Hydrochloric Acid → 3-(1-(4-fluorophenyl)-1H-indazol-5-yl)-2,3-diphenylpropanoic acid
Reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[C:16]3[C:11](=[CH:12][C:13]([CH:17]([C:29]4[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=4)[CH:18]([C:23]4[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=4)[C:19]([O:21]C)=[O:20])=[CH:14][CH:15]=3)[CH:10]=[N:9]2)=[CH:4][CH:3]=1.Cl>[OH-].[Na+].CO.CS(C)=O>[F:1][C:2]1[CH:3]=[CH:4][C:5]([N:8]2[C:16]3[C:11](=[CH:12][C:13]([CH:17]([C:29]4[CH:30]=[CH:31][CH:32]=[CH:33][CH:34]=4)[CH:18]([C:23]4[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=4)[C:19]([OH:21])=[O:20])=[CH:14][CH:15]=3)[CH:10]=[N:9]2)=[CH:6][CH:7]=1Participants
4
Procedure
Methyl 3-(1-(4-fluorophenyl)-1H-indazol-5-yl)-2,3-diphenylpropanoate (346 mg, 0.77 mmol) was heated to 100 C overnight in a mixture of 2 M NaOH/MeOH/DMSO (1:1:1). The next day, the reaction was cooled, acidified to pH 5 with HCl and extracted 2× EtOAc. The organic layers were washed with water×2, dried over MgSO4, filtered, concentrated in vacuo, and purified by HPLC to give 245 mg (73% yield) of acid 3-(1-(4-fluorophenyl)-1H-indazol-5-yl)-2,3-diphenylpropanoic acid. MS found: (M+H)+=389.
Workup
- temperatureThe next day, the reaction was cooled
- extractionextracted 2× EtOAc
- washThe organic layers were washed with water×2
- dry with materialdried over MgSO4
- filtrationfiltered
- concentrationconcentrated in vacuo
- custompurified by HPLC
Sources & evidence
- ORD record
- ord-4a1a10f9e279425992082fe44cfe6f17
- Source dataset
- uspto-grants-2012_06
- Patent number
- US08198311B2
Reaction notes
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