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Hydrochloric Acid → N-(phenylsulfonyl)-benzo-1,2,3-thiadiazole-7-carboxylic acid amide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Pyridine | HCID 1049 | — |
| 反応物 | Benzenesulfonamide | HCID 7370 | — |
| 反応物 | 1,2,3-Benzothiadiazole-7-carbonyl chloride | HCID 18377607 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | N-(phenylsulfonyl)-benzo-1,2,3-thiadiazole-7-carboxylic acid amide | HCID 54415936 | — |
反応手順
3.2 g of benzenesulfonamide are introduced at from 0°-5° C. into 50 ml of abs. pyridine and, while stirring at that temperature, a solution of 3.9 g of benzo-1,2,3-thiadiazole-7-carboxylic acid chloride in20 ml of methylene chloride is added dropwise. The mixture is stirred overnight and then poured onto ice-water, rendered slightly acidic with hydrochloric acid and extracted with methylene chloride, and the extracts are washed with water, dried and concentrated by evaporation. The residue is dissolved warm in tetrahydrofuran, treated with some silica gel, filtered, concentrated by evaporation and then recrystallised from tetrahydrofuran/hexane. The title compound resulting melts at 231°-233° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05051436 |
| 出典データセット | uspto-grants-1991_09 |
| ORD ID | ord-4fd4ff4754b84b008f3ee20d61297533 |
| 出典メモ | uspto-grants-1991_09 |