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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 721466생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/721466

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물ThiophosgeneHCID 10040—
반응물(2-Aminopropyl)diethylamineHCID 16643481—
반응물4-((6,7-Dimethoxyquinolin-4-yl)oxy)-2,5-dimethylanilineHCID 21890421—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물N-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]-2,5-dimethylphenyl}-N'-(3-diethylaminopropyl)thioureaHCID 2189084149%

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07135466B2
출처 데이터셋uspto-grants-2006_11
ORD IDord-60117da95c1f4c6c90c299545c39ad9c
출처 메모uspto-grants-2006_11