CA2871222A1 - Substituted pyrazole compounds as crac modulators - Google Patents
Substituted pyrazole compounds as crac modulators Download PDFInfo
- Publication number
- CA2871222A1 CA2871222A1 CA 2871222 CA2871222A CA2871222A1 CA 2871222 A1 CA2871222 A1 CA 2871222A1 CA 2871222 CA2871222 CA 2871222 CA 2871222 A CA2871222 A CA 2871222A CA 2871222 A1 CA2871222 A1 CA 2871222A1
- Authority
- CA
- Canada
- Prior art keywords
- substituted
- pyrazol
- methyl
- unsubstituted
- pyridin
- 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.)
- Abandoned
Links
- NOIXNOMHHWGUTG-UHFFFAOYSA-N 2-[[4-[4-pyridin-4-yl-1-(2,2,2-trifluoroethyl)pyrazol-3-yl]phenoxy]methyl]quinoline Chemical class C=1C=C(OCC=2N=C3C=CC=CC3=CC=2)C=CC=1C1=NN(CC(F)(F)F)C=C1C1=CC=NC=C1 NOIXNOMHHWGUTG-UHFFFAOYSA-N 0.000 title description 3
- 150000001875 compounds Chemical class 0.000 claims abstract description 238
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 101
- 201000010099 disease Diseases 0.000 claims abstract description 55
- 208000035475 disorder Diseases 0.000 claims abstract description 46
- 150000003839 salts Chemical class 0.000 claims abstract description 24
- 239000011575 calcium Substances 0.000 claims abstract description 17
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims abstract description 16
- 229910052791 calcium Inorganic materials 0.000 claims abstract description 16
- 208000011580 syndromic disease Diseases 0.000 claims abstract description 14
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 13
- 150000001669 calcium Chemical class 0.000 claims abstract description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 62
- 238000000034 method Methods 0.000 claims description 62
- -1 nitro, hydroxyl Chemical group 0.000 claims description 60
- 229910052736 halogen Inorganic materials 0.000 claims description 39
- 150000002367 halogens Chemical class 0.000 claims description 39
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 34
- 125000000623 heterocyclic group Chemical group 0.000 claims description 30
- 239000002904 solvent Substances 0.000 claims description 29
- 239000001257 hydrogen Substances 0.000 claims description 28
- 229910052739 hydrogen Inorganic materials 0.000 claims description 28
- 125000001188 haloalkyl group Chemical group 0.000 claims description 26
- 125000003118 aryl group Chemical group 0.000 claims description 22
- 206010028980 Neoplasm Diseases 0.000 claims description 19
- 229910052757 nitrogen Inorganic materials 0.000 claims description 17
- 208000024172 Cardiovascular disease Diseases 0.000 claims description 16
- 230000015572 biosynthetic process Effects 0.000 claims description 16
- 125000001072 heteroaryl group Chemical group 0.000 claims description 16
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 16
- 125000003545 alkoxy group Chemical group 0.000 claims description 15
