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HRID 1629687作成日:2026年10月26日

Imidazole → Acetic Acid 5-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-(tert-butyl-diphenyl-silanyloxy)-2-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl Ester

https://huagongshe.com/reaction/1629687

反応式

関与物質

役割名称HCID仕込み量
反応物ImidazoleHCID 795—
反応物Ethyl AcetateHCID 8857—
反応物tert-ButyldiphenylchlorosilaneHCID 94078—
反応物Acetic Acid 5-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-2-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-4-hydroxy-tetrahydro-furan-3-yl EsterHCID 131728048—
溶媒DimethylformamideHCID 6228—
生成物Acetic Acid 5-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-(tert-butyl-diphenyl-silanyloxy)-2-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl EsterHCID 131728049—

反応手順

The preparation of tert-butyldiphenylsilyl ethers is a common, routine procedure (Protective Groups in Organic Synthesis, 3rd edition, 1999, pp. 141-144 and references therein, Greene, T. W. and Wuts, P. G. M., eds, Wiley-Interscience, New York). In general, a solution of one eq. of 7 and imidazole (3.5 eq.) in anhydrous N,N-dimethylformamide (DMF) is treated with tert-butyldiphenylsilyl chloride (1.2 eq.). After stirring at room temperature for several hours, the reaction mixture is poured into ethyl acetate and washed extensively with water and saturated brine solution. The resulting organic solution is dried over anhydrous sodium sulfate, filtered, evaporated, and purified by silica gel chromatography to give Compound 8.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08791083B2
出典データセットuspto-grants-2014_07
ORD IDord-9b707518f77946ecadffd64834428d37
出典メモuspto-grants-2014_07