Hydrochloric Acid → HCID 23567019, compound
Reaction equation
C([O:3][C:4](=[O:32])[CH2:5][C:6]1[CH:11]=[CH:10][C:9]([C:12]2[CH:17]=[CH:16][C:15]([C:18]([F:28])([CH3:27])[CH2:19][NH:20][S:21]([CH:24]([CH3:26])[CH3:25])(=[O:23])=[O:22])=[CH:14][CH:13]=2)=[CH:8][C:7]=1[N+:29]([O-:31])=[O:30])C.[OH-].[Na+].Cl>C(O)C.O>[F:28][C:18]([C:15]1[CH:14]=[CH:13][C:12]([C:9]2[CH:10]=[CH:11][C:6]([CH2:5][C:4]([OH:32])=[O:3])=[C:7]([N+:29]([O-:31])=[O:30])[CH:8]=2)=[CH:17][CH:16]=1)([CH3:27])[CH2:19][NH:20][S:21]([CH:24]([CH3:25])[CH3:26])(=[O:22])=[O:23]Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
To a solution of {4′-[1-fluoro-1-methyl-2-(propane-2-sulfonylamino)-ethyl]-3-nitro-biphenyl-4-yl}-acetic acid ethyl ester. (0.341 g, 0.731 mmol, prepared in example 47) in Ethanol (5.0 mL) is added a solution of 6.7% NaOH (15.0 mL) and the resulting mixture is stirred under N2 at ambient temperature for 72 h. The mixture is diluted with H2O (100 mL) and acidified with 37% HCl. Extraction with EtOAc followed by drying (MgSO4), filtration, and evaporation of the filtrate in vacuo gives the title compound.
Workup
- extractionExtraction with EtOAc
- customby drying
- filtration(MgSO4), filtration, and evaporation of the filtrate in vacuo
Sources & evidence
- ORD record
- ord-172cc3b7beac4d98a4056960e863a923
- Source dataset
- uspto-grants-2006_04
- Patent number
- US07034045B1
Reaction notes
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