JP2008533117A5 - - Google Patents
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- Publication number
- JP2008533117A5 JP2008533117A5 JP2008501397A JP2008501397A JP2008533117A5 JP 2008533117 A5 JP2008533117 A5 JP 2008533117A5 JP 2008501397 A JP2008501397 A JP 2008501397A JP 2008501397 A JP2008501397 A JP 2008501397A JP 2008533117 A5 JP2008533117 A5 JP 2008533117A5
- Authority
- JP
- Japan
- Prior art keywords
- thiazolo
- tetrahydro
- cyclobutyl
- azepine
- azepin
- 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.)
- Withdrawn
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- 125000000217 alkyl group Chemical group 0.000 claims 29
- 150000001875 compounds Chemical class 0.000 claims 19
- 125000003118 aryl group Chemical group 0.000 claims 10
- 125000004321 azepin-2-yl group Chemical group [H]N1C([H])=C([H])C([H])=C([H])C([H])=C1* 0.000 claims 10
- 229910052736 halogen Inorganic materials 0.000 claims 9
- 125000000623 heterocyclic group Chemical group 0.000 claims 9
- 150000002367 halogens Chemical class 0.000 claims 8
- 125000001072 heteroaryl group Chemical group 0.000 claims 8
- 229910052739 hydrogen Inorganic materials 0.000 claims 7
- 239000001257 hydrogen Substances 0.000 claims 7
- 150000003839 salts Chemical class 0.000 claims 6
- 239000012453 solvate Substances 0.000 claims 6
- 125000000753 cycloalkyl group Chemical group 0.000 claims 5
- WUFMUYFEWPBICZ-UHFFFAOYSA-N 5-[3-(6-cyclobutyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl)pyrrolidin-1-yl]pyridine-2-carbonitrile Chemical compound C1=NC(C#N)=CC=C1N1CC(C=2SC=3CCN(CCC=3N=2)C2CCC2)CC1 WUFMUYFEWPBICZ-UHFFFAOYSA-N 0.000 claims 4
- 229910002091 carbon monoxide Inorganic materials 0.000 claims 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 4
- 229910052760 oxygen Inorganic materials 0.000 claims 4
- 125000001424 substituent group Chemical group 0.000 claims 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 3
- 208000012902 Nervous system disease Diseases 0.000 claims 3
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 claims 3
- 125000004093 cyano group Chemical group *C#N 0.000 claims 3
- 150000002431 hydrogen Chemical class 0.000 claims 3
- -1 hydroxy, cyano, amino Chemical group 0.000 claims 3
- 239000008194 pharmaceutical composition Substances 0.000 claims 3
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims 2
- GVFNIRHEMHBGKK-UHFFFAOYSA-N 1-[4-(6-cyclobutyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl)phenyl]-3-methylimidazolidin-2-one Chemical compound O=C1N(C)CCN1C1=CC=C(C=2SC=3CCN(CCC=3N=2)C2CCC2)C=C1 GVFNIRHEMHBGKK-UHFFFAOYSA-N 0.000 claims 2
- RVMLJMMOHPMSBM-UHFFFAOYSA-N 1-[4-(6-cyclobutyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl)phenyl]imidazolidin-2-one Chemical compound O=C1NCCN1C1=CC=C(C=2SC=3CCN(CCC=3N=2)C2CCC2)C=C1 RVMLJMMOHPMSBM-UHFFFAOYSA-N 0.000 claims 2
