1-(3-Aminobenzo[B]thiophen-2-YL)ethanone → (E)-2-cinnamoyl-3-amino-6-fluoro-benzo[b]thiophene
Reaction equation
[NH2:1][C:2]1[C:3]2[CH:13]=[CH:12][C:11]([F:14])=[CH:10][C:4]=2[S:5][C:6]=1[C:7](=[O:9])[CH3:8].N[C:16]1[C:17]2[CH:27]=[CH:26][CH:25]=[CH:24][C:18]=2SC=1C(=O)C>>[C:7]([C:6]1[S:5][C:4]2[CH:10]=[C:11]([F:14])[CH:12]=[CH:13][C:3]=2[C:2]=1[NH2:1])(=[O:9])/[CH:8]=[CH:16]/[C:17]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:18]=1Participants
3
Procedure
The procedure was similar to step S3C, while the starting material was 17B in stead of 3B.
Sources & evidence
- ORD record
- ord-21f0ccd74d854158a89c94db9ce12426
- Source dataset
- uspto-grants-2015_03
- Patent number
- US08969373B2
Reaction notes
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