1H-1,2,4-Triazole, 1-methyl- → N-methoxy-N,1-dimethyl-1H-1,2,4-triazole-5-carboxamide

HRID 577833Notes

Reaction equation

HRID 577833 reaction equation
[CH3:1][N:2]1[CH:6]=[N:5][CH:4]=[N:3]1.[CH3:7][O:8][N:9]([CH3:13])[C:10](Cl)=[O:11]>C(#N)C.CCOCC>[CH3:7][O:8][N:9]([CH3:13])[C:10]([C:6]1[N:2]([CH3:1])[N:3]=[CH:4][N:5]=1)=[O:11]

Participants

5

Procedure

A mixture of 1-methyl-1H-1,2,4-triazole (3.15 mL, 55.56 mmol) and methoxy(methyl)carbamic chloride (7.55 g, 61.11 mmol) in acetonitrile (60 mL) was cooled in an ice water bath before addition of TEA (8.52 mL, 61.11 mmol). The mixture was allowed to slowly warm to room temperature and was then stirred overnight. The material was diluted with ether and solids were filtered and rinsed well with ether. The filtrate was concentrated and the residue was taken up in ether. Insoluble solids were filtered off and rinsed well with additional ether. The filtrate was concentrated to give and oil that was chromatographed on silica gel (100% CH2Cl2 followed by gradient elution to 40% EtOAc in CH2Cl2) to afford product as an oil that slowly solidified. 6.13 g (65% yield).

Workup

  1. filtrationwere filtered
  2. washrinsed well with ether
  3. concentrationThe filtrate was concentrated
  4. filtrationInsoluble solids were filtered off
  5. washrinsed well with additional ether
  6. concentrationThe filtrate was concentrated
  7. customto give
  8. customoil that was chromatographed on silica gel (100% CH2Cl2 followed by gradient elution to 40% EtOAc in CH2Cl2)
  9. customto afford product as an oil that

Sources & evidence

ORD record
ord-a4fe73bb234841bda188763e9b353d0a
Source dataset
uspto-grants-2015_05
Patent number
US09040528B2

Reaction notes

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