Phosphorus oxychloride → Ethyl 4-chloro-6-methyl-2-oxo-1,2-dihydropyridine-3-carboxylate

HRID 1513566Notes

Reaction equation

HRID 1513566 reaction equation
O[C:2]1[CH:7]=[C:6]([CH3:8])[NH:5][C:4](=[O:9])[C:3]=1[C:10]([O:12][CH2:13][CH3:14])=[O:11].P(Cl)(Cl)([Cl:17])=O.[Cl-].C([N+](CC)(CC)CC)CCC>C(#N)C>[Cl:17][C:2]1[CH:7]=[C:6]([CH3:8])[NH:5][C:4](=[O:9])[C:3]=1[C:10]([O:12][CH2:13][CH3:14])=[O:11]

Participants

5

Conditions

Temperature
40 °C

Procedure

A mixture of ethyl 4-hydroxy-6-methyl-2-oxo-1,2-dihydropyridine-3-carboxylate (3.00 g, 15.2 mmol), phosphorus oxychloride (7.75 mL), n-butyltriethylammonium chloride (13.8 g, 60.8 mmol) and acetonitrile (60 mL) was stirred at 40° C. for 30 min and under refluxing conditions for 30 min. After cooling, the reaction mixture was concentrated under reduced pressure, water was added to the residue and the mixture was extracted with ethyl acetate. The extract was washed with brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was washed with ethyl acetate-hexane mixed solution, and dried under reduced pressure to give the title compound (1.45 g, 44%) as a white powder.

Workup

  1. temperatureAfter cooling
  2. concentrationthe reaction mixture was concentrated under reduced pressure, water
  3. additionwas added to the residue
  4. extractionthe mixture was extracted with ethyl acetate
  5. washThe extract was washed with brine
  6. dry with materialdried over magnesium sulfate
  7. concentrationconcentrated under reduced pressure
  8. washThe residue was washed with ethyl acetate-hexane mixed solution
  9. customdried under reduced pressure

Sources & evidence

ORD record
ord-edd2d8dc3cc74ca1b023a46516c0b0b8
Source dataset
uspto-grants-2012_07
Patent number
US08217176B2

Reaction notes

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