Sodium methanethiolate → 3-Pyridinecarboxamide, 5-mercapto-N,N-dimethyl-

HRID 2101678Notes

Reaction equation

HRID 2101678 reaction equation
C[S-:2].[Na+].Br[C:5]1[CH:6]=[C:7]([C:11]([N:13]([CH3:15])[CH3:14])=[O:12])[CH:8]=[N:9][CH:10]=1>CN(C)C=O>[SH:2][C:5]1[CH:6]=[C:7]([C:11]([N:13]([CH3:15])[CH3:14])=[O:12])[CH:8]=[N:9][CH:10]=1

Participants

4

Conditions

Temperature
100 °C

Procedure

Sodium thiomethoxide (3 g) was added to a stirred solution of 5-bromo-N,N-dimethyl-3-pyridinecarboxamide (2.5 g, WO2000055168) in N,N-dimethylformamide (40 ml) and the suspension stirred at 100° C. for 4 h. The solvent was concentrated in vacuo, the residue dissolved in 2M sodium hydroxide (35 ml) and water (50 ml), and the solution washed with chloroform (4×75 ml). The aqueous layer was acidified with 2M hydrochloric acid to pH 4 and extracted with chloroform (5×80 ml), and the combined organic layers were washed with brine (20 ml), dried over magnesium sulphate and concentrated in vacuo to give the title compound as an orange oil (1.8 g).

Workup

  1. concentrationThe solvent was concentrated in vacuo
  2. dissolutionthe residue dissolved in 2M sodium hydroxide (35 ml)
  3. washwater (50 ml), and the solution washed with chloroform (4×75 ml)
  4. extractionextracted with chloroform (5×80 ml)
  5. washthe combined organic layers were washed with brine (20 ml)
  6. dry with materialdried over magnesium sulphate
  7. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-bdd4718a5ece49509fb4b8470c6407ca
Source dataset
uspto-grants-2009_08
Patent number
US07572915B2

Reaction notes

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