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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1496638Generated: October 26, 2026

Triethylamine → 5-methyl-1-(2,2,2-trifluoro-1-trifluoromethyl-ethyl)-1H-pyrazole-4-carboxylic acid pyridazin-4-ylamide

https://huagongshe.com/reaction/1496638

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-AminopyridazineHCID 298492—
Reactant5-Methyl-1-[2,2,2-trifluoro-1-(trifluoromethyl)ethyl]pyrazole-4-carbonyl chlorideHCID 89157399—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product5-methyl-1-(2,2,2-trifluoro-1-trifluoromethyl-ethyl)-1H-pyrazole-4-carboxylic acid pyridazin-4-ylamideHCID 8915705290%

Reaction Conditions

Temperature22.5 °C

Reaction Steps

A solution of 398 mg 5-methyl-1-[2,2,2-trifluoro-1-(trifluoromethyl)ethyl]pyrazole-4-carbonyl chloride in 10 ml CH2Cl2 was added dropwise to a solution of 185 mg pyridazin-4-amine and 750 mg triethylamine in 30 ml CH2Cl2 at 0° C. The mixture was stirred at 20-25° C. for about 68 h, diluted with 25 ml ethylacetate, washed with 3×15 ml sat. aq. NH4Cl solution, dried over MgSO4 and evaporated. Purification by flash chromatography (CH2Cl2/MeOH) gave 160 mg of the title compound (90% purity). HPLC-MS (Method 1): RT 2.278 min, m/z [MH]+ 354.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09198422B2
Source datasetuspto-grants-2015_12
ORD IDord-88b83d26ba4340d3a383441a52ae6a09
Source noteuspto-grants-2015_12