SK58995A3 - Nitric spirocyclic compounds, method of their production pharmaceutical agents which contains thereof and their use - Google Patents
Nitric spirocyclic compounds, method of their production pharmaceutical agents which contains thereof and their use Download PDFInfo
- Publication number
- SK58995A3 SK58995A3 SK589-95A SK58995A SK58995A3 SK 58995 A3 SK58995 A3 SK 58995A3 SK 58995 A SK58995 A SK 58995A SK 58995 A3 SK58995 A3 SK 58995A3
- Authority
- SK
- Slovakia
- Prior art keywords
- formula
- azaspiro
- nitrogen
- group
- compound
- Prior art date
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- 150000001875 compounds Chemical class 0.000 title claims abstract description 145
- 238000000034 method Methods 0.000 title claims description 25
- 238000004519 manufacturing process Methods 0.000 title claims description 9
- 239000008177 pharmaceutical agent Substances 0.000 title 1
- -1 sulphamoyl Chemical group 0.000 claims abstract description 22
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 21
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 19
- 238000011282 treatment Methods 0.000 claims abstract description 18
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 15
- 150000003839 salts Chemical class 0.000 claims abstract description 13
- 208000019901 Anxiety disease Diseases 0.000 claims abstract description 7
- 208000008589 Obesity Diseases 0.000 claims abstract description 7
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims abstract description 7
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 7
- 230000036506 anxiety Effects 0.000 claims abstract description 7
- 125000001624 naphthyl group Chemical group 0.000 claims abstract description 7
- 235000020824 obesity Nutrition 0.000 claims abstract description 7
- 125000001424 substituent group Chemical group 0.000 claims abstract description 7
- 208000019022 Mood disease Diseases 0.000 claims abstract description 6
- 125000003342 alkenyl group Chemical group 0.000 claims abstract description 3
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims abstract description 3
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims abstract description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 51
- 229910052757 nitrogen Inorganic materials 0.000 claims description 26
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims description 23
- 125000004432 carbon atom Chemical group C* 0.000 claims description 20
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 17
- 229910052739 hydrogen Inorganic materials 0.000 claims description 13
- 239000001257 hydrogen Substances 0.000 claims description 12
- 239000003814 drug Substances 0.000 claims description 11
- 239000008194 pharmaceutical composition Substances 0.000 claims description 10
- AEQNEEYHZFISTP-UHFFFAOYSA-N 5-(4-chlorophenyl)-1-azaspiro[5.5]undec-4-ene Chemical compound C1=CC(Cl)=CC=C1C1=CCCNC11CCCCC1 AEQNEEYHZFISTP-UHFFFAOYSA-N 0.000 claims description 9
- 238000002360 preparation method Methods 0.000 claims description 9
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 7
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 7
- 125000004189 3,4-dichlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(Cl)C([H])=C1* 0.000 claims description 4
- 125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 claims description 4
- 239000003153 chemical reaction reagent Substances 0.000 claims description 4
- 229910052801 chlorine Inorganic materials 0.000 claims description 4
- 125000005843 halogen group Chemical group 0.000 claims description 4
