JP2008088090A - 2位に置換基を有する光学活性キヌクリジノール類の製造方法 - Google Patents
2位に置換基を有する光学活性キヌクリジノール類の製造方法 Download PDFInfo
- Publication number
- JP2008088090A JP2008088090A JP2006269642A JP2006269642A JP2008088090A JP 2008088090 A JP2008088090 A JP 2008088090A JP 2006269642 A JP2006269642 A JP 2006269642A JP 2006269642 A JP2006269642 A JP 2006269642A JP 2008088090 A JP2008088090 A JP 2008088090A
- Authority
- JP
- Japan
- Prior art keywords
- quinuclidinone
- group
- general formula
- substituent
- optically active
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 125000001424 substituent group Chemical group 0.000 title claims abstract description 92
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 20
- FSNYTEYOTCTPSO-UHFFFAOYSA-N 1-azabicyclo[2.2.2]octan-2-ol Chemical class C1CN2C(O)CC1CC2 FSNYTEYOTCTPSO-UHFFFAOYSA-N 0.000 title description 4
- ZKMZPXWMMSBLNO-UHFFFAOYSA-N 1-azabicyclo[2.2.2]octan-3-one Chemical class C1CC2C(=O)CN1CC2 ZKMZPXWMMSBLNO-UHFFFAOYSA-N 0.000 claims abstract description 31
- IVLICPVPXWEGCA-UHFFFAOYSA-N 3-quinuclidinol Chemical class C1C[C@@H]2C(O)C[N@]1CC2 IVLICPVPXWEGCA-UHFFFAOYSA-N 0.000 claims abstract description 25
- 150000001875 compounds Chemical class 0.000 claims abstract description 24
- 150000004696 coordination complex Chemical class 0.000 claims abstract description 15
- 238000000034 method Methods 0.000 claims description 47
- -1 hydride group Chemical group 0.000 claims description 45
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 19
- 125000000217 alkyl group Chemical group 0.000 claims description 13
- 229910052703 rhodium Inorganic materials 0.000 claims description 10
- 239000010948 rhodium Chemical group 0.000 claims description 10
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical group [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 claims description 10
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical group [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 claims description 9
- 125000004432 carbon atom Chemical group C* 0.000 claims description 9
- 229910052741 iridium Chemical group 0.000 claims description 9
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical group [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 claims description 9
- 125000001624 naphthyl group Chemical group 0.000 claims description 9
- 229910052707 ruthenium Inorganic materials 0.000 claims description 9
- 229910052799 carbon Inorganic materials 0.000 claims description 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 5
- 125000000058 cyclopentadienyl group Chemical group C1(=CC=CC1)* 0.000 claims description 5
- 239000001257 hydrogen Substances 0.000 claims description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims description 5
- 239000000203 mixture Substances 0.000 claims description 5
- 125000005842 heteroatom Chemical group 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- 125000002723 alicyclic group Chemical group 0.000 claims description 3
- 125000000129 anionic group Chemical group 0.000 claims description 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 3
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 3
- 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 description 3
- 125000003837 (C1-C20) alkyl group Chemical group 0.000 claims description 2
- DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 claims description 2
- 241000723346 Cinnamomum camphora Species 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 229960000846 camphor Drugs 0.000 claims description 2
- 229930008380 camphor Natural products 0.000 claims description 2
- 125000005010 perfluoroalkyl group Chemical group 0.000 claims description 2
- 239000003905 agrochemical Substances 0.000 abstract description 3
- 239000003814 drug Substances 0.000 abstract description 3
- 239000004973 liquid crystal related substance Substances 0.000 abstract description 2
- 239000000463 material Substances 0.000 abstract description 2
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical group CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 42
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 33
- 239000003054 catalyst Substances 0.000 description 28
- 238000006243 chemical reaction Methods 0.000 description 24
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 19
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 18
- 230000003287 optical effect Effects 0.000 description 17
- 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 16
- 235000019253 formic acid Nutrition 0.000 description 16
- 239000002585 base Substances 0.000 description 15
- FJXLZNSVOSVTPH-UHFFFAOYSA-N 1-azabicyclo[2.2.2]octan-2-one Chemical class C1CN2C(=O)CC1CC2 FJXLZNSVOSVTPH-UHFFFAOYSA-N 0.000 description 13
- 239000002904 solvent Substances 0.000 description 13
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 12
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 12
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 12
- 239000000758 substrate Substances 0.000 description 12
- 239000000852 hydrogen donor Substances 0.000 description 10
- 238000006722 reduction reaction Methods 0.000 description 10
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 9
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 239000003446 ligand Substances 0.000 description 9
- 239000000047 product Substances 0.000 description 8
- 230000002194 synthesizing effect Effects 0.000 description 7
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical group CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 6
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 6
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 6
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 5
- 238000005481 NMR spectroscopy Methods 0.000 description 5
- 239000012327 Ruthenium complex Substances 0.000 description 5
- 150000001298 alcohols Chemical class 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- 239000000543 intermediate Substances 0.000 description 5
- UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 5
- 238000003786 synthesis reaction Methods 0.000 description 5
- RXWKHZXQGODLGQ-UHFFFAOYSA-N 2,2-dipropyl-6-(pyridin-2-ylmethyl)-1-azabicyclo[2.2.2]octan-5-one Chemical compound CCCC1(CCC)CC(C2=O)CCN1C2CC1=CC=CC=N1 RXWKHZXQGODLGQ-UHFFFAOYSA-N 0.000 description 4
- CKDDUULIRPQPSS-UHFFFAOYSA-N 2-(pyridin-3-ylmethyl)-1-azabicyclo[2.2.2]octan-3-ol Chemical compound OC1C(CC2)CCN2C1CC1=CC=CN=C1 CKDDUULIRPQPSS-UHFFFAOYSA-N 0.000 description 4
- XXDZIVYAWMMIJB-UHFFFAOYSA-N 2-benzhydryl-5-propyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound CCCC1CN2CCC1C(=O)C2C(C=1C=CC=CC=1)C1=CC=CC=C1 XXDZIVYAWMMIJB-UHFFFAOYSA-N 0.000 description 4
- KFYIMQOZNMWSCN-UHFFFAOYSA-N 2-benzhydryl-6-propyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound CCCC1CC(C2=O)CCN1C2C(C=1C=CC=CC=1)C1=CC=CC=C1 KFYIMQOZNMWSCN-UHFFFAOYSA-N 0.000 description 4
