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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 721498생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/721498

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물ThiophosgeneHCID 10040—
반응물4-[(6,7-Dimethoxyquinolin-4-yl)oxy]anilineHCID 11594543—
반응물(2-Aminopropyl)diethylamineHCID 16643481—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물N-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]phenyl}-N'-(2-diethylaminopropyl)thioureaHCID 21890370—

반응 단계

4-[(6,7-Dimethoxy-4-quinolyl)oxy]aniline (50 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 14 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 (25 mg, yield %).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07135466B2
출처 데이터셋uspto-grants-2006_11
ORD IDord-6464900ee49a4b6caef9412bed6f0731
출처 메모uspto-grants-2006_11