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HRID 24625作成日:2026年10月26日
Ethyl Acetate → 4-(3,4-Dichlorophenyl)-6-methyl-2-phenyl-1,4-dihydropyrimidine-5-carboxylic acid (3-phenylpropyl) amide
https://huagongshe.com/reaction/24625
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ethyl Acetate | HCID 8857 | — |
| 反応物 | Benzamidine, hydrochloride | HCID 80289 | — |
| 反応物 | Sodium Acetate | HCID 517045 | — |
| 反応物 | 2-acetyl-3-(3,4-dichlorophenyl)-N-(3-phenylpropyl)acrylamide | HCID 86586027 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 4-(3,4-Dichlorophenyl)-6-methyl-2-phenyl-1,4-dihydropyrimidine-5-carboxylic acid (3-phenylpropyl) amide | HCID 20758885 | — |
反応手順
100 mg (0.266 mmol) of 2-acetyl-3-(3,4-dichlorophenyl)-N-(3-phenylpropyl)acrylamide was dissolved in 2 ml of DMF. 63.0 mg (0.400 mmol) of benzamidine hydrochloride and 26.0 mg (0.317 mmol) of sodium acetate were added to the obtained solution, and they were stirred at 60° C. overnight. Ethyl acetate was added to the reaction mixture and then the obtained mixture was washed with 1 N hydrochloric acid, saturated aqueous sodium hydrogencarbonate solution and saturated aqueous sodium chloride solution. The organic layer was dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The residue was purified by the silica gel chromatography (hexane/ethyl acetate=1/3) to obtain the title compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06855716B2 |
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| 出典データセット | uspto-grants-2005_02 |
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| ORD ID | ord-65f56a4908a64ba0a57887f19df6bc8a |
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| 出典メモ | uspto-grants-2005_02 |
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