- KVWJVHIFCGCJFS-UHFFFAOYSA-N 2-benzyl-5-propyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound CCCC1CN2CCC1C(=O)C2CC1=CC=CC=C1 KVWJVHIFCGCJFS-UHFFFAOYSA-N 0.000 description 4
- VTVHMXRWADEDAM-UHFFFAOYSA-N 2-benzyl-6-propyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound CCCC1CC(C2=O)CCN1C2CC1=CC=CC=C1 VTVHMXRWADEDAM-UHFFFAOYSA-N 0.000 description 4
- MOSVREIKDQHXSA-UHFFFAOYSA-N 2-methyl-5,5-dipropyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound C1CC2C(CCC)(CCC)CN1C(C)C2=O MOSVREIKDQHXSA-UHFFFAOYSA-N 0.000 description 4
- SMVZEFPDEGMAHZ-UHFFFAOYSA-N 2-methyl-5-propyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound C1CC2C(CCC)CN1C(C)C2=O SMVZEFPDEGMAHZ-UHFFFAOYSA-N 0.000 description 4
- XITYPGZVFRYXBD-UHFFFAOYSA-N 6-methyl-2-propyl-1-azabicyclo[2.2.2]octan-5-one Chemical compound C1CN2C(CCC)CC1C(=O)C2C XITYPGZVFRYXBD-UHFFFAOYSA-N 0.000 description 4
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 4
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 4
- 150000001412 amines Chemical class 0.000 description 4
- 125000001153 fluoro group Chemical group F* 0.000 description 4
- 150000002367 halogens Chemical group 0.000 description 4
- 238000004128 high performance liquid chromatography Methods 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- CTQNGGLPUBDAKN-UHFFFAOYSA-N o-dimethylbenzene Natural products CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 4
- 230000002829 reductive effect Effects 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- GKIOTMSOXQMART-UHFFFAOYSA-N 2-benzhydryl-1-azabicyclo[2.2.2]octan-3-ol Chemical compound OC1C(CC2)CCN2C1C(C=1C=CC=CC=1)C1=CC=CC=C1 GKIOTMSOXQMART-UHFFFAOYSA-N 0.000 description 3
- PQSXXBSNZJLXMQ-UHFFFAOYSA-N 2-benzhydryl-1-azabicyclo[2.2.2]octan-3-one Chemical compound O=C1C(CC2)CCN2C1C(C=1C=CC=CC=1)C1=CC=CC=C1 PQSXXBSNZJLXMQ-UHFFFAOYSA-N 0.000 description 3
- UVGXMMSWOFQAPO-UHFFFAOYSA-N 2-benzhydryl-5,5-dipropyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound CCCC1(CCC)CN2CCC1C(=O)C2C(C=1C=CC=CC=1)C1=CC=CC=C1 UVGXMMSWOFQAPO-UHFFFAOYSA-N 0.000 description 3
- MSXVEPNJUHWQHW-UHFFFAOYSA-N 2-methylbutan-2-ol Chemical compound CCC(C)(C)O MSXVEPNJUHWQHW-UHFFFAOYSA-N 0.000 description 3
- WOFXARVQBPLJRX-UHFFFAOYSA-N 5,5-dipropyl-2-(pyridin-2-ylmethyl)-1-azabicyclo[2.2.2]octan-3-one Chemical compound CCCC1(CCC)CN2CCC1C(=O)C2CC1=CC=CC=N1 WOFXARVQBPLJRX-UHFFFAOYSA-N 0.000 description 3
- LBUAFFIOZVMHFQ-UHFFFAOYSA-N 5-propyl-2-(pyridin-2-ylmethyl)-1-azabicyclo[2.2.2]octan-3-one Chemical compound CCCC1CN2CCC1C(=O)C2CC1=CC=CC=N1 LBUAFFIOZVMHFQ-UHFFFAOYSA-N 0.000 description 3
- KCFMIJLAHBTEDS-UHFFFAOYSA-N 6-benzyl-2,2-dipropyl-1-azabicyclo[2.2.2]octan-5-one Chemical compound CCCC1(CCC)CC(C2=O)CCN1C2CC1=CC=CC=C1 KCFMIJLAHBTEDS-UHFFFAOYSA-N 0.000 description 3
- DUHUIJLLDDMRPR-UHFFFAOYSA-N 6-propyl-2-(pyridin-2-ylmethyl)-1-azabicyclo[2.2.2]octan-3-one Chemical compound CCCC1CC(C2=O)CCN1C2CC1=CC=CC=N1 DUHUIJLLDDMRPR-UHFFFAOYSA-N 0.000 description 3
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- VURFVHCLMJOLKN-UHFFFAOYSA-N Diphosphine Natural products PP VURFVHCLMJOLKN-UHFFFAOYSA-N 0.000 description 3
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 3
- AZFNGPAYDKGCRB-XCPIVNJJSA-M [(1s,2s)-2-amino-1,2-diphenylethyl]-(4-methylphenyl)sulfonylazanide;chlororuthenium(1+);1-methyl-4-propan-2-ylbenzene Chemical compound [Ru+]Cl.CC(C)C1=CC=C(C)C=C1.C1=CC(C)=CC=C1S(=O)(=O)[N-][C@@H](C=1C=CC=CC=1)[C@@H](N)C1=CC=CC=C1 AZFNGPAYDKGCRB-XCPIVNJJSA-M 0.000 description 3
- 239000012300 argon atmosphere Substances 0.000 description 3
- 150000001728 carbonyl compounds Chemical class 0.000 description 3
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 150000002894 organic compounds Chemical class 0.000 description 3
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 3
- 230000001766 physiological effect Effects 0.000 description 3
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical group CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 3
- 238000001953 recrystallisation Methods 0.000 description 3
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
- AUHZEENZYGFFBQ-UHFFFAOYSA-N 1,3,5-trimethylbenzene Chemical compound CC1=CC(C)=CC(C)=C1 AUHZEENZYGFFBQ-UHFFFAOYSA-N 0.000 description 2
- IVSZLXZYQVIEFR-UHFFFAOYSA-N 1,3-Dimethylbenzene Natural products CC1=CC=CC(C)=C1 IVSZLXZYQVIEFR-UHFFFAOYSA-N 0.000 description 2
- LLZCQCYOESCOOC-UHFFFAOYSA-N 2,2,6-trimethyl-1-azabicyclo[2.2.2]octan-5-one Chemical compound C1CC2CC(C)(C)N1C(C)C2=O LLZCQCYOESCOOC-UHFFFAOYSA-N 0.000 description 2
- FPAGQWYWDXUUJY-UHFFFAOYSA-N 2,2-dibutyl-6-(pyridin-2-ylmethyl)-1-azabicyclo[2.2.2]octan-5-one Chemical compound CCCCC1(CCCC)CC(C2=O)CCN1C2CC1=CC=CC=N1 FPAGQWYWDXUUJY-UHFFFAOYSA-N 0.000 description 2
- RUFFEEJUPBPPAN-UHFFFAOYSA-N 2,2-dibutyl-6-methyl-1-azabicyclo[2.2.2]octan-5-one Chemical compound C1CN2C(CCCC)(CCCC)CC1C(=O)C2C RUFFEEJUPBPPAN-UHFFFAOYSA-N 0.000 description 2
- ZFGLSJWGABUTFP-UHFFFAOYSA-N 2,2-diethyl-6-(pyridin-2-ylmethyl)-1-azabicyclo[2.2.2]octan-5-one Chemical compound CCC1(CC)CC(C2=O)CCN1C2CC1=CC=CC=N1 ZFGLSJWGABUTFP-UHFFFAOYSA-N 0.000 description 2
- DJVFJIYIFWSUQL-UHFFFAOYSA-N 2,2-diethyl-6-methyl-1-azabicyclo[2.2.2]octan-5-one Chemical compound C1CN2C(CC)(CC)CC1C(=O)C2C DJVFJIYIFWSUQL-UHFFFAOYSA-N 0.000 description 2
- CBTIYRBOGIBSIL-UHFFFAOYSA-N 2,2-dimethyl-6-(pyridin-2-ylmethyl)-1-azabicyclo[2.2.2]octan-5-one Chemical compound CC1(C)CC(C2=O)CCN1C2CC1=CC=CC=N1 CBTIYRBOGIBSIL-UHFFFAOYSA-N 0.000 description 2
- UGXFJIIDSQDTTP-UHFFFAOYSA-N 2,2-dipropyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound C1CC2CCN1C(CCC)(CCC)C2=O UGXFJIIDSQDTTP-UHFFFAOYSA-N 0.000 description 2
- NQOFXQIWWUXGEJ-UHFFFAOYSA-N 2,5,5-trimethyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound C1CC2C(=O)C(C)N1CC2(C)C NQOFXQIWWUXGEJ-UHFFFAOYSA-N 0.000 description 2
- GKZRXVSTWICJDD-UHFFFAOYSA-N 2,5-dibenzyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound C=1C=CC=CC=1CC1CN2CCC1C(=O)C2CC1=CC=CC=C1 GKZRXVSTWICJDD-UHFFFAOYSA-N 0.000 description 2
- FGZCXPAKNQCBAB-UHFFFAOYSA-N 2,5-dimethyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound C1CC2C(C)CN1C(C)C2=O FGZCXPAKNQCBAB-UHFFFAOYSA-N 0.000 description 2
- ARQXJRQZMROTFG-UHFFFAOYSA-N 2,6-dibenzyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound C=1C=CC=CC=1CC1C(=O)C(C2)CCN1C2CC1=CC=CC=C1 ARQXJRQZMROTFG-UHFFFAOYSA-N 0.000 description 2
- INWCRGWSNNRQAD-UHFFFAOYSA-N 2,6-dimethyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound C1CN2C(C)CC1C(=O)C2C INWCRGWSNNRQAD-UHFFFAOYSA-N 0.000 description 2
- WJXSGKYIBQDKNF-UHFFFAOYSA-N 2-benzhydryl-4-propyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound C1CC(CCC)(C2=O)CCN1C2C(C=1C=CC=CC=1)C1=CC=CC=C1 WJXSGKYIBQDKNF-UHFFFAOYSA-N 0.000 description 2
- XEKDKMJQUTWETM-UHFFFAOYSA-N 2-benzhydryl-5,5-dibutyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound CCCCC1(CCCC)CN2CCC1C(=O)C2C(C=1C=CC=CC=1)C1=CC=CC=C1 XEKDKMJQUTWETM-UHFFFAOYSA-N 0.000 description 2
