関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Vesnarinone | HCID 5663 | — |
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | Benzyl Chloride | HCID 7503 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 1-Benzyl-6-[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]-3,4-dihydrocarbostyril hemihydrate | HCID 88739270 | — |
反応手順
6-[4-(3,4-Dimethoxybenzoyl)-1-piperazinyl]-3,4-dihydrocarbostyril (500 mg) and 70 mg of 60% oily sodium hydride were mixed with 5 ml of DMF and stirred at room temperature for 1 hour. Then, to the mixture was added dropwise 3 ml of DMF solution containing 0.17 ml of benzylchloride. After stirring for 4 hours at room temperature, the reaction mixture was poured into a large amount of water and organic substances were extracted with chloroform. The chloroform layer was washed with water and dehydrated. Chloroform was distilled off and the residue was recrystallized from ethanol to give 150 mg of 1-benzyl-6-[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]-3,4-dihydrocarbostyril hemihydrate, m.p. 131.5°-132.5° C., yellow powders. Elemental Analysis for
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04415572 |
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| 出典データセット | uspto-grants-1983_11 |
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| ORD ID | ord-9f8f5f37da7c44aab41dab4ec74ca058 |
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| 出典メモ | uspto-grants-1983_11 |
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