Anthranilic Acid → HCID 21786232, compound
Reaction equation
[C:1]([OH:10])(=[O:9])[C:2]1[C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[NH2:4].[F:11][C:12]1[CH:19]=[CH:18][C:15]([CH:16]=O)=[CH:14][CH:13]=1.C1(C)C=CC(S(O)(=O)=O)=CC=1.[BH4-].[Na+]>C1(C)C=CC=CC=1>[F:11][C:12]1[CH:19]=[CH:18][C:15]([CH2:16][NH:4][C:3]2[CH:5]=[CH:6][CH:7]=[CH:8][C:2]=2[C:1]([OH:10])=[O:9])=[CH:14][CH:13]=1Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of anthranilic acid (1.37 g, 1.0 mmol), 4-fluorobenzaldehyde (1.24 g, 1.0 mmol), and p-toluenesulfonic acid mohohydrate (0.025 g, 0.13 mmol) in 30 mL of anhydrous toluene was stirred at reflux for 1 h, then cooled to RT and NaBH4 (1.1 g) was added. The mixture was stirred at RT for 30 min, then quenched with MeOH. The volatiles were removed under reduced pressure and the residue was taken up in water. AcOH was added to bring pH to 4, and the mixture was extracted with EtOAc. The combined organic portions were washed with brine, dried over MgSO4, filtered, condensed, and the residue was purified by flash column chromatography to give the titled compound. MS (ES+): 246.0 (M+H)+. Calc'd for C14H12FNO2-245.09.
Workup
- temperatureat reflux for 1 h
- stirringThe mixture was stirred at RT for 30 min
- customquenched with MeOH
- customThe volatiles were removed under reduced pressure
- additionAcOH was added
- extractionthe mixture was extracted with EtOAc
- washThe combined organic portions were washed with brine
- dry with materialdried over MgSO4
- filtrationfiltered
- customcondensed
- customthe residue was purified by flash column chromatography
Sources & evidence
- ORD record
- ord-95dc91a3c6f34da4afd65de48675042a
- Source dataset
- uspto-grants-2007_12
- Patent number
- US07307088B2
Reaction notes
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