- CJORXZHGWAOQGG-UHFFFAOYSA-N 2-benzhydryl-5,5-diethyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound CCC1(CC)CN2CCC1C(=O)C2C(C=1C=CC=CC=1)C1=CC=CC=C1 CJORXZHGWAOQGG-UHFFFAOYSA-N 0.000 description 2
- LFOCOZWJQHYCST-UHFFFAOYSA-N 2-benzhydryl-5,5-dimethyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound CC1(C)CN2CCC1C(=O)C2C(C=1C=CC=CC=1)C1=CC=CC=C1 LFOCOZWJQHYCST-UHFFFAOYSA-N 0.000 description 2
- ZHAVRAIQVBPSEB-UHFFFAOYSA-N 2-benzhydryl-5-benzyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)C1C(=O)C2CCN1CC2CC1=CC=CC=C1 ZHAVRAIQVBPSEB-UHFFFAOYSA-N 0.000 description 2
- UEZIRCHXWQMTDI-UHFFFAOYSA-N 2-benzhydryl-5-butyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound CCCCC1CN2CCC1C(=O)C2C(C=1C=CC=CC=1)C1=CC=CC=C1 UEZIRCHXWQMTDI-UHFFFAOYSA-N 0.000 description 2
- RPUDZIAZYRPPLT-UHFFFAOYSA-N 2-benzhydryl-5-ethyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound CCC1CN2CCC1C(=O)C2C(C=1C=CC=CC=1)C1=CC=CC=C1 RPUDZIAZYRPPLT-UHFFFAOYSA-N 0.000 description 2
- OWEJSEIQAOTTKX-UHFFFAOYSA-N 2-benzhydryl-5-methyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound CC1CN2CCC1C(=O)C2C(C=1C=CC=CC=1)C1=CC=CC=C1 OWEJSEIQAOTTKX-UHFFFAOYSA-N 0.000 description 2
- REFZETRHPLXYPU-UHFFFAOYSA-N 2-benzhydryl-5-tert-butyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound CC(C)(C)C1CN2CCC1C(=O)C2C(C=1C=CC=CC=1)C1=CC=CC=C1 REFZETRHPLXYPU-UHFFFAOYSA-N 0.000 description 2
- FYGZFDURIOTELQ-UHFFFAOYSA-N 2-benzhydryl-6-butyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound CCCCC1CC(C2=O)CCN1C2C(C=1C=CC=CC=1)C1=CC=CC=C1 FYGZFDURIOTELQ-UHFFFAOYSA-N 0.000 description 2
- UBALTGNDPVTKBM-UHFFFAOYSA-N 2-benzhydryl-6-ethyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound CCC1CC(C2=O)CCN1C2C(C=1C=CC=CC=1)C1=CC=CC=C1 UBALTGNDPVTKBM-UHFFFAOYSA-N 0.000 description 2
- DCZSANVKFPLIRZ-UHFFFAOYSA-N 2-benzhydryl-6-methyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound CC1CC(C2=O)CCN1C2C(C=1C=CC=CC=1)C1=CC=CC=C1 DCZSANVKFPLIRZ-UHFFFAOYSA-N 0.000 description 2
- COLQHXANZSDSJL-UHFFFAOYSA-N 2-benzyl-1-azabicyclo[2.2.2]octan-3-ol Chemical compound OC1C(CC2)CCN2C1CC1=CC=CC=C1 COLQHXANZSDSJL-UHFFFAOYSA-N 0.000 description 2
- AHDBTNDXCMLRHB-UHFFFAOYSA-N 2-benzyl-4-propyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound C1CC(CCC)(C2=O)CCN1C2CC1=CC=CC=C1 AHDBTNDXCMLRHB-UHFFFAOYSA-N 0.000 description 2
- OFRDBXIQCQUHOG-UHFFFAOYSA-N 2-benzyl-5,5-dibutyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound CCCCC1(CCCC)CN2CCC1C(=O)C2CC1=CC=CC=C1 OFRDBXIQCQUHOG-UHFFFAOYSA-N 0.000 description 2
- BWFFTROTLKBRJR-UHFFFAOYSA-N 2-benzyl-5,5-diethyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound CCC1(CC)CN2CCC1C(=O)C2CC1=CC=CC=C1 BWFFTROTLKBRJR-UHFFFAOYSA-N 0.000 description 2
- XRSQOGAJRRSVDM-UHFFFAOYSA-N 2-benzyl-5,5-dimethyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound CC1(C)CN2CCC1C(=O)C2CC1=CC=CC=C1 XRSQOGAJRRSVDM-UHFFFAOYSA-N 0.000 description 2
- QGXHYRIKWMWKQA-UHFFFAOYSA-N 2-benzyl-5,5-dipropyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound CCCC1(CCC)CN2CCC1C(=O)C2CC1=CC=CC=C1 QGXHYRIKWMWKQA-UHFFFAOYSA-N 0.000 description 2
- VMSCHEHJCQNYTJ-UHFFFAOYSA-N 2-benzyl-5-butyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound CCCCC1CN2CCC1C(=O)C2CC1=CC=CC=C1 VMSCHEHJCQNYTJ-UHFFFAOYSA-N 0.000 description 2
- WVHBYRIIFALBEO-UHFFFAOYSA-N 2-benzyl-5-ethyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound CCC1CN2CCC1C(=O)C2CC1=CC=CC=C1 WVHBYRIIFALBEO-UHFFFAOYSA-N 0.000 description 2
- HLUGYKFPWOWPMG-UHFFFAOYSA-N 2-benzyl-5-methyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound CC1CN2CCC1C(=O)C2CC1=CC=CC=C1 HLUGYKFPWOWPMG-UHFFFAOYSA-N 0.000 description 2
- BBOYBDBHHSJVBL-UHFFFAOYSA-N 2-benzyl-5-tert-butyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound CC(C)(C)C1CN2CCC1C(=O)C2CC1=CC=CC=C1 BBOYBDBHHSJVBL-UHFFFAOYSA-N 0.000 description 2
- HFNVMFBSLIUCEF-UHFFFAOYSA-N 2-benzyl-6-ethyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound CCC1CC(C2=O)CCN1C2CC1=CC=CC=C1 HFNVMFBSLIUCEF-UHFFFAOYSA-N 0.000 description 2
- NRYGUZISBMUICY-UHFFFAOYSA-N 2-benzyl-6-methyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound CC1CC(C2=O)CCN1C2CC1=CC=CC=C1 NRYGUZISBMUICY-UHFFFAOYSA-N 0.000 description 2
- SEFWWHJTVHPLQM-UHFFFAOYSA-N 2-benzyl-6-methyl-1-azabicyclo[2.2.2]octan-5-one Chemical compound O=C1C(C)N2CCC1CC2CC1=CC=CC=C1 SEFWWHJTVHPLQM-UHFFFAOYSA-N 0.000 description 2
- JYORZYVFVKJZPK-UHFFFAOYSA-N 2-benzyl-6-tert-butyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound CC(C)(C)C1CC(C2=O)CCN1C2CC1=CC=CC=C1 JYORZYVFVKJZPK-UHFFFAOYSA-N 0.000 description 2
- OTSCEMCYLOTCHM-UHFFFAOYSA-N 2-butyl-1-azabicyclo[2.2.2]octan-5-one Chemical compound C1CN2C(CCCC)CC1C(=O)C2 OTSCEMCYLOTCHM-UHFFFAOYSA-N 0.000 description 2
- UVXMEDKACNVVPR-UHFFFAOYSA-N 2-ethyl-6-methyl-1-azabicyclo[2.2.2]octan-5-one Chemical compound C1CN2C(CC)CC1C(=O)C2C UVXMEDKACNVVPR-UHFFFAOYSA-N 0.000 description 2
- WOQOVHITYXJLGO-UHFFFAOYSA-N 2-methyl-4-propyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound C1CN2CCC1(CCC)C(=O)C2C WOQOVHITYXJLGO-UHFFFAOYSA-N 0.000 description 2
- VFONENVCMZLYMX-UHFFFAOYSA-N 2-methyl-6,6-di(propan-2-yl)-1-azabicyclo[2.2.2]octan-3-one Chemical compound C1CN2C(C(C)C)(C(C)C)CC1C(=O)C2C VFONENVCMZLYMX-UHFFFAOYSA-N 0.000 description 2
- NMCLUBHACHXWQO-UHFFFAOYSA-N 2-tert-butyl-6-methyl-1-azabicyclo[2.2.2]octan-5-one Chemical compound C1CC2CC(C(C)(C)C)N1C(C)C2=O NMCLUBHACHXWQO-UHFFFAOYSA-N 0.000 description 2
- UTDAGHZGKXPRQI-UHFFFAOYSA-N 4-[4-[4-(4-aminophenoxy)phenyl]sulfonylphenoxy]aniline Chemical compound C1=CC(N)=CC=C1OC1=CC=C(S(=O)(=O)C=2C=CC(OC=3C=CC(N)=CC=3)=CC=2)C=C1 UTDAGHZGKXPRQI-UHFFFAOYSA-N 0.000 description 2
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 description 2
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 description 2
- 125000000590 4-methylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 2
- XXQXIPAQCOZMEI-UHFFFAOYSA-N 5,5-dibutyl-2-methyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound C1CC2C(CCCC)(CCCC)CN1C(C)C2=O XXQXIPAQCOZMEI-UHFFFAOYSA-N 0.000 description 2
- BMTMKMSZTHNVJZ-UHFFFAOYSA-N 5,5-diethyl-2-(pyridin-2-ylmethyl)-1-azabicyclo[2.2.2]octan-3-one Chemical compound CCC1(CC)CN2CCC1C(=O)C2CC1=CC=CC=N1 BMTMKMSZTHNVJZ-UHFFFAOYSA-N 0.000 description 2
- QIMYVQFMOWPKGG-UHFFFAOYSA-N 5,5-diethyl-2-methyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound C1CC2C(CC)(CC)CN1C(C)C2=O QIMYVQFMOWPKGG-UHFFFAOYSA-N 0.000 description 2
- FZEYVWMJUMRXST-UHFFFAOYSA-N 5,5-dimethyl-2-(pyridin-2-ylmethyl)-1-azabicyclo[2.2.2]octan-3-one Chemical compound CC1(C)CN2CCC1C(=O)C2CC1=CC=CC=N1 FZEYVWMJUMRXST-UHFFFAOYSA-N 0.000 description 2
- LKNVKZZXYBQCJZ-UHFFFAOYSA-N 5-butyl-2-(pyridin-2-ylmethyl)-1-azabicyclo[2.2.2]octan-3-one Chemical compound CCCCC1CN2CCC1C(=O)C2CC1=CC=CC=N1 LKNVKZZXYBQCJZ-UHFFFAOYSA-N 0.000 description 2
