Reaction equation
[F:1][C:2]1[CH:3]=[C:4]2[C:9](=[C:10]([OH:12])[CH:11]=1)[N:8]=[C:7]([CH3:13])[CH:6]=[CH:5]2.C(=O)([O-])[O-].[K+].[K+].C(#N)C.O.Cl[C:25]([F:35])([F:34])C(C1C=CC=CC=1)=O>>[F:34][CH:25]([F:35])[O:12][C:10]1[CH:11]=[C:2]([F:1])[CH:3]=[C:4]2[C:9]=1[N:8]=[C:7]([CH3:13])[CH:6]=[CH:5]2Participants
Conditions
- Temperature
- 80 °C
Procedure
To a mixture of 6-fluoro-2-methylquinolin-8-ol (0.15 g, 0.85 mmol) and potassium carbonate (4.2 g, 30 mmol) in acetonitrile (3.4 mL, 0.85 mmol) and water (3.4 mL, 0.85 mmol) was added 2-chloro-2,2-difluoroacetophenone (0.62 mL, 4.2 mmol). The vessel was sealed and the mixture was heated at 80° C. for 4 hours. The cooled reaction mixture was extracted with diethyl ether (2×30 mL), and the combined organic extracts were dried over magnesium sulfate, filtered and concentrated under reduced pressure at ambient temperature The resulting residue was purified by reverse phase chromatography on a C18 column (0-100% acetonitrile/water). Aqueous fractions containing the product were combined and extracted with diethyl ether (2×100 mL). The combined organic extracts were dried over magnesium sulfate, filtered and concentrated under reduced pressure at ambient temperature providing the title compound. Presence of water was noted and the material taken on as is assuming theoretical yield obtained (0.19 g, 100%).
Workup
- customThe vessel was sealed
- customThe cooled reaction mixture
- extractionwas extracted with diethyl ether (2×30 mL)
- dry with materialthe combined organic extracts were dried over magnesium sulfate
- filtrationfiltered
- concentrationconcentrated under reduced pressure at ambient temperature The resulting residue
- customwas purified by reverse phase chromatography on a C18 column (0-100% acetonitrile/water)
- additionAqueous fractions containing the product
- extractionextracted with diethyl ether (2×100 mL)
- dry with materialThe combined organic extracts were dried over magnesium sulfate
- filtrationfiltered
- concentrationconcentrated under reduced pressure at ambient temperature
Sources & evidence
- ORD record
- ord-75c94b7ae1fc4b6fba7882526e3a2fab
- Source dataset
- uspto-grants-2014_11
- Patent number
- US08889704B2
Linked notes
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