JP5145218B2 - ヒスタミンｈ３アンタゴニストとしてのピラゾロ［３，４−ｄ］アゼピン誘導体 - Google Patents
ヒスタミンｈ３アンタゴニストとしてのピラゾロ［３，４−ｄ］アゼピン誘導体 Download PDFInfo
- Publication number
- JP5145218B2 JP5145218B2 JP2008519862A JP2008519862A JP5145218B2 JP 5145218 B2 JP5145218 B2 JP 5145218B2 JP 2008519862 A JP2008519862 A JP 2008519862A JP 2008519862 A JP2008519862 A JP 2008519862A JP 5145218 B2 JP5145218 B2 JP 5145218B2
- Authority
- JP
- Japan
- Prior art keywords
- tetrahydropyrazolo
- alkyl
- azepin
- mmol
- phenyl
- 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.)
- Expired - Fee Related
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- 239000003395 histamine H3 receptor antagonist Substances 0.000 title 1
- RMUDBHOUKWNOLH-UHFFFAOYSA-N pyrazolo[3,4-d]azepine Chemical class C1=CN=CC=C2C=NN=C21 RMUDBHOUKWNOLH-UHFFFAOYSA-N 0.000 title 1
- 208000012902 Nervous system disease Diseases 0.000 claims abstract description 6
- 150000001875 compounds Chemical class 0.000 claims description 190
- 125000000217 alkyl group Chemical group 0.000 claims description 127
- -1 hydroxy, cyano, amino Chemical group 0.000 claims description 119
- 125000000623 heterocyclic group Chemical group 0.000 claims description 49
- 125000001424 substituent group Chemical group 0.000 claims description 49
- 239000001257 hydrogen Substances 0.000 claims description 34
- 229910052739 hydrogen Inorganic materials 0.000 claims description 34
- 150000003839 salts Chemical class 0.000 claims description 34
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 29
- 125000003118 aryl group Chemical group 0.000 claims description 28
- 229910052736 halogen Inorganic materials 0.000 claims description 28
- 150000002367 halogens Chemical class 0.000 claims description 28
- 229910052757 nitrogen Inorganic materials 0.000 claims description 26
- 229910052760 oxygen Inorganic materials 0.000 claims description 24
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 22
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 21
- 125000001072 heteroaryl group Chemical group 0.000 claims description 20
- 229910052799 carbon Inorganic materials 0.000 claims description 19
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 16
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 13
- XYOVOXDWRFGKEX-UHFFFAOYSA-N azepine Chemical compound N1C=CC=CC=C1 XYOVOXDWRFGKEX-UHFFFAOYSA-N 0.000 claims description 12
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 12
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 12
- 239000012453 solvate Substances 0.000 claims description 11
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 claims description 9
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims description 9
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 9
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 8
- SOAXOIPIFFFTDI-UHFFFAOYSA-N 2-(4-bromophenyl)-6-cyclobutyl-4,5,7,8-tetrahydropyrazolo[3,4-d]azepine Chemical compound C1=CC(Br)=CC=C1N1N=C2CCN(C3CCC3)CCC2=C1 SOAXOIPIFFFTDI-UHFFFAOYSA-N 0.000 claims description 7
- 208000010877 cognitive disease Diseases 0.000 claims description 7
- 239000000126 substance Substances 0.000 claims description 7
- 208000028698 Cognitive impairment Diseases 0.000 claims description 6
- 201000010099 disease Diseases 0.000 claims description 6
- SWGKYHKUYIKLDC-UHFFFAOYSA-N 1-[4-(6-cyclobutyl-4,5,7,8-tetrahydropyrazolo[3,4-d]azepin-2-yl)phenyl]pyrrolidin-2-one Chemical compound O=C1CCCN1C1=CC=C(N2N=C3CCN(CCC3=C2)C2CCC2)C=C1 SWGKYHKUYIKLDC-UHFFFAOYSA-N 0.000 claims description 5
- PCCHYOUYRRGEJP-UHFFFAOYSA-N 1-[5-(6-cyclobutyl-4,5,7,8-tetrahydropyrazolo[3,4-d]azepin-2-yl)pyridin-2-yl]pyrrolidin-2-one Chemical compound O=C1CCCN1C1=CC=C(N2N=C3CCN(CCC3=C2)C2CCC2)C=N1 PCCHYOUYRRGEJP-UHFFFAOYSA-N 0.000 claims description 5
