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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 622014Generated: October 29, 2026

1,1'-Carbonyldiimidazole → HCID 14390378, compound

https://huagongshe.com/reaction/622014

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant1-methyl-1H-pyrrole-2-ethylamineHCID 565058—
Reactant4-chlorophenyl-3H-imidazo[4,5-b]pyridine-3-acetic acidHCID 14390457—
SolventTetrahydrofuranHCID 8028—
ProductHCID 14390378HCID 1439037863%

Reaction Steps

A suspension of 2-(4-chlorophenyl)-3H-imidazo[4,5-b]pyridine-3-acetic acid (5.0 g, 0.0174 mole), 1,1'-carbonyldimidazole (2.82 g, 0.0174 mole) and dry tetrahydrofuran (100 ml) was stirred at room temperature for 3 hr with a stream of nitrogen bubbling through it. A solution of 2-(2-aminoethyl)-1-methylpyrrole (5.40 g, 0.0435 mole) in tetrahydrofuran (6 ml) was added and the mixture was stirred at room temperature under nitrogen overnight. The solvent was evaporated under reduced pressure and the resulting oil was triturated in water (100 ml) which caused a solid to form. The solid was collected by filtration, rinsed twice with water, twice with 5% potassium hydroxide solution and twice again with water. The solid was dissolved in hot isopropyl alcohol and filtered hot. Water was added to the cloud point. Upon cooling, a solid precipitated which was collected by filtration, rinsed with water, and dried under high vacuum at 50° C. overnight to give 4.31 g (63%) of title compound, mp 171°-172.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04824951
Source datasetuspto-grants-1989_04
ORD IDord-3b1cad00d08a45c19bd8f94b2d700061
Source noteuspto-grants-1989_04