돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2198487생성일: 2026년 10월 25일

Dimethylformamide → N-(1-Ethyl-3-piperidyl)-4-(8-trifluoromethyl-4-quinolylamino)benzamide

https://huagongshe.com/reaction/2198487

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Sodium CarbonateHCID 10340—
반응물3-amino-N-ethylpiperidineHCID 98094—
반응물4-(8-Trifluoromethyl-4-quinolylamino)benzoic acid hydrochloride monohydrateHCID 70545502—
촉매Thionyl ChlorideHCID 24386—
용매WaterHCID 962—
용매ChloroformHCID 6212—
생성물N-(1-Ethyl-3-piperidyl)-4-(8-trifluoromethyl-4-quinolylamino)benzamideHCID 2052013937%

반응 단계

11.6 Grams (0.03 mole) of 4-(8-trifluoromethyl-4-quinolylamino)benzoic acid hydrochloride monohydrate were refluxed in thionyl chloride containing a few drops of dimethyl formamide for one hour. The thionyl chloride was evaporated and 50 milliliters of benzene were added and evaporated. The resulting acid chloride hydrochloride was added in portions with stirring to a cooled mixture of 3.84 grams (0.03 mole) of 3-amino-1-ethylpiperidine in 80 milliliters of chloroform and 31.8 grams (0.3 mole) of sodium carbonate in 100 milliliters of water. The product began to precipitate almost at once, and the mixture was stirred vigorously for two hours, and allowed to stand overnight. Filtration gave a solid which was stirred in water, collected and dried. The resulting solid was dissolved in an ethanol:chloroform mixture and chromatographed on an alumine column made up in chloroform. Elution with chloroform gave 4.9 grams (37%) of title compound as a pale yellow solid, melting point 177°-178° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04357333
출처 데이터셋uspto-grants-1982_11
ORD IDord-3328dc48c13a419da6dfce9ddbcfcab7
출처 메모uspto-grants-1982_11