ES2554353T3 - Moduladores de transportadores del casete de unión a ATP - Google Patents
Moduladores de transportadores del casete de unión a ATP Download PDFInfo
- Publication number
- ES2554353T3 ES2554353T3 ES07755298.2T ES07755298T ES2554353T3 ES 2554353 T3 ES2554353 T3 ES 2554353T3 ES 07755298 T ES07755298 T ES 07755298T ES 2554353 T3 ES2554353 T3 ES 2554353T3
- Authority
- ES
- Spain
- Prior art keywords
- independently
- optionally substituted
- halogen
- aliphatic
- ring
- 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.)
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- 150000001875 compounds Chemical class 0.000 claims abstract description 5
- 239000003937 drug carrier Substances 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 125000001931 aliphatic group Chemical group 0.000 abstract description 35
- 229910052736 halogen Inorganic materials 0.000 abstract description 29
- 125000004093 cyano group Chemical group *C#N 0.000 abstract description 26
- 150000002367 halogens Chemical class 0.000 abstract description 25
- -1 -OH Chemical group 0.000 abstract description 23
- 229910052739 hydrogen Inorganic materials 0.000 abstract description 20
- 239000001257 hydrogen Substances 0.000 abstract description 20
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract description 20
- 125000001072 heteroaryl group Chemical group 0.000 abstract description 16
- 125000000623 heterocyclic group Chemical group 0.000 abstract description 13
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract description 13
- 125000003118 aryl group Chemical group 0.000 abstract description 10
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract description 9
- 125000004429 atom Chemical group 0.000 abstract description 8
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract description 8
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract description 7
- 125000005842 heteroatom Chemical group 0.000 abstract description 5
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract description 5
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 abstract description 4
- 125000002950 monocyclic group Chemical group 0.000 abstract description 3
- 229910052760 oxygen Inorganic materials 0.000 abstract description 3
- 229910052717 sulfur Inorganic materials 0.000 abstract description 3
- 125000005843 halogen group Chemical group 0.000 abstract 4
- 150000003839 salts Chemical class 0.000 abstract 2
- 125000002619 bicyclic group Chemical group 0.000 abstract 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 9
- 150000002431 hydrogen Chemical group 0.000 description 9
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 7
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- 125000003545 alkoxy group Chemical group 0.000 description 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 5
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 description 4
- 125000001041 indolyl group Chemical group 0.000 description 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- HARUWJZORCBAAL-UHFFFAOYSA-N 6-(chloromethyl)-2,3-dihydro-1,4-benzodioxine Chemical compound O1CCOC2=CC(CCl)=CC=C21 HARUWJZORCBAAL-UHFFFAOYSA-N 0.000 description 3
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000012074 organic phase Substances 0.000 description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 125000001424 substituent group Chemical group 0.000 description 3
- 125000003107 substituted aryl group Chemical group 0.000 description 3
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 3
- ZONLKONEGHMVBB-UHFFFAOYSA-N 2-(2,3-dihydro-1,4-benzodioxin-6-yl)acetonitrile Chemical compound O1CCOC2=CC(CC#N)=CC=C21 ZONLKONEGHMVBB-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 239000007832 Na2SO4 Substances 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 239000012267 brine Substances 0.000 description 2
- 125000002837 carbocyclic group Chemical group 0.000 description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 2
- YMGUBTXCNDTFJI-UHFFFAOYSA-N cyclopropanecarboxylic acid Chemical compound OC(=O)C1CC1 YMGUBTXCNDTFJI-UHFFFAOYSA-N 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 125000004043 oxo group Chemical group O=* 0.000 description 2
- 125000004430 oxygen atom Chemical group O* 0.000 description 2
- 229910052938 sodium sulfate Inorganic materials 0.000 description 2
- 235000011152 sodium sulphate Nutrition 0.000 description 2
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 2
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 2
- BJHIKXHVCXFQLS-UHFFFAOYSA-N 1,3,4,5,6-pentahydroxyhexan-2-one Chemical compound OCC(O)C(O)C(O)C(=O)CO BJHIKXHVCXFQLS-UHFFFAOYSA-N 0.000 description 1
- NZZVDTIYQUASAT-UHFFFAOYSA-N 1-(1,3-benzodioxol-5-yl)cyclopropane-1-carboxylic acid Chemical compound C=1C=C2OCOC2=CC=1C1(C(=O)O)CC1 NZZVDTIYQUASAT-UHFFFAOYSA-N 0.000 description 1
