Sodium Hydroxide → HCID 178527299, compound
Reaction equation
[C:1]1([S:7]([CH2:10][C:11]2[CH:17]=[CH:16][CH:15]=[CH:14][C:12]=2[NH2:13])(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[N:18]([O-])=O.[Na+].[OH-].[Na+]>Cl.O>[C:1]1([S:7]([C:10]2[C:11]3[C:12](=[CH:14][CH:15]=[CH:16][CH:17]=3)[NH:13][N:18]=2)(=[O:8])=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
A stirred solution of 2-[(phenylsulfonyl)methyl]aniline (247 mg, 1.00 mmol) in 4N HCl (50 ml) is treated with a solution of NaNO2 (100 mg, 1.5 mmol) in water at ice-bath temperatures, stirred for 30 min., neutralized with 10% NaOH and filtered. The filtercake is dissolved in CH2Cl2, dried over MgSO4 and concentrated in vacuo to afford the title product as a tan solid, 240 mg (93% yield), mp 118° C., identified by mass spectral and HNMR analyses.
Workup
- filtrationfiltered
- dissolutionThe filtercake is dissolved in CH2Cl2
- dry with materialdried over MgSO4
- concentrationconcentrated in vacuo
Sources & evidence
- ORD record
- ord-5f2e2a8016b74183b19bf1047688235a
- Source dataset
- uspto-grants-2006_02
- Patent number
- US06995176B2
Reaction notes
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