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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 82144생성일: 2026년 10월 24일

7-[(1S)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-methylethyl]-4-chloro-7H-pyrrolo[2,3-d]pyrimidine → 7-[(1S)-2-{[tert-Butyl(dimethyl)silyl]oxy}-1-methylethyl]-7H-pyrrolo[2,3-d]pyrimidine

https://huagongshe.com/ko/reaction/82144

반응식

참여 물질

역할이름HCID투입량
반응물7-[(1S)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-methylethyl]-4-chloro-7H-pyrrolo[2,3-d]pyrimidineHCID 86672078—
촉매PalladiumHCID 23938—
용매AmmoniaHCID 222—
용매EthanolHCID 702—
생성물7-[(1S)-2-{[tert-Butyl(dimethyl)silyl]oxy}-1-methylethyl]-7H-pyrrolo[2,3-d]pyrimidineHCID 7081766994%

반응 단계

Palladium (10% on carbon, 18 g) was added to 7-[(1S)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-methylethyl]-4-chloro-7H-pyrrolo[2,3-d]pyrimidine (182 g, 558 mmol) (see Preparation 1) in ethanol (900 mL) and concentrated ammonia solution (100 mL) and hydrogenated (60 psi, 20° C.) for 18 hours. The reaction mixture was filtered through Arbocel™ and the filtrate was evaporated in vacuo. Diethyl ether (300 mL) was added to the residue and the mixture was filtered. The filtrate was evaporated in vacuo to afford the title compound as an orange oil in 94% yield, 162.7 g.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846698B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-4597911af295450aaca7933c8a0f5f58
출처 메모uspto-grants-2014_09