RU2517194C2 - Пирролопиридины как ингибиторы киназы - Google Patents

Info

Publication number

RU2517194C2

RU2517194C2 RU2010150786/04A RU2010150786A RU2517194C2 RU 2517194 C2 RU2517194 C2 RU 2517194C2 RU 2010150786/04 A RU2010150786/04 A RU 2010150786/04A RU 2010150786 A RU2010150786 A RU 2010150786A RU 2517194 C2 RU2517194 C2 RU 2517194C2

Authority

RU

Russia

Prior art keywords

alkyl

hydrogen

phenyl

cycloalkyl

membered

Prior art date

2008-05-13

Links

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• 229940043355 kinase inhibitor Drugs 0.000 title description 2
• 239000003757 phosphotransferase inhibitor Substances 0.000 title description 2
• 150000005255 pyrrolopyridines Chemical class 0.000 title 1
• 239000001257 hydrogen Substances 0.000 claims abstract description 331
• 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 331
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 260
• -1 heteocycles Chemical group 0.000 claims abstract description 244
• 150000001875 compounds Chemical class 0.000 claims abstract description 241
• 229910052736 halogen Inorganic materials 0.000 claims abstract description 197
• 150000002367 halogens Chemical group 0.000 claims abstract description 197
• 125000000623 heterocyclic group Chemical group 0.000 claims abstract description 162
• 150000002431 hydrogen Chemical group 0.000 claims abstract description 154
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 148
• 125000004429 atom Chemical group 0.000 claims abstract description 141
• 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims abstract description 126
• 238000000034 method Methods 0.000 claims abstract description 121
• 229920006395 saturated elastomer Polymers 0.000 claims abstract description 114
• 125000001072 heteroaryl group Chemical group 0.000 claims abstract description 108
• 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims abstract description 101
• IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract description 97
• 125000000217 alkyl group Chemical group 0.000 claims abstract description 97
• 125000003118 aryl group Chemical group 0.000 claims abstract description 94
• 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 75
• 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 claims abstract description 69
• 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 60
• 125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 59
• 201000010099 disease Diseases 0.000 claims abstract description 56
• 125000005842 heteroatom Chemical group 0.000 claims abstract description 55
• QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 52
• 229910052760 oxygen Inorganic materials 0.000 claims abstract description 50
• 239000001301 oxygen Substances 0.000 claims abstract description 50
• NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 49
• 150000003839 salts Chemical class 0.000 claims abstract description 46
• 230000003463 hyperproliferative effect Effects 0.000 claims abstract description 37
• 101000777293 Homo sapiens Serine/threonine-protein kinase Chk1 Proteins 0.000 claims abstract description 35
• 102100031081 Serine/threonine-protein kinase Chk1 Human genes 0.000 claims abstract description 34
• 125000002618 bicyclic heterocycle group Chemical group 0.000 claims abstract description 29
• 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 29
• 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 20
• 101000777277 Homo sapiens Serine/threonine-protein kinase Chk2 Proteins 0.000 claims abstract description 19
• 102100031075 Serine/threonine-protein kinase Chk2 Human genes 0.000 claims abstract description 19
• 208000035475 disorder Diseases 0.000 claims abstract description 19
• 125000006727 (C1-C6) alkenyl group Chemical group 0.000 claims abstract description 12
• 125000003342 alkenyl group Chemical group 0.000 claims abstract description 11
• 230000002401 inhibitory effect Effects 0.000 claims abstract description 5
• 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 claims description 78
• 238000011282 treatment Methods 0.000 claims description 57
• 239000012623 DNA damaging agent Substances 0.000 claims description 52
• 206010028980 Neoplasm Diseases 0.000 claims description 50
• 229910052717 sulfur Inorganic materials 0.000 claims description 43
• 239000011593 sulfur Chemical group 0.000 claims description 43
• 201000011510 cancer Diseases 0.000 claims description 40
• 125000001424 substituent group Chemical group 0.000 claims description 35
• 229910052731 fluorine Inorganic materials 0.000 claims description 32
