関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Chlorosulfonic acid | HCID 24638 | — |
| 反応物 | Thieno(2,3-b)pyridine | HCID 289928 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 生成物 | Thieno[2,3-b]pyridine-3-sulfonyl chloride | HCID 18614041 | — |
反応手順
A solution of thieno[2,3-b]pyridine (0.70 g, 5.2 mmoles), prepared as described in Example 1 (A), in chlorosulfonic acid, (7 ml) was heated to 100° C. for 15 minutes, then cooled to ambient temperature and added to ice (100 ml). The pH of the aqueous phase as adjusted to 8 with sat. NaHCO3, then extracted with CHCl3 (2×125 ml). The organic phase was dried (MgSO4), filtered and concentrated to collect 0.95 g (78%) of the title compound as a tan solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US06545014B2 |
|---|
| 出典データセット | uspto-grants-2003_04 |
|---|
| ORD ID | ord-71052d30862c4bfa9eac36eb5b8295ed |
|---|
| 出典メモ | uspto-grants-2003_04 |
|---|