EA025356B1 - Антагонисты trpm8 - Google Patents
Антагонисты trpm8 Download PDFInfo
- Publication number
- EA025356B1 EA025356B1 EA201491213A EA201491213A EA025356B1 EA 025356 B1 EA025356 B1 EA 025356B1 EA 201491213 A EA201491213 A EA 201491213A EA 201491213 A EA201491213 A EA 201491213A EA 025356 B1 EA025356 B1 EA 025356B1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- thiazole
- carboxylate
- ethyl
- oxy
- fluorophenyl
- Prior art date
Links
- 239000005557 antagonist Substances 0.000 title abstract description 27
- 102000003610 TRPM8 Human genes 0.000 title abstract 3
- 101150111302 Trpm8 gene Proteins 0.000 title abstract 3
- 150000001875 compounds Chemical class 0.000 claims abstract description 285
- 230000000694 effects Effects 0.000 claims abstract description 29
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 25
- 208000002193 Pain Diseases 0.000 claims abstract description 23
- 238000011282 treatment Methods 0.000 claims abstract description 22
- 230000036407 pain Effects 0.000 claims abstract description 21
- 201000010099 disease Diseases 0.000 claims abstract description 13
- 208000023504 respiratory system disease Diseases 0.000 claims abstract description 8
- 208000020016 psychiatric disease Diseases 0.000 claims abstract description 7
- 208000003251 Pruritus Diseases 0.000 claims abstract description 6
- 208000028867 ischemia Diseases 0.000 claims abstract description 6
- 230000007803 itching Effects 0.000 claims abstract description 5
- 230000004770 neurodegeneration Effects 0.000 claims abstract description 5
- 208000006011 Stroke Diseases 0.000 claims abstract description 4
- -1 (trifluoromethyl) benzyl Chemical group 0.000 claims description 124
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims description 37
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 37
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 18
- 239000011734 sodium Substances 0.000 claims description 18
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 13
- 239000003814 drug Substances 0.000 claims description 12
- NJIJXHPIIHCJKS-UHFFFAOYSA-N ethyl 2-(3-fluorophenyl)-4-hydroxy-1,3-thiazole-5-carboxylate Chemical compound CCOC(=O)c1sc(nc1O)-c1cccc(F)c1 NJIJXHPIIHCJKS-UHFFFAOYSA-N 0.000 claims description 12
- 125000004180 3-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(F)=C1[H] 0.000 claims description 11
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 11
- HTQNUGGPEURDFS-UHFFFAOYSA-N ethyl 4-hydroxy-2-(4-methylphenyl)-1,3-thiazole-5-carboxylate Chemical compound CCOC(=O)c1sc(nc1O)-c1ccc(C)cc1 HTQNUGGPEURDFS-UHFFFAOYSA-N 0.000 claims description 11
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims description 11
- TVKXJECNMMOPNE-UHFFFAOYSA-N 2-(3-fluorophenyl)-4-hydroxy-1,3-thiazole-5-carboxylic acid Chemical compound OC(=O)c1sc(nc1O)-c1cccc(F)c1 TVKXJECNMMOPNE-UHFFFAOYSA-N 0.000 claims description 10
