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4-Amino-3-methylbenzenesulfonic acid → Pyridinium 4-(acetylamino)-3-methylbenzenesulfonate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-Amino-3-methylbenzenesulfonic acid | HCID 7384 | — |
| 反応物 | Acetic Anhydride | HCID 7918 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 生成物 | Pyridinium 4-(acetylamino)-3-methylbenzenesulfonate | HCID 22251061 | — |
反応手順
For example, commercially available 2-aminotoluene-5-sulfonic acid was allowed to react with acetic anhydride in pyridine to afford pyridinium 4-(acetylamino)-3-methylbenzenesulfonate (Scheme V). The resulting salt was then allowed to react with sodium hydroxide to afford the corresponding sodium salt, sodium 4-(acetylamino)-3-methylbenzenesulfonate. The salt was then allowed to react with thionyl chloride to afford the intermediate sulfonyl chloride, followed by reaction with ammonia and subsequent deprotection by reaction with aqueous hydrochloric acid in ethanol to afford the desired sulfonamide.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06995283B2 |
| 出典データセット | uspto-grants-2006_02 |
| ORD ID | ord-5e2ea6ffbfc54c3993c8992b4a289042 |
| 出典メモ | uspto-grants-2006_02 |