- WDOQMVLDSMTVKP-UHFFFAOYSA-N 1-(1,3-dihydro-2-benzofuran-5-yl)cyclopropane-1-carboxylic acid Chemical compound C=1C=C2COCC2=CC=1C1(C(=O)O)CC1 WDOQMVLDSMTVKP-UHFFFAOYSA-N 0.000 description 1
- RRWKJVZZARHFPB-UHFFFAOYSA-N 1-(1-benzofuran-5-yl)cyclopropane-1-carboxylic acid Chemical compound C=1C=C2OC=CC2=CC=1C1(C(=O)O)CC1 RRWKJVZZARHFPB-UHFFFAOYSA-N 0.000 description 1
- HBLYKIRKVAVJLQ-UHFFFAOYSA-N 1-(1-benzofuran-6-yl)cyclopropane-1-carboxylic acid Chemical compound C=1C=C2C=COC2=CC=1C1(C(=O)O)CC1 HBLYKIRKVAVJLQ-UHFFFAOYSA-N 0.000 description 1
- YMTWFOQAQOMXRP-UHFFFAOYSA-N 1-(1-methylbenzimidazol-5-yl)cyclopropane-1-carboxylic acid Chemical compound C=1C=C2N(C)C=NC2=CC=1C1(C(O)=O)CC1 YMTWFOQAQOMXRP-UHFFFAOYSA-N 0.000 description 1
- PONCYYKNRUMPBJ-UHFFFAOYSA-N 1-(1-methylbenzotriazol-5-yl)cyclopropane-1-carboxylic acid Chemical compound C=1C=C2N(C)N=NC2=CC=1C1(C(O)=O)CC1 PONCYYKNRUMPBJ-UHFFFAOYSA-N 0.000 description 1
- UFFAEXWKGYYSSQ-UHFFFAOYSA-N 1-(1h-indol-5-yl)cyclopropane-1-carboxylic acid Chemical compound C=1C=C2NC=CC2=CC=1C1(C(=O)O)CC1 UFFAEXWKGYYSSQ-UHFFFAOYSA-N 0.000 description 1
- IELWGOUPQRHXLS-UHFFFAOYSA-N 1-(2,2-difluoro-1,3-benzodioxol-5-yl)cyclopropane-1-carboxylic acid Chemical compound C=1C=C2OC(F)(F)OC2=CC=1C1(C(=O)O)CC1 IELWGOUPQRHXLS-UHFFFAOYSA-N 0.000 description 1
- RKHLGXXHPSCJJL-UHFFFAOYSA-N 1-(2,2-dimethyl-1,3-benzodioxol-5-yl)cyclopropane-1-carboxylic acid Chemical compound C1=C2OC(C)(C)OC2=CC=C1C1(C(O)=O)CC1 RKHLGXXHPSCJJL-UHFFFAOYSA-N 0.000 description 1
- QVXPITFURMQHIV-UHFFFAOYSA-N 1-(2,3-dihydro-1,4-benzodioxin-6-yl)cyclopropane-1-carboxylic acid Chemical compound C=1C=C2OCCOC2=CC=1C1(C(=O)O)CC1 QVXPITFURMQHIV-UHFFFAOYSA-N 0.000 description 1
- UNYWNRTZUCJKPY-UHFFFAOYSA-N 1-(2,3-dihydro-1-benzofuran-5-yl)cyclopropane-1-carboxylic acid Chemical compound C=1C=C2OCCC2=CC=1C1(C(=O)O)CC1 UNYWNRTZUCJKPY-UHFFFAOYSA-N 0.000 description 1
- DDBSEHVRDVYHRQ-UHFFFAOYSA-N 1-(2,3-dihydro-1-benzofuran-6-yl)cyclopropane-1-carboxylic acid Chemical compound C=1C=C2CCOC2=CC=1C1(C(=O)O)CC1 DDBSEHVRDVYHRQ-UHFFFAOYSA-N 0.000 description 1
- CZPYUTXQDVNAFL-UHFFFAOYSA-N 1-(2-methoxyphenyl)cyclopropane-1-carboxylic acid Chemical compound COC1=CC=CC=C1C1(C(O)=O)CC1 CZPYUTXQDVNAFL-UHFFFAOYSA-N 0.000 description 1
- KNYGHQQOCHYYSP-UHFFFAOYSA-N 1-(2-methyl-3h-benzimidazol-5-yl)cyclopropane-1-carboxylic acid Chemical compound C=1C=C2NC(C)=NC2=CC=1C1(C(O)=O)CC1 KNYGHQQOCHYYSP-UHFFFAOYSA-N 0.000 description 1
- RHPXKWHEJOXWEH-UHFFFAOYSA-N 1-(2-oxo-3h-1,3-benzoxazol-5-yl)cyclopropane-1-carboxylic acid Chemical compound C=1C=C2OC(=O)NC2=CC=1C1(C(=O)O)CC1 RHPXKWHEJOXWEH-UHFFFAOYSA-N 0.000 description 1
- PGJOQLCGZQSXCU-UHFFFAOYSA-N 1-(2h-benzotriazol-5-yl)cyclopropane-1-carboxylic acid Chemical compound C=1C=C2NN=NC2=CC=1C1(C(=O)O)CC1 PGJOQLCGZQSXCU-UHFFFAOYSA-N 0.000 description 1
- YSWZECDCQZHATN-UHFFFAOYSA-N 1-(3,3-dimethyl-2h-1-benzofuran-5-yl)cyclopropane-1-carboxylic acid Chemical compound C1=C2C(C)(C)COC2=CC=C1C1(C(O)=O)CC1 YSWZECDCQZHATN-UHFFFAOYSA-N 0.000 description 1
- BYUXTEWDOBYESO-UHFFFAOYSA-N 1-(3,4-difluorophenyl)cyclopropane-1-carboxylic acid Chemical compound C=1C=C(F)C(F)=CC=1C1(C(=O)O)CC1 BYUXTEWDOBYESO-UHFFFAOYSA-N 0.000 description 1
- HLADYMRXHXVWDP-UHFFFAOYSA-N 1-(3,4-dihydro-2h-chromen-6-yl)cyclopropane-1-carboxylic acid Chemical compound C=1C=C2OCCCC2=CC=1C1(C(=O)O)CC1 HLADYMRXHXVWDP-UHFFFAOYSA-N 0.000 description 1
- GHJFLVNGRUWTLC-UHFFFAOYSA-N 1-(3,4-dihydroxyphenyl)cyclopropane-1-carboxylic acid Chemical compound C=1C=C(O)C(O)=CC=1C1(C(=O)O)CC1 GHJFLVNGRUWTLC-UHFFFAOYSA-N 0.000 description 1
- FELRPROQUKLRFC-UHFFFAOYSA-N 1-(3,4-dimethoxyphenyl)cyclopropane-1-carboxylic acid Chemical compound C1=C(OC)C(OC)=CC=C1C1(C(O)=O)CC1 FELRPROQUKLRFC-UHFFFAOYSA-N 0.000 description 1
- YAGVSCARZZXXKU-UHFFFAOYSA-N 1-(3-chloro-4-hydroxyphenyl)cyclopropane-1-carboxylic acid Chemical compound C=1C=C(O)C(Cl)=CC=1C1(C(=O)O)CC1 YAGVSCARZZXXKU-UHFFFAOYSA-N 0.000 description 1
- IJNNWPMZHGIFOW-UHFFFAOYSA-N 1-(3-chloro-4-methoxyphenyl)cyclopropane-1-carboxylic acid Chemical compound C1=C(Cl)C(OC)=CC=C1C1(C(O)=O)CC1 IJNNWPMZHGIFOW-UHFFFAOYSA-N 0.000 description 1
- JKIHCIJMQGMLOG-UHFFFAOYSA-N 1-(3-fluoro-4-methoxyphenyl)cyclopropane-1-carboxylic acid Chemical compound C1=C(F)C(OC)=CC=C1C1(C(O)=O)CC1 JKIHCIJMQGMLOG-UHFFFAOYSA-N 0.000 description 1
- DQALANWWCRLIPZ-UHFFFAOYSA-N 1-(3-hydroxy-4-methoxyphenyl)cyclopropane-1-carboxylic acid Chemical compound C1=C(O)C(OC)=CC=C1C1(C(O)=O)CC1 DQALANWWCRLIPZ-UHFFFAOYSA-N 0.000 description 1
- HNUPNADNJWDNFR-UHFFFAOYSA-N 1-(3-hydroxyphenyl)cyclopropane-1-carboxylic acid Chemical compound C=1C=CC(O)=CC=1C1(C(=O)O)CC1 HNUPNADNJWDNFR-UHFFFAOYSA-N 0.000 description 1
- OJHMCTKCWHHFRP-UHFFFAOYSA-N 1-(3-methoxy-4-phenylmethoxyphenyl)cyclopropane-1-carboxylic acid Chemical compound COC1=CC(C2(CC2)C(O)=O)=CC=C1OCC1=CC=CC=C1 OJHMCTKCWHHFRP-UHFFFAOYSA-N 0.000 description 1
