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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 495031생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/495031

반응식

참여 물질

역할이름HCID투입량
반응물Cesium fluorideHCID 25953—
반응물Methyl 6-amino-2,5-dichloropyrimidine-4-carboxylateHCID 312630—
반응물2-(4-Chloro-2-fluoro-3-methoxyphenyl)-1,3,2-dioxaborinaneHCID 57782419—
촉매HCID 178418476HCID 178418476—
용매WaterHCID 962—
용매1,2-DimethoxyethaneHCID 8071—
생성물6-Amino-2-(4-chloro-2-fluoro-3-methoxyphenyl)-5-chloropyrimidine-4-carboxylic acid methyl esterHCID 1665680153.5%

반응 조건

온도80 °C

반응 단계

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):

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07538214B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-2a908c9352944840aa079bc20e42e430
출처 메모uspto-grants-2009_05