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HRID 75541作成日:2026年10月25日

Isothiocyanatotrimethylsilane → 6-(2,6-Dimethoxypyridin-3-yl)-1-(2-hydroxyethyl)-2-thioxo-2,3-dihydropyrimidin-4(1H)-one

https://huagongshe.com/reaction/75541

反応式

関与物質

役割名称HCID仕込み量
反応物IsothiocyanatotrimethylsilaneHCID 75297—
反応物HCID 86684678HCID 86684678—
溶媒2-MethyltetrahydrofuranHCID 7301—
溶媒Ethyl AcetateHCID 8857—
生成物6-(2,6-Dimethoxypyridin-3-yl)-1-(2-hydroxyethyl)-2-thioxo-2,3-dihydropyrimidin-4(1H)-oneHCID 8668467916%

反応条件

温度80 °C

反応手順

To a solution of (Z)-ethyl 3-(2,6-dimethoxypyridin-3-yl)-3-((2-hydroxyethyl)amino)acrylate (100 mg, 0.34 mmol) in 2-MeTHF (1.0 mL) was added (trimethylsilyl)isothiocyanate (0.30 mL, 2.0 mmol) and the reaction mixture was heated at 80° C. for 4 hours. The cooled reaction mixture was diluted with EtOAc and washed with a saturated aqueous sodium bicarbonate solution. The layers were separated and the organic layer was concentrated in vacuo. The residue was triturated with MeOH and the resulting solids were collected by vacuum filtration to give the title compound (16 mg, 16%) as a white solid.

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-57d982c63b564ccf8f14e28d8af23c19
出典メモuspto-grants-2014_09