- VZWORUHCRUFYEY-UHFFFAOYSA-N 1-[4-(6-cyclobutyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl)phenyl]pyrrolidin-2-one Chemical compound O=C1CCCN1C1=CC=C(C=2SC=3CCN(CCC=3N=2)C2CCC2)C=C1 VZWORUHCRUFYEY-UHFFFAOYSA-N 0.000 claims 2
- AVGWDAZNMDHRLW-UHFFFAOYSA-N 5-[4-(6-cyclobutyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl)piperidin-1-yl]-n,n-dimethylpyridine-2-carboxamide Chemical compound C1=NC(C(=O)N(C)C)=CC=C1N1CCC(C=2SC=3CCN(CCC=3N=2)C2CCC2)CC1 AVGWDAZNMDHRLW-UHFFFAOYSA-N 0.000 claims 2
- DXAMKIWWMUKGFJ-UHFFFAOYSA-N 5-[4-(6-cyclobutyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl)piperidin-1-yl]pyridine-2-carbonitrile Chemical compound C1=NC(C#N)=CC=C1N1CCC(C=2SC=3CCN(CCC=3N=2)C2CCC2)CC1 DXAMKIWWMUKGFJ-UHFFFAOYSA-N 0.000 claims 2
- BZIMEWAWRGVTEM-UHFFFAOYSA-N 6-cyclobutyl-2-[1-(6-methylpyridin-3-yl)pyrrolidin-3-yl]-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepine Chemical compound C1=NC(C)=CC=C1N1CC(C=2SC=3CCN(CCC=3N=2)C2CCC2)CC1 BZIMEWAWRGVTEM-UHFFFAOYSA-N 0.000 claims 2
- MXNROENSEHWVOE-UHFFFAOYSA-N [4-(6-cyclobutyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl)piperidin-1-yl]-(5-methylpyridin-3-yl)methanone Chemical compound CC1=CN=CC(C(=O)N2CCC(CC2)C=2SC=3CCN(CCC=3N=2)C2CCC2)=C1 MXNROENSEHWVOE-UHFFFAOYSA-N 0.000 claims 2
- FTVIUIXLKVOCFD-UHFFFAOYSA-N [4-(6-cyclobutyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl)piperidin-1-yl]-(6-methylpyridin-2-yl)methanone Chemical compound CC1=CC=CC(C(=O)N2CCC(CC2)C=2SC=3CCN(CCC=3N=2)C2CCC2)=N1 FTVIUIXLKVOCFD-UHFFFAOYSA-N 0.000 claims 2
- 125000003545 alkoxy group Chemical group 0.000 claims 2
- 229910052799 carbon Inorganic materials 0.000 claims 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 2
- JJESDBWWAOIYRI-UHFFFAOYSA-N (3-chlorophenyl)-[4-(6-cyclobutyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl)piperidin-1-yl]methanone Chemical compound ClC1=CC=CC(C(=O)N2CCC(CC2)C=2SC=3CCN(CCC=3N=2)C2CCC2)=C1 JJESDBWWAOIYRI-UHFFFAOYSA-N 0.000 claims 1
- PYQRZFDCHITHKJ-UHFFFAOYSA-N (4-chlorophenyl)-[4-(6-cyclobutyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl)piperidin-1-yl]methanone Chemical compound C1=CC(Cl)=CC=C1C(=O)N1CCC(C=2SC=3CCN(CCC=3N=2)C2CCC2)CC1 PYQRZFDCHITHKJ-UHFFFAOYSA-N 0.000 claims 1
- YGHXJMJGWRFTPW-UHFFFAOYSA-N 1-[4-(6-cyclohexyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl)phenyl]-3-methylimidazolidin-2-one Chemical compound O=C1N(C)CCN1C1=CC=C(C=2SC=3CCN(CCC=3N=2)C2CCCCC2)C=C1 YGHXJMJGWRFTPW-UHFFFAOYSA-N 0.000 claims 1
- YLVZOKZFPLFDOV-UHFFFAOYSA-N 1-[4-(6-cyclopentyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl)phenyl]-3-methylimidazolidin-2-one Chemical compound O=C1N(C)CCN1C1=CC=C(C=2SC=3CCN(CCC=3N=2)C2CCCC2)C=C1 YLVZOKZFPLFDOV-UHFFFAOYSA-N 0.000 claims 1