- 125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 claims description 3
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 3
- 229910052731 fluorine Inorganic materials 0.000 claims description 3
- 125000001153 fluoro group Chemical group F* 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- 125000002524 organometallic group Chemical group 0.000 claims description 3
- 125000006595 (C1-C3) alkylsulfinyl group Chemical group 0.000 claims description 2
- 125000004455 (C1-C3) alkylthio group Chemical group 0.000 claims description 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 2
- IMYYHIKSXBGUMR-UHFFFAOYSA-N 10-(4-chlorophenyl)-6-azaspiro[4.5]dec-9-ene Chemical compound C1=CC(Cl)=CC=C1C1=CCCNC11CCCC1 IMYYHIKSXBGUMR-UHFFFAOYSA-N 0.000 claims description 2
- 125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 claims description 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 2
- OVEXPYLNKKNTRR-UHFFFAOYSA-N 4-(1-azaspiro[5.5]undec-4-en-5-yl)phenol Chemical compound C1=CC(O)=CC=C1C1=CCCNC11CCCCC1 OVEXPYLNKKNTRR-UHFFFAOYSA-N 0.000 claims description 2
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims description 2
- 125000004203 4-hydroxyphenyl group Chemical group [H]OC1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 claims description 2
- JVZGGPPZXNLGDH-UHFFFAOYSA-N 5-(3,4-dichlorophenyl)-1-azaspiro[5.5]undec-4-ene Chemical compound C1=C(Cl)C(Cl)=CC=C1C1=CCCNC11CCCCC1 JVZGGPPZXNLGDH-UHFFFAOYSA-N 0.000 claims description 2
- AHLYCRMSQUMMHN-UHFFFAOYSA-N 5-(3-chlorophenyl)-1-azaspiro[5.5]undec-4-ene Chemical compound ClC1=CC=CC(C=2C3(CCCCC3)NCCC=2)=C1 AHLYCRMSQUMMHN-UHFFFAOYSA-N 0.000 claims description 2
- BUWCCHHWRDLWDT-UHFFFAOYSA-N 5-(4-chlorophenyl)-1-(2-methoxyethyl)-1-azaspiro[5.5]undec-4-ene Chemical compound C1CCCCC11N(CCOC)CCC=C1C1=CC=C(Cl)C=C1 BUWCCHHWRDLWDT-UHFFFAOYSA-N 0.000 claims description 2
- VVSWWDQOULQHEP-UHFFFAOYSA-N 5-(4-chlorophenyl)-1-methyl-1-azaspiro[5.5]undec-4-ene Chemical compound C1CCCCC11N(C)CCC=C1C1=CC=C(Cl)C=C1 VVSWWDQOULQHEP-UHFFFAOYSA-N 0.000 claims description 2
- GIQWQGSOQMNOLG-UHFFFAOYSA-N 5-(4-fluorophenyl)-1-azaspiro[5.5]undec-4-ene Chemical compound C1=CC(F)=CC=C1C1=CCCNC11CCCCC1 GIQWQGSOQMNOLG-UHFFFAOYSA-N 0.000 claims description 2
- JBGKFUIOAIZBKS-UHFFFAOYSA-N 5-(4-methoxyphenyl)-1-azaspiro[5.5]undecane Chemical compound C1=CC(OC)=CC=C1C1C2(CCCCC2)NCCC1 JBGKFUIOAIZBKS-UHFFFAOYSA-N 0.000 claims description 2
- MTMFRLUBCJFUIT-UHFFFAOYSA-N 5-(4-phenylphenyl)-1-azaspiro[5.5]undec-4-ene Chemical compound C1CCCCC21C(C=1C=CC(=CC=1)C=1C=CC=CC=1)=CCCN2 MTMFRLUBCJFUIT-UHFFFAOYSA-N 0.000 claims description 2
- IETRNLHYOREMMT-UHFFFAOYSA-N 5-[3-(trifluoromethyl)phenyl]-1-azaspiro[5.5]undec-4-ene Chemical compound FC(F)(F)C1=CC=CC(C=2C3(CCCCC3)NCCC=2)=C1 IETRNLHYOREMMT-UHFFFAOYSA-N 0.000 claims description 2
- AQOOBZOCCPZGPX-UHFFFAOYSA-N 5-naphthalen-2-yl-1-azaspiro[5.5]undec-4-ene Chemical compound C1CCCCC21C(C=1C=C3C=CC=CC3=CC=1)=CCCN2 AQOOBZOCCPZGPX-UHFFFAOYSA-N 0.000 claims description 2
- RTSDKWWFBSVFFY-UHFFFAOYSA-N 5-phenyl-1-azaspiro[5.5]undec-4-ene Chemical compound C1CCCCC21C(C=1C=CC=CC=1)=CCCN2 RTSDKWWFBSVFFY-UHFFFAOYSA-N 0.000 claims description 2
- 239000007818 Grignard reagent Substances 0.000 claims description 2
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims description 2
- SOVOPSCRHKEUNJ-UHFFFAOYSA-N dec-4-ene Chemical compound CCCCCC=CCCC SOVOPSCRHKEUNJ-UHFFFAOYSA-N 0.000 claims description 2
- 239000003085 diluting agent Substances 0.000 claims description 2
- 150000004795 grignard reagents Chemical class 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical class 0.000 claims description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 2
