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HRID 245280作成日:2026年10月23日

4-Chloro-2-fluoro-3-methoxyphenylboronic acid → 6-Amino-2-(4-chloro-2-fluoro-3-methoxyphenyl)pyrimidine-4-carboxylic acid methyl ester

https://huagongshe.com/ja/reaction/245280

反応式

関与物質

役割名称HCID仕込み量
反応物4-Chloro-2-fluoro-3-methoxyphenylboronic acidHCID 44129706—
反応物Methyl 6-amino-2-chloropyrimidine-4-carboxylateHCID 53396493—
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)pyrimidine-4-carboxylic acid methyl esterHCID 5943208353.5%

反応条件

温度80 °C

反応手順

6-Amino-2-chloropyrimidine-4-carboxylic acid methyl ester (2.25 g, 12 mmol, 4-chloro-2-fluoro-3-methoxyphenylboronic acid (3.27 g, 16 mmol), and bis(triphenylphosphine)palladium(II) dichloride (842 mg, 1.2 mmol) were combined in 12 mL of 1,2-dimethoxyethane and 12 mL of water. The reaction mixture was heated at 80° C. for 2 h and the cooled reaction mixture was partitioned between ethyl acetate and water. The organic phase was washed with water, dried, and concentrated under vacuum. The product was purified by flash chromatography on silica gel to yield the title compound (2.0 g, 53.5% yield): mp 188-190° C.: 1H NMR (CDCl3) δ 7.66 (dd, 1H), 7.22 (dd, 1H), 7.14 (s, 1H), 5.25 (br s, 2H), 4.0 (s, 3H), 3.99 (s, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08658791B2
出典データセットuspto-grants-2014_02
ORD IDord-8cbee6570fb84ca3b9e972863db6d1d8
出典メモuspto-grants-2014_02