NO327005B1 - Acetylenderivaer som har mGluR5 antagonistisk aktivitet - Google Patents
Acetylenderivaer som har mGluR5 antagonistisk aktivitet Download PDFInfo
- Publication number
- NO327005B1 NO327005B1 NO20042673A NO20042673A NO327005B1 NO 327005 B1 NO327005 B1 NO 327005B1 NO 20042673 A NO20042673 A NO 20042673A NO 20042673 A NO20042673 A NO 20042673A NO 327005 B1 NO327005 B1 NO 327005B1
- Authority
- NO
- Norway
- Prior art keywords
- hydroxy
- carboxylic acid
- phenylethynyl
- ethyl ester
- cyclohexyl
- Prior art date
Links
- 102000012777 Metabotropic Glutamate 5 Receptor Human genes 0.000 title claims description 6
- 108010065028 Metabotropic Glutamate 5 Receptor Proteins 0.000 title claims description 6
- 150000000475 acetylene derivatives Chemical class 0.000 title description 2
- 230000003042 antagnostic effect Effects 0.000 title description 2
- 150000001875 compounds Chemical class 0.000 claims description 52
- 238000000034 method Methods 0.000 claims description 24
- -1 tetrahydrofuran- 3yl Chemical group 0.000 claims description 23
- 150000003839 salts Chemical group 0.000 claims description 22
- 239000002253 acid Substances 0.000 claims description 21
- 229910052739 hydrogen Inorganic materials 0.000 claims description 18
- 239000001257 hydrogen Substances 0.000 claims description 18
- 239000012458 free base Substances 0.000 claims description 15
- 125000000217 alkyl group Chemical group 0.000 claims description 14
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- 239000003814 drug Substances 0.000 claims description 6
- 150000002431 hydrogen Chemical group 0.000 claims description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 6
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 6
- MIROVSIAGIUZPP-UHFFFAOYSA-N ethyl 5-[2-(3-chlorophenyl)ethynyl]-5-hydroxy-2,3,4,4a,6,7,8,8a-octahydroquinoline-1-carboxylate Chemical compound CCOC(=O)N1CCCC2C1CCCC2(O)C#CC1=CC=CC(Cl)=C1 MIROVSIAGIUZPP-UHFFFAOYSA-N 0.000 claims description 5
- GRNSGJOKGICXGO-UHFFFAOYSA-N tert-butyl 4-oxo-3,3a,5,6,7,7a-hexahydro-2h-indole-1-carboxylate Chemical compound C1CCC(=O)C2C1N(C(=O)OC(C)(C)C)CC2 GRNSGJOKGICXGO-UHFFFAOYSA-N 0.000 claims description 5
- 208000019901 Anxiety disease Diseases 0.000 claims description 4
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- CFBZCLJIZQGFNC-UHFFFAOYSA-N [5-[2-(3-chlorophenyl)ethynyl]-5-hydroxy-2,3,4,4a,6,7,8,8a-octahydroquinolin-1-yl]-(furan-2-yl)methanone Chemical compound C=1C=CC(Cl)=CC=1C#CC1(O)CCCC2C1CCCN2C(=O)C1=CC=CO1 CFBZCLJIZQGFNC-UHFFFAOYSA-N 0.000 claims description 4
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- SNPPWIUOZRMYNY-UHFFFAOYSA-N bupropion Chemical compound CC(C)(C)NC(C)C(=O)C1=CC=CC(Cl)=C1 SNPPWIUOZRMYNY-UHFFFAOYSA-N 0.000 claims description 4
- 229940088679 drug related substance Drugs 0.000 claims description 4
- JATWRGYZPSSPIF-UHFFFAOYSA-N ethyl n-[3-[2-(3-fluorophenyl)ethynyl]-3-hydroxycyclohexyl]carbamate Chemical compound C1C(NC(=O)OCC)CCCC1(O)C#CC1=CC=CC(F)=C1 JATWRGYZPSSPIF-UHFFFAOYSA-N 0.000 claims description 4