- ZSVDVQPHRFNSMG-UHFFFAOYSA-N 1-[4-(6-ethyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl)phenyl]-3-methylimidazolidin-2-one Chemical compound S1C=2CCN(CC)CCC=2N=C1C(C=C1)=CC=C1N1CCN(C)C1=O ZSVDVQPHRFNSMG-UHFFFAOYSA-N 0.000 claims 1
- JSIBKAHJYBHGFF-UHFFFAOYSA-N 1-[4-[6-(cyclohexylmethyl)-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl]phenyl]-3-methylimidazolidin-2-one Chemical compound O=C1N(C)CCN1C1=CC=C(C=2SC=3CCN(CC4CCCCC4)CCC=3N=2)C=C1 JSIBKAHJYBHGFF-UHFFFAOYSA-N 0.000 claims 1
- FDQDCCGVWABUQA-UHFFFAOYSA-N 1-[4-[6-(cyclopropylmethyl)-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl]phenyl]-3-methylimidazolidin-2-one Chemical compound O=C1N(C)CCN1C1=CC=C(C=2SC=3CCN(CC4CC4)CCC=3N=2)C=C1 FDQDCCGVWABUQA-UHFFFAOYSA-N 0.000 claims 1
- KNTSKCCSKLRVDW-UHFFFAOYSA-N 1-[5-(6-cyclobutyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl)pyridin-2-yl]-3-methylimidazolidin-2-one Chemical compound O=C1N(C)CCN1C1=CC=C(C=2SC=3CCN(CCC=3N=2)C2CCC2)C=N1 KNTSKCCSKLRVDW-UHFFFAOYSA-N 0.000 claims 1
- FCKBSFHPXHYQIF-UHFFFAOYSA-N 1-[5-(6-cyclobutyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl)pyridin-2-yl]pyrrolidin-2-one Chemical compound O=C1CCCN1C1=CC=C(C=2SC=3CCN(CCC=3N=2)C2CCC2)C=N1 FCKBSFHPXHYQIF-UHFFFAOYSA-N 0.000 claims 1
- ZLIWIVSLGCGFLS-UHFFFAOYSA-N 1-methyl-3-[4-[6-(2-methylpropyl)-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl]phenyl]imidazolidin-2-one Chemical compound S1C=2CCN(CC(C)C)CCC=2N=C1C(C=C1)=CC=C1N1CCN(C)C1=O ZLIWIVSLGCGFLS-UHFFFAOYSA-N 0.000 claims 1
- NGNYCAXHGYNGLH-UHFFFAOYSA-N 2-(2-chloropyrimidin-5-yl)-6-cyclobutyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepine Chemical compound C1=NC(Cl)=NC=C1C(S1)=NC2=C1CCN(C1CCC1)CC2 NGNYCAXHGYNGLH-UHFFFAOYSA-N 0.000 claims 1
- YXCBMVKTMYRQHH-UHFFFAOYSA-N 2-(4-bromophenyl)-6-cyclobutyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepine Chemical compound C1=CC(Br)=CC=C1C(S1)=NC2=C1CCN(C1CCC1)CC2 YXCBMVKTMYRQHH-UHFFFAOYSA-N 0.000 claims 1
- SOSZRSSOEUVNSJ-UHFFFAOYSA-N 2-(6-chloropyridin-3-yl)-6-cyclobutyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepine Chemical compound C1=NC(Cl)=CC=C1C(S1)=NC2=C1CCN(C1CCC1)CC2 SOSZRSSOEUVNSJ-UHFFFAOYSA-N 0.000 claims 1
- SPGRSHYTPNOOMK-UHFFFAOYSA-N 3-(6-cyclobutyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl)benzonitrile Chemical compound N#CC1=CC=CC(C=2SC=3CCN(CCC=3N=2)C2CCC2)=C1 SPGRSHYTPNOOMK-UHFFFAOYSA-N 0.000 claims 1
- AOTYOKVTTWNHCA-UHFFFAOYSA-N 3-[4-(6-cyclobutyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl)phenyl]-1,3-oxazolidin-2-one Chemical compound O=C1OCCN1C1=CC=C(C=2SC=3CCN(CCC=3N=2)C2CCC2)C=C1 AOTYOKVTTWNHCA-UHFFFAOYSA-N 0.000 claims 1