- KXDAEFPNCMNJSK-UHFFFAOYSA-N benzene carboxamide Natural products NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 claims description 15
- 208000023275 Autoimmune disease Diseases 0.000 claims description 14
- 206010061218 Inflammation Diseases 0.000 claims description 14
- 201000011510 cancer Diseases 0.000 claims description 14
- 230000004054 inflammatory process Effects 0.000 claims description 14
- 239000002253 acid Substances 0.000 claims description 13
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 13
- 238000002360 preparation method Methods 0.000 claims description 13
- 208000010668 atopic eczema Diseases 0.000 claims description 12
- 238000010168 coupling process Methods 0.000 claims description 12
- 125000004438 haloalkoxy group Chemical group 0.000 claims description 12
- 210000000056 organ Anatomy 0.000 claims description 12
- 230000008569 process Effects 0.000 claims description 12
- 238000007112 amidation reaction Methods 0.000 claims description 11
- 150000001408 amides Chemical class 0.000 claims description 11
- 238000005859 coupling reaction Methods 0.000 claims description 11
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 11
- 125000003342 alkenyl group Chemical group 0.000 claims description 10
- 230000000172 allergic effect Effects 0.000 claims description 10
- 230000009435 amidation Effects 0.000 claims description 10
- 239000003153 chemical reaction reagent Substances 0.000 claims description 10
- 230000008878 coupling Effects 0.000 claims description 10
- 125000004122 cyclic group Chemical group 0.000 claims description 10
- 201000006417 multiple sclerosis Diseases 0.000 claims description 10
- 230000002829 reductive effect Effects 0.000 claims description 9
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 8
- UCPYLLCMEDAXFR-UHFFFAOYSA-N triphosgene Chemical compound ClC(Cl)(Cl)OC(=O)OC(Cl)(Cl)Cl UCPYLLCMEDAXFR-UHFFFAOYSA-N 0.000 claims description 8
- 125000000000 cycloalkoxy group Chemical group 0.000 claims description 7
- 238000007254 oxidation reaction Methods 0.000 claims description 7
- NWZSZGALRFJKBT-KNIFDHDWSA-N (2s)-2,6-diaminohexanoic acid;(2s)-2-hydroxybutanedioic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O.NCCCC[C@H](N)C(O)=O NWZSZGALRFJKBT-KNIFDHDWSA-N 0.000 claims description 6
- NAWXUBYGYWOOIX-SFHVURJKSA-N (2s)-2-[[4-[2-(2,4-diaminoquinazolin-6-yl)ethyl]benzoyl]amino]-4-methylidenepentanedioic acid Chemical compound C1=CC2=NC(N)=NC(N)=C2C=C1CCC1=CC=C(C(=O)N[C@@H](CC(=C)C(O)=O)C(O)=O)C=C1 NAWXUBYGYWOOIX-SFHVURJKSA-N 0.000 claims description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 6
- 125000000392 cycloalkenyl group Chemical group 0.000 claims description 6
- IKDUDTNKRLTJSI-UHFFFAOYSA-N hydrazine monohydrate Substances O.NN IKDUDTNKRLTJSI-UHFFFAOYSA-N 0.000 claims description 6
- 230000003647 oxidation Effects 0.000 claims description 6
- 206010039073 rheumatoid arthritis Diseases 0.000 claims description 6