- 230000000848 glutamatergic effect Effects 0.000 claims description 4
- ZFPZEYHRWGMJCV-ZHALLVOQSA-N mavoglurant Chemical compound C([C@]1(O)CCC[C@@H]2[C@H]1CCN2C(=O)OC)#CC1=CC=CC(C)=C1 ZFPZEYHRWGMJCV-ZHALLVOQSA-N 0.000 claims description 4
- 230000001404 mediated effect Effects 0.000 claims description 4
- GWKUSCMPEHTLOL-UHFFFAOYSA-N n-[3-hydroxy-3-[2-(3-methylphenyl)ethynyl]cyclohexyl]acetamide Chemical compound C1C(NC(=O)C)CCCC1(O)C#CC1=CC=CC(C)=C1 GWKUSCMPEHTLOL-UHFFFAOYSA-N 0.000 claims description 4
- 230000008054 signal transmission Effects 0.000 claims description 4
- MAUUZUNIDQAWQB-UHFFFAOYSA-N tert-butyl n-[3-hydroxy-3-[2-(3-methoxyphenyl)ethynyl]cyclohexyl]carbamate Chemical compound COC1=CC=CC(C#CC2(O)CC(CCC2)NC(=O)OC(C)(C)C)=C1 MAUUZUNIDQAWQB-UHFFFAOYSA-N 0.000 claims description 4
- 206010008120 Cerebral ischaemia Diseases 0.000 claims description 3
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- 208000005392 Spasm Diseases 0.000 claims description 3
- OOHWRZMAIUHACJ-PMRGXDQWSA-N [(3r)-oxolan-3-yl] 4-hydroxy-4-(2-phenylethynyl)-3,3a,5,6,7,7a-hexahydro-2h-indole-1-carboxylate Chemical compound C=1C=CC=CC=1C#CC1(O)CCCC2C1CCN2C(=O)O[C@@H]1CCOC1 OOHWRZMAIUHACJ-PMRGXDQWSA-N 0.000 claims description 3
- 206010002026 amyotrophic lateral sclerosis Diseases 0.000 claims description 3
- 229960001058 bupropion Drugs 0.000 claims description 3
- YQWKJPIHRNCFRR-UHFFFAOYSA-N cyclopropyl-[7-hydroxy-7-[2-(3-methylphenyl)ethynyl]-3,3a,4,5,6,7a-hexahydro-1h-isoindol-2-yl]methanone Chemical compound CC1=CC=CC(C#CC2(O)C3CN(CC3CCC2)C(=O)C2CC2)=C1 YQWKJPIHRNCFRR-UHFFFAOYSA-N 0.000 claims description 3
- 239000003937 drug carrier Substances 0.000 claims description 3
- 206010015037 epilepsy Diseases 0.000 claims description 3
- CWSTVFBFMPWZTK-UHFFFAOYSA-N ethyl 4-[2-(3-fluorophenyl)ethynyl]-4-hydroxy-3,3a,5,6,7,7a-hexahydro-2h-indole-1-carboxylate Chemical compound CCOC(=O)N1CCC2C1CCCC2(O)C#CC1=CC=CC(F)=C1 CWSTVFBFMPWZTK-UHFFFAOYSA-N 0.000 claims description 3
- WIPRRMYYUMAMPJ-UHFFFAOYSA-N ethyl 5-hydroxy-5-(2-phenylethynyl)-2,3,4,4a,6,7,8,8a-octahydroquinoline-1-carboxylate Chemical compound CCOC(=O)N1CCCC2C1CCCC2(O)C#CC1=CC=CC=C1 WIPRRMYYUMAMPJ-UHFFFAOYSA-N 0.000 claims description 3
- ZUHRWLSVTMLWEN-UHFFFAOYSA-N ethyl n-[3-(2-phenylethynyl)cyclohex-2-en-1-yl]carbamate Chemical compound CCOC(=O)NC1CCCC(C#CC=2C=CC=CC=2)=C1 ZUHRWLSVTMLWEN-UHFFFAOYSA-N 0.000 claims description 3
- OLWRARXBPQTFTR-UHFFFAOYSA-N ethyl n-[3-hydroxy-3-[2-(3-methylphenyl)ethynyl]cyclohexyl]carbamate Chemical compound C1C(NC(=O)OCC)CCCC1(O)C#CC1=CC=CC(C)=C1 OLWRARXBPQTFTR-UHFFFAOYSA-N 0.000 claims description 3
- 208000028867 ischemia Diseases 0.000 claims description 3
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- 230000007803 itching Effects 0.000 claims description 3
- 201000006417 multiple sclerosis Diseases 0.000 claims description 3
- PLRSDRSEJPEAED-UHFFFAOYSA-N n-[3-[2-(3-fluorophenyl)ethynyl]-3-hydroxycyclohexyl]acetamide Chemical compound C1C(NC(=O)C)CCCC1(O)C#CC1=CC=CC(F)=C1 PLRSDRSEJPEAED-UHFFFAOYSA-N 0.000 claims description 3
