Water → HCID 70984374, compound

HRID 339042

Reaction equation

HRID 339042 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]2

Participants

6

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

  1. customThe vessel was sealed
  2. customThe cooled reaction mixture
  3. extractionwas extracted with diethyl ether (2×30 mL)
  4. dry with materialthe combined organic extracts were dried over magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated under reduced pressure at ambient temperature The resulting residue
  7. customwas purified by reverse phase chromatography on a C18 column (0-100% acetonitrile/water)
  8. additionAqueous fractions containing the product
  9. extractionextracted with diethyl ether (2×100 mL)
  10. dry with materialThe combined organic extracts were dried over magnesium sulfate
  11. filtrationfiltered
  12. 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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