Hydrochloric Acid → (R)-2-amino-3-(pyridin-2-yl)propanamide hydrochloride
反応式
[NH2:1][C:2](=[O:19])[C@H:3]([NH:11]C(=O)OC(C)(C)C)[CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][N:6]=1.[ClH:20]>>[ClH:20].[NH2:11][C@H:3]([CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][N:6]=1)[C:2]([NH2:1])=[O:19]参加物
3
実験手順
A solution of (R)-tert-butyl 1-amino-1-oxo-3-(pyridin-2-yl)propan-2-ylcarbamate (280 mg, 0.739 mmol) in aq. 6N HCl (8 mL) was stirred at room temperature for 2 h. It was then concentrated in vacuo to give (R)-2-amino-3-(pyridin-2-yl)propanamide hydrochloride (170 mg).
後処理
- concentrationIt was then concentrated in vacuo
出典と根拠
- ORDレコード
- ord-beec39d9180e4d63b74b5c63d5450de0
- 出典データセット
- uspto-grants-2014_09
- 特許番号
- US08846928B2
反応ノート
読み込み中…