- QDPGLLVOMJRZBJ-UHFFFAOYSA-N 5-butyl-2-methyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound C1CC2C(CCCC)CN1C(C)C2=O QDPGLLVOMJRZBJ-UHFFFAOYSA-N 0.000 description 2
- UKJXXVGEUOXBKS-UHFFFAOYSA-N 5-ethyl-2-(pyridin-2-ylmethyl)-1-azabicyclo[2.2.2]octan-3-one Chemical compound CCC1CN2CCC1C(=O)C2CC1=CC=CC=N1 UKJXXVGEUOXBKS-UHFFFAOYSA-N 0.000 description 2
- FZEGIMQMRWCWDS-UHFFFAOYSA-N 5-ethyl-2-methyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound C1CC2C(CC)CN1C(C)C2=O FZEGIMQMRWCWDS-UHFFFAOYSA-N 0.000 description 2
- VYRNEPXHLSMNIJ-UHFFFAOYSA-N 5-methyl-2-(pyridin-2-ylmethyl)-1-azabicyclo[2.2.2]octan-3-one Chemical compound CC1CN2CCC1C(=O)C2CC1=CC=CC=N1 VYRNEPXHLSMNIJ-UHFFFAOYSA-N 0.000 description 2
- FYWLPIZPIDAVMO-UHFFFAOYSA-N 5-tert-butyl-2-(pyridin-2-ylmethyl)-1-azabicyclo[2.2.2]octan-3-one Chemical compound CC(C)(C)C1CN2CCC1C(=O)C2CC1=CC=CC=N1 FYWLPIZPIDAVMO-UHFFFAOYSA-N 0.000 description 2
- AFPDPVFVEVXXLB-UHFFFAOYSA-N 5-tert-butyl-2-methyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound C1CC2C(C(C)(C)C)CN1C(C)C2=O AFPDPVFVEVXXLB-UHFFFAOYSA-N 0.000 description 2
- YQGUCFUBUMUBCD-UHFFFAOYSA-N 6-benzhydryl-2,2-dibutyl-1-azabicyclo[2.2.2]octan-5-one Chemical compound CCCCC1(CCCC)CC(C2=O)CCN1C2C(C=1C=CC=CC=1)C1=CC=CC=C1 YQGUCFUBUMUBCD-UHFFFAOYSA-N 0.000 description 2
- NWBUETIQJCUIAA-UHFFFAOYSA-N 6-benzhydryl-2,2-diethyl-1-azabicyclo[2.2.2]octan-5-one Chemical compound CCC1(CC)CC(C2=O)CCN1C2C(C=1C=CC=CC=1)C1=CC=CC=C1 NWBUETIQJCUIAA-UHFFFAOYSA-N 0.000 description 2
- GYCKISNIIFHXOD-UHFFFAOYSA-N 6-benzhydryl-2,2-dimethyl-1-azabicyclo[2.2.2]octan-5-one Chemical compound CC1(C)CC(C2=O)CCN1C2C(C=1C=CC=CC=1)C1=CC=CC=C1 GYCKISNIIFHXOD-UHFFFAOYSA-N 0.000 description 2
- OAWNXIOMFOFARQ-UHFFFAOYSA-N 6-benzhydryl-2,2-dipropyl-1-azabicyclo[2.2.2]octan-5-one Chemical compound CCCC1(CCC)CC(C2=O)CCN1C2C(C=1C=CC=CC=1)C1=CC=CC=C1 OAWNXIOMFOFARQ-UHFFFAOYSA-N 0.000 description 2
- NBGIPWZBQQUINB-UHFFFAOYSA-N 6-benzyl-2,2-dibutyl-1-azabicyclo[2.2.2]octan-5-one Chemical compound CCCCC1(CCCC)CC(C2=O)CCN1C2CC1=CC=CC=C1 NBGIPWZBQQUINB-UHFFFAOYSA-N 0.000 description 2
- XATNDUZJMPTREB-UHFFFAOYSA-N 6-benzyl-2,2-diethyl-1-azabicyclo[2.2.2]octan-5-one Chemical compound CCC1(CC)CC(C2=O)CCN1C2CC1=CC=CC=C1 XATNDUZJMPTREB-UHFFFAOYSA-N 0.000 description 2
- HAAAMFRENIPNQY-UHFFFAOYSA-N 6-benzyl-2,2-dimethyl-1-azabicyclo[2.2.2]octan-5-one Chemical compound CC1(C)CC(C2=O)CCN1C2CC1=CC=CC=C1 HAAAMFRENIPNQY-UHFFFAOYSA-N 0.000 description 2
- QIVVLMIOKMQFCB-UHFFFAOYSA-N 6-butyl-2-(pyridin-2-ylmethyl)-1-azabicyclo[2.2.2]octan-3-one Chemical compound CCCCC1CC(C2=O)CCN1C2CC1=CC=CC=N1 QIVVLMIOKMQFCB-UHFFFAOYSA-N 0.000 description 2
- FJIMISGFJNWVPK-UHFFFAOYSA-N 6-ethyl-2-(pyridin-2-ylmethyl)-1-azabicyclo[2.2.2]octan-3-one Chemical compound CCC1CC(C2=O)CCN1C2CC1=CC=CC=N1 FJIMISGFJNWVPK-UHFFFAOYSA-N 0.000 description 2
- QGRLLPBDURQZHK-UHFFFAOYSA-N 6-methyl-2,2-dipropyl-1-azabicyclo[2.2.2]octan-5-one Chemical compound C1CN2C(CCC)(CCC)CC1C(=O)C2C QGRLLPBDURQZHK-UHFFFAOYSA-N 0.000 description 2
- PTCNSMFYPRUZCA-UHFFFAOYSA-N 6-methyl-2-(pyridin-2-ylmethyl)-1-azabicyclo[2.2.2]octan-3-one Chemical compound CC1CC(C2=O)CCN1C2CC1=CC=CC=N1 PTCNSMFYPRUZCA-UHFFFAOYSA-N 0.000 description 2
- MZOVIUNAYCFOJD-UHFFFAOYSA-N 6-tert-butyl-2-(pyridin-2-ylmethyl)-1-azabicyclo[2.2.2]octan-3-one Chemical compound CC(C)(C)C1CC(C2=O)CCN1C2CC1=CC=CC=N1 MZOVIUNAYCFOJD-UHFFFAOYSA-N 0.000 description 2
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- URLKBWYHVLBVBO-UHFFFAOYSA-N Para-Xylene Chemical group CC1=CC=C(C)C=C1 URLKBWYHVLBVBO-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
- 239000013543 active substance Substances 0.000 description 2
- 239000005456 alcohol based solvent Substances 0.000 description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- 238000009876 asymmetric hydrogenation reaction Methods 0.000 description 2
- 238000011914 asymmetric synthesis Methods 0.000 description 2
- 150000001555 benzenes Chemical group 0.000 description 2
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 2
- MUALRAIOVNYAIW-UHFFFAOYSA-N binap Chemical compound C1=CC=CC=C1P(C=1C(=C2C=CC=CC2=CC=1)C=1C2=CC=CC=C2C=CC=1P(C=1C=CC=CC=1)C=1C=CC=CC=1)C1=CC=CC=C1 MUALRAIOVNYAIW-UHFFFAOYSA-N 0.000 description 2
- 125000001246 bromo group Chemical group Br* 0.000 description 2
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 208000015114 central nervous system disease Diseases 0.000 description 2
- 125000001309 chloro group Chemical group Cl* 0.000 description 2
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 2
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 2
- SQNZJJAZBFDUTD-UHFFFAOYSA-N durene Chemical compound CC1=CC(C)=C(C)C=C1C SQNZJJAZBFDUTD-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000004210 ether based solvent Substances 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 238000005984 hydrogenation reaction Methods 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- XCYJPXQACVEIOS-UHFFFAOYSA-N meta-isopropyltoluene Natural products CC(C)C1=CC=CC(C)=C1 XCYJPXQACVEIOS-UHFFFAOYSA-N 0.000 description 2
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 125000004043 oxo group Chemical group O=* 0.000 description 2
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 2
- HFPZCAJZSCWRBC-UHFFFAOYSA-N p-cymene Chemical compound CC(C)C1=CC=C(C)C=C1 HFPZCAJZSCWRBC-UHFFFAOYSA-N 0.000 description 2
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- UOHMMEJUHBCKEE-UHFFFAOYSA-N prehnitene Chemical compound CC1=CC=C(C)C(C)=C1C UOHMMEJUHBCKEE-UHFFFAOYSA-N 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 2
- 235000017557 sodium bicarbonate Nutrition 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 2
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- QBYIENPQHBMVBV-HFEGYEGKSA-N (2R)-2-hydroxy-2-phenylacetic acid Chemical compound O[C@@H](C(O)=O)c1ccccc1.O[C@@H](C(O)=O)c1ccccc1 QBYIENPQHBMVBV-HFEGYEGKSA-N 0.000 description 1
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 description 1
- ZXMGHDIOOHOAAE-UHFFFAOYSA-N 1,1,1-trifluoro-n-(trifluoromethylsulfonyl)methanesulfonamide Chemical group FC(F)(F)S(=O)(=O)NS(=O)(=O)C(F)(F)F ZXMGHDIOOHOAAE-UHFFFAOYSA-N 0.000 description 1
- YPEOCTSXLWIZSO-UHFFFAOYSA-N 1,3-dimethylcyclopenta-1,3-diene Chemical compound CC1=CC(C)=CC1 YPEOCTSXLWIZSO-UHFFFAOYSA-N 0.000 description 1
- WWRCMNKATXZARA-UHFFFAOYSA-N 1-Isopropyl-2-methylbenzene Chemical compound CC(C)C1=CC=CC=C1C WWRCMNKATXZARA-UHFFFAOYSA-N 0.000 description 1
- LNETULKMXZVUST-UHFFFAOYSA-N 1-naphthoic acid Chemical group C1=CC=C2C(C(=O)O)=CC=CC2=C1 LNETULKMXZVUST-UHFFFAOYSA-N 0.000 description 1
- 238000005160 1H NMR spectroscopy Methods 0.000 description 1
- YXMOGYHTCFHCJS-UHFFFAOYSA-N 2,2-dibutyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound C1CC2CCN1C(CCCC)(CCCC)C2=O YXMOGYHTCFHCJS-UHFFFAOYSA-N 0.000 description 1
