JP2014525444A5 - - Google Patents
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- Publication number
- JP2014525444A5 JP2014525444A5 JP2014528513A JP2014528513A JP2014525444A5 JP 2014525444 A5 JP2014525444 A5 JP 2014525444A5 JP 2014528513 A JP2014528513 A JP 2014528513A JP 2014528513 A JP2014528513 A JP 2014528513A JP 2014525444 A5 JP2014525444 A5 JP 2014525444A5
- Authority
- JP
- Japan
- Prior art keywords
- oxadiazol
- pyridine
- imidazo
- carboxamide
- methylphenyl
- 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.)
- Granted
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- -1 C 1 -C 6 alkyl Chemical group 0.000 claims 69
- 125000005842 heteroatom Chemical group 0.000 claims 43
- 150000001875 compounds Chemical class 0.000 claims 27
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 22
- 229910052760 oxygen Inorganic materials 0.000 claims 22
- 125000003003 spiro group Chemical group 0.000 claims 22
- 229910052717 sulfur Inorganic materials 0.000 claims 20
- ZMBYQTGAXZOMOO-UHFFFAOYSA-N imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=CC=CN2C(C(=O)N)=CN=C21 ZMBYQTGAXZOMOO-UHFFFAOYSA-N 0.000 claims 19
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 18
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims 17
- 125000001424 substituent group Chemical group 0.000 claims 15
- DFPAKSUCGFBDDF-UHFFFAOYSA-N Nicotinamide Chemical compound NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 claims 14
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 claims 12
- 125000005843 halogen group Chemical group 0.000 claims 12
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 12
- 125000006163 5-membered heteroaryl group Chemical group 0.000 claims 11
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 8
- WNXJIVFYUVYPPR-UHFFFAOYSA-N 1,3-dioxolane Chemical compound C1COCO1 WNXJIVFYUVYPPR-UHFFFAOYSA-N 0.000 claims 8
- SHQSVMDWKBRBGB-UHFFFAOYSA-N cyclobutanone Chemical compound O=C1CCC1 SHQSVMDWKBRBGB-UHFFFAOYSA-N 0.000 claims 8
- BGTOWKSIORTVQH-UHFFFAOYSA-N cyclopentanone Chemical compound O=C1CCCC1 BGTOWKSIORTVQH-UHFFFAOYSA-N 0.000 claims 8
- 235000005152 nicotinamide Nutrition 0.000 claims 7
- 239000011570 nicotinamide Substances 0.000 claims 7
- 229910052799 carbon Inorganic materials 0.000 claims 6
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 6
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 claims 6
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims 5
- IZXIZTKNFFYFOF-UHFFFAOYSA-N 2-Oxazolidone Chemical compound O=C1NCCO1 IZXIZTKNFFYFOF-UHFFFAOYSA-N 0.000 claims 5
- YZCKVEUIGOORGS-OUBTZVSYSA-N Deuterium Chemical compound [2H] YZCKVEUIGOORGS-OUBTZVSYSA-N 0.000 claims 5
- 125000000217 alkyl group Chemical group 0.000 claims 5
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 5
- 229910052805 deuterium Inorganic materials 0.000 claims 5
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 claims 4
- 208000022559 Inflammatory bowel disease Diseases 0.000 claims 4
- 125000003118 aryl group Chemical group 0.000 claims 4
- 201000010099 disease Diseases 0.000 claims 4
- 229910052739 hydrogen Inorganic materials 0.000 claims 4
- 208000002551 irritable bowel syndrome Diseases 0.000 claims 4
- VBSCTWFMHAWPSW-UHFFFAOYSA-N n-[5-[5-(3-hydroxy-3-methylcyclobutyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=C(NC(=O)C=2N3C=CC=CC3=NC=2)C(C)=CC=C1C(N=1)=NOC=1C1CC(C)(O)C1 VBSCTWFMHAWPSW-UHFFFAOYSA-N 0.000 claims 4
- 125000006582 (C5-C6) heterocycloalkyl group Chemical group 0.000 claims 3
- 125000004793 2,2,2-trifluoroethoxy group Chemical group FC(CO*)(F)F 0.000 claims 3
- KTHXBEHDVMTNOH-UHFFFAOYSA-N cyclobutanol Chemical compound OC1CCC1 KTHXBEHDVMTNOH-UHFFFAOYSA-N 0.000 claims 3
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 3
- 125000002757 morpholinyl group Chemical group 0.000 claims 3
- 125000004193 piperazinyl group Chemical group 0.000 claims 3
- 125000003386 piperidinyl group Chemical group 0.000 claims 3
- 208000002815 pulmonary hypertension Diseases 0.000 claims 3
