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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 3649생성일: 2026년 10월 23일

Imidazole → 5'-O-tert-Butyldimethylsilylthymidine

https://huagongshe.com/ko/reaction/3649

반응식

참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물ThymidineHCID 5789—
반응물tert-Butyldimethylsilyl chlorideHCID 28928—
용매DimethylformamideHCID 6228—
생성물5'-O-tert-ButyldimethylsilylthymidineHCID 1025125970.1%

반응 단계

To a solution of 2.42 g (10 mmol) thymidine in 15 ml DMF was added 1.7 g (25 mmol) imidazole and 1.6 g (10.6 mmol) tert-butyldimethyl silyl chloride. The solution was stirred at room temperature for 3 hours. DMF was then removed in vacuo and the residue was dissolved in 150 ml of ethyl acetate. The solution was washed with water and the organic layer was dried over MgSO4. After removing the solvent, the solid was recrystallized with ethyl acetate/pentane to obtain 2.5 g pure 5'-O-(tert-butyldimethylsilyl) thymidine 1 (70% yield).: m.p. 193°-194° C.; 1H NMR (500 MHz, CDCl3) δ9.0 (s, 1H, NH), 7.50 (s, 1H, H-6), 6.36 (dd, J=5.8, 8.1 Hz, 1H, H-1'), 4.44 (m, 1H, H-3'), 4.03 (m, 1H, H-4'), 3.85 (m, 2H, H-5'), 2.66 (d, J=3.8 Hz, 1H, OH), 2.35 (m, 1H, H-2'), 2.07 (m, 1H, H-2'), 1.89 (s, 3H, C=CMe), 0.89 (s, 9H, CMe3), 0.09 (s, 6H, SiMe2); --NMR (125 MHz, CDCl3) δ163.8 (C-4), 150.4 (C-2), 135.4 (C-6), 110.9 (C-5), 87.2 (C-4'), 85.0 (C-1'), 72.6 (C-3'), 63.6 (C-5'), 41.1 (C-2'), 25.9 (SiCMe3), 18.3 (SiCMe3), 12.5 (C=CMe), -5.4 (SiMe2), -5.5 (SiMe2).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05734041
출처 데이터셋uspto-grants-1998_03
ORD IDord-18d0c7be8ef340e5b002ed0b9fb78e76
출처 메모uspto-grants-1998_03