- ITHFMUBXKDEFPT-UHFFFAOYSA-N 2-(4-fluorophenyl)-4-hydroxy-1,3-thiazole-5-carboxylic acid Chemical compound OC(=O)c1sc(nc1O)-c1ccc(F)cc1 ITHFMUBXKDEFPT-UHFFFAOYSA-N 0.000 claims description 10
- GTTLQUWXZGMKGX-UHFFFAOYSA-N chembl1377190 Chemical compound OC1=C(C(=O)OCC)SC(C=2C=CC(Cl)=CC=2)=N1 GTTLQUWXZGMKGX-UHFFFAOYSA-N 0.000 claims description 10
- 208000013403 hyperactivity Diseases 0.000 claims description 10
- 208000004296 neuralgia Diseases 0.000 claims description 10
- 229910052708 sodium Inorganic materials 0.000 claims description 10
- IBVOCILLCZTWKT-UHFFFAOYSA-N 2-(4-chlorophenyl)-4-(methoxymethoxy)-1,3-thiazole-5-carbonitrile Chemical compound S1C(C#N)=C(OCOC)N=C1C1=CC=C(Cl)C=C1 IBVOCILLCZTWKT-UHFFFAOYSA-N 0.000 claims description 9
- FPLQXRZLRODTMM-UHFFFAOYSA-N ethyl 2-(4-fluorophenyl)-4-hydroxy-1,3-thiazole-5-carboxylate Chemical compound CCOC(=O)c1sc(nc1O)-c1ccc(F)cc1 FPLQXRZLRODTMM-UHFFFAOYSA-N 0.000 claims description 9
- QKRYFBKKMLYRHO-UHFFFAOYSA-N chembl65312 Chemical compound OC1=C(C(=O)OCC)SC(C=2C=CC=CC=2)=N1 QKRYFBKKMLYRHO-UHFFFAOYSA-N 0.000 claims description 8
- 239000008194 pharmaceutical composition Substances 0.000 claims description 8
- 125000004299 tetrazol-5-yl group Chemical group [H]N1N=NC(*)=N1 0.000 claims description 8
- QCLLVUJFJHPWKW-UHFFFAOYSA-N 2-(3-fluorophenyl)-5-(5-methyl-1,2,4-oxadiazol-3-yl)-1,3-oxazol-4-ol Chemical compound Cc1nc(no1)-c1oc(nc1O)-c1cccc(F)c1 QCLLVUJFJHPWKW-UHFFFAOYSA-N 0.000 claims description 7
- LCEWMKKEBKMJMD-UHFFFAOYSA-N 2-(3-fluorophenyl)-5-(5-methyl-1,2,4-oxadiazol-3-yl)-1,3-thiazol-4-ol Chemical compound Cc1nc(no1)-c1sc(nc1O)-c1cccc(F)c1 LCEWMKKEBKMJMD-UHFFFAOYSA-N 0.000 claims description 7
- BWJCGZISWJGCQH-UHFFFAOYSA-N 2-(4-chlorophenyl)-4-(methoxymethoxy)-1,3-thiazole-5-carboxamide Chemical compound S1C(C(N)=O)=C(OCOC)N=C1C1=CC=C(Cl)C=C1 BWJCGZISWJGCQH-UHFFFAOYSA-N 0.000 claims description 7
- VSTOXGIORCTKQC-UHFFFAOYSA-N 2-(4-chlorophenyl)-4-(methoxymethoxy)-1,3-thiazole-5-carboxylic acid Chemical compound S1C(C(O)=O)=C(OCOC)N=C1C1=CC=C(Cl)C=C1 VSTOXGIORCTKQC-UHFFFAOYSA-N 0.000 claims description 7
- YTBXQOVLYUPQLG-UHFFFAOYSA-N 2-(4-chlorophenyl)-4-hydroxy-1,3-thiazole-5-carboxylic acid Chemical compound OC(=O)c1sc(nc1O)-c1ccc(Cl)cc1 YTBXQOVLYUPQLG-UHFFFAOYSA-N 0.000 claims description 7
- MOXAICOPIPZILF-UHFFFAOYSA-N 2-(4-chlorophenyl)-5-(2H-tetrazol-5-yl)-1,3-thiazol-4-ol Chemical compound Oc1nc(sc1-c1nnn[nH]1)-c1ccc(Cl)cc1 MOXAICOPIPZILF-UHFFFAOYSA-N 0.000 claims description 7
- OBPZBZRLFJAFAB-UHFFFAOYSA-N 3-[4-[(4-chlorophenyl)methoxy]-2-(3-fluorophenyl)-1,3-oxazol-5-yl]-5-methyl-1,2,4-oxadiazole Chemical compound O1C(C)=NC(C2=C(N=C(O2)C=2C=C(F)C=CC=2)OCC=2C=CC(Cl)=CC=2)=N1 OBPZBZRLFJAFAB-UHFFFAOYSA-N 0.000 claims description 7
- HPCDMKKZYVBIBD-UHFFFAOYSA-N 4-[(2-chlorophenyl)methoxy]-2-(4-methylphenyl)-1,3-thiazole-5-carboxylic acid Chemical compound C1=CC(C)=CC=C1C1=NC(OCC=2C(=CC=CC=2)Cl)=C(C(O)=O)S1 HPCDMKKZYVBIBD-UHFFFAOYSA-N 0.000 claims description 7