- 125000003226 pyrazolyl group Chemical group 0.000 claims 3
- 125000001425 triazolyl group Chemical group 0.000 claims 3
- 125000001359 1,2,3-triazol-4-yl group Chemical group [H]N1N=NC([*])=C1[H] 0.000 claims 2
- HVLLSFSZBNWGEY-UHFFFAOYSA-N 7-cyano-n-[5-[5-(3,3-difluorocyclobutyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=C(NC(=O)C=2N3C=CC(=CC3=NC=2)C#N)C(C)=CC=C1C(N=1)=NOC=1C1CC(F)(F)C1 HVLLSFSZBNWGEY-UHFFFAOYSA-N 0.000 claims 2
- 206010007559 Cardiac failure congestive Diseases 0.000 claims 2
- 208000004248 Familial Primary Pulmonary Hypertension Diseases 0.000 claims 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims 2
- 101000692455 Homo sapiens Platelet-derived growth factor receptor beta Proteins 0.000 claims 2
- 102100026547 Platelet-derived growth factor receptor beta Human genes 0.000 claims 2
- 206010064911 Pulmonary arterial hypertension Diseases 0.000 claims 2
- 201000008937 atopic dermatitis Diseases 0.000 claims 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims 2
- 125000002962 imidazol-1-yl group Chemical group [*]N1C([H])=NC([H])=C1[H] 0.000 claims 2
- 125000003037 imidazol-2-yl group Chemical group [H]N1C([*])=NC([H])=C1[H] 0.000 claims 2
- 125000002883 imidazolyl group Chemical group 0.000 claims 2
- RHJXTZUDRRZZBR-UHFFFAOYSA-N n-[2-methyl-5-[5-(3-oxocyclobutyl)-1,2,4-oxadiazol-3-yl]phenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=C(NC(=O)C=2N3C=CC=CC3=NC=2)C(C)=CC=C1C(N=1)=NOC=1C1CC(=O)C1 RHJXTZUDRRZZBR-UHFFFAOYSA-N 0.000 claims 2
- PZQWOZMFFXZLHP-UHFFFAOYSA-N n-[5-[5-(3,3-difluorocyclobutyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl]-7-methylimidazo[1,2-a]pyridine-3-carboxamide Chemical compound C=1N=C2C=C(C)C=CN2C=1C(=O)NC(C(=CC=1)C)=CC=1C(N=1)=NOC=1C1CC(F)(F)C1 PZQWOZMFFXZLHP-UHFFFAOYSA-N 0.000 claims 2
- YYJQXSJQDPOQPK-UHFFFAOYSA-N n-[5-[5-(3,3-difluorocyclobutyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=C(NC(=O)C=2N3C=CC=CC3=NC=2)C(C)=CC=C1C(N=1)=NOC=1C1CC(F)(F)C1 YYJQXSJQDPOQPK-UHFFFAOYSA-N 0.000 claims 2
- HAJVNPLYVSZWRG-CYBMUJFWSA-N n-[5-[5-[(1r)-2,2-difluorocyclopropyl]-1,2,4-oxadiazol-3-yl]-2-methylphenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=C(NC(=O)C=2N3C=CC=CC3=NC=2)C(C)=CC=C1C(N=1)=NOC=1[C@H]1CC1(F)F HAJVNPLYVSZWRG-CYBMUJFWSA-N 0.000 claims 2
- RHNJOZCVGSBEAG-KBPBESRZSA-N n-[5-[5-[(1r,2s)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl]-2-methylphenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=C(NC(=O)C=2N3C=CC=CC3=NC=2)C(C)=CC=C1C(N=1)=NOC=1[C@H]1C[C@@H]1F RHNJOZCVGSBEAG-KBPBESRZSA-N 0.000 claims 2
- HAJVNPLYVSZWRG-ZDUSSCGKSA-N n-[5-[5-[(1s)-2,2-difluorocyclopropyl]-1,2,4-oxadiazol-3-yl]-2-methylphenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=C(NC(=O)C=2N3C=CC=CC3=NC=2)C(C)=CC=C1C(N=1)=NOC=1[C@@H]1CC1(F)F HAJVNPLYVSZWRG-ZDUSSCGKSA-N 0.000 claims 2
- RHNJOZCVGSBEAG-ZIAGYGMSSA-N n-[5-[5-[(1s,2r)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl]-2-methylphenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=C(NC(=O)C=2N3C=CC=CC3=NC=2)C(C)=CC=C1C(N=1)=NOC=1[C@@H]1C[C@H]1F RHNJOZCVGSBEAG-ZIAGYGMSSA-N 0.000 claims 2
- AHHWIHXENZJRFG-UHFFFAOYSA-N oxetane Chemical compound C1COC1 AHHWIHXENZJRFG-UHFFFAOYSA-N 0.000 claims 2
- 125000004194 piperazin-1-yl group Chemical group [H]N1C([H])([H])C([H])([H])N(*)C([H])([H])C1([H])[H] 0.000 claims 2
- 125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims 2
- 125000004574 piperidin-2-yl group Chemical group N1C(CCCC1)* 0.000 claims 2
- 125000004483 piperidin-3-yl group Chemical group N1CC(CCC1)* 0.000 claims 2
- 125000004482 piperidin-4-yl group Chemical group N1CCC(CC1)* 0.000 claims 2
- 201000008312 primary pulmonary hypertension Diseases 0.000 claims 2
- 125000004353 pyrazol-1-yl group Chemical group [H]C1=NN(*)C([H])=C1[H] 0.000 claims 2
- WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 claims 2
- 208000017520 skin disease Diseases 0.000 claims 2
- 125000004495 thiazol-4-yl group Chemical group S1C=NC(=C1)* 0.000 claims 2
