FI94241B - Förfarande för framställning av nya terapeutiskt användbara 1,3-disubstituerade piperidinderivat - Google Patents
Förfarande för framställning av nya terapeutiskt användbara 1,3-disubstituerade piperidinderivat Download PDFInfo
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- FI94241B FI94241B FI893326A FI893326A FI94241B FI 94241 B FI94241 B FI 94241B FI 893326 A FI893326 A FI 893326A FI 893326 A FI893326 A FI 893326A FI 94241 B FI94241 B FI 94241B
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- Finland
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- alkyl
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- -1 1,3-disubstituted piperidine Chemical class 0.000 title claims abstract description 66
- 238000002360 preparation method Methods 0.000 title claims description 84
- 238000000034 method Methods 0.000 title claims description 50
- 230000008569 process Effects 0.000 title claims description 15
- 150000001875 compounds Chemical class 0.000 claims abstract description 161
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 40
- 239000001257 hydrogen Substances 0.000 claims abstract description 15
- 150000003839 salts Chemical class 0.000 claims abstract description 15
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims abstract description 4
- 238000006243 chemical reaction Methods 0.000 claims description 57
- 125000000217 alkyl group Chemical group 0.000 claims description 53
- 239000000203 mixture Substances 0.000 claims description 50
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 27
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 claims description 18
- 239000002253 acid Substances 0.000 claims description 17
- 230000002829 reductive effect Effects 0.000 claims description 15
- 125000003545 alkoxy group Chemical group 0.000 claims description 14
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 14
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 12
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 claims description 11
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims description 10
- 229910021529 ammonia Inorganic materials 0.000 claims description 10
- NDKBVBUGCNGSJJ-UHFFFAOYSA-M benzyltrimethylammonium hydroxide Chemical compound [OH-].C[N+](C)(C)CC1=CC=CC=C1 NDKBVBUGCNGSJJ-UHFFFAOYSA-M 0.000 claims description 10
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 9
- 150000008064 anhydrides Chemical class 0.000 claims description 9
- 239000012280 lithium aluminium hydride Substances 0.000 claims description 9
- 150000001412 amines Chemical class 0.000 claims description 8
- PFKFTWBEEFSNDU-UHFFFAOYSA-N carbonyldiimidazole Chemical compound C1=CN=CN1C(=O)N1C=CN=C1 PFKFTWBEEFSNDU-UHFFFAOYSA-N 0.000 claims description 8
- 239000003054 catalyst Substances 0.000 claims description 8
- 239000003638 chemical reducing agent Substances 0.000 claims description 8
- 229910052801 chlorine Inorganic materials 0.000 claims description 8
- 229910052794 bromium Inorganic materials 0.000 claims description 7
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 6
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 claims description 6
- 229910002092 carbon dioxide Inorganic materials 0.000 claims description 6
- 229910002091 carbon monoxide Inorganic materials 0.000 claims description 6
- 229910052736 halogen Inorganic materials 0.000 claims description 6
- 150000002367 halogens Chemical class 0.000 claims description 6
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims description 5
- 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 claims description 5
- 230000002378 acidificating effect Effects 0.000 claims description 5
- 229910052799 carbon Inorganic materials 0.000 claims description 5
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 5
- 150000002431 hydrogen Chemical class 0.000 claims description 5
- 239000012948 isocyanate Substances 0.000 claims description 5
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 5
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 5
- 125000003277 amino group Chemical group 0.000 claims description 4
- 125000004185 ester group Chemical group 0.000 claims description 4
- 150000002148 esters Chemical class 0.000 claims description 4
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims description 4
