関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | Sodium Acetate | HCID 517045 | — |
| 反応物 | Aminomalononitrile p-toluenesulphonate | HCID 563049 | — |
| 反応物 | 3-amino-N-cyclopropyl-4-methylbenzamide | HCID 11983854 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Ethyl orthoformate | HCID 31214 | — |
| 生成物 | 3-[5-amino-4-(4-methyl-benzoyl)-pyrazol-1-yl]-N-cyclopropyl-4-methyl-benzamide | HCID 11164703 | 30% |
反応手順
A mixture of 3-amino-N-cyclopropyl-4-methyl-benzamide 1 (380 mg, 2.0 mmol) in 2.0 mL of triethyl orthoformate was stirred at 120° C. in microwave for 20 minutes. The solvent was removed under reduced pressure. The residue was dissolved in 5 mL of acetic acid and then was added aminomalononitrile p-toluenesulfonate (506 mg, 2.0 mmol) and sodium acetate (164 mg, 2.0 mmol). The reaction mixture was stirred at room temperature overnight. The mixture was diluted with 20 mL of water and then its pH was adjusted to 8.0 by aqueous NaOH. The resulting mixture was extracted with EtOAc (3×50 mL). The combined organic layers were washed with water (10 mL) and brine (10 mL), dried over MgSO4, filtered and concentrated in vacuo evaporated. The residue was purified by silica gel column chromatography (10/1, methylene chloride:methanol) to give 3-(5-amino-4-cyano-imidazol-1-yl)-N-cyclopropyl-4-methyl-benzamide 3 as a colorless solid (170 mg, 30%). HPLC (4 minute gradient) tR=1.39 min; MS m/z 282 [M+H].
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07863314B2 |
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| 出典データセット | uspto-grants-2011_01 |
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| ORD ID | ord-58d9bc116e3d41c3b7a02aebc0b2eda8 |
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| 出典メモ | uspto-grants-2011_01 |
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