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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 74864생성일: 2026년 10월 24일

1,2-Epoxy-3-methoxypropane → (S)-3-((2-(5-chloro-1-tosyl-1H-pyrrolo[2,3-b]pyridin-3-yl)-5-fluoropyrimidin-4-ylamino)piperidin-1-yl)-3-methoxypropan-2-ol

https://huagongshe.com/ko/reaction/74864

반응식

참여 물질

역할이름HCID투입량
반응물1,2-Epoxy-3-methoxypropaneHCID 13589—
반응물2-[5-chloro-1-(p-tolylsulfonyl)pyrrolo[2,3-b]pyridin-3-yl]-5-fluoro-N-[(3S)-3-piperidyl]pyrimidin-4-amineHCID 67285119—
용매EthanolHCID 702—
생성물(S)-3-((2-(5-chloro-1-tosyl-1H-pyrrolo[2,3-b]pyridin-3-yl)-5-fluoropyrimidin-4-ylamino)piperidin-1-yl)-3-methoxypropan-2-olHCID 86762718—

반응 조건

온도140 °C

반응 단계

To a solution of 2-[5-chloro-1-(p-tolylsulfonyl)pyrrolo[5,4-b]pyridin-3-yl]-5-fluoro-N-[(3S)-3-piperidyl]pyrimidin-4-amine, 1c, (0.20 g, 0.40 mmol) in ethanol was added 2-(methoxymethyl)oxirane (0.04 mL, 0.40 mmol). The reaction mixture was heated in a microwave reactor at 140° C. for 5 minutes. The reaction was evaporated to dryness and the resulting residue was purified via silica gel chromatography (0-10% MeOH: CH2Cl2) to afford the desired product (1d).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08829007B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-36f9b358ed36485fb98f406c9949dab4
출처 메모uspto-grants-2014_09