Ethanol → HCID 20230482, compound
Reaction equation
Cl.[OH:2][C:3]1[CH:13]=[CH:12][C:11]([CH:14]([Cl:20])[CH2:15][NH:16][CH:17]([CH3:19])[CH3:18])=[CH:10][C:4]=1[NH:5][S:6]([CH3:9])(=[O:8])=[O:7].[CH2:21]([OH:23])[CH3:22]>>[ClH:20].[OH:2][C:3]1[CH:13]=[CH:12][C:11]([CH:14]([O:23][CH2:21][CH3:22])[CH2:15][NH:16][CH:17]([CH3:19])[CH3:18])=[CH:10][C:4]=1[NH:5][S:6]([CH3:9])(=[O:8])=[O:7]Participants
3
Procedure
A 1 g sample of 2'-hydroxy-5'-[1-chloro-2-(isopropylamino)ethyl]methanesulfonanilide hydrochloride is added to 10 ml of absolute ethanol and heated at reflux for 30 minutes. The mixture is evaporated to dryness and the residue is washed with ethyl ether thus yielding the product compound.
Workup
- temperatureheated
- temperatureat reflux for 30 minutes
- customThe mixture is evaporated to dryness
- washthe residue is washed with ethyl ether
- customthus yielding the product compound
Sources & evidence
- ORD record
- ord-1fc1fd7e6e2a415fa1eddd20d3b23058
- Source dataset
- uspto-grants-1983_09
- Patent number
- US04404224
Reaction notes
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