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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1817448생성일: 2026년 10월 24일

Triethylamine → N-[1-(3,4-Difluorophenyl)ethyl]-N'-(2-fluoro-4-{[6-methoxy-7-(3-morpholinopropoxy)-4-quinolyl]oxy}phenyl)urea

https://huagongshe.com/ko/reaction/1817448

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물TriphosgeneHCID 94429—
반응물1-(3,4-Difluorophenyl)ethanamineHCID 3815974—
반응물2-Fluoro-4-{[6-methoxy-7-(3-morpholinopropoxy)-4-quinolyl]oxy}-anilineHCID 69057905—
용매ChloroformHCID 6212—
생성물N-[1-(3,4-Difluorophenyl)ethyl]-N'-(2-fluoro-4-{[6-methoxy-7-(3-morpholinopropoxy)-4-quinolyl]oxy}phenyl)ureaHCID 1037154177.2%

반응 단계

2-Fluoro-4-{[6-methoxy-7-(3-morpholinopropoxy)-4-quinolyl]oxy}-aniline (30 mg) was dissolved in chloroform (3 ml) and triethylamine (0.3 ml) to prepare a solution. A solution of triphosgene (17 mg) in chloroform (0.2 ml) was then added to the solution, and the mixture was stirred at room temperature for 25 min. Next, a solution of 1-(3,4-difluorophenyl)ethylamine (14 mg) in chloroform (0.2 ml) was added thereto, and the mixture was stirred at room temperature for 5 hr. The stirred mixture was purified by chromatography on silica gel using chloroform/methanol for development to give the title compound (27 mg, yield 60%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07598258B2
출처 데이터셋uspto-grants-2009_10
ORD IDord-ff61ca87a7114d0fa029322f29caa7a0
출처 메모uspto-grants-2009_10