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HRID 1008341作成日:2026年10月25日

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

https://huagongshe.com/reaction/1008341

反応式

関与物質

役割名称HCID仕込み量
反応物PropylamineHCID 7852—
反応物TriethylamineHCID 8471—
反応物TriphosgeneHCID 94429—
反応物4-{[7-(Benzyloxy)-6-methoxy-4-quinazolinyl]oxy}-2-chloroanilineHCID 22667232—
溶媒ChloroformHCID 6212—
生成物N-(4-{[7-(Benzyloxy)-6-methoxy-4-quinazolinyl]oxy}-2-chlorophenyl)-N'-propylureaHCID 2266703563%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06797823B1
出典データセットuspto-grants-2004_09
ORD IDord-c1859057389c4602b7c7592af4c438bc
出典メモuspto-grants-2004_09