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Triethylamine → 1-benzyl-3-phenyl-1H-pyrazol-5-amine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Benzoylacetonitrile | HCID 64799 | — |
| 反応物 | Benzylhydrazine dihydrochloride | HCID 146540 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 1-benzyl-3-phenyl-1H-pyrazol-5-amine | HCID 684746 | 82.3% |
反応手順
2.9 g of α-cyanoacetophenone and 3.9 g of benzyl hydrazine dihydrochloride were suspended in 50 mL of ethanol. The reaction solution was added with 6.0 ml of triethylamine at room temperature, and heated under reflux for 4 hours. The solvent was evaporated, and the residue was added with water, extracted with ethyl acetate, and dried over anhydrous sodium sulfate. After distilling off the solvent, the residue was purified and separated by silica gel column chromatography (ethyl acetate:n-hexane=1:4), to afford 4.1 g of the title compound as a yellow needle powder.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07429609B2 |
| 出典データセット | uspto-grants-2008_09 |
| ORD ID | ord-ab741d29a856446f992b176cf69abef4 |
| 出典メモ | uspto-grants-2008_09 |