Sodium Hydroxide → HCID 19029742, compound
Reaction equation
[Cl:1][C:2]1[CH:15]=[CH:14][C:13]2[S:12][C:11]3[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=3)[N:5]([CH2:16][CH2:17][CH2:18][N:19]3[CH:23]=[CH:22][CH:21]=[C:20]3[C:24]([O:26]C)=[O:25])[C:4]=2[CH:3]=1.[OH-].[Na+]>C(O)C.CS(C)=O>[ClH:1].[Cl:1][C:2]1[CH:15]=[CH:14][C:13]2[S:12][C:11]3[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=3)[N:5]([CH2:16][CH2:17][CH2:18][N:19]3[CH:23]=[CH:22][CH:21]=[C:20]3[C:24]([OH:26])=[O:25])[C:4]=2[CH:3]=1Participants
6
Reactant 2
Product 2
Reagents, catalysts & solvents 2
Procedure
3.99 g (10 mmol) of the compound obtained in Example 11 are dissolved in 15 ml of ethanol and 7.5 ml of dimethyl sulfoxide. 0.8 g (20 mmol) of sodium hydroxide (in 1N solution) is added and the mixture is heated under reflux for 7 hours, with stirring. After acidification with a 1N hydrochloric acid solution and customary treatment of the organic phases, 3.62 g of the expected product are obtained.
Workup
- temperaturethe mixture is heated
- temperatureunder reflux for 7 hours
Sources & evidence
- ORD record
- ord-1d93a4260cd141419656fa0e2031ae9a
- Source dataset
- uspto-grants-1997_08
- Patent number
- US05654323
Reaction notes
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