- DGBYHHMLWZHXBJ-UHFFFAOYSA-N 1-methyl-3-[4-[6-(2-methylpropyl)-4,5,7,8-tetrahydropyrazolo[3,4-d]azepin-2-yl]phenyl]imidazolidin-2-one Chemical compound N1=C2CCN(CC(C)C)CCC2=CN1C(C=C1)=CC=C1N1CCN(C)C1=O DGBYHHMLWZHXBJ-UHFFFAOYSA-N 0.000 claims description 5
- 208000024827 Alzheimer disease Diseases 0.000 claims description 5
- KMROEJOHJJYSOS-UHFFFAOYSA-N n-methyl-4-[6-(2-methylpropyl)-4,5,7,8-tetrahydropyrazolo[3,4-d]azepin-2-yl]benzamide Chemical compound C1=CC(C(=O)NC)=CC=C1N1N=C2CCN(CC(C)C)CCC2=C1 KMROEJOHJJYSOS-UHFFFAOYSA-N 0.000 claims description 5
- 230000001225 therapeutic effect Effects 0.000 claims description 5
- DTFNQANOSNEOCD-UHFFFAOYSA-N 1-[4-(6-cyclobutyl-4,5,7,8-tetrahydropyrazolo[3,4-d]azepin-2-yl)phenyl]-3-methylimidazolidin-2-one Chemical compound O=C1N(C)CCN1C1=CC=C(N2N=C3CCN(CCC3=C2)C2CCC2)C=C1 DTFNQANOSNEOCD-UHFFFAOYSA-N 0.000 claims description 4
- XUXLXFNWTHSVDU-UHFFFAOYSA-N 1-[4-(6-cyclohexyl-4,5,7,8-tetrahydropyrazolo[3,4-d]azepin-2-yl)phenyl]pyrrolidin-2-one Chemical compound O=C1CCCN1C1=CC=C(N2N=C3CCN(CCC3=C2)C2CCCCC2)C=C1 XUXLXFNWTHSVDU-UHFFFAOYSA-N 0.000 claims description 4
- UNFFLKKHVRORSL-UHFFFAOYSA-N 1-[4-(6-ethyl-4,5,7,8-tetrahydropyrazolo[3,4-d]azepin-2-yl)phenyl]pyrrolidin-2-one Chemical compound N1=C2CCN(CC)CCC2=CN1C(C=C1)=CC=C1N1CCCC1=O UNFFLKKHVRORSL-UHFFFAOYSA-N 0.000 claims description 4
- BKADWIISZKEYEA-UHFFFAOYSA-N 1-methyl-3-[4-(6-propan-2-yl-4,5,7,8-tetrahydropyrazolo[3,4-d]azepin-2-yl)phenyl]imidazolidin-2-one Chemical compound N1=C2CCN(C(C)C)CCC2=CN1C(C=C1)=CC=C1N1CCN(C)C1=O BKADWIISZKEYEA-UHFFFAOYSA-N 0.000 claims description 4
- KQGXBEQKKDNBEF-UHFFFAOYSA-N 3-[4-(6-propan-2-yl-4,5,7,8-tetrahydropyrazolo[3,4-d]azepin-2-yl)phenyl]-1,3-oxazolidin-2-one Chemical compound N1=C2CCN(C(C)C)CCC2=CN1C(C=C1)=CC=C1N1CCOC1=O KQGXBEQKKDNBEF-UHFFFAOYSA-N 0.000 claims description 4
- BYXQPVYYCODYFR-UHFFFAOYSA-N 6-cyclobutyl-2-(4-methylsulfonylphenyl)-4,5,7,8-tetrahydropyrazolo[3,4-d]azepine Chemical compound C1=CC(S(=O)(=O)C)=CC=C1N1N=C2CCN(C3CCC3)CCC2=C1 BYXQPVYYCODYFR-UHFFFAOYSA-N 0.000 claims description 4
- SCYQCPUBNNKNFU-UHFFFAOYSA-N 6-cyclobutyl-2-phenyl-4,5,7,8-tetrahydropyrazolo[3,4-d]azepine Chemical compound C1CCC1N1CCC2=NN(C=3C=CC=CC=3)C=C2CC1 SCYQCPUBNNKNFU-UHFFFAOYSA-N 0.000 claims description 4
- 150000002431 hydrogen Chemical class 0.000 claims description 4
- KMPBTRDNKULAIB-UHFFFAOYSA-N n,n-dimethyl-4-[6-(2-methylpropyl)-4,5,7,8-tetrahydropyrazolo[3,4-d]azepin-2-yl]benzamide Chemical compound N1=C2CCN(CC(C)C)CCC2=CN1C1=CC=C(C(=O)N(C)C)C=C1 KMPBTRDNKULAIB-UHFFFAOYSA-N 0.000 claims description 4
- PFKVVKZVZKQJIY-UHFFFAOYSA-N 1-[4-(6-cyclopentyl-4,5,7,8-tetrahydropyrazolo[3,4-d]azepin-2-yl)phenyl]pyrrolidin-2-one Chemical compound O=C1CCCN1C1=CC=C(N2N=C3CCN(CCC3=C2)C2CCCC2)C=C1 PFKVVKZVZKQJIY-UHFFFAOYSA-N 0.000 claims description 3
- NHLUUDFTIYLGCR-UHFFFAOYSA-N 1-[4-(6-propan-2-yl-4,5,7,8-tetrahydropyrazolo[3,4-d]azepin-2-yl)phenyl]pyrrolidin-2-one Chemical compound N1=C2CCN(C(C)C)CCC2=CN1C(C=C1)=CC=C1N1CCCC1=O NHLUUDFTIYLGCR-UHFFFAOYSA-N 0.000 claims description 3
- FBLPODTYWKUWKU-UHFFFAOYSA-N 1-[4-[6-(cyclopropylmethyl)-4,5,7,8-tetrahydropyrazolo[3,4-d]azepin-2-yl]phenyl]pyrrolidin-2-one Chemical compound O=C1CCCN1C1=CC=C(N2N=C3CCN(CC4CC4)CCC3=C2)C=C1 FBLPODTYWKUWKU-UHFFFAOYSA-N 0.000 claims description 3
- QYXNJPQHJBBEBP-UHFFFAOYSA-N 3-[4-(6-cyclobutyl-4,5,7,8-tetrahydropyrazolo[3,4-d]azepin-2-yl)phenyl]-1,3-oxazolidin-2-one Chemical compound O=C1OCCN1C1=CC=C(N2N=C3CCN(CCC3=C2)C2CCC2)C=C1 QYXNJPQHJBBEBP-UHFFFAOYSA-N 0.000 claims description 3
- ULDBTTCHMFJGSK-UHFFFAOYSA-N 3-[4-[6-(2-methylpropyl)-4,5,7,8-tetrahydropyrazolo[3,4-d]azepin-2-yl]phenyl]-1,3-oxazolidin-2-one Chemical compound N1=C2CCN(CC(C)C)CCC2=CN1C(C=C1)=CC=C1N1CCOC1=O ULDBTTCHMFJGSK-UHFFFAOYSA-N 0.000 claims description 3
