戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 253701作成日:2026年10月26日

Methyl acetoacetate → 4(3H)-Pyrimidinone, 6-methyl-2-[2-(trifluoromethyl)phenyl]-

https://huagongshe.com/reaction/253701

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl acetoacetateHCID 7757—
反応物Sodium ethoxideHCID 2723922—
反応物2-TrifluoromethylbenzamidineHCID 3266509—
溶媒EthanolHCID 702—
生成物4(3H)-Pyrimidinone, 6-methyl-2-[2-(trifluoromethyl)phenyl]-HCID 13585083550.2%

反応手順

A mixture of 2-trifluoromethyl-benzamidine (2.13 g, 4 mmol) and sodium ethoxide (0.83 g, 12 mmol) in ethanol (20 mL) was treated with methyl acetoacetate (0.44 mL, 4 mmol) and heated at for 24 hours. The reaction was cooled, concentrated, diluted with water and acidified with 2 N hydrochloric acid. The resulting solution was extracted with ethyl acetate, dried over sodium sulfate and concentrated. Purification by flash chromatography [SiO2, methanol:dichloromethane (3:97)] provided the title compound (0.51 g, 50% yield) as a yellow solid; 1H-NMR (500 MHz, DMSO-d6) δ 12.7 (br s, 1H), 7.9 (m, 1H), 7.8 (m, 2H), 7.7 (m, 1H), 6.3 (s, 1H), 2.21 (s, 3H) ppm; MS (FIA) 255.0 (M+H); Rt (Method A) 2.578 minutes.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07872129B2
出典データセットuspto-grants-2011_01
ORD IDord-498c478e0ede464c8788cf90134de9c7
出典メモuspto-grants-2011_01