2-Acetylbenzo[b]thiophene → HCID 66582176, compound
Reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[O:12][N:11]=[C:10]([CH3:13])[C:9]=2[NH2:14])=[CH:4][CH:3]=1.[S:15]1[C:19]([C:20](=O)[CH3:21])=[CH:18][C:17]2[CH:23]=[CH:24][CH:25]=[CH:26][C:16]1=2>>[S:15]1[C:19]([CH:20]([NH:14][C:9]2[C:10]([CH3:13])=[N:11][O:12][C:8]=2[C:5]2[CH:4]=[CH:3][C:2]([Br:1])=[CH:7][CH:6]=2)[CH3:21])=[CH:18][C:17]2[CH:23]=[CH:24][CH:25]=[CH:26][C:16]1=2Participants
3
Procedure
Prepared according to the procedure described in Example 24, Step 1, using 5-(4-bromo-phenyl)-3-methyl-isoxazol-4-ylamine and 1-benzo[b]thiophen-2-yl-ethanone.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-b060c3a4f5e84ae59342f8be70639dad
- Source dataset
- uspto-grants-2015_07
- Patent number
- US09090573B2
Reaction notes
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