Water → HCID 18373452, compound
Reaction equation
[CH2:1]([O:3][CH2:4][CH2:5][NH:6][S:7]([C:10]1[C:15]([Cl:16])=[CH:14][CH:13]=[C:12]([N+:17]([O-:19])=[O:18])[C:11]=1Cl)(=[O:9])=[O:8])[CH3:2].[H-].[Na+].[OH2:23]>>[CH2:1]([O:3][CH2:4][CH2:5][NH:6][S:7]([C:10]1[C:15]([Cl:16])=[CH:14][CH:13]=[C:12]([N+:17]([O-:19])=[O:18])[C:11]=1[OH:23])(=[O:9])=[O:8])[CH3:2]Participants
4
Procedure
Following the general hydrolysis procedure outlined in example 15, N-(2-ethoxyethyl)-2,6-dichloro-3-nitrobenzenesulfonamide (1.78 g, 5.16 mmol), 80% NaH (0.46 g, 15.48mmol) and water (111 μL, 6.20mmol) were reacted. The crude product (1.63 g) was carried onto the next step without purification. LC-MS (m/z) 325.0(M+).
Workup
- customthe general hydrolysis procedure
- customwere reacted
- customThe crude product (1.63 g) was carried onto the next step without purification
Sources & evidence
- ORD record
- ord-cbfa3feee9eb45ceb31aa931910e19ba
- Source dataset
- uspto-grants-2002_12
- Patent number
- US06500863B1
Reaction notes
Loading…