Isobutyryl chloride → HCID 11702640, compound
Reaction equation
[CH3:1][N:2]1[C:6]([C:7]2[S:11][C:10]([NH2:12])=[N:9][C:8]=2[C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)=[N:5][N:4]=[N:3]1.[C:19](Cl)(=[O:23])[CH:20]([CH3:22])[CH3:21]>>[CH3:1][N:2]1[C:6]([C:7]2[S:11][C:10]([NH:12][C:19](=[O:23])[CH:20]([CH3:22])[CH3:21])=[N:9][C:8]=2[C:13]2[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=2)=[N:5][N:4]=[N:3]1Participants
3
Procedure
Prepared from 5-(1-methyl-1H-tetrazol-5-yl)-4-phenyl-thiazol-2-ylamine and isobutyryl chloride.
Sources & evidence
- ORD record
- ord-c4f19650f8374e6283dc4d9e3e6e38a6
- Source dataset
- uspto-grants-2011_03
- Patent number
- US07910613B2
Reaction notes
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