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Butyl isocyanate → N-(n-butylcarbamoyl)-4-ethoxycarbonyl-1-(2-pyridyl)pyrazole-5-sulfonamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Butyl isocyanate | HCID 8110 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 4-Ethoxycarbonyl-1-(2-pyridyl)pyrazole-5-sulfonamide | HCID 14049155 | — |
| 溶媒 | Acetone | HCID 180 | — |
| 生成物 | N-(n-butylcarbamoyl)-4-ethoxycarbonyl-1-(2-pyridyl)pyrazole-5-sulfonamide | HCID 19839374 | 95.2% |
反応手順
To a 70 ml acetone mixture of 8.5 g of 4-ethoxycarbonyl-1-(2-pyridyl)pyrazole-5-sulfonamide and 6.0 g of anhydrous potassium carbonate, added was 3.3 g of n-butylisocyanate at room temperature, followed by heating under reflux for 3 hours. After the reaction was completed, acetone was evaporated under reduced pressure, and then the residue was emptied into ice water to filter insolbles off, and then the filtrate was precipitated with hydrochloric acid. Crystals precipitated was filtered, washed with water and dried to obtain 10.8 g of N-(n-butylcarbamoyl)-4-ethoxycarbonyl-1-(2-pyridyl)pyrazole-5-sulfonamide. m.p.: 180° to 181° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04881965 |
| 出典データセット | uspto-grants-1989_11 |
| ORD ID | ord-f49a1aa730cb47e18a9058c083cdc71e |
| 出典メモ | uspto-grants-1989_11 |