化工社化工社 化学情報印刷レポート · 研究参考用
Hydrogen chloride-ethyl acetate → 5-Fluoro-1-methyl-1H-indole-2-sulfonic acid (2-methanesulfonyl-4-piperidin-4-yl-phenyl)-amide hydrochloride
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrogen chloride-ethyl acetate | HCID 21866389 | — |
| 反応物 | 4-[4-(5-Fluoro-1-methyl-1H-indole-2-sulfonylamino)-3-methanesulfonyl-phenyl]piperidine-1-carboxylic acid tert-butyl ester | HCID 59759964 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | 5-Fluoro-1-methyl-1H-indole-2-sulfonic acid (2-methanesulfonyl-4-piperidin-4-yl-phenyl)-amide hydrochloride | HCID 24967039 | — |
反応手順
A solution of 4-[4-(5-fluoro-1-methyl-1H-indole-2-sulfonylamino)-3-methanesulfonyl-phenyl]-piperidine-1-carboxylic acid tert-butyl ester (0.019 g) was treated with 2.5 N HCl/ethyl acetate (2.5 ml). The reaction mixture was stirred at rt for 3 h, then ether (20 ml) was added. The precipitate was collected, washed with ether and dried under high vacuum over P2O5 to produce the title compound (0.014 g) as an off-white amorphous powder. MS (ISN): 464.0 (M−H)−
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08158655B2 |
| 出典データセット | uspto-grants-2012_04 |
| ORD ID | ord-502df8c6ead4455bb40016696d5a237d |
| 出典メモ | uspto-grants-2012_04 |