TWI725998B - 化合物或其可藥用鹽、藥物組合物及其用途 - Google Patents
化合物或其可藥用鹽、藥物組合物及其用途 Download PDFInfo
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- TWI725998B TWI725998B TW105134694A TW105134694A TWI725998B TW I725998 B TWI725998 B TW I725998B TW 105134694 A TW105134694 A TW 105134694A TW 105134694 A TW105134694 A TW 105134694A TW I725998 B TWI725998 B TW I725998B
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- Prior art keywords
- azabicyclo
- ylethynyl
- pyridin
- hex
- compound
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- 150000001875 compounds Chemical class 0.000 title claims abstract description 114
- 150000003839 salts Chemical class 0.000 title claims abstract description 26
- 239000008194 pharmaceutical composition Substances 0.000 title claims abstract description 7
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 15
- -1 5-( 1-(Pyridin-2-ylethynyl)-3-azabicyclo[3.1.0]hex-3-yl)nicotinic cyanide Chemical compound 0.000 claims description 61
- 125000000217 alkyl group Chemical group 0.000 claims description 40
- 125000001424 substituent group Chemical group 0.000 claims description 40
- 125000003118 aryl group Chemical group 0.000 claims description 38
- 125000001072 heteroaryl group Chemical group 0.000 claims description 34
- 229910052736 halogen Inorganic materials 0.000 claims description 26
- 125000002950 monocyclic group Chemical group 0.000 claims description 26
- 125000002619 bicyclic group Chemical group 0.000 claims description 18
- 125000005842 heteroatom Chemical group 0.000 claims description 17
- 229910052760 oxygen Inorganic materials 0.000 claims description 14
- 229910052717 sulfur Inorganic materials 0.000 claims description 13
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 10
- 201000010099 disease Diseases 0.000 claims description 8
- 150000002367 halogens Chemical class 0.000 claims description 7
- 229910052757 nitrogen Inorganic materials 0.000 claims description 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 7
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 6
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 6
- 125000005143 heteroarylsulfonyl group Chemical group 0.000 claims description 6
- 125000003373 pyrazinyl group Chemical group 0.000 claims description 6
- 125000002098 pyridazinyl group Chemical group 0.000 claims description 6
- 125000000335 thiazolyl group Chemical group 0.000 claims description 6
- 125000004391 aryl sulfonyl group Chemical group 0.000 claims description 5
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims description 4
- 208000019022 Mood disease Diseases 0.000 claims description 4
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 claims description 4
- 125000005098 aryl alkoxy carbonyl group Chemical group 0.000 claims description 4
- 239000003937 drug carrier Substances 0.000 claims description 4
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 claims description 4
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 4
- VXECEOVRTRIWBW-UHFFFAOYSA-N (6-chloropyridin-3-yl)-[1-(2-pyridin-2-ylethynyl)-3-azabicyclo[3.1.0]hexan-3-yl]methanone Chemical compound ClC1=CC=C(C=N1)C(=O)N1CC2(CC2C1)C#CC1=NC=CC=C1 VXECEOVRTRIWBW-UHFFFAOYSA-N 0.000 claims description 3
