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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602383Generated: October 30, 2026

Water → HCID 67061319, compound

https://huagongshe.com/reaction/602383

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiisopropylethylamineHCID 81531—
Reactant1H-Pyrazol-5-amine, 3-methyl-1-(4-methylphenyl)-HCID 112855—
Reactant3-Iodo-4-methylbenzoic acidHCID 621640—
SolventDichloromethaneHCID 6344—
SolventThionyl ChlorideHCID 24386—
ProductHCID 67061319HCID 6706131986%

Reaction Conditions

Temperature80 °C

Reaction Steps

3-Iodo-4-methylbenzoic acid (1.00 g, 3.89 mmol) was dissolved in thionyl chloride (12.5 mL) and was stirred at 80° C. for 1.75 hours, then thionyl chloride was evaporated under reduced pressure. The reaction mixture was dissolved in methylene chloride (10.0 mL) and the solution was added with a solution of 5-amino-3-methyl-1-(p-tolyl)pyrazole (0.728 g, 3.89 mmol) and N,N-diisopropylethylamine (0.678 mL, 3.89 mmol) in methylene chloride (10.0 mL), followed by stirring at room temperature overnight. After the reaction mixture was added with water and extracted with ethyl acetate, the organic layer was washed with saturated aqueous sodium hydrogencarbonate solution, saturated aqueous ammonium chloride solution and water, followed by drying over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (ethyl acetate/hexane=1/4) to obtain 3-iodo-4-methyl-N-[5-methyl-2-(p-tolyl)-2H-pyrazol-3-yl]benzamide (1.44 g, 86%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07906522B2
Source datasetuspto-grants-2011_03
ORD IDord-f7d70882243c4ebe972aa05f12360632
Source noteuspto-grants-2011_03