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1-Fluoro-3-isocyanato-5-(trifluoromethyl)benzene → 2-acetylamino-4-{4-[3-(3-fluoro-5-trifluoromethylphenyl)ureido]phenyl}-1H-pyrrole-3-carboxamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1-Fluoro-3-isocyanato-5-(trifluoromethyl)benzene | HCID 3445672 | — |
| 反応物 | 2-acetylamino-4-(4-aminophenyl)-1H-pyrrole-3-carboxamide | HCID 69061860 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 2-acetylamino-4-{4-[3-(3-fluoro-5-trifluoromethylphenyl)ureido]phenyl}-1H-pyrrole-3-carboxamide | HCID 57845551 | 41.8% |
反応手順
0.061 cm3 (0.426 mmol) of 3-fluoro-5-trifluoromethylphenyl isocyanate is added at room temperature to a suspension of 100 mg (0.387 mmol) of 2-acetylamino-4-(4-aminophenyl)-1H-pyrrole-3-carboxamide in 5 cm3 of anhydrous tetrahydrofuran. The reaction medium is stirred at room temperature for 24 hours, cooled in a water-ice bath and then filtered on sintered glass. The solid collected is washed with a small amount of dichloromethane and cyclohexane and then dried under vacuum. 75 mg of 2-acetylamino-4-{4-[3-(3-fluoro-5-trifluoromethylphenyl)ureido]phenyl}-1H-pyrrole-3-carboxamide are obtained in the form of a beige solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07592365B2 |
| 出典データセット | uspto-grants-2009_09 |
| ORD ID | ord-4cd57cb910dd432b8625224f499fdc1c |
| 出典メモ | uspto-grants-2009_09 |