- 125000006283 4-chlorobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1Cl)C([H])([H])* 0.000 claims description 7
- QGFFUALUHPYUGQ-UHFFFAOYSA-N 4-hydroxy-2-(4-methylphenyl)-1,3-thiazole-5-carboxylic acid Chemical compound Cc1ccc(cc1)-c1nc(O)c(s1)C(O)=O QGFFUALUHPYUGQ-UHFFFAOYSA-N 0.000 claims description 7
- 208000035475 disorder Diseases 0.000 claims description 7
- ZYPFJCNOBJBQAW-UHFFFAOYSA-N ethyl 2-(3-chlorophenyl)-4-[(2-chlorophenyl)methoxy]-1,3-thiazole-5-carboxylate Chemical compound CCOC(=O)C=1SC(C=2C=C(Cl)C=CC=2)=NC=1OCC1=CC=CC=C1Cl ZYPFJCNOBJBQAW-UHFFFAOYSA-N 0.000 claims description 7
- JVTYXNJWURWOLV-UHFFFAOYSA-N ethyl 2-(3-fluorophenyl)-4-hydroxy-1,3-oxazole-5-carboxylate Chemical compound CCOC(=O)c1oc(nc1O)-c1cccc(F)c1 JVTYXNJWURWOLV-UHFFFAOYSA-N 0.000 claims description 7
- JWOAWAWCNCDTIP-UHFFFAOYSA-N ethyl 2-(4-chlorophenyl)-4-(methoxymethoxy)-1,3-thiazole-5-carboxylate Chemical compound COCOC1=C(C(=O)OCC)SC(C=2C=CC(Cl)=CC=2)=N1 JWOAWAWCNCDTIP-UHFFFAOYSA-N 0.000 claims description 7
- NAAIPCYIRFKODY-UHFFFAOYSA-N ethyl 2-(4-chlorophenyl)-4-[(2-chlorophenyl)methoxy]-1,3-thiazole-5-carboxylate Chemical compound CCOC(=O)C=1SC(C=2C=CC(Cl)=CC=2)=NC=1OCC1=CC=CC=C1Cl NAAIPCYIRFKODY-UHFFFAOYSA-N 0.000 claims description 7
- HAWGINGHSGYHJO-UHFFFAOYSA-N ethyl 2-(4-fluorophenyl)-4-[(2-methylpropan-2-yl)oxycarbonylamino]-1,3-thiazole-5-carboxylate Chemical compound CC(C)(C)OC(=O)NC1=C(C(=O)OCC)SC(C=2C=CC(F)=CC=2)=N1 HAWGINGHSGYHJO-UHFFFAOYSA-N 0.000 claims description 7
- ZYWMFWQPWIYMDQ-UHFFFAOYSA-N ethyl 2-(4-methylphenyl)-4-(2-methylpropoxy)-1,3-thiazole-5-carboxylate Chemical compound CC(C)COC1=C(C(=O)OCC)SC(C=2C=CC(C)=CC=2)=N1 ZYWMFWQPWIYMDQ-UHFFFAOYSA-N 0.000 claims description 7
- DJXXLZXDFIZYAV-UHFFFAOYSA-N ethyl 2-phenyl-4-phenylmethoxy-1,3-thiazole-5-carboxylate Chemical compound CCOC(=O)C=1SC(C=2C=CC=CC=2)=NC=1OCC1=CC=CC=C1 DJXXLZXDFIZYAV-UHFFFAOYSA-N 0.000 claims description 7
- XXQQHPGTWUSZLV-UHFFFAOYSA-N ethyl 4-(2-aminoethylamino)-2-(4-chlorophenyl)-1,3-thiazole-5-carboxylate Chemical compound NCCNC1=C(C(=O)OCC)SC(C=2C=CC(Cl)=CC=2)=N1 XXQQHPGTWUSZLV-UHFFFAOYSA-N 0.000 claims description 7
- RJWSCGGRYXRAMT-UHFFFAOYSA-N ethyl 4-[(3-chlorophenyl)methoxy]-2-(3-fluorophenyl)-1,3-thiazole-5-carboxylate Chemical compound CCOC(=O)C=1SC(C=2C=C(F)C=CC=2)=NC=1OCC1=CC=CC(Cl)=C1 RJWSCGGRYXRAMT-UHFFFAOYSA-N 0.000 claims description 7
- WRTHLFGZMSTFER-UHFFFAOYSA-N ethyl 4-[2-(methylamino)ethylamino]-2-(4-methylphenyl)-1,3-thiazole-5-carboxylate Chemical compound CNCCNC1=C(C(=O)OCC)SC(C=2C=CC(C)=CC=2)=N1 WRTHLFGZMSTFER-UHFFFAOYSA-N 0.000 claims description 7
- FRKLLEYVAMRCNV-UHFFFAOYSA-N ethyl 4-hydroxy-2-(4-methylphenyl)-1,3-oxazole-5-carboxylate Chemical compound CCOC(=O)c1oc(nc1O)-c1ccc(C)cc1 FRKLLEYVAMRCNV-UHFFFAOYSA-N 0.000 claims description 7
