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HRID 245287作成日:2026年10月26日

Water → 6-Amino-2-(4-chloro-2-fluoro-3-methoxyphenyl)-5-((E)-propenyl)pyrimidine-4-carboxylic acid methyl ester

https://huagongshe.com/reaction/245287

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Cesium fluorideHCID 25953—
反応物((1E)-prop-1-en-1-yl)boronic acidHCID 6157276—
反応物6-Amino-5-bromo-2-(4-chloro-2-fluoro-3-methoxyphenyl)-pyrimidine-4-carboxylic acid methyl esterHCID 59432116—
触媒HCID 178418476HCID 178418476—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物6-Amino-2-(4-chloro-2-fluoro-3-methoxyphenyl)-5-((E)-propenyl)pyrimidine-4-carboxylic acid methyl esterHCID 59432121—

反応手順

6-Amino-5-bromo-2-(4-chloro-2-fluoro-3-methoxyphenyl)-pyrimidine-4-carboxylic acid methyl ester (400 mg, 1.02 mmol), trans-propenyl boronic acid (2132 mg, 1.54 mmol), bis(triphenylphosphine)palladium(II) dichloride (72 mg, 0.1 mmol), and cesium fluoride (311 mg, 2.05 mmol) were combined in 1,2-dimethoxyethane (2 mL) and water (2 mL) and heated at 100° C. for 15 min in a CEM microwave reactor. The cooled reaction mixture was partitioned between ethyl acetate and water; and the organic phase was dried and concentrated. The product was purified by flash chromatography on silica gel (hexane/ethyl acetate gradient) then purified again by reverse phase HPLC to yield the title compound: mp 133-135° C.: 1H NMR (CDCl3) δ 7.63 (m, 1H), 7.22 (m, 1H), 6.43 (m, 1H), 6.12 (m, 1H), 5.35 (br s, 2H), 3.99 (d, 3H), 3.94 (s, 3H), 1.94 (dd, 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-9233e964877444ffa28b2a7314cce935
出典メモuspto-grants-2014_02