- OKGXVHRWLUXELM-UHFFFAOYSA-N 1-(3-methoxyphenyl)cyclopropane-1-carboxylic acid Chemical compound COC1=CC=CC(C2(CC2)C(O)=O)=C1 OKGXVHRWLUXELM-UHFFFAOYSA-N 0.000 description 1
- WDHARPWQZYVRJH-UHFFFAOYSA-N 1-(3-methyl-1,2-benzoxazol-5-yl)cyclopropane-1-carboxylic acid Chemical compound C1=C2C(C)=NOC2=CC=C1C1(C(O)=O)CC1 WDHARPWQZYVRJH-UHFFFAOYSA-N 0.000 description 1
- HVCJDJBLQHCTFY-UHFFFAOYSA-N 1-(3h-benzimidazol-5-yl)cyclopropane-1-carboxylic acid Chemical compound C=1C=C2NC=NC2=CC=1C1(C(=O)O)CC1 HVCJDJBLQHCTFY-UHFFFAOYSA-N 0.000 description 1
- QQYJLBPFNCLOMD-UHFFFAOYSA-N 1-(4-chloro-3-hydroxyphenyl)cyclopropane-1-carboxylic acid Chemical compound C=1C=C(Cl)C(O)=CC=1C1(C(=O)O)CC1 QQYJLBPFNCLOMD-UHFFFAOYSA-N 0.000 description 1
- HMAIOQOQPGCPKW-UHFFFAOYSA-N 1-(4-chloro-3-methoxyphenyl)cyclopropane-1-carboxylic acid Chemical compound C1=C(Cl)C(OC)=CC(C2(CC2)C(O)=O)=C1 HMAIOQOQPGCPKW-UHFFFAOYSA-N 0.000 description 1
- WTRVVRPSILRMNP-UHFFFAOYSA-N 1-(4-chloro-3-phenylmethoxyphenyl)cyclopropane-1-carboxylic acid Chemical compound C=1C=C(Cl)C(OCC=2C=CC=CC=2)=CC=1C1(C(=O)O)CC1 WTRVVRPSILRMNP-UHFFFAOYSA-N 0.000 description 1
- UPNXUJXIIZGXLQ-UHFFFAOYSA-N 1-(4-chlorophenyl)cyclohexane-1-carboxylic acid Chemical compound C=1C=C(Cl)C=CC=1C1(C(=O)O)CCCCC1 UPNXUJXIIZGXLQ-UHFFFAOYSA-N 0.000 description 1
- QJNFJEMGWIQMJT-UHFFFAOYSA-N 1-(4-chlorophenyl)cyclopentane-1-carboxylic acid Chemical compound C=1C=C(Cl)C=CC=1C1(C(=O)O)CCCC1 QJNFJEMGWIQMJT-UHFFFAOYSA-N 0.000 description 1
- YAHLWSGIQJATGG-UHFFFAOYSA-N 1-(4-chlorophenyl)cyclopropane-1-carboxylic acid Chemical compound C=1C=C(Cl)C=CC=1C1(C(=O)O)CC1 YAHLWSGIQJATGG-UHFFFAOYSA-N 0.000 description 1
- AOGCLMKYKRLDAB-UHFFFAOYSA-N 1-(4-hydroxy-4-methoxy-2,3-dihydrochromen-6-yl)cyclopropane-1-carboxylic acid Chemical compound C1=C2C(OC)(O)CCOC2=CC=C1C1(C(O)=O)CC1 AOGCLMKYKRLDAB-UHFFFAOYSA-N 0.000 description 1
- MBSAMXWFQMZRNE-UHFFFAOYSA-N 1-(4-methoxy-3-methylphenyl)cyclopropane-1-carboxylic acid Chemical compound C1=C(C)C(OC)=CC=C1C1(C(O)=O)CC1 MBSAMXWFQMZRNE-UHFFFAOYSA-N 0.000 description 1
- ZZXMORPBGYOROB-UHFFFAOYSA-N 1-(4-methoxy-3-phenylmethoxyphenyl)cyclopropane-1-carboxylic acid Chemical compound COC1=CC=C(C2(CC2)C(O)=O)C=C1OCC1=CC=CC=C1 ZZXMORPBGYOROB-UHFFFAOYSA-N 0.000 description 1
- JKJAJSWMKTWWJS-UHFFFAOYSA-N 1-(4-methoxyphenyl)cyclohexane-1-carboxylic acid Chemical compound C1=CC(OC)=CC=C1C1(C(O)=O)CCCCC1 JKJAJSWMKTWWJS-UHFFFAOYSA-N 0.000 description 1
- OMMROWIAJMZSLF-UHFFFAOYSA-N 1-(4-methoxyphenyl)cyclopentane-1-carboxylic acid Chemical compound C1=CC(OC)=CC=C1C1(C(O)=O)CCCC1 OMMROWIAJMZSLF-UHFFFAOYSA-N 0.000 description 1
- WCPFQQHADRJANG-UHFFFAOYSA-N 1-(4-methoxyphenyl)cyclopropane-1-carboxylic acid Chemical compound C1=CC(OC)=CC=C1C1(C(O)=O)CC1 WCPFQQHADRJANG-UHFFFAOYSA-N 0.000 description 1
- JONFWIWGPHCFLV-UHFFFAOYSA-N 1-(4-oxo-2,3-dihydrochromen-6-yl)cyclopropane-1-carboxylic acid Chemical compound C=1C=C2OCCC(=O)C2=CC=1C1(C(=O)O)CC1 JONFWIWGPHCFLV-UHFFFAOYSA-N 0.000 description 1
- CWIRUFZXQCNXLK-UHFFFAOYSA-N 1-(7-chloro-1,3-benzodioxol-5-yl)cyclopropane-1-carboxylic acid Chemical compound C=1C=2OCOC=2C(Cl)=CC=1C1(C(=O)O)CC1 CWIRUFZXQCNXLK-UHFFFAOYSA-N 0.000 description 1
- IREXTUHKNSCNHV-UHFFFAOYSA-N 1-(7-fluoro-1,3-benzodioxol-5-yl)cyclopropane-1-carboxylic acid Chemical compound C=1C=2OCOC=2C(F)=CC=1C1(C(=O)O)CC1 IREXTUHKNSCNHV-UHFFFAOYSA-N 0.000 description 1
- TVBHFGQXOHONQC-UHFFFAOYSA-N 1-(7-methoxy-1,3-benzodioxol-5-yl)cyclopropane-1-carboxylic acid Chemical compound C=1C=2OCOC=2C(OC)=CC=1C1(C(O)=O)CC1 TVBHFGQXOHONQC-UHFFFAOYSA-N 0.000 description 1
- HQBNLJOWTODEPR-UHFFFAOYSA-N 1-[3-(hydroxymethyl)-4-methoxyphenyl]cyclopropane-1-carboxylic acid Chemical compound C1=C(CO)C(OC)=CC=C1C1(C(O)=O)CC1 HQBNLJOWTODEPR-UHFFFAOYSA-N 0.000 description 1
- WLYQHMMKMYCFAP-UHFFFAOYSA-N 1-[4-(trifluoromethoxy)phenyl]cyclopropane-1-carboxylic acid Chemical compound C=1C=C(OC(F)(F)F)C=CC=1C1(C(=O)O)CC1 WLYQHMMKMYCFAP-UHFFFAOYSA-N 0.000 description 1
- QXXHHHWXFHPNOS-UHFFFAOYSA-N 1-phenylcyclohexane-1-carboxylic acid Chemical compound C=1C=CC=CC=1C1(C(=O)O)CCCCC1 QXXHHHWXFHPNOS-UHFFFAOYSA-N 0.000 description 1
- RHPCYZLXNNRRMB-UHFFFAOYSA-N 1-phenylcyclopentane-1-carboxylic acid Chemical compound C=1C=CC=CC=1C1(C(=O)O)CCCC1 RHPCYZLXNNRRMB-UHFFFAOYSA-N 0.000 description 1
- IWWCCNVRNHTGLV-UHFFFAOYSA-N 1-phenylcyclopropane-1-carboxylic acid Chemical compound C=1C=CC=CC=1C1(C(=O)O)CC1 IWWCCNVRNHTGLV-UHFFFAOYSA-N 0.000 description 1
- MAKLRUMKFWTSAY-UHFFFAOYSA-N 1-spiro[1,3-benzodioxole-2,1'-cyclobutane]-5-ylcyclopropane-1-carboxylic acid Chemical compound C=1C=C2OC3(CCC3)OC2=CC=1C1(C(=O)O)CC1 MAKLRUMKFWTSAY-UHFFFAOYSA-N 0.000 description 1
- FFLHNBGNAWYMRH-UHFFFAOYSA-N 2,3-dihydro-1,4-benzodioxin-6-ylmethanol Chemical compound O1CCOC2=CC(CO)=CC=C21 FFLHNBGNAWYMRH-UHFFFAOYSA-N 0.000 description 1
