4-Fluorobenzoyl chloride → HCID 22283414, compound
Reaction equation
[C:1]([NH:4][C:5]1[C:13]2[S:12][C:11]([NH2:14])=[N:10][C:9]=2[C:8]([O:15][CH3:16])=[CH:7][CH:6]=1)(=[O:3])[CH3:2].[F:17][C:18]1[CH:26]=[CH:25][C:21]([C:22](Cl)=[O:23])=[CH:20][CH:19]=1>>[C:1]([NH:4][C:5]1[C:13]2[S:12][C:11]([NH:14][C:22](=[O:23])[C:21]3[CH:25]=[CH:26][C:18]([F:17])=[CH:19][CH:20]=3)=[N:10][C:9]=2[C:8]([O:15][CH3:16])=[CH:7][CH:6]=1)(=[O:3])[CH3:2]Participants
3
Procedure
Using 7-acetylamino-4-methoxy-benzothiazol-2-ylamine and 4-fluoro-benzoyl chloride the title compound was obtained as a tan solid (25% yield), MS: m/e=359.1 (M+H+).
Sources & evidence
- ORD record
- ord-69c30a3280934b1f818583ed4f8978fb
- Source dataset
- uspto-grants-2008_01
- Patent number
- US07317007B2
Reaction notes
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