- 125000004496 thiazol-5-yl group Chemical group S1C=NC=C1* 0.000 claims 2
- 125000000335 thiazolyl group Chemical group 0.000 claims 2
- 125000005869 (methoxyethoxy)methanyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])OC([H])([H])* 0.000 claims 1
- 125000006432 1-methyl cyclopropyl group Chemical group [H]C([H])([H])C1(*)C([H])([H])C1([H])[H] 0.000 claims 1
- GVNVAWHJIKLAGL-UHFFFAOYSA-N 2-(cyclohexen-1-yl)cyclohexan-1-one Chemical compound O=C1CCCCC1C1=CCCCC1 GVNVAWHJIKLAGL-UHFFFAOYSA-N 0.000 claims 1
- WMOGDCLNSOMBFC-UHFFFAOYSA-N 2-[4-[3-[[5-[5-(3,3-difluorocyclobutyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl]carbamoyl]imidazo[1,2-a]pyridin-6-yl]pyrazol-1-yl]acetic acid Chemical compound CC1=CC=C(C=2N=C(ON=2)C2CC(F)(F)C2)C=C1NC(=O)C(N1C=2)=CN=C1C=CC=2C=1C=NN(CC(O)=O)C=1 WMOGDCLNSOMBFC-UHFFFAOYSA-N 0.000 claims 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims 1
- PYJGRPRPIMKYEB-UHFFFAOYSA-N 3-n-[5-[5-(3,3-difluorocyclobutyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl]imidazo[1,2-a]pyridine-3,6-dicarboxamide Chemical compound C1=C(NC(=O)C=2N3C=C(C=CC3=NC=2)C(N)=O)C(C)=CC=C1C(N=1)=NOC=1C1CC(F)(F)C1 PYJGRPRPIMKYEB-UHFFFAOYSA-N 0.000 claims 1
- ZFFHSMSEOODFLB-UHFFFAOYSA-N 6-cyano-n-[5-[5-(3,3-difluorocyclobutyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=C(NC(=O)C=2N3C=C(C=CC3=NC=2)C#N)C(C)=CC=C1C(N=1)=NOC=1C1CC(F)(F)C1 ZFFHSMSEOODFLB-UHFFFAOYSA-N 0.000 claims 1
- HGFPSCQSKGUSQU-UHFFFAOYSA-N 6-fluoro-n-[5-[5-(3-hydroxy-3-methylcyclobutyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=C(NC(=O)C=2N3C=C(F)C=CC3=NC=2)C(C)=CC=C1C(N=1)=NOC=1C1CC(C)(O)C1 HGFPSCQSKGUSQU-UHFFFAOYSA-N 0.000 claims 1
- GYBSZVNBXDIORM-UHFFFAOYSA-N 6-fluoro-n-[5-[5-(3-hydroxycyclobutyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=C(NC(=O)C=2N3C=C(F)C=CC3=NC=2)C(C)=CC=C1C(N=1)=NOC=1C1CC(O)C1 GYBSZVNBXDIORM-UHFFFAOYSA-N 0.000 claims 1
- DXOREGNPVAKXRD-UHFFFAOYSA-N 6-fluoro-n-[5-[5-[1-(methoxymethyl)cyclobutyl]-1,2,4-oxadiazol-3-yl]-2-methylphenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound N=1C(C=2C=C(NC(=O)C=3N4C=C(F)C=CC4=NC=3)C(C)=CC=2)=NOC=1C1(COC)CCC1 DXOREGNPVAKXRD-UHFFFAOYSA-N 0.000 claims 1
- QYWKXTQLSWTQAM-UHFFFAOYSA-N 6-fluoro-n-[5-[5-[3-hydroxy-3-(trifluoromethyl)cyclobutyl]-1,2,4-oxadiazol-3-yl]-2-methylphenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=C(NC(=O)C=2N3C=C(F)C=CC3=NC=2)C(C)=CC=C1C(N=1)=NOC=1C1CC(O)(C(F)(F)F)C1 QYWKXTQLSWTQAM-UHFFFAOYSA-N 0.000 claims 1
- RFSJBIGRJQSQJP-UHFFFAOYSA-N 7-fluoro-n-[5-[5-[3-hydroxy-3-(trifluoromethyl)cyclobutyl]-1,2,4-oxadiazol-3-yl]-2-methylphenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=C(NC(=O)C=2N3C=CC(F)=CC3=NC=2)C(C)=CC=C1C(N=1)=NOC=1C1CC(O)(C(F)(F)F)C1 RFSJBIGRJQSQJP-UHFFFAOYSA-N 0.000 claims 1
- 206010002198 Anaphylactic reaction Diseases 0.000 claims 1
- 208000023275 Autoimmune disease Diseases 0.000 claims 1
- PCBZRNYXXCIELG-WYFCWLEVSA-N COC1=CC=C(C[C@H](NC(=O)OC2CCCC3(C2)OOC2(O3)C3CC4CC(C3)CC2C4)C(=O)N[C@@H]2[C@@H](CO)O[C@H]([C@@H]2O)N2C=NC3=C2N=CN=C3N(C)C)C=C1 Chemical compound COC1=CC=C(C[C@H](NC(=O)OC2CCCC3(C2)OOC2(O3)C3CC4CC(C3)CC2C4)C(=O)N[C@@H]2[C@@H](CO)O[C@H]([C@@H]2O)N2C=NC3=C2N=CN=C3N(C)C)C=C1 PCBZRNYXXCIELG-WYFCWLEVSA-N 0.000 claims 1
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 claims 1
- 101150065749 Churc1 gene Proteins 0.000 claims 1
- 206010012434 Dermatitis allergic Diseases 0.000 claims 1
- 206010012438 Dermatitis atopic Diseases 0.000 claims 1
- 206010016654 Fibrosis Diseases 0.000 claims 1
- 206010051066 Gastrointestinal stromal tumour Diseases 0.000 claims 1
- 206010020772 Hypertension Diseases 0.000 claims 1
- 108091000080 Phosphotransferase Proteins 0.000 claims 1
- 102100038239 Protein Churchill Human genes 0.000 claims 1
- 102000016971 Proto-Oncogene Proteins c-kit Human genes 0.000 claims 1
- 108010014608 Proto-Oncogene Proteins c-kit Proteins 0.000 claims 1
- 206010039085 Rhinitis allergic Diseases 0.000 claims 1
- 206010039710 Scleroderma Diseases 0.000 claims 1