- HUAOQQIUUYXNFN-UHFFFAOYSA-N 4-(4-methoxyphenyl)oxane-4-carboxylic acid Chemical compound C1=CC(OC)=CC=C1C1(C(O)=O)CCOCC1 HUAOQQIUUYXNFN-UHFFFAOYSA-N 0.000 description 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 description 1
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 description 1
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 1
- 229910006124 SOCl2 Inorganic materials 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 125000005605 benzo group Chemical group 0.000 description 1
- SIKJAQJRHWYJAI-UHFFFAOYSA-N benzopyrrole Natural products C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 1
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 description 1
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004115 pentoxy group Chemical group [*]OC([H])([H])C([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- MNWBNISUBARLIT-UHFFFAOYSA-N sodium cyanide Chemical compound [Na+].N#[C-] MNWBNISUBARLIT-UHFFFAOYSA-N 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 125000000547 substituted alkyl group Chemical group 0.000 description 1
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- Pain & Pain Management (AREA)
Abstract
Un compuesto de fórmula Ic:**Fórmula** o una sal farmacéuticamente aceptable del mismo, en la que R1 es -ZAR4, en el que cada ZA es independientemente un enlace o una cadena alifática C1-6 ramificada o lineal en el que hasta dos unidades de carbono de ZA están opcionalmente e independientemente sustituidas con - CO-, -CS-, -CONRA-, -CONRANRA-, -CO2- -OCO-, -NRACO2-, -O-, -NRACONRA-, -OCONRA-, -NRANRA-, - NRACO-, -S-, -SO-, -SO2- -NRA-, -SO2NRA-, -NRASO2- o -NRASO2NRA-, Cada R4 es independientemente RA, halógeno, -OH, -NH2, 20 -NO2, -CN o -OCF3, Cada RA es independientemente hidrógeno, un alifático, un cicloalifático, heterocicloalifático, un arilo o un heteroarilo; Cada R2 es independientemente -ZBR5, en el que cada ZB es independientemente un enlace o una cadena alifática C1-6 ramificada o lineal opcionalmente sustituida con halógeno, -OH, ciano, cicloalifático C3-10, heterocicloalifático de 3-10 miembros, arilo monocíclico o bicíclico de 8-12 miembros, heteroarilo de 4-15 miembros, o combinaciones de los mismos, en el que hasta dos unidades de carbono de ZB están opcionalmente e independientemente sustituidas con -CO-, -CS-, -CONRB-, -CONRBNRB-, -CO2-, -OCO-, - NRBCO2-, -O-, -NRBCONRB-, -OCONRB-, -NRBNRB-, -NRBCO-, -S-, -SO-, -SO2-, -NRB-, -SO2NRB-, -NRBSO2- o - NRBSO2NRB-, Cada R5 es independientemente RB, halógeno, -OH, -NH2, -NO2, -CN, -CF3 o -OCF3, Cada RB es independientemente hidrógeno, un alifático C3-10, un cicloalifático C3-10, un heterocicloalifático de 3- 10 miembros, un arilo monocíclico o bicíclico de 8-12 miembros, o un heteroarilo de 4-15 miembros; o, dos grupos R2 cualquiera adyacentes junto con los átomos a los que están unidos forman un carbociclo o un heterociclo; Anillo A es un anillo monocíclico de 3-7 miembros que tiene 0-3 heteroátomos seleccionados de N, O y S; Anillo B es un grupo que tiene la fórmula Ia:**Fórmula** o una sal farmacéuticamente aceptable del mismo, en la que p es 0-2, Cada R3 y R'3 es independientemente -ZCR6, en el que cada ZC es independientemente un enlace o una cadena alifática C1-6 ramificada o lineal opcionalmente sustituida con halógeno, hidroxi, o combinaciones de los mismos, en la que hasta dos unidades de carbono de ZC 50 están opcionalmente e independientemente sustituidas con -CO-, -CS-, -CONRC-, -CONRCNRC-, -CO2-, -OCO-, -NRCCO2-, -O-, -NRCCONRC-, -OCONRC-, - NRCNRC-, -NRCCO-, -S-, -SO-, -SO2-, -NRC-, -SO2NRC-, -NRCSO2- o -NRCSO2NRC-, Cada R6 es independientemente RC, halógeno, -OH, -NH2, -NO2, -CN o -OCF3, Cada RC es independientemente hidrógeno, un alifático opcionalmente sustituido con halógeno, hidroxi, o combinaciones de los mismos, un cicloalifático opcionalmente sustituido con alifático, halógeno, hidroxi, nitro, ciano, o combinaciones de los mismos, un heterocicloalifático opcionalmente sustituido con alifático, halógeno, hidroxi, nitro, ciano, o combinaciones de los mismos, un arilo o un heteroarilo, cualquiera de los cuales puede estar opcionalmente sustituido con halógeno, hidroxi, o combinaciones de los mismos, o, dos grupos R3 cualquiera adyacentes junto con los átomos a los que están unidos forman un heterociclo; y n es 1-3, a condición de que cuando el anillo A sea ciclopentilo sin sustituir, n sea 1, R2 sea 4-cloro y R1 sea hidrógeno, entonces el anillo B no sea 2-(terc-butil)indol-5-ilo, o (2,6-diclorofenil(carbonil))-3-metil-1H-indol-5-ilo; y cuando el anillo A sea ciclopentilo sin sustituir, n sea 0 y R1 sea hidrógeno, entonces el anillo B no sea**Fórmula**
Description
