1,4-Dioxane hydrochloride → rel-[(3R,4S)-3-fluoro-4-methoxypiperidin-4-yl]methanol hydrochloride
反応式
[ClH:1].O1CCOCC1.[F:8][C@H:9]1[C@:14]([CH2:17][OH:18])([O:15][CH3:16])[CH2:13][CH2:12][N:11](C(OC(C)(C)C)=O)[CH2:10]1>>[ClH:1].[F:8][C@H:9]1[C@:14]([CH2:17][OH:18])([O:15][CH3:16])[CH2:13][CH2:12][NH:11][CH2:10]1参加物
3
実験手順
4M hydrochloric acid/dioxane solution (11.4 ml) was added to tert-butyl rel-(3R,4S)-3-fluoro-4-(hydroxymethyl)-4-methoxypiperidine-1-carboxylate (800 mg) and stirring was performed at room temperature for 1 hour. Concentration under reduced pressure gave rel-[(3R,4S)-3-fluoro-4-methoxypiperidin-4-yl]methanol hydrochloride (606 mg).
後処理
- concentrationConcentration under reduced pressure
出典と根拠
- ORDレコード
- ord-32a86b90b6574e46927b6e095637c6ef
- 出典データセット
- uspto-grants-2014_09
- 特許番号
- US08822688B2
反応ノート
読み込み中…