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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 217571생성일: 2026년 10월 25일

tert-Butyldimethylsilyl chloride → 9-[(2R,4R,5R)-4-[tert-butyl(dimethyl)silyl]-5-[[tert-butyl(dimethyl)silyl]oxymethyl]-4-hydroxyoxolan-2-yl]-3H-purin-6-one

https://huagongshe.com/reaction/217571

반응식

참여 물질

역할이름HCID투입량
반응물tert-Butyldimethylsilyl chlorideHCID 28928—
반응물HCID 178521064HCID 178521064—
용매DimethylformamideHCID 6228—
생성물9-[(2R,4R,5R)-4-[tert-butyl(dimethyl)silyl]-5-[[tert-butyl(dimethyl)silyl]oxymethyl]-4-hydroxyoxolan-2-yl]-3H-purin-6-oneHCID 178455233—

반응 단계

A solution of TBSCl (1.91 g, 12.67 mmol) was added to a solution of 2′-deoxyinosine (1.00 g, 3.96 mmol) and imidiazole (1.73 g, 25.34 mmol) in anhydrous DMF (3 mL) at 0° C. under nitrogen atmosphere. The reaction mixture was gradually warmed to room temperature and stirred for 12 hours. The mixture was then concentrated in vacuo, dissolved in CH2Cl2 (100 mL), washed twice with water (50 mL), dried over anhydrous Na2SO4, concentrated in vacuo, and purified by silica gel chromatography to yield 3′,5′-O-bis-tert-butyldimethylsilyl-2′-deoxyinosine dA.n9 (1.58 g, 83%) as a white powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08198029B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-84ad6101302d452794849dc43974e84d
출처 메모uspto-grants-2012_06