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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 616762생성일: 2026년 10월 25일

Carbamic acid, ethyl ester → 2-(3-ethoxycarbonyl-N-methyl-3-aza-propanamido)-5-chlorobenzophenone hydrochloride

https://huagongshe.com/reaction/616762

반응식

참여 물질

역할이름HCID투입량
반응물Carbamic acid, ethyl esterHCID 5641—
반응물TriethylamineHCID 8471—
반응물N-(2-benzoyl-4-chlorophenyl)-2-bromo-N-methylacetamideHCID 76099—
용매O-XyleneHCID 7237—
생성물2-(3-ethoxycarbonyl-N-methyl-3-aza-propanamido)-5-chlorobenzophenone hydrochlorideHCID 70628768158.8%

반응 단계

7.3 g of 2-(N-methyl-bromoacetamido)-5-chlorobenzophenone are heated in 200 ml of anhydrous xylene with 2.2 g of triethylamine and 2 g of urethane (NH2COOC2H5) for 12 hours under reflux whilst stirring. The triethylamine hydrobromide which has precipitated is filtered off with suction after cooling, the filtrate is extracted by shaking with three times 250 ml of water and the organic phase is dried over potassium carbonate, filtered and evaporated in vacuo. The oily residue is dissolved in 400 ml of anhydrous diethyl ether and filtered and 6.5 g of 2-(3-ethoxycarbonyl-N-methyl-3-aza-propanamido)-5-chlorobenzophenone hydrochloride (79% of theory), with a melting point of 156°-158°, are obtained by passing dry hydrogen chloride gas into the ethereal solution.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04075409
출처 데이터셋uspto-grants-1978_02
ORD IDord-6c8e637e7eac4613b994871ae2ec23ad
출처 메모uspto-grants-1978_02