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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 11792생성일: 2026년 10월 24일

Aniline → 3-(4-Chloro-2-phenylamino-pyrimidin-5-yl)-2-(4-methoxy-phenyl)-propionic acid methyl ester

https://huagongshe.com/ko/reaction/11792

반응식

참여 물질

역할이름HCID투입량
반응물AnilineHCID 6115—
반응물DiisopropylethylamineHCID 81531—
반응물3-(2,4-Dichloro-pyrimidin-5-yl)-2-(4-methoxy-phenyl)-propionic acid methyl esterHCID 21044312—
용매1-ButanolHCID 263—
용매Ethyl AcetateHCID 8857—
생성물3-(4-Chloro-2-phenylamino-pyrimidin-5-yl)-2-(4-methoxy-phenyl)-propionic acid methyl esterHCID 21044314—

반응 조건

온도100 °C

반응 단계

To a solution of 3-(2,4-dichloro-pyrimidin-5-yl)-2-(4-methoxy-phenyl)-propionic acid methyl ester (341 mg, 1.0 mmol) (from Example 1d supra) in n-butanol (10 mL) was added aniline (200 mg, 2.15 mmol) (Aldrich) followed by N,N-diisopropylethylamine (258 mg, 2.0 mmol) (Aldrich) and the reaction mixture was heated at 100° C. for 12 hours. After cooling, the reaction mixture was diluted with ethyl acetate (100 mL) and successively washed with saturated aqueous ammonium chloride solution (30 mL), water (30 mL) and brine (30 mL), dried over anhydrous sodium sulfate, filtered, and concentrated in vacuo. The crude product was purified by flash column chromatography (silica gel) to give 3-(4-chloro-2-phenylamino-pyrimidin-5-yl)-2-(4-methoxy-phenyl)-propionic acid methyl ester. (Yield 45.1 mg, 11.3%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07098332B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-0fc233a13f9f4025aae8312c9520c8fc
출처 메모uspto-grants-2006_08