Dimethylformamide → 5-Bromo-1,3-thiazole-2-carboxamide

HRID 1366172Notes

Reaction equation

HRID 1366172 reaction equation
[Br:1][C:2]1[S:6][C:5]([C:7]([OH:9])=O)=[N:4][CH:3]=1.C(Cl)(=O)C(Cl)=O.C[N:17](C=O)C>ClCCl>[Br:1][C:2]1[S:6][C:5]([C:7]([NH2:17])=[O:9])=[N:4][CH:3]=1

Participants

5

Procedure

To 5-bromo-thiazole-2-carboxylic acid (0.267 g, 0.128 mmol) suspended in dry dichloromethane (30 mL) are added oxalyl chloride (0.22 mL, 0.257 mmol) and a drop of DMF. The reaction is stirred for 1 hour at room temperature. The solvent is evaporated and the resultant crude is dissolved in 7M NE3 in MeOH. The reaction mixture is stirred overnight at room temperature. After evaporation of the solvent, the residue is dissolved in dichloromethane and washed with 1M NaOH. The organic phase is dried over MgSO4, filtered and evaporated. The residue is purified by silica gel column chromatography eluting with 95:5 DCM:MeOH to give the title compound (33.8 mg, 25%).

Workup

  1. customThe solvent is evaporated
  2. dissolutionthe resultant crude is dissolved in 7M
  3. stirringThe reaction mixture is stirred overnight at room temperature
  4. customAfter evaporation of the solvent
  5. dissolutionthe residue is dissolved in dichloromethane
  6. washwashed with 1M NaOH
  7. dry with materialThe organic phase is dried over MgSO4
  8. filtrationfiltered
  9. customevaporated
  10. customThe residue is purified by silica gel column chromatography
  11. washeluting with 95:5 DCM

Sources & evidence

ORD record
ord-b79b796a9dc34f50884b6e0d3e7cf53d
Source dataset
uspto-grants-2011_02
Patent number
US07893058B2

Reaction notes

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