 sedative agent Substances 0.000 claims description 3
208000020401 Depressive disease Diseases 0.000 claims description 2
239000002841 Lewis acid Substances 0.000 claims description 2
125000004414 alkyl thio group Chemical group 0.000 claims description 2
CHIHQLCVLOXUJW-UHFFFAOYSA-N benzoic anhydride Chemical compound C=1C=CC=CC=1C(=O)OC(=O)C1=CC=CC=C1 CHIHQLCVLOXUJW-UHFFFAOYSA-N 0.000 claims description 2
PASDCCFISLVPSO-UHFFFAOYSA-N benzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1 PASDCCFISLVPSO-UHFFFAOYSA-N 0.000 claims description 2
230000007062 hydrolysis Effects 0.000 claims description 2
238000006460 hydrolysis reaction Methods 0.000 claims description 2
150000007517 lewis acids Chemical class 0.000 claims description 2
125000004435 hydrogen atom Chemical group [H]* 0.000 claims 11
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 3
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 3
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 3
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 3
229910052794 bromium Inorganic materials 0.000 claims 3
239000011737 fluorine Substances 0.000 claims 3
125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
LKPHQEUGIIWIIQ-UHFFFAOYSA-N 1-(4-fluorophenyl)hex-5-en-1-one Chemical group FC1=CC=C(C(=O)CCCC=C)C=C1 LKPHQEUGIIWIIQ-UHFFFAOYSA-N 0.000 claims 1
GNFTZDOKVXKIBK-UHFFFAOYSA-N 3-(2-methoxyethoxy)benzohydrazide Chemical compound COCCOC1=CC=CC(C(=O)NN)=C1 GNFTZDOKVXKIBK-UHFFFAOYSA-N 0.000 claims 1
230000002378 acidificating effect Effects 0.000 claims 1
150000008064 anhydrides Chemical class 0.000 claims 1
125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 claims 1
125000005359 phenoxyalkyl group Chemical group 0.000 claims 1
230000001624 sedative effect Effects 0.000 claims 1
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 202
229910052757 nitrogen Inorganic materials 0.000 description 146
229910052799 carbon Inorganic materials 0.000 description 144
239000000203 mixture Substances 0.000 description 135
239000000243 solution Substances 0.000 description 128
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 104
125000005605 benzo group Chemical group 0.000 description 86
239000003921 oil Substances 0.000 description 84
235000019198 oils Nutrition 0.000 description 84
NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 83
238000004458 analytical method Methods 0.000 description 72
HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 68
CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 64
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 55
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 52
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 49
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 45
UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 42
NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 42
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 40
CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 39
239000012458 free base Substances 0.000 description 38
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 36
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 33
229910052943 magnesium sulfate Inorganic materials 0.000 description 32
235000019341 magnesium sulphate Nutrition 0.000 description 32
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 29
239000000047 product Substances 0.000 description 28
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 26
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 24
239000007787 solid Substances 0.000 description 23
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 22
KZMGYPLQYOPHEL-UHFFFAOYSA-N Boron trifluoride etherate Chemical compound FB(F)F.CCOCC KZMGYPLQYOPHEL-UHFFFAOYSA-N 0.000 description 22
235000017557 sodium bicarbonate Nutrition 0.000 description 21
229910000030 sodium bicarbonate Inorganic materials 0.000 description 21
239000011780 sodium chloride Substances 0.000 description 21
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 20
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 18
229910000042 hydrogen bromide Inorganic materials 0.000 description 18
239000000843 powder Substances 0.000 description 18
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 18
239000005977 Ethylene Substances 0.000 description 17
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 16
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 16
KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 15
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 15
239000013078 crystal Substances 0.000 description 15
HWJHWSBFPPPIPD-UHFFFAOYSA-N ethoxyethane;propan-2-one Chemical compound CC(C)=O.CCOCC HWJHWSBFPPPIPD-UHFFFAOYSA-N 0.000 description 15
239000005457 ice water Substances 0.000 description 15
239000012312 sodium hydride Substances 0.000 description 15
