反応式
O1C2C=CC(C[C:11](Cl)=[O:12])=CC=2OC1.CO[C:16]1[CH:21]=[CH:20][C:19]([O:22]C)=[CH:18][C:17]=1[C:24]1[S:28][C:27]([NH:29][C:30](=[O:39])[C:31]2[C:36]([F:37])=[CH:35][CH:34]=[CH:33][C:32]=2[F:38])=[N:26][C:25]=1[CH3:40].[Br:41]Br>>[Br:41][C:21]1[C:20]2[O:12][CH2:11][O:22][C:19]=2[CH:18]=[C:17]([C:24]2[S:28][C:27]([NH:29][C:30](=[O:39])[C:31]3[C:36]([F:37])=[CH:35][CH:34]=[CH:33][C:32]=3[F:38])=[N:26][C:25]=2[CH3:40])[CH:16]=1参加物
4
実験手順
Compound 56 was prepared from 2-(benzo[d][1,3]dioxol-5-yl)acetyl chloride in the similar manner as described for the preparation of Compound 55 with the exception that 2 equivalents of bromine was used.
出典と根拠
- ORDレコード
- ord-4cbb285ef03145899b6a62dfe55242cb
- 出典データセット
- uspto-grants-2013_06
- 特許番号
- US08455658B2
関連ノート
読み込み中…