- APJQLFKODBWPDL-UHFFFAOYSA-N 4-(6-cyclobutyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl)-n-ethylbenzamide Chemical compound C1=CC(C(=O)NCC)=CC=C1C(S1)=NC2=C1CCN(C1CCC1)CC2 APJQLFKODBWPDL-UHFFFAOYSA-N 0.000 claims 1
- RDFKBDPHVJMWFC-UHFFFAOYSA-N 4-(6-cyclobutyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl)-n-methylbenzamide Chemical compound C1=CC(C(=O)NC)=CC=C1C(S1)=NC2=C1CCN(C1CCC1)CC2 RDFKBDPHVJMWFC-UHFFFAOYSA-N 0.000 claims 1
- OGZGDVSJDJSXRL-UHFFFAOYSA-N 4-(6-cyclobutyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl)-n-methylpiperidine-1-carboxamide Chemical compound C1CN(C(=O)NC)CCC1C(S1)=NC2=C1CCN(C1CCC1)CC2 OGZGDVSJDJSXRL-UHFFFAOYSA-N 0.000 claims 1
- ABTJPHUBNMVYRC-UHFFFAOYSA-N 4-(6-cyclobutyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl)benzamide Chemical compound C1=CC(C(=O)N)=CC=C1C(S1)=NC2=C1CCN(C1CCC1)CC2 ABTJPHUBNMVYRC-UHFFFAOYSA-N 0.000 claims 1
- NWISRHCDYAIVGL-UHFFFAOYSA-N 4-(6-cyclobutyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl)benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1C(S1)=NC2=C1CCN(C1CCC1)CC2 NWISRHCDYAIVGL-UHFFFAOYSA-N 0.000 claims 1
- OAJQEKCJHNEGFM-UHFFFAOYSA-N 4-(6-cyclobutyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl)benzonitrile Chemical compound C1=CC(C#N)=CC=C1C(S1)=NC2=C1CCN(C1CCC1)CC2 OAJQEKCJHNEGFM-UHFFFAOYSA-N 0.000 claims 1
- AHWJFRMVTYDAFH-UHFFFAOYSA-N 4-[3-(6-cyclobutyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl)pyrrolidine-1-carbonyl]benzonitrile Chemical compound C=1C=C(C#N)C=CC=1C(=O)N(C1)CCC1C(SC=1CC2)=NC=1CCN2C1CCC1 AHWJFRMVTYDAFH-UHFFFAOYSA-N 0.000 claims 1
- HYUJTDMDPUQHJI-UHFFFAOYSA-N 4-[4-(6-cyclobutyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl)phenyl]morpholine Chemical compound C1CCC1N1CCC(SC(=N2)C=3C=CC(=CC=3)N3CCOCC3)=C2CC1 HYUJTDMDPUQHJI-UHFFFAOYSA-N 0.000 claims 1
- NMAJUNHZWKZQLX-UHFFFAOYSA-N 4-[4-(6-cyclobutyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl)piperidin-1-yl]benzonitrile Chemical compound C1=CC(C#N)=CC=C1N1CCC(C=2SC=3CCN(CCC=3N=2)C2CCC2)CC1 NMAJUNHZWKZQLX-UHFFFAOYSA-N 0.000 claims 1
- XGJNVHKCNGYJST-UHFFFAOYSA-N 4-[4-(6-cyclobutyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl)piperidine-1-carbonyl]benzonitrile Chemical compound C=1C=C(C#N)C=CC=1C(=O)N(CC1)CCC1C(SC=1CC2)=NC=1CCN2C1CCC1 XGJNVHKCNGYJST-UHFFFAOYSA-N 0.000 claims 1
- RBQKBTJTROCBND-UHFFFAOYSA-N 4-[5-(6-cyclobutyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl)pyridin-2-yl]morpholine Chemical compound C1CCC1N1CCC(SC(=N2)C=3C=NC(=CC=3)N3CCOCC3)=C2CC1 RBQKBTJTROCBND-UHFFFAOYSA-N 0.000 claims 1
- INCVZKRMUFWNJO-UHFFFAOYSA-N 5-(6-cyclobutyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl)-1H-pyrimidin-2-one Chemical compound N1C(=O)N=CC(C=2SC=3CCN(CCC=3N=2)C2CCC2)=C1 INCVZKRMUFWNJO-UHFFFAOYSA-N 0.000 claims 1
