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HRID 1375833作成日:2026年10月27日

Pentylamine → N-{2-Chloro-4-[(6,7-dimethoxy-4-quinazolinyl)oxy]phenyl}-N'-pentylurea

https://huagongshe.com/reaction/1375833

反応式

関与物質

役割名称HCID仕込み量
反応物PentylamineHCID 8060—
反応物TriphosgeneHCID 94429—
反応物Sodium BicarbonateHCID 516892—
反応物2-Chloro-4-((6,7-dimethoxyquinazolin-4-yl)oxy)anilineHCID 21889899—
溶媒ChloroformHCID 6212—
溶媒TriethylamineHCID 8471—
生成物N-{2-Chloro-4-[(6,7-dimethoxy-4-quinazolinyl)oxy]phenyl}-N'-pentylureaHCID 2266709449%

反応手順

2-Chloro-4-[(6,7-dimethoxy-4-quinazolinyl)oxy]-aniline (50 mg) was dissolved in chloroform (5 ml) and triethylamine (1 ml), and a solution of triphosgene (45 mg) in chloroform was then added to the solution. The mixture was stirred at room temperature for 30 min. Next, amylamine (26 μl) was added to the reaction solution, and the mixture was stirred at room temperature for additional 30 min. A saturated aqueous sodium hydrogencarbonate solution was added to the reaction solution, and the mixture was extracted with chloroform. The chloroform layer was dried over anhydrous sodium sulfate. The solvent was removed by distillation under the reduced pressure. The residue was purified by HPLC by development with chloroform/methanol to give 33 mg (yield 49%) 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-6d7ca8244a1d4821a73c962b82d1f1c1
出典メモuspto-grants-2007_01