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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 916680Generated: October 29, 2026

Cyclohexylamine → HCID 58961386, compound

https://huagongshe.com/reaction/916680

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexylamineHCID 7965—
ReactantSodium BicarbonateHCID 516892—
ReactantTrimethylaluminumHCID 16682925—
ReactantHCID 66885880HCID 66885880—
SolventDichloromethaneHCID 6344—
SolventHeptaneHCID 8900—
ProductHCID 58961386HCID 58961386—

Reaction Steps

Part C: Cyclohexylamine (0.91 ml, 8 mmol) is dissolved in dichloromethane (20 ml) and (CH3)3Al (4 ml of a 2 M solution in heptane, 8 mmol) is added. The resulting mixture is stirred for 10 minutes at room temperature and ethyl 1-(4-chlorophenyl)2-(2,4-dichlorophenyl)-5-(pyrolidin-1-ylmethyl)-1H-imidazole4-carboxylate (1.8 gram, 3.8 mmol) is added. The resulting mixture is stirred at room temperature for 16 hours, poured into an aqueous NaHCO3 solution, stirred for 30 minutes and filtered over hyflo. The filtrated is twice extracted with dichloromethane. The organic layers are dried over Na2SO4, filtered and concentrated in vacuo. Subsequent purification with flash chromatography (dichloromethane/methanol=98/2 (v/v)) gives N-cyclohexyl-1-(4-chlorophenyl )-2-(2,4-dichlorophenyl)-5-(pyrrolidin-1-ylmethyl)-1H-imidazole-4-carboxamide, compound 1 (1.06 gram, 53% yield). Melting point: 155-157° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07271189B2
Source datasetuspto-grants-2007_09
ORD IDord-c86c6289f0f54b65849ee163df7dd7c5
Source noteuspto-grants-2007_09