- DVSDBMFJEQPWNO-UHFFFAOYSA-N methyllithium Chemical compound C[Li] DVSDBMFJEQPWNO-UHFFFAOYSA-N 0.000 claims description 4
- NVBFHJWHLNUMCV-UHFFFAOYSA-N sulfamide Chemical compound NS(N)(=O)=O NVBFHJWHLNUMCV-UHFFFAOYSA-N 0.000 claims description 4
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims description 3
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 3
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims description 3
- 150000001351 alkyl iodides Chemical class 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 239000001569 carbon dioxide Substances 0.000 claims description 3
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 claims description 3
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims description 3
- 229910052740 iodine Inorganic materials 0.000 claims description 3
- NXPHGHWWQRMDIA-UHFFFAOYSA-M magnesium;carbanide;bromide Chemical compound [CH3-].[Mg+2].[Br-] NXPHGHWWQRMDIA-UHFFFAOYSA-M 0.000 claims description 3
- 125000005948 methanesulfonyloxy group Chemical group 0.000 claims description 3
- MUJIDPITZJWBSW-UHFFFAOYSA-N palladium(2+) Chemical compound [Pd+2] MUJIDPITZJWBSW-UHFFFAOYSA-N 0.000 claims description 3
- 125000002252 acyl group Chemical group 0.000 claims description 2
- 150000007928 imidazolide derivatives Chemical class 0.000 claims description 2
- 239000011734 sodium Substances 0.000 claims description 2
- 229910052708 sodium Inorganic materials 0.000 claims description 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 2
- 239000004922 lacquer Substances 0.000 claims 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims 1
- 125000005036 alkoxyphenyl group Chemical group 0.000 claims 1
- 125000005982 diphenylmethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 1
- JBFYUZGYRGXSFL-UHFFFAOYSA-N imidazolide Chemical compound C1=C[N-]C=N1 JBFYUZGYRGXSFL-UHFFFAOYSA-N 0.000 claims 1
- 229910001629 magnesium chloride Inorganic materials 0.000 claims 1
- 229910001641 magnesium iodide Inorganic materials 0.000 claims 1
- FJWLWIRHZOHPIY-UHFFFAOYSA-N potassium;hydroiodide Chemical compound [K].I FJWLWIRHZOHPIY-UHFFFAOYSA-N 0.000 claims 1
- 125000001424 substituent group Chemical group 0.000 abstract description 7
- 210000002460 smooth muscle Anatomy 0.000 abstract description 4
- 201000010099 disease Diseases 0.000 abstract description 3
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract description 3
- 230000004899 motility Effects 0.000 abstract description 3
- 125000001475 halogen functional group Chemical group 0.000 abstract 1
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 158
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 135
- 239000000243 solution Substances 0.000 description 60
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 59
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 57
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 56
- 238000004458 analytical method Methods 0.000 description 55
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 48
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 47
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 40
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 34
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 32
- 239000012230 colorless oil Substances 0.000 description 32
- 238000004587 chromatography analysis Methods 0.000 description 31
- 239000003480 eluent Substances 0.000 description 29
- 239000000377 silicon dioxide Substances 0.000 description 29
- 239000003921 oil Substances 0.000 description 27
- 235000019198 oils Nutrition 0.000 description 27
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 26
- 229910000029 sodium carbonate Inorganic materials 0.000 description 23
- FVAUCKIRQBBSSJ-UHFFFAOYSA-M sodium iodide Inorganic materials [Na+].[I-] FVAUCKIRQBBSSJ-UHFFFAOYSA-M 0.000 description 23
- 239000007787 solid Substances 0.000 description 22
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 21
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 20
- 235000019341 magnesium sulphate Nutrition 0.000 description 20
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 19
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 19
- 239000012044 organic layer Substances 0.000 description 19
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 18
