4-Methylphenyl isocyanate → N-[[(4-methylphenyl)amino]carbonyl]-2-benzofuransulfonamide
Reaction equation
[O:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[CH:3]=[C:2]1[S:10]([NH2:13])(=[O:12])=[O:11].[CH3:14][C:15]1[CH:20]=[CH:19][C:18]([N:21]=[C:22]=[O:23])=[CH:17][CH:16]=1>>[CH3:14][C:15]1[CH:20]=[CH:19][C:18]([NH:21][C:22]([NH:13][S:10]([C:2]2[O:1][C:5]3[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=3[CH:3]=2)(=[O:11])=[O:12])=[O:23])=[CH:17][CH:16]=1Participants
3
Procedure
2-Benzofuransulfonamide (7.6 mmol), prepared as described in Preparation 2, was reacted with 4-methylphenylisocyanate (7.6 mmol) as described in Preparation 2 to obtain 1.6 g of the title product as a solid.
Workup
- customas described in Preparation 2
- customas described in Preparation 2
Sources & evidence
- ORD record
- ord-46a5b4abb87d48ecbf829cc3c05b8fa7
- Source dataset
- uspto-grants-1993_12
- Patent number
- US05270329
Reaction notes
Loading…