229910000104 sodium hydride Inorganic materials 0.000 description 15
239000002253 acid Substances 0.000 description 13
238000006243 chemical reaction Methods 0.000 description 13
239000003480 eluent Substances 0.000 description 13
229910052717 sulfur Inorganic materials 0.000 description 13
239000010410 layer Substances 0.000 description 12
238000001953 recrystallisation Methods 0.000 description 12
229920006395 saturated elastomer Polymers 0.000 description 12
239000000741 silica gel Substances 0.000 description 12
229910002027 silica gel Inorganic materials 0.000 description 12
MUVGBRLYRTVCSM-UHFFFAOYSA-N 4-(2-fluorophenyl)-1-methylpiperidin-4-ol Chemical compound C1CN(C)CCC1(O)C1=CC=CC=C1F MUVGBRLYRTVCSM-UHFFFAOYSA-N 0.000 description 11
235000011087 fumaric acid Nutrition 0.000 description 11
239000000725 suspension Substances 0.000 description 11
229960000583 acetic acid Drugs 0.000 description 10
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 9
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 9
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
239000003153 chemical reaction reagent Substances 0.000 description 9
239000002027 dichloromethane extract Substances 0.000 description 9
239000011976 maleic acid Substances 0.000 description 9
238000002844 melting Methods 0.000 description 9
AZUYLZMQTIKGSC-UHFFFAOYSA-N 1-[6-[4-(5-chloro-6-methyl-1H-indazol-4-yl)-5-methyl-3-(1-methylindazol-5-yl)pyrazol-1-yl]-2-azaspiro[3.3]heptan-2-yl]prop-2-en-1-one Chemical compound ClC=1C(=C2C=NNC2=CC=1C)C=1C(=NN(C=1C)C1CC2(CN(C2)C(C=C)=O)C1)C=1C=C2C=NN(C2=CC=1)C AZUYLZMQTIKGSC-UHFFFAOYSA-N 0.000 description 8
239000012362 glacial acetic acid Substances 0.000 description 8
238000010438 heat treatment Methods 0.000 description 8
230000008018 melting Effects 0.000 description 8
238000003756 stirring Methods 0.000 description 8
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 7
150000001412 amines Chemical class 0.000 description 7
238000010828 elution Methods 0.000 description 7
150000002431 hydrogen Chemical group 0.000 description 7
IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 7
229910000041 hydrogen chloride Inorganic materials 0.000 description 7
239000011734 sodium Substances 0.000 description 7
229910052708 sodium Inorganic materials 0.000 description 7
VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 6
MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 6
239000000908 ammonium hydroxide Substances 0.000 description 6
MDKXBBPLEGPIRI-UHFFFAOYSA-N ethoxyethane;methanol Chemical compound OC.CCOCC MDKXBBPLEGPIRI-UHFFFAOYSA-N 0.000 description 6
DLLJVQNYBYOKGS-UHFFFAOYSA-N ethoxyethane;pentane Chemical compound CCCCC.CCOCC DLLJVQNYBYOKGS-UHFFFAOYSA-N 0.000 description 6
239000012044 organic layer Substances 0.000 description 6
TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 6
239000002244 precipitate Substances 0.000 description 6
239000012265 solid product Substances 0.000 description 6
239000003795 chemical substances by application Substances 0.000 description 5
239000012043 crude product Substances 0.000 description 5
239000012259 ether extract Substances 0.000 description 5
239000000706 filtrate Substances 0.000 description 5
238000001914 filtration Methods 0.000 description 5
239000000155 melt Substances 0.000 description 5
LGRLWUINFJPLSH-UHFFFAOYSA-N methanide Chemical compound [CH3-] LGRLWUINFJPLSH-UHFFFAOYSA-N 0.000 description 5
125000006216 methylsulfinyl group Chemical group [H]C([H])([H])S(*)=O 0.000 description 5
239000008188 pellet Substances 0.000 description 5
UXGVMFHEKMGWMA-UHFFFAOYSA-N 2-benzofuran Chemical compound C1=CC=CC2=COC=C21 UXGVMFHEKMGWMA-UHFFFAOYSA-N 0.000 description 4
MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 4
OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 4
RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 4
239000002585 base Substances 0.000 description 4
239000012455 biphasic mixture Substances 0.000 description 4
239000002775 capsule Substances 0.000 description 4
238000001816 cooling Methods 0.000 description 4
125000004356 hydroxy functional group Chemical group O* 0.000 description 4
150000002689 maleic acids Chemical class 0.000 description 4
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
LBYBALOVMJPDIW-UHFFFAOYSA-N 1-(4-chlorophenyl)spiro[1h-2-benzothiophene-3,4'-piperidine] Chemical compound C1=CC(Cl)=CC=C1C1C2=CC=CC=C2C2(CCNCC2)S1 LBYBALOVMJPDIW-UHFFFAOYSA-N 0.000 description 3
LYTMVABTDYMBQK-UHFFFAOYSA-N 2-benzothiophene Chemical compound C1=CC=CC2=CSC=C21 LYTMVABTDYMBQK-UHFFFAOYSA-N 0.000 description 3
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 3
WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
241000124008 Mammalia Species 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