- FBCIOSJGCBSUPO-UHFFFAOYSA-N 3-methyl-5-[4-(6-propan-2-yl-4,5,7,8-tetrahydropyrazolo[3,4-d]azepin-2-yl)phenyl]-1,2,4-oxadiazole Chemical compound N1=C2CCN(C(C)C)CCC2=CN1C(C=C1)=CC=C1C1=NC(C)=NO1 FBCIOSJGCBSUPO-UHFFFAOYSA-N 0.000 claims description 3
- OSKJMVLSHZZCLF-UHFFFAOYSA-N 3-methyl-5-[4-[6-(2-methylpropyl)-4,5,7,8-tetrahydropyrazolo[3,4-d]azepin-2-yl]phenyl]-1,2,4-oxadiazole Chemical compound N1=C2CCN(CC(C)C)CCC2=CN1C(C=C1)=CC=C1C1=NC(C)=NO1 OSKJMVLSHZZCLF-UHFFFAOYSA-N 0.000 claims description 3
- JSPMYAZGTGJOAI-UHFFFAOYSA-N 4-(6-cyclobutyl-4,5,7,8-tetrahydropyrazolo[3,4-d]azepin-2-yl)benzamide Chemical compound C1=CC(C(=O)N)=CC=C1N1N=C2CCN(C3CCC3)CCC2=C1 JSPMYAZGTGJOAI-UHFFFAOYSA-N 0.000 claims description 3
- YLZHGJSNBVVMHA-UHFFFAOYSA-N 4-(6-cyclobutyl-4,5,7,8-tetrahydropyrazolo[3,4-d]azepin-2-yl)benzonitrile Chemical compound C1=CC(C#N)=CC=C1N1N=C2CCN(C3CCC3)CCC2=C1 YLZHGJSNBVVMHA-UHFFFAOYSA-N 0.000 claims description 3
- NXNUSIGCWNWZFT-UHFFFAOYSA-N 4-(6-cyclopentyl-4,5,7,8-tetrahydropyrazolo[3,4-d]azepin-2-yl)benzamide Chemical compound C1=CC(C(=O)N)=CC=C1N1N=C2CCN(C3CCCC3)CCC2=C1 NXNUSIGCWNWZFT-UHFFFAOYSA-N 0.000 claims description 3
- ULJXVGFBRBQVFN-UHFFFAOYSA-N 4-(6-propan-2-yl-4,5,7,8-tetrahydropyrazolo[3,4-d]azepin-2-yl)benzamide Chemical compound N1=C2CCN(C(C)C)CCC2=CN1C1=CC=C(C(N)=O)C=C1 ULJXVGFBRBQVFN-UHFFFAOYSA-N 0.000 claims description 3
- NZGTZGNHBYHCHG-UHFFFAOYSA-N 4-[(6-cyclobutyl-4,5,7,8-tetrahydropyrazolo[3,4-d]azepin-2-yl)methyl]benzonitrile Chemical compound C1=CC(C#N)=CC=C1CN1N=C2CCN(C3CCC3)CCC2=C1 NZGTZGNHBYHCHG-UHFFFAOYSA-N 0.000 claims description 3
- XSZLCHNKJCBKCB-UHFFFAOYSA-N 4-[4-(6-cyclobutyl-4,5,7,8-tetrahydropyrazolo[3,4-d]azepin-2-yl)phenyl]morpholine Chemical compound C1CCC1N1CCC2=NN(C=3C=CC(=CC=3)N3CCOCC3)C=C2CC1 XSZLCHNKJCBKCB-UHFFFAOYSA-N 0.000 claims description 3
- WRTSWARSQLNKPU-UHFFFAOYSA-N 4-[6-(2-methylpropyl)-4,5,7,8-tetrahydropyrazolo[3,4-d]azepin-2-yl]benzamide Chemical compound N1=C2CCN(CC(C)C)CCC2=CN1C1=CC=C(C(N)=O)C=C1 WRTSWARSQLNKPU-UHFFFAOYSA-N 0.000 claims description 3
- IRXCERGGZYNFJI-UHFFFAOYSA-N 6-cyclobutyl-2-(4-piperidin-1-ylphenyl)-4,5,7,8-tetrahydropyrazolo[3,4-d]azepine Chemical compound C1CCC1N1CCC2=NN(C=3C=CC(=CC=3)N3CCCCC3)C=C2CC1 IRXCERGGZYNFJI-UHFFFAOYSA-N 0.000 claims description 3
- RUGQPDGXAJMLNQ-UHFFFAOYSA-N 6-cyclobutyl-2-(4-pyrrolidin-1-ylphenyl)-4,5,7,8-tetrahydropyrazolo[3,4-d]azepine Chemical compound C1CCC1N1CCC2=NN(C=3C=CC(=CC=3)N3CCCC3)C=C2CC1 RUGQPDGXAJMLNQ-UHFFFAOYSA-N 0.000 claims description 3
- IUMZUJYPSCQKNK-UHFFFAOYSA-N 6-cyclobutyl-2-[1-(6-methylpyridin-3-yl)piperidin-4-yl]-4,5,7,8-tetrahydropyrazolo[3,4-d]azepine Chemical compound C1=NC(C)=CC=C1N1CCC(N2N=C3CCN(CCC3=C2)C2CCC2)CC1 IUMZUJYPSCQKNK-UHFFFAOYSA-N 0.000 claims description 3
- LNUZKOYKRTWVLK-UHFFFAOYSA-N n-[4-(6-cyclobutyl-4,5,7,8-tetrahydropyrazolo[3,4-d]azepin-2-yl)phenyl]methanesulfonamide Chemical compound C1=CC(NS(=O)(=O)C)=CC=C1N1N=C2CCN(C3CCC3)CCC2=C1 LNUZKOYKRTWVLK-UHFFFAOYSA-N 0.000 claims description 3
- 208000015122 neurodegenerative disease Diseases 0.000 claims description 3
- 230000002265 prevention Effects 0.000 claims description 3
- NUCUHFOXKYAJSO-UHFFFAOYSA-N 1-[4-(6-cyclopentyl-4,5,7,8-tetrahydropyrazolo[3,4-d]azepin-2-yl)phenyl]-3-methylimidazolidin-2-one Chemical compound O=C1N(C)CCN1C1=CC=C(N2N=C3CCN(CCC3=C2)C2CCCC2)C=C1 NUCUHFOXKYAJSO-UHFFFAOYSA-N 0.000 claims description 2
- QZEZLNQKBWZPDJ-UHFFFAOYSA-N 1-[4-[6-(2-methylpropyl)-4,5,7,8-tetrahydropyrazolo[3,4-d]azepin-2-yl]phenyl]pyrrolidin-2-one Chemical compound N1=C2CCN(CC(C)C)CCC2=CN1C(C=C1)=CC=C1N1CCCC1=O QZEZLNQKBWZPDJ-UHFFFAOYSA-N 0.000 claims description 2
