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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1799399Generated: November 2, 2026

Cyclohexylamine → HCID 59516147, compound

https://huagongshe.com/reaction/1799399

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexylamineHCID 7965—
ReactantOxalyl chlorideHCID 65578—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 28606431HCID 28606431—
CatalystDimethylformamideHCID 6228—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 59516147HCID 59516147—

Reaction Steps

1-(4-bromophenyl)-5-cyclopropyl-pyrazole-4-carboxylic acid (Intermediate #30) (237 mg, 0.77 mmol) was suspended in DCM (5 mL). One drop of DMF was added and then oxalyl chloride (200 μL, 2.32 mmol) was added slowly. The reaction mixture was stirred at ambient temperature for 4 h and then evaporated under reduced pressure. The residue was to dissolved in DCM (5 mL) and added to a solution of cyclohexylamine (97 μL, 0.85 mmol) and DIPEA (403 μL, 2.32 mmol) in DCM (5 mL). The mixture was stirred at ambient for 24 h and then water, (10 mL) was added and the mixture passed through a phase separating filter. The product was recovered from the filtrate by flash column chromatography (SiO2, elution gradient 0-100% EtOAc in isohexane). Pure fractions were combined and evaporated to give 1-(4-bromophenyl)-N-cyclohexyl-5-cyclopropyl-pyrazole-4-carboxamide as white solid. (277 mg, 92%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08344016B2
Source datasetuspto-grants-2013_01
ORD IDord-de0ed89739754a598c02982667df7507
Source noteuspto-grants-2013_01