239000008346 aqueous phase Substances 0.000 description 3
SLUNEGLMXGHOLY-UHFFFAOYSA-N benzene;hexane Chemical compound CCCCCC.C1=CC=CC=C1 SLUNEGLMXGHOLY-UHFFFAOYSA-N 0.000 description 3
230000037396 body weight Effects 0.000 description 3
239000006185 dispersion Substances 0.000 description 3
230000000694 effects Effects 0.000 description 3
ZKQFHRVKCYFVCN-UHFFFAOYSA-N ethoxyethane;hexane Chemical compound CCOCC.CCCCCC ZKQFHRVKCYFVCN-UHFFFAOYSA-N 0.000 description 3
239000000284 extract Substances 0.000 description 3
229910052736 halogen Inorganic materials 0.000 description 3
150000002367 halogens Chemical group 0.000 description 3
150000002688 maleic acid derivatives Chemical class 0.000 description 3
239000012074 organic phase Substances 0.000 description 3
239000012071 phase Substances 0.000 description 3
238000000746 purification Methods 0.000 description 3
239000000126 substance Substances 0.000 description 3
MKJIEFSOBYUXJB-HOCLYGCPSA-N (3S,11bS)-9,10-dimethoxy-3-isobutyl-1,3,4,6,7,11b-hexahydro-2H-pyrido[2,1-a]isoquinolin-2-one Chemical compound C1CN2C[C@H](CC(C)C)C(=O)C[C@H]2C2=C1C=C(OC)C(OC)=C2 MKJIEFSOBYUXJB-HOCLYGCPSA-N 0.000 description 2
QVVIRWZJPSLRTI-UHFFFAOYSA-N 1-(3,4-dichlorophenyl)spiro[1h-2-benzothiophene-3,4'-piperidine] Chemical compound C1=C(Cl)C(Cl)=CC=C1C1C2=CC=CC=C2C2(CCNCC2)S1 QVVIRWZJPSLRTI-UHFFFAOYSA-N 0.000 description 2
HUUPVABNAQUEJW-UHFFFAOYSA-N 1-methylpiperidin-4-one Chemical compound CN1CCC(=O)CC1 HUUPVABNAQUEJW-UHFFFAOYSA-N 0.000 description 2
PAMIQIKDUOTOBW-UHFFFAOYSA-N 1-methylpiperidine Chemical compound CN1CCCCC1 PAMIQIKDUOTOBW-UHFFFAOYSA-N 0.000 description 2
SLPUTJFVMJPMKV-UHFFFAOYSA-N 1-methylpyrrolidin-3-one Chemical compound CN1CCC(=O)C1 SLPUTJFVMJPMKV-UHFFFAOYSA-N 0.000 description 2
RVRFZPWZHBSUEN-UHFFFAOYSA-N 1-phenylspiro[1h-2-benzothiophene-3,4'-piperidine] Chemical compound C1CNCCC21C1=CC=CC=C1C(C=1C=CC=CC=1)S2 RVRFZPWZHBSUEN-UHFFFAOYSA-N 0.000 description 2
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 2
VKOARTZZDBBIGG-UHFFFAOYSA-N 4-(2,5-difluorophenyl)-1-methylpiperidin-4-ol Chemical compound C1CN(C)CCC1(O)C1=CC(F)=CC=C1F VKOARTZZDBBIGG-UHFFFAOYSA-N 0.000 description 2
ORRMRODLTDXQKV-UHFFFAOYSA-N 4-[1-(2-chlorophenyl)spiro[1h-2-benzothiophene-3,4'-piperidine]-1'-yl]-1-(4-fluorophenyl)butan-1-one;ethene Chemical group C=C.C1=CC(F)=CC=C1C(=O)CCCN1CCC2(C3=CC=CC=C3C(S2)C=2C(=CC=CC=2)Cl)CC1 ORRMRODLTDXQKV-UHFFFAOYSA-N 0.000 description 2
ZOXJGFHDIHLPTG-BJUDXGSMSA-N Boron-10 Chemical compound [10B] ZOXJGFHDIHLPTG-BJUDXGSMSA-N 0.000 description 2
108010010803 Gelatin Proteins 0.000 description 2
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
241000699670 Mus sp. Species 0.000 description 2
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 2
229930006000 Sucrose Natural products 0.000 description 2
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 2
239000004480 active ingredient Substances 0.000 description 2
125000003342 alkenyl group Chemical group 0.000 description 2
125000004453 alkoxycarbonyl group Chemical group 0.000 description 2
239000000935 antidepressant agent Substances 0.000 description 2
229940005513 antidepressants Drugs 0.000 description 2
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 2
239000012230 colorless oil Substances 0.000 description 2
238000004440 column chromatography Methods 0.000 description 2
238000002425 crystallisation Methods 0.000 description 2
230000008025 crystallization Effects 0.000 description 2
125000001316 cycloalkyl alkyl group Chemical group 0.000 description 2
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XXXVLCJYTVYXPB-UHFFFAOYSA-N ethene;1-(4-fluorophenyl)-4-[1-(2-fluorophenyl)spiro[1h-2-benzothiophene-3,4'-piperidine]-1'-yl]butan-1-one Chemical group C=C.C1=CC(F)=CC=C1C(=O)CCCN1CCC2(C3=CC=CC=C3C(S2)C=2C(=CC=CC=2)F)CC1 XXXVLCJYTVYXPB-UHFFFAOYSA-N 0.000 description 2
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CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 1
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KYAIBVZDNUDUJE-UHFFFAOYSA-N spiro[1h-2-benzothiophene-3,4'-piperidine] Chemical compound C12=CC=CC=C2CSC21CCNCC2 KYAIBVZDNUDUJE-UHFFFAOYSA-N 0.000 description 1
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Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/10—Spiro-condensed systems
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/24—Antidepressants
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/26—Psychostimulants, e.g. nicotine, ***e
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D211/40—Oxygen atoms
- C07D211/44—Oxygen atoms attached in position 4
- C07D211/52—Oxygen atoms attached in position 4 having an aryl radical as the second substituent in position 4
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D211/54—Sulfur atoms