- 229940021182 non-steroidal anti-inflammatory drug Drugs 0.000 claims description 3
- 208000020016 psychiatric disease Diseases 0.000 claims description 3
- 201000000980 schizophrenia Diseases 0.000 claims description 3
- 208000018198 spasticity Diseases 0.000 claims description 3
- 208000011117 substance-related disease Diseases 0.000 claims description 3
- PQTUGQRVYKKHJX-UHFFFAOYSA-N tert-butyl 7-hydroxy-7-(2-phenylethynyl)-3,3a,4,5,6,7a-hexahydro-1h-isoindole-2-carboxylate Chemical compound C12CN(C(=O)OC(C)(C)C)CC2CCCC1(O)C#CC1=CC=CC=C1 PQTUGQRVYKKHJX-UHFFFAOYSA-N 0.000 claims description 3
- SOOMTUHFRGROGM-UHFFFAOYSA-N tert-butyl n-[3-hydroxy-3-[2-(3-methylphenyl)ethynyl]cyclohexyl]carbamate Chemical compound CC1=CC=CC(C#CC2(O)CC(CCC2)NC(=O)OC(C)(C)C)=C1 SOOMTUHFRGROGM-UHFFFAOYSA-N 0.000 claims description 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 2
- 201000006474 Brain Ischemia Diseases 0.000 claims description 2
- 206010010904 Convulsion Diseases 0.000 claims description 2
- NMIXTTBVZMBIHL-WOIUINJBSA-N [(3ar,4s,7ar)-4-hydroxy-4-[2-(3-methylphenyl)ethynyl]-3,3a,5,6,7,7a-hexahydro-2h-indol-1-yl]-(furan-2-yl)methanone Chemical compound CC1=CC=CC(C#C[C@@]2(O)[C@H]3[C@H](N(CC3)C(=O)C=3OC=CC=3)CCC2)=C1 NMIXTTBVZMBIHL-WOIUINJBSA-N 0.000 claims description 2
- OOHWRZMAIUHACJ-GGQJKKPXSA-N [(3s)-oxolan-3-yl] 4-hydroxy-4-(2-phenylethynyl)-3,3a,5,6,7,7a-hexahydro-2h-indole-1-carboxylate Chemical compound C=1C=CC=CC=1C#CC1(O)CCCC2C1CCN2C(=O)O[C@H]1CCOC1 OOHWRZMAIUHACJ-GGQJKKPXSA-N 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 206010008118 cerebral infarction Diseases 0.000 claims description 2
- 230000036461 convulsion Effects 0.000 claims description 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 2
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 claims description 2
- CRRWFEQGFGDINN-QWFCFKBJSA-N ethyl (3ar,4s,7ar)-4-hydroxy-4-[2-(3-methylphenyl)ethynyl]-3,3a,5,6,7,7a-hexahydro-2h-indole-1-carboxylate Chemical compound C([C@]1(O)CCC[C@@H]2[C@H]1CCN2C(=O)OCC)#CC1=CC=CC(C)=C1 CRRWFEQGFGDINN-QWFCFKBJSA-N 0.000 claims description 2
- ILFYTTLEALYKPG-UHFFFAOYSA-N ethyl 4-(2-phenylethynyl)-2,3,5,6,7,7a-hexahydroindole-1-carboxylate Chemical compound C1CCC2N(C(=O)OCC)CCC2=C1C#CC1=CC=CC=C1 ILFYTTLEALYKPG-UHFFFAOYSA-N 0.000 claims description 2
- UXDUZBZETAVXED-UHFFFAOYSA-N ethyl 4-[2-(3-methoxyphenyl)ethynyl]-2,3,5,6,7,7a-hexahydroindole-1-carboxylate Chemical compound C1CCC2N(C(=O)OCC)CCC2=C1C#CC1=CC=CC(OC)=C1 UXDUZBZETAVXED-UHFFFAOYSA-N 0.000 claims description 2
- NPYOBWOVEFAZLC-UHFFFAOYSA-N ethyl 4-[2-(3-methylphenyl)ethynyl]-2,3,5,6,7,7a-hexahydroindole-1-carboxylate Chemical compound C1CCC2N(C(=O)OCC)CCC2=C1C#CC1=CC=CC(C)=C1 NPYOBWOVEFAZLC-UHFFFAOYSA-N 0.000 claims description 2
- CRRWFEQGFGDINN-UHFFFAOYSA-N ethyl 4-hydroxy-4-[2-(3-methylphenyl)ethynyl]-3,3a,5,6,7,7a-hexahydro-2h-indole-1-carboxylate Chemical compound CCOC(=O)N1CCC2C1CCCC2(O)C#CC1=CC=CC(C)=C1 CRRWFEQGFGDINN-UHFFFAOYSA-N 0.000 claims description 2