- 206010067584 Type 1 diabetes mellitus Diseases 0.000 claims 1
- 208000024780 Urticaria Diseases 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 201000010105 allergic rhinitis Diseases 0.000 claims 1
- 230000036783 anaphylactic response Effects 0.000 claims 1
- 208000003455 anaphylaxis Diseases 0.000 claims 1
- 208000006673 asthma Diseases 0.000 claims 1
- 208000010668 atopic eczema Diseases 0.000 claims 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 230000009787 cardiac fibrosis Effects 0.000 claims 1
- 208000019425 cirrhosis of liver Diseases 0.000 claims 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 1
- 208000035475 disorder Diseases 0.000 claims 1
- 239000003814 drug Substances 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 230000004761 fibrosis Effects 0.000 claims 1
- 201000011243 gastrointestinal stromal tumor Diseases 0.000 claims 1
- 210000003630 histaminocyte Anatomy 0.000 claims 1
- 208000027866 inflammatory disease Diseases 0.000 claims 1
- 210000004072 lung Anatomy 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 201000006512 mast cell neoplasm Diseases 0.000 claims 1
- 208000006971 mastocytoma Diseases 0.000 claims 1
- 208000008585 mastocytosis Diseases 0.000 claims 1
- 201000001441 melanoma Diseases 0.000 claims 1
- 208000030159 metabolic disease Diseases 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims 1
- 201000006417 multiple sclerosis Diseases 0.000 claims 1
- STTCYAFMCPPVTG-UHFFFAOYSA-N n-[2-fluoro-5-[5-(3-methylidenecyclobutyl)-1,2,4-oxadiazol-3-yl]phenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=C(NC(=O)C=2N3C=CC=CC3=NC=2)C(F)=CC=C1C(N=1)=NOC=1C1CC(=C)C1 STTCYAFMCPPVTG-UHFFFAOYSA-N 0.000 claims 1
- XHGVWDXFZUEHRV-UHFFFAOYSA-N n-[2-methyl-5-[5-(2-oxospiro[3.3]heptan-6-yl)-1,2,4-oxadiazol-3-yl]phenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=C(NC(=O)C=2N3C=CC=CC3=NC=2)C(C)=CC=C1C(N=1)=NOC=1C(C1)CC21CC(=O)C2 XHGVWDXFZUEHRV-UHFFFAOYSA-N 0.000 claims 1
- VCGZRAXATKIMPO-UHFFFAOYSA-N n-[2-methyl-5-[5-(3-methylidenecyclobutyl)-1,2,4-oxadiazol-3-yl]phenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=C(NC(=O)C=2N3C=CC=CC3=NC=2)C(C)=CC=C1C(N=1)=NOC=1C1CC(=C)C1 VCGZRAXATKIMPO-UHFFFAOYSA-N 0.000 claims 1
- GYZVPSXFDGNLTL-UHFFFAOYSA-N n-[2-methyl-5-[5-(3-morpholin-4-ylcyclobutyl)-1,2,4-oxadiazol-3-yl]phenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=C(NC(=O)C=2N3C=CC=CC3=NC=2)C(C)=CC=C1C(N=1)=NOC=1C(C1)CC1N1CCOCC1 GYZVPSXFDGNLTL-UHFFFAOYSA-N 0.000 claims 1
- CMKHFELGXWLQSX-UHFFFAOYSA-N n-[2-methyl-5-[5-(3-oxocyclopentyl)-1,2,4-oxadiazol-3-yl]phenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=C(NC(=O)C=2N3C=CC=CC3=NC=2)C(C)=CC=C1C(N=1)=NOC=1C1CCC(=O)C1 CMKHFELGXWLQSX-UHFFFAOYSA-N 0.000 claims 1
- YPJQEOYEDWLTPQ-UHFFFAOYSA-N n-[2-methyl-5-[5-(3-propan-2-yloxyiminocyclobutyl)-1,2,4-oxadiazol-3-yl]phenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1C(=NOC(C)C)CC1C1=NC(C=2C=C(NC(=O)C=3N4C=CC=CC4=NC=3)C(C)=CC=2)=NO1 YPJQEOYEDWLTPQ-UHFFFAOYSA-N 0.000 claims 1
- TUZSVQWAIOHMAN-UHFFFAOYSA-N n-[2-methyl-5-[5-(5-oxaspiro[3.4]octan-2-yl)-1,2,4-oxadiazol-3-yl]phenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=C(NC(=O)C=2N3C=CC=CC3=NC=2)C(C)=CC=C1C(N=1)=NOC=1C(C1)CC21CCCO2 TUZSVQWAIOHMAN-UHFFFAOYSA-N 0.000 claims 1
- AJALWDBRAVSTFX-UHFFFAOYSA-N n-[2-methyl-5-[5-[(2,2,3,3-tetrafluorocyclobutyl)oxymethyl]-1,2,4-oxadiazol-3-yl]phenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=C(NC(=O)C=2N3C=CC=CC3=NC=2)C(C)=CC=C1C(N=1)=NOC=1COC1CC(F)(F)C1(F)F AJALWDBRAVSTFX-UHFFFAOYSA-N 0.000 claims 1
- BFENDVJZXZZBMZ-HAQQTFLXSA-N n-[2-methyl-5-[5-[(7r)-7-methyl-5,8-dioxaspiro[3.4]octan-2-yl]-1,2,4-oxadiazol-3-yl]phenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound O1[C@H](C)COC11CC(C=2ON=C(N=2)C=2C=C(NC(=O)C=3N4C=CC=CC4=NC=3)C(C)=CC=2)C1 BFENDVJZXZZBMZ-HAQQTFLXSA-N 0.000 claims 1
- BFENDVJZXZZBMZ-LCVZGFTISA-N n-[2-methyl-5-[5-[(7s)-7-methyl-5,8-dioxaspiro[3.4]octan-2-yl]-1,2,4-oxadiazol-3-yl]phenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound O1[C@@H](C)COC11CC(C=2ON=C(N=2)C=2C=C(NC(=O)C=3N4C=CC=CC4=NC=3)C(C)=CC=2)C1 BFENDVJZXZZBMZ-LCVZGFTISA-N 0.000 claims 1
