1-Pyrrolidineacetamide, 3-hydroxy-2-oxo-, (+-)- → (R/S)-2-(3-hydroxy-2-oxo-1-pyrrolidinyl)propionamide
反応式
[OH:1][CH:2]1[CH2:6][CH2:5][N:4]([CH2:7][C:8]([NH2:10])=[O:9])[C:3]1=[O:11].O[CH:13]1CCN(C(C)C(OCC)=O)C1=O>>[OH:1][CH:2]1[CH2:6][CH2:5][N:4]([CH:7]([CH3:13])[C:8]([NH2:10])=[O:9])[C:3]1=[O:11]参加物
3
実験手順
According to the process described in paragraph (b) of Example 1, from ethyl (R/S)-2-(3-hydroxy-2-oxo-1-pyrrolidinyl)propionate there is obtained, after chromatographic filtration on silica gel (granular size 0.2-0.5 mm), elution with acetonitrile/ethanol (1:1) and crystallization from acetonitrile, (R/S)-2-(3-hydroxy-2-oxo-1-pyrrolidinyl)propionamide of melting point 139°-141°.
後処理
- customthere is obtained
- filtrationafter chromatographic filtration
- washon silica gel (granular size 0.2-0.5 mm), elution
- customwith acetonitrile/ethanol (1:1) and crystallization from acetonitrile, (R/S)-2-(3-hydroxy-2-oxo-1-pyrrolidinyl)propionamide of melting point 139°-141°
出典と根拠
- ORDレコード
- ord-662c44b38db042d5a82f56d7f4bf9fe2
- 出典データセット
- uspto-grants-1984_10
- 特許番号
- US04476308
反応ノート
読み込み中…