- HNFMHECDJPDLJL-UHFFFAOYSA-N ethyl 4-methoxy-2-(4-methylphenyl)-1,3-thiazole-5-carboxylate Chemical compound COC1=C(C(=O)OCC)SC(C=2C=CC(C)=CC=2)=N1 HNFMHECDJPDLJL-UHFFFAOYSA-N 0.000 claims description 7
- 229910052736 halogen Inorganic materials 0.000 claims description 7
- 150000002367 halogens Chemical class 0.000 claims description 7
- 208000021722 neuropathic pain Diseases 0.000 claims description 7
- 229910052698 phosphorus Inorganic materials 0.000 claims description 7
- GXNYVWKROULFFG-UHFFFAOYSA-N 2-(3-chlorophenyl)-4-[(2-chlorophenyl)methoxy]-1,3-thiazole-5-carboxylic acid Chemical compound OC(=O)C=1SC(C=2C=C(Cl)C=CC=2)=NC=1OCC1=CC=CC=C1Cl GXNYVWKROULFFG-UHFFFAOYSA-N 0.000 claims description 6
- GGBOHTHBMRGLOH-UHFFFAOYSA-N 2-(3-chlorophenyl)-4-[(4-chlorophenyl)methoxy]-1,3-thiazole-5-carboxylic acid Chemical compound OC(=O)C=1SC(C=2C=C(Cl)C=CC=2)=NC=1OCC1=CC=C(Cl)C=C1 GGBOHTHBMRGLOH-UHFFFAOYSA-N 0.000 claims description 6
- OKEASJIKYMBOPX-UHFFFAOYSA-N 2-(3-fluorophenyl)-4-[4-(trifluoromethyl)benzoyl]oxy-1,3-thiazole-5-carboxylic acid Chemical compound OC(=O)C=1SC(C=2C=C(F)C=CC=2)=NC=1OC(=O)C1=CC=C(C(F)(F)F)C=C1 OKEASJIKYMBOPX-UHFFFAOYSA-N 0.000 claims description 6
- IRJQYQYQQAMGFW-UHFFFAOYSA-N 2-(3-fluorophenyl)-4-[[4-(trifluoromethyl)phenyl]methoxy]-1,3-thiazole-5-carboxylic acid Chemical compound OC(=O)C=1SC(C=2C=C(F)C=CC=2)=NC=1OCC1=CC=C(C(F)(F)F)C=C1 IRJQYQYQQAMGFW-UHFFFAOYSA-N 0.000 claims description 6
- DDWBYSWMVFQQGO-UHFFFAOYSA-N 2-(3-fluorophenyl)-5-(1-methyltetrazol-5-yl)-1,3-thiazol-4-ol Chemical compound Cn1nnnc1-c1sc(nc1O)-c1cccc(F)c1 DDWBYSWMVFQQGO-UHFFFAOYSA-N 0.000 claims description 6
- FVWOOMDCHNGWNY-UHFFFAOYSA-N 2-(3-fluorophenyl)-5-(5-methyl-1H-1,2,4-triazol-3-yl)-1,3-thiazol-4-ol Chemical compound Cc1nnc([nH]1)-c1sc(nc1O)-c1cccc(F)c1 FVWOOMDCHNGWNY-UHFFFAOYSA-N 0.000 claims description 6
- LHIYFYBPQCTBSB-UHFFFAOYSA-N 2-(4-chlorophenyl)-4-[(2-chlorophenyl)methoxy]-1,3-thiazole-5-carboxylic acid Chemical compound OC(=O)C=1SC(C=2C=CC(Cl)=CC=2)=NC=1OCC1=CC=CC=C1Cl LHIYFYBPQCTBSB-UHFFFAOYSA-N 0.000 claims description 6
- SQJOVAOFGKZPIC-UHFFFAOYSA-N 2-(4-chlorophenyl)-4-[(4-chlorophenyl)methoxy]-1,3-thiazole-5-carboxylic acid Chemical compound OC(=O)C=1SC(C=2C=CC(Cl)=CC=2)=NC=1OCC1=CC=C(Cl)C=C1 SQJOVAOFGKZPIC-UHFFFAOYSA-N 0.000 claims description 6
- VXESVNMXBWMVDG-UHFFFAOYSA-N 2-(4-chlorophenyl)-5-(1-methyltetrazol-5-yl)-1,3-thiazol-4-ol Chemical compound Cn1nnnc1-c1sc(nc1O)-c1ccc(Cl)cc1 VXESVNMXBWMVDG-UHFFFAOYSA-N 0.000 claims description 6
- IBWIODBONDUNGG-UHFFFAOYSA-N 2-(4-chlorophenyl)-5-(5-methyl-1,2,4-oxadiazol-3-yl)-1,3-thiazol-4-ol Chemical compound Cc1nc(no1)-c1sc(nc1O)-c1ccc(Cl)cc1 IBWIODBONDUNGG-UHFFFAOYSA-N 0.000 claims description 6
- PNWAABHVBOSNJO-UHFFFAOYSA-N 2-(4-chlorophenyl)-5-(5-methyl-1,3,4-oxadiazol-2-yl)-1,3-thiazol-4-ol Chemical compound Cc1nnc(o1)-c1sc(nc1O)-c1ccc(Cl)cc1 PNWAABHVBOSNJO-UHFFFAOYSA-N 0.000 claims description 6
