돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 11793생성일: 2026년 10월 25일

6-Methoxy-3-pyridinylamine → 3-[2-(6-Methoxy-pyridin-3-ylamino)-4-phenylamino-pyrimidin-5-yl]-2-(4-methoxy-phenyl)-propionic acid methyl ester

https://huagongshe.com/reaction/11793

반응식

참여 물질

역할이름HCID투입량
반응물6-Methoxy-3-pyridinylamineHCID 81121—
반응물3-(2-Chloro-4-phenylamino-pyrimidin-5-yl)-2-(4-methoxy-phenyl)-propionic acid methyl esterHCID 21044315—
용매Ethyl AcetateHCID 8857—
생성물3-[2-(6-Methoxy-pyridin-3-ylamino)-4-phenylamino-pyrimidin-5-yl]-2-(4-methoxy-phenyl)-propionic acid methyl esterHCID 21044318—

반응 조건

온도110 °C

반응 단계

A mixture of 3-(2-chloro-4-phenylamino-pyrimidin-5-yl)-2-(4-methoxy-phenyl)-propionic acid methyl ester (40 mg, 0.1 mmol) (from Example 12b supra) and 5-amino-2-methoxypyridine (37.2 mg, 0.3 mmol) (Aldrich) was heated at 110° C. for 4 hours. After cooling, the reaction mixture was diluted with ethyl acetate (50 mL) and successively washed with saturated aqueous ammonium chloride solution (10 mL), water (10 mL) and brine (10 mL), dried over anhydrous sodium sulfate, filtered, and concentrated in vacuo to give crude 3-[2-(6-methoxy-pyridin-3-ylamino)-4-phenylamino-pyrimidin-5-yl]-2-(4-methoxy-phenyl)-propionic acid methyl ester as a dark-red solid which was used in the next step without further purification. (Yield 47.1 mg, 96.8%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07098332B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-4ec5039ca5784a64aa34542cd4a45e8b
출처 메모uspto-grants-2006_08