Hydrochloric Acid → HCID 21533306, compound
Reaction equation
[Cl:1][C:2]1[C:3]([S:14][CH:15]([CH3:17])[CH3:16])=[CH:4][C:5]2[S:10](=[O:12])(=[O:11])[NH:9]C=[N:7][C:6]=2[CH:13]=1.Cl>[OH-].[Na+]>[S:10]([C:5]1[CH:4]=[C:3]([S:14][CH:15]([CH3:16])[CH3:17])[C:2]([Cl:1])=[CH:13][C:6]=1[NH2:7])(=[O:11])(=[O:12])[NH2:9]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
6-Chloro-7-isopropylthio-1,2,4-benzothiadiazine-1,1-dioxide (0.03 mole), prepared as described in Example 2, is dissolved in 10% aqueous sodium hydroxide (50 ml.) and heated on the steam bath for 1 hour. The solution is chilled, acidified with hydrochloric acid and the product upon recrystallization from a mixture of ethanol and water melts at 137°-138° C.
Workup
- temperatureheated on the steam bath for 1 hour
- temperatureThe solution is chilled
- customthe product upon recrystallization
- additionfrom a mixture of ethanol and water melts at 137°-138° C.
Sources & evidence
- ORD record
- ord-4f06499fe9b3438bb27bbbaf3300be14
- Source dataset
- uspto-grants-1976_06
- Patent number
- US03960854
Reaction notes
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