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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 721907생성일: 2026년 10월 25일

Thionyl Chloride → N-{4-[(6,7-Dimethoxy-4-quinazolinyl)oxy]phenyl}-N'-[3-(2-methylphenyl)propanoyl]thiourea

https://huagongshe.com/reaction/721907

반응식

참여 물질

역할이름HCID투입량
반응물Thionyl ChlorideHCID 24386—
반응물3-(2-Methylphenyl)propionic acidHCID 30938—
반응물4-(6,7-Dimethoxyquinazolin-4-yloxy)anilineHCID 11616363—
반응물3-(2-Methylphenyl)propanoyl chlorideHCID 13029201—
반응물3-(2-Methylphenyl)propanoyl isothiocyanateHCID 21890701—
용매EthanolHCID 702—
용매TolueneHCID 1140—
생성물N-{4-[(6,7-Dimethoxy-4-quinazolinyl)oxy]phenyl}-N'-[3-(2-methylphenyl)propanoyl]thioureaHCID 2188995757%

반응 조건

온도100 °C

반응 단계

Toluene (20 ml) and thionyl chloride (1 ml) were added to commercially available 3-(2-methylphenyl)propanoic acid (80 mg), and the mixture was heated at 100° C. for one hr. The solvent was removed by distillation, and 3-(2-methylphenyl)propanoyl isothiocyanate was prepared using the resultant 3-(2-methylphenyl)propanoyl chloride as a starting compound according to the description of the literature. 4-[(6,7-Dimethoxy-4-quinazolinyl)oxy]aniline (50 mg) was dissolved in toluene (5 ml) and ethanol (1 ml) to prepare a solution. A solution of 3-(2-methylphenyl)propanoyl isothiocyanate in ethanol (1 ml) was then added to the solution, and the mixture was stirred at room temperature for 2 hr. The reaction solution was concentrated, and the residue was purified by chromatography on silica gel using chloroform/acetone for development to give the title compound (48 mg, yield 57%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07135466B2
출처 데이터셋uspto-grants-2006_11
ORD IDord-35ea3f3fc5f64d2f83ebe787358ae9e2
출처 메모uspto-grants-2006_11