- HCTJDJPBZMKQNZ-UHFFFAOYSA-N 2,2-diethyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound C1CC2CCN1C(CC)(CC)C2=O HCTJDJPBZMKQNZ-UHFFFAOYSA-N 0.000 description 1
- SPEQMFXWAHTACU-UHFFFAOYSA-N 2,2-dimethyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound C1CC2CCN1C(C)(C)C2=O SPEQMFXWAHTACU-UHFFFAOYSA-N 0.000 description 1
- ZLBMNQVDRHQUJV-UHFFFAOYSA-N 2,4-dibenzyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound C1CN2CCC1(CC=1C=CC=CC=1)C(=O)C2CC1=CC=CC=C1 ZLBMNQVDRHQUJV-UHFFFAOYSA-N 0.000 description 1
- USCJCIIGOQMGLR-UHFFFAOYSA-N 2,4-dimethyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound C1CC2(C)CCN1C(C)C2=O USCJCIIGOQMGLR-UHFFFAOYSA-N 0.000 description 1
- LKXMIMXBWNPWEK-UHFFFAOYSA-N 2-(pyridin-2-ylmethyl)-1-azabicyclo[2.2.2]octan-3-one Chemical compound O=C1C(CC2)CCN2C1CC1=CC=CC=N1 LKXMIMXBWNPWEK-UHFFFAOYSA-N 0.000 description 1
- RCZTVWXBZKSDRO-UHFFFAOYSA-N 2-benzhydryl-4-benzyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound C1CN2CCC1(CC=1C=CC=CC=1)C(=O)C2C(C=1C=CC=CC=1)C1=CC=CC=C1 RCZTVWXBZKSDRO-UHFFFAOYSA-N 0.000 description 1
- HELJORDIPWSWBP-UHFFFAOYSA-N 2-benzhydryl-4-butyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound C1CC(CCCC)(C2=O)CCN1C2C(C=1C=CC=CC=1)C1=CC=CC=C1 HELJORDIPWSWBP-UHFFFAOYSA-N 0.000 description 1
- XCBRZQIAJBUGIP-UHFFFAOYSA-N 2-benzhydryl-4-ethyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound C1CC(CC)(C2=O)CCN1C2C(C=1C=CC=CC=1)C1=CC=CC=C1 XCBRZQIAJBUGIP-UHFFFAOYSA-N 0.000 description 1
- UADPCWHZWJWVKH-UHFFFAOYSA-N 2-benzhydryl-4-methyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound C1CC(C)(C2=O)CCN1C2C(C=1C=CC=CC=1)C1=CC=CC=C1 UADPCWHZWJWVKH-UHFFFAOYSA-N 0.000 description 1
- XTBIKDMVFQWFRL-UHFFFAOYSA-N 2-benzhydryl-4-tert-butyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound C1CC(C(C)(C)C)(C2=O)CCN1C2C(C=1C=CC=CC=1)C1=CC=CC=C1 XTBIKDMVFQWFRL-UHFFFAOYSA-N 0.000 description 1
- QQKMXYGQNQDZPX-UHFFFAOYSA-N 2-benzhydryl-6,6-di(propan-2-yl)-1-azabicyclo[2.2.2]octan-3-one Chemical compound CC(C)C1(C(C)C)CC(C2=O)CCN1C2C(C=1C=CC=CC=1)C1=CC=CC=C1 QQKMXYGQNQDZPX-UHFFFAOYSA-N 0.000 description 1
- UGYHGZBKZOGBMP-UHFFFAOYSA-N 2-benzyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound O=C1C(CC2)CCN2C1CC1=CC=CC=C1 UGYHGZBKZOGBMP-UHFFFAOYSA-N 0.000 description 1
- ZMLDTDTUQNMDGG-UHFFFAOYSA-N 2-benzyl-4-butyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound C1CC(CCCC)(C2=O)CCN1C2CC1=CC=CC=C1 ZMLDTDTUQNMDGG-UHFFFAOYSA-N 0.000 description 1
- TXGBIJISBFJLCL-UHFFFAOYSA-N 2-benzyl-4-ethyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound C1CC(CC)(C2=O)CCN1C2CC1=CC=CC=C1 TXGBIJISBFJLCL-UHFFFAOYSA-N 0.000 description 1
- WIJMVVHIESMIQN-UHFFFAOYSA-N 2-benzyl-4-methyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound C1CC(C)(C2=O)CCN1C2CC1=CC=CC=C1 WIJMVVHIESMIQN-UHFFFAOYSA-N 0.000 description 1
- BXGAEIFFJKINML-UHFFFAOYSA-N 2-benzyl-4-tert-butyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound C1CC(C(C)(C)C)(C2=O)CCN1C2CC1=CC=CC=C1 BXGAEIFFJKINML-UHFFFAOYSA-N 0.000 description 1
- RDTCWFOELVZRDY-UHFFFAOYSA-N 2-benzyl-6,6-di(propan-2-yl)-1-azabicyclo[2.2.2]octan-3-one Chemical compound CC(C)C1(C(C)C)CC(C2=O)CCN1C2CC1=CC=CC=C1 RDTCWFOELVZRDY-UHFFFAOYSA-N 0.000 description 1
- YYLOBFDZYJZLLK-UHFFFAOYSA-N 2-benzyl-6-butyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound CCCCC1CC(C2=O)CCN1C2CC1=CC=CC=C1 YYLOBFDZYJZLLK-UHFFFAOYSA-N 0.000 description 1
- OQWMKHBPXUEJET-UHFFFAOYSA-N 2-butyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound C1CC2CCN1C(CCCC)C2=O OQWMKHBPXUEJET-UHFFFAOYSA-N 0.000 description 1
- YXMCKYBIXUPZRP-UHFFFAOYSA-N 2-butyl-6-methyl-1-azabicyclo[2.2.2]octan-5-one Chemical compound C1CN2C(CCCC)CC1C(=O)C2C YXMCKYBIXUPZRP-UHFFFAOYSA-N 0.000 description 1
- HGTFCYLHGGFUSJ-UHFFFAOYSA-N 2-ethyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound C1CC2CCN1C(CC)C2=O HGTFCYLHGGFUSJ-UHFFFAOYSA-N 0.000 description 1
- LGOHLIRGPFPGKT-UHFFFAOYSA-N 2-methyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound C1CC2CCN1C(C)C2=O LGOHLIRGPFPGKT-UHFFFAOYSA-N 0.000 description 1
- UOBYKYZJUGYBDK-UHFFFAOYSA-N 2-naphthoic acid Chemical group C1=CC=CC2=CC(C(=O)O)=CC=C21 UOBYKYZJUGYBDK-UHFFFAOYSA-N 0.000 description 1
- LWMLPRIFDATEIJ-UHFFFAOYSA-N 2-propyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound C1CC2CCN1C(CCC)C2=O LWMLPRIFDATEIJ-UHFFFAOYSA-N 0.000 description 1
- DKZFMFKOKYWEHB-UHFFFAOYSA-N 2-propyl-1-azabicyclo[2.2.2]octan-5-one Chemical compound C1CN2C(CCC)CC1C(=O)C2 DKZFMFKOKYWEHB-UHFFFAOYSA-N 0.000 description 1
- 125000006479 2-pyridyl methyl group Chemical group [H]C1=C([H])C([H])=C([H])C(=N1)C([H])([H])* 0.000 description 1
- NZBRANADQSRSPE-UHFFFAOYSA-N 2-tert-butyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound C1CC2CCN1C(C(C)(C)C)C2=O NZBRANADQSRSPE-UHFFFAOYSA-N 0.000 description 1
- LPRIHYORUUWIGJ-UHFFFAOYSA-N 4-benzyl-2-(pyridin-2-ylmethyl)-1-azabicyclo[2.2.2]octan-3-one Chemical compound C1CN2CCC1(CC=1C=CC=CC=1)C(=O)C2CC1=CC=CC=N1 LPRIHYORUUWIGJ-UHFFFAOYSA-N 0.000 description 1
- WIDLJVGCTHZABL-UHFFFAOYSA-N 4-benzyl-2-methyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound O=C1C(C)N(CC2)CCC12CC1=CC=CC=C1 WIDLJVGCTHZABL-UHFFFAOYSA-N 0.000 description 1
- COVNNYYFYMIFCH-UHFFFAOYSA-N 4-butyl-2-methyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound C1CN2CCC1(CCCC)C(=O)C2C COVNNYYFYMIFCH-UHFFFAOYSA-N 0.000 description 1
- WHEOFXHTIBACND-UHFFFAOYSA-N 4-ethyl-2-(pyridin-2-ylmethyl)-1-azabicyclo[2.2.2]octan-3-one Chemical compound C1CC(CC)(C2=O)CCN1C2CC1=CC=CC=N1 WHEOFXHTIBACND-UHFFFAOYSA-N 0.000 description 1
- DJJKFRRBNDOCMB-UHFFFAOYSA-N 4-ethyl-2-methyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound C1CN2CCC1(CC)C(=O)C2C DJJKFRRBNDOCMB-UHFFFAOYSA-N 0.000 description 1
- SDINNEUSJWDRJU-UHFFFAOYSA-N 4-methyl-2-(pyridin-2-ylmethyl)-1-azabicyclo[2.2.2]octan-3-one Chemical compound C1CC(C)(C2=O)CCN1C2CC1=CC=CC=N1 SDINNEUSJWDRJU-UHFFFAOYSA-N 0.000 description 1
- AWJYXLWZDCXPMK-UHFFFAOYSA-N 4-propyl-2-(pyridin-2-ylmethyl)-1-azabicyclo[2.2.2]octan-3-one Chemical compound C1CC(CCC)(C2=O)CCN1C2CC1=CC=CC=N1 AWJYXLWZDCXPMK-UHFFFAOYSA-N 0.000 description 1
- PHTBGMHQENLJKC-UHFFFAOYSA-N 4-tert-butyl-2-methyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound C1CC2(C(C)(C)C)CCN1C(C)C2=O PHTBGMHQENLJKC-UHFFFAOYSA-N 0.000 description 1
- WGTSXPBOFHUXAE-UHFFFAOYSA-N 5,5-di(propan-2-yl)-2-(pyridin-2-ylmethyl)-1-azabicyclo[2.2.2]octan-3-one Chemical compound CC(C)C1(C(C)C)CN2CCC1C(=O)C2CC1=CC=CC=N1 WGTSXPBOFHUXAE-UHFFFAOYSA-N 0.000 description 1
- ZZMMERGREUWVLD-UHFFFAOYSA-N 5,5-dibutyl-2-(pyridin-2-ylmethyl)-1-azabicyclo[2.2.2]octan-3-one Chemical compound CCCCC1(CCCC)CN2CCC1C(=O)C2CC1=CC=CC=N1 ZZMMERGREUWVLD-UHFFFAOYSA-N 0.000 description 1
- ASKKDMKRHPGUBH-UHFFFAOYSA-N 5-benzyl-2-methyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound O=C1C(C)N(C2)CCC1C2CC1=CC=CC=C1 ASKKDMKRHPGUBH-UHFFFAOYSA-N 0.000 description 1