• 241000124008 Mammalia Species 0.000 claims description 31
• 239000003112 inhibitor Substances 0.000 claims description 31
• 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 31
• 125000006239 protecting group Chemical group 0.000 claims description 29
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 28
• 238000006243 chemical reaction Methods 0.000 claims description 24
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 24
• UWKQSNNFCGGAFS-XIFFEERXSA-N irinotecan Chemical compound C1=C2C(CC)=C3CN(C(C4=C([C@@](C(=O)OC4)(O)CC)C=4)=O)C=4C3=NC2=CC=C1OC(=O)N(CC1)CCC1N1CCCCC1 UWKQSNNFCGGAFS-XIFFEERXSA-N 0.000 claims description 21
• SDUQYLNIPVEERB-QPPQHZFASA-N gemcitabine Chemical compound O=C1N=C(N)C=CN1[C@H]1C(F)(F)[C@H](O)[C@@H](CO)O1 SDUQYLNIPVEERB-QPPQHZFASA-N 0.000 claims description 20
• 229960005277 gemcitabine Drugs 0.000 claims description 20
• 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims description 20
• UHDGCWIWMRVCDJ-CCXZUQQUSA-N Cytarabine Chemical compound O=C1N=C(N)C=CN1[C@H]1[C@@H](O)[C@H](O)[C@@H](CO)O1 UHDGCWIWMRVCDJ-CCXZUQQUSA-N 0.000 claims description 19
• 229910052801 chlorine Inorganic materials 0.000 claims description 19
• 229960004768 irinotecan Drugs 0.000 claims description 19
• GAGWJHPBXLXJQN-UORFTKCHSA-N Capecitabine Chemical compound C1=C(F)C(NC(=O)OCCCCC)=NC(=O)N1[C@H]1[C@H](O)[C@H](O)[C@@H](C)O1 GAGWJHPBXLXJQN-UORFTKCHSA-N 0.000 claims description 18
• BPEGJWRSRHCHSN-UHFFFAOYSA-N Temozolomide Chemical compound O=C1N(C)N=NC2=C(C(N)=O)N=CN21 BPEGJWRSRHCHSN-UHFFFAOYSA-N 0.000 claims description 18
• DQLATGHUWYMOKM-UHFFFAOYSA-L cisplatin Chemical compound N[Pt](N)(Cl)Cl DQLATGHUWYMOKM-UHFFFAOYSA-L 0.000 claims description 18
• 229960004316 cisplatin Drugs 0.000 claims description 18
• GAGWJHPBXLXJQN-UHFFFAOYSA-N Capecitabine Natural products C1=C(F)C(NC(=O)OCCCCC)=NC(=O)N1C1C(O)C(O)C(C)O1 GAGWJHPBXLXJQN-UHFFFAOYSA-N 0.000 claims description 17
• GHASVSINZRGABV-UHFFFAOYSA-N Fluorouracil Chemical compound FC1=CNC(=O)NC1=O GHASVSINZRGABV-UHFFFAOYSA-N 0.000 claims description 17
• 229960004117 capecitabine Drugs 0.000 claims description 17
• 229910052799 carbon Inorganic materials 0.000 claims description 17
• 229960002949 fluorouracil Drugs 0.000 claims description 17
• 229960004964 temozolomide Drugs 0.000 claims description 17
• KLWPJMFMVPTNCC-UHFFFAOYSA-N Camptothecin Natural products CCC1(O)C(=O)OCC2=C1C=C3C4Nc5ccccc5C=C4CN3C2=O KLWPJMFMVPTNCC-UHFFFAOYSA-N 0.000 claims description 16
• VSJKWCGYPAHWDS-FQEVSTJZSA-N camptothecin Chemical compound C1=CC=C2C=C(CN3C4=CC5=C(C3=O)COC(=O)[C@]5(O)CC)C4=NC2=C1 VSJKWCGYPAHWDS-FQEVSTJZSA-N 0.000 claims description 16
• 229940127093 camptothecin Drugs 0.000 claims description 16
• VSJKWCGYPAHWDS-UHFFFAOYSA-N dl-camptothecin Natural products C1=CC=C2C=C(CN3C4=CC5=C(C3=O)COC(=O)C5(O)CC)C4=NC2=C1 VSJKWCGYPAHWDS-UHFFFAOYSA-N 0.000 claims description 16
• 239000003814 drug Substances 0.000 claims description 16
• 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 15
• 238000004519 manufacturing process Methods 0.000 claims description 15
• 229910052794 bromium Inorganic materials 0.000 claims description 14
• 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 11
• 150000001412 amines Chemical class 0.000 claims description 9
• 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 9
• 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 9
• 239000000546 pharmaceutical excipient Substances 0.000 claims description 9
• 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 8
• 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims description 7
• 125000004312 morpholin-2-yl group Chemical group [H]N1C([H])([H])C([H])([H])OC([H])(*)C1([H])[H] 0.000 claims description 7
• 125000000246 pyrimidin-2-yl group Chemical group [H]C1=NC(*)=NC([H])=C1[H] 0.000 claims description 7
• 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 7
• 125000004192 tetrahydrofuran-2-yl group Chemical group [H]C1([H])OC([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 7
• 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims description 6
• 125000004207 3-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(OC([H])([H])[H])=C1[H] 0.000 claims description 6
• 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims description 6
• 238000005859 coupling reaction Methods 0.000 claims description 6
• 125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 claims description 6
• 125000004180 3-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(F)=C1[H] 0.000 claims description 5
• 238000011319 anticancer therapy Methods 0.000 claims description 5