- XYZWHNNWYMUKOW-UHFFFAOYSA-N 2-[1-(2-pyridin-2-ylethynyl)-3-azabicyclo[3.1.0]hexan-3-yl]pyridine-4-carbonitrile Chemical compound N1=C(C=CC=C1)C#CC12CN(CC2C1)C=1C=C(C#N)C=CN=1 XYZWHNNWYMUKOW-UHFFFAOYSA-N 0.000 claims description 3
- VZWOXDYRBDIHMA-UHFFFAOYSA-N 2-methyl-1,3-thiazole Chemical compound CC1=NC=CS1 VZWOXDYRBDIHMA-UHFFFAOYSA-N 0.000 claims description 3
- AGZMRMJGSWURSB-UHFFFAOYSA-N 3-(5-fluoropyridin-3-yl)-1-(2-pyridin-2-ylethynyl)-3-azabicyclo[3.1.0]hexane Chemical compound FC=1C=C(C=NC=1)N1CC2(CC2C1)C#CC1=NC=CC=C1 AGZMRMJGSWURSB-UHFFFAOYSA-N 0.000 claims description 3
- BGDPWJGYSUFIEL-UHFFFAOYSA-N 3-(5-fluoropyridin-3-yl)-1-[2-(6-methylpyridin-2-yl)ethynyl]-3-azabicyclo[3.1.0]hexane Chemical compound FC=1C=C(C=NC=1)N1CC2(CC2C1)C#CC1=NC(=CC=C1)C BGDPWJGYSUFIEL-UHFFFAOYSA-N 0.000 claims description 3
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 claims description 3
- 150000001335 aliphatic alkanes Chemical class 0.000 claims description 3
- 125000003368 amide group Chemical group 0.000 claims description 3
- 125000004104 aryloxy group Chemical group 0.000 claims description 3
- 208000029560 autism spectrum disease Diseases 0.000 claims description 3
- 239000003814 drug Substances 0.000 claims description 3
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 3
- JZAOWBFWHIBGBX-UHFFFAOYSA-N (3-chlorophenyl)-[1-[2-(2-methyl-1,3-thiazol-4-yl)ethynyl]-3-azabicyclo[3.1.0]hexan-3-yl]methanone Chemical compound ClC=1C=C(C=CC=1)C(=O)N1CC2(CC2C1)C#CC=1N=C(SC=1)C JZAOWBFWHIBGBX-UHFFFAOYSA-N 0.000 claims description 2
- SRKDGOFYDUMUQM-UHFFFAOYSA-N (3-fluorophenyl)-[1-(2-pyridin-2-ylethynyl)-3-azabicyclo[3.1.0]hexan-3-yl]methanone Chemical compound FC=1C=C(C=CC=1)C(=O)N1CC2(CC2C1)C#CC1=NC=CC=C1 SRKDGOFYDUMUQM-UHFFFAOYSA-N 0.000 claims description 2
- LQHJNSXNAFLXGX-UHFFFAOYSA-N (3-fluorophenyl)-[1-[2-(6-methylpyridin-2-yl)ethynyl]-3-azabicyclo[3.1.0]hexan-3-yl]methanone Chemical compound FC=1C=C(C=CC=1)C(=O)N1CC2(CC2C1)C#CC1=NC(=CC=C1)C LQHJNSXNAFLXGX-UHFFFAOYSA-N 0.000 claims description 2
- FTRRTKIOAAHQNS-UHFFFAOYSA-N (4-chlorophenyl)-[1-(2-pyridin-2-ylethynyl)-3-azabicyclo[3.1.0]hexan-3-yl]methanone Chemical compound ClC1=CC=C(C=C1)C(=O)N1CC2(CC2C1)C#CC1=NC=CC=C1 FTRRTKIOAAHQNS-UHFFFAOYSA-N 0.000 claims description 2
- KTSTZYAYOJYVDV-UHFFFAOYSA-N (5-chloropyridin-3-yl)-[1-(2-pyridin-2-ylethynyl)-3-azabicyclo[3.1.0]hexan-3-yl]methanone Chemical compound ClC=1C=C(C=NC=1)C(=O)N1CC2(CC2C1)C#CC1=NC=CC=C1 KTSTZYAYOJYVDV-UHFFFAOYSA-N 0.000 claims description 2
- GHPGNSRANXVTCZ-UHFFFAOYSA-N 1-(2-pyridin-2-ylethynyl)-3-[4-(trifluoromethoxy)phenyl]-3-azabicyclo[3.1.0]hexane Chemical compound N1=C(C=CC=C1)C#CC12CN(CC2C1)C1=CC=C(C=C1)OC(F)(F)F GHPGNSRANXVTCZ-UHFFFAOYSA-N 0.000 claims description 2
- PYKGETOIFSHXNK-UHFFFAOYSA-N 1-[1-(2-pyridin-2-ylethynyl)-3-azabicyclo[3.1.0]hexan-3-yl]pentan-1-one Chemical compound N1=C(C=CC=C1)C#CC12CN(CC2C1)C(CCCC)=O PYKGETOIFSHXNK-UHFFFAOYSA-N 0.000 claims description 2
- YHUAGAGVBHHASJ-UHFFFAOYSA-N 1-[1-[2-(2-methyl-1,3-thiazol-4-yl)ethynyl]-3-azabicyclo[3.1.0]hexan-3-yl]pentan-1-one Chemical compound CC=1SC=C(N=1)C#CC12CN(CC2C1)C(CCCC)=O YHUAGAGVBHHASJ-UHFFFAOYSA-N 0.000 claims description 2