- 229920006395 saturated elastomer Polymers 0.000 claims description 6
- 208000006673 asthma Diseases 0.000 claims description 5
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 5
- 208000027866 inflammatory disease Diseases 0.000 claims description 5
- 238000007363 ring formation reaction Methods 0.000 claims description 5
- 208000022559 Inflammatory bowel disease Diseases 0.000 claims description 4
- 206010033645 Pancreatitis Diseases 0.000 claims description 4
- 201000004681 Psoriasis Diseases 0.000 claims description 4
- 230000001684 chronic effect Effects 0.000 claims description 4
- 150000002148 esters Chemical class 0.000 claims description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
- 206010002556 Ankylosing Spondylitis Diseases 0.000 claims description 3
- 125000006615 aromatic heterocyclic group Chemical group 0.000 claims description 3
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 3
- 208000033808 peripheral neuropathy Diseases 0.000 claims description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
- 208000006545 Chronic Obstructive Pulmonary Disease Diseases 0.000 claims description 2
- 201000001263 Psoriatic Arthritis Diseases 0.000 claims description 2
- 208000036824 Psoriatic arthropathy Diseases 0.000 claims description 2
- 239000003638 chemical reducing agent Substances 0.000 claims description 2
- 201000008482 osteoarthritis Diseases 0.000 claims description 2
- 230000001590 oxidative effect Effects 0.000 claims description 2
- 150000002431 hydrogen Chemical class 0.000 claims 9
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims 2
- JSGMIUDHQQMUOD-UHFFFAOYSA-N 1-[5-[1-[5-[(2,6-difluorophenyl)methylamino]pyridin-2-yl]-5-(trifluoromethyl)pyrazol-3-yl]-2,2-dimethyl-1,3,4-oxadiazol-3-yl]ethanone Chemical compound O1C(C)(C)N(C(=O)C)N=C1C1=NN(C=2N=CC(NCC=3C(=CC=CC=3F)F)=CC=2)C(C(F)(F)F)=C1 JSGMIUDHQQMUOD-UHFFFAOYSA-N 0.000 claims 1
- RMVMTHZVTFCKCG-UHFFFAOYSA-N 2,3,4-trifluoro-n-[5-[3-(4-methyl-5-oxo-1,3,4-oxadiazol-2-yl)-5-(trifluoromethyl)pyrazol-1-yl]pyridin-2-yl]benzamide Chemical compound O1C(=O)N(C)N=C1C1=NN(C=2C=NC(NC(=O)C=3C(=C(F)C(F)=CC=3)F)=CC=2)C(C(F)(F)F)=C1 RMVMTHZVTFCKCG-UHFFFAOYSA-N 0.000 claims 1
- IMAYNKZXZYASJM-UHFFFAOYSA-N 2,3-difluoro-n-[5-[3-(4-methyl-5-oxo-1,3,4-oxadiazol-2-yl)-5-(trifluoromethyl)pyrazol-1-yl]pyridin-2-yl]benzamide Chemical compound O1C(=O)N(C)N=C1C1=NN(C=2C=NC(NC(=O)C=3C(=C(F)C=CC=3)F)=CC=2)C(C(F)(F)F)=C1 IMAYNKZXZYASJM-UHFFFAOYSA-N 0.000 claims 1
- PQNXHEPRHRBNMM-UHFFFAOYSA-N 2,3-dimethyl-n-[5-[3-(4-methyl-5-oxo-1,3,4-oxadiazol-2-yl)-5-(trifluoromethyl)pyrazol-1-yl]pyridin-2-yl]benzamide Chemical compound CC1=CC=CC(C(=O)NC=2N=CC(=CC=2)N2C(=CC(=N2)C=2OC(=O)N(C)N=2)C(F)(F)F)=C1C PQNXHEPRHRBNMM-UHFFFAOYSA-N 0.000 claims 1
- AYPAMJXATAOZSH-UHFFFAOYSA-N 2,4,5-trifluoro-n-[5-[3-(4-methyl-5-oxo-1,3,4-oxadiazol-2-yl)-5-(trifluoromethyl)pyrazol-1-yl]pyridin-2-yl]benzamide Chemical compound O1C(=O)N(C)N=C1C1=NN(C=2C=NC(NC(=O)C=3C(=CC(F)=C(F)C=3)F)=CC=2)C(C(F)(F)F)=C1 AYPAMJXATAOZSH-UHFFFAOYSA-N 0.000 claims 1