- TWVFVZDAGLYQKN-UHFFFAOYSA-N 5-(6-cyclobutyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl)-n-methylpyrazine-2-carboxamide Chemical compound C1=NC(C(=O)NC)=CN=C1C(S1)=NC2=C1CCN(C1CCC1)CC2 TWVFVZDAGLYQKN-UHFFFAOYSA-N 0.000 claims 1
- ZVFZYFSORBEUBH-UHFFFAOYSA-N 5-(6-cyclobutyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl)-n-methylpyridine-2-carboxamide Chemical compound C1=NC(C(=O)NC)=CC=C1C(S1)=NC2=C1CCN(C1CCC1)CC2 ZVFZYFSORBEUBH-UHFFFAOYSA-N 0.000 claims 1
- SSXWYPXUESEVTG-UHFFFAOYSA-N 5-(6-cyclobutyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl)pyridine-2-carbonitrile Chemical compound C1=NC(C#N)=CC=C1C(S1)=NC2=C1CCN(C1CCC1)CC2 SSXWYPXUESEVTG-UHFFFAOYSA-N 0.000 claims 1
- BWKSPZHVGXFVPD-UHFFFAOYSA-N 5-(6-cyclobutyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl)pyridine-2-carboxamide Chemical compound C1=NC(C(=O)N)=CC=C1C(S1)=NC2=C1CCN(C1CCC1)CC2 BWKSPZHVGXFVPD-UHFFFAOYSA-N 0.000 claims 1
- LOMSQGIKFZLYTD-UHFFFAOYSA-N 5-(6-cyclobutyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl)pyridine-2-carboxylic acid Chemical compound C1=NC(C(=O)O)=CC=C1C(S1)=NC2=C1CCN(C1CCC1)CC2 LOMSQGIKFZLYTD-UHFFFAOYSA-N 0.000 claims 1
- AVGKKMYFTPYADB-UHFFFAOYSA-N 5-(6-cyclobutyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl)pyrimidine-2-carbonitrile Chemical compound C1=NC(C#N)=NC=C1C(S1)=NC2=C1CCN(C1CCC1)CC2 AVGKKMYFTPYADB-UHFFFAOYSA-N 0.000 claims 1
- ITTSBLBFNODHJE-UHFFFAOYSA-N 5-[3-(6-cyclobutyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl)pyrrolidin-1-yl]pyridine-3-carbonitrile Chemical compound N#CC1=CN=CC(N2CC(CC2)C=2SC=3CCN(CCC=3N=2)C2CCC2)=C1 ITTSBLBFNODHJE-UHFFFAOYSA-N 0.000 claims 1
- QMBBZFQXLXNVEX-UHFFFAOYSA-N 5-[4-(6-cyclobutyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl)piperidin-1-yl]-n-methylpyridine-2-carboxamide Chemical compound C1=NC(C(=O)NC)=CC=C1N1CCC(C=2SC=3CCN(CCC=3N=2)C2CCC2)CC1 QMBBZFQXLXNVEX-UHFFFAOYSA-N 0.000 claims 1
- BDKLWAUFRJERTL-UHFFFAOYSA-N 5-[4-(6-cyclobutyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl)piperidin-1-yl]pyridine-2-carboxamide Chemical compound C1=NC(C(=O)N)=CC=C1N1CCC(C=2SC=3CCN(CCC=3N=2)C2CCC2)CC1 BDKLWAUFRJERTL-UHFFFAOYSA-N 0.000 claims 1
- DGLSFKHHVVNPBJ-UHFFFAOYSA-N 5-[4-(6-cyclobutyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl)piperidin-1-yl]pyridine-2-carboxylic acid Chemical compound C1=NC(C(=O)O)=CC=C1N1CCC(C=2SC=3CCN(CCC=3N=2)C2CCC2)CC1 DGLSFKHHVVNPBJ-UHFFFAOYSA-N 0.000 claims 1
- WWPVRQKZMFSHRJ-UHFFFAOYSA-N 5-[4-(6-cyclobutyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl)piperidin-1-yl]pyridine-3-carbonitrile Chemical compound N#CC1=CN=CC(N2CCC(CC2)C=2SC=3CCN(CCC=3N=2)C2CCC2)=C1 WWPVRQKZMFSHRJ-UHFFFAOYSA-N 0.000 claims 1
