Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1709492Generated: October 31, 2026

Cyclohexylamine → HCID 14390289, compound

https://huagongshe.com/reaction/1709492

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexylamineHCID 7965—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant4-chlorophenyl-3H-imidazo[4,5-b]pyridine-3-acetic acidHCID 14390457—
SolventTetrahydrofuranHCID 8028—
ProductHCID 14390289HCID 1439028973%

Reaction Steps

Under nitrogen bubbling, a mixture of 2-(4-chlorophenyl)-3H-imidazo[4,5-b]pyridine-3-acetic acid (4.0 g, 0.014 mole) and 1,1'-carbonyldiimidazole (2.27 g, 0.014 mole) in 150 ml of tetrahydrofuran was stirred at room temperature for 3 hours. Cyclohexylamine (2.77 g, 0.028 mole) was added and the reaction mixture was allowed to stir at room temperature overnight. The tetrahydrofuran was evaporated to dryness and the residue was treated with water. The solid was collected by filtration, washed with water, and dried under high vacuum over the weekend. The solid was recrystallized from isopropyl alcohol-95% ethanol, collected by filtration, washed with water, and dried under high vacuum at 50° C. overnight to give 3.75 g (73%) of crystals, mp 240°-241° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04948800
Source datasetuspto-grants-1990_08
ORD IDord-6f9d82e240ea4d75be12624e057d19bf
Source noteuspto-grants-1990_08