- SYZOSLGACBALGR-UHFFFAOYSA-N 5-methyl-1-azabicyclo[2.2.2]octan-3-one Chemical compound C1CC2C(C)CN1CC2=O SYZOSLGACBALGR-UHFFFAOYSA-N 0.000 description 1
- 208000024827 Alzheimer disease Diseases 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- JWFBZIIWQPFQST-UHFFFAOYSA-N C1CN2CCC1C(=O)C2CC3=CC=CC=C3C(C4=CC=CC=C4)C5=CC=CC=C5 Chemical compound C1CN2CCC1C(=O)C2CC3=CC=CC=C3C(C4=CC=CC=C4)C5=CC=CC=C5 JWFBZIIWQPFQST-UHFFFAOYSA-N 0.000 description 1
- VPSULBJUKFCKKU-UHFFFAOYSA-N CC1=C(C(=C(C1(C)[Ir])C)C)C Chemical compound CC1=C(C(=C(C1(C)[Ir])C)C)C VPSULBJUKFCKKU-UHFFFAOYSA-N 0.000 description 1
- SAXQOYZKDFVDTH-UHFFFAOYSA-N CC1=C(C(=C(C1(C)[Rh])C)C)C Chemical compound CC1=C(C(=C(C1(C)[Rh])C)C)C SAXQOYZKDFVDTH-UHFFFAOYSA-N 0.000 description 1
- NBGZRWXLOZPNHG-UHFFFAOYSA-N CCCC1CN2CCC1C(=O)C2(C)C3=CC=CC=N3 Chemical compound CCCC1CN2CCC1C(=O)C2(C)C3=CC=CC=N3 NBGZRWXLOZPNHG-UHFFFAOYSA-N 0.000 description 1
- LSPHULWDVZXLIL-UHFFFAOYSA-N Camphoric acid Natural products CC1(C)C(C(O)=O)CCC1(C)C(O)=O LSPHULWDVZXLIL-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 108010009685 Cholinergic Receptors Proteins 0.000 description 1
- DIWVBIXQCNRCFE-UHFFFAOYSA-N DL-alpha-Methoxyphenylacetic acid Chemical compound COC(C(O)=O)C1=CC=CC=C1 DIWVBIXQCNRCFE-UHFFFAOYSA-N 0.000 description 1
- GSNUFIFRDBKVIE-UHFFFAOYSA-N DMF Natural products CC1=CC=C(C)O1 GSNUFIFRDBKVIE-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical group CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- QECVIPBZOPUTRD-UHFFFAOYSA-N N=S(=O)=O Chemical group N=S(=O)=O QECVIPBZOPUTRD-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- IWYDHOAUDWTVEP-UHFFFAOYSA-N R-2-phenyl-2-hydroxyacetic acid Natural products OC(=O)C(O)C1=CC=CC=C1 IWYDHOAUDWTVEP-UHFFFAOYSA-N 0.000 description 1
- 244000028419 Styrax benzoin Species 0.000 description 1
- 235000000126 Styrax benzoin Nutrition 0.000 description 1
- 235000008411 Sumatra benzointree Nutrition 0.000 description 1
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 1
- 102000034337 acetylcholine receptors Human genes 0.000 description 1
- 125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 229910000272 alkali metal oxide Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 229960002130 benzoin Drugs 0.000 description 1
- 125000001231 benzoyloxy group Chemical group C(C1=CC=CC=C1)(=O)O* 0.000 description 1
- WHGYBXFWUBPSRW-FOUAGVGXSA-N beta-cyclodextrin Chemical compound OC[C@H]([C@H]([C@@H]([C@H]1O)O)O[C@H]2O[C@@H]([C@@H](O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O3)[C@H](O)[C@H]2O)CO)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@@H]3O[C@@H]1CO WHGYBXFWUBPSRW-FOUAGVGXSA-N 0.000 description 1
- 229960004853 betadex Drugs 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- LSPHULWDVZXLIL-QUBYGPBYSA-N camphoric acid Chemical compound CC1(C)[C@H](C(O)=O)CC[C@]1(C)C(O)=O LSPHULWDVZXLIL-QUBYGPBYSA-N 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000007810 chemical reaction solvent Substances 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 238000004440 column chromatography Methods 0.000 description 1
- 150000003997 cyclic ketones Chemical class 0.000 description 1
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 1
- 238000010511 deprotection reaction Methods 0.000 description 1
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- KTWOOEGAPBSYNW-UHFFFAOYSA-N ferrocene Chemical group [Fe+2].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 KTWOOEGAPBSYNW-UHFFFAOYSA-N 0.000 description 1
- 125000004216 fluoromethyl group Chemical group [H]C([H])(F)* 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 235000019382 gum benzoic Nutrition 0.000 description 1
- YUWFEBAXEOLKSG-UHFFFAOYSA-N hexamethylbenzene Chemical compound CC1=C(C)C(C)=C(C)C(C)=C1C YUWFEBAXEOLKSG-UHFFFAOYSA-N 0.000 description 1
- IHPDTPWNFBQHEB-UHFFFAOYSA-N hydrobenzoin Chemical compound C=1C=CC=CC=1C(O)C(O)C1=CC=CC=C1 IHPDTPWNFBQHEB-UHFFFAOYSA-N 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000006317 isomerization reaction Methods 0.000 description 1
- 239000005453 ketone based solvent Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- JILPJDVXYVTZDQ-UHFFFAOYSA-N lithium methoxide Chemical compound [Li+].[O-]C JILPJDVXYVTZDQ-UHFFFAOYSA-N 0.000 description 1
- 229960002510 mandelic acid Drugs 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- NHQZWDCNEJJOGT-UHFFFAOYSA-N n-(2-amino-1,2-diphenylethyl)-2,4,6-trimethylbenzenesulfonamide Chemical compound CC1=CC(C)=CC(C)=C1S(=O)(=O)NC(C=1C=CC=CC=1)C(N)C1=CC=CC=C1 NHQZWDCNEJJOGT-UHFFFAOYSA-N 0.000 description 1
- IHGSMBVTJBJICR-UHFFFAOYSA-N n-(2-amino-1,2-diphenylethyl)-3,5-dimethylbenzenesulfonamide Chemical compound CC1=CC(C)=CC(S(=O)(=O)NC(C(N)C=2C=CC=CC=2)C=2C=CC=CC=2)=C1 IHGSMBVTJBJICR-UHFFFAOYSA-N 0.000 description 1
- XJPRQBJPIQYZTG-UHFFFAOYSA-N n-(2-amino-1,2-diphenylethyl)-4-chlorobenzenesulfonamide Chemical compound C=1C=CC=CC=1C(N)C(C=1C=CC=CC=1)NS(=O)(=O)C1=CC=C(Cl)C=C1 XJPRQBJPIQYZTG-UHFFFAOYSA-N 0.000 description 1
- PKJIJTOTTMMAHF-UHFFFAOYSA-N n-(2-amino-1,2-diphenylethyl)-4-methoxybenzenesulfonamide Chemical compound C1=CC(OC)=CC=C1S(=O)(=O)NC(C=1C=CC=CC=1)C(N)C1=CC=CC=C1 PKJIJTOTTMMAHF-UHFFFAOYSA-N 0.000 description 1
- UOPFIWYXBIHPIP-UHFFFAOYSA-N n-(2-amino-1,2-diphenylethyl)-4-methylbenzenesulfonamide Chemical compound C1=CC(C)=CC=C1S(=O)(=O)NC(C=1C=CC=CC=1)C(N)C1=CC=CC=C1 UOPFIWYXBIHPIP-UHFFFAOYSA-N 0.000 description 1
- WSXSGNTYACLUNV-UHFFFAOYSA-N n-(2-amino-1,2-diphenylethyl)-4-tert-butylbenzenesulfonamide Chemical compound C1=CC(C(C)(C)C)=CC=C1S(=O)(=O)NC(C=1C=CC=CC=1)C(N)C1=CC=CC=C1 WSXSGNTYACLUNV-UHFFFAOYSA-N 0.000 description 1
- FSRRNSLQEDUDTP-UHFFFAOYSA-N n-(2-amino-1,2-diphenylethyl)methanesulfonamide Chemical compound C=1C=CC=CC=1C(NS(=O)(=O)C)C(N)C1=CC=CC=C1 FSRRNSLQEDUDTP-UHFFFAOYSA-N 0.000 description 1
- ZDIGAPCVRZZXDB-UHFFFAOYSA-N n-(2-amino-1,2-diphenylethyl)naphthalene-2-sulfonamide Chemical compound C=1C=CC=CC=1C(N)C(NS(=O)(=O)C=1C=C2C=CC=CC2=CC=1)C1=CC=CC=C1 ZDIGAPCVRZZXDB-UHFFFAOYSA-N 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000005457 optimization Methods 0.000 description 1
- 125000002524 organometallic group Chemical group 0.000 description 1
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 description 1
- NFHFRUOZVGFOOS-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.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 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 1
- 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 description 1
- BEZDDPMMPIDMGJ-UHFFFAOYSA-N pentamethylbenzene Chemical compound CC1=CC(C)=C(C)C(C)=C1C BEZDDPMMPIDMGJ-UHFFFAOYSA-N 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- WQKGAJDYBZOFSR-UHFFFAOYSA-N potassium;propan-2-olate Chemical compound [K+].CC(C)[O-] WQKGAJDYBZOFSR-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000003890 substance P antagonist Substances 0.000 description 1