- NUJUIGFVMNONIJ-UHFFFAOYSA-N 5-[4-(6-cyclobutyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl)piperidine-1-carbonyl]pyridine-2-carbonitrile Chemical compound C=1C=C(C#N)N=CC=1C(=O)N(CC1)CCC1C(SC=1CC2)=NC=1CCN2C1CCC1 NUJUIGFVMNONIJ-UHFFFAOYSA-N 0.000 claims 1
- HWMACOXIHLFZBK-UHFFFAOYSA-N 5-[5-(6-cyclobutyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl)pyridin-2-yl]-3-methyl-1,2,4-oxadiazole Chemical compound CC1=NOC(C=2N=CC(=CC=2)C=2SC=3CCN(CCC=3N=2)C2CCC2)=N1 HWMACOXIHLFZBK-UHFFFAOYSA-N 0.000 claims 1
- HIRZXBANJRNRGX-UHFFFAOYSA-N 6-(6-cyclobutyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl)-n-methylpyridine-3-carboxamide Chemical compound N1=CC(C(=O)NC)=CC=C1C(S1)=NC2=C1CCN(C1CCC1)CC2 HIRZXBANJRNRGX-UHFFFAOYSA-N 0.000 claims 1
- COVWKBKVYSUUTK-UHFFFAOYSA-N 6-(6-cyclobutyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl)pyridine-3-carbonitrile Chemical compound N1=CC(C#N)=CC=C1C(S1)=NC2=C1CCN(C1CCC1)CC2 COVWKBKVYSUUTK-UHFFFAOYSA-N 0.000 claims 1
- YBMAQOPLYKMTRY-UHFFFAOYSA-N 6-(6-cyclobutyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl)pyridine-3-carboxylic acid Chemical compound N1=CC(C(=O)O)=CC=C1C(S1)=NC2=C1CCN(C1CCC1)CC2 YBMAQOPLYKMTRY-UHFFFAOYSA-N 0.000 claims 1
- LXDYIVJGTBVLND-UHFFFAOYSA-N 6-(6-cyclopentyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-yl)pyridine-3-carbonitrile Chemical compound N1=CC(C#N)=CC=C1C(S1)=NC2=C1CCN(C1CCCC1)CC2 LXDYIVJGTBVLND-UHFFFAOYSA-N 0.000 claims 1
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| PCT/GB2006/000846 WO2006097691A1 (en) | 2005-03-14 | 2006-03-10 | Fused thiazole derivatives having affinity for the histamine h3 receptor |
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| ES (1) | ES2321028T3 (enExample) |
| IL (1) | IL185869A0 (enExample) |
| MA (1) | MA29339B1 (enExample) |
| MX (1) | MX2007011211A (enExample) |
| NO (1) | NO20074977L (enExample) |
| WO (1) | WO2006097691A1 (enExample) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0513886D0 (en) | 2005-07-06 | 2005-08-10 | Glaxo Group Ltd | Novel compounds |
| US9108948B2 (en) | 2006-06-23 | 2015-08-18 | Abbvie Inc. | Cyclopropyl amine derivatives |
| CN101472887A (zh) | 2006-06-23 | 2009-07-01 | 艾博特公司 | 作为组胺h3受体调节物的环丙胺衍生物 |
| US8283360B2 (en) | 2008-12-19 | 2012-10-09 | Merck Sharp & Dohme Corp. | Bicyclic heterocyclic derivatives and methods of use thereof |
| US20110245267A1 (en) * | 2008-12-19 | 2011-10-06 | Schering Plough Corporation | Piperidine and piperazine derivatives and methods of use thereof |
| US9186353B2 (en) * | 2009-04-27 | 2015-11-17 | Abbvie Inc. | Treatment of osteoarthritis pain |
| HUE028435T2 (en) * | 2010-09-02 | 2016-12-28 | Suven Life Sciences Ltd | Heterocyclic compounds as histamine H3 receptor ligands |