- RWZMAPPEUKYVHM-UHFFFAOYSA-N 2-(4-methylphenyl)-4-[4-(trifluoromethyl)benzoyl]oxy-1,3-thiazole-5-carboxylic acid Chemical compound C1=CC(C)=CC=C1C1=NC(OC(=O)C=2C=CC(=CC=2)C(F)(F)F)=C(C(O)=O)S1 RWZMAPPEUKYVHM-UHFFFAOYSA-N 0.000 claims description 6
- 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 claims description 6
- OVRBITSOHARNPZ-UHFFFAOYSA-N 2-phenyl-4-[4-(trifluoromethyl)benzoyl]oxy-1,3-thiazole-5-carboxylic acid Chemical compound OC(=O)C=1SC(C=2C=CC=CC=2)=NC=1OC(=O)C1=CC=C(C(F)(F)F)C=C1 OVRBITSOHARNPZ-UHFFFAOYSA-N 0.000 claims description 6
- OIOLMYRKDIDFFD-UHFFFAOYSA-N 2-phenyl-4-[[4-(trifluoromethyl)phenyl]methoxy]-1,3-thiazole-5-carboxylic acid Chemical compound OC(=O)C=1SC(C=2C=CC=CC=2)=NC=1OCC1=CC=C(C(F)(F)F)C=C1 OIOLMYRKDIDFFD-UHFFFAOYSA-N 0.000 claims description 6
- LGJPWXQJFZLYNY-UHFFFAOYSA-N 2-phenyl-4-phenylmethoxy-1,3-thiazole-5-carboxylic acid Chemical compound OC(=O)C=1SC(C=2C=CC=CC=2)=NC=1OCC1=CC=CC=C1 LGJPWXQJFZLYNY-UHFFFAOYSA-N 0.000 claims description 6
- ACBXRLZLZZXFJY-UHFFFAOYSA-N 4-(2-aminoethylamino)-2-(4-methylphenyl)-1,3-thiazole-5-carboxylic acid Chemical compound C1=CC(C)=CC=C1C1=NC(NCCN)=C(C(O)=O)S1 ACBXRLZLZZXFJY-UHFFFAOYSA-N 0.000 claims description 6
- WCTHAEUXJNZZHZ-UHFFFAOYSA-N 4-[(2-chlorophenyl)methoxy]-2-(3-fluorophenyl)-1,3-thiazole-5-carboxylic acid Chemical compound OC(=O)C=1SC(C=2C=C(F)C=CC=2)=NC=1OCC1=CC=CC=C1Cl WCTHAEUXJNZZHZ-UHFFFAOYSA-N 0.000 claims description 6
- KUVWDOMRCCLBEQ-UHFFFAOYSA-N 4-[(2-chlorophenyl)methoxy]-2-(4-fluorophenyl)-1,3-thiazole-5-carboxylic acid Chemical compound OC(=O)C=1SC(C=2C=CC(F)=CC=2)=NC=1OCC1=CC=CC=C1Cl KUVWDOMRCCLBEQ-UHFFFAOYSA-N 0.000 claims description 6
- PPDFIBBWLGDHEZ-UHFFFAOYSA-N 4-[(2-chlorophenyl)methoxy]-2-phenyl-1,3-thiazole-5-carboxylic acid Chemical compound OC(=O)C=1SC(C=2C=CC=CC=2)=NC=1OCC1=CC=CC=C1Cl PPDFIBBWLGDHEZ-UHFFFAOYSA-N 0.000 claims description 6
- NDBQQRVYGHAIRY-UHFFFAOYSA-N 4-[(4-chlorophenyl)methoxy]-2-(4-methylphenyl)-1,3-thiazole-5-carboxylic acid Chemical compound C1=CC(C)=CC=C1C1=NC(OCC=2C=CC(Cl)=CC=2)=C(C(O)=O)S1 NDBQQRVYGHAIRY-UHFFFAOYSA-N 0.000 claims description 6
- MZGZVGRKSZNFCL-UHFFFAOYSA-N 4-[(4-chlorophenyl)methoxy]-2-phenyl-1,3-thiazole-5-carboxylic acid Chemical compound OC(=O)C=1SC(C=2C=CC=CC=2)=NC=1OCC1=CC=C(Cl)C=C1 MZGZVGRKSZNFCL-UHFFFAOYSA-N 0.000 claims description 6
- XTVBCQMMVFNPHP-UHFFFAOYSA-N 4-[2-(methylamino)ethylamino]-2-(4-methylphenyl)-1,3-thiazole-5-carboxylic acid Chemical compound S1C(C(O)=O)=C(NCCNC)N=C1C1=CC=C(C)C=C1 XTVBCQMMVFNPHP-UHFFFAOYSA-N 0.000 claims description 6
- YKGZUJNWHSCMEJ-UHFFFAOYSA-N 4-methoxy-2-(4-methylphenyl)-1,3-thiazole-5-carboxylic acid Chemical compound S1C(C(O)=O)=C(OC)N=C1C1=CC=C(C)C=C1 YKGZUJNWHSCMEJ-UHFFFAOYSA-N 0.000 claims description 6
- 208000005615 Interstitial Cystitis Diseases 0.000 claims description 6
- 125000005605 benzo group Chemical group 0.000 claims description 6
