Water → HCID 18520196, compound
Reaction equation
[Cl:1][C:2]1[N:3]=[C:4]([C:33]2[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=2)[N:5]([CH2:9][C:10]2[CH:15]=[CH:14][C:13]([S:16]([C:19]3[CH:24]=[CH:23][CH:22]=[CH:21][C:20]=3[S:25]([N:28]=CN(C)C)(=[O:27])=[O:26])(=[O:18])=[O:17])=[CH:12][CH:11]=2)[C:6]=1[CH:7]=[O:8].O>CCO.Cl>[Cl:1][C:2]1[N:3]=[C:4]([C:33]2[CH:34]=[CH:35][CH:36]=[CH:37][CH:38]=2)[N:5]([CH2:9][C:10]2[CH:15]=[CH:14][C:13]([S:16]([C:19]3[CH:24]=[CH:23][CH:22]=[CH:21][C:20]=3[S:25]([NH2:28])(=[O:26])=[O:27])(=[O:17])=[O:18])=[CH:12][CH:11]=2)[C:6]=1[CH:7]=[O:8]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
230 mg of 2-[4-(4-chloro-5-formyl-2-phenylimidazol-1-ylmethyl)benzenesulfonyl]-N-dimethylaminomethylenebenzenesulfonamide are refluxed for 2 h in 3 ml of EtOH and 3 ml of a saturated aqueous HCl solution. The reaction mixture is allowed to cool and poured onto 10 ml of water, and the product is filtered off. Chromatography on silica gel using MTB yields 151 mg of an amorphous solid.
Workup
- temperatureto cool
- filtrationthe product is filtered off
Sources & evidence
- ORD record
- ord-3c250b97b83a4d398c0c4c72c6eb4cf9
- Source dataset
- uspto-grants-2003_06
- Patent number
- US06573288B1
Reaction notes
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