• 239000003937 drug carrier Substances 0.000 claims description 5
• 125000005931 tert-butyloxycarbonyl group Chemical group [H]C([H])([H])C(OC(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 5
• 238000002560 therapeutic procedure Methods 0.000 claims description 5
• 125000004214 1-pyrrolidinyl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 claims description 4
• 230000029936 alkylation Effects 0.000 claims description 4
• 238000005804 alkylation reaction Methods 0.000 claims description 4
• 230000001093 anti-cancer Effects 0.000 claims description 4
• 125000000555 isopropenyl group Chemical group [H]\C([H])=C(\*)C([H])([H])[H] 0.000 claims description 4
• 125000004307 pyrazin-2-yl group Chemical group [H]C1=C([H])N=C(*)C([H])=N1 0.000 claims description 4
• 125000004262 quinoxalin-2-yl group Chemical group [H]C1=NC2=C([H])C([H])=C([H])C([H])=C2N=C1* 0.000 claims description 4
• 125000006432 1-methyl cyclopropyl group Chemical group [H]C([H])([H])C1(*)C([H])([H])C1([H])[H] 0.000 claims description 3
• 125000001847 2-phenylcyclopropyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C1([H])C([H])([H])C1([H])* 0.000 claims description 3
• 125000004566 azetidin-1-yl group Chemical group N1(CCC1)* 0.000 claims description 3
• 238000010511 deprotection reaction Methods 0.000 claims description 3
• 238000007306 functionalization reaction Methods 0.000 claims description 2
• 230000002265 prevention Effects 0.000 claims description 2
• OLBVUFHMDRJKTK-UHFFFAOYSA-N [N].[O] Chemical group [N].[O] OLBVUFHMDRJKTK-UHFFFAOYSA-N 0.000 claims 4
• 239000011737 fluorine Substances 0.000 claims 1
• 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract description 10
• 239000000126 substance Substances 0.000 abstract description 8
• 230000000694 effects Effects 0.000 abstract description 4
• 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 9
• 239000005864 Sulphur Substances 0.000 abstract 6
• 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 3
• 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
• OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 162
• XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 160
• YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 105
• 239000000203 mixture Substances 0.000 description 102
• VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 96
• 239000011541 reaction mixture Substances 0.000 description 95
• 239000007787 solid Substances 0.000 description 90
• WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical group C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 86
• 125000004043 oxo group Chemical group O=* 0.000 description 85
• 239000000243 solution Substances 0.000 description 82
• RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 62
• 235000019439 ethyl acetate Nutrition 0.000 description 57
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 56
• 238000004895 liquid chromatography mass spectrometry Methods 0.000 description 49
• 239000002904 solvent Substances 0.000 description 49
• 238000000451 chemical ionisation Methods 0.000 description 47
• ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 46
• PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 43
• 229910052938 sodium sulfate Inorganic materials 0.000 description 43
• 235000011152 sodium sulphate Nutrition 0.000 description 43
• 239000012267 brine Substances 0.000 description 37
• HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 37
• 230000014759 maintenance of location Effects 0.000 description 34
• LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 31
• HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 30
• 239000003921 oil Substances 0.000 description 30
• VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 29
• VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 25
• 239000000741 silica gel Substances 0.000 description 23
• 229910002027 silica gel Inorganic materials 0.000 description 23
• 210000004027 cell Anatomy 0.000 description 22
• 238000001914 filtration Methods 0.000 description 22
• 238000003818 flash chromatography Methods 0.000 description 22
• 201000009030 Carcinoma Diseases 0.000 description 21
• ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 21
• WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 20
• JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 20
• MMWRGWQTAMNAFC-UHFFFAOYSA-N 1,2-dihydropyridine Chemical group C1NC=CC=C1 MMWRGWQTAMNAFC-UHFFFAOYSA-N 0.000 description 18
• DTQVDTLACAAQTR-UHFFFAOYSA-N trifluoroacetic acid Substances OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 18