- QVWMCWWQUPRRBT-UHFFFAOYSA-N ethyl 2-(3-chlorophenyl)-4-hydroxy-1,3-thiazole-5-carboxylate Chemical compound OC1=C(C(=O)OCC)SC(C=2C=C(Cl)C=CC=2)=N1 QVWMCWWQUPRRBT-UHFFFAOYSA-N 0.000 claims description 6
- ZTXPJMSAFRSRQX-UHFFFAOYSA-N ethyl 2-(4-chlorophenyl)-4-[(3-chlorophenyl)methoxy]-1,3-thiazole-5-carboxylate Chemical compound CCOC(=O)C=1SC(C=2C=CC(Cl)=CC=2)=NC=1OCC1=CC=CC(Cl)=C1 ZTXPJMSAFRSRQX-UHFFFAOYSA-N 0.000 claims description 6
- JOPKMIZQXTZPOC-UHFFFAOYSA-N ethyl 2-(4-chlorophenyl)-4-[2-(propylamino)ethylamino]-1,3-thiazole-5-carboxylate Chemical compound S1C(C(=O)OCC)=C(NCCNCCC)N=C1C1=CC=C(Cl)C=C1 JOPKMIZQXTZPOC-UHFFFAOYSA-N 0.000 claims description 6
- TVZQRYJIBOLLHJ-UHFFFAOYSA-N ethyl 2-(4-fluorophenyl)-4-(trifluoromethylsulfonyloxy)-1,3-thiazole-5-carboxylate Chemical compound FC(F)(F)S(=O)(=O)OC1=C(C(=O)OCC)SC(C=2C=CC(F)=CC=2)=N1 TVZQRYJIBOLLHJ-UHFFFAOYSA-N 0.000 claims description 6
- QYAKKXGJLSBNJN-UHFFFAOYSA-N ethyl 2-(4-methylphenyl)-4-(phenylcarbamoylamino)-1,3-thiazole-5-carboxylate Chemical compound CCOC(=O)C=1SC(C=2C=CC(C)=CC=2)=NC=1NC(=O)NC1=CC=CC=C1 QYAKKXGJLSBNJN-UHFFFAOYSA-N 0.000 claims description 6
- BDPWIJQLVXPZML-UHFFFAOYSA-N ethyl 2-(4-methylphenyl)-4-[[4-(trifluoromethyl)benzoyl]amino]-1,3-thiazole-5-carboxylate Chemical compound CCOC(=O)C=1SC(C=2C=CC(C)=CC=2)=NC=1NC(=O)C1=CC=C(C(F)(F)F)C=C1 BDPWIJQLVXPZML-UHFFFAOYSA-N 0.000 claims description 6
- OZAQRBPRKKUZCR-UHFFFAOYSA-N ethyl 2-[4-(2-fluorophenyl)phenyl]-4-hydroxy-1,3-thiazole-5-carboxylate Chemical compound CCOC(=O)c1sc(nc1O)-c1ccc(cc1)-c1ccccc1F OZAQRBPRKKUZCR-UHFFFAOYSA-N 0.000 claims description 6
- PRIPNLJZMWEWRE-UHFFFAOYSA-N ethyl 2-[4-[(2-fluorophenyl)methoxy]phenyl]-4-hydroxy-1,3-thiazole-5-carboxylate Chemical compound CCOC(=O)c1sc(nc1O)-c1ccc(OCc2ccccc2F)cc1 PRIPNLJZMWEWRE-UHFFFAOYSA-N 0.000 claims description 6
- ZSHLGNUPFVWFJY-UHFFFAOYSA-N ethyl 2-phenyl-4-[4-(trifluoromethyl)benzoyl]oxy-1,3-thiazole-5-carboxylate Chemical compound CCOC(=O)C=1SC(C=2C=CC=CC=2)=NC=1OC(=O)C1=CC=C(C(F)(F)F)C=C1 ZSHLGNUPFVWFJY-UHFFFAOYSA-N 0.000 claims description 6
- UHECOXPCGQYXBE-UHFFFAOYSA-N ethyl 4-(2-aminoethoxy)-2-(4-chlorophenyl)-1,3-thiazole-5-carboxylate Chemical compound NCCOC1=C(C(=O)OCC)SC(C=2C=CC(Cl)=CC=2)=N1 UHECOXPCGQYXBE-UHFFFAOYSA-N 0.000 claims description 6
- KRCWBHRGSVAELC-UHFFFAOYSA-N ethyl 4-(2-aminoethylamino)-2-(4-methylphenyl)-1,3-thiazole-5-carboxylate Chemical compound NCCNC1=C(C(=O)OCC)SC(C=2C=CC(C)=CC=2)=N1 KRCWBHRGSVAELC-UHFFFAOYSA-N 0.000 claims description 6
- AQUOSENVZNZRMV-UHFFFAOYSA-N ethyl 4-(benzylamino)-2-(3-fluorophenyl)-1,3-thiazole-5-carboxylate Chemical compound CCOC(=O)C=1SC(C=2C=C(F)C=CC=2)=NC=1NCC1=CC=CC=C1 AQUOSENVZNZRMV-UHFFFAOYSA-N 0.000 claims description 6
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Classifications
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- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
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- A—HUMAN NECESSITIES