- ZTSBMHAPDJMGKM-UHFFFAOYSA-N n-[2-methyl-5-[5-[1-(trifluoromethyl)cyclopropyl]-1,2,4-oxadiazol-3-yl]phenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=C(NC(=O)C=2N3C=CC=CC3=NC=2)C(C)=CC=C1C(N=1)=NOC=1C1(C(F)(F)F)CC1 ZTSBMHAPDJMGKM-UHFFFAOYSA-N 0.000 claims 1
- MVWCFRFJCKNFKP-UHFFFAOYSA-N n-[2-methyl-5-[5-[3-(1,2,4-triazol-1-yl)cyclobutyl]-1,2,4-oxadiazol-3-yl]phenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=C(NC(=O)C=2N3C=CC=CC3=NC=2)C(C)=CC=C1C(N=1)=NOC=1C(C1)CC1N1C=NC=N1 MVWCFRFJCKNFKP-UHFFFAOYSA-N 0.000 claims 1
- BHYADCWMERYDNF-UHFFFAOYSA-N n-[2-methyl-5-[5-[3-(2-morpholin-4-ylethoxyimino)cyclobutyl]-1,2,4-oxadiazol-3-yl]phenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=C(NC(=O)C=2N3C=CC=CC3=NC=2)C(C)=CC=C1C(N=1)=NOC=1C(C1)CC1=NOCCN1CCOCC1 BHYADCWMERYDNF-UHFFFAOYSA-N 0.000 claims 1
- AXOIMIICKSYXMT-UHFFFAOYSA-N n-[2-methyl-5-[5-[3-(4-methylpiperazin-1-yl)cyclobutyl]-1,2,4-oxadiazol-3-yl]phenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1CN(C)CCN1C1CC(C=2ON=C(N=2)C=2C=C(NC(=O)C=3N4C=CC=CC4=NC=3)C(C)=CC=2)C1 AXOIMIICKSYXMT-UHFFFAOYSA-N 0.000 claims 1
- LEKPOEMXPKTFIQ-UHFFFAOYSA-N n-[3-[5-(3,3-difluorocyclobutyl)-1,2,4-oxadiazol-3-yl]-2,6-dimethylphenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound CC1=C(NC(=O)C=2N3C=CC=CC3=NC=2)C(C)=CC=C1C(N=1)=NOC=1C1CC(F)(F)C1 LEKPOEMXPKTFIQ-UHFFFAOYSA-N 0.000 claims 1
- TVLMBEXTOHTRNS-UHFFFAOYSA-N n-[5-(3-cyclopropyl-1,2,4-oxadiazol-5-yl)-2-methylphenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=C(NC(=O)C=2N3C=CC=CC3=NC=2)C(C)=CC=C1C(ON=1)=NC=1C1CC1 TVLMBEXTOHTRNS-UHFFFAOYSA-N 0.000 claims 1
- XBZQIWZQXUSRKJ-UHFFFAOYSA-N n-[5-(5-cyclobutyl-1,2,4-oxadiazol-3-yl)-2-fluorophenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=C(NC(=O)C=2N3C=CC=CC3=NC=2)C(F)=CC=C1C(N=1)=NOC=1C1CCC1 XBZQIWZQXUSRKJ-UHFFFAOYSA-N 0.000 claims 1
- LAAFMNKBPFCIJU-UHFFFAOYSA-N n-[5-(5-cyclobutyl-1,2,4-oxadiazol-3-yl)-2-methylphenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=C(NC(=O)C=2N3C=CC=CC3=NC=2)C(C)=CC=C1C(N=1)=NOC=1C1CCC1 LAAFMNKBPFCIJU-UHFFFAOYSA-N 0.000 claims 1
- ZGOBVKLRYAOXSK-UHFFFAOYSA-N n-[5-(5-cyclopentyl-1,2,4-oxadiazol-3-yl)-2-methylphenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=C(NC(=O)C=2N3C=CC=CC3=NC=2)C(C)=CC=C1C(N=1)=NOC=1C1CCCC1 ZGOBVKLRYAOXSK-UHFFFAOYSA-N 0.000 claims 1
- IACBZSGWVMFOJV-UHFFFAOYSA-N n-[5-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)-2-methylphenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=C(NC(=O)C=2N3C=CC=CC3=NC=2)C(C)=CC=C1C(N=1)=NOC=1C1CC1 IACBZSGWVMFOJV-UHFFFAOYSA-N 0.000 claims 1
- CITATNXHTLRWAC-UHFFFAOYSA-N n-[5-[(3,3-difluorocyclobutyl)carbamoyl]-2-methylphenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=C(NC(=O)C=2N3C=CC=CC3=NC=2)C(C)=CC=C1C(=O)NC1CC(F)(F)C1 CITATNXHTLRWAC-UHFFFAOYSA-N 0.000 claims 1
- UMMDASRURJTCCN-UHFFFAOYSA-N n-[5-[3-(3,3-difluorocyclobutyl)-1,2,4-oxadiazol-5-yl]-2-methylphenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=C(NC(=O)C=2N3C=CC=CC3=NC=2)C(C)=CC=C1C(ON=1)=NC=1C1CC(F)(F)C1 UMMDASRURJTCCN-UHFFFAOYSA-N 0.000 claims 1
- KZDMOSVLZIBBNH-UHFFFAOYSA-N n-[5-[5-(1-aminocyclobutyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=C(NC(=O)C=2N3C=CC=CC3=NC=2)C(C)=CC=C1C(N=1)=NOC=1C1(N)CCC1 KZDMOSVLZIBBNH-UHFFFAOYSA-N 0.000 claims 1
- WLBKDTIWZLBQKG-UHFFFAOYSA-N n-[5-[5-(1-aminocyclopropyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=C(NC(=O)C=2N3C=CC=CC3=NC=2)C(C)=CC=C1C(N=1)=NOC=1C1(N)CC1 WLBKDTIWZLBQKG-UHFFFAOYSA-N 0.000 claims 1
- HAJVNPLYVSZWRG-UHFFFAOYSA-N n-[5-[5-(2,2-difluorocyclopropyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=C(NC(=O)C=2N3C=CC=CC3=NC=2)C(C)=CC=C1C(N=1)=NOC=1C1CC1(F)F HAJVNPLYVSZWRG-UHFFFAOYSA-N 0.000 claims 1
- VVYKXEVSEJUERS-UHFFFAOYSA-N n-[5-[5-(2-hydroxycyclopropyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=C(NC(=O)C=2N3C=CC=CC3=NC=2)C(C)=CC=C1C(N=1)=NOC=1C1CC1O VVYKXEVSEJUERS-UHFFFAOYSA-N 0.000 claims 1