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 18
- 235000017550 sodium carbonate Nutrition 0.000 description 16
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 15
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 14
- 238000010992 reflux Methods 0.000 description 14
- 239000007858 starting material Substances 0.000 description 14
- 239000003960 organic solvent Substances 0.000 description 13
- 235000017557 sodium bicarbonate Nutrition 0.000 description 13
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 13
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 12
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 12
- 238000007792 addition Methods 0.000 description 11
- 238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 11
- 239000002585 base Substances 0.000 description 10
- 239000010410 layer Substances 0.000 description 10
- QJPQVXSHYBGQGM-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 QJPQVXSHYBGQGM-UHFFFAOYSA-N 0.000 description 10
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 10
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 10
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 9
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 9
- 229920006395 saturated elastomer Polymers 0.000 description 9
- 229910052938 sodium sulfate Inorganic materials 0.000 description 9
- 235000011152 sodium sulphate Nutrition 0.000 description 9
- 239000002904 solvent Substances 0.000 description 9
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 9
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 8
- 238000009835 boiling Methods 0.000 description 8
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 8
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 8
- 235000009518 sodium iodide Nutrition 0.000 description 8
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 8
- 239000000284 extract Substances 0.000 description 7
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 6
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 6
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 239000000725 suspension Substances 0.000 description 6
- 210000003932 urinary bladder Anatomy 0.000 description 6
- KMCBERWUSATVKV-UHFFFAOYSA-N FC1=CC=C(C=C1)C1N(CCCC1)OC Chemical compound FC1=CC=C(C=C1)C1N(CCCC1)OC KMCBERWUSATVKV-UHFFFAOYSA-N 0.000 description 5
- 229960000583 acetic acid Drugs 0.000 description 5
- 235000011054 acetic acid Nutrition 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 5
- 210000003405 ileum Anatomy 0.000 description 5
- 229910000027 potassium carbonate Inorganic materials 0.000 description 5
- 239000011347 resin Substances 0.000 description 5
- 229920005989 resin Polymers 0.000 description 5
- 229910000104 sodium hydride Inorganic materials 0.000 description 5
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 5
- ODVLMCWNGKLROU-UHFFFAOYSA-N 2-(1,3-benzodioxol-5-yl)acetic acid Chemical compound OC(=O)CC1=CC=C2OCOC2=C1 ODVLMCWNGKLROU-UHFFFAOYSA-N 0.000 description 4
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 4
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 4
- 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
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 4
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 4
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 4
- 229940121948 Muscarinic receptor antagonist Drugs 0.000 description 4
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 4
- QILSFLSDHQAZET-UHFFFAOYSA-N diphenylmethanol Chemical compound C=1C=CC=CC=1C(O)C1=CC=CC=C1 QILSFLSDHQAZET-UHFFFAOYSA-N 0.000 description 4
- 239000000706 filtrate Substances 0.000 description 4
- QARBMVPHQWIHKH-UHFFFAOYSA-N methanesulfonyl chloride Chemical compound CS(Cl)(=O)=O QARBMVPHQWIHKH-UHFFFAOYSA-N 0.000 description 4
- KDLHZDBZIXYQEI-UHFFFAOYSA-N palladium Substances [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 4
- 239000012312 sodium hydride Substances 0.000 description 4
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical class O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 4
- FWPIDFUJEMBDLS-UHFFFAOYSA-L tin(II) chloride dihydrate Chemical group O.O.Cl[Sn]Cl FWPIDFUJEMBDLS-UHFFFAOYSA-L 0.000 description 4
- 210000003437 trachea Anatomy 0.000 description 4
