反応式
[C:1]([O:5][C:6](=[O:23])[NH:7][CH:8]([C:15]1[CH:20]=[CH:19][C:18]([Cl:21])=[C:17]([Cl:22])[CH:16]=1)[C:9](=[O:14])N(OC)C)([CH3:4])([CH3:3])[CH3:2].[Br:24][C:25]1[CH:26]=[CH:27][C:28](I)=[C:29]([CH3:31])[CH:30]=1>>[C:1]([O:5][C:6](=[O:23])[NH:7][CH:8]([C:15]1[CH:20]=[CH:19][C:18]([Cl:21])=[C:17]([Cl:22])[CH:16]=1)[C:9]([C:28]1[CH:27]=[CH:26][C:25]([Br:24])=[CH:30][C:29]=1[CH3:31])=[O:14])([CH3:2])([CH3:3])[CH3:4]参加物
3
実験手順
The title compound was prepared from rac-[(3,4-dichloro-phenyl)-(methoxy-methyl-carbamoyl)-methyl]-carbamic acid tert-butyl ester (Intermediate 9) and 5-bromo-2-iodotoluene in analogy to Example 1a): MS (ISP): 473.9 (M+H)+ and 373.9 ((M-Boc)+H)+.
出典と根拠
- ORDレコード
- ord-104d2032f4aa4238bc658a7bdd393eed
- 出典データセット
- uspto-grants-2013_02
- 特許番号
- US08367838B2
関連ノート
読み込み中…