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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 31379Generated: October 25, 2026

2-(Ethoxymethylene)propanedinitrile → 5-amino-1-(2-fluoro-4-methanesulfonyl-phenyl)-1H-pyrazole-4-carbonitrile

https://huagongshe.com/reaction/31379

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Ethoxymethylene)propanedinitrileHCID 67152—
Reactant[2-Fluoro-4-(methylsulfonyl)phenyl]hydrazineHCID 2782739—
SolventMethanolHCID 887—
Product5-amino-1-(2-fluoro-4-methanesulfonyl-phenyl)-1H-pyrazole-4-carbonitrileHCID 21897593—

Reaction Conditions

Temperature-6 °C

Reaction Steps

To a stirred suspension of 2-fluoro-4-methylsulfonylphenyl hydrazine (1) (4.0336 Kg; 1 eq) (commercially available from, e.g., Peakdale Molecular, Ltd.) in methanol (12.7723 Kg) was added a suspension of ethoxymethylene malononitrile (2.6564 Kg, 1.101 equivalents) in methanol (11.212 Kg) at a rate sufficiently slow to maintain the reaction mixture at −10° to 0° C. with reactor jacket cooling. After the addition had been completed, the reaction mixture was stirred for 1 hour at −6° C. and then heated to reflux for 5 hours, at which time the reaction mixture gave a pyrazole (3): hydrazine (1) HPLC peak area ratio of 105:1. Solvent (20.5153 Kg) was then distilled off the reaction mixture at atmospheric pressure, leaving a residue having less than 20% of the original volume. The resulting mixture was used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07425630B2
Source datasetuspto-grants-2008_09
ORD IDord-2cf28deae1a344dd9efb094b5ca7a968
Source noteuspto-grants-2008_09