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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1641885생성일: 2026년 10월 26일

Triphenylphosphine → (1S,4R)-4-(2,6-Dichloro-9H-purin-9-yl)cyclopent-2-en-1-ol

https://huagongshe.com/reaction/1641885

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물2,6-DichloropurineHCID 5324412—
반응물rac-(1R,4S)-4-hydroxycyclopent-2-en-1-yl acetateHCID 10154103—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
생성물(1S,4R)-4-(2,6-Dichloro-9H-purin-9-yl)cyclopent-2-en-1-olHCID 10378467—

반응 단계

2,6-Dichloropurine (10 g, 52.90 mmol), (1S,4R)-cis 4-Acetoxy-2-cyclopenten-1-ol (10 g. 70.40 mmol), tris(dibenzylideneacetone)dipalladium(0) (3.20 g, 3.50 mmol) and polymer supported triphenylphosphine (˜3 mmol/g, 11.60 g, 35.00 mmol) are placed in an oven-dried flask under an atmosphere of argon. Dry deoxygenated THF (80 mL) is added and the reaction mixture is stirred gently for 5 minutes. Triethylamine (20 mL) is added and the reaction mixture is stirred at 50° C. The reaction is shown to be complete by LCMS after 1 hour. The reaction mixture is allowed to cool, the polymer supported triphenylphosphine is filtered off and the solvent is removed in vacuo. The title compound is obtained after purification by flash column chromatography (silica, dichloromethane/methanol 25:1). 1H nmr (CDCl3, 400 MHz); 8.30 (s, 1H), 6.40 (m, 1H), 5.90 (m, 1H), 5.50 (m, 1H), 4.95 (m, 1H), 3.05 (m, 1H), 2.10 (m, 1H), MS (ES+) m/e 271 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08114877B2
출처 데이터셋uspto-grants-2012_02
ORD IDord-333a776e6099421ab78e06437482da7c
출처 메모uspto-grants-2012_02