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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598774Generated: October 30, 2026

Cyclohexylamine → 2-(4-Methoxyphenyl)-5-methyl-2H-pyrazole-3-carboxylic acid cyclohexylamide

https://huagongshe.com/reaction/598774

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexylamineHCID 7965—
Reactant1-(4-Methoxyphenyl)-3-methyl-1H-pyrazole-5-carboxylic acidHCID 2769599—
CatalystDimethyl SulfoxideHCID 679—
SolventDichloromethaneHCID 6344—
Product2-(4-Methoxyphenyl)-5-methyl-2H-pyrazole-3-carboxylic acid cyclohexylamideHCID 5825680262%

Reaction Steps

2-(4-Methoxyphenyl)-5-methyl-2H-pyrazole-3-carboxylic acid (752 mg, 3.24 mmol) was suspended in methylene chloride (25 mL) and DMSO (3 drops) was added. After the reaction was stirred at room temperature for 1 hour, it was concentrated in vacuo. The residue was diluted twice with methylene chloride (60 mL) and concentrated to dryness. The residue was diluted again with methylene chloride (45 mL), cyclohexylamine (650 μL, 5.68 mmol) was added, and the reaction was stirred at room temperature for 1 hour. The reaction was diluted further with methylene chloride, washed with NaOH (10%) and 1 N HCl, then dried over Na2SO4. Concentration gave 630 mg of the title compound, which was used in the next reaction without further purification. LC-MS (C18H23N3O2 calculated 313) m/z 314 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897634B2
Source datasetuspto-grants-2011_03
ORD IDord-8b3054f1b876447e90f785aa9c91b76f
Source noteuspto-grants-2011_03