- UTZALURJTZPLMS-UHFFFAOYSA-N 1-[5-(6-propan-2-yl-4,5,7,8-tetrahydropyrazolo[3,4-d]azepin-2-yl)pyridin-2-yl]pyrrolidin-2-one Chemical compound N1=C2CCN(C(C)C)CCC2=CN1C(C=N1)=CC=C1N1CCCC1=O UTZALURJTZPLMS-UHFFFAOYSA-N 0.000 claims description 2
- XEZCPAVXKBUPRY-UHFFFAOYSA-N 3-[4-(6-cyclopentyl-4,5,7,8-tetrahydropyrazolo[3,4-d]azepin-2-yl)phenyl]-1,3-oxazolidin-2-one Chemical compound O=C1OCCN1C1=CC=C(N2N=C3CCN(CCC3=C2)C2CCCC2)C=C1 XEZCPAVXKBUPRY-UHFFFAOYSA-N 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 5
- MGKKZYOFKNDJGD-UHFFFAOYSA-N 3-[4-(6-cyclobutyl-4,5,7,8-tetrahydropyrazolo[3,4-d]azepin-2-yl)phenyl]-1-methylimidazolidine-2,4-dione Chemical compound O=C1N(C)CC(=O)N1C1=CC=C(N2N=C3CCN(CCC3=C2)C2CCC2)C=C1 MGKKZYOFKNDJGD-UHFFFAOYSA-N 0.000 claims 1
- 239000000203 mixture Substances 0.000 abstract description 273
- 238000000034 method Methods 0.000 abstract description 85
- 238000002360 preparation method Methods 0.000 abstract description 20
- 239000005557 antagonist Substances 0.000 abstract description 11
- 208000025966 Neurological disease Diseases 0.000 abstract description 4
- 230000000144 pharmacologic effect Effects 0.000 abstract description 3
- 230000008569 process Effects 0.000 abstract description 3
- 208000020016 psychiatric disease Diseases 0.000 abstract description 3
- 150000003217 pyrazoles Chemical class 0.000 abstract description 3
- 230000000926 neurological effect Effects 0.000 abstract description 2
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 777
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 452
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 178
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 159
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 134
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 111
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 96
- 229910021529 ammonia Inorganic materials 0.000 description 89
- 239000000243 solution Substances 0.000 description 86
- 238000012799 strong cation exchange Methods 0.000 description 83
- 239000002904 solvent Substances 0.000 description 77
- 229910052786 argon Inorganic materials 0.000 description 67
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 63
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 58
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 57
- 239000012321 sodium triacetoxyborohydride Substances 0.000 description 51
- 238000003756 stirring Methods 0.000 description 49
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 44
- 238000010992 reflux Methods 0.000 description 43
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 42
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 40
- 239000000741 silica gel Substances 0.000 description 40
- 229910002027 silica gel Inorganic materials 0.000 description 40
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 39
- 239000000047 product Substances 0.000 description 38
- 235000011054 acetic acid Nutrition 0.000 description 37
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 36
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 33
- 238000006243 chemical reaction Methods 0.000 description 32
- 238000004440 column chromatography Methods 0.000 description 31
- NTYJJOPFIAHURM-UHFFFAOYSA-N Histamine Chemical compound NCCC1=CN=CN1 NTYJJOPFIAHURM-UHFFFAOYSA-N 0.000 description 30
- 239000011541 reaction mixture Substances 0.000 description 30
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 29
- 235000019341 magnesium sulphate Nutrition 0.000 description 29
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 29
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 28
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 27
- AMIMRNSIRUDHCM-UHFFFAOYSA-N Isopropylaldehyde Chemical compound CC(C)C=O AMIMRNSIRUDHCM-UHFFFAOYSA-N 0.000 description 26