- 150000002900 organolithium compounds Chemical group 0.000 claims description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 2
- SDTYFWAQLSIEBH-UHFFFAOYSA-N undec-3-ene Chemical compound CCCCCCCC=CCC SDTYFWAQLSIEBH-UHFFFAOYSA-N 0.000 claims description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 6
- 208000020401 Depressive disease Diseases 0.000 claims 2
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- 239000011737 fluorine Substances 0.000 claims 1
- 230000007062 hydrolysis Effects 0.000 claims 1
- 238000006460 hydrolysis reaction Methods 0.000 claims 1
- 125000004644 alkyl sulfinyl group Chemical group 0.000 abstract 1
- 125000004414 alkyl thio group Chemical group 0.000 abstract 1
- 125000001589 carboacyl group Chemical group 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 125000001475 halogen functional group Chemical group 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 144
- 239000000203 mixture Substances 0.000 description 123
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 117
- 239000007787 solid Substances 0.000 description 114
- 239000000243 solution Substances 0.000 description 96
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 81
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 76
- 239000002904 solvent Substances 0.000 description 75
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 75
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 70
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 56
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 54
- 238000001914 filtration Methods 0.000 description 46
- 239000000047 product Substances 0.000 description 41
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 39
- 239000000284 extract Substances 0.000 description 36
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 35
- 235000019341 magnesium sulphate Nutrition 0.000 description 35
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 30
- 229920006395 saturated elastomer Polymers 0.000 description 29
- 238000006243 chemical reaction Methods 0.000 description 27
- 238000010992 reflux Methods 0.000 description 27
- 239000003921 oil Substances 0.000 description 22
- 235000019198 oils Nutrition 0.000 description 22
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 20
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 20
- 239000000126 substance Substances 0.000 description 19
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 17
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 16
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 15
- 229910000027 potassium carbonate Inorganic materials 0.000 description 15
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 14
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 13
- 238000004821 distillation Methods 0.000 description 13
- 239000003826 tablet Substances 0.000 description 13
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 12
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 12
- 239000000706 filtrate Substances 0.000 description 12
- 241000700159 Rattus Species 0.000 description 10
- 239000005457 ice water Substances 0.000 description 10
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 9
- 239000003795 chemical substances by application Substances 0.000 description 9
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 9
- 238000002844 melting Methods 0.000 description 9
- 230000008018 melting Effects 0.000 description 9
- 239000000741 silica gel Substances 0.000 description 9
- 229910002027 silica gel Inorganic materials 0.000 description 9