- LQDHVNHVHAYANB-UHFFFAOYSA-N 1-(2-bromoethyl)-3-methoxybenzene Chemical compound COC1=CC=CC(CCBr)=C1 LQDHVNHVHAYANB-UHFFFAOYSA-N 0.000 description 3
- JADSGOFBFPTCHG-UHFFFAOYSA-N 2-(1,3-benzodioxol-5-yl)ethanol Chemical compound OCCC1=CC=C2OCOC2=C1 JADSGOFBFPTCHG-UHFFFAOYSA-N 0.000 description 3
- KFDVPJUYSDEJTH-UHFFFAOYSA-N 4-ethenylpyridine Chemical compound C=CC1=CC=NC=C1 KFDVPJUYSDEJTH-UHFFFAOYSA-N 0.000 description 3
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- 229910010082 LiAlH Inorganic materials 0.000 description 3
- 239000012359 Methanesulfonyl chloride Substances 0.000 description 3
- PHSPJQZRQAJPPF-UHFFFAOYSA-N N-alpha-Methylhistamine Chemical compound CNCCC1=CN=CN1 PHSPJQZRQAJPPF-UHFFFAOYSA-N 0.000 description 3
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 3
- 239000013543 active substance Substances 0.000 description 3
- 239000002168 alkylating agent Substances 0.000 description 3
- 229940100198 alkylating agent Drugs 0.000 description 3
- SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 description 3
- 229940092714 benzenesulfonic acid Drugs 0.000 description 3
- 239000004305 biphenyl Substances 0.000 description 3
- WCTZPQWLFWZYJE-UHFFFAOYSA-N bis(4-fluorophenyl)methanol Chemical compound C=1C=C(F)C=CC=1C(O)C1=CC=C(F)C=C1 WCTZPQWLFWZYJE-UHFFFAOYSA-N 0.000 description 3
- 230000008602 contraction Effects 0.000 description 3
- 238000007796 conventional method Methods 0.000 description 3
- SHFJWMWCIHQNCP-UHFFFAOYSA-M hydron;tetrabutylazanium;sulfate Chemical compound OS([O-])(=O)=O.CCCC[N+](CCCC)(CCCC)CCCC SHFJWMWCIHQNCP-UHFFFAOYSA-M 0.000 description 3
- 239000000543 intermediate Substances 0.000 description 3
- 238000001990 intravenous administration Methods 0.000 description 3
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 3
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 229910017604 nitric acid Inorganic materials 0.000 description 3
- 125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 description 3
- 239000002504 physiological saline solution Substances 0.000 description 3
- 238000000746 purification Methods 0.000 description 3
- 238000001953 recrystallisation Methods 0.000 description 3
- 230000009467 reduction Effects 0.000 description 3
- 210000005245 right atrium Anatomy 0.000 description 3
- 239000012279 sodium borohydride Substances 0.000 description 3
- 229910000033 sodium borohydride Inorganic materials 0.000 description 3
- 230000003595 spectral effect Effects 0.000 description 3
- 210000001519 tissue Anatomy 0.000 description 3
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 3
- OXHPTABOQVHKLN-UHFFFAOYSA-N 1-(2-bromoethyl)-4-methoxybenzene Chemical compound COC1=CC=C(CCBr)C=C1 OXHPTABOQVHKLN-UHFFFAOYSA-N 0.000 description 2
- ASOKPJOREAFHNY-UHFFFAOYSA-N 1-Hydroxybenzotriazole Chemical compound C1=CC=C2N(O)N=NC2=C1 ASOKPJOREAFHNY-UHFFFAOYSA-N 0.000 description 2
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- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 125000004458 methylaminocarbonyl group Chemical group [H]N(C(*)=O)C([H])([H])[H] 0.000 description 1
- AQIAIZBHFAKICS-UHFFFAOYSA-N methylaminomethyl Chemical compound [CH2]NC AQIAIZBHFAKICS-UHFFFAOYSA-N 0.000 description 1
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N monoethanolamine hydrochloride Natural products NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
- 229910000069 nitrogen hydride Inorganic materials 0.000 description 1
- 239000010502 orange oil Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- PIBWKRNGBLPSSY-UHFFFAOYSA-L palladium(II) chloride Chemical compound Cl[Pd]Cl PIBWKRNGBLPSSY-UHFFFAOYSA-L 0.000 description 1
- 238000007911 parenteral administration Methods 0.000 description 1
- 230000002572 peristaltic effect Effects 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 239000003444 phase transfer catalyst Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 238000000053 physical method Methods 0.000 description 1
- 150000003053 piperidines Chemical class 0.000 description 1
- 125000003386 piperidinyl group Chemical group 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 210000001747 pupil Anatomy 0.000 description 1
- 125000003373 pyrazinyl group Chemical group 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 208000023504 respiratory system disease Diseases 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 230000000284 resting effect Effects 0.000 description 1
