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HRID 1817448作成日:2026年10月25日

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

https://huagongshe.com/reaction/1817448

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物TriphosgeneHCID 94429—
反応物1-(3,4-Difluorophenyl)ethanamineHCID 3815974—
反応物2-Fluoro-4-{[6-methoxy-7-(3-morpholinopropoxy)-4-quinolyl]oxy}-anilineHCID 69057905—
溶媒ChloroformHCID 6212—
生成物N-[1-(3,4-Difluorophenyl)ethyl]-N'-(2-fluoro-4-{[6-methoxy-7-(3-morpholinopropoxy)-4-quinolyl]oxy}phenyl)ureaHCID 1037154177.2%

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07598258B2
出典データセットuspto-grants-2009_10
ORD IDord-ff61ca87a7114d0fa029322f29caa7a0
出典メモuspto-grants-2009_10