- HOUHCIQJQCZGDU-UHFFFAOYSA-N 1-[1-[2-(6-chloropyridin-2-yl)ethynyl]-3-azabicyclo[3.1.0]hexan-3-yl]-2-methylpropan-1-one Chemical compound ClC1=CC=CC(=N1)C#CC12CN(CC2C1)C(C(C)C)=O HOUHCIQJQCZGDU-UHFFFAOYSA-N 0.000 claims description 2
- KNDOFIXPZYCNLL-UHFFFAOYSA-N 2,2-dimethyl-1-[1-(2-pyridin-2-ylethynyl)-3-azabicyclo[3.1.0]hexan-3-yl]propan-1-one Chemical compound CC(C(=O)N1CC2(CC2C1)C#CC1=NC=CC=C1)(C)C KNDOFIXPZYCNLL-UHFFFAOYSA-N 0.000 claims description 2
- SDXHWDHDPNOTOM-UHFFFAOYSA-N 2,2-dimethyl-1-[1-[2-(2-methyl-1,3-thiazol-4-yl)ethynyl]-3-azabicyclo[3.1.0]hexan-3-yl]propan-1-one Chemical compound CC(C(=O)N1CC2(CC2C1)C#CC=1N=C(SC=1)C)(C)C SDXHWDHDPNOTOM-UHFFFAOYSA-N 0.000 claims description 2
- RWCNOTNVDWUPDK-UHFFFAOYSA-N 2-methyl-1-[1-[2-(2-methyl-1,3-thiazol-4-yl)ethynyl]-3-azabicyclo[3.1.0]hexan-3-yl]propan-1-one Chemical compound CC(C(=O)N1CC2(CC2C1)C#CC=1N=C(SC=1)C)C RWCNOTNVDWUPDK-UHFFFAOYSA-N 0.000 claims description 2
- FIAAAJATPWDIEE-UHFFFAOYSA-N 2-methyl-1-[1-[2-(6-methylpyridin-2-yl)ethynyl]-3-azabicyclo[3.1.0]hexan-3-yl]propan-1-one Chemical compound CC(C(=O)N1CC2(CC2C1)C#CC1=NC(=CC=C1)C)C FIAAAJATPWDIEE-UHFFFAOYSA-N 0.000 claims description 2
- WOYWTLBNAYSLEE-UHFFFAOYSA-N 2-phenyl-1-[1-(2-pyridin-2-ylethynyl)-3-azabicyclo[3.1.0]hexan-3-yl]ethanone Chemical compound C1(=CC=CC=C1)CC(=O)N1CC2(CC2C1)C#CC1=NC=CC=C1 WOYWTLBNAYSLEE-UHFFFAOYSA-N 0.000 claims description 2
- XRTOCUTVIAEUHK-UHFFFAOYSA-N 3-(2-chlorophenyl)sulfonyl-1-(2-pyridin-2-ylethynyl)-3-azabicyclo[3.1.0]hexane Chemical compound ClC1=C(C=CC=C1)S(=O)(=O)N1CC2(CC2C1)C#CC1=NC=CC=C1 XRTOCUTVIAEUHK-UHFFFAOYSA-N 0.000 claims description 2
- NRLMOBIDIVRKGO-UHFFFAOYSA-N 3-(2-fluorophenyl)-1-(2-pyridin-2-ylethynyl)-3-azabicyclo[3.1.0]hexane Chemical compound FC1=C(C=CC=C1)N1CC2(CC2C1)C#CC1=NC=CC=C1 NRLMOBIDIVRKGO-UHFFFAOYSA-N 0.000 claims description 2
- WNPNSGRJGZAXDD-UHFFFAOYSA-N 3-(2-fluorophenyl)sulfonyl-1-(2-pyridin-2-ylethynyl)-3-azabicyclo[3.1.0]hexane Chemical compound FC1=C(C=CC=C1)S(=O)(=O)N1CC2(CC2C1)C#CC1=NC=CC=C1 WNPNSGRJGZAXDD-UHFFFAOYSA-N 0.000 claims description 2
- VOOLGEDNKZKXCN-UHFFFAOYSA-N 3-(3,5-difluorophenyl)-1-(2-pyrimidin-2-ylethynyl)-3-azabicyclo[3.1.0]hexane Chemical compound FC=1C=C(C=C(C=1)F)N1CC2(CC2C1)C#CC1=NC=CC=N1 VOOLGEDNKZKXCN-UHFFFAOYSA-N 0.000 claims description 2
- IJRRLBIJFYZFRM-UHFFFAOYSA-N 3-(3-chloro-5-fluorophenyl)-1-(2-pyridin-2-ylethynyl)-3-azabicyclo[3.1.0]hexane Chemical compound ClC=1C=C(C=C(C=1)F)N1CC2(CC2C1)C#CC1=NC=CC=C1 IJRRLBIJFYZFRM-UHFFFAOYSA-N 0.000 claims description 2
- YAGQUOVWLDODNN-UHFFFAOYSA-N 3-(3-chlorophenyl)-1-(2-pyridin-2-ylethynyl)-3-azabicyclo[3.1.0]hexane Chemical compound ClC=1C=C(C=CC=1)N1CC2(CC2C1)C#CC1=NC=CC=C1 YAGQUOVWLDODNN-UHFFFAOYSA-N 0.000 claims description 2
- PSMGEHUVWDNIKB-UHFFFAOYSA-N 3-(3-fluorophenyl)-1-(2-pyrimidin-2-ylethynyl)-3-azabicyclo[3.1.0]hexane Chemical compound FC=1C=C(C=CC=1)N1CC2(CC2C1)C#CC1=NC=CC=N1 PSMGEHUVWDNIKB-UHFFFAOYSA-N 0.000 claims description 2
- YXUHFVOJNORMBN-UHFFFAOYSA-N 3-(4-chloro-2-fluorophenyl)-1-(2-pyridin-2-ylethynyl)-3-azabicyclo[3.1.0]hexane Chemical compound ClC1=CC(=C(C=C1)N1CC2(CC2C1)C#CC1=NC=CC=C1)F YXUHFVOJNORMBN-UHFFFAOYSA-N 0.000 claims description 2