- 208000026451 salivation Diseases 0.000 description 1
- 229940125723 sedative agent Drugs 0.000 description 1
- 239000000932 sedative agent Substances 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000012258 stirred mixture Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical compound ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 150000003892 tartrate salts Chemical class 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 238000011287 therapeutic dose Methods 0.000 description 1
- BISQTCXKVNCDDA-UHFFFAOYSA-N thiepine Chemical compound S1C=CC=CC=C1 BISQTCXKVNCDDA-UHFFFAOYSA-N 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/02—Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
-
- 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
- A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
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- 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
- C07D211/42—Oxygen atoms attached in position 3 or 5
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/06—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
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- Chemical & Material Sciences (AREA)
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- Urology & Nephrology (AREA)
- Pulmonology (AREA)
- Endocrinology (AREA)
- Reproductive Health (AREA)
- Hydrogenated Pyridines (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Steroid Compounds (AREA)
Claims (9)
1. Förfarande för framställning av nya terapeutlskt användbara (3R,S)- och (3R)-former av 1,3-disubstituerade 5 piperidinderivat med formeln I och farmaceutiskt godtag-bara syraadditionssalter därav, R*0-f ^N-CH-CH-R (J) « kj 2 2 1 vilken formel R1 är en grupp med formeln 15 γ γ x ^ \ ^ eller 20 där symbolerna Y, som kan vara lika eller ollka, betecknar väte, halogen eller alkyl; X är -(CH2)2-, -CH=CH-, -CH2-S-, -CH20-, -S- eller -O-; och R är en grupp med formeln ·. 25 R2 "61 . o- . tr 30 • -• · -f\ »5 T"'}) 35 eller ^ . 94241 105 där R2 och R3 betecknar oberoende av varandra väte, C^-alkyl, hyroxi-iC^-alkyl), hydroxl, C^-alkoxi, halogen, trifluormetyl, nitro, cyano, sulfamoyl, -COiCj^-al-5 kyl), -OCO( C^-alkyl), -CO^C^-alkyl), en grupp - (CH2 )nCONR6R7, - (CH2 ) nOCONR6R7, -(CH2)nNR8R9 eller NHS02NH2, varvid R6 och R7 betecknar oberoende av varandra väte eller Cj^-alkyl, n är 0, 1 eller 2, och Re och R9 betecknar oberoende av varandra väte eller C1.4-alkyl eller Re är väte 10 och R9 är -S02(C1_4-alkyl), -COiCj^-alkyl) eller -C0NH( -alkyl); eller R2 och R3 bildar tillsammans, dä de är bundna tili närliggande kolatomer, en grupp med formeln -0(CH2)e0-, där m är 1, 2 eller 3, -0(CH2)2- eller -(CH2)3-;
15 R4 är H, Cj^-alkyl eller -C0NH2; och R5 är H, C^-alkyl eller C^-alkoxi; förutsatt att, dä R1 är difenylmetyl, sä är R ej fenyl, ifall föreningen med formeln I har (3R,S)-formen, kännetecknat därav, att 20 A) (3R,S)- eller (3R)-formen av en förening med formeln r1o—fNH u där R1 betecknar samma som ovan, omsätts med en förening med formeln QCH2CH2R (III), där R betecknar samma som ovan och Q är Cl, Br, I eller metansulfonyloxi, eller 30 B) (3R,S)- eller (3R)-formen av en förening med formeln ‘ · · R10-i^VN-C0CH2R Il (iv) 35 94241 106 där R och R1 betecknar sanuna som ovan, reduceras med ett oorganlskt reduktionsmedel,eller C) (3R,S)- eller (3R)-formen av en förening med formeln 5 HO- 10 där R betecknar sanuna som ovan, omsätts med en förening med formeln R1Q ’, där R1 betecknar samma som ovan och Q' är Cl eller Br, eller D) för framställning av (3R,S)- eller (3R)-formen av en förening med formeln (I), där R är Q-* 0- Ό 20 där R5 betecknar samma som ovan, omsätts (3R,S)- eller (3R)-formen av en förening med formeln RX0-f^NH där R1 betecknar samma som ovan, med en förening med formeln RCH=CH2, där R betecknar samma som ovan, eventuellt 1 närvaro av en sur eller basisk katalysator, eller 30 E) för framställning av (3R,S)- eller (3R)-formen ! av en förening med formeln (1), där R är JT\ 35 ^s/^cohHj • k 94241 107 (i) omsätts (3R,S)- eller (3R)-formen av en för-enlng med formeln (I), där R är ^ ^ , först med 5 en stark bas och därefter med koldloxld för erhällande av (3R,S)- eller (3R)-formen av en förenlng med formeln (I), där R är II ; och /XS/^C00H 10 (11) av den sä framställda karboxlförenlngen bildas en aktlv ester eller ett imidazolidderivat, varefter föl-jer behandllng med ammonlak; varefter, om sä önskas, utförs ett eller flera av följande steg: 15 a) d4 ätminstone den ena av R2 och R3 betecknar en grupp -COjiCj^-alkyl), reduceras nämnda estergrupp tili gruppen -CHOH? b) dä ätminstone den ena av R2 och R3 betecknar hydroxi, omvandlas nämnda hydroxigrupp tili en grupp 20 -0C0( C^-alkyl) genom att acylera med en C^-alkanoylklorid eller -bromid eller med en C^-alkansyraanhydrid; c) dä ätminstone den ena av R2 och R3 betecknar en grupp -C0(C1.3-alkyl), reduceras nämnda alkanoylgrupp tili en grupp -CH(OH) (C1.3-alkyl); : 25 d) d4 ätminstone den ena av R2 och R3 betecknar en grupp -C02(C1.4-alkyl), reduceras nämnda estergrupp tili en grupp -C0NR6R7 genom reaktion med ammonlak eller en lämplig amin R6R7NH, där R6 och R7 betecknar samma som ovan; e) dä ätminstone den ena av R2 och R3 betecknar nit- 30 ro, reduceras nämnda nitrogrupp tili gruppen -NH2; / f) dä ätminstone den ena av R2 och R3 betecknar ami no, omvandlas nämnda aminogrupp tili en grupp -NHSOjiC^-alkyl) genom reaktion med en C1.4-alkansulfonylklorid eller -bromid eller med en C^-alkansulfonsyraanhydrid; 94241 108 g) dä ätminstone den ena av R2 och R3 betecknar en grupp -(CH2)nNH2, där n är 0, 1 eller 2, omvandlas nämnda grupp tili en grupp - (CH2 )nNHC0( C^-alkyl) genom reaktion med en C^-alkanoylklorid eller -bromid eller med en C^- 5 alkansyraanhydrid; h) dä ätminstone den ena av R2 och R3 betecknar amino, omvandlas nämnda aminogrupp tili gruppen -NHS02NH2 genom reaktion med en sulfamid; i) dä ätminstone den ena av R2 och R3 betecknar 10 hydroxi, omvandlas nämnda hydroxigrupp tili en grupp C:_4-alkoxi genom reaktion med en stark bas, varefter följer behandling med en C1.4-alkyljodid; j ) dä ätminstone den ena av R2 och R3 betecknar en grupp -(CH2)n0H, där n är 0, 1 eller 2, omvandlas nämnda 15 grupp tili en grupp -(CH^OCONHiC^-alkyl) genom reaktion med ett C^-alkylisocyanat; k) dä ätminstone den ena av R2 och R3 betecknar gruppen -CH20H, omvandlas nämnda hydroximetylgrupp tili en grupp -CH2NR8R9, där R8 och R9 betecknar oberoende av var- 20 andra väte eller C1.4-alkyl, genom reaktion först med en tionylklorid och därefter med ammoniak eller en lämplig amin R8R9NH; l) dä ätminstone den ena av R2 och R3 betecknar gruppen -C0CH3, omvandlas nämnda acetylgrupp tili gruppen : 25 -C(OH)(CH3)2 genom reaktion med antingen metyl- litium eller metylmagnesiumbromid, -klorid eller -jodid; m) dä ätminstone den ena av R2 och R3 betecknar jod, omvandlas nämnda jodsubstituent tili en grupp -COjiC^-alkyl) genom reaktion med en blandning av kolmonoxid, en 30 bas, en C^-alkanol och en palladium(Il)katalysator; n) dä ätminstone den ena av R2 och R3 betecknar cya-no, reduceras nämnda cyanosubstituent tili gruppen -CH2NH2; o) dä ätminstone den ena av R2 och R3 betecknar en grupp - (CH2 )nNH2, där n är 0, 1 eller 2, omvandlas nämnda 35 grupp tili en grupp -(CHj^NHCONHiC^-alkyl) genom reaktion med ett C1.4-alkylisocyanat; 94241 109 p) dä ätminstone den ena av R2 och R3 betecknar C^-alkoxi, omvandlas nämnda alkoxlgrupp till en hydroxi-grupp genom behandling med en C1.4-alkantlol i närvaro av en stark bas; och 5 q) en förening med fonneln (I) omvandlas till ett farmaceutlskt godtagbart syraadditionssalt.
2. Förfarande enligt patentkravet 1, känne-t e c k n a t därav, att förfarandealternativet A) utförs 1 närvaro av en syraacceptor. 10 3. Förfarande enligt patentkravet 1 eller 2, kännetecknat därav, att Q är Cl eller Br och förfarandealternativet A) utförs 1 närvaro av natrium-eller kallumjodld.
4. Förfarande enligt patentkravet 1, känne- 15 tecknat därav, att förfarandealternativet B) utförs genom att som reduktlonsmedel använda litiumaluminiumhyd- rld.
5. Förfarande enligt patentkravet 1, kännetecknat därav, att förfarandealternativet D) ut- 20 förs genom att som katalysator använda N-bensyltrimetylam-moniumhydroxid ("Triton B"):
6. Förfarande enligt patentkravet 1, kännetecknat därav, att förfarandealternativet E) utförs genom att använda n-butyllitium som stark bas 1 steg : 25 (1), och imidazoliden bildas 1 steg (il) genom att använda 1,1'-karbonyldiimidazol.
