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

HRID 600555Notes

Reaction equation

HRID 600555 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 minutes in a 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 with ethyl acetate (2×30 mL). The organic extracts 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) and brine (10 mL) and dried (MgSO4). The volatiles were removed under reduced pressure to afford the product (68 mg). 1H NMR δ (400 MHZ, CDCl3): 7.20 (1H, br s), 8.72 (1H, s), 9.21-9.21 (1H, m); m/z 157 (M−H)+.

Workup

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

Sources & evidence

ORD record
ord-d903815d55db4075b857b04ae9d89a82
Source dataset
uspto-grants-2011_03
Patent number
US07902200B2

Reaction notes

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