Sodium Carbonate → 5-chloro-1-methyl-1H-imidazole-4-carbaldehyde

HRID 577068Notes

Reaction equation

HRID 577068 reaction equation
P(Cl)(Cl)(Cl)=O.[ClH:6].[NH2:7][CH2:8][C:9]([NH:11][CH3:12])=O.[C:13](=[O:16])([O-])[O-].[Na+].[Na+].[C:19](=O)([O-])[O-].[K+].[K+]>O1CCOCC1.CN(C=O)C>[Cl:6][C:9]1[N:11]([CH3:12])[CH:19]=[N:7][C:8]=1[CH:13]=[O:16]

Participants

7

Procedure

Phosphoryl trichloride (1 mL, 11 mmol) was added slowly to a 0° C. solution of DMF (22 mL), followed by 2-amino-N-methylacetamide hydrochloride (2.5 g, 20 mmol). The mixture was warmed at room temperature and stirred at 60° C. before phosphoryl trichloride (35 mL, 390 mmol) was added slowly. The solution was stirred at 90° C. overnight. After cooling to room temperature, the mixture was poured into ice/water (500 mL). Solid sodium carbonate was added until pH 6-7 was reached. The mixture was extracted with DCM (4×150 mL). The organic extracts were combined, dried over MgSO4, filtered, evaporated, and dried in vacuo. The residue was dissolved in water (10 mL) and 1,4-dioxane (20 mL) before potassium carbonate (10 g, 72.3 mmol) was added. The mixture was stirred at 60° C. for 4 hours. The mixture was evaporated to dryness. The residue was treated with 50% EtOAc/Et2O (250 mL). The solid was removed by filtration. The filtrate was recovered, evaporated, and dried in vacuo, affording 5-chloro-1-methyl-1H-imidazole-4-carbaldehyde (476 mg, 23% yield). The product was used without further purification.

Workup

  1. additionwas added slowly
  2. temperatureAfter cooling to room temperature
  3. extractionThe mixture was extracted with DCM (4×150 mL)
  4. dry with materialdried over MgSO4
  5. filtrationfiltered
  6. customevaporated
  7. customdried in vacuo
  8. dissolutionThe residue was dissolved in water (10 mL)
  9. stirringThe mixture was stirred at 60° C. for 4 hours
  10. customThe mixture was evaporated to dryness
  11. additionThe residue was treated with 50% EtOAc/Et2O (250 mL)
  12. customThe solid was removed by filtration
  13. customThe filtrate was recovered
  14. customevaporated
  15. customdried in vacuo

Sources & evidence

ORD record
ord-1ac908414aaf4173b9d22423e094e0bf
Source dataset
uspto-grants-2015_05
Patent number
US09040538B2

Reaction notes

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