反応式
C([N:8]1[CH2:13][C:12](=[O:14])[NH:11][C:10](=[O:15])[CH2:9]1)C1C=CC=CC=1.[ClH:16]>CO.O.CO.[Pd]>[ClH:16].[NH:11]1[C:12](=[O:14])[CH2:13][NH:8][CH2:9][C:10]1=[O:15]参加物
6
実験手順
To a solution of 4-benzylpiperazine-2,6-dione (which may be prepared in accordance with the experimental described in Example 4, step 1; 2.0 g, 9.8 mmol) in a mixture of methanol/H2O (65 mL/28 mL) were added a solution of HCl 1N in methanol (23.8 mL) and Pd/C (10% wet, 0.2% wt., 400 mg). The reaction mixture was degassed 3 times with hydrogen/vacuum prior to its overnight stirring under hydrogen (P=1 atm). The reaction mixture was then filtered on Clarcel® and washed with methanol. The filtrate was finally concentrated to dryness and the residue was precipitated from a mixture of methanol and ether. The title product was obtained as a beige solid (418 mg, 28%).
後処理
- customThe reaction mixture was degassed 3 times with hydrogen/vacuum
- filtrationThe reaction mixture was then filtered on Clarcel®
- washwashed with methanol
- concentrationThe filtrate was finally concentrated to dryness
- customthe residue was precipitated from a mixture of methanol and ether
出典と根拠
- ORDレコード
- ord-b0b194addb7145c8b35b2a3dd49b637c
- 出典データセット
- uspto-grants-2014_01
- 特許番号
- US08623865B2
関連ノート
読み込み中…