- DNXIKVLOVZVMQF-UHFFFAOYSA-N (3beta,16beta,17alpha,18beta,20alpha)-17-hydroxy-11-methoxy-18-[(3,4,5-trimethoxybenzoyl)oxy]-yohimban-16-carboxylic acid, methyl ester Natural products C1C2CN3CCC(C4=CC=C(OC)C=C4N4)=C4C3CC2C(C(=O)OC)C(O)C1OC(=O)C1=CC(OC)=C(OC)C(OC)=C1 DNXIKVLOVZVMQF-UHFFFAOYSA-N 0.000 description 8
- LCQMZZCPPSWADO-UHFFFAOYSA-N Reserpilin Natural products COC(=O)C1COCC2CN3CCc4c([nH]c5cc(OC)c(OC)cc45)C3CC12 LCQMZZCPPSWADO-UHFFFAOYSA-N 0.000 description 8
- 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 8
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 8
- 235000019270 ammonium chloride Nutrition 0.000 description 8
- 230000037396 body weight Effects 0.000 description 8
- 239000003054 catalyst Substances 0.000 description 8
- 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 8
- 229960003147 reserpine Drugs 0.000 description 8
- 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 8
- 239000011734 sodium Substances 0.000 description 8
- 229910052708 sodium Inorganic materials 0.000 description 8
- 206010015995 Eyelid ptosis Diseases 0.000 description 7
- 241000699670 Mus sp. Species 0.000 description 7
- 238000009835 boiling Methods 0.000 description 7
- 239000002775 capsule Substances 0.000 description 7
- 239000008367 deionised water Substances 0.000 description 7
- 229910021641 deionized water Inorganic materials 0.000 description 7
- 238000003818 flash chromatography Methods 0.000 description 7
- 239000012299 nitrogen atmosphere Substances 0.000 description 7
- 201000003004 ptosis Diseases 0.000 description 7
- SCYVXIWGVDSXFA-UHFFFAOYSA-N 1-azaspiro[5.5]undecan-5-one Chemical compound O=C1CCCNC11CCCCC1 SCYVXIWGVDSXFA-UHFFFAOYSA-N 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 6
- 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 6
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 6
- 239000004480 active ingredient Substances 0.000 description 6
- 239000002585 base Substances 0.000 description 6
- 238000000354 decomposition reaction Methods 0.000 description 6
- KYOSRZBFVVSBKY-UHFFFAOYSA-N ethyl 1-[(4-ethoxy-4-oxobutyl)amino]cyclohexane-1-carboxylate Chemical compound CCOC(=O)CCCNC1(C(=O)OCC)CCCCC1 KYOSRZBFVVSBKY-UHFFFAOYSA-N 0.000 description 6
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 6
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 6
- 229910052938 sodium sulfate Inorganic materials 0.000 description 6
- 235000011152 sodium sulphate Nutrition 0.000 description 6
- 239000000725 suspension Substances 0.000 description 6
- RSJKGSCJYJTIGS-UHFFFAOYSA-N undecane Chemical compound CCCCCCCCCCC RSJKGSCJYJTIGS-UHFFFAOYSA-N 0.000 description 6
- MIOKDJADFPYYIM-UHFFFAOYSA-N 5-(4-chlorophenyl)-1-azaspiro[5.5]undecan-5-ol Chemical compound C=1C=C(Cl)C=CC=1C1(O)CCCNC11CCCCC1 MIOKDJADFPYYIM-UHFFFAOYSA-N 0.000 description 5
- 239000012043 crude product Substances 0.000 description 5
- 239000003480 eluent Substances 0.000 description 5
- 239000012458 free base Substances 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- 230000001225 therapeutic effect Effects 0.000 description 5
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 4
- CDEMHJCJMMOFMB-UHFFFAOYSA-M ClC1=CC=C([Mg]Br)C=C1 Chemical compound ClC1=CC=C([Mg]Br)C=C1 CDEMHJCJMMOFMB-UHFFFAOYSA-M 0.000 description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 4
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 4
- 238000010533 azeotropic distillation Methods 0.000 description 4
- KUAFMPWKUNNUEC-UHFFFAOYSA-N ethyl 1-aminocyclohexane-1-carboxylate Chemical compound CCOC(=O)C1(N)CCCCC1 KUAFMPWKUNNUEC-UHFFFAOYSA-N 0.000 description 4