- ZHEFVZXPIAVBPS-UHFFFAOYSA-N 2,4-difluoro-n-[5-[3-(4-methyl-5-oxo-1,3,4-oxadiazol-2-yl)-5-(trifluoromethyl)pyrazol-1-yl]pyridin-2-yl]benzamide Chemical compound O1C(=O)N(C)N=C1C1=NN(C=2C=NC(NC(=O)C=3C(=CC(F)=CC=3)F)=CC=2)C(C(F)(F)F)=C1 ZHEFVZXPIAVBPS-UHFFFAOYSA-N 0.000 claims 1
- XQOGDJFYJQKXSA-UHFFFAOYSA-N 2,6-difluoro-n-[5-[3-(4-methyl-5-oxo-1,3,4-oxadiazol-2-yl)-5-(trifluoromethyl)pyrazol-1-yl]pyridin-2-yl]benzamide Chemical compound O1C(=O)N(C)N=C1C1=NN(C=2C=NC(NC(=O)C=3C(=CC=CC=3F)F)=CC=2)C(C(F)(F)F)=C1 XQOGDJFYJQKXSA-UHFFFAOYSA-N 0.000 claims 1
- DUOBBXAAIXFNGC-UHFFFAOYSA-N 2,6-difluoro-n-[6-[3-(4-methyl-5-oxo-1,2,4-oxadiazol-3-yl)-5-(trifluoromethyl)pyrazol-1-yl]pyridin-3-yl]benzamide Chemical compound O1C(=O)N(C)C(C2=NN(C(=C2)C(F)(F)F)C=2N=CC(NC(=O)C=3C(=CC=CC=3F)F)=CC=2)=N1 DUOBBXAAIXFNGC-UHFFFAOYSA-N 0.000 claims 1
- IZUDTMPPIYNGSB-UHFFFAOYSA-N 2,6-difluoro-n-[6-[3-(4-methyl-5-oxo-1,3,4-oxadiazol-2-yl)-5-(trifluoromethyl)pyrazol-1-yl]pyridin-3-yl]benzamide Chemical compound O1C(=O)N(C)N=C1C1=NN(C=2N=CC(NC(=O)C=3C(=CC=CC=3F)F)=CC=2)C(C(F)(F)F)=C1 IZUDTMPPIYNGSB-UHFFFAOYSA-N 0.000 claims 1
- QQNZLXYBTGFCFN-UHFFFAOYSA-N 2,6-difluoro-n-[6-[3-[5-(hydroxymethyl)-5-methyl-4h-1,2-oxazol-3-yl]-5-(trifluoromethyl)pyrazol-1-yl]pyridin-3-yl]benzamide Chemical compound O1C(C)(CO)CC(C2=NN(C(=C2)C(F)(F)F)C=2N=CC(NC(=O)C=3C(=CC=CC=3F)F)=CC=2)=N1 QQNZLXYBTGFCFN-UHFFFAOYSA-N 0.000 claims 1
- MYVWTGOYPVOLAM-UHFFFAOYSA-N 2,6-difluoro-n-[6-[5-(4-methyl-5-oxo-1,3,4-oxadiazol-2-yl)-3-(trifluoromethyl)pyrazol-1-yl]pyridin-3-yl]benzamide Chemical compound O1C(=O)N(C)N=C1C1=CC(C(F)(F)F)=NN1C(N=C1)=CC=C1NC(=O)C1=C(F)C=CC=C1F MYVWTGOYPVOLAM-UHFFFAOYSA-N 0.000 claims 1
- UILVOUAQWAKPBV-UHFFFAOYSA-N 2,6-difluoro-n-[6-[5-(trifluoromethyl)-3-(1,4,4-trimethyl-5-oxopyrazol-3-yl)pyrazol-1-yl]pyridin-3-yl]benzamide Chemical compound CC1(C)C(=O)N(C)N=C1C1=NN(C=2N=CC(NC(=O)C=3C(=CC=CC=3F)F)=CC=2)C(C(F)(F)F)=C1 UILVOUAQWAKPBV-UHFFFAOYSA-N 0.000 claims 1
- GNPAFVPTPRRZLY-UHFFFAOYSA-N 2,6-difluoro-n-[6-[5-methyl-3-(4-methyl-5-oxo-1,3,4-oxadiazol-2-yl)pyrazol-1-yl]pyridin-3-yl]benzamide Chemical compound CC1=CC(C=2OC(=O)N(C)N=2)=NN1C(N=C1)=CC=C1NC(=O)C1=C(F)C=CC=C1F GNPAFVPTPRRZLY-UHFFFAOYSA-N 0.000 claims 1
- XMQCELZJEUYNPD-UHFFFAOYSA-N 2-chloro-6-fluoro-n-[5-[3-(4-methyl-5-oxo-1,3,4-oxadiazol-2-yl)-5-(trifluoromethyl)pyrazol-1-yl]pyridin-2-yl]benzamide Chemical compound O1C(=O)N(C)N=C1C1=NN(C=2C=NC(NC(=O)C=3C(=CC=CC=3F)Cl)=CC=2)C(C(F)(F)F)=C1 XMQCELZJEUYNPD-UHFFFAOYSA-N 0.000 claims 1
- YNDZTORGEOHJMX-UHFFFAOYSA-N 2-chloro-6-fluoro-n-[6-[3-(4-methyl-5-oxo-1,3,4-oxadiazol-2-yl)-5-(trifluoromethyl)pyrazol-1-yl]pyridin-3-yl]benzamide Chemical compound O1C(=O)N(C)N=C1C1=NN(C=2N=CC(NC(=O)C=3C(=CC=CC=3F)Cl)=CC=2)C(C(F)(F)F)=C1 YNDZTORGEOHJMX-UHFFFAOYSA-N 0.000 claims 1