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ciano, o combinaciones de los mismos, un heterocicloalifático opcionalmente sustituido con alifático, halógeno, hidroxi, nitro, ciano, o combinaciones de los mismos, un arilo o un heteroarilo, cualquiera de los cuales puede estar opcionalmente sustituido con halógeno, hidroxi, o combinaciones de los mismos, o, dos grupos R3 cualquiera adyacentes junto con los átomos a los que están unidos forman un heterociclo; y n es 1-3, a condición de que cuando el anillo A sea ciclopentilo sin sustituir, n sea 1, R2 sea 4-cloro y R1 sea hidrógeno, entonces el anillo B no sea 2-(terc-butil)indol-5-ilo, o (2,6-diclorofenil(carbonil))-3-metil-1H-indol-5-ilo; y cuando el anillo A sea ciclopentilo sin sustituir, n sea 0 y R1 sea hidrógeno, entonces el anillo B no sea
o
B. Compuestos específicos
1. Grupo R1
R1 es -ZAR4, en el que cada ZA es independientemente un enlace o una cadena alifática C1-6 ramificada o lineal ZA
opcionalmente sustituida en la que hasta dos unidades de carbono de están opcionalmente e independientemente sustituidas con -CO-, -CS-, -CONRA-, -CONRANRA-, -CO2-, -OCO-, -NRACO2-, -O-, -NRACONRA-, -OCONRA-, -NRANRA-, -NRACO-, -S-, -SO-, -SO2-, -NRA-, -SO2NRA-, -NRASO2-o -NRASO2NRA-. Cada R4 es independientemente RA, halógeno, -OH, -NH2, -NO2, -CN o -OCF3. Cada RA es independientemente hidrógeno, un alifático opcionalmente sustituido, un cicloalifático opcionalmente sustituido, un heterocicloalifático opcionalmente sustituido, un arilo opcionalmente sustituido o un heteroarilo opcionalmente sustituido.
En varias realizaciones, R1 es -ZAR4, en el que cada ZA es independientemente un enlace o una cadena alifática C1-6 ramificada o lineal opcionalmente sustituida y cada R4 es hidrógeno.
En otras realizaciones, R1 es -ZAR4, en el que cada ZA es un enlace y cada R4 es hidrógeno.
2. Grupo R2
Cada R2 es independientemente -ZBR5, en el que cada ZB es independientemente un enlace o una cadena alifática ZB
C1-6 ramificada o lineal opcionalmente sustituida en la que hasta dos unidades de carbono de están opcionalmente e independientemente sustituidas con -CO-, -CS-, -CONRB-, -CONRBNRB-, -CO2-, -OCO-, -NRBCO2-, -O-, -NRBCONRB-, -OCONRB-, -NRBNRB-, -NRBCO-, -S-, -SO-, -SO2-, -NRB-, -SO2NRB-, -NRBSO2-o -NRBSO2NRB-.
RB RB
Cada R5 es independientemente , halógeno, -OH,-NH2, -NO2, -CN, -CF3, o -OCF3. Cada es independientemente hidrógeno, un alifático opcionalmente sustituido, un cicloalifático opcionalmente sustituido, un heterocicloalifático opcionalmente sustituido, un arilo opcionalmente sustituido o un heteroarilo opcionalmente sustituido. Alternativamente, dos grupos R2 cualquiera adyacentes junto con los átomos a los que están unidos forman un carbociclo opcionalmente sustituido o un heterociclo o heteroarilo opcionalmente sustituido.
En varias realizaciones, R2 es un alifático opcionalmente sustituido. Por ejemplo, R2 es una cadena alifática C1-6 ramificada o lineal opcionalmente sustituida. En otros ejemplos, R2 es una cadena de alquilo C1-6 ramificada o lineal opcionalmente sustituida, una cadena de alquenilo C2-6 ramificada o lineal opcionalmente sustituida, o una cadena de alquinilo C2-6 ramificada o lineal opcionalmente sustituida. En realizaciones alternativas, R2 es una cadena alifática C1-6 ramificada o lineal que está opcionalmente sustituida con 1-3 de halógeno, hidroxi, ciano, cicloalifático, heterocicloalifático, arilo, heteroarilo, o combinaciones de los mismos. Por ejemplo, R2 es un alquilo C1-6 ramificado o lineal que está opcionalmente sustituido con 1-3 de halógeno, hidroxi, ciano, cicloalifático, heterocicloalifático, arilo, heteroarilo, o combinaciones de los mismos. En todavía otros ejemplos, R2 es un metilo, etilo, propilo, butilo, isopropilo o terc-butilo, cada uno de los cuales está opcionalmente sustituido con 1-3 de halógeno, hidroxi, ciano,
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arilo, heteroarilo, cicloalifático o heterocicloalifático. En todavía otros ejemplos, R2 es un metilo, etilo, propilo, butilo, isopropilo o terc-butilo, cada uno de los cuales está sin sustituir. En varias otras realizaciones, R2 es un alcoxi C1-5 ramificado o lineal opcionalmente sustituido. Por ejemplo, R2 es un alcoxi C1-5 que está opcionalmente sustituido con 1-3 de hidroxi, arilo, heteroarilo, cicloalifático, heterocicloalifático o
5 combinaciones de los mismos. En otros ejemplos, R2 es un metoxi, etoxi, propoxi, butoxi o pentoxi, cada uno de los cuales está opcionalmente sustituido con 1-3 de hidroxi, arilo, heteroarilo, cicloalifático, heterocicloalifático, o combinaciones de los mismos.
En otras realizaciones, R2 es hidroxi, halógeno o ciano. 10 En varias realizaciones, R2 es -ZBR5, y ZB es independientemente un enlace o una cadena alifática C1-4 ramificada o ZB
lineal opcionalmente sustituida en la que hasta dos unidades de carbono de están opcionalmente e independientemente sustituidas con -C(O)-, -O-, -S-, -S(O)2-o -NH-, y R5 es RB, halógeno, -OH, -NH2, -NO2, -CN, -CF3 o -OCF3, y RB es hidrógeno o arilo.
