反応式
C([O:8][C:9]1[C:10](=[O:16])[CH:11]=[C:12]([CH3:15])[NH:13][CH:14]=1)C1C=CC=CC=1>CO.O.[Pd]>[OH:8][C:9]1[C:10](=[O:16])[CH:11]=[C:12]([CH3:15])[NH:13][CH:14]=1参加物
5
実験手順
A solution of 5-benzyloxy-2-methyl-1H-pyridin-4-one (2 g, 9.29 mmol) in methanol (30 ml) and water (8 ml) was placed in a Parr bottle. 10% Pd/C was added and the mixture was hydrogenated at 50 psi for 3 hours. A bed of CELITE™ was placed on a sintered glass, and washed with 0.1N HCl and then water. The content in the Parr bottle was removed from the Parr hydrogenator and flushed with nitrogen. The solution was filtered under suction. The filtrate was evaporated to give a white solid (820 mg, 70% yield).
後処理
- washwashed with 0.1N HCl
- customThe content in the Parr bottle was removed from the Parr hydrogenator
- customflushed with nitrogen
- filtrationThe solution was filtered under suction
- customThe filtrate was evaporated
出典と根拠
- ORDレコード
- ord-6b12319e6d6a4f97a51545aa6925c4e6
- 出典データセット
- uspto-grants-2011_09
- 特許番号
- US08026261B2
関連ノート
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