- MZDPQHBQZDEWHF-UHFFFAOYSA-N 2-chloro-n-[5-[3-(4-methyl-5-oxo-1,3,4-oxadiazol-2-yl)-5-(trifluoromethyl)pyrazol-1-yl]pyridin-2-yl]benzamide Chemical compound O1C(=O)N(C)N=C1C1=NN(C=2C=NC(NC(=O)C=3C(=CC=CC=3)Cl)=CC=2)C(C(F)(F)F)=C1 MZDPQHBQZDEWHF-UHFFFAOYSA-N 0.000 claims 1
- ORKLJPPTJJDBHY-UHFFFAOYSA-N 2-chloro-n-[6-[3-(5,5-dimethyl-4-oxo-1,2-oxazol-3-yl)-5-(trifluoromethyl)pyrazol-1-yl]pyridin-3-yl]-6-fluorobenzamide Chemical compound O=C1C(C)(C)ON=C1C1=NN(C=2N=CC(NC(=O)C=3C(=CC=CC=3F)Cl)=CC=2)C(C(F)(F)F)=C1 ORKLJPPTJJDBHY-UHFFFAOYSA-N 0.000 claims 1
- XQDNMZTZVAEIBO-UHFFFAOYSA-N 2-fluoro-6-methyl-n-[5-[3-(4-methyl-5-oxo-1,3,4-oxadiazol-2-yl)-5-(trifluoromethyl)pyrazol-1-yl]pyridin-2-yl]benzamide Chemical compound CC1=CC=CC(F)=C1C(=O)NC1=CC=C(N2C(=CC(=N2)C=2OC(=O)N(C)N=2)C(F)(F)F)C=N1 XQDNMZTZVAEIBO-UHFFFAOYSA-N 0.000 claims 1
- ZHQMBDLIXOOORN-UHFFFAOYSA-N 2-fluoro-6-methyl-n-[6-[3-(4-methyl-5-oxo-1,3,4-oxadiazol-2-yl)-5-(trifluoromethyl)pyrazol-1-yl]pyridin-3-yl]benzamide Chemical compound CC1=CC=CC(F)=C1C(=O)NC1=CC=C(N2C(=CC(=N2)C=2OC(=O)N(C)N=2)C(F)(F)F)N=C1 ZHQMBDLIXOOORN-UHFFFAOYSA-N 0.000 claims 1
- XMWGYVBDUMYCAV-UHFFFAOYSA-N 2-fluoro-6-methyl-n-[6-[5-(4-methyl-5-oxo-1,3,4-oxadiazol-2-yl)-3-(trifluoromethyl)pyrazol-1-yl]pyridin-3-yl]benzamide Chemical compound CC1=CC=CC(F)=C1C(=O)NC1=CC=C(N2C(=CC(=N2)C(F)(F)F)C=2OC(=O)N(C)N=2)N=C1 XMWGYVBDUMYCAV-UHFFFAOYSA-N 0.000 claims 1
- XUQDUFMXPOARND-UHFFFAOYSA-N 2-fluoro-n-[5-[3-(4-methyl-5-oxo-1,3,4-oxadiazol-2-yl)-5-(trifluoromethyl)pyrazol-1-yl]pyridin-2-yl]benzamide Chemical compound O1C(=O)N(C)N=C1C1=NN(C=2C=NC(NC(=O)C=3C(=CC=CC=3)F)=CC=2)C(C(F)(F)F)=C1 XUQDUFMXPOARND-UHFFFAOYSA-N 0.000 claims 1
- JSNBTOKZNZSWED-UHFFFAOYSA-N 2-methyl-n-[5-[3-(4-methyl-5-oxo-1,3,4-oxadiazol-2-yl)-5-(trifluoromethyl)pyrazol-1-yl]pyridin-2-yl]benzamide Chemical compound CC1=CC=CC=C1C(=O)NC1=CC=C(N2C(=CC(=N2)C=2OC(=O)N(C)N=2)C(F)(F)F)C=N1 JSNBTOKZNZSWED-UHFFFAOYSA-N 0.000 claims 1
- JAOWWZWFIITTSH-UHFFFAOYSA-N 3-[1-[5-[(2,6-difluorobenzoyl)amino]pyridin-2-yl]-5-(trifluoromethyl)pyrazol-3-yl]-5-methyl-4h-1,2-oxazole-5-carboxamide Chemical compound O1C(C)(C(N)=O)CC(C2=NN(C(=C2)C(F)(F)F)C=2N=CC(NC(=O)C=3C(=CC=CC=3F)F)=CC=2)=N1 JAOWWZWFIITTSH-UHFFFAOYSA-N 0.000 claims 1
- MFRAPLCCPFMEGR-UHFFFAOYSA-N 3-[1-[5-[(2,6-difluorophenyl)methylamino]pyridin-2-yl]-5-(trifluoromethyl)pyrazol-3-yl]-4-methyl-1,2,4-oxadiazol-5-one Chemical compound O1C(=O)N(C)C(C2=NN(C(=C2)C(F)(F)F)C=2N=CC(NCC=3C(=CC=CC=3F)F)=CC=2)=N1 MFRAPLCCPFMEGR-UHFFFAOYSA-N 0.000 claims 1
- YKXRTNHMWUNZKG-UHFFFAOYSA-N 4-ethyl-n-[5-[3-(4-methyl-5-oxo-1,3,4-oxadiazol-2-yl)-5-(trifluoromethyl)pyrazol-1-yl]pyridin-2-yl]benzamide Chemical compound C1=CC(CC)=CC=C1C(=O)NC1=CC=C(N2C(=CC(=N2)C=2OC(=O)N(C)N=2)C(F)(F)F)C=N1 YKXRTNHMWUNZKG-UHFFFAOYSA-N 0.000 claims 1
