2,2-Dimethylethenylboronic acid → N-(2-Cyano-4-(2-methylprop-1-enyl)phenyl)sulfamide
Reaction equation
[C:1]([C:3]1[CH:8]=[C:7](Br)[CH:6]=[CH:5][C:4]=1[NH:10][S:11]([NH2:14])(=[O:13])=[O:12])#[N:2].[CH3:15][C:16]([CH3:21])=[CH:17]B(O)O>>[C:1]([C:3]1[CH:8]=[C:7]([CH:15]=[C:16]([CH3:21])[CH3:17])[CH:6]=[CH:5][C:4]=1[NH:10][S:11]([NH2:14])(=[O:13])=[O:12])#[N:2]Participants
3
Procedure
Prepared as in Example 77a from N-(2-cyano-4-bromophenyl)sulfamide (Example 83b) and 2-methylprop-1-enylboronic acid.
Sources & evidence
- ORD record
- ord-49ffb972738641268f9c28fd2d724143
- Source dataset
- uspto-grants-2014_01
- Patent number
- US08633186B2
Reaction notes
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