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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4099생성일: 2026년 10월 23일

Triethylamine → 4-Methyl-N-[2-(6-bromo-1,2,3,4-tetrahydro-1-quinolinyl)phenyl]piperazinecarboxamide maleate

https://huagongshe.com/ko/reaction/4099

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Phenyl chloroformateHCID 15891—
반응물1-MethylpiperazineHCID 53167—
반응물Maleic AcidHCID 444266—
반응물1-(2-Aminophenyl)-6-bromo-1,2,3,4-tetrahydroquinolineHCID 13812932—
용매EthanolHCID 702—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물4-Methyl-N-[2-(6-bromo-1,2,3,4-tetrahydro-1-quinolinyl)phenyl]piperazinecarboxamide maleateHCID 7040717861%

반응 단계

A stirred solution, under nitrogen, of 1-(2-aminophenyl)-6-bromo-1,2,3,4-tetrahydroquinoline (21.2 g, 0.070 mole) and triethylamine (10.1 g, 0.10 mole) in dichloromethane (200 ml) was cooled to 0° C. Then there was added dropwise phenylchloroformate (15.7 g, 0.10 mole) at such a rate as to keep the reaction temperature below 5° C. The addition took 30 minutes. The mixture was stirred for 1 hour at ice-bath temperature, 2 hours at room temperature, and N-methylpiperazine (28.1 g, 0.28 mole) dissolved in dichloromethane (30 ml) was added dropwise over a 45 minute period. The solution was stirred for 3 hours and an additional charge of N-methylpiperazine (14.05 g, 0.14 mole) dissolved in dichloromethane (15 ml) was added, and the mixture was stirred overnight. Water (250 ml) was added with vigorous stirring. The layers were separated and the organic phase was washed twice with water, dried over anhydrous sodium sulfate and concentrated. The residue was dissolved in ethanol (200 ml), with heating, and treated with a warm solution of maleic acid (8.93 g, 0.077 mole) in ethanol (100 ml). The maleate salt was collected to give 23.2 g (61%) of product. Recrystallization from methanol afforded the analytical sample, mp 172°-174° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04723003
출처 데이터셋uspto-grants-1988_02
ORD IDord-c8d324b564d0491d91020d54c175f9db
출처 메모uspto-grants-1988_02