- NQSKTONEMVXXOY-UHFFFAOYSA-N 3-(4-chlorophenyl)-1-(2-pyridin-2-ylethynyl)-3-azabicyclo[3.1.0]hexane Chemical compound ClC1=CC=C(C=C1)N1CC2(CC2C1)C#CC1=NC=CC=C1 NQSKTONEMVXXOY-UHFFFAOYSA-N 0.000 claims description 2
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- GLQMDADCZCMFFM-UHFFFAOYSA-N 3-(5-fluoropyridin-2-yl)-1-(2-pyridin-2-ylethynyl)-3-azabicyclo[3.1.0]hexane Chemical compound FC=1C=CC(=NC=1)N1CC2(CC2C1)C#CC1=NC=CC=C1 GLQMDADCZCMFFM-UHFFFAOYSA-N 0.000 claims description 2
- UYTXNBPVMVNBSF-UHFFFAOYSA-N 3-(benzenesulfonyl)-1-(2-pyridin-2-ylethynyl)-3-azabicyclo[3.1.0]hexane Chemical compound C1(=CC=CC=C1)S(=O)(=O)N1CC2(CC2C1)C#CC1=NC=CC=C1 UYTXNBPVMVNBSF-UHFFFAOYSA-N 0.000 claims description 2
- AFXIRFMTXCQKKT-UHFFFAOYSA-N 3-[1-(2-pyridin-2-ylethynyl)-3-azabicyclo[3.1.0]hexan-3-yl]benzonitrile Chemical compound N1=C(C=CC=C1)C#CC12CN(CC2C1)C=1C=C(C#N)C=CC=1 AFXIRFMTXCQKKT-UHFFFAOYSA-N 0.000 claims description 2
- IKUDBSKONSPSTH-UHFFFAOYSA-N 3-[1-(2-pyrimidin-2-ylethynyl)-3-azabicyclo[3.1.0]hexan-3-yl]benzonitrile Chemical compound N1=C(N=CC=C1)C#CC12CN(CC2C1)C=1C=C(C#N)C=CC=1 IKUDBSKONSPSTH-UHFFFAOYSA-N 0.000 claims description 2
- QTCJDVUVURTYLI-UHFFFAOYSA-N 3-[1-(6-chloropyridin-2-yl)-3-azabicyclo[3.1.0]hexan-3-yl]-5-fluorobenzonitrile Chemical compound ClC1=CC=CC(=N1)C12CN(CC2C1)C=1C=C(C#N)C=C(C=1)F QTCJDVUVURTYLI-UHFFFAOYSA-N 0.000 claims description 2
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- HVIXKKSJSQREQX-UHFFFAOYSA-N 3-[1-[2-(2-methyl-1,3-thiazol-4-yl)ethynyl]-3-azabicyclo[3.1.0]hexan-3-yl]benzonitrile Chemical compound CC=1SC=C(N=1)C#CC12CN(CC2C1)C=1C=C(C#N)C=CC=1 HVIXKKSJSQREQX-UHFFFAOYSA-N 0.000 claims description 2
- 125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 claims description 2
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Classifications
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- 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
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- C—CHEMISTRY; METALLURGY
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- 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
- C07D401/08—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 alicyclic rings
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- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
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- A61K31/4025—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil not condensed and containing further heterocyclic rings, e.g. cromakalim
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- A61K31/4164—1,3-Diazoles
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- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/4965—Non-condensed pyrazines
- A61K31/497—Non-condensed pyrazines containing further heterocyclic rings
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- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/501—Pyridazines; Hydrogenated pyridazines not condensed and containing further heterocyclic rings
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- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