• 238000004587 chromatography analysis Methods 0.000 description 17
• DBAOFQCSAQXIIN-UHFFFAOYSA-N n-(5-bromo-4-fluoro-1h-pyrrolo[2,3-b]pyridin-3-yl)pyridine-3-carboxamide Chemical compound C1=2C(F)=C(Br)C=NC=2NC=C1NC(=O)C1=CC=CN=C1 DBAOFQCSAQXIIN-UHFFFAOYSA-N 0.000 description 17
• QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 16
• QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 16
• 239000000725 suspension Substances 0.000 description 16
• 230000015572 biosynthetic process Effects 0.000 description 15
• KDLHZDBZIXYQEI-UHFFFAOYSA-N palladium Substances [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 15
• LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 14
• 239000000706 filtrate Substances 0.000 description 14
• 239000012223 aqueous fraction Substances 0.000 description 13
• 239000012298 atmosphere Substances 0.000 description 13
• 229910052763 palladium Inorganic materials 0.000 description 13
• 238000003786 synthesis reaction Methods 0.000 description 12
• RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 11
• VZHJRYVFKSFRKL-UHFFFAOYSA-N 5-bromo-4-fluoro-1h-pyrrolo[2,3-b]pyridin-3-amine Chemical compound C1=C(Br)C(F)=C2C(N)=CNC2=N1 VZHJRYVFKSFRKL-UHFFFAOYSA-N 0.000 description 11
• NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 11
• 206010025323 Lymphomas Diseases 0.000 description 11
• UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical class [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 11
• 239000003054 catalyst Substances 0.000 description 11
• 238000000926 separation method Methods 0.000 description 11
• 239000011734 sodium Substances 0.000 description 11
• WUOQXNWMYLFAHT-UHFFFAOYSA-N tert-butyl n-piperidin-3-ylcarbamate Chemical compound CC(C)(C)OC(=O)NC1CCCNC1 WUOQXNWMYLFAHT-UHFFFAOYSA-N 0.000 description 11
• PVNIIMVLHYAWGP-UHFFFAOYSA-N Niacin Chemical compound OC(=O)C1=CC=CN=C1 PVNIIMVLHYAWGP-UHFFFAOYSA-N 0.000 description 10
• 239000002246 antineoplastic agent Substances 0.000 description 10
• UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 10
• 238000004366 reverse phase liquid chromatography Methods 0.000 description 10
• ZEFGUWRQFNTGGX-UHFFFAOYSA-N 1,6-dihydropyridazine Chemical compound C1NN=CC=C1 ZEFGUWRQFNTGGX-UHFFFAOYSA-N 0.000 description 9
• HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 9
• 108091000080 Phosphotransferase Proteins 0.000 description 9
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• 239000012047 saturated solution Substances 0.000 description 9
• 238000003756 stirring Methods 0.000 description 9
• WUOQXNWMYLFAHT-MRVPVSSYSA-N tert-butyl n-[(3r)-piperidin-3-yl]carbamate Chemical compound CC(C)(C)OC(=O)N[C@@H]1CCCNC1 WUOQXNWMYLFAHT-MRVPVSSYSA-N 0.000 description 9
• IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 8
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• 206010039491 Sarcoma Diseases 0.000 description 8
• 230000002159 abnormal effect Effects 0.000 description 8
• 238000007792 addition Methods 0.000 description 8
• 239000007864 aqueous solution Substances 0.000 description 8
• 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 8
• 125000000524 functional group Chemical group 0.000 description 8
• 125000004433 nitrogen atom Chemical group N* 0.000 description 8
• 239000000047 product Substances 0.000 description 8
• FPGGTKZVZWFYPV-UHFFFAOYSA-M tetrabutylammonium fluoride Chemical compound [F-].CCCC[N+](CCCC)(CCCC)CCCC FPGGTKZVZWFYPV-UHFFFAOYSA-M 0.000 description 8
• 206010009944 Colon cancer Diseases 0.000 description 7
• 206010033128 Ovarian cancer Diseases 0.000 description 7
• 239000010410 layer Substances 0.000 description 7
• 239000000463 material Substances 0.000 description 7
• 206010041823 squamous cell carcinoma Diseases 0.000 description 7
• MVXVYAKCVDQRLW-UHFFFAOYSA-N 1h-pyrrolo[2,3-b]pyridine Chemical class C1=CN=C2NC=CC2=C1 MVXVYAKCVDQRLW-UHFFFAOYSA-N 0.000 description 6
• AOTXEIQACILNKS-UHFFFAOYSA-N 5-chloro-4-fluoro-1h-pyrrolo[2,3-b]pyridin-3-amine Chemical compound C1=C(Cl)C(F)=C2C(N)=CNC2=N1 AOTXEIQACILNKS-UHFFFAOYSA-N 0.000 description 6
• JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 6
• 208000000035 Osteochondroma Diseases 0.000 description 6
• 206010061535 Ovarian neoplasm Diseases 0.000 description 6
• YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
• HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 6
• 208000006990 cholangiocarcinoma Diseases 0.000 description 6
• 125000005843 halogen group Chemical group 0.000 description 6
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