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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1008341생성일: 2026년 10월 24일

Propylamine → N-(4-{[7-(Benzyloxy)-6-methoxy-4-quinazolinyl]oxy}-2-chlorophenyl)-N'-propylurea

https://huagongshe.com/ko/reaction/1008341

반응식

참여 물질

역할이름HCID투입량
반응물PropylamineHCID 7852—
반응물TriethylamineHCID 8471—
반응물TriphosgeneHCID 94429—
반응물4-{[7-(Benzyloxy)-6-methoxy-4-quinazolinyl]oxy}-2-chloroanilineHCID 22667232—
용매ChloroformHCID 6212—
생성물N-(4-{[7-(Benzyloxy)-6-methoxy-4-quinazolinyl]oxy}-2-chlorophenyl)-N'-propylureaHCID 2266703563%

반응 단계

4-{[7-(Benzyloxy)-6-methoxy-4-quinazolinyl]oxy}-2-chloroaniline (12.2 g) was dissolved in anhydrous chloroform. Triethylamine (8.4 ml) was then added to the solution, and the mixture was stirred at room temperature. Separately, triphosgene (4.5 g) was dissolved in anhydrous chloroform (12 ml), and the solution was added dropwise to the mixed solution. The mixture was stirred at room temperature for 20 min, and n-propylamine (4.9 ml) was then added thereto, followed by stirring at room temperature for additional one hr to precipitate a white solid. This solid was collected by filtration and was then washed with chloroform to give rib 9.4 g (yield 63%) of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06797823B1
출처 데이터셋uspto-grants-2004_09
ORD IDord-c1859057389c4602b7c7592af4c438bc
출처 메모uspto-grants-2004_09