- 238000001308 synthesis method Methods 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- CZDYPVPMEAXLPK-UHFFFAOYSA-N tetramethylsilane Chemical compound C[Si](C)(C)C CZDYPVPMEAXLPK-UHFFFAOYSA-N 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- RKBCYCFRFCNLTO-UHFFFAOYSA-N triisopropylamine Chemical compound CC(C)N(C(C)C)C(C)C RKBCYCFRFCNLTO-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D453/00—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids
- C07D453/02—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids containing not further condensed quinuclidine ring systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
2位に置換基を有する光学活性3−キヌクリジノール類、特に医薬、農薬等に利用される光学活性な生理活性化合物、または液晶材料等の合成中間体として有用な2位に置換基を有する光学活性シス−3−キヌクリジノール類の製造方法を提供する。
【解決手段】
本発明の2位に置換基を有する光学活性3−キヌクリジノール類の製造方法は、所定の金属錯体の存在下において、2位に置換基を有する3−キヌクリジノン類と水素を供与する化合物とを反応させる。
【選択図】なし
Description
2−メチル−4−メチル−3−キヌクリジノン、2−メチル−4−エチル−3−キヌクリジノン、2−メチル−4−n−プロピル−3−キヌクリジノン、2−メチル−4−i−プロピル−3−キヌクリジノン、2−メチル−4−ブチル−3−キヌクリジノン、2−メチル−4−t−ブチル−3−キヌクリジノン、2−メチル−4−ベンジル−3−キヌクリジノン、2−ベンジル−4−メチル−3−キヌクリジノン、2−ベンジル−4−エチル−3−キヌクリジノン、2−ベンジル−4−n−プロピル−3−キヌクリジノン、2−ベンジル−4−i−プロピル−3−キヌクリジノン、2−ベンジル−4−ブチル−3−キヌクリジノン、2−ベンジル−4−t−ブチル−3−キヌクリジノン、2−ベンジル−4−ベンジル−3−キヌクリジノン、2−ジフェニルメチル−4−メチル−3−キヌクリジノン、2−ジフェニルメチル−4−エチル−3−キヌクリジノン、2−ジフェニルメチル−4−n−プロピル−3−キヌクリジノン、2−ジフェニルメチル−4−i−プロピル−3−キヌクリジノン、2−ジフェニルメチル−4−ブチル−3−キヌクリジノン、2−ジフェニルメチル−4−t−ブチル−3−キヌクリジノン、2−ジフェニルメチル−4−ベンジル−3−キヌクリジノン、2−ピリジルメチル−4−メチル−3−キヌクリジノン、2−ピリジルメチル−4−エチル−3−キヌクリジノン、2−ピリジルメチル−4−n−プロピル−3−キヌクリジノン、2−ピリジルメチル−4−i−プロピル−3−キヌクリジノン、2−ピリジルメチル−4−ブチル−3−キヌクリジノン、2−ピリジルメチル−4−t−ブチル−3−キヌクリジノン、2−ピリジルメチル−4−ベンジル−3−キヌクリジノン、
2−メチル−5−メチル−3−キヌクリジノン、2−メチル−5,5−ジメチル−3−キヌクリジノン、2−メチル−5−エチル−3−キヌクリジノン、2−メチル−5,5−ジエチル−3−キヌクリジノン、2−メチル−5−n−プロピル−3−キヌクリジノン、2−メチル−5,5−ジn−プロピル−3−キヌクリジノン、2−メチル−5−i−プロピル−3−キヌクリジノン、2−メチル−5,5−ジi−プロピル−3−キヌクリジノン、2−メチル−5−ブチル−3−キヌクリジノン、2−メチル−5,5−ジブチル−3−キヌクリジノン、2−メチル−5−t−ブチル−3−キヌクリジノン、2−メチル−5−ベンジル−3−キヌクリジノン、
2−メチル−6−メチル−3−キヌクリジノン、2−メチル−6,6−ジメチル−3−キヌクリジノン、2−メチル−6−エチル−3−キヌクリジノン、2−メチル−6,6−ジエチル−3−キヌクリジノン、2−メチル−6−n−プロピル−3−キヌクリジノン、2−メチル−6,6−ジn−プロピル−3−キヌクリジノン、2−メチル−6−i−プロピル−3−キヌクリジノン、2−メチル−6,6−ジi−プロピル−3−キヌクリジノン、6−ブチル−3−キヌクリジノン、2−メチル−6,6−ジブチル−3−キヌクリジノン、2−メチル−6−t−ブチル−3−キヌクリジノン、2−メチル−6−ベンジル−3−キヌクリジノン、
2−メチル−7−メチル−3−キヌクリジノン、2−メチル−7,7−ジメチル−3−キヌクリジノン、2−メチル−7−エチル−3−キヌクリジノン、2−メチル−7,7−ジエチル−3−キヌクリジノン、2−メチル−7−n−プロピル−3−キヌクリジノン、2−メチル−7,7−ジn−プロピル−3−キヌクリジノン、2−メチル−7−i−プロピル−3−キヌクリジノン、2−メチル−7,7−ジi−プロピル−3−キヌクリジノン、2−メチル−7−ブチル−3−キヌクリジノン、2−メチル−7,7−ジブチル−3−キヌクリジノン、2−メチル−7−t−ブチル−3−キヌクリジノン、2−メチル−7−ベンジル−3−キヌクリジノン、
2−メチル−8−メチル−3−キヌクリジノン、2−メチル−8,8−ジメチル−3−キヌクリジノン、2−メチル−8−エチル−3−キヌクリジノン、2−メチル−8,8−ジエチル−3−キヌクリジノン、2−メチル−8−n−プロピル−3−キヌクリジノン、2−メチル−8,8−ジn−プロピル−3−キヌクリジノン、2−メチル−8−i−プロピル−3−キヌクリジノン、2−メチル−8,8−ジi−プロピル−3−キヌクリジノン、2−メチル−8−ブチル−3−キヌクリジノン、2−メチル−8,8−ジブチル−3−キヌクリジノン、2−メチル−8−t−ブチル−3−キヌクリジノン、8−メチル−3−キヌクリジノン、2−ベンジル−8−メチル−3−キヌクリジノン、2−ベンジル−8,8−ジメチル−3−キヌクリジノン、2−ベンジル−8−エチル−3−キヌクリジノン、2−ベンジル−8,8−ジエチル−3−キヌクリジノン、2−ベンジル−8−n−プロピル−3−キヌクリジノン、2−ベンジル−8,8−n−プロピル−3−キヌクリジノン、2−ベンジル−8−i−プロピル−3−キヌクリジノン、2−ベンジル−8,8−i−プロピル−3−キヌクリジノン、2−ベンジル−8−ブチル−3−キヌクリジノン、2−ベンジル−8,8−ジブチル−3−キヌクリジノン、2−ベンジル−8−t−ブチル−3−キヌクリジノン、2,8−ジベンジル−3−キヌクリジノン、
NMR:LA400型装置(400MHz)
(日本電子(株)製)
内部標準物質:1H−NMR・・・テトラメチルシラン
外部標準物質:31P−NMR・・・85%リン酸
光学純度:ガスクロマトグラフィ−
Chirasil−DEX CB(0.25mm×25m、DF=0.25μm)
(CHROMPACK社製)
BETA DEX 120(0.25mm×30m、DF=0.25μm)
(SUPELCO社製)
:高速液体クロマトグラフィ−
(株)島津製作所製
また、実施例中のee%はエナンチオマ−過剰率を示し、S/Cは触媒に対する基質のモル比を示す。
光学活性−シス−2−ジフェニルメチル−3−キヌクリジノ−ルの製造
ラセミ−2−ジフェニルメチル−3−キヌクリジノン0.511g(1.75mmol)、トリエチルアミン0.49ml(3.51mmol)、ギ酸0.33ml(1.75mmol)(ギ酸/トリエチルアミン=5/2対基質モル比)、RuCl[(S,S)−Tsdpen](p−cymene)5.5mg(8.6×10−3mmol、S/C=200)を、アルゴン雰囲気下に20mLシュレンクに入れ、40℃にて19時間攪拌した。反応液に飽和炭酸水素ナトリウム水溶液を加えて塩基性にした後、析出粉末を濾集して目的物を収率86%で得た。NMRから、シス体のみの2−ジフェニルメチル−3−キヌクリジノールが得られたことを確認した。また、HPLC(Daicel Chiralcel OD−H,Hexane/2−propanol/diethylamine=80/20/0.1,0.5mL/min,25℃、シス体中2種の光学異性体のレテンションタイムは11.3minおよび26.5min)により光学純度を測定した結果、99%eeであり、光学活性−シス−2−ジフェニルメチル−3−キヌクリジノールが生成したことが判明した。
光学活性−シス−2−ジフェニルメチル−3−キヌクリジノールの製造
ラセミ−2−ジフェニルメチル−3−キヌクリジノン0.511g(1.75mmol)、トリエチルアミン0.49mL(3.51mmol)、ギ酸0.33mL(1.75mmol)(ギ酸/トリエチルアミン=5/2対基質モル比)、RuCl[(S,S)−Tsdpen](p−cymene)5.5mg(8.6×10−3mmol、S/C=200)、溶媒としてN,N−ジメチルホルムアミド2mLを、アルゴン雰囲気下に20mLシュレンクに入れ、40℃にて19時間攪拌した。反応液に飽和炭酸水素ナトリウム水溶液を加えて塩基性にした後、析出粉末を濾集して目的物を90%収率で得た。NMRから、シス体のみの2−ジフェニルメチル−3−キヌクリジノールが得られたことを確認した。また、光学純度は、99%eeであった。
光学活性−シス−2−ジフェニルメチル−3−キヌクリジノールの製造
RuCl[(R,R)−Tsdpen](mesitylene)を使用した以外は、実施例2と同様の条件で反応を行ない、95%eeのシス−2−ジフェニルメチル−3−キヌクリジノールを収率43%で得た。
光学活性2−(3−ピリジニルメチル)−3−キヌクリジノールの合成
ラセミ−2−(3−ピリジニルメチル)−3−キヌクリジノン0.518g(2.39mmol)トリエチルアミン0.65ml(4.66mmol)、ギ酸0.44mL(11.7mmol)(ギ酸/トリエチルアミン=5/2対基質モル比)、RuCl[(S,S)−Tsdpen](p−cymene)5.5mg(8.6×10−3mmol、S/C=200)を、アルゴン雰囲気下に20mLシュレンクに入れ、40℃にて19時間攪拌した。反応液をジクロロメタンに希釈して、炭酸カリウムで中和し、固体をろ過により除去した後、濃縮乾固して目的物を収率49%で得た。NMRから、一方のジアステレオマ−のみの2−(3−ピリジニルメチル)−3−キヌクリジノールが得られたことを確認した。また、HPLC(Daicel Chiralcel OD−Hを2本直列接続, Hexane/2−propanol/diethylamine=80/20/0.1, 0.3mL/min,25℃、得られたジアステレオマー中2種の光学異性体のレテンションタイムは64.0minおよび83.2min)により光学純度を測定した結果、85%eeであった。
光学活性2−(3−ピリジニルメチル)−3−キヌクリジノールの合成
Cp*IrCl[(S,S)−Tsdpen]を使用した以外は、実施例4と同様の条件で反応を行ない、71%eeの光学活性2−(3−ピリジニルメチル)−3−キヌクリジノールを単一のジアステレオマーとして収率100%で得た。
光学活性2−ベンジル−3−キヌクリジノールの合成
ラセミ−2−ベンジル−3−キヌクリジノンを反応した以外は、実施例1と同様の条件で反応を行ない、93%eeの光学活性2−ベンジル−3−キヌクリジノールを単一のジアステレオマーとして収率100%で得た。
Claims (9)
- 2位に置換基を有する光学活性3−キヌクリジノール類の製造方法であって、下記一般式(1)
- 請求項1または2に記載の一般式(1)または一般式(2)中のMがルテニウムである、請求項1または2に記載の方法。
- 請求項1または2に記載の一般式(1)または一般式(2)中のMがイリジウムである、請求項1または2に記載の方法。
- 請求項1または2に記載の一般式(1)または一般式(2)中のMがロジウムである、請求項1または2に記載の方法。
- 2位に置換基を有する光学活性3−キヌクリジノール類がジアステレオ選択的かつエナンチオ選択的に得られることを特徴とする、請求項1〜3のいずれかに記載の方法。
- 請求項7に記載の一般式(3)〜(6)中のR5が、置換基を有してもよい、ジフェニルメチル基、3−ピリジルメチル基またはベンジル基である、請求項7に記載の方法。
- 請求項1〜5のいずれかに記載の一般式(1)または一般式(2)で表される金属錯体の、2位に置換基を有する光学活性3−キヌクリジノール類の製造への使用。
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2006269642A JP5172124B2 (ja) | 2006-09-29 | 2006-09-29 | 2位に置換基を有する光学活性キヌクリジノール類の製造方法 |
US11/906,103 US7687630B2 (en) | 2006-09-29 | 2007-09-28 | Method for producing optically active quinuclidinols having one or more substituted groups at the 2-position |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2006269642A JP5172124B2 (ja) | 2006-09-29 | 2006-09-29 | 2位に置換基を有する光学活性キヌクリジノール類の製造方法 |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2008088090A true JP2008088090A (ja) | 2008-04-17 |
JP5172124B2 JP5172124B2 (ja) | 2013-03-27 |
Family
ID=39261853
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2006269642A Expired - Fee Related JP5172124B2 (ja) | 2006-09-29 | 2006-09-29 | 2位に置換基を有する光学活性キヌクリジノール類の製造方法 |
Country Status (2)
Country | Link |
---|---|
US (1) | US7687630B2 (ja) |
JP (1) | JP5172124B2 (ja) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8436181B2 (en) | 2007-09-06 | 2013-05-07 | Nippon Soda Co., Ltd. | Production process of optically active 3-quinuclidinol derivative |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2009023941A (ja) * | 2007-07-19 | 2009-02-05 | Kanto Chem Co Inc | 有機金属化合物及びそれを用いた光学活性アルコール類の製造方法 |
