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6-Chloro-2-benzothiazolamine → N-(6-Chloro-2-benzothiazolyl)-8-hydroxy-7-quinolinecarboxamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 6-Chloro-2-benzothiazolamine | HCID 7226 | — |
| 反応物 | Phosphorus trichloride | HCID 24387 | — |
| 反応物 | 8-Hydroxyquinoline-7-carboxylic Acid | HCID 231363 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | N-(6-Chloro-2-benzothiazolyl)-8-hydroxy-7-quinolinecarboxamide | HCID 18372733 | 54.9% |
反応手順
A solution of 8-hydroxyquinoline-7-carboxylic acid (0.30 g) of Preparation 1 in 75 mL xylenes is heated to reflux. PCl3 (0.07 mL) is added dropwise and the mixture stirred for 15 minutes. 2-Amino-6-chlorobenzothiazole (0.31 g) is added in one portion and the reaction refluxed overnight. The reaction is cooled to room temperature and H2O is added to quench excess PCl3. After stirring the solution for 30 minutes, a yellow solid is filtered, dried, and recrystallized from DMSO to give the title product (0.31 g).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06310211B1 |
| 出典データセット | uspto-grants-2001_10 |
| ORD ID | ord-16d3c32698fa40ed92a53875ed296c77 |
| 出典メモ | uspto-grants-2001_10 |