돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 721462생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/721462

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물ThiophosgeneHCID 10040—
반응물(2-Aminopropyl)diethylamineHCID 16643481—
반응물4-[(6,7-Dimethoxy-4-quinolyl)oxy]-2,3-dimethylanilineHCID 21890439—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물N-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]-2,3-dimethylphenyl}-N'-(3-diethylaminopropyl)thioureaHCID 2189060945%

반응 단계

4-[(6,7-Dimethoxy-4-quinolyl)oxy]-2,3-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 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 (36 mg, yield 45%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07135466B2
출처 데이터셋uspto-grants-2006_11
ORD IDord-f52d6f4111274753834c3f9763d514d6
출처 메모uspto-grants-2006_11