戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 495031作成日:2026年10月26日

Cesium fluoride → 6-Amino-2-(4-chloro-2-fluoro-3-methoxyphenyl)-5-chloropyrimidine-4-carboxylic acid methyl ester

https://huagongshe.com/reaction/495031

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium fluorideHCID 25953—
反応物Methyl 6-amino-2,5-dichloropyrimidine-4-carboxylateHCID 312630—
反応物2-(4-Chloro-2-fluoro-3-methoxyphenyl)-1,3,2-dioxaborinaneHCID 57782419—
触媒HCID 178418476HCID 178418476—
溶媒WaterHCID 962—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物6-Amino-2-(4-chloro-2-fluoro-3-methoxyphenyl)-5-chloropyrimidine-4-carboxylic acid methyl esterHCID 1665680153.5%

反応条件

温度80 °C

反応手順

6-Amino-2,5-dichloropyrimidine-4-carboxylic acid methyl ester (888 mg, 4 mmol), 2-(4-chloro-2-fluoro-3-methoxyphenyl)-[1,3,2]-dioxaborinane (1.47 g, 6 mmol), bis(triphenylphosphine)palladium(II) dichloride (280 mg, 0.4 mmol), and cesium fluoride (1.21 g, 8 mmol) were combined in 8 mL of 1,2-dimethoxyethane and 8 mL of water. The reaction mixture was heated at 80° C. for 3 hours and the cooled reaction mixture was partitioned between ethyl acetate and water. The organic phase was washed with water, dried, and concentrated. The product was purified by column chromatography (ethyl acetate/hexane gradient) then purified again by column chromatography (methylene chloride/ethyl acetate gradient) to yield 6-amino-5-chloro-2-(4-chloro-2-fluoro-3-methoxyphenyl) pyrimidine-4-carboxylic acid methyl ester (738 mg, 53.5% yield):

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07538214B2
出典データセットuspto-grants-2009_05
ORD IDord-2a908c9352944840aa079bc20e42e430
出典メモuspto-grants-2009_05