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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2198488생성일: 2026년 10월 24일

Dimethylformamide → N-(2-diethylaminoethyl)-N-ethyl-4-(8-trifluoromethyl-4-quinolylamino)benzamide

https://huagongshe.com/ko/reaction/2198488

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Sodium CarbonateHCID 10340—
반응물TriethylethylenediamineHCID 66040—
반응물4-(8-Trifluoromethyl-4-quinolylamino)benzoic acid hydrochloride monohydrateHCID 70545502—
촉매Thionyl ChlorideHCID 24386—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
용매ChloroformHCID 6212—
생성물N-(2-diethylaminoethyl)-N-ethyl-4-(8-trifluoromethyl-4-quinolylamino)benzamideHCID 2052014964%

반응 단계

11.6 Grams (0.03 mole) of 4-(8-trifluoromethyl-4-quinolylamino)benzoic acid hydrochloride monohydrate were refluxed in 80 milliliters of thionyl chloride containing two drops of dimethyl formamide for 11/2 hours. The thionyl chloride was evaporated off 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 4.32 grams (0.03 mole) of N,N,N'-triethyl ethylenediamine in 80 milliliters of chloroform and 31.8 grams (0.3 mole) of sodium carbonate in 100 milliliters of water. The mixture was stirred for one hour, and allowed to stand overnight. The chloroform layer was separated and dried and the chloroform evaporated to give a gummy solid, which was largely taken up in ether. On concentration of this solution a colourless solid crystallised out, which was collected to give 8.8 grams (63% yield) of N-(2-diethylaminoethyl)-N-ethyl-4-(8-trifluoromethyl-4-quinolylamino)benzamide quarter hydrate, m.p. 151°-152° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04357333
출처 데이터셋uspto-grants-1982_11
ORD IDord-040fa951ae274dd09b72d85c9cc46476
출처 메모uspto-grants-1982_11