CN112679433A (zh) * | 2019-10-18 | 2021-04-20 | 浙江九洲药业股份有限公司 | 一种艾利西平的制备方法 |
CN112707899B (zh) * | 2019-10-24 | 2023-10-17 | 东莞市东阳光动物保健药品有限公司 | 一种奎宁醇的制备方法 |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0578354A (ja) * | 1991-02-11 | 1993-03-30 | Merck Sharp & Dohme Ltd | アザ二環式化合物、これを含有する医薬組成物及び治療のための使用方法 |
JP2000256234A (ja) * | 1999-03-03 | 2000-09-19 | Mitsubishi Chemicals Corp | 光学活性1,2−ジオール類の製造方法 |
JP2001104795A (ja) * | 1999-10-13 | 2001-04-17 | Mitsubishi Chemicals Corp | ルテニウム触媒組成物 |
JP2002531564A (ja) * | 1998-12-11 | 2002-09-24 | アール・ジェイ・レイノルズ・タバコ・カンパニー | ピリジル−橋頭誘導体およびそれらの類縁体、医用組成物およびニコチン性コリン作用性受容体の阻害物質としてのそれらの使用 |
JP2003201269A (ja) * | 2001-10-31 | 2003-07-18 | Kanto Chem Co Inc | 光学活性アミノアルコールおよびその中間体の製造方法 |
WO2004031155A1 (en) * | 2002-10-07 | 2004-04-15 | Novartis Ag | ENANTIOSELECTIVE PROCESS FOR THE PREPARATION OF BOTH ENANTIOMERS OF 10,11-DIHYDRO-10-HYDROXY-5H-DIBENZ [b,f]AZEPINE-5-CARBOXAMIDE AND NEW CRYSTAL FORMS THEREOF |
JP2004526788A (ja) * | 2001-04-19 | 2004-09-02 | ファルマシア・アンド・アップジョン・カンパニー | 疾患治療用の置換型アザ二環式基(ニコチン性アセチルコリン受容体アンタゴニスト) |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2731377B2 (ja) | 1994-12-07 | 1998-03-25 | 科学技術振興事業団 | 光学活性アルコール類の製造方法 |
CA2164685C (en) * | 1994-12-07 | 2005-03-08 | Takeshi Ohkuma | Method for producing an alcohol |
ATE194342T1 (de) | 1996-01-19 | 2000-07-15 | Lonza Ag | Verfahren zur herstellung von optisch aktivem 3- chinuclidinol |
MX9706944A (es) | 1996-09-12 | 1998-08-30 | Pfizer | Quinuclidinas sustituidas con tetrazolilo como antagonistas de la sustancia p. |
JP4004123B2 (ja) | 1997-12-26 | 2007-11-07 | 独立行政法人科学技術振興機構 | ルテニウム錯体を触媒とするアルコール化合物の製造方法 |
JPH11322649A (ja) | 1998-03-16 | 1999-11-24 | Mitsubishi Chemical Corp | 光学活性アルコールの製造方法 |
IL142810A0 (en) * | 2000-05-03 | 2002-03-10 | Pfizer Prod Inc | Pharmaceutical uses for fluoroalkoxybenzylamino derivatives of nitrogen containing heterocycles |
JP3566955B2 (ja) * | 2001-12-28 | 2004-09-15 | 関東化学株式会社 | 新規ルテニウム錯体およびこれを触媒として用いるアルコール化合物の製造方法 |
JP2003277380A (ja) | 2002-03-20 | 2003-10-02 | Kawaken Fine Chem Co Ltd | 光学活性3−キヌクリジノールの製造方法 |
JP3569280B1 (ja) | 2003-03-07 | 2004-09-22 | 川研ファインケミカル株式会社 | 光学活性アルコールの製造方法 |
EP1601635B1 (en) | 2003-03-07 | 2008-01-09 | Kawaken Fine Chemicals Co., Ltd. | Process for producing optically active alcohol in the presence of rhodium, a chiral ferrocenyldiphosphine and an optically active diamine |
JP2005298411A (ja) * | 2004-04-13 | 2005-10-27 | Kawaken Fine Chem Co Ltd | 光学活性アルコールの製造方法 |
JP4490211B2 (ja) * | 2004-08-27 | 2010-06-23 | 高砂香料工業株式会社 | 光学活性3−キヌクリジノール類の製造方法 |
-
2006
- 2006-09-29 JP JP2006269642A patent/JP5172124B2/ja not_active Expired - Fee Related
-
2007
- 2007-09-28 US US11/906,103 patent/US7687630B2/en not_active Expired - Fee Related
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0578354A (ja) * | 1991-02-11 | 1993-03-30 | Merck Sharp & Dohme Ltd | アザ二環式化合物、これを含有する医薬組成物及び治療のための使用方法 |
JP2002531564A (ja) * | 1998-12-11 | 2002-09-24 | アール・ジェイ・レイノルズ・タバコ・カンパニー | ピリジル−橋頭誘導体およびそれらの類縁体、医用組成物およびニコチン性コリン作用性受容体の阻害物質としてのそれらの使用 |
JP2000256234A (ja) * | 1999-03-03 | 2000-09-19 | Mitsubishi Chemicals Corp | 光学活性1,2−ジオール類の製造方法 |
JP2001104795A (ja) * | 1999-10-13 | 2001-04-17 | Mitsubishi Chemicals Corp | ルテニウム触媒組成物 |
JP2004526788A (ja) * | 2001-04-19 | 2004-09-02 | ファルマシア・アンド・アップジョン・カンパニー | 疾患治療用の置換型アザ二環式基(ニコチン性アセチルコリン受容体アンタゴニスト) |
JP2003201269A (ja) * | 2001-10-31 | 2003-07-18 | Kanto Chem Co Inc | 光学活性アミノアルコールおよびその中間体の製造方法 |
WO2004031155A1 (en) * | 2002-10-07 | 2004-04-15 | Novartis Ag | ENANTIOSELECTIVE PROCESS FOR THE PREPARATION OF BOTH ENANTIOMERS OF 10,11-DIHYDRO-10-HYDROXY-5H-DIBENZ [b,f]AZEPINE-5-CARBOXAMIDE AND NEW CRYSTAL FORMS THEREOF |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8436181B2 (en) | 2007-09-06 | 2013-05-07 | Nippon Soda Co., Ltd. | Production process of optically active 3-quinuclidinol derivative |
JP5244113B2 (ja) * | 2007-09-06 | 2013-07-24 | 日本曹達株式会社 | 光学活性3−キヌクリジノール誘導体の製造方法 |
US8759524B2 (en) | 2007-09-06 | 2014-06-24 | Nippon Soda Co., Ltd. | Production process of optically active 3-quinuclidinol derivative |
Also Published As
Publication number | Publication date |
---|---|
US20080081911A1 (en) | 2008-04-03 |
US7687630B2 (en) | 2010-03-30 |
JP5172124B2 (ja) | 2013-03-27 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP1276745B1 (en) | Ruthenium-diphosphine complexes and their use as catalysts | |
US7601667B2 (en) | Sulfonate catalyst and method of producing alcohol compound using the same | |
WO2018060512A1 (en) | Process for preparing chiral amines | |
JP2008184398A (ja) | キラルなイリジウムアクア錯体およびそれを用いた光学活性ヒドロキシ化合物の製造方法 | |
JP5372771B2 (ja) | プロセス | |
JP5172124B2 (ja) | 2位に置換基を有する光学活性キヌクリジノール類の製造方法 | |
JP4722037B2 (ja) | 光学活性アルコールの製法 | |
US20090216019A1 (en) | Process for Production of Optically Active Quinuclidinols | |
EP2264000B1 (en) | Method for producing optically active aminoalcohol compound using ruthenium compound | |
AU2011301115B2 (en) | Biaryl diphosphine ligands, intermediates of the same and their use in asymmetric catalysis | |
JP2005525426A (ja) | ルテニウム錯体を触媒として用いた不活性イミンの水素添加法 | |
US9328079B2 (en) | Process for producing optically active amine | |
JP5232374B2 (ja) | 2位に置換基を有する光学活性キヌクリジノール類の製造方法 | |
JP2912572B2 (ja) | 光学活性アミン類の製造方法 | |
JP5507931B2 (ja) | 芳香族複素環をもつ光学活性アルコールの製造方法 | |
JP2003277380A (ja) | 光学活性3−キヌクリジノールの製造方法 | |
US20120309997A1 (en) | Enantiomerically Enriched Aminodiphosphines as Ligands for the Preparation of Catalysts for Asymmetric Synthesis | |
JP2005306804A (ja) | 光学活性3−キヌクリジノールの製造方法 | |
EP1601635A1 (en) | Process for producing optically active alcohol in the presence of rhodium, a chiral ferrocenyldiphosphine and an optically active diamine | |
JP2007106734A (ja) | 新規な光学活性遷移金属錯体,及びその製造方法 | |
KR100425526B1 (ko) | 키랄 디포스핀 화합물 및 이를 이용한 비대칭 반응 | |
TWI510472B (zh) | 立體選擇性製備吡唑羧醯胺之方法 | |
JP5087395B2 (ja) | スルホナート触媒及びそれを利用したアルコール化合物の製法 | |
WO2005056513A1 (en) | Asymmetric imine hydrogenation processes | |
JP2006063028A (ja) | 光学活性3−キヌクリジノール類の製造方法 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
RD04 | Notification of resignation of power of attorney |
Free format text: JAPANESE INTERMEDIATE CODE: A7424 Effective date: 20081024 |
|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20090929 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20100630 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20120228 |
|
A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20120229 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20120427 |
|
TRDD | Decision of grant or rejection written | ||
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20121211 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20121226 |
|
R150 | Certificate of patent or registration of utility model |
Ref document number: 5172124 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
LAPS | Cancellation because of no payment of annual fees |