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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1709474Generated: October 30, 2026

N,N-Dimethylethylenediamine → HCID 14390264, compound

https://huagongshe.com/reaction/1709474

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylethylenediamineHCID 66053—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant2-(3-Chlorophenyl)-3H-imidazo[4,5-b]pyridine-3-acetic acidHCID 14390454—
SolventTetrahydrofuranHCID 8028—
ProductHCID 14390264HCID 14390264479.8%

Reaction Steps

A solution of 2-(3-chlorophenyl)-3H-imidazo[4,5-b]pyridine-3-acetic acid (6.7 g, 0.00233 mole), 1,1'-carbonyldiimidazole (4.0 g, 0.0245 mole), and anhydrous tetrahydrofuran (150 ml) was stirred at room temperature with a stream of nitrogen bubbling through for 21/2 hours. The nitrogen flow was stopped and a solution of N,N-dimethylethylenediamine (2.3 g, 0.0257 mole) in dry tetrahydrofuran (50 ml) was stirred at room temperature under nitrogen for 2 hours. The reaction was concentrated in vacuo and partitioned between methylene chloride (75 ml) and water (75 ml). The layers were separated and the aqueous portion washed with methylene chloride (25 ml). The combined organic portions were washed with potassium bicarbonate solution (2×50 ml), water (25 ml), dried over sodium sulfate, and concentrated in vacuo. The solid residue, 5.7 g (68%) was recrystallized from isopropyl alcohol-isopropyl ether to give 4.0 g of off-white granular solid, mp 124°-125° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04948800
Source datasetuspto-grants-1990_08
ORD IDord-f49b4bbd707c429e90d81a068aa30f3a
Source noteuspto-grants-1990_08