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 26
- 239000012043 crude product Substances 0.000 description 26
- 210000004027 cell Anatomy 0.000 description 24
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 23
- SHQSVMDWKBRBGB-UHFFFAOYSA-N cyclobutanone Chemical compound O=C1CCC1 SHQSVMDWKBRBGB-UHFFFAOYSA-N 0.000 description 23
- 229910021595 Copper(I) iodide Inorganic materials 0.000 description 21
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 21
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical class [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 21
- 238000004587 chromatography analysis Methods 0.000 description 19
- OPQARKPSCNTWTJ-UHFFFAOYSA-L copper(ii) acetate Chemical compound [Cu+2].CC([O-])=O.CC([O-])=O OPQARKPSCNTWTJ-UHFFFAOYSA-L 0.000 description 19
- 230000002829 reductive effect Effects 0.000 description 19
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- 150000002923 oximes Chemical class 0.000 description 1
- 125000000466 oxiranyl group Chemical group 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 238000007911 parenteral administration Methods 0.000 description 1
- 108010091212 pepstatin Proteins 0.000 description 1
- FAXGPCHRFPCXOO-LXTPJMTPSA-N pepstatin A Chemical compound OC(=O)C[C@H](O)[C@H](CC(C)C)NC(=O)[C@H](C)NC(=O)C[C@H](O)[C@H](CC(C)C)NC(=O)[C@H](C(C)C)NC(=O)[C@H](C(C)C)NC(=O)CC(C)C FAXGPCHRFPCXOO-LXTPJMTPSA-N 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 208000033808 peripheral neuropathy Diseases 0.000 description 1
- 229960003531 phenolsulfonphthalein Drugs 0.000 description 1
- UYWQUFXKFGHYNT-UHFFFAOYSA-N phenylmethyl ester of formic acid Natural products O=COCC1=CC=CC=C1 UYWQUFXKFGHYNT-UHFFFAOYSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 239000002953 phosphate buffered saline Substances 0.000 description 1
- 125000004592 phthalazinyl group Chemical group C1(=NN=CC2=CC=CC=C12)* 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 108060006633 protein kinase Proteins 0.000 description 1
- 235000018102 proteins Nutrition 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 125000001042 pteridinyl group Chemical group N1=C(N=CC2=NC=CN=C12)* 0.000 description 1
- 125000000561 purinyl group Chemical group N1=C(N=C2N=CNC2=C1)* 0.000 description 1
- 125000004309 pyranyl group Chemical group O1C(C=CC=C1)* 0.000 description 1
- 125000003373 pyrazinyl group Chemical group 0.000 description 1
- 125000003226 pyrazolyl group Chemical group 0.000 description 1
- 125000002098 pyridazinyl group Chemical group 0.000 description 1
- 125000004076 pyridyl group Chemical group 0.000 description 1
- 125000000714 pyrimidinyl group Chemical group 0.000 description 1
- 125000000168 pyrrolyl group Chemical group 0.000 description 1
- 125000002294 quinazolinyl group Chemical group N1=C(N=CC2=CC=CC=C12)* 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 description 1
- 125000001567 quinoxalinyl group Chemical group N1=C(C=NC2=CC=CC=C12)* 0.000 description 1
- 125000004621 quinuclidinyl group Chemical group N12C(CC(CC1)CC2)* 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000006722 reduction reaction Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 206010039073 rheumatoid arthritis Diseases 0.000 description 1
- 238000011808 rodent model Methods 0.000 description 1
- 229960001860 salicylate Drugs 0.000 description 1
- YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical compound OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 239000012047 saturated solution Substances 0.000 description 1
- 201000000980 schizophrenia Diseases 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000006152 selective media Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 208000019116 sleep disease Diseases 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 230000000707 stereoselective effect Effects 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 239000012258 stirred mixture Substances 0.000 description 1