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- C—CHEMISTRY; METALLURGY
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/30—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D263/34—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D263/36—One oxygen atom
- C07D263/40—One oxygen atom attached in position 4
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- C—CHEMISTRY; METALLURGY
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- C07D—HETEROCYCLIC COMPOUNDS
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- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/30—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D263/34—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D263/36—One oxygen atom
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- C07D—HETEROCYCLIC COMPOUNDS
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- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D277/56—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
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- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing aromatic rings
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| EP12178327 | 2012-07-27 | ||
| PCT/EP2012/076147 WO2013092711A1 (en) | 2011-12-19 | 2012-12-19 | Trpm8 antagonists |
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| EP2481727A1 (en) * | 2011-01-28 | 2012-08-01 | Dompe S.p.A. | TRPM8 receptor antagonists |
| SMT201800351T1 (it) | 2011-12-19 | 2018-09-13 | Dompe Farm Spa | Antagonisti trpm8 |
| CA2908365C (en) | 2013-05-24 | 2023-02-28 | Nestec S.A. | Treatment or prevention of non-inflammatory neuronal damage from brain trauma and strokes using linalool |
| US10294243B2 (en) | 2014-06-05 | 2019-05-21 | Bayer Cropscience Aktiengesellschaft | Bicyclic compounds as pesticides |
| SI3157918T1 (sl) | 2014-06-23 | 2019-05-31 | Dompe Farmaceutici S.P.A. | 2-aril-4-hidroksi-1,3-tiazolni derivati, uporabni kot inhibitorji TRPM8 pri zdravljenju nevralgije, bolečine, KOPB in astme |
| JP6865743B2 (ja) | 2015-10-01 | 2021-04-28 | フィルメニッヒ インコーポレイテッドFirmenich Incorporated | Trpm8の活性調節因子として有用な化合物 |
| EP3184524A1 (en) * | 2015-12-21 | 2017-06-28 | Dompé farmaceutici S.p.A. | 4-hydroxy-2-phenyl-1,3-thiazol-5-yl methanone derivatives as trpm8 antagonists |
| JP6943887B2 (ja) | 2016-06-13 | 2021-10-06 | 田辺三菱製薬株式会社 | 血管運動症状を治療または予防するための組成物および方法 |
| WO2018117166A1 (ja) * | 2016-12-21 | 2018-06-28 | キッセイ薬品工業株式会社 | チアゾール誘導体、またはその薬理学的に許容される塩 |
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| US4153607A (en) * | 1977-03-28 | 1979-05-08 | Basf Aktiengesellschaft | Process for the production of 4,5-disubstituted thiazoles |
| US5614520A (en) * | 1990-11-30 | 1997-03-25 | Teijin Limited | 2-arylthiazole derivatives and pharmaceutical composition thereof |
| EP1321463A1 (en) * | 2001-12-21 | 2003-06-25 | Shire Biochem Inc. | Thiazole derivatives and their use for the treatment or prevention of Flavivirus infections |