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Medicinal Chemistry (AREA)
Psychiatry (AREA)
Neurology (AREA)
Neurosurgery (AREA)
Bioinformatics & Cheminformatics (AREA)
Chemical Kinetics & Catalysis (AREA)
General Chemical & Material Sciences (AREA)
Engineering & Computer Science (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Biomedical Technology (AREA)
Pharmacology & Pharmacy (AREA)
Life Sciences & Earth Sciences (AREA)
Animal Behavior & Ethology (AREA)
General Health & Medical Sciences (AREA)
Public Health (AREA)
Veterinary Medicine (AREA)
Pain & Pain Management (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)

NO784039A 1977-12-02 1978-12-01 Substituerte 1,3-dihydrospiro(benzo(c)thiofener) NO784039L (no)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US85717777A	1977-12-02	1977-12-02
US94890878A	1978-10-05	1978-10-05

Publications (1)

Publication Number	Publication Date
NO784039L true NO784039L (no)	1979-06-06

Family

ID=27127396

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO784039A NO784039L (no)	1977-12-02	1978-12-01	Substituerte 1,3-dihydrospiro(benzo(c)thiofener)

Country Status (15)

Country	Link
EP (1)	EP0002283B1 (fi)
JP (1)	JPS5498775A (fi)
AT (1)	AT371468B (fi)
AU (1)	AU522997B2 (fi)
CA (1)	CA1122985A (fi)
DE (1)	DE2862307D1 (fi)
DK (1)	DK547278A (fi)
EG (1)	EG13536A (fi)
FI (1)	FI783664A (fi)
GR (1)	GR74052B (fi)
HU (1)	HU179984B (fi)
IL (1)	IL56094A0 (fi)
NO (1)	NO784039L (fi)
NZ (1)	NZ189057A (fi)
PT (1)	PT68855A (fi)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR2519636A2 (en) *	1982-01-14	1983-07-18	Delalande Sa	Spiro iso:benzofuran and iso:benzothiophene derivs. - with anticonvulsant and analgesic activities
FR2498603A1 (fr) *	1981-01-29	1982-07-30	Delalande Sa	Nouveaux derives spiro-1 isobenzofuranniques et spiro-1 isobenzothiopheniques, leur procede de preparation et leur application en therapeutique
NZ243065A (en) *	1991-06-13	1995-07-26	Lundbeck & Co As H	Piperidine derivatives and pharmaceutical compositions

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3959475A (en) *	1973-12-12	1976-05-25	American Hoechst Corporation	Substituted 1,3-dihydrospiro(isobenzofuran)s