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- 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
- C07D401/14—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 three or more hetero rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
Landscapes
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- Chemical Kinetics & Catalysis (AREA)
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- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
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| CNCN201510713865.7 | 2015-10-28 | ||
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| WOPCT/CN2016/102946 | 2016-10-21 | ||
| PCT/CN2016/102946 WO2017071536A1 (en) | 2015-10-28 | 2016-10-21 | Pyrrolidine derivatives |
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| TW201718542A TW201718542A (zh) | 2017-06-01 |
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| CN113616656B (zh) | 2014-03-19 | 2023-02-17 | 无限药品股份有限公司 | 用于治疗PI3K-γ介导的障碍的杂环化合物 |
| AU2016322552B2 (en) | 2015-09-14 | 2021-03-25 | Infinity Pharmaceuticals, Inc. | Solid forms of isoquinolinone derivatives, process of making, compositions comprising, and methods of using the same |
| CN106632243B (zh) * | 2015-10-28 | 2019-03-15 | 华领医药技术(上海)有限公司 | 吡咯烷衍生物 |
| KR102740618B1 (ko) * | 2021-11-17 | 2024-12-10 | 유노비아 주식회사 | 아이속사졸 유도체의 제조 방법 및 그의 중간체 |
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| TW201116532A (en) * | 2009-08-05 | 2011-05-16 | Merz Pharma Gmbh & Co Kgaa | Metabotropic glutamate receptor modulators |
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2018
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|---|---|---|---|---|
| WO2014124560A1 (en) * | 2013-02-18 | 2014-08-21 | Hua Medicine (Shanghai) Ltd. | Mglur regulators |
Non-Patent Citations (1)
| Title |
|---|
| Intramolecular Alkynylcyclopropanation of Olefins Catalyzed by Bi(OTf)3: Stereoselective Synthesis of 1‐Alkynyl‐3‐azabicyclo[3.1.0]hexanes * |
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| AU2016345244A1 (en) | 2018-04-26 |
| MX385587B (es) | 2025-03-18 |
| AU2016345244B2 (en) | 2020-07-09 |
| CN106632243A (zh) | 2017-05-10 |
| RU2740019C1 (ru) | 2020-12-30 |
| JP6877771B2 (ja) | 2021-05-26 |
| CA3000794A1 (en) | 2017-05-04 |
| JP2018532778A (ja) | 2018-11-08 |
| WO2017071536A1 (en) | 2017-05-04 |
| IL258517B (en) | 2020-05-31 |
| EP3371163A1 (en) | 2018-09-12 |
| ZA201802235B (en) | 2019-07-31 |
| IL258517A (en) | 2018-05-31 |
| BR112018008204B1 (pt) | 2023-12-26 |
| CN108349935B (zh) | 2021-02-05 |
| HK1254456A1 (en) | 2019-07-19 |
| EP3371163B1 (en) | 2022-03-30 |
| HUE058899T2 (hu) | 2022-09-28 |
| BR112018008204A2 (pt) | 2018-12-18 |
| KR20180070693A (ko) | 2018-06-26 |
| TW201718542A (zh) | 2017-06-01 |
| CN106632243B (zh) | 2019-03-15 |
| US10328054B2 (en) | 2019-06-25 |
| CA3000794C (en) | 2024-01-16 |
| MX2018004868A (es) | 2018-11-09 |
| KR102815874B1 (ko) | 2025-06-02 |
| CN108349935A (zh) | 2018-07-31 |
| US20180318254A1 (en) | 2018-11-08 |
| EP3371163A4 (en) | 2019-05-01 |
| ES2922978T3 (es) | 2022-09-22 |
| DK3371163T3 (da) | 2022-07-04 |
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