| US20100160289A1 (en) * | 2008-12-18 | 2010-06-24 | Macielag Mark J | Sulfonamides as trpm8 modulators |
| WO2010125831A1 (en) * | 2009-05-01 | 2010-11-04 | Raqualia Pharma Inc. | Sulfamoyl benzoic acid derivatives as trpm8 antagonists |
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| JPS59220687A (ja) * | 1983-05-30 | 1984-12-12 | 株式会社日立製作所 | 直接サイクル型軽水原子炉一次冷却系の腐食環境抑制設備 |
| US20080214654A1 (en) | 2004-10-13 | 2008-09-04 | Bayer Healthcare Ag | Substituted Benzyloxy-Phenylmethylamide Derivatives |
| WO2007017094A1 (en) | 2005-08-04 | 2007-02-15 | Bayer Healthcare Ag | Substituted benzyloxy-phenylmethylcarbamate derivatives |
| WO2007017092A1 (en) | 2005-08-04 | 2007-02-15 | Bayer Healthcare Ag | Substituted 4-benzyloxy-benzoic acid amide derivatives |
| WO2007017093A1 (en) | 2005-08-04 | 2007-02-15 | Bayer Healthcare Ag | Substituted 2-benzyloxy-benzoic acid amide derivatives |
| WO2007080109A1 (en) | 2006-01-16 | 2007-07-19 | Bayer Healthcare Ag | Substituded benzyloxy-phenylmethylurea derivatives |
| WO2007089031A1 (en) * | 2006-02-01 | 2007-08-09 | Takeda Pharmaceutical Company Limited | Piperidine derivatives as tachykinin receptor antagonists |
| CA2651865C (en) | 2006-05-10 | 2015-11-24 | Janssen Pharmaceutica N.V. | Cold menthol receptor-1 antagonists |
| EP2183239B1 (en) | 2007-07-18 | 2012-08-22 | Janssen Pharmaceutica, N.V. | Sulfonamides as trpm8 modulators |
| WO2010103381A1 (en) | 2009-03-13 | 2010-09-16 | Glenmark Pharmaceuticals S.A. | Spirocyclic piperidine derivatives as trpm 8 modulators |
| WO2012036233A1 (ja) * | 2010-09-17 | 2012-03-22 | 塩野義製薬株式会社 | メラニン凝集ホルモン受容体アンタゴニスト活性を有する縮合へテロ環誘導体 |
| SMT201800351T1 (it) | 2011-12-19 | 2018-09-13 | Dompe Farm Spa | Antagonisti trpm8 |
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2012
- 2012-12-19 SM SM20180351T patent/SMT201800351T1/it unknown
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- 2012-12-19 HU HUE12812229A patent/HUE038407T2/hu unknown
- 2012-12-19 LT LTEP12812229.8T patent/LT2793883T/lt unknown
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- 2012-12-19 JP JP2014547975A patent/JP6238906B2/ja active Active
- 2012-12-19 WO PCT/EP2012/076147 patent/WO2013092711A1/en not_active Ceased
- 2012-12-19 ME MEP-2018-177A patent/ME03038B/me unknown
- 2012-12-19 US US14/366,796 patent/US9585875B2/en active Active
- 2012-12-19 CN CN201280069993.7A patent/CN104220069B/zh active Active
- 2012-12-19 TR TR2018/08861T patent/TR201808861T4/tr unknown
- 2012-12-19 RS RS20180793A patent/RS57389B1/sr unknown
- 2012-12-19 PT PT128122298T patent/PT2793883T/pt unknown
- 2012-12-19 EA EA201491213A patent/EA025356B1/ru unknown
- 2012-12-19 KR KR1020147019697A patent/KR102000319B1/ko active Active
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- 2017-06-19 JP JP2017119493A patent/JP2017197564A/ja not_active Withdrawn
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