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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 466240생성일: 2026년 10월 24일

Imidazole → (1R,2S,3R,5R)-3-[6-Amino-9H-purin-9-yl]-5-[((2,3-dimethylbut-2-yl)dimethylsilyloxy)methyl]-1,2-cyclopentanediol

https://huagongshe.com/ko/reaction/466240

반응식

참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물DimethylformamideHCID 6228—
반응물AristeromycinHCID 65269—
반응물Dimethylthexylsilyl chlorideHCID 144239—
용매WaterHCID 962—
생성물(1R,2S,3R,5R)-3-[6-Amino-9H-purin-9-yl]-5-[((2,3-dimethylbut-2-yl)dimethylsilyloxy)methyl]-1,2-cyclopentanediolHCID 15089637—

반응 단계

A mixture of aristeromycin (50 g) and dimethylformamide (250 ml) was stirred at room temperature and imidazole (50 g) and then dimethylthexylsilyl chloride (10 ml) were added. Three further 10 ml portions of dimethylthexylsilyl chloride were added after 20 min, 1 h and 1.75 h. After 4 h the resulting mixture was poured into rapidly stirred water (2.5 L). The suspension was filtered and the residue washed with water (2×250 ml). The air dried solid was added to di-isopropyl ether (500 ml) and stirred for 20 min. The suspension was filtered and the residue collected, stirred with diethyl ether (500 ml) and filtered to give the title compound (49 g); 1H nmr (DMSO-d6) δ8.13 (1H), 8.09 (1H), 7.18 (2H), 5.03-4.93 (1H), 4.76-4.60 (2H), 4.41-4.28 (1H), 3.88-3.78 (1H), 3.72-3.57 (2H), 2.28-1.70 (3H), 1.67-1.52 (1H), 0.95-0.75 (12H), 0.1 (6H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05155112
출처 데이터셋uspto-grants-1992_10
ORD IDord-c0be78fd77224f0b9ea87f495985fd6e
출처 메모uspto-grants-1992_10