돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 441241생성일: 2026년 10월 25일

Methanol → 1-{4-[2-(4-Methylphenyl)benzoylamino]benzoyl}-1,2,3,4-tetrahydroquinoline

https://huagongshe.com/reaction/441241

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물TriethylamineHCID 8471—
반응물(4-aminophenyl)(3,4-dihydroquinolin-1(2H)-yl)methanoneHCID 2984117—
용매ChloroformHCID 6212—
용매DichloromethaneHCID 6344—
생성물1-{4-[2-(4-Methylphenyl)benzoylamino]benzoyl}-1,2,3,4-tetrahydroquinolineHCID 10503544—

반응 단계

To a solution of 2-(4-methylphenyl)benzoic acid (140 mg) in dichloromethane (5 ml) were added oxalyl chloride (133 mg) and a few drop of N,N-dimethylformamide and the solution was stirred at ambient temperature for 2 hours. Dichloromethane was evaporated in vacuo to give an acid chloride as an oil and the oil was added to a mixture of 1-(4-aminobenzoyl)-1,2,3,4-tetrahydroquinoline (166 mg) and triethylamine (0.14 ml) in dichloromethane (20 ml). The mixture was stirred at ambient temperature for 2 hours, washed successively with diluted hydrogen chloride, water and brine and dried over magnesium sulfate. The solvent was evaporated in vacuo to give an oil and the oil was subjected to silica gel column (30 g, 1% methanol in chloroform) to give 1-{4-[2-(4-methylphenyl)benzoylamino]benzoyl}-1,2,3,4-tetrahydroquinoline (202 mg) as an amorphous solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05521170
출처 데이터셋uspto-grants-1996_05
ORD IDord-f4e7c6fdea184ac1af3418aa2524b819
출처 메모uspto-grants-1996_05