戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 6862作成日:2026年10月25日

2-Bromo-3-hydroxyacrylaldehyde → 2-(Pyridin-2-ylamino)thiazole-5-carbaldehyde

https://huagongshe.com/reaction/6862

反応式

関与物質

役割名称HCID仕込み量
反応物2-Bromo-3-hydroxyacrylaldehydeHCID 170565—
反応物Sodium AcetateHCID 517045—
反応物1-(2-Pyridyl)-2-thioureaHCID 1490491—
溶媒AcetoneHCID 180—
生成物2-(Pyridin-2-ylamino)thiazole-5-carbaldehydeHCID 2201905852%

反応条件

温度75 °C

反応手順

To a solution of 1-(2-pyridyl)-2-thiourea (765 mg, 5.0 mmol) in acetone (14 mL) was added slowly 2-bromo-3-hydroxypropenal (755 mg, 5.0 mmol, for preparation see J. Org. Chem. 28, 3243, 1963) in acetone (14 mL) over a period of 5 min. After stirring for 1.5 h, a precipitate formed. The solids were separated, washed with acetone (10 mL) and then taken into mixed solvent (ethanol/water=1/1, 9 mL). To this suspension was added sodium acetate (1.23 g, 15.0 mmol) and the resulting mixture was heated at 75° C. for 1 h. After cooling to RT, the mixture was filtered and the solids were washed with water (10 mL), and dried in vacuo to provide compound A, 2-(pyridin-2-ylamino)-thiazole-5-carbaldehyde (533 mg, 52%) as a solid. LC/MS; (M+H)+=206

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07084160B2
出典データセットuspto-grants-2006_08
ORD IDord-c0f346fd6672465c92d63410e95e866a
出典メモuspto-grants-2006_08