15 En varias realizaciones, dos grupos R2 adyacentes forman un carbociclo opcionalmente sustituido o un heterociclo opcionalmente sustituido. Por ejemplo, dos grupos R2 adyacentes forman un carbociclo opcionalmente sustituido o un heterociclo opcionalmente sustituido, cualquiera de los cuales está condensado con el fenilo de fórmula I, en el que el carbociclo o heterociclo tiene la fórmula Ib:
20
30 Cada uno de Z1, Z2, Z3, Z4 y Z5 es independientemente un enlace, -CR7R'7-, -C(O)-, -NR7-o -O-; cada R7 es independientemente -ZDR8, en el que cada ZD es independientemente un enlace o una cadena alifática C1-6 ramificada o lineal opcionalmente sustituida en la que hasta dos unidades de carbono de ZD están opcionalmente e independientemente sustituidas con -CO-, -CS-, -CONRD-, -CO2-, -OCO-, -NRDCO2-, -O-, -NRDCONRD-, -OCONRD-, -NRDNRD-, -NRDCO-, -S-, -SO-, -SO2-, -NRD-, -SO2NRD-, -NRDSO2-o -NRDSO2NRD-. Cada R8 es
35 independientemente RD, halógeno, -OH, -NH2, -NO2, -CN,-CF3 o -OCF3. Cada RD es independientemente hidrógeno, un cicloalifático opcionalmente sustituido, un heterocicloalifático opcionalmente sustituido, un arilo opcionalmente sustituido o un heteroarilo opcionalmente sustituido. Cada R'7 es independientemente hidrógeno, alifático C1-6 opcionalmente sustituido, hidroxi, halógeno, ciano, nitro, o combinaciones de los mismos. Alternativamente, dos grupos R7 cualquiera adyacentes junto con los átomos a los que están unidos forman un anillo carbocíclico de 3-7
40 miembros opcionalmente sustituido, tal como un anillo de ciclobutilo opcionalmente sustituido, o dos grupos R7 y R'7 cualquiera junto con el átomo o átomos a los que están unidos forman un anillo carbocíclico o un anillo heterocarbocíclico de 3-7 miembros opcionalmente sustituido.
En varios otros ejemplos, dos grupos R2 adyacentes forman un carbociclo opcionalmente sustituido. Por ejemplo,
45 dos grupos R2 adyacentes forman un carbociclo de 5-7 miembros opcionalmente sustituido que está opcionalmente sustituido con 1-3 de halógeno, hidroxi, ciano, oxo, ciano, alcoxi, alquilo, o combinaciones de los mismos. En otro ejemplo, dos grupos R2 adyacentes forman un carbociclo de 5-6 miembros que está opcionalmente sustituido con 13 de halógeno, hidroxi, ciano, oxo, ciano, alcoxi, alquilo, o combinaciones de los mismos. En otro ejemplo adicional, dos grupos R2 adyacentes forman un carbociclo de 5-7 miembros sin sustituir.
50 En ejemplos alternativos, dos grupos R2 adyacentes forman un heterociclo opcionalmente sustituido. Por ejemplo, dos grupos R2 adyacentes forman un heterociclo de 5-7 miembros opcionalmente sustituido que tiene 1-3 heteroátomos independientemente seleccionados de N, O y S. En varios ejemplos, dos grupos R2 adyacentes forman un heterociclo de 5-6 miembros opcionalmente sustituido que tiene 1-2 átomos de oxígeno. En otros
55 ejemplos, dos grupos R2 adyacentes forman un heterociclo de 5-7 miembros sin sustituir que tiene 1-2 átomos de oxígeno. En otras realizaciones, dos grupos R2 adyacentes forman un anillo seleccionado de:
15
30 En ejemplos alternativos, dos grupos R2 adyacentes forman un carbociclo opcionalmente sustituido o un heterociclo opcionalmente sustituido, y un tercer grupo R2 está unido a cualquier posición químicamente factible sobre el fenilo de fórmula I. Por ejemplo, un carbociclo opcionalmente sustituido o un heterociclo opcionalmente sustituido, ambos de los cuales están formados por dos grupos R2 adyacentes; un tercer grupo R2; y el fenilo de fórmula I forman un grupo que tiene la fórmula Ic:
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Z1, Z2, Z3, Z4 y Z5 se han definido anteriormente en la fórmula Ib, y R2 se ha definido anteriormente en la fórmula I.
En varias realizaciones, cada grupo R2 está seleccionado independientemente de hidrógeno, halógeno, -OCH3, -OH, -CH2OH, -CH3 y -OCF3, y/o dos grupos R2 adyacentes junto con los átomos a los que están unidos forman
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opcionalmente sustituido. Por ejemplo, R3 es un (heterocicloalifático)carbonilo opcionalmente sustituido que tiene 1-3 heteroátomos independientemente seleccionados de N, O y S. En otros ejemplos, R3 es un (heterocicloalifático)carbonilo opcionalmente sustituido que tiene 1-3 heteroátomos independientemente seleccionados de N y O. En todavía otros ejemplos, R3 es un (heterocicloalifático)carbonilo monocíclico de 4-7
5 miembros opcionalmente sustituido que tiene 1-3 heteroátomos independientemente seleccionados de N y O. Alternativamente, R3 es (piperidin-1-il)carbonilo, (pirrolidin-1-il)carbonilo o (morfolin-4-il)carbonilo, (piperazin-1il)carbonilo, cada uno de los cuales está opcionalmente sustituido con 1-3 de halógeno, hidroxi, ciano, nitro, o alifático.
10 En todavía más casos, R3 es (alifático)amido opcionalmente sustituido tal como (alifático(amino(carbonilo)) que está unido a la posición 2 o 3 sobre el anillo de indol de fórmula Ia. En algunas realizaciones, R3 es un (alquil(amino))carbonilo opcionalmente sustituido que está unido a la posición 2 o 3 sobre el anillo de indol de fórmula Ia. En otras realizaciones, R3 es un (alifático(amino))carbonilo lineal o ramificado opcionalmente sustituido que está unido a la posición 2 o 3 sobre el anillo de indol de fórmula Ia. En varios ejemplos, R3 es (N,N
15 dimetil(amino))carbonilo, (metil(amino))carbonilo, (etil(amino))carbonilo, (propil(amino))carbonilo, (prop-2il(amino))carbonilo, (dimetil(but-2-il(amino)))carbonilo, (terc-butil(amino))carbonilo, (butil(amino))carbonilo, cada uno de los cuales está opcionalmente sustituido con 1-3 de halógeno, hidroxi, cicloalifático, heterocicloalifático, arilo, heteroarilo, o combinaciones de los mismos.