- PRQIMGZKFRUZFL-UHFFFAOYSA-N ethyl 7-[2-(3-cyanophenyl)ethynyl]-7-hydroxy-3,3a,4,5,6,7a-hexahydro-1h-isoindole-2-carboxylate Chemical compound C12CN(C(=O)OCC)CC2CCCC1(O)C#CC1=CC=CC(C#N)=C1 PRQIMGZKFRUZFL-UHFFFAOYSA-N 0.000 claims description 2
- FSKINSVZNATXMA-UHFFFAOYSA-N ethyl 7-hydroxy-7-[2-(3-methylphenyl)ethynyl]-3,3a,4,5,6,7a-hexahydro-1h-isoindole-2-carboxylate Chemical compound C12CN(C(=O)OCC)CC2CCCC1(O)C#CC1=CC=CC(C)=C1 FSKINSVZNATXMA-UHFFFAOYSA-N 0.000 claims description 2
- CBYGJJTXZOIYCV-UHFFFAOYSA-N ethyl 7-hydroxy-7-[2-(4-methylphenyl)ethynyl]-3,3a,4,5,6,7a-hexahydro-1h-isoindole-2-carboxylate Chemical compound C12CN(C(=O)OCC)CC2CCCC1(O)C#CC1=CC=C(C)C=C1 CBYGJJTXZOIYCV-UHFFFAOYSA-N 0.000 claims description 2
- BVAIXRYWZUMDMR-UHFFFAOYSA-N furan-2-yl-[7-hydroxy-7-[2-(3-methylphenyl)ethynyl]-3,3a,4,5,6,7a-hexahydro-1h-isoindol-2-yl]methanone Chemical compound CC1=CC=CC(C#CC2(O)C3CN(CC3CCC2)C(=O)C=2OC=CC=2)=C1 BVAIXRYWZUMDMR-UHFFFAOYSA-N 0.000 claims description 2
- 125000002541 furyl group Chemical group 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical class 0.000 claims description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 2
- 125000002757 morpholinyl group Chemical group 0.000 claims description 2
- YVNZPJZOIIBHQN-UHFFFAOYSA-N n-[3-hydroxy-3-[2-(3-methoxyphenyl)ethynyl]cyclohexyl]acetamide Chemical compound COC1=CC=CC(C#CC2(O)CC(CCC2)NC(C)=O)=C1 YVNZPJZOIIBHQN-UHFFFAOYSA-N 0.000 claims description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- 239000008024 pharmaceutical diluent Substances 0.000 claims description 2
- 125000004193 piperazinyl group Chemical group 0.000 claims description 2
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 claims description 2
- 125000004494 ethyl ester group Chemical group 0.000 claims 3
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 claims 2
- FEYFOLRTFYMDRW-UHFFFAOYSA-N ethyl 4-[2-(3-chlorophenyl)ethynyl]-4-hydroxy-3,3a,5,6,7,7a-hexahydro-2h-indole-1-carboxylate Chemical compound CCOC(=O)N1CCC2C1CCCC2(O)C#CC1=CC=CC(Cl)=C1 FEYFOLRTFYMDRW-UHFFFAOYSA-N 0.000 claims 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 1
- USPQFPYFSLLRES-UHFFFAOYSA-N 4-[2-(3-chlorophenyl)ethynyl]-1-methylsulfonyl-3,3a,5,6,7,7a-hexahydro-2h-indol-4-ol Chemical compound CS(=O)(=O)N1CCC2C1CCCC2(O)C#CC1=CC=CC(Cl)=C1 USPQFPYFSLLRES-UHFFFAOYSA-N 0.000 claims 1
- ANRMILBHZXLLOI-UHFFFAOYSA-N 4-[2-(3-chlorophenyl)ethynyl]-4-hydroxy-3,3a,5,6,7,7a-hexahydro-2H-indole-1-carboxylic acid Chemical compound OC1(C2CCN(C2CCC1)C(=O)O)C#CC1=CC(=CC=C1)Cl ANRMILBHZXLLOI-UHFFFAOYSA-N 0.000 claims 1
- OUTMOSXAPQLFAI-UHFFFAOYSA-N 4-hydroxy-4-(2-phenylethynyl)-3,3a,5,6,7,7a-hexahydro-2h-indole-1-carboxylic acid Chemical compound OC(=O)N1CCC2C1CCCC2(O)C#CC1=CC=CC=C1 OUTMOSXAPQLFAI-UHFFFAOYSA-N 0.000 claims 1
- 125000004217 4-methoxybenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1OC([H])([H])[H])C([H])([H])* 0.000 claims 1
- PXZKSWLKUIOJGZ-UHFFFAOYSA-N [5-[2-(3-chlorophenyl)ethynyl]-5-hydroxy-2,3,4,4a,6,7,8,8a-octahydroquinolin-1-yl]-morpholin-4-ylmethanone Chemical compound C=1C=CC(Cl)=CC=1C#CC1(O)CCCC2C1CCCN2C(=O)N1CCOCC1 PXZKSWLKUIOJGZ-UHFFFAOYSA-N 0.000 claims 1
