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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Carbamic acid, ethyl ester | HCID 5641 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | N-(2-benzoyl-4-chlorophenyl)-2-bromo-N-methylacetamide | HCID 76099 | — |
| 溶媒 | O-Xylene | HCID 7237 | — |
| 生成物 | 2-(3-ethoxycarbonyl-N-methyl-3-aza-propanamido)-5-chlorobenzophenone hydrochloride | HCID 70628768 | 158.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04075409 |
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| 出典データセット | uspto-grants-1978_02 |
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| ORD ID | ord-6c8e637e7eac4613b994871ae2ec23ad |
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| 出典メモ | uspto-grants-1978_02 |
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