돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 19489생성일: 2026년 10월 23일

Imidazole → 5-Amino-3-(5'-o-tert-butyl-dimethylsilanyl-beta-d-ribofuranosyl)-3h-thiazolo[4,5-d]pyrimidin-2-one

https://huagongshe.com/ko/reaction/19489

반응식

참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물tert-Butyldimethylsilyl chlorideHCID 28928—
반응물5-Amino-3-(2',3,5'-tri-O-acetyl-beta-D-ribofuranosyl)-3H-thiazolo[4,5-d]pyrimidin-2-oneHCID 11633267—
용매DimethylformamideHCID 6228—
생성물5-Amino-3-(5'-o-tert-butyl-dimethylsilanyl-beta-d-ribofuranosyl)-3h-thiazolo[4,5-d]pyrimidin-2-oneHCID 6670770652%

반응 단계

To a solution of 79 (0.68 g, 2.28 mmol) in DMF (10 mL) was added imidazole (0.54 g, 7.93 mmol) and tert-butyldimethylsilyl chloride (0.68 g, 4.56 mmol) sequentially. The reaction mixture was stirred at room temperature for 2 h, at which point it was concentrated and purified by flash column chromatography (silica, MeOH/CHCl3; gradient=5-20%) to afford 0.49 g (52%) 87 as a white solid: 1H (400 MHz, d6-DMSO) δ 8.33 (s, 1H), 6.87 (s, 2H), 5.90 (d, J=4.0 Hz, 1H), 5.33 (d, J=5.6 Hz, 1H), 5.00 (d, J=5.2 Hz, 1H), 4.79 (q, J=5.2 Hz, 1H), 4.16 (q, J=5.2 Hz, 1H), 3.77 (m, 2H), 3.64 (dd, J=12.0, 7.2 Hz, 1H), 0.84 (s, 9H), 0.00 (s, 6H); MS (+)-ES [M+H]+ m/z 415.4.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745415B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-09e741117e3544bd96272e936487c8e8
출처 메모uspto-grants-2010_06