- UKPZLGWRKFEYLP-UHFFFAOYSA-N 5-[1-[5-[(2,6-difluorophenyl)methylamino]pyridin-2-yl]-5-(fluoromethyl)pyrazol-3-yl]-3-methyl-1,3,4-oxadiazol-2-one Chemical compound O1C(=O)N(C)N=C1C1=NN(C=2N=CC(NCC=3C(=CC=CC=3F)F)=CC=2)C(CF)=C1 UKPZLGWRKFEYLP-UHFFFAOYSA-N 0.000 claims 1
- ZVANEPHBQQBZKJ-UHFFFAOYSA-N 5-[1-[5-[(2,6-difluorophenyl)methylamino]pyridin-2-yl]-5-(trifluoromethyl)pyrazol-3-yl]-3-methyl-1,3,4-oxadiazol-2-one Chemical compound O1C(=O)N(C)N=C1C1=NN(C=2N=CC(NCC=3C(=CC=CC=3F)F)=CC=2)C(C(F)(F)F)=C1 ZVANEPHBQQBZKJ-UHFFFAOYSA-N 0.000 claims 1
- MCNDZJVJQRYGRE-UHFFFAOYSA-N 5-[1-[5-[(2,6-difluorophenyl)methylamino]pyridin-2-yl]-5-methylpyrazol-3-yl]-3-methyl-1,3,4-oxadiazol-2-one Chemical compound CC1=CC(C=2OC(=O)N(C)N=2)=NN1C(N=C1)=CC=C1NCC1=C(F)C=CC=C1F MCNDZJVJQRYGRE-UHFFFAOYSA-N 0.000 claims 1
- PNRASTKJGQVKGW-UHFFFAOYSA-N 5-[1-[5-[(2-chloro-6-fluorophenyl)methylamino]pyridin-2-yl]-5-(trifluoromethyl)pyrazol-3-yl]-2,4,4-trimethylpyrazol-3-one Chemical compound CC1(C)C(=O)N(C)N=C1C1=NN(C=2N=CC(NCC=3C(=CC=CC=3F)Cl)=CC=2)C(C(F)(F)F)=C1 PNRASTKJGQVKGW-UHFFFAOYSA-N 0.000 claims 1
- YKPQGGSMTQQEES-UHFFFAOYSA-N 5-[1-[5-[(2-chloro-6-fluorophenyl)methylamino]pyridin-2-yl]-5-(trifluoromethyl)pyrazol-3-yl]-3-methyl-1,3,4-oxadiazol-2-one Chemical compound O1C(=O)N(C)N=C1C1=NN(C=2N=CC(NCC=3C(=CC=CC=3F)Cl)=CC=2)C(C(F)(F)F)=C1 YKPQGGSMTQQEES-UHFFFAOYSA-N 0.000 claims 1
- UGPUZBYDFZBPOL-UHFFFAOYSA-N 5-[1-[6-[(2,6-difluorophenyl)methylamino]pyridin-3-yl]-5-(trifluoromethyl)pyrazol-3-yl]-3-methyl-1,3,4-oxadiazol-2-one Chemical compound O1C(=O)N(C)N=C1C1=NN(C=2C=NC(NCC=3C(=CC=CC=3F)F)=CC=2)C(C(F)(F)F)=C1 UGPUZBYDFZBPOL-UHFFFAOYSA-N 0.000 claims 1
- BKJBZDDHDCTQHT-UHFFFAOYSA-N 5-[1-[6-[(2-chloro-6-fluorophenyl)methylamino]pyridin-3-yl]-5-(trifluoromethyl)pyrazol-3-yl]-3-methyl-1,3,4-oxadiazol-2-one Chemical compound O1C(=O)N(C)N=C1C1=NN(C=2C=NC(NCC=3C(=CC=CC=3F)Cl)=CC=2)C(C(F)(F)F)=C1 BKJBZDDHDCTQHT-UHFFFAOYSA-N 0.000 claims 1
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Rheumatology (AREA)
- Pulmonology (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Pain & Pain Management (AREA)
- Dermatology (AREA)
- Immunology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IN6/KOL/2012 | 2012-05-02 | ||
| IN6KO2012 | 2012-05-02 | ||
| IN1474/KOL/2012 | 2012-12-28 | ||
| IN1474KO2012 | 2012-12-28 | ||
| PCT/IB2013/053446 WO2013164773A1 (en) | 2012-05-02 | 2013-05-01 | Substituted pyrazole compounds as crac modulators |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2871222A1 true CA2871222A1 (en) | 2013-11-07 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA 2871222 Abandoned CA2871222A1 (en) | 2012-05-02 | 2013-05-01 | Substituted pyrazole compounds as crac modulators |
Country Status (7)
| Country | Link |
|---|---|
| US (2) | US9409898B2 (enExample) |
| EP (1) | EP2844656A1 (enExample) |
| AU (1) | AU2013255441B2 (enExample) |
| CA (1) | CA2871222A1 (enExample) |
| IN (1) | IN2014MN02127A (enExample) |
| WO (1) | WO2013164773A1 (enExample) |
