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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 527033생성일: 2026년 10월 25일

Pyrrolidine → N-((1R,3S)-3-(2-(5-chloro-1H-pyrrolo[2,3-b]pyridin-3-yl)-5-fluoropyrimidin-4-ylamino)-1-methylcyclohexyl)pyrrolidine-1-carboxamide

https://huagongshe.com/reaction/527033

반응식

참여 물질

역할이름HCID투입량
반응물PyrrolidineHCID 31268—
반응물2-(5-chloro-1H-pyrrolo[2,3-b]pyridin-3-yl)-5-fluoro-N-((1S,3R)-3-isocyanato-3-methylcyclohexyl)pyrimidin-4-amineHCID 86667437—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물N-((1R,3S)-3-(2-(5-chloro-1H-pyrrolo[2,3-b]pyridin-3-yl)-5-fluoropyrimidin-4-ylamino)-1-methylcyclohexyl)pyrrolidine-1-carboxamideHCID 68008126—

반응 단계

A solution of 2-(5-chloro-1H-pyrrolo[2,3-b]pyridin-3-yl)-5-fluoro-N-((1S,3R)-3-isocyanato-3-methylcyclohexyl)pyrimidin-4-amine, 52m, (0.035 g, 0.087 mmol) in 3 mL of NMP with 0.5 mL of pyrrolidine was warmed to 200° C. in a microwave for 30 minutes. The reaction was then concentrated in vacuo and purified by reverse phase HPLC chromatography, yielding 8.7 mg of desired product as a tan solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09345708B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-44f04ce23e9e4331ad5fe9fa4098f847
출처 메모uspto-grants-2016_05