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HRID 1375778作成日:2026年10月27日

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

https://huagongshe.com/reaction/1375778

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 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US07169789B2
出典データセットuspto-grants-2007_01
ORD IDord-263184a99e0f44e3a30224fdb6040f40
出典メモuspto-grants-2007_01