| WO2012037258A1 (en) | 2010-09-16 | 2012-03-22 | Abbott Laboratories | Processes for preparing 1,2-substituted cyclopropyl derivatives |
| WO2013151982A1 (en) | 2012-04-03 | 2013-10-10 | Arena Pharmaceuticals, Inc. | Methods and compounds useful in treating pruritus, and methods for identifying such compounds |
| EP2647377A1 (en) | 2012-04-06 | 2013-10-09 | Sanofi | Use of an h3 receptor antagonist for the treatment of alzheimer's disease |
| US10662157B2 (en) | 2016-04-06 | 2020-05-26 | Sumitomo Chemical Company, Limited | Heterocyclic compound |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4324580A1 (de) * | 1993-07-22 | 1995-01-26 | Thomae Gmbh Dr K | Bicyclische Heterocyclen, diese Verbindungen enthaltende Arzneimittel und Verfahren zu ihrer Herstellung |
| DE4427838A1 (de) | 1994-08-05 | 1996-02-08 | Thomae Gmbh Dr K | Kondensierte Azepinderivate, diese Verbindungen enthaltende Arzneimittel und Verfahren zu ihrer Herstellung |
| JPH1017569A (ja) | 1996-07-05 | 1998-01-20 | Yamanouchi Pharmaceut Co Ltd | 置換チアゾール誘導体を有効成分とする医薬及び新規化合物 |
| EP1173438A1 (en) | 1999-04-16 | 2002-01-23 | Novo Nordisk A/S | Substituted imidazoles, their preparation and use |
| GB0224083D0 (en) | 2002-10-16 | 2002-11-27 | Glaxo Group Ltd | Novel compounds |
| US8466143B2 (en) | 2003-07-23 | 2013-06-18 | Exelixis, Inc. | Azepine derivatives as pharmaceutical agents |
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2006
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- 2006-03-10 WO PCT/GB2006/000846 patent/WO2006097691A1/en not_active Ceased
- 2006-03-10 US US11/908,532 patent/US20080161289A1/en not_active Abandoned
- 2006-03-10 KR KR1020077020994A patent/KR20070113225A/ko not_active Withdrawn
- 2006-03-10 AT AT06710058T patent/ATE420091T1/de not_active IP Right Cessation
- 2006-03-10 MX MX2007011211A patent/MX2007011211A/es unknown
- 2006-03-10 JP JP2008501397A patent/JP2008533117A/ja not_active Withdrawn
- 2006-03-10 EA EA200701984A patent/EA200701984A1/ru unknown
- 2006-03-10 CA CA002601644A patent/CA2601644A1/en not_active Abandoned
- 2006-03-10 AU AU2006224440A patent/AU2006224440A1/en not_active Abandoned
- 2006-03-10 BR BRPI0608437-0A patent/BRPI0608437A2/pt not_active IP Right Cessation
- 2006-03-10 DE DE602006004714T patent/DE602006004714D1/de active Active
- 2006-03-10 EP EP06710058A patent/EP1858900B1/en active Active
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2007
- 2007-09-10 IL IL185869A patent/IL185869A0/en unknown
- 2007-09-24 MA MA30235A patent/MA29339B1/fr unknown
- 2007-10-02 NO NO20074977A patent/NO20074977L/no not_active Application Discontinuation
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