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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 79439생성일: 2026년 10월 24일

Triethylamine → 7-((2,2-dimethyl-1,3-dioxolan-4-yl)methoxy)-N-(3-ethyl-1-((6-methylpyridin-2-yl)methyl)-1H-indazol-4-yl)imidazo[1,2-a]pyridine-3-carboxamide

https://huagongshe.com/ko/reaction/79439

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2,4,6-Trichlorobenzoyl chlorideHCID 2733703—
반응물Lithium HexamethyldisilazideHCID 2733832—
반응물3-ethyl-((6-methylpyridin-2-yl)methyl)-1H-indazol-4-amineHCID 67259804—
반응물7-((2,2-Dimethyl-1,3-dioxolan-4-yl)methoxy)imidazo[1,2-a]pyridine-3-carboxylic acidHCID 67260183—
용매TetrahydrofuranHCID 8028—
생성물7-((2,2-dimethyl-1,3-dioxolan-4-yl)methoxy)-N-(3-ethyl-1-((6-methylpyridin-2-yl)methyl)-1H-indazol-4-yl)imidazo[1,2-a]pyridine-3-carboxamideHCID 6725948316.3%

반응 단계

To a stirred mixture of 7-((2,2-dimethyl-1,3-dioxolan-4-yl)methoxy)imidazo[1,2-a]pyridine-3-carboxylic acid (128 mg, 0.44 mmol) in tetrahydrofuran (6 mL), under nitrogen, was added 2,4,6-trichlorobenzoyl chloride (115 mg, 0.47 mmol) and triethylamine (51 mg, 0.51 mmol). The mixture was stirred for 30 minutes. To the reaction mixture was added 3-ethyl-1-((6-methylpyridin-2-yl)methyl)-1H-indazol-4-amine (90 mg, 0.34 mmol), followed by lithium bis(trimethylsilyl)amide (1.7 mL, 1.7 mmol; 1M solution in tetrahydrofuran). The mixture was concentrated under reduced pressure and purified by flash chromatography on silica, eluting with dichloromethane/methanol (10:1) to give 7-((2,2-dimethyl-1,3-dioxolan-4-yl)methoxy)-N-(3-ethyl-1-((6-methylpyridin-2-yl)methyl)-1H-indazol-4-yl)imidazo[1,2-a]pyridine-3-carboxamide (30 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841455B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-cfe31da9445f4dc0b44f22515a3a8b99
출처 메모uspto-grants-2014_09