- RQTXMIDDKRXCCI-UHFFFAOYSA-N [7-hydroxy-7-[2-(3-methylphenyl)ethynyl]-3,3a,4,5,6,7a-hexahydro-1h-isoindol-2-yl]-pyridin-3-ylmethanone Chemical compound CC1=CC=CC(C#CC2(O)C3CN(CC3CCC2)C(=O)C=2C=NC=CC=2)=C1 RQTXMIDDKRXCCI-UHFFFAOYSA-N 0.000 claims 1
- PLKJVWTVHCOBFF-UHFFFAOYSA-N ethyl 4-(2-phenylethynyl)-2,3,3a,6,7,7a-hexahydroindole-1-carboxylate Chemical compound CCOC(=O)N1CCC2C1CCC=C2C#CC1=CC=CC=C1 PLKJVWTVHCOBFF-UHFFFAOYSA-N 0.000 claims 1
- RUDJFNPIFRHEMI-UHFFFAOYSA-N ethyl 5-hydroxy-5-[2-(3-methylphenyl)ethynyl]-2,3,4,4a,6,7,8,8a-octahydroquinoline-1-carboxylate Chemical compound CCOC(=O)N1CCCC2C1CCCC2(O)C#CC1=CC=CC(C)=C1 RUDJFNPIFRHEMI-UHFFFAOYSA-N 0.000 claims 1
- UGBZUTABUHFIBE-UHFFFAOYSA-N ethyl 7-[2-(3-fluorophenyl)ethynyl]-7-hydroxy-3,3a,4,5,6,7a-hexahydro-1h-isoindole-2-carboxylate Chemical compound C12CN(C(=O)OCC)CC2CCCC1(O)C#CC1=CC=CC(F)=C1 UGBZUTABUHFIBE-UHFFFAOYSA-N 0.000 claims 1
- PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 claims 1
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 claims 1
- 150000004702 methyl esters Chemical class 0.000 claims 1
- 239000000041 non-steroidal anti-inflammatory agent Substances 0.000 claims 1
- UOUFRTFWWBCVPV-UHFFFAOYSA-N tert-butyl 4-(2,4-dioxo-1H-thieno[3,2-d]pyrimidin-3-yl)piperidine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1CCC(CC1)n1c(=O)[nH]c2ccsc2c1=O UOUFRTFWWBCVPV-UHFFFAOYSA-N 0.000 claims 1
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 93
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 69
- 239000011734 sodium Substances 0.000 description 42
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 41
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 40
- 238000000589 high-performance liquid chromatography-mass spectrometry Methods 0.000 description 37
- 239000000203 mixture Substances 0.000 description 28
- 239000000243 solution Substances 0.000 description 28
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 27
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- 239000011541 reaction mixture Substances 0.000 description 23
- 239000000741 silica gel Substances 0.000 description 23
- 229910002027 silica gel Inorganic materials 0.000 description 23
- 238000002330 electrospray ionisation mass spectrometry Methods 0.000 description 22
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 20
- 239000003795 chemical substances by application Substances 0.000 description 20
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 15
- 238000005160 1H NMR spectroscopy Methods 0.000 description 14
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 12
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
- 239000003921 oil Substances 0.000 description 12
- 235000019198 oils Nutrition 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- 239000012074 organic phase Substances 0.000 description 10
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 9
- 239000000047 product Substances 0.000 description 9
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 7
- 238000005481 NMR spectroscopy Methods 0.000 description 7