- 208000023516 stroke disease Diseases 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- 150000003456 sulfonamides Chemical class 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 239000000829 suppository Substances 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 230000002889 sympathetic effect Effects 0.000 description 1
- 238000002636 symptomatic treatment Methods 0.000 description 1
- 230000016978 synaptic transmission, cholinergic Effects 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 229940095064 tartrate Drugs 0.000 description 1
- SMIGUQBCGWRCHP-UHFFFAOYSA-N tert-butyl 2-[4-(methanesulfonamido)phenyl]-4,5,7,8-tetrahydropyrazolo[3,4-d]azepine-6-carboxylate Chemical compound N1=C2CCN(C(=O)OC(C)(C)C)CCC2=CN1C1=CC=C(NS(C)(=O)=O)C=C1 SMIGUQBCGWRCHP-UHFFFAOYSA-N 0.000 description 1
- PMLBUVZPRKXMOX-UHFFFAOYSA-N tert-butyl 4-oxoazepane-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1CCCC(=O)CC1 PMLBUVZPRKXMOX-UHFFFAOYSA-N 0.000 description 1
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 description 1
- 125000003039 tetrahydroisoquinolinyl group Chemical group C1(NCCC2=CC=CC=C12)* 0.000 description 1
- 125000001412 tetrahydropyranyl group Chemical group 0.000 description 1
- 125000003507 tetrahydrothiofenyl group Chemical group 0.000 description 1
- 125000004632 tetrahydrothiopyranyl group Chemical group S1C(CCCC1)* 0.000 description 1
- 125000005247 tetrazinyl group Chemical group N1=NN=NC(=C1)* 0.000 description 1
- 125000003831 tetrazolyl group Chemical group 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 125000001113 thiadiazolyl group Chemical group 0.000 description 1
- 125000000335 thiazolyl group Chemical group 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- 125000002088 tosyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1C([H])([H])[H])S(*)(=O)=O 0.000 description 1
- BWHOZHOGCMHOBV-BQYQJAHWSA-N trans-benzylideneacetone Chemical compound CC(=O)\C=C\C1=CC=CC=C1 BWHOZHOGCMHOBV-BQYQJAHWSA-N 0.000 description 1
- 125000004306 triazinyl group Chemical group 0.000 description 1
- 125000001425 triazolyl group Chemical group 0.000 description 1
- 125000002827 triflate group Chemical group FC(S(=O)(=O)O*)(F)F 0.000 description 1
- 125000004044 trifluoroacetyl group Chemical group FC(C(=O)*)(F)F 0.000 description 1
- 125000004205 trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/06—Antimigraine agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/08—Antiepileptics; Anticonvulsants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/22—Anxiolytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/24—Antidepressants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Public Health (AREA)
- Life Sciences & Earth Sciences (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Veterinary Medicine (AREA)
- Neurology (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Hospice & Palliative Care (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0513886.2 | 2005-07-06 | ||
| GBGB0513886.2A GB0513886D0 (en) | 2005-07-06 | 2005-07-06 | Novel compounds |
| PCT/EP2006/006613 WO2007025596A1 (en) | 2005-07-06 | 2006-07-04 | Pyrazolo [3 , 4-d] azepine derivatives as histamine h3 antagonists |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2009500366A JP2009500366A (ja) | 2009-01-08 |
| JP2009500366A5 JP2009500366A5 (OSRAM) | 2009-08-20 |
| JP5145218B2 true JP5145218B2 (ja) | 2013-02-13 |
Family
ID=34856781
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2008519862A Expired - Fee Related JP5145218B2 (ja) | 2005-07-06 | 2006-07-04 | ヒスタミンｈ３アンタゴニストとしてのピラゾロ［３，４−ｄ］アゼピン誘導体 |