- XBPOBCXHALHJFP-UHFFFAOYSA-N ethyl 4-bromobutanoate Chemical compound CCOC(=O)CCCBr XBPOBCXHALHJFP-UHFFFAOYSA-N 0.000 description 4
- 239000008187 granular material Substances 0.000 description 4
- 239000000546 pharmaceutical excipient Substances 0.000 description 4
- 239000002244 precipitate Substances 0.000 description 4
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 4
- NHDODQWIKUYWMW-UHFFFAOYSA-N 1-bromo-4-chlorobenzene Chemical compound ClC1=CC=C(Br)C=C1 NHDODQWIKUYWMW-UHFFFAOYSA-N 0.000 description 3
- CYNYIHKIEHGYOZ-UHFFFAOYSA-N 1-bromopropane Chemical compound CCCBr CYNYIHKIEHGYOZ-UHFFFAOYSA-N 0.000 description 3
- 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 3
- WIRHNQRAWGCAKV-UHFFFAOYSA-N 5-(4-chlorophenyl)-1-azaspiro[5.5]undec-4-ene;hydrochloride Chemical compound Cl.C1=CC(Cl)=CC=C1C1=CCCNC11CCCCC1 WIRHNQRAWGCAKV-UHFFFAOYSA-N 0.000 description 3
- JCDFAIIYTCOHPX-UHFFFAOYSA-N 5-(4-methoxyphenyl)-1-azaspiro[5.5]undec-4-ene;hydrochloride Chemical compound Cl.C1=CC(OC)=CC=C1C1=CCCNC11CCCCC1 JCDFAIIYTCOHPX-UHFFFAOYSA-N 0.000 description 3
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- 150000002148 esters Chemical class 0.000 description 1
- FQTIYMRSUOADDK-UHFFFAOYSA-N ethyl 3-bromopropanoate Chemical compound CCOC(=O)CCBr FQTIYMRSUOADDK-UHFFFAOYSA-N 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 230000004399 eye closure Effects 0.000 description 1
- 239000012065 filter cake Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000008098 formaldehyde solution Substances 0.000 description 1
- WBJINCZRORDGAQ-UHFFFAOYSA-N formic acid ethyl ester Natural products CCOC=O WBJINCZRORDGAQ-UHFFFAOYSA-N 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 1
- VZCYOOQTPOCHFL-OWOJBTEDSA-L fumarate(2-) Chemical class [O-]C(=O)\C=C\C([O-])=O VZCYOOQTPOCHFL-OWOJBTEDSA-L 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 239000012362 glacial acetic acid Substances 0.000 description 1
- 235000013922 glutamic acid Nutrition 0.000 description 1
- 239000004220 glutamic acid Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 150000004677 hydrates Chemical class 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 230000002631 hypothermal effect Effects 0.000 description 1
- 239000007943 implant Substances 0.000 description 1
- 239000003701 inert diluent Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000001990 intravenous administration Methods 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- ZLVXBBHTMQJRSX-VMGNSXQWSA-N jdtic Chemical compound C1([C@]2(C)CCN(C[C@@H]2C)C[C@H](C(C)C)NC(=O)[C@@H]2NCC3=CC(O)=CC=C3C2)=CC=CC(O)=C1 ZLVXBBHTMQJRSX-VMGNSXQWSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000003446 ligand Substances 0.000 description 1
- 239000000314 lubricant Substances 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
- 150000002688 maleic acid derivatives Chemical class 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- AFVFQIVMOAPDHO-UHFFFAOYSA-M methanesulfonate group Chemical class CS(=O)(=O)[O-] AFVFQIVMOAPDHO-UHFFFAOYSA-M 0.000 description 1
- 229940098779 methanesulfonic acid Drugs 0.000 description 1
- 230000011987 methylation Effects 0.000 description 1
- 238000007069 methylation reaction Methods 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 239000003883 ointment base Substances 0.000 description 1
- 239000010502 orange oil Substances 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000000312 peanut oil Substances 0.000 description 1
- 235000019271 petrolatum Nutrition 0.000 description 1
- 229940066842 petrolatum Drugs 0.000 description 1
