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HRID 55551作成日:2026年10月26日

Thymidine → 5'-O-tert-Butyldimethylsilylthymidine

https://huagongshe.com/reaction/55551

反応式

関与物質

役割名称HCID仕込み量
反応物ThymidineHCID 5789—
反応物TriethylamineHCID 8471—
反応物tert-Butyldimethylsilyl chlorideHCID 28928—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物5'-O-tert-ButyldimethylsilylthymidineHCID 1025125988.4%

反応手順

5'-O-tert-Butyldimethylsilylthymidine (Compound 2, Table I) was prepared by dissolving thymidine (25 g, 0.10 mole), 4-N,N-dimethylaminopyridine (3.15 g, 0.026 mole) and triethylamine (13.5 g, 18.6 ml, 0.13 mole) in 200 ml of dry N,N-dimethylformamide under a stream of argon. 19.4 g (0.13 mol) tert-butyldimethylchlorosilane was added to the dissolved mixture, with the entire mixture then being stirred for six hours before evaporation of the solvent. The resulting gum was dissolved in 30 ml ethyl acetate and the solution extracted with 10 ml saturated sodium bicarbonate solution, 30 ml water and 30 ml brine. Following drying of the organic layer, the residue was purified by flash chromatography using dichloromethane/ethanol (50/1) as eluent. Evaporation of the product-containing fractions yielded 31.5 g of the desired 5'-O-tert-butyldimethylsilylthymidine as a white foam (86% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05625050
出典データセットuspto-grants-1997_04
ORD IDord-d4b5a0253f064b57881e8da5d1fae4d0
出典メモuspto-grants-1997_04