反応式
[CH2:1]([O:5][C:6]1[CH:14]=[CH:13][C:9]([C:10](Cl)=[O:11])=[C:8]([CH2:15][CH2:16]Cl)[CH:7]=1)[CH2:2][CH2:3][CH3:4].[C:18]([O:22][C:23](=[O:39])[NH:24][CH2:25][C@H:26]1[CH2:30][CH2:29][N:28]([C:31]2[CH:36]=[CH:35][C:34]([NH2:37])=[CH:33][C:32]=2[F:38])[CH2:27]1)([CH3:21])([CH3:20])[CH3:19]>>[C:18]([O:22][C:23](=[O:39])[NH:24][CH2:25][C@H:26]1[CH2:30][CH2:29][N:28]([C:31]2[CH:36]=[CH:35][C:34]([N:37]3[CH2:16][CH2:15][C:8]4[C:9](=[CH:13][CH:14]=[C:6]([O:5][CH2:1][CH2:2][CH2:3][CH3:4])[CH:7]=4)[C:10]3=[O:11])=[CH:33][C:32]=2[F:38])[CH2:27]1)([CH3:21])([CH3:19])[CH3:20]参加物
3
実験手順
4-Butoxy-2-(2-chloroethyl)benzoyl chloride was reacted by method A with [(R)-1-(4-amino-2-fluorophenyl)pyrrolidin-3-yl]methylcarbamic acid tert-butyl ester. The product with the molecular weight of 511.64 (C29H38FN3O4) was obtained in this way; MS (ESI): 512 (M+H+).
後処理
- customThe product with the molecular weight of 511.64 (C29H38FN3O4) was obtained in this way
出典と根拠
- ORDレコード
- ord-69de3f758ca34cd18c6b024b8196e36a
- 出典データセット
- uspto-grants-2014_09
- 特許番号
- US08822495B2
関連ノート
読み込み中…