Water → HCID 18373494, compound
Reaction equation
[CH:1]([O:4][CH2:5][CH2:6][NH:7][S:8]([C:11]1[C:16]([Cl:17])=[CH:15][CH:14]=[C:13]([N+:18]([O-:20])=[O:19])[C:12]=1Cl)(=[O:10])=[O:9])([CH3:3])[CH3:2].[H-].[Na+].[OH2:24]>>[CH:1]([O:4][CH2:5][CH2:6][NH:7][S:8]([C:11]1[C:16]([Cl:17])=[CH:15][CH:14]=[C:13]([N+:18]([O-:20])=[O:19])[C:12]=1[OH:24])(=[O:10])=[O:9])([CH3:3])[CH3:2]Participants
4
Procedure
Following the general hydrolysis procedure outlined in example 15, N-(2-isopropoxyethyl)-2,6-dichloro-3-nitrobenzenesulfonamide (1.635 g, 4.58 mmol), 60% NaH (0.41 g, 13.74 mmol) and water (0.099 mL, 5.50 mmol) were reacted. The crude product (1.676 g) was carried on to the next step without purification. LC-MS (m/z) 340 (M-H)+.
Workup
- customthe general hydrolysis procedure
- customwere reacted
- customThe crude product (1.676 g) was carried on to the next step without purification
Sources & evidence
- ORD record
- ord-b6b8ab4a977d4a9281d8b2370661fc9c
- Source dataset
- uspto-grants-2002_12
- Patent number
- US06500863B1
Reaction notes
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