Country Status (27)
| Country | Link |
|---|---|
| US (1) | US7888347B2 (OSRAM) |
| EP (1) | EP1899350B1 (OSRAM) |
| JP (1) | JP5145218B2 (OSRAM) |
| KR (1) | KR20080037651A (OSRAM) |
| CN (1) | CN101258154B (OSRAM) |
| AT (1) | ATE467636T1 (OSRAM) |
| AU (1) | AU2006286897A1 (OSRAM) |
| BR (1) | BRPI0612719A2 (OSRAM) |
| CA (1) | CA2614232A1 (OSRAM) |
| CR (1) | CR9622A (OSRAM) |
| CY (1) | CY1110711T1 (OSRAM) |
| DE (1) | DE602006014273D1 (OSRAM) |
| DK (1) | DK1899350T3 (OSRAM) |
| EA (1) | EA013600B1 (OSRAM) |
| ES (1) | ES2345841T3 (OSRAM) |
| GB (1) | GB0513886D0 (OSRAM) |
| HR (1) | HRP20100401T1 (OSRAM) |
| IL (1) | IL188184A0 (OSRAM) |
| MA (1) | MA29623B1 (OSRAM) |
| MX (1) | MX2008000383A (OSRAM) |
| NO (1) | NO20080563L (OSRAM) |
| PL (1) | PL1899350T3 (OSRAM) |
| PT (1) | PT1899350E (OSRAM) |
| SI (1) | SI1899350T1 (OSRAM) |
| UA (1) | UA93047C2 (OSRAM) |
| WO (1) | WO2007025596A1 (OSRAM) |
| ZA (1) | ZA200710798B (OSRAM) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MX2008016343A (es) | 2006-06-23 | 2009-01-19 | Abbott Lab | Derivados ciclopropil amina como moduladores del receptro de histamina h3. |
| US9108948B2 (en) | 2006-06-23 | 2015-08-18 | Abbvie Inc. | Cyclopropyl amine derivatives |
| EP2205596A1 (en) | 2007-09-24 | 2010-07-14 | Comentis, Inc. | (3-hydroxy-4-amino-butan-2-yl) -3- (2-thiazol-2-yl-pyrrolidine-1-carbonyl) benzamide derivatives and related compounds as beta-secretase inhibitors for treating |
| US9186353B2 (en) * | 2009-04-27 | 2015-11-17 | Abbvie Inc. | Treatment of osteoarthritis pain |
| US8853390B2 (en) | 2010-09-16 | 2014-10-07 | Abbvie Inc. | Processes for preparing 1,2-substituted cyclopropyl derivatives |
| CN102952139B (zh) * | 2011-08-30 | 2016-08-10 | 上海药明康德新药开发有限公司 | 反式-3a-氟吡咯烷[3,4-C]并环化合物及其制备方法 |
| 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 |
| JO3407B1 (ar) | 2012-05-31 | 2019-10-20 | Eisai R&D Man Co Ltd | مركبات رباعي هيدرو بيرازولو بيريميدين |
| US9910887B2 (en) * | 2013-04-25 | 2018-03-06 | Facebook, Inc. | Variable search query vertical access |
| SG11201810292YA (en) * | 2016-05-25 | 2018-12-28 | Akarna Therapeutics Ltd | Fused bicyclic compounds for the treatment of disease |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20010079778A (ko) * | 1998-09-09 | 2001-08-22 | 이시하라 겐조 | 제초제로 유용한 융합-벤젠 유도체 |
| AU3956900A (en) * | 1999-04-16 | 2000-11-02 | Boehringer Ingelheim International Gmbh | Substituted imidazoles, their preparation and use |
| JP2001220390A (ja) | 2000-02-09 | 2001-08-14 | Yamanouchi Pharmaceut Co Ltd | 縮合ピラゾール誘導体 |
| AU2003229535A1 (en) * | 2002-06-06 | 2003-12-22 | Novo Nordisk A/S | Substituted hexahydropyrrolo(1,2-a)pyrazines, octahydropyrido(1,2-a)pyrazines and decahydropyrazino(1,2-a)azepines |
| US6770597B2 (en) | 2002-07-17 | 2004-08-03 | Ishihara Sangyo Kaisha, Ltd. | Benzohydrazide derivatives as herbicides and desiccant compositions containing them |
| EP1527074A1 (en) | 2002-07-25 | 2005-05-04 | Pharmacia Italia S.p.A. | Bicyclo-pyrazoles active as kinase inhibitors, process for their preparation and pharmaceutical compositions comprising them |
| EP1539704A1 (en) * | 2002-08-20 | 2005-06-15 | Eli Lilly And Company | Substituted azepines as histamine h3 receptor antagonists, preparation and therapeutic uses |
| GB0224083D0 (en) | 2002-10-16 | 2002-11-27 | Glaxo Group Ltd | Novel compounds |
| GB0224557D0 (en) | 2002-10-22 | 2002-11-27 | Glaxo Group Ltd | Novel compounds |
| CA2509413C (en) | 2002-12-20 | 2012-05-01 | Glaxo Group Limited | Benzazepine derivatives for the treatment of neurological disorders |
| CN103788089A (zh) * | 2003-09-17 | 2014-05-14 | 詹森药业有限公司 | 作为血清素受体调节剂的稠合杂环化合物 |
| GB0329214D0 (en) | 2003-12-17 | 2004-01-21 | Glaxo Group Ltd | Novel compounds |