| ZA (1) | ZA201407668B (enExample) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
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| WO2015197188A1 (en) * | 2014-06-24 | 2015-12-30 | Grünenthal GmbH | Pyrazolyl-based carboxamides as crac inhibitors |
| WO2015197187A1 (en) * | 2014-06-24 | 2015-12-30 | Grünenthal GmbH | Pyrazolyl-based carboxamides v |
| CN107847548B (zh) | 2015-05-18 | 2022-06-14 | 贝思以色列女会吏医学中心公司 | P物质、肥大细胞脱颗粒抑制剂和周围神经病 |
| JP2022508468A (ja) | 2018-09-14 | 2022-01-19 | ルヒゼン ファーマスティカルズ アクツィエンゲゼルシャフト | Ｃｒａｃ阻害剤およびコルチコステロイドを含む組成物ならびにそれらの使用方法 |
| AU2019387370A1 (en) | 2018-11-30 | 2021-06-10 | Nuvation Bio Inc. | Pyrrole and pyrazole compounds and methods of use thereof |
| WO2020244968A1 (en) | 2019-06-06 | 2020-12-10 | Basf Se | Fungicidal n-(pyrid-3-yl)carboxamides |
| CN110604735B (zh) * | 2019-09-18 | 2022-10-25 | 华东师范大学 | 一种治疗肝纤维化、硬皮病的化合物及其应用 |
| WO2021063735A1 (en) | 2019-10-02 | 2021-04-08 | Basf Se | New bicyclic pyridine derivatives |
Family Cites Families (27)
| Publication number | Priority date | Publication date | Assignee | Title |
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| AU751139B2 (en) | 1997-10-13 | 2002-08-08 | Astellas Pharma Inc. | Amide derivative |
| CA2327185A1 (en) * | 1998-04-08 | 1999-10-14 | Abbott Laboratories | Pyrazole inhibitors of cytokine production |
| US6506747B1 (en) | 1998-06-05 | 2003-01-14 | Boehringer Ingelheim Pharmaceuticals, Inc. | Substituted 1-(4-aminophenyl)pyrazoles and their use as anti-inflammatory agents |
| NZ545447A (en) | 2003-07-23 | 2010-03-26 | Synta Pharmaceuticals Corp | Compounds for inflammation and immune-related uses |
| KR20070057965A (ko) | 2004-09-21 | 2007-06-07 | 신타 파마슈티칼스 코프. | 염증 및 면역 관련 용도를 위한 화합물 |
| WO2006083477A2 (en) | 2005-01-07 | 2006-08-10 | Synta Pharmaceuticals Corp. | Compounds for inflammation and immune-related uses |
| AU2006208045B2 (en) | 2005-01-25 | 2012-08-30 | Synta Pharmaceuticals Corp. | Compounds for inflammation and immune-related uses |
| WO2006081389A1 (en) | 2005-01-25 | 2006-08-03 | Synta Pharmaceuticals Corp. | Thiophene compounds for inflammation and immune-related uses |
| CA2640090A1 (en) | 2006-01-25 | 2007-08-02 | Synta Pharmaceuticals Corp. | Substituted aromatic compounds for inflammation and immune-related uses |
| CA2639913A1 (en) | 2006-01-25 | 2007-08-02 | Synta Pharmaceutical Corp. | Phenyl and pyridyl compounds for inflammation and immune-related uses |
| JP2009528273A (ja) | 2006-01-25 | 2009-08-06 | シンタ ファーマシューティカルズ コーポレーション | 炎症および免疫関連使用用の置換ビアリール化合物 |
| AU2007211276B2 (en) | 2006-01-31 | 2013-06-06 | Synta Pharmaceuticals Corp. | Pyridylphenyl compounds for inflammation and immune-related uses |
| TW200911800A (en) | 2007-08-01 | 2009-03-16 | Synta Pharmaceuticals Corp | Pyridine compounds for inflammation and immune-related uses |
| RU2465272C2 (ru) | 2007-09-10 | 2012-10-27 | КалсиМедика, Инк. | Соединения, моделирующие внутриклеточный кальций |