20 En otras realizaciones, R3 es un (alcoxi)carbonilo opcionalmente sustituido. Por ejemplo, R3 es (metoxi)carbonilo, (etoxi)carbonilo, (propoxi)carbonilo, o (butoxi)carbonilo, cada uno de los cuales está opcionalmente sustituido con 13 de halógeno, hidroxi, o combinaciones de los mismos. En varios casos, R3 es un alifático C1-6 lineal o ramificado opcionalmente sustituido. Por ejemplo, R3 es un alquilo C1-6 lineal o ramificado opcionalmente sustituido. En otros ejemplos, R3 es independientemente un metilo, etilo, propilo, butilo, isopropilo o terc-butilo opcionalmente sustituido,
25 cada uno de los cuales está opcionalmente sustituido con 1-3 de halógeno, hidroxi, ciano, nitro, o combinación de los mismos En otras realizaciones, R3 es un cicloalifático C3-6 opcionalmente sustituido. Realizaciones a modo de ejemplo incluyen ciclopropilo, 1-metil-cicloprop-1-ilo, etc. En otros ejemplos, p es 2 y los dos sustituyentes R3 están unidos al indol de fórmula Ia en las posiciones 2,4 o 2,6 o 2,7. Realizaciones a modo de ejemplo incluyen 6-F, 3-( alifático C1-6 o cicloalifático C3-6 opcionalmente sustituido); 7-F-2-(-(alifático C1-6 o cicloalifático C3-6 opcionalmente
30 sustituido)), 4F-2-(alifático C1-6 o cicloalifático C3-6 opcionalmente sustituido); 7-CN-2-(alifático C1-6 o cicloalifático C3-6 opcionalmente sustituido); 7-Me-2-(alifático C1-6 o cicloalifático C3-6 opcionalmente sustituido) y 7-OMe-2-(alifático C16 o cicloalifático C3-6 opcionalmente sustituido).
En varias realizaciones, R3 es hidrógeno. En varios casos, R3 es un alifático C1-6 lineal o ramificado opcionalmente 35 sustituido. En otras realizaciones, R3 es un cicloalifático C3-6 opcionalmente sustituido.
En varias realizaciones, R3 es uno seleccionado de: -H, -CH3, -CH2OH, -CH2CH3, -CH2CH2OH, -CH2CH2CH3, -NH2, halógeno, -OCH3, -CN, -CF3, -C(O)OCH2CH3, -S(O)2CH3, -CH2NH2, -C(O)NH2,
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cualquiera del alifático o cicloalifático está opcionalmente sustituido con hasta 4 sustituyentes -OH. En otra realización, RC es hidrógeno, o alquilo C1-6 opcionalmente sustituido con hasta 4 sustituyentes -OH.
En otras realizaciones, R'3 es hidrógeno o
en la que R31 es H o un alifático C1-2 que está opcionalmente sustituido con 1-3 de halógeno, -OH, o combinaciones de los mismos. R32 es -L-R33, en el que L es un enlace, -CH2-, -CH2O-, -CH2NHS(O)2-, -CH2C(O)-, -CH2NHC(O)-o
15 CH2NH-; y R33 es hidrógeno, o alifático C1-2, cicloalifático, heterocicloalifático, o heteroarilo, cada uno de los cuales está opcionalmente sustituido con 1 de -OH, -NH2, o -CN. Por ejemplo, en una realización, R31 es hidrógeno y R32 es alifático C1-2 opcionalmente sustituido con -OH, -NH2 o -CN.
En varias realizaciones, R'3 está seleccionado independientemente de uno de los siguientes: -H, -CH3, -CH2CH3, 20 C(O)CH3, -CH2CH2OH, -C(O)OCH3,
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6-Clorometil-2,3-dihidro-benzo[1,4]dioxina
Se agitó una mezcla de (2,3-dihidro-benzo[1,4]dioxin-6-il)metanol (10,6 g) en SOCl2 (10 ml) a temperatura ambiente durante 10 min y luego se vertió en agua con hielo. Se separó la fase orgánica y la fase acuosa se extrajo con diclorometano (50 ml × 3). Las fases orgánicas combinadas se lavaron con NaHCO3 (disolución sat), agua y salmuera, se secaron sobre Na2SO4 y se concentraron a sequedad para obtener 6-clorometil-2,3-dihidrobenzo[1,4]dioxina (12 g, 88 % durante dos etapas), que se usó directamente en la siguiente etapa.
2-(2,3-Dihidrobenzo[b][1,4]dioxin-6-il)acetonitrilo
Se agitó una mezcla de 6-clorometil-2,3-dihidro-benzo[1,4]dioxina (12,5 g, 67,7 mmoles) y NaCN (4,30 g, 87,8 mmoles) en DMSO (50 ml) a ta durante 1 h. La mezcla se vertió en agua (150 ml) y a continuación se extrajo con diclorometano (50 ml × 4). Las fases orgánicas combinadas se lavaron con agua (50 ml × 2) y salmuera (50 ml), se secaron sobre Na2SO4 y se concentraron a sequedad. El residuo se purificó por columna (éter de petróleo/acetato de etilo 50:1) sobre gel de sílice para obtener 2-(2,3-dihidrobenzo[b][1,4]dioxin-6-il)acetonitrilo como un aceite amarillo (10,2 g, 86 %), RMN 1H (300 MHz, CDCl3) δ 6,78-6,86 (m, 3H), 4,25 (s, 4H), 3,63 (s, 2H).
La siguiente Tabla 2 contiene una lista de elementos estructurales de ácido carboxílico que estuvieron comercialmente disponibles, o se prepararon por uno de los tres métodos descritos anteriormente:
Tabla 2: Elementos estructurales de ácido carboxílico.
- Nombre
- Estructura
- 1-benzo[1,3]dioxol-5-ilciclopropano-1-ácido carboxílico
-
imagen110
- 1-(2,2-difluorobenzo[1,3]dioxol-5-il)ciclopropano-1-ácido carboxílico
-
imagen111
- 1-(3,4-dihidroxifenil)ciclopropano acido carboxílico
-
imagen112
- 1-(3-metoxifenil)ciclopropano-1-ácido carboxilico
-
imagen113
- 1-(2-metoxifenil)ciclopropano-1-ácido carboxílico
-
imagen114
- 1-[4-(trifluorometoxi)fenil]ciclopropano-1-ácido carboxílico
-
imagen115
- 1-(2,2-dimetilbenzo[d][1,3]dioxol-5-il)ciclopropano ácido carboxílico
-
imagen116
104 105 106 107 108
- Nombre
- Estructura
- tetrahidro-4-(4-metoxifenil)-2H-piran-4-ácido carboxílico
-
imagen117
- 1-fenilciclopropano-1-ácido carboxílico
-
imagen118
- 1-(4-metoxifenil)ciclopropano-1-ácido carboxílico
-
imagen119
- 1-(4-clorofenil)ciclopropano-1-ácido carboxílico
-
imagen120
- 1-(3-hidroxifenil)ciclopropano ácido carboxílico
-
imagen121
- 1-fenilciclopentano ácido carboxílico
-
imagen122