- CXAIUYZBLYTVTR-UHFFFAOYSA-N n-[5-[5-(2-hydroxyspiro[3.3]heptan-6-yl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=C(NC(=O)C=2N3C=CC=CC3=NC=2)C(C)=CC=C1C(N=1)=NOC=1C(C1)CC21CC(O)C2 CXAIUYZBLYTVTR-UHFFFAOYSA-N 0.000 claims 1
- QVVZVIMTCBNZEO-UHFFFAOYSA-N n-[5-[5-(3,3-difluorocyclobutyl)-1,2,4-oxadiazol-3-yl]-2,4-dimethylphenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=C(NC(=O)C=2N3C=CC=CC3=NC=2)C(C)=CC(C)=C1C(N=1)=NOC=1C1CC(F)(F)C1 QVVZVIMTCBNZEO-UHFFFAOYSA-N 0.000 claims 1
- XCRIYMJWHVQZPI-UHFFFAOYSA-N n-[5-[5-(3,3-difluorocyclobutyl)-1,2,4-oxadiazol-3-yl]-2-fluorophenyl]-6-(5-methyl-1h-1,2,4-triazol-3-yl)imidazo[1,2-a]pyridine-3-carboxamide Chemical compound N1C(C)=NN=C1C1=CN2C(C(=O)NC=3C(=CC=C(C=3)C=3N=C(ON=3)C3CC(F)(F)C3)F)=CN=C2C=C1 XCRIYMJWHVQZPI-UHFFFAOYSA-N 0.000 claims 1
- XCXUYGGKVTVWJA-UHFFFAOYSA-N n-[5-[5-(3,3-difluorocyclobutyl)-1,2,4-oxadiazol-3-yl]-2-fluorophenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=C(NC(=O)C=2N3C=CC=CC3=NC=2)C(F)=CC=C1C(N=1)=NOC=1C1CC(F)(F)C1 XCXUYGGKVTVWJA-UHFFFAOYSA-N 0.000 claims 1
- FZYVKXRUCUFWPT-UHFFFAOYSA-N n-[5-[5-(3,3-difluorocyclobutyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl]-6-(1,3-thiazol-4-yl)imidazo[1,2-a]pyridine-3-carboxamide Chemical compound CC1=CC=C(C=2N=C(ON=2)C2CC(F)(F)C2)C=C1NC(=O)C(N1C=2)=CN=C1C=CC=2C1=CSC=N1 FZYVKXRUCUFWPT-UHFFFAOYSA-N 0.000 claims 1
- UYLMYXBJJAZNJX-UHFFFAOYSA-N n-[5-[5-(3,3-difluorocyclobutyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl]-6-(1-hydroxyethyl)imidazo[1,2-a]pyridine-3-carboxamide Chemical compound N12C=C(C(O)C)C=CC2=NC=C1C(=O)NC(C(=CC=1)C)=CC=1C(N=1)=NOC=1C1CC(F)(F)C1 UYLMYXBJJAZNJX-UHFFFAOYSA-N 0.000 claims 1
- RMXVIPAFTSRMND-UHFFFAOYSA-N n-[5-[5-(3,3-difluorocyclobutyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl]-6-(1h-pyrazol-4-yl)imidazo[1,2-a]pyridine-3-carboxamide Chemical compound CC1=CC=C(C=2N=C(ON=2)C2CC(F)(F)C2)C=C1NC(=O)C(N1C=2)=CN=C1C=CC=2C=1C=NNC=1 RMXVIPAFTSRMND-UHFFFAOYSA-N 0.000 claims 1
- JHFRDCLISNAGNN-UHFFFAOYSA-N n-[5-[5-(3,3-difluorocyclobutyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl]-6-(2-fluoroethoxymethyl)imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=C(NC(=O)C=2N3C=C(COCCF)C=CC3=NC=2)C(C)=CC=C1C(N=1)=NOC=1C1CC(F)(F)C1 JHFRDCLISNAGNN-UHFFFAOYSA-N 0.000 claims 1
- BZTQGSHQRMAQQH-UHFFFAOYSA-N n-[5-[5-(3,3-difluorocyclobutyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl]-6-(3-hydroxy-3-methylbutyl)imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=C(NC(=O)C=2N3C=C(CCC(C)(C)O)C=CC3=NC=2)C(C)=CC=C1C(N=1)=NOC=1C1CC(F)(F)C1 BZTQGSHQRMAQQH-UHFFFAOYSA-N 0.000 claims 1
- XCYDGRAVLMZAMV-UHFFFAOYSA-N n-[5-[5-(3,3-difluorocyclobutyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl]-6-(hydroxymethyl)imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=C(NC(=O)C=2N3C=C(CO)C=CC3=NC=2)C(C)=CC=C1C(N=1)=NOC=1C1CC(F)(F)C1 XCYDGRAVLMZAMV-UHFFFAOYSA-N 0.000 claims 1
- SRDBLOPEORGLEG-UHFFFAOYSA-N n-[5-[5-(3,3-difluorocyclobutyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl]-6-(methoxymethyl)imidazo[1,2-a]pyridine-3-carboxamide Chemical compound N12C=C(COC)C=CC2=NC=C1C(=O)NC(C(=CC=1)C)=CC=1C(N=1)=NOC=1C1CC(F)(F)C1 SRDBLOPEORGLEG-UHFFFAOYSA-N 0.000 claims 1
- ZHTTUPZLXLKBER-UHFFFAOYSA-N n-[5-[5-(3,3-difluorocyclobutyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl]-6-[(2-oxo-1,3-oxazolidin-3-yl)methyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound CC1=CC=C(C=2N=C(ON=2)C2CC(F)(F)C2)C=C1NC(=O)C(N1C=2)=CN=C1C=CC=2CN1CCOC1=O ZHTTUPZLXLKBER-UHFFFAOYSA-N 0.000 claims 1
- WLWRVOASHCUSOL-CALCHBBNSA-N n-[5-[5-(3,3-difluorocyclobutyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl]-6-[(2r,6s)-2,6-dimethylmorpholin-4-yl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1[C@@H](C)O[C@@H](C)CN1C1=CN2C(C(=O)NC=3C(=CC=C(C=3)C=3N=C(ON=3)C3CC(F)(F)C3)C)=CN=C2C=C1 WLWRVOASHCUSOL-CALCHBBNSA-N 0.000 claims 1