- 239000002831 pharmacologic agent Substances 0.000 description 1
- DLYUQMMRRRQYAE-UHFFFAOYSA-N phosphorus pentoxide Inorganic materials O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000002953 preparative HPLC Methods 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000005932 reductive alkylation reaction Methods 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 238000009738 saturating Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 1
- BEOOHQFXGBMRKU-UHFFFAOYSA-N sodium cyanoborohydride Chemical compound [Na+].[B-]C#N BEOOHQFXGBMRKU-UHFFFAOYSA-N 0.000 description 1
- 239000012453 solvate Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000008174 sterile solution Substances 0.000 description 1
- 210000002784 stomach Anatomy 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 150000003890 succinate salts Chemical class 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000000829 suppository Substances 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 150000003892 tartrate salts Chemical class 0.000 description 1
- 229940124597 therapeutic agent Drugs 0.000 description 1
- 238000011200 topical administration Methods 0.000 description 1
- 239000012049 topical pharmaceutical composition Substances 0.000 description 1
- 230000037317 transdermal delivery Effects 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 230000004580 weight loss Effects 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
- 239000002076 α-tocopherol Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D221/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00
- C07D221/02—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00 condensed with carbocyclic rings or ring systems
- C07D221/20—Spiro-condensed ring 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
- A61P25/20—Hypnotics; Sedatives
-
- 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, cocaine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Psychiatry (AREA)
- Anesthesiology (AREA)
- Child & Adolescent Psychology (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Diabetes (AREA)
- Pain & Pain Management (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Steroid Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Indole Compounds (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB929223445A GB9223445D0 (en) | 1992-11-09 | 1992-11-09 | Therapeutic agents |
| PCT/EP1993/002951 WO1994011346A1 (en) | 1992-11-09 | 1993-10-23 | Aza spiro alkanes derivatives as therapeutic agents |
| CN94105852A CN1113911A (zh) | 1992-11-09 | 1994-05-07 | 治疗剂 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SK58995A3 true SK58995A3 (en) | 1995-10-11 |
Family
ID=37075771
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SK589-95A SK58995A3 (en) | 1992-11-09 | 1993-10-23 | Nitric spirocyclic compounds, method of their production pharmaceutical agents which contains thereof and their use |
Country Status (27)
| Country | Link |
|---|---|
| US (1) | US5610161A (xx) |
| EP (1) | EP0667860B1 (xx) |
| JP (1) | JPH08502985A (xx) |
| CN (1) | CN1113911A (xx) |
| AT (1) | ATE169907T1 (xx) |
| AU (1) | AU5338194A (xx) |
| BG (1) | BG99608A (xx) |
| BR (1) | BR9307388A (xx) |
| CA (1) | CA2148582A1 (xx) |
| CZ (1) | CZ117595A3 (xx) |
| DE (1) | DE69320488T2 (xx) |
| DK (1) | DK0667860T3 (xx) |
| ES (1) | ES2118977T3 (xx) |
| FI (1) | FI952205A0 (xx) |
| GB (1) | GB9223445D0 (xx) |
| HR (1) | HRP931384A2 (xx) |
| HU (2) | HUT71554A (xx) |
| IL (1) | IL107486A0 (xx) |
| IN (1) | IN176828B (xx) |
| LT (1) | LT3421B (xx) |
| MX (1) | MX9306951A (xx) |
| NO (1) | NO951798L (xx) |
