Methyl 5-chloropyrazine-2-carboxylate → 5-Chloropyrazinoic acid

HRID 1989966Notes

Reaction equation

HRID 1989966 reaction equation
C[O:2][C:3]([C:5]1[CH:10]=[N:9][C:8]([Cl:11])=[CH:7][N:6]=1)=[O:4].[Cl-].[Li+].C(=O)(O)[O-].[Na+]>C(#N)C.CN(C=O)C.O>[Cl:11][C:8]1[N:9]=[CH:10][C:5]([C:3]([OH:4])=[O:2])=[N:6][CH:7]=1

Participants

7

Conditions

Temperature
160 °C

Procedure

To a solution of methyl-5-chloropyrazine-2-carboxylate (120 mg, 0.70 mmol) in a mixture of acetonitrile (2 mL) and DMF (1 mL) was added lithium chloride (295 mg, 6.95 mmol). The suspension was heated to 160° C. for 5 mins in a Smith creator microwave after which time the reaction was diluted with water (10 mL). Saturated sodium bicarbonate solution (20 mL) was added and the aqueous layered extracted twice with ethyl acetate (30 mL). The combined organics were discarded and the aqueous layer adjusted to pH 4 with 1N hydrochloric acid. The aqueous phase was extracted twice with ethyl acetate (20 mL) and the combined organics washed with water (2×20 mL), brine (10 mL) and dried (MgSO4). The volatiles were removed to give the title compound as a colourless solid (68 mg).

Workup

  1. extractionthe aqueous layered extracted twice with ethyl acetate (30 mL)
  2. extractionThe aqueous phase was extracted twice with ethyl acetate (20 mL)
  3. washthe combined organics washed with water (2×20 mL), brine (10 mL)
  4. dry with materialdried (MgSO4)
  5. customThe volatiles were removed

Sources & evidence

ORD record
ord-7ca2d101e9e843348622bbd8c720edf5
Source dataset
uspto-grants-2010_01
Patent number
US07642263B2

Reaction notes

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