Hydrochloric Acid → HCID 54529973, compound
Reaction equation
C([N:4]1[CH2:9][CH2:8][N:7]([C:10]2[CH:15]=[CH:14][C:13]([NH:16][S:17]([CH3:20])(=[O:19])=[O:18])=[C:12]([CH3:21])[CH:11]=2)[CH2:6][CH2:5]1)(=O)C.Cl>>[CH3:20][S:17]([NH:16][C:13]1[CH:14]=[CH:15][C:10]([N:7]2[CH2:8][CH2:9][NH:4][CH2:5][CH2:6]2)=[CH:11][C:12]=1[CH3:21])(=[O:18])=[O:19]Participants
3
Procedure
1-Acetyl-4-(4-methanesulphonamido-3-methylphenyl)piperazine (5.93 g) and 2N aqueous hydrochloric acid (85 ml) were refluxed for 2 hours, cooled, evaporated to low bulk, basified with sodium carbonate to pH 9-10 and extracted with 5×100 ml 5% methanol in dichloromethane. The organic layers were combined and evaporated to give the title compound as a brown foam, (4.78 g), m.p. 79°-81°.
Workup
- temperaturecooled
- customevaporated to low bulk
- extractionextracted with 5×100 ml 5% methanol in dichloromethane
- customevaporated
Sources & evidence
- ORD record
- ord-b04bc5d87aef4a85979f86901be91526
- Source dataset
- uspto-grants-1989_01
- Patent number
- US04797401
Reaction notes
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