| PL (1) | PL308754A1 (xx) |
| SI (1) | SI9300584A (xx) |
| SK (1) | SK58995A3 (xx) |
| WO (1) | WO1994011346A1 (xx) |
| ZA (1) | ZA938302B (xx) |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3218540A1 (de) * | 1982-05-17 | 1983-11-24 | Hoechst Ag, 6230 Frankfurt | Spiro-2-aza-alkan-3-carbonitrile, verfahren zu ihrer herstellung und ihre verwendung |
| US4430335A (en) * | 1983-02-09 | 1984-02-07 | Hoechst-Roussel Pharmaceuticals Inc. | Substituted 1-azaspiro[4,5]decanes and their analgesic compositions |
-
1992
- 1992-11-09 GB GB929223445A patent/GB9223445D0/en active Pending
-
1993
- 1993-10-23 WO PCT/EP1993/002951 patent/WO1994011346A1/en active IP Right Grant
- 1993-10-23 CZ CZ951175A patent/CZ117595A3/cs unknown
- 1993-10-23 DK DK93923549T patent/DK0667860T3/da active
- 1993-10-23 EP EP93923549A patent/EP0667860B1/en not_active Expired - Lifetime
- 1993-10-23 JP JP6511646A patent/JPH08502985A/ja active Pending
- 1993-10-23 AT AT93923549T patent/ATE169907T1/de not_active IP Right Cessation
- 1993-10-23 CA CA002148582A patent/CA2148582A1/en not_active Abandoned
- 1993-10-23 ES ES93923549T patent/ES2118977T3/es not_active Expired - Lifetime
- 1993-10-23 SK SK589-95A patent/SK58995A3/sk unknown
- 1993-10-23 US US08/424,388 patent/US5610161A/en not_active Expired - Fee Related
- 1993-10-23 PL PL93308754A patent/PL308754A1/xx unknown
- 1993-10-23 DE DE69320488T patent/DE69320488T2/de not_active Expired - Fee Related
- 1993-10-23 AU AU53381/94A patent/AU5338194A/en not_active Abandoned
- 1993-10-23 BR BR9307388-7A patent/BR9307388A/pt not_active Application Discontinuation
- 1993-10-23 HU HU9501317A patent/HUT71554A/hu unknown
- 1993-10-28 IN IN696MA1993 patent/IN176828B/en unknown
- 1993-11-04 IL IL10748693A patent/IL107486A0/xx unknown
- 1993-11-08 ZA ZA938302A patent/ZA938302B/xx unknown
- 1993-11-08 MX MX9306951A patent/MX9306951A/es unknown
- 1993-11-09 HR HR931384A patent/HRP931384A2/hr not_active Application Discontinuation
- 1993-11-09 SI SI9300584A patent/SI9300584A/sl unknown
- 1993-11-09 LT LTIP1450A patent/LT3421B/lt not_active IP Right Cessation
-
1994
- 1994-05-07 CN CN94105852A patent/CN1113911A/zh active Pending
-
1995
- 1995-05-02 BG BG99608A patent/BG99608A/bg unknown
- 1995-05-08 FI FI952205A patent/FI952205A0/fi unknown
- 1995-05-08 NO NO951798A patent/NO951798L/no unknown
- 1995-06-30 HU HU95P/P00690P patent/HU211867A9/hu unknown
Also Published As
| Publication number | Publication date |
|---|---|
| HUT71554A (en) | 1995-12-28 |
| AU5338194A (en) | 1994-06-08 |
| DK0667860T3 (da) | 1999-05-25 |
| MX9306951A (es) | 1995-01-31 |
| FI952205A (fi) | 1995-05-08 |
| FI952205A0 (fi) | 1995-05-08 |
| ZA938302B (en) | 1994-05-09 |
| ATE169907T1 (de) | 1998-09-15 |
| ES2118977T3 (es) | 1998-10-01 |
| HRP931384A2 (en) | 1994-12-31 |
| BG99608A (bg) | 1995-08-28 |
| WO1994011346A1 (en) | 1994-05-26 |
| US5610161A (en) | 1997-03-11 |
| LT3421B (en) | 1995-09-25 |
| LTIP1450A (en) | 1994-10-25 |
| BR9307388A (pt) | 1999-08-31 |
| GB9223445D0 (en) | 1992-12-23 |
| PL308754A1 (en) | 1995-08-21 |
| NO951798D0 (no) | 1995-05-08 |
| CA2148582A1 (en) | 1994-05-26 |
| JPH08502985A (ja) | 1996-04-02 |
| HU9501317D0 (en) | 1995-06-28 |
| DE69320488D1 (de) | 1998-09-24 |
| IL107486A0 (en) | 1994-02-27 |
| CZ117595A3 (en) | 1995-12-13 |
| EP0667860A1 (en) | 1995-08-23 |
| HU211867A9 (en) | 1995-12-28 |
| SI9300584A (en) | 1994-06-30 |
| EP0667860B1 (en) | 1998-08-19 |
| NO951798L (no) | 1995-05-31 |
| IN176828B (xx) | 1996-09-21 |
| DE69320488T2 (de) | 1998-12-24 |
| CN1113911A (zh) | 1995-12-27 |
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