| WO2009076454A2 (en) | 2007-12-12 | 2009-06-18 | Calcimedica, Inc. | Compounds that modulate intracellular calcium |
| CA2734500A1 (en) | 2008-08-27 | 2010-03-11 | Calcimedica Inc. | Compounds that modulate intracellular calcium |
| US8524763B2 (en) | 2008-09-22 | 2013-09-03 | Calcimedica, Inc. | Inhibitors of store operated calcium release |
| AU2009300318A1 (en) | 2008-10-01 | 2010-04-08 | Synta Pharmaceuticals Corp. | Compounds for inflammation and immune-related uses |
| US8618307B2 (en) | 2009-09-16 | 2013-12-31 | Calcimedica, Inc. | Compounds that modulate intracellular calcium |
| US8377970B2 (en) * | 2009-10-08 | 2013-02-19 | Rhizen Pharmaceuticals Sa | Modulators of calcium release-activated calcium channel |
| WO2012022487A1 (de) | 2010-08-20 | 2012-02-23 | Grünenthal GmbH | Substituierte cyclische carboxamid- und harnstoff-derivate als liganden des vanilloid-rezeptors |
| JP5387541B2 (ja) | 2010-10-29 | 2014-01-15 | 住友電装株式会社 | グロメット |
| AP3341A (en) * | 2010-10-30 | 2015-07-31 | Lupin Ltd | Oxazoline and isoxazoline derivatives as crac modulators |
| JP2013545740A (ja) | 2010-11-10 | 2013-12-26 | グリュネンタール・ゲゼルシャフト・ミト・ベシュレンクテル・ハフツング | バニロイド受容体リガンドとしての置換された複素芳香族カルボキサミド誘導体および尿素誘導体 |
| EP2704701B1 (en) | 2011-05-03 | 2018-01-03 | PRCL Research Inc. | Compounds for inflammation and immune-related uses |
| WO2013059677A1 (en) | 2011-10-19 | 2013-04-25 | Calcimedica, Inc. | Compounds that modulate intracellular calcium |
| EP2768810A1 (en) | 2011-10-19 | 2014-08-27 | Calcimedica, Inc. | Compounds that modulate intracellular calcium |
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2013
- 2013-05-01 AU AU2013255441A patent/AU2013255441B2/en not_active Expired - Fee Related
- 2013-05-01 IN IN2127MUN2014 patent/IN2014MN02127A/en unknown
- 2013-05-01 WO PCT/IB2013/053446 patent/WO2013164773A1/en not_active Ceased
- 2013-05-01 US US14/398,161 patent/US9409898B2/en not_active Expired - Fee Related
- 2013-05-01 EP EP13722112.3A patent/EP2844656A1/en not_active Withdrawn
- 2013-05-01 CA CA 2871222 patent/CA2871222A1/en not_active Abandoned
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2014
- 2014-10-22 ZA ZA2014/07668A patent/ZA201407668B/en unknown
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2016
- 2016-06-28 US US15/194,795 patent/US20160304507A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| EP2844656A1 (en) | 2015-03-11 |
| US20160304507A1 (en) | 2016-10-20 |
| ZA201407668B (en) | 2015-11-25 |
| IN2014MN02127A (enExample) | 2015-09-11 |
| AU2013255441A1 (en) | 2014-11-13 |
| WO2013164773A1 (en) | 2013-11-07 |
| US20150111925A1 (en) | 2015-04-23 |
| AU2013255441B2 (en) | 2017-11-09 |
| US9409898B2 (en) | 2016-08-09 |
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| Date | Code | Title | Description |
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| FZDE | Dead |
Effective date: 20190501 |