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 7
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 7
- 239000003480 eluent Substances 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- 241001465754 Metazoa Species 0.000 description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 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
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 6
- 238000000746 purification Methods 0.000 description 6
- 229910052938 sodium sulfate Inorganic materials 0.000 description 6
- 235000011152 sodium sulphate Nutrition 0.000 description 6
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 6
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- 239000011780 sodium chloride Substances 0.000 description 1
- 239000012312 sodium hydride Substances 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 239000007962 solid dispersion Substances 0.000 description 1
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- 230000005477 standard model Effects 0.000 description 1
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- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 1
- MRMYRYLVMIZVQM-MXWKQRLJSA-N tert-butyl (3ar,4s,7ar)-4-hydroxy-2,3,3a,4,5,6,7,7a-octahydroindole-1-carboxylate Chemical compound [C@H]1([C@H](CCC2)O)[C@@H]2N(C(=O)OC(C)(C)C)CC1 MRMYRYLVMIZVQM-MXWKQRLJSA-N 0.000 description 1
- ZAPZZFRGOMWRCG-WOIUINJBSA-N tert-butyl (3ar,4s,7ar)-4-hydroxy-4-[2-(3-methylphenyl)ethynyl]-3,3a,5,6,7,7a-hexahydro-2h-indole-1-carboxylate Chemical compound CC1=CC=CC(C#C[C@@]2(O)[C@H]3[C@H](N(CC3)C(=O)OC(C)(C)C)CCC2)=C1 ZAPZZFRGOMWRCG-WOIUINJBSA-N 0.000 description 1
- GRNSGJOKGICXGO-UWVGGRQHSA-N tert-butyl (3as,7as)-4-oxo-3,3a,5,6,7,7a-hexahydro-2h-indole-1-carboxylate Chemical compound C1CCC(=O)[C@@H]2[C@H]1N(C(=O)OC(C)(C)C)CC2 GRNSGJOKGICXGO-UWVGGRQHSA-N 0.000 description 1
- NIISILKXKMNSLC-UHFFFAOYSA-N tert-butyl 7-hydroxy-7-[2-(3-methylphenyl)ethynyl]-3,3a,4,5,6,7a-hexahydro-1h-isoindole-2-carboxylate Chemical compound CC1=CC=CC(C#CC2(O)C3CN(CC3CCC2)C(=O)OC(C)(C)C)=C1 NIISILKXKMNSLC-UHFFFAOYSA-N 0.000 description 1
- SGPWUVURFSJYQO-UHFFFAOYSA-N tert-butyl 7-oxo-3,3a,4,5,6,7a-hexahydro-1h-isoindole-2-carboxylate Chemical compound C1CCC(=O)C2CN(C(=O)OC(C)(C)C)CC21 SGPWUVURFSJYQO-UHFFFAOYSA-N 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 230000000472 traumatic effect Effects 0.000 description 1
- CWMFRHBXRUITQE-UHFFFAOYSA-N trimethylsilylacetylene Chemical group C[Si](C)(C)C#C CWMFRHBXRUITQE-UHFFFAOYSA-N 0.000 description 1
- 238000000825 ultraviolet detection Methods 0.000 description 1
- 229940087652 vioxx Drugs 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
- 229940018503 zyban Drugs 0.000 description 1
Classifications
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- 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
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Landscapes
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- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Indole Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Quinoline Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyridine Compounds (AREA)
