反応式
C1([C@@H](N2CCCC2)CO)C=CC=CC=1.[C:15]1([C@H:21](O)[CH2:22][N:23]2[CH2:27][CH2:26][CH2:25][CH2:24]2)[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1.[CH3:29][NH:30][C:31]1[CH:40]=[CH:39][C:34]([C:35]([O:37][CH3:38])=[O:36])=[CH:33][CH:32]=1>>[C:15]1([C@H:21]([N:30]([C:31]2[CH:40]=[CH:39][C:34]([C:35]([O:37][CH3:38])=[O:36])=[CH:33][CH:32]=2)[CH3:29])[CH2:22][N:23]2[CH2:27][CH2:26][CH2:25][CH2:24]2)[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1参加物
4
実験手順
This was prepared from the mixture of 2-(R)-phenyl-2-(pyrrolidin-1-yl)ethanol and 1-(S)-phenyl-2-(pyrrolidin-1-yl)ethanol and methyl 4-methylaminobenzoate in 52% yield according to a procedure similar to that described in Example 1 (i).
出典と根拠
- ORDレコード
- ord-1b882b7d06eb46a5aa6fbbab842066cb
- 出典データセット
- uspto-grants-2001_11
- 特許番号
- US06313302B2
関連ノート
読み込み中…