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HRID 721466作成日:2026年10月27日

Triethylamine → N-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]-2,5-dimethylphenyl}-N'-(3-diethylaminopropyl)thiourea

https://huagongshe.com/reaction/721466

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(2-Aminopropyl)diethylamineHCID 16643481—
反応物4-((6,7-Dimethoxyquinolin-4-yl)oxy)-2,5-dimethylanilineHCID 21890421—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物N-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]-2,5-dimethylphenyl}-N'-(3-diethylaminopropyl)thioureaHCID 2189084149%

反応手順

4-[(6,7-Dimethoxy-4-quinolyl)oxy]-2,5-dimethylaniline (51 mg) was dissolved in N,N-dimethylformamide (2 ml) and triethylamine (1 ml) to prepare a solution. Thiophosgene (51 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 16 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 (38 mg, yield 49%).

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-60117da95c1f4c6c90c299545c39ad9c
出典メモuspto-grants-2006_11