戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 616762作成日:2026年10月26日

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

https://huagongshe.com/reaction/616762

反応式

関与物質

役割名称HCID仕込み量
反応物Carbamic acid, ethyl esterHCID 5641—
反応物TriethylamineHCID 8471—
反応物N-(2-benzoyl-4-chlorophenyl)-2-bromo-N-methylacetamideHCID 76099—
溶媒O-XyleneHCID 7237—
生成物2-(3-ethoxycarbonyl-N-methyl-3-aza-propanamido)-5-chlorobenzophenone hydrochlorideHCID 70628768158.8%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04075409
出典データセットuspto-grants-1978_02
ORD IDord-6c8e637e7eac4613b994871ae2ec23ad
出典メモuspto-grants-1978_02