Water → HCID 18373485, compound
Reaction equation
[CH2:1]([NH:3][S:4]([C:7]1[C:12]([Cl:13])=[CH:11][CH:10]=[C:9]([N+:14]([O-:16])=[O:15])[C:8]=1Cl)(=[O:6])=[O:5])[CH3:2].[H-].[Na+].[OH2:20]>>[CH2:1]([NH:3][S:4]([C:7]1[C:12]([Cl:13])=[CH:11][CH:10]=[C:9]([N+:14]([O-:16])=[O:15])[C:8]=1[OH:20])(=[O:6])=[O:5])[CH3:2]Participants
4
Procedure
Following the general hydrolysis procedure outlined in example 15, N-ethyl-2,6dichloro-3-nitrobenzenesulfonamide (1.16 g, 3.88mmol), 60% NaH (466 mg, 11.64 mmol) and water (70 μL, 3.88 mmol) were reacted. The crude product (1.34 g) was carried on to the next step without purification. 1H NMR (MeOD-d4): δ 8.07 (d, 1H), 7.25 (d, 1H), 3.05 (q, 2H), 1.12 (t, 3H).
Workup
- customthe general hydrolysis procedure
- customwere reacted
- customThe crude product (1.34 g) was carried on to the next step without purification
Sources & evidence
- ORD record
- ord-ff26e2cdcc364f09ae3124a577ba6a5d
- Source dataset
- uspto-grants-2002_12
- Patent number
- US06500863B1
Reaction notes
Loading…