7. Förfarande enligt patentkravet 1, kännetecknat därav, att man framställer en förening med formeln I, där R1 är ΟψΟ och R är ^ XX>. 94241 110
8. Förfarande enligt patentkravet 7, k ft n ηβ-'t e c k n a t därav, att man framställer en förening med formeln a;jo 9. (3R,S)- eller (3R)-formen av en förening med formeln IV eller VI,
15 R10—-|^V"N-C0CH2R Kj (iv> H0 N-CH2CH2R' (VI> 20 l^J vilka formler R och R1 betecknar samma som i patentkravet 1 och R’ är 2-, 3- eller 4-C1_4-alkoxifenyl.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB8816365 | 1988-07-08 | ||
| GB888816365A GB8816365D0 (en) | 1988-07-08 | 1988-07-08 | Therapeutic agents |
Publications (4)
| Publication Number | Publication Date |
|---|---|
| FI893326A0 FI893326A0 (sv) | 1989-07-07 |
| FI893326A FI893326A (sv) | 1990-01-09 |
| FI94241B true FI94241B (sv) | 1995-04-28 |
| FI94241C FI94241C (sv) | 1995-08-10 |
Family
ID=10640168
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI893326A FI94241C (sv) | 1988-07-08 | 1989-07-07 | Förfarande för framställning av nya terapeutiskt användbara 1,3-disubstituerade piperidinderivat |
Country Status (28)
| Country | Link |
|---|---|
| US (1) | US5089505A (sv) |
| EP (1) | EP0350309B1 (sv) |
| JP (2) | JPH0739388B2 (sv) |
| KR (1) | KR930002728B1 (sv) |
| CN (1) | CN1022914C (sv) |
| AT (1) | ATE82262T1 (sv) |
| AU (1) | AU602453B2 (sv) |
| CA (1) | CA1336833C (sv) |
| DD (1) | DD284011A5 (sv) |
| DE (1) | DE68903437T2 (sv) |
| DK (1) | DK337589A (sv) |
| EG (1) | EG18853A (sv) |
| ES (1) | ES2052917T3 (sv) |
| FI (1) | FI94241C (sv) |
| GB (1) | GB8816365D0 (sv) |
| GR (1) | GR3006595T3 (sv) |
| HU (1) | HUT50771A (sv) |
| IE (1) | IE63438B1 (sv) |
| IL (1) | IL90792A0 (sv) |
| MX (1) | MX16728A (sv) |
| MY (1) | MY106976A (sv) |
| NO (1) | NO892828L (sv) |
| NZ (1) | NZ229865A (sv) |
| PL (2) | PL161887B1 (sv) |
| PT (1) | PT91081B (sv) |
| RU (2) | RU1838307C (sv) |
| YU (1) | YU135389A (sv) |
| ZA (1) | ZA895175B (sv) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5231104A (en) * | 1988-07-08 | 1993-07-27 | Pfizer Inc. | 1-arylethyl-3-substituted piperidines |
| GB9000301D0 (en) * | 1990-01-06 | 1990-03-07 | Pfizer Ltd | Piperidine & pyrrolidine derivatives |
| GB9208230D0 (en) * | 1992-04-14 | 1992-05-27 | Pfizer Ltd | Treatment of delayed gastric emptying |
| US5340826A (en) * | 1993-02-04 | 1994-08-23 | Pfizer Inc. | Pharmaceutical agents for treatment of urinary incontinence |
| GB9400600D0 (en) * | 1994-01-14 | 1994-03-09 | Pfizer Ltd | Treatment of motion seckness |
| EP1156807A4 (en) * | 1998-12-18 | 2002-04-03 | Du Pont Pharm Co | N-UREIDOALKYL-PIPERIDINES FOR USE AS MODULATORS OF THE ACTIVITY OF CHIMIOKIN RECEPTORS |
| US6525069B1 (en) | 1998-12-18 | 2003-02-25 | Bristol-Myers Squibb Pharma Co. | N-ureidoalkyl-piperidines as modulators of chemokine receptor activity |
| US6331541B1 (en) | 1998-12-18 | 2001-12-18 | Soo S. Ko | N-ureidoalkyl-piperidines as modulators of chemokine receptor activity |
| CA2348923A1 (en) | 1998-12-18 | 2000-06-22 | Dean A. Wacker | N-ureidoalkyl-piperidines as modulators of chemokine receptor activity |
| KR20010101287A (ko) * | 1998-12-18 | 2001-11-14 | 블레어 큐. 퍼거슨 | 케모킨 수용체 활성의 조절자로서 ｎ-우레이도알킬-피페리딘 |
| US6897234B2 (en) | 1999-12-17 | 2005-05-24 | Bristol-Myers Squibb Pharma Company | N-ureidoalkyl-piperidines as modulators of chemokine receptor activity |
| AU2001273129A1 (en) | 2000-06-30 | 2002-01-14 | Bristol-Myers Squibb Pharma Company | N-ureidoheterocycloaklyl-piperidines as modulators of chemokine receptor activity |