- DKWKCRFGHXIPLX-UHFFFAOYSA-N n-[5-[5-(3,3-difluorocyclobutyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl]-6-[1-(2-methoxyethyl)-5-methyl-1,2,4-triazol-3-yl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound N1=C(C)N(CCOC)N=C1C1=CN2C(C(=O)NC=3C(=CC=C(C=3)C=3N=C(ON=3)C3CC(F)(F)C3)C)=CN=C2C=C1 DKWKCRFGHXIPLX-UHFFFAOYSA-N 0.000 claims 1
- FLGYJSZOORSFEH-UHFFFAOYSA-N n-[5-[5-(3,3-difluorocyclobutyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl]-6-[[4-(2-hydroxyethyl)piperazin-1-yl]methyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound CC1=CC=C(C=2N=C(ON=2)C2CC(F)(F)C2)C=C1NC(=O)C(N1C=2)=CN=C1C=CC=2CN1CCN(CCO)CC1 FLGYJSZOORSFEH-UHFFFAOYSA-N 0.000 claims 1
- XHQBPWQRZZIMAA-UHFFFAOYSA-N n-[5-[5-(3,3-difluorocyclobutyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl]-6-fluoroimidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=C(NC(=O)C=2N3C=C(F)C=CC3=NC=2)C(C)=CC=C1C(N=1)=NOC=1C1CC(F)(F)C1 XHQBPWQRZZIMAA-UHFFFAOYSA-N 0.000 claims 1
- CYHBIKSLEMCECT-UHFFFAOYSA-N n-[5-[5-(3,3-difluorocyclobutyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl]-6-methylimidazo[1,2-a]pyridine-3-carboxamide Chemical compound N12C=C(C)C=CC2=NC=C1C(=O)NC(C(=CC=1)C)=CC=1C(N=1)=NOC=1C1CC(F)(F)C1 CYHBIKSLEMCECT-UHFFFAOYSA-N 0.000 claims 1
- FWLZXDPPLHJPDB-UHFFFAOYSA-N n-[5-[5-(3,3-difluorocyclobutyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl]-7-(2-oxopyrrolidin-1-yl)imidazo[1,2-a]pyridine-3-carboxamide Chemical compound CC1=CC=C(C=2N=C(ON=2)C2CC(F)(F)C2)C=C1NC(=O)C(N1C=C2)=CN=C1C=C2N1CCCC1=O FWLZXDPPLHJPDB-UHFFFAOYSA-N 0.000 claims 1
- IZCWSKVYLGKJTN-UHFFFAOYSA-N n-[5-[5-(3,3-difluorocyclobutyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl]-7-(2h-triazol-4-yl)imidazo[1,2-a]pyridine-3-carboxamide Chemical compound CC1=CC=C(C=2N=C(ON=2)C2CC(F)(F)C2)C=C1NC(=O)C(N1C=C2)=CN=C1C=C2C1=CNN=N1 IZCWSKVYLGKJTN-UHFFFAOYSA-N 0.000 claims 1
- FDAOKJLCACKIFM-UHFFFAOYSA-N n-[5-[5-(3,3-difluorocyclobutyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl]-7-(difluoromethoxy)imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=C(NC(=O)C=2N3C=CC(OC(F)F)=CC3=NC=2)C(C)=CC=C1C(N=1)=NOC=1C1CC(F)(F)C1 FDAOKJLCACKIFM-UHFFFAOYSA-N 0.000 claims 1
- YIDCEVNXBMMFHY-UHFFFAOYSA-N n-[5-[5-(3,3-difluorocyclobutyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl]-7-[1-(2-hydroxyethyl)triazol-4-yl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound CC1=CC=C(C=2N=C(ON=2)C2CC(F)(F)C2)C=C1NC(=O)C(N1C=C2)=CN=C1C=C2C1=CN(CCO)N=N1 YIDCEVNXBMMFHY-UHFFFAOYSA-N 0.000 claims 1
- WZGYVSALYZWXML-UHFFFAOYSA-N n-[5-[5-(3,3-difluorocyclobutyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl]-7-fluoroimidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=C(NC(=O)C=2N3C=CC(F)=CC3=NC=2)C(C)=CC=C1C(N=1)=NOC=1C1CC(F)(F)C1 WZGYVSALYZWXML-UHFFFAOYSA-N 0.000 claims 1
- SMXOEIFIDKLKCI-UHFFFAOYSA-N n-[5-[5-(3,3-difluorocyclobutyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl]-7-piperidin-4-ylimidazo[1,2-a]pyridine-3-carboxamide Chemical compound CC1=CC=C(C=2N=C(ON=2)C2CC(F)(F)C2)C=C1NC(=O)C(N1C=C2)=CN=C1C=C2C1CCNCC1 SMXOEIFIDKLKCI-UHFFFAOYSA-N 0.000 claims 1
- QMMUKLCBLNXISU-UHFFFAOYSA-N n-[5-[5-(3,3-difluorocyclobutyl)-1,3,4-oxadiazol-2-yl]-2-methylphenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=C(NC(=O)C=2N3C=CC=CC3=NC=2)C(C)=CC=C1C(O1)=NN=C1C1CC(F)(F)C1 QMMUKLCBLNXISU-UHFFFAOYSA-N 0.000 claims 1
- HHUBMCNSFFNTCO-UHFFFAOYSA-N n-[5-[5-(3,3-dimethylcyclobutyl)-1,2,4-oxadiazol-3-yl]-2-fluorophenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1C(C)(C)CC1C1=NC(C=2C=C(NC(=O)C=3N4C=CC=CC4=NC=3)C(F)=CC=2)=NO1 HHUBMCNSFFNTCO-UHFFFAOYSA-N 0.000 claims 1
- CYRMRQSGQSZIHP-UHFFFAOYSA-N n-[5-[5-(3,3-dimethylcyclobutyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=C(NC(=O)C=2N3C=CC=CC3=NC=2)C(C)=CC=C1C(N=1)=NOC=1C1CC(C)(C)C1 CYRMRQSGQSZIHP-UHFFFAOYSA-N 0.000 claims 1
- DQBZLRRBDNJYLN-UHFFFAOYSA-N n-[5-[5-(3-aminocyclobutyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=C(NC(=O)C=2N3C=CC=CC3=NC=2)C(C)=CC=C1C(N=1)=NOC=1C1CC(N)C1 DQBZLRRBDNJYLN-UHFFFAOYSA-N 0.000 claims 1
