Reaction equation
[S:1](Cl)(=[O:4])(=[O:3])[NH2:2].[C:6]1([CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][OH:17])[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1>>[S:1]([O:17][CH2:16][CH2:15][CH2:14][CH2:13][CH2:12][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)(=[O:4])(=[O:3])[NH2:2]Participants
3
Procedure
The title compound was prepared by procedures of Example 33 from sulfamoyl chloride and 5-phenyl-1-pentanol. The oil obtained was further purified by chromatography using a column with methylene chloride as eluting agent. Evaporation of appropriate fractions gave a viscous oil which solidified on standing. The solid was recrystallized from ethyl ether-petroleum ether (bp range 30°-60° C.) to give the title compound as white solid, mp 63°-66° C. in 60% yield.
Workup
- customThe oil obtained
- customwas further purified by chromatography
- washas eluting agent
- customEvaporation of appropriate fractions
- customgave a viscous oil which
- customThe solid was recrystallized from ethyl ether-petroleum ether (bp range 30°-60° C.)
Sources & evidence
- ORD record
- ord-d622221d020a4ad3ac702acd8004e9ad
- Source dataset
- uspto-grants-1993_12
- Patent number
- US05273993
Linked notes
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