| EP1318988A2 (en) * | 2000-09-11 | 2003-06-18 | Sepracor, Inc. | Ligands for monoamine receptors and transporters, and methods of use thereof (neurotransmission) |
| US6508872B2 (en) * | 2001-02-26 | 2003-01-21 | Hewlett-Packard Company | Lightfast additive molecule for inkjet ink |
| WO2008144602A1 (en) * | 2007-05-18 | 2008-11-27 | Auspex Pharmaceuticals, Inc. | Deuterated zamifenacin derivatives |
| US9365553B2 (en) * | 2010-05-27 | 2016-06-14 | Aska Pharmaceutical Co., Ltd. | Heterocyclic compound and H1 receptor antagonist |
| CN107129453B (zh) * | 2016-02-26 | 2019-10-11 | 中国科学院大连化学物理研究所 | 化合物、毒蕈碱m受体拮抗剂、组合物及应用 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA541598A (en) * | 1957-05-28 | Levy Joseph | N-substituted-4-benzhydryl etherpiperidines and method for obtaining the same | |
| GB688345A (en) * | 1951-02-19 | 1953-03-04 | Greenwood And Hughes Ltd | Improvements in sanitary liquid traps |
| US2745837A (en) * | 1954-01-21 | 1956-05-15 | Schering Corp | Benzhydryl ethers of alkyl piperidinols |
| GB780027A (en) * | 1955-01-20 | 1957-07-31 | Schering Corp | 3-piperidyl ethers and thioethers |
| US2974146A (en) * | 1956-02-24 | 1961-03-07 | Lakeside Lab Inc | 3-piperidyl benzhydryl ethers |
| NL237664A (sv) * | 1959-04-01 |
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1988
- 1988-07-08 GB GB888816365A patent/GB8816365D0/en active Pending
-
1989
- 1989-06-29 IL IL90792A patent/IL90792A0/xx not_active IP Right Cessation
- 1989-07-05 MY MYPI89000908A patent/MY106976A/en unknown
- 1989-07-06 PT PT91081A patent/PT91081B/pt not_active IP Right Cessation
- 1989-07-06 EP EP89306881A patent/EP0350309B1/en not_active Expired - Lifetime
- 1989-07-06 DD DD89330509A patent/DD284011A5/de not_active IP Right Cessation
- 1989-07-06 YU YU01353/89A patent/YU135389A/xx unknown
- 1989-07-06 CA CA000604882A patent/CA1336833C/en not_active Expired - Fee Related
- 1989-07-06 US US07/376,263 patent/US5089505A/en not_active Expired - Fee Related
- 1989-07-06 DE DE8989306881T patent/DE68903437T2/de not_active Expired - Fee Related
- 1989-07-06 AT AT89306881T patent/ATE82262T1/de not_active IP Right Cessation
- 1989-07-06 ES ES89306881T patent/ES2052917T3/es not_active Expired - Lifetime
- 1989-07-06 EG EG32789A patent/EG18853A/xx active
- 1989-07-07 HU HU893449A patent/HUT50771A/hu unknown
- 1989-07-07 FI FI893326A patent/FI94241C/sv not_active IP Right Cessation
- 1989-07-07 NO NO89892828A patent/NO892828L/no unknown
- 1989-07-07 RU SU894614534A patent/RU1838307C/ru active
- 1989-07-07 KR KR1019890009671A patent/KR930002728B1/ko not_active IP Right Cessation
- 1989-07-07 PL PL89280474A patent/PL161887B1/pl unknown
- 1989-07-07 IE IE220289A patent/IE63438B1/en not_active IP Right Cessation
- 1989-07-07 PL PL89283209A patent/PL162318B1/pl unknown
- 1989-07-07 AU AU37971/89A patent/AU602453B2/en not_active Ceased
- 1989-07-07 DK DK337589A patent/DK337589A/da not_active Application Discontinuation
- 1989-07-07 ZA ZA895175A patent/ZA895175B/xx unknown
- 1989-07-07 MX MX1672889A patent/MX16728A/es unknown
- 1989-07-07 NZ NZ229865A patent/NZ229865A/en unknown
- 1989-07-08 CN CN89104933A patent/CN1022914C/zh not_active Expired - Fee Related
- 1989-07-10 JP JP1177854A patent/JPH0739388B2/ja not_active Expired - Fee Related
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1990
- 1990-09-17 RU SU904831151A patent/RU1836364C/ru active
-
1992
- 1992-12-21 GR GR920403003T patent/GR3006595T3/el unknown
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1994
- 1994-07-26 JP JP6173882A patent/JPH07157469A/ja active Pending
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| MM | Patent lapsed |
Owner name: PFIZER INC. |