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HRID 75557作成日:2026年10月25日

Isothiocyanatotrimethylsilane → Ethyl 2-(6-(2,4-dimethoxyphenyl)-4-oxo-2-thioxo-3,4-dihydropyrimidin-1(2H)-yl)acetate

https://huagongshe.com/reaction/75557

反応式

関与物質

役割名称HCID仕込み量
反応物IsothiocyanatotrimethylsilaneHCID 75297—
反応物Ethylacetate heptaneHCID 21899848—
反応物(Z)-Methyl 3-(2,4-dimethoxyphenyl)-3-((2-ethoxy-2-oxoethyl)amino)acrylateHCID 86684695—
溶媒2-MethyltetrahydrofuranHCID 7301—
生成物Ethyl 2-(6-(2,4-dimethoxyphenyl)-4-oxo-2-thioxo-3,4-dihydropyrimidin-1(2H)-yl)acetateHCID 86684696—

反応条件

温度110 °C

反応手順

To a solution of (Z)-methyl 3-(2,4-dimethoxyphenyl)-3-((2-ethoxy-2-oxoethyl)amino)acrylate (4.68 g, 15.1 mmol) in 2-methyltetrahydrofuran (38 mL) was added (trimethylsilyl)isothiocyanate (12.9 mL, 90.8 mmol). The resulting solution was purged with nitrogen gas for 3 times, and the mixture was heated at 110° C. for 18 hours. The mixture was cooled down to room temperature and the solvent was removed under reduced pressure to give a red solid. This residue was suspended in a mixture of 3:1 heptane/EtOAc (200 mL), and it was stirred at room temperature for 1 hour. The solid was filtered, and triturated with CH2Cl2 (100 mL), concentrated under reduced pressure and dried under vacuum the title compound (4.42 g, 87%) as a pink solid. This material was used without further purification in the next step.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08835449B2
出典データセットuspto-grants-2014_09
ORD IDord-5356724165aa47ea97f6a12f0ced82f0
出典メモuspto-grants-2014_09