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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1634082Generated: October 25, 2026

1,2-Dichloroethane → N-{4-[3,5-bis(Trifluoromethyl)pyrazol-1-yl]phenyl}cyclohexanecarboxamide

https://huagongshe.com/reaction/1634082

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantCyclohexanecarboxylic acidHCID 7413—
Reactant2-DimethylaminopyridineHCID 21885—
Reactant4-(3,5-Bis(trifluoromethyl)-1H-pyrazol-1-yl)anilineHCID 2740668—
SolventDichloromethaneHCID 6344—
ProductN-{4-[3,5-bis(Trifluoromethyl)pyrazol-1-yl]phenyl}cyclohexanecarboxamideHCID 10158140—

Reaction Steps

A mixture of cyclohexanecarboxylic acid (0.10 g, 0.8 mmol) and EDC (0.077 g, 0.4 mmol) in CH2Cl2 (1.5 mL) was stirred for 15 minutes. 1(4′-Aminophenyl)-3,5-bis(trifluoromethyl)pyrazole (0.059 g, 0.2 mmol) was added followed by dimethylaminopyridine (0.01 g, 0.1 mmol). After 3 hours the mixture was diluted with CH2Cl2 (50 mL), washed with 10% NaHCO3 (2×50 mL), brine (3×25mL), and dried over anhydrous Na2SO4. Evaporation of the solvent gave the above-named compound as a solid that crystallized from benzene (0.075 g, 92%): mp 178-180° C.; 1H NMR (CDCl3) δ 1.35 (3H, m), 1.66 (2H, m), 1.75 (1H, m), 1.85 (2H, m), 2.0 (2H, m), 2.3 (1H, m), 7.08 (1H, s), 7.45 (1H, d, J=8.5 Hz), 7.75 (2H, d, J=8.5 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06506747B1
Source datasetuspto-grants-2003_01
ORD IDord-4ad2f92fc19141c88a5b7543995421ed
Source noteuspto-grants-2003_01