2-Piperidinecarboxamide, (R)- → Ammonia
反応式
[NH:1]1[CH2:6][CH2:5][CH2:4][CH2:3][C@@H:2]1[C:7]([NH2:9])=[O:8].[CH2:10]1[CH:12]([CH:13](O)C#[N:15])[CH2:11]1>>[CH:12]1([CH2:13][N:1]2[CH2:6][CH2:5][CH2:4][CH2:3][C@@H:2]2[C:7]([NH2:9])=[O:8])[CH2:10][CH2:11]1.[NH3:15]参加物
4
実験手順
The title compound was prepared by a similar method to preparation 57 from (2R)-2-piperidinecarboxamide [see preparation 68] and cyclopropylcarboxaldehye. The crude compound was purified by column chromatography on silica gel using dichloromethane:methanol:0.88 ammonia (92:7:1) as the eluant to afford the product as a white solid, (44%).
後処理
- customThe crude compound was purified by column chromatography on silica gel
出典と根拠
- ORDレコード
- ord-6963233142bf412bb88afc8a3ea64a00
- 出典データセット
- uspto-grants-2001_01
- 特許番号
- US06180627B2
反応ノート
読み込み中…