化工社化工社 化学情報印刷レポート · 研究参考用
Thionyl Chloride → 2-Trifluoromethyl-n-[4-(6-methoxy-1,3-benzothiazol-2-yl)phenyl]-4-(methoxy)benzamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Thionyl Chloride | HCID 24386 | — |
| 反応物 | 4-(6-Methoxy-1,3-benzothiazol-2-yl)aniline | HCID 391870 | — |
| 反応物 | 4-methoxy-2-(trifluoromethyl)benzoic Acid | HCID 2775294 | — |
| 反応物 | 4-Methoxy-3-(trifluoromethyl)benzoyl chloride | HCID 2775298 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 生成物 | 2-Trifluoromethyl-n-[4-(6-methoxy-1,3-benzothiazol-2-yl)phenyl]-4-(methoxy)benzamide | HCID 67240460 | 46% |
反応手順
A stirred mixture of 4-methoxy-2-trifluoromethylbenzoic acid (0.50 g, 2.27 mmol) and thionyl chloride (9 ml) was heated under reflux for 4 h. After cooling to room temperature, the excess reagent was removed under reduced pressure to give crude acid chloride. The amide was prepared as described in the Amide Coupling section using the crude 4-methoxy-5-trifluoromethylbenzoyl chloride and 2-(4-aminophenyl)-6-methoxybenzo thiazole (0.58 g, 2.27 mmol) in dry pyridine (15 ml) to give the title compound (0.478 g, 46%) as pale yellow needles after work-up and recrystallisation from acetic acid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08895313B2 |
| 出典データセット | uspto-grants-2014_11 |
| ORD ID | ord-d3daccfe68cc4410bdbac4b9d5eab2e2 |
| 出典メモ | uspto-grants-2014_11 |