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HRID 721455作成日:2026年10月26日

Triethylamine → N-{4-[(6,7-Dimethoxy-4-quinazolinyl)oxy]phenyl}-N'-(3-diethylaminopropyl)thiourea

https://huagongshe.com/reaction/721455

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物ThiophosgeneHCID 10040—
反応物4-(6,7-Dimethoxyquinazolin-4-yloxy)anilineHCID 11616363—
反応物(2-Aminopropyl)diethylamineHCID 16643481—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物N-{4-[(6,7-Dimethoxy-4-quinazolinyl)oxy]phenyl}-N'-(3-diethylaminopropyl)thioureaHCID 2188998812%

反応手順

4-[(6,7-Dimethoxy-4-quinazolinyl)oxy]aniline (50 mg) was dissolved in N,N-dimethylformamide (2 ml) and triethylamine (1 ml) to prepare a solution. Thiophosgene (50 mg) was then added to the solution, and the mixture was stirred at room temperature for 6 hr. Next, N,N-diethylpropylenediamine (50 mg) was added thereto, and the mixture was further stirred at room temperature for 15 hr. Ethyl acetate was added to the reaction solution, followed by washing with water and saturated brine in that order. The organic layer was then dried over anhydrous sodium sulfate. The solvent was removed by distillation under the reduced pressure, and the residue was purified by HPLC using chloroform/methanol for development to give the title compound (10 mg, yield 12%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07135466B2
出典データセットuspto-grants-2006_11
ORD IDord-f6751be79ae04707bf0e40138e54490e
出典メモuspto-grants-2006_11