Sodium Cyanide → 5-Bromopyrimidine-2-carbonitrile

HRID 641454Notes

Reaction equation

HRID 641454 reaction equation
[C-:1]#[N:2].[Na+].[Br:4][C:5]1[CH:6]=[N:7][C:8](Cl)=[N:9][CH:10]=1>CN(C)C=O.O>[Br:4][C:5]1[CH:6]=[N:7][C:8]([C:1]#[N:2])=[N:9][CH:10]=1

Participants

5

Procedure

Sodium cyanide (2.30 g, 46.6 mmol) was dissolved in dimethylformamide (60 ml) and treated with 5-bromo-2-chloropyrimidine (6.0 g, 31.1 mmol). The resulting mixture was stirred at room temperature for 18 hours, diluted with water and extracted with dichloromethane. The dichloromethane extracts were combined, washed with water, dried (magnesium sulphate), filtered and concentrated in vacuo. The crude product was purified by column chromatography eluting with a mixture of ethyl acetate:hexane (1:4) to afford the title compound (D38).

Workup

  1. extractionextracted with dichloromethane
  2. washwashed with water
  3. dry with materialdried (magnesium sulphate)
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo
  6. customThe crude product was purified by column chromatography
  7. washeluting with a mixture of ethyl acetate:hexane (1:4)

Sources & evidence

ORD record
ord-1b412fef8fcc4ddd9002dc988ee2fb9a
Source dataset
uspto-grants-2010_04
Patent number
US07696193B2

Reaction notes

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