- GBSLZTPHUKSUFS-UHFFFAOYSA-N n-[5-[5-(3-cyclopropyl-3-hydroxycyclobutyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1=C(NC(=O)C=2N3C=CC=CC3=NC=2)C(C)=CC=C1C(N=1)=NOC=1C(C1)CC1(O)C1CC1 GBSLZTPHUKSUFS-UHFFFAOYSA-N 0.000 claims 1
- ALCOLPSSMDCYTE-UHFFFAOYSA-N n-[5-[5-(3-ethoxyiminocyclobutyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1C(=NOCC)CC1C1=NC(C=2C=C(NC(=O)C=3N4C=CC=CC4=NC=3)C(C)=CC=2)=NO1 ALCOLPSSMDCYTE-UHFFFAOYSA-N 0.000 claims 1
- YGXKCHDRBDRTQD-UHFFFAOYSA-N n-[5-[5-(3-ethylcyclobutyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl]imidazo[1,2-a]pyridine-3-carboxamide Chemical compound C1C(CC)CC1C1=NC(C=2C=C(NC(=O)C=3N4C=CC=CC4=NC=3)C(C)=CC=2)=NO1 YGXKCHDRBDRTQD-UHFFFAOYSA-N 0.000 claims 1
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| CN103965190A (zh) * | 2014-05-20 | 2014-08-06 | 定陶县友帮化工有限公司 | 一种咪唑并[1,2-a]吡啶-3-甲酸的合成方法 |
| BR112017028318B1 (pt) | 2015-07-02 | 2024-02-20 | Janssen Sciences Ireland Uc | Composto antibacteriano, seu uso, processo para sua preparação,produto que o contém, composição farmacêutica e combinação |
| US10059708B2 (en) * | 2016-04-26 | 2018-08-28 | Northwestern University | Therapeutic targeting of the interleukin 1 receptor-associated kinase 4 (IRAK4) in leukemias characterized by rearrangements in the mixed lineage leukemia gene (MLL-r) |
| BR112018076126A2 (pt) | 2016-06-16 | 2019-03-26 | Janssen Sciences Ireland Unlimited Company | compostos heterocíclicos como antibacterianos |
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| CA3041679A1 (en) | 2016-10-27 | 2018-05-03 | Lawrence S. ZISMAN | Combination therapy for treating pulmonary hypertension |
| EP4417262A3 (en) | 2017-03-01 | 2024-11-27 | Janssen Sciences Ireland Unlimited Company | Combination therapy |
| CN111039946A (zh) * | 2018-10-15 | 2020-04-21 | 上海轶诺药业有限公司 | 一类咪唑并芳环类化合物的制备和应用 |
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| CN114761006A (zh) | 2019-11-08 | 2022-07-15 | Inserm(法国国家健康医学研究院) | 对激酶抑制剂产生耐药性的癌症的治疗方法 |
| WO2021148581A1 (en) | 2020-01-22 | 2021-07-29 | Onxeo | Novel dbait molecule and its use |
| WO2021187486A1 (ja) * | 2020-03-17 | 2021-09-23 | 大日本住友製薬株式会社 | オキサジアゾール誘導体 |
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| WO2025256609A1 (en) * | 2024-06-13 | 2025-12-18 | Third Harmonic Bio, Inc. | Crystalline forms of a selective c-kit kinase inhibitor |
| WO2025259929A1 (en) * | 2024-06-13 | 2025-12-18 | Third Harmonic Bio, Inc. | COMPOUNDS AND COMPOSITIONS AS c-Kit KINASE INHIBITORS |
| CN121181581A (zh) * | 2024-06-21 | 2025-12-23 | 上海美悦生物科技发展有限公司 | 一种稠杂环化合物、其制备方法和用途 |
| CN121426815A (zh) * | 2024-07-30 | 2026-01-30 | 上海美悦生物科技发展有限公司 | 一种杂环化合物、其制备方法和用途 |
| WO2026032333A1 (zh) * | 2024-08-06 | 2026-02-12 | 上海美悦生物科技发展有限公司 | 一种杂环化合物、其制备方法和用途 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9518993D0 (en) * | 1995-09-16 | 1995-11-15 | Agrevo Uk Ltd | Fungicides |
| US20070072861A1 (en) * | 2000-03-27 | 2007-03-29 | Barbara Roniker | Method of using cyclooxygenase-2 inhibitors in the prevention of cardiovascular disorders |
| AU2003251561A1 (en) | 2002-06-20 | 2004-01-06 | Beacon Looms, Inc. | Knitted electrical conductor fabric |
| JP2007524596A (ja) | 2003-02-28 | 2007-08-30 | トランスフォーム・ファーマシューティカルズ・インコーポレイテッド | 共結晶医薬組成物 |
| US7754717B2 (en) | 2005-08-15 | 2010-07-13 | Amgen Inc. | Bis-aryl amide compounds and methods of use |
| BRPI0718677A2 (pt) | 2006-11-03 | 2013-11-26 | Irm Llc | Compostos e composições como inibidores de quinases proteicas |
| AU2011329233A1 (en) * | 2010-11-15 | 2013-05-23 | Abbvie Deutschland Gmbh & Co Kg | NAMPT and ROCK inhibitors |
| JP2014525450A (ja) * | 2011-09-01 | 2014-09-29 | アイアールエム・リミテッド・ライアビリティ・カンパニー | ｃ−Ｋｉｔキナーゼ阻害剤としての化合物および組成物 |
| EA201490537A1 (ru) * | 2011-09-01 | 2014-07-30 | АйАрЭм ЭлЭлСи | СОЕДИНЕНИЯ И КОМПОЗИЦИИ В КАЧЕСТВЕ ИНГИБИТОРОВ КИНАЗЫ C-Kit |
| EP2751104B1 (en) * | 2011-09-01 | 2019-09-25 | Novartis AG | Compounds and compositions as c-kit kinase inhibitors |
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