Dimethylamine → HCID 10126912, compound
Reaction equation
[CH3:1][NH:2][CH3:3].[Cl:4][C:5]1[C:10]([Cl:11])=[CH:9][CH:8]=[CH:7][C:6]=1[S:12]([N:15]([C:24]1[C:29]([O:30][CH3:31])=[N:28][C:27](Cl)=[C:26]([Cl:33])[N:25]=1)COCC[Si](C)(C)C)(=[O:14])=[O:13]>O1CCCC1>[Cl:4][C:5]1[C:10]([Cl:11])=[CH:9][CH:8]=[CH:7][C:6]=1[S:12]([NH:15][C:24]1[C:29]([O:30][CH3:31])=[N:28][C:27]([N:2]([CH3:3])[CH3:1])=[C:26]([Cl:33])[N:25]=1)(=[O:13])=[O:14]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Prepared by the method of Example 67 using dimethylamine (5 mL of a 2M solution in tetrahydrofuran) and 2,3-dichloro-N-(5,6-dichloro-3-methoxy-2-pyrazinyl)-N-{[2-(trimethylsilyl)ethoxy]methyl}benzenesulfonamide (0.1 g). Yield 0.015g.
Sources & evidence
- ORD record