1978
- 1978-11-29 EG EG677/78A patent/EG13536A/xx active
- 1978-11-30 AU AU42073/78A patent/AU522997B2/en not_active Expired
- 1978-11-30 NZ NZ189057A patent/NZ189057A/xx unknown
- 1978-11-30 FI FI783664A patent/FI783664A/fi unknown
- 1978-11-30 PT PT68855A patent/PT68855A/pt unknown
- 1978-11-30 IL IL56094A patent/IL56094A0/xx unknown
- 1978-12-01 DK DK547278A patent/DK547278A/da not_active Application Discontinuation
- 1978-12-01 AT AT0860978A patent/AT371468B/de not_active IP Right Cessation
- 1978-12-01 NO NO784039A patent/NO784039L/no unknown
- 1978-12-01 CA CA317,255A patent/CA1122985A/en not_active Expired
- 1978-12-01 HU HU78HO2118A patent/HU179984B/hu unknown
- 1978-12-01 GR GR57790A patent/GR74052B/el unknown
- 1978-12-02 JP JP14865078A patent/JPS5498775A/ja active Pending
- 1978-12-04 EP EP78101554A patent/EP0002283B1/de not_active Expired
- 1978-12-04 DE DE7878101554T patent/DE2862307D1/de not_active Expired

Also Published As

Publication number	Publication date
CA1122985A (en)	1982-05-04
AU522997B2 (en)	1982-07-08
DK547278A (da)	1978-12-01
IL56094A0 (en)	1979-01-31
PT68855A (en)	1978-12-01
ATA860978A (de)	1982-11-15
EP0002283B1 (de)	1983-08-24
JPS5498775A (en)	1979-08-03
AT371468B (de)	1983-06-27
HU179984B (en)	1983-01-28
NZ189057A (en)	1982-03-23
GR74052B (fi)	1984-06-06
AU4207378A (en)	1979-06-07
EG13536A (en)	1981-12-31
DE2862307D1 (en)	1983-09-29
EP0002283A1 (de)	1979-06-13
FI783664A (fi)	1979-06-03

Publication	Publication Date	Title
US3341538A (en)	1967-09-12	Certain 2, 6-methano-3-benzazocines
KR100212231B1 (ko)	1999-08-02	불안 해소 효과를 갖는 피페리딘 유도체
IE902706A1 (en)	1991-02-27	Spirocyclic Antipsychotic Agents
WO2007038138A2 (en)	2007-04-05	Amido compounds and their use as pharmaceuticals
CA1246563A (en)	1988-12-13	3-arylcarbonyl- and 3-cycloalkylcarbonyl-1-aminoalkyl- 1h-indoles useful as analgesics
US4110459A (en)	1978-08-29	Benzoylpiperidylalkylindoles in alleviating pain
CA1055945A (en)	1979-06-05	Pharmaceutical compositions and method of producing antipsychotic activity without extrapyramidal symptoms
CA1132988A (en)	1982-10-05	N-¬3-(4-fluorobenzoyl)propyl\|spiro¬dihydro- benzofuranpiperidine and -pyrrolidine\|s, derivatives thereof, process for their manufacture and their use as medicaments
US4800212A (en)	1989-01-24	Pyrrolidone-2 compounds and anti-hypertensive use thereof
US3320265A (en)	1967-05-16	6-phenyl-1, 2, 3, 4, 5, 6-hexahydro-2, 6-methano-3-benzazocines
US4209625A (en)	1980-06-24	Spiro[indoline-3,4'-piperidine]s
NO784039L (no)	1979-06-06	Substituerte 1,3-dihydrospiro(benzo(c)thiofener)
US4409229A (en)	1983-10-11	Antidepressive and tranquilizing substituted 1,3-dihydrospiro[benzo(c)thiophene]s
US4524207A (en)	1985-06-18	Process for preparing substituted 1,3-dihydrospiro[benzo(c)thiophene]s
US4379933A (en)	1983-04-12	Process for preparing spiro[indoline-3,4'-piperidine]s
US4307235A (en)	1981-12-22	Spiro[indoline-3,4'-piperidine]s
PT93503A (pt)	1990-11-07	Processo para a preparacao de derivados de quinolinicos e de composicoes farmaceuticas que os contem
US4667039A (en)	1987-05-19	11-substituted 5H,11H-pyrrolo(2,1-C) (1,4)benzoxazepines as antipsychotic and analgesic agents
US4345081A (en)	1982-08-17	Spiro[indoline-3,4'-piperidine]s
EP0102034B1 (en)	1988-04-20	Spiro(2h-1,4-benzodioxepin-3(5h)4'-piperidine and 3'-pyrrolidino) compounds, a process for preparing the same and their use as medicaments
HU185633B (en)	1985-03-28	Process for preparing phenyl-quinolizidine derivatives
US4477667A (en)	1984-10-16	Spiro[indoline-3,4'-piperidine]s and related compounds
US4408050A (en)	1983-10-04	Spiro(indoline-3,4'-piperidine) and related compounds
US4379932A (en)	1983-04-12	Process for preparing spiro[indoline-3,4'-piperidine]s
US4024265A (en)	1977-05-17	Benzo[5,6]cyclohepta[1,2-c]pyridines