HCID 19096124, compound → 4-Phenoxy-3-sulfamoylbenzoic acid
Reaction equation
C[O:2][C:3](=[O:21])[C:4]1[CH:9]=[C:8]([S:10](=[O:13])(=[O:12])[NH2:11])[C:7]([O:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)=[CH:6][CH:5]=1>[OH-].[Na+]>[O:14]([C:7]1[C:8]([S:10](=[O:13])(=[O:12])[NH2:11])=[CH:9][C:4]([C:3]([OH:21])=[O:2])=[CH:5][CH:6]=1)[C:15]1[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
6.2 g of 3-N-(3-azabicyclo-[3.2.0]-heptano)-4-phenoxy-5-sulphamylbenzoic acid methyl ester are suspended in 60 ml of 1 N NaOH and the suspension is heated on the waterbath until a clear solution is formed. The acid is then precipitated with 2 N HCl, while stirring well, and is recrystallised from glacial acetic acid.
Workup
- temperaturethe suspension is heated on the waterbath until a clear solution
- customis formed
- customThe acid is then precipitated with 2 N HCl
- customis recrystallised from glacial acetic acid
Sources & evidence
- ORD record
- ord-5b47d70dcdd749a2b2db0a096a253e8a
- Source dataset
- uspto-grants-1978_09
- Patent number
- US04111953
Reaction notes
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