- 1-(2-oxo-2,3-dihidrobenzo[d]oxazol-5-il)ciclopropano ácido carboxílico
-
imagen123
- 1-(benzofuran-5-il)ciclopropano ácido carboxílico
-
imagen124
- 1-(4-metoxifenil)ciclohexano ácido carboxílico
-
imagen125
- 1-(4-clorofenil)ciclohexano ácido carboxílico
-
imagen126
- 1-(2,3-dihidrobenzofuran-5-il)ciclopropano ácido carboxílico
-
imagen127
- 1-(3,3-dimethil-2,3-dihidrobenzofuran-5-il)ciclopropano ácido carboxílico
-
imagen128
- Nombre
- Estructura
- 1-(7-metoxibenzo[d][1,3]dioxol-5-il)ciclopropano ácido carboxílico
-
imagen129
- 1-(3-hidroxi-4-metoxifenil)ciclopropano ácido carboxílico
-
imagen130
- 1-(4-cloro-3-hidroxifenil)ciclopropano ácido carboxílico
-
imagen131
- 1-(3-(benziloxi)-4-clorofenil)ciclopropano ácido carboxílico
-
imagen132
- 1-(4-clorofenil)ciclopentano ácido carboxílico
-
imagen133
- 1-(3-(benziloxi)-4-metoxifenil)ciclopropano ácido carboxílico
-
imagen134
- 1-(3-cloro-4-metoxifenil)ciclopropano ácido carboxílico
-
imagen135
- 1-(3-fluoro-4-metoxifenil)ciclopropano ácido carboxílico
-
imagen136
- 1-(4-metoxi-3-metilfenil)ciclopropano ácido carboxílico
-
imagen137
- 1-(4-(benziloxi)-3-metoxifenil)ciclopropano ácido carboxílico
-
imagen138
- 1-(4-cloro-3-metoxifenil)ciclopropano ácido carboxílico
-
imagen139
- 1-(3-cloro-4-hidroxifenil)ciclopropano ácido carboxílico
-
imagen140
- Nombre
- Estructura
- 1-(3-(hidroximetil)-4-metoxifenil)ciclopropano ácido carboxilico
-
imagen141
- 1-(4-metoxifenil)ciclopentano ácido carboxilico
-
imagen142
- 1-fenilciclohexano ácido carboxilico
-
imagen143
- 1-(3,4-dimetoxifenil)ciclopropano ácido carboxilico
-
imagen144
- 1-(7-chlorobenzo[d][1,3]dioxol-5-il)ciclopropano ácido carboxilico
-
imagen145
- 1-(benzo[djoxazol-5-il)ciclopropano ácido carboxilico
-
imagen146
- 1-(7-fluorobenzo[d][1,3]dioxol-5-il)ciclopropano ácido carboxilico
-
imagen147
- 1-(3,4-difluorofenil)ciclopropano ácido carboxilico
-
imagen148
- 1-(1H-indol-5-il)ciclopropano ácido carboxilico
-
imagen149
- 1-(1H-benzo[d]imidazol-5-il)ciclopropano ácido carboxilico
-
imagen150
- 1-(2-metil-1H-benzo[d]imidazol-5-il)ciclopropano ácido carboxilico
-
imagen151
- 1-(-metil-1H-benzo[d]imidazol-5-il)ciclopropano ácido carboxilico
-
imagen152
- 1-(3-metilbenzo[d]isoxazol-5-il)ciclopropano ácido carboxilico
-
imagen153
- Nombre
- Estructura
- 1-(spiro[benzo[d][1,3]dioxol-2,1’-ciclobutano]-5-il)ciclopropano ácido carboxílico
-
imagen154
- 1-(1H-benzo[d][1,2,3]triazol-5-il)ciclopropano ácido carboxílico
-
imagen155
- 1-(1-metil-1H-benzo[d][1,2,3]triazol-5-il)ciclopropano ácido carboxílico
-
imagen156
- 1-(1,3-dihidroisobenzofuran-5-il)ciclopropano ácido carboxílico
-
imagen157
- 1-(6-fluorobenzo[d][1,3]dioxol-5-il)ciclopropano ácido carboxílico
-
imagen158
- 1-(2,3-dihidrobenzofuran-6-il)ciclopropano ácido carboxílico
-
imagen159
- 1-(chroman-6-il)ciclopropano ácido carboxílico
-
imagen160
- 1-(4-hidroxy-4-methoxychroman-6-il)ciclopropano ácido carboxílico
-
imagen161
- 1-(4-oxochroman-6-il)ciclopropano ácido carboxílico
-
imagen162
- 1-(3,4-dicloorofenil)ciclopropano ácido carboxílico
-
imagen163
- 1-(2,3-dihidrobenzo[b][1,4]dioxin-6-il)ciclopropano ácido carboxílico
-
imagen164
- 1-(benzofuran-6-il)ciclopropano ácido carboxílico
-
imagen165
Claims (2)
-
imagen1 imagen2 imagen3 imagen4 imagen5 imagen6 imagen7 199imagen8 imagen9 imagen10 imagen11 imagen12 imagen13 imagen14 imagen15 imagen16 208 209imagen17 imagen18 imagen19 imagen20 imagen21 213 214imagen22 imagen23 imagen24 imagen25 imagen26 218 219imagen27 imagen28 imagen29 imagen30 imagen31 223 29. El compuesto de la reivindicación 28, en el que el compuesto esimagen32 imagen33 - 30. Una composición farmacéutica que comprende un compuesto como se describe en cualquiera de las reivindicaciones 1-29 y un vehículo farmacéuticamente aceptable.224
imagen34 imagen35 imagen36 imagen37 imagen38 229imagen39 imagen40 imagen41 imagen42 imagen43 234imagen44 imagen45 imagen46 imagen47 imagen48 239imagen49 imagen50 imagen51 imagen52 imagen53 244 245imagen54 imagen55 imagen56 imagen57 imagen58 249 250imagen59 imagen60
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ES07755298.2T Active ES2554353T3 (es) | 2006-04-07 | 2007-04-09 | Moduladores de transportadores del casete de unión a ATP |
ES16155334.2T Active ES2659364T3 (es) | 2006-04-07 | 2007-04-09 | Moduladores de transportadores del casete de unión a ATP |
ES17209175T Active ES2882684T3 (es) | 2006-04-07 | 2007-04-09 | Preparación de moduladores de transportadores del casete de unión a ATP |
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ES17209175T Active ES2882684T3 (es) | 2006-04-07 | 2007-04-09 | Preparación de moduladores de transportadores del casete de unión a ATP |
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US (9) | US7776905B2 (es) |
EP (5) | EP3882245A1 (es) |
JP (3) | JP5420395B2 (es) |
CN (2) | CN101460489A (es) |
AU (1) | AU2007235260B2 (es) |
BR (1) | BRPI0710965B8 (es) |
CA (2) | CA2648719C (es) |
CY (3) | CY1116979T1 (es) |
DK (3) | DK2007756T3 (es) |
ES (4) | ES2580803T3 (es) |
HU (4) | HUE026145T2 (es) |
IL (1) | IL194576A (es) |
IN (1) | IN2014KN02423A (es) |
LT (1) | LT3091011T (es) |
MX (1) | MX2008012945A (es) |
NZ (3) | NZ571803A (es) |
PL (4) | PL3327016T3 (es) |
PT (3) | PT3091011T (es) |
RU (1) | RU2451018C2 (es) |
SI (4) | SI2674428T1 (es) |
WO (1) | WO2007117715A2 (es) |
ZA (1) | ZA200809290B (es) |
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