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PCT/EP2002/013670 WO2003047581A1 (en) | 2001-12-04 | 2002-12-03 | Acetylene derivatives having mglur 5 antagonistic activity |
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US7772188B2 (en) | 2003-01-28 | 2010-08-10 | Ironwood Pharmaceuticals, Inc. | Methods and compositions for the treatment of gastrointestinal disorders |
GB0325956D0 (en) * | 2003-11-06 | 2003-12-10 | Addex Pharmaceuticals Sa | Novel compounds |
EP1734963A4 (en) | 2004-04-02 | 2008-06-18 | Merck & Co Inc | METHOD FOR TREATING PEOPLE WITH METABOLIC AND ANTHROPOMETRIC DISORDER |
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EP2272509A1 (en) * | 2006-09-11 | 2011-01-12 | Novartis AG | New Uses of metabotropic glutamate receptors |
MX354786B (es) | 2007-06-04 | 2018-03-21 | Synergy Pharmaceuticals Inc | Agonistas de guanilato ciclasa utiles para el tratamiento de trastornos gastrointestinales, inflamacion, cancer y otros trastornos. |
US8969514B2 (en) | 2007-06-04 | 2015-03-03 | Synergy Pharmaceuticals, Inc. | Agonists of guanylate cyclase useful for the treatment of hypercholesterolemia, atherosclerosis, coronary heart disease, gallstone, obesity and other cardiovascular diseases |
TW200924745A (en) * | 2007-10-12 | 2009-06-16 | Novartis Ag | Organic compounds |
AU2012254934B2 (en) * | 2007-10-12 | 2013-10-17 | Novartis Ag | Metabotropic glutamate receptor modulators for the treatment of Parkinson's disease |
CA2726917C (en) | 2008-06-04 | 2018-06-26 | Synergy Pharmaceuticals Inc. | Agonists of guanylate cyclase useful for the treatment of gastrointestinal disorders, inflammation, cancer and other disorders |
CN102131503A (zh) * | 2008-06-30 | 2011-07-20 | 诺瓦提斯公司 | 用于治疗帕金森病的包含mGluR调节剂的组合产品 |
NZ590753A (en) | 2008-08-12 | 2012-06-29 | Novartis Ag | Processes for the preparation of 4-oxo-octahydro-indole-1-carbocylic acid methyl ester and derivatives thereof |
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US20120157464A1 (en) | 2009-07-23 | 2012-06-21 | Novartis Ag | Use of azabicycloalkyl derivatives or pyrrolidine-2-one derivatives for the treatment or prevention of ataxia |
TWI558398B (zh) | 2009-09-22 | 2016-11-21 | 諾華公司 | 菸鹼乙醯膽鹼受體α7活化劑之用途 |
WO2011048150A1 (en) | 2009-10-20 | 2011-04-28 | Novartis Ag | Use of 1h-quinazoline-2,4-diones |
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BR112012033290A2 (pt) | 2010-06-24 | 2016-11-22 | Novartis Ag | uso de 1h-quinazolina-2,4-dionas |
US9616097B2 (en) | 2010-09-15 | 2017-04-11 | Synergy Pharmaceuticals, Inc. | Formulations of guanylate cyclase C agonists and methods of use |
WO2012084873A1 (en) | 2010-12-20 | 2012-06-28 | Novartis Ag | 4- (hetero) aryl - ethynyl - octahydro - indole - 1 - carboxylic acid esters |
EP2668159A1 (en) | 2011-01-24 | 2013-12-04 | Novartis AG | 4-tolyl-ethynyl-octahydro-indole-1-ester derivatives |
JP2014503568A (ja) | 2011-01-27 | 2014-02-13 | ノバルティス アーゲー | ニコチン酸アセチルコリン受容体α7活性化因子の使用 |
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