| GB0405628D0 (en) | 2004-03-12 | 2004-04-21 | Glaxo Group Ltd | Novel compounds |
| GB0408083D0 (en) | 2004-04-08 | 2004-05-12 | Glaxo Group Ltd | Novel compounds |
| PE20060302A1 (es) | 2004-06-18 | 2006-04-08 | Glaxo Group Ltd | Derivados de benzazepina como antagonistas del receptor h3 |
| GB0418267D0 (en) | 2004-08-16 | 2004-09-15 | Glaxo Group Ltd | Novel compounds |
| EP1833796A1 (en) | 2004-12-07 | 2007-09-19 | Glaxo Group Limited | Indenyl derivatives and use thereof for the treatment of neurological disorders |
| ES2321028T3 (es) | 2005-03-14 | 2009-06-01 | Glaxo Group Limited | Derivados de tiazol condensados que tienen afinidad por el receptor h3 de histamina. |
-
2005
- 2005-07-06 GB GBGB0513886.2A patent/GB0513886D0/en not_active Ceased
-
2006
- 2006-07-04 PL PL06818218T patent/PL1899350T3/pl unknown
- 2006-07-04 DE DE602006014273T patent/DE602006014273D1/de active Active
- 2006-07-04 CA CA002614232A patent/CA2614232A1/en not_active Abandoned
- 2006-07-04 ES ES06818218T patent/ES2345841T3/es active Active
- 2006-07-04 BR BRPI0612719-3A patent/BRPI0612719A2/pt not_active IP Right Cessation
- 2006-07-04 AT AT06818218T patent/ATE467636T1/de active
- 2006-07-04 PT PT06818218T patent/PT1899350E/pt unknown
- 2006-07-04 HR HR20100401T patent/HRP20100401T1/hr unknown
- 2006-07-04 WO PCT/EP2006/006613 patent/WO2007025596A1/en not_active Ceased
- 2006-07-04 DK DK06818218.7T patent/DK1899350T3/da active
- 2006-07-04 EP EP06818218A patent/EP1899350B1/en active Active
- 2006-07-04 AU AU2006286897A patent/AU2006286897A1/en not_active Abandoned
- 2006-07-04 MX MX2008000383A patent/MX2008000383A/es active IP Right Grant
- 2006-07-04 EA EA200800264A patent/EA013600B1/ru not_active IP Right Cessation
- 2006-07-04 US US11/994,689 patent/US7888347B2/en not_active Expired - Fee Related
- 2006-07-04 UA UAA200800190A patent/UA93047C2/ru unknown
- 2006-07-04 KR KR1020087000265A patent/KR20080037651A/ko not_active Ceased
- 2006-07-04 SI SI200630733T patent/SI1899350T1/sl unknown
- 2006-07-04 JP JP2008519862A patent/JP5145218B2/ja not_active Expired - Fee Related
- 2006-07-04 CN CN2006800322776A patent/CN101258154B/zh not_active Expired - Fee Related
-
2007
- 2007-12-12 ZA ZA200710798A patent/ZA200710798B/xx unknown
- 2007-12-17 IL IL188184A patent/IL188184A0/en unknown
- 2007-12-20 CR CR9622A patent/CR9622A/es not_active Application Discontinuation
-
2008
- 2008-01-09 MA MA30562A patent/MA29623B1/fr unknown
- 2008-01-30 NO NO20080563A patent/NO20080563L/no not_active Application Discontinuation
-
2010
- 2010-07-29 CY CY20101100713T patent/CY1110711T1/el unknown
Also Published As
| Publication number | Publication date |
|---|---|
| BRPI0612719A2 (pt) | 2010-11-30 |
| EP1899350B1 (en) | 2010-05-12 |
| PT1899350E (pt) | 2010-07-21 |
| WO2007025596A1 (en) | 2007-03-08 |
| MA29623B1 (fr) | 2008-07-01 |
| EP1899350A1 (en) | 2008-03-19 |
| AU2006286897A1 (en) | 2007-03-08 |
| KR20080037651A (ko) | 2008-04-30 |
| PL1899350T3 (pl) | 2010-10-29 |
| DE602006014273D1 (de) | 2010-06-24 |
| ATE467636T1 (de) | 2010-05-15 |
| NO20080563L (no) | 2008-02-01 |
| CN101258154B (zh) | 2011-01-19 |
| JP2009500366A (ja) | 2009-01-08 |
| IL188184A0 (en) | 2008-03-20 |
| CY1110711T1 (el) | 2015-06-10 |
| CA2614232A1 (en) | 2007-03-08 |
| US20080176832A1 (en) | 2008-07-24 |
| DK1899350T3 (da) | 2010-09-06 |
| ES2345841T3 (es) | 2010-10-04 |
| GB0513886D0 (en) | 2005-08-10 |
| SI1899350T1 (sl) | 2010-09-30 |
| EA013600B1 (ru) | 2010-06-30 |
| MX2008000383A (es) | 2008-03-07 |
| US7888347B2 (en) | 2011-02-15 |
| HRP20100401T1 (hr) | 2010-09-30 |
| CN101258154A (zh) | 2008-09-03 |
| EA200800264A1 (ru) | 2008-06-30 |
| UA93047C2 (ru) | 2011-01-10 |
| ZA200710798B (en) | 2008-11-26 |
| CR9622A (es) | 2008-04-10 |
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