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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 279952Generated: October 30, 2026

Dimethylformamide → 1H-Pyrazole-4-carboxamide, 5-cyano-N-methyl-1-phenyl-

https://huagongshe.com/reaction/279952

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantMethylamineHCID 6329—
ReactantSodium CyanideHCID 8929—
ReactantEthyl 5-chloro-1-phenyl-1H-pyrazole-4-carboxylateHCID 13608341—
SolventWaterHCID 962—
Product1H-Pyrazole-4-carboxamide, 5-cyano-N-methyl-1-phenyl-HCID 163675—

Reaction Conditions

Temperature100 °C

Reaction Steps

A 100 ml 3-neck round bottom flask was charged with 12.0 g (0.048 mol) of 99.1% pure 5-chloro-1-phenyl-1H-pyrazole-4-carboxylic acid, ethyl ester, 4.7 g (0.096 mol) of sodium cyanide and 28.8 ml of DMF. The resulting mixture was heated at approximately 100° C. for 6 hours and then stirred at room temperature overnight. Thirteen grams (0.17 mol) of 40% aqueous methylamine were added to the reaction mixture dropwise. The reaction mixture was stirred at room temperature for 61/2 hours and 28.8 ml of water was added. The mixture was stirred for 30 minutes and the precipitated solid was collected by filtration. The resulting solid was washed with water and vacuum dried to afford 9.2 g of 5-cyano-1-phenyl-N-methyl-1H-pyrazole-4-carboxamide. The corrected yield was 73.4% and purity of the final product by high pressure liquid chromatography was 85.8%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04587348
Source datasetuspto-grants-1986_05
ORD IDord-86267b547f5b4481a172f217c06b3af0
Source noteuspto-grants-1986_05