돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2198485생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/2198485

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물TriethylethylenediamineHCID 66040—
반응물2-(8-Trifluoromethyl-4-quinolylamino)benzoic acid hydrochloride dihydrateHCID 70546379—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
용매ChloroformHCID 6212—
용매Thionyl ChlorideHCID 24386—
생성물N-(2-diethylaminoethyl)-N-ethyl-2-(8-trifluoromethyl-4-quinolylamino)benzamideHCID 2052014046.2%

반응 단계

12.1 Grams (0.03 mole) of 2-(8-trifluoromethyl-4-quinolylamino)benzoic acid hydrochloride dihydrate were refluxed in 80 milliliters of thionyl chloride for half an hour. A yellow solid precipitated. 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'-triethylethylenediamine 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 an oil, which could not be solidified. The oil was dissolved in ether and purified by chromatography on an alumina (type H) column. Elution with ether/chloroform (50:50) gave a pale yellow oil which was kept under vacuum for four days when it gradually solidified to give 6.35 grams (46% yield) of title compound of melting point 112°-113° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04357333
출처 데이터셋uspto-grants-1982_11
ORD IDord-dd65826eaac2415690c96a7254070999
출처 메모uspto-grants-1982_11