Dimethylformamide → HCID 51000274, compound

HRID 245381Notes

Reaction equation

HRID 245381 reaction equation
[Cl:1][C:2]1[N:7]=[C:6]([C:8]([OH:10])=O)[CH:5]=[N:4][CH:3]=1.C(Cl)(=O)C(Cl)=O.CN(C=O)C.Cl.[CH3:23][NH:24][O:25][CH3:26]>C(Cl)Cl>[Cl:1][C:2]1[N:7]=[C:6]([C:8]([N:24]([O:25][CH3:26])[CH3:23])=[O:10])[CH:5]=[N:4][CH:3]=1

Participants

6

Procedure

To a 100 ml round bottom flask, 6-chloropyrazine-2-carboxylic acid (1 g, 6.31 mmol) was suspended in dry CH2Cl2 (30 ml). Oxalyl chloride (3.78 ml, 7.57 mmol) was added along with a few drop of DMF, the mixture was stirred at room temperature for 12 hrs, N,O-Dimethylhydroxylamine hydrochloride (0.800 g, 8.20 mmol) was added, the resulting mixture was cooled down to 5° C., TEA (2.64 ml, 18.92 mmol) was added via a dropping funnel, the reaction mixture was stirred at room temperature for 30 minutes, filtered and the filter cake was washed with EtOAc, the combined filtrate was washed with saturated sodium bicarbonate and brine, concentrated to an oil, purified on silica gel with Hexanes/EtOAc solvents to give product (1.06 g).

Workup

  1. temperaturethe resulting mixture was cooled down to 5° C.
  2. stirringthe reaction mixture was stirred at room temperature for 30 minutes
  3. filtrationfiltered
  4. washthe filter cake was washed with EtOAc
  5. washthe combined filtrate was washed with saturated sodium bicarbonate and brine
  6. concentrationconcentrated to an oil
  7. custompurified on silica gel with Hexanes/EtOAc solvents

Sources & evidence

ORD record
ord-dd231f383a044db8a46f39a537ce2298
Source dataset
uspto-grants-2014_02
Patent number
US08658641B2

Reaction notes

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