Hydrochloric Acid → 2-(6-Aminopyridin-3-yl)-2-methylpropanoic acid hydrochloride
反応式
CC1(C)[N:7]([C:8]2[N:13]=[CH:12][C:11]([C:14]([CH3:21])([CH3:20])[C:15]([O:17]CC)=[O:16])=[CH:10][CH:9]=2)C(=O)C2C=CC=CC=2O1.[ClH:28]>>[ClH:28].[NH2:7][C:8]1[N:13]=[CH:12][C:11]([C:14]([CH3:21])([CH3:20])[C:15]([OH:17])=[O:16])=[CH:10][CH:9]=1参加物
3
反応条件
- 温度
- 100 °C
実験手順
A stirred mixture of ethyl 2-[6-(2,2-dimethyl-4-oxo-4H-1,3-benzoxazin-3-yl)-pyridin-3-yl]-2-methylpropanoate (13.3 g, 36.1 mmol) in concentrated HCl (50 mL) was heated at 100° C. overnight. After cooling to ambient temperature, the reaction mixture was concentrated in vacuo and the residue washed exhaustively with chloroform to give the title compound as a solid (6.90 g).
後処理
- temperatureAfter cooling to ambient temperature
- concentrationthe reaction mixture was concentrated in vacuo
- washthe residue washed exhaustively with chloroform
出典と根拠
- ORDレコード
- ord-478ebf1ddeb24a4ca5e5ee936b248136
- 出典データセット
- uspto-grants-2000_08
- 特許番号
- US06110931
反応ノート
読み込み中…