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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 526915생성일: 2026년 10월 26일

(R)-(+)-1-Boc-3-aminopyrrolidine → (R)-((S)-tetrahydrofuran-3-yl) 3-(2-(5-chloro-1H-pyrrolo[2,3-b]pyridin-3-yl)-5-fluoropyrimidin-4-ylamino)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/526915

반응식

참여 물질

역할이름HCID투입량
반응물(R)-(+)-1-Boc-3-aminopyrrolidineHCID 854070—
반응물Carbonic Acid 2,5-Dioxopyrrolidin-1-yl (S)-Tetrahydrofuran-3-yl EsterHCID 11229944—
반응물(S)-2-(5-chloro-1H-pyrrolo[2,3-b]pyridin-3-yl)-5-fluoro-N-(1-(methylsulfonyl)pyrrolidin-3-yl)pyrimidin-4-amineHCID 68008525—
생성물(R)-((S)-tetrahydrofuran-3-yl) 3-(2-(5-chloro-1H-pyrrolo[2,3-b]pyridin-3-yl)-5-fluoropyrimidin-4-ylamino)pyrrolidine-1-carboxylateHCID 6800788647%

반응 단계

According to the procedure for compound 398 using (R)-tert-butyl 3-aminopyrrolidine-1-carboxylate and (S)-2,5-dioxopyrrolidin-1-yl tetrahydrofuran-3-yl carbonate afforded 19.8 mg (47% yield) of 424 as a solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09345708B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-e39f8134e463413cbe90d9547f34e926
출처 메모uspto-grants-2016_05