Hydrochloric Acid → N-[3-[2-(phenylsulphonyl)-diazenyl]-5-bromophenyl]-N-methylacetamide
Reaction equation
[NH2:1][C:2]1[CH:3]=[C:4]([N:9]([CH3:13])[C:10](=[O:12])[CH3:11])[CH:5]=[C:6]([Br:8])[CH:7]=1.Cl.[N:15]([O-])=O.[Na+].[Na+].[C:20]1([S:26]([O-:28])=[O:27])[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1>O>[C:20]1([S:26]([N:15]=[N:1][C:2]2[CH:3]=[C:4]([N:9]([CH3:13])[C:10](=[O:12])[CH3:11])[CH:5]=[C:6]([Br:8])[CH:7]=2)(=[O:28])=[O:27])[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 0 °C
Procedure
0.243 g (0.001 mol) of N-(3-amino-5-bromophenyl)-N-methylacetamide was suspended in 5 ml of water, treated with 0.2 ml (0.002 mol) of HCl (37%) and cooled to 0° C. A solution of 0.069 g (0.001 mol) of NaNO2 in 1 ml of water was added thereto, the mixture was stirred at 0° C. for 5 min. and subsequently at room temperature for 10 min. and finally treated with a solution of 0.25 g (0.0015 mol) of benzenesulphinic acid sodium salt in 5 ml of water. The reaction mixture was treated in an ultrasound bath for 10 min. and subsequently partitioned in water/ethyl acetate. The organic phase was washed with sat. sodium chloride solution, dried over MgSO4, filtered and freed from solvent. The residue was chromatographed on silica gel with 1% MeOH in dichloromethane. There was obtained 0.23 g (58%) of N-[3-[2-(phenylsulphonyl)-diazenyl]-5-bromophenyl]-N-methylacetamide as a brown oil. MS (ISN): me/e=456, 454 (C15H14BrN3O3S- +NaOAc).
Workup
- additionThe reaction mixture was treated in an ultrasound bath for 10 min.
- customsubsequently partitioned in water/ethyl acetate
- washThe organic phase was washed with sat. sodium chloride solution
- dry with materialdried over MgSO4
- filtrationfiltered
- customThe residue was chromatographed on silica gel with 1% MeOH in dichloromethane
Sources & evidence
- ORD record
- ord-da728c472665437a8557e3cff09bb101
- Source dataset
- uspto-grants-1999_11
- Patent number
- US05990105
Reaction notes
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