Hydrochloric Acid → HCID 67578298, compound
Reaction equation
[CH2:1]([C:5]1[C:14](=[O:15])[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][C:12]=2[S:16][CH3:17])[NH:7][C:6]=1[C:18]([O:20]CC)=[O:19])[CH2:2][CH2:3][CH3:4].[OH-].[Na+].[ClH:25]>O>[ClH:25].[CH2:1]([C:5]1[C:14](=[O:15])[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][C:12]=2[S:16][CH3:17])[NH:7][C:6]=1[C:18]([OH:20])=[O:19])[CH2:2][CH2:3][CH3:4]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
0.63 g of the product of Step B in 10 ml of a N sodium hydroxide solution was stirred for 2 hours at reflux and the mixture was poured into ice-cooled water, acidified with concentrated hydrochloric acid, separated, washed with water, dried and impasted in 100 ml of ethyl acetate to obtain 495 mg of the desired product melting at 240° C.
Workup
- temperatureat reflux
- additionthe mixture was poured into ice-
- customseparated
- washwashed with water
- customdried
Sources & evidence
- ORD record
- ord-7adcf8afe6f64748a05e9576b7295553
- Source dataset
- uspto-grants-1999_11
- Patent number
- US05985894
Reaction notes
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