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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2351709Generated: October 31, 2026

Chloride → 2-(4-Chlorophenyl)-N-[4-(dimethylamino)phenyl]-3H-imidazo[4,5-b]pyridine-3-acetamide

https://huagongshe.com/reaction/2351709

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorideHCID 312—
ReactantTriethylamineHCID 8471—
Reactant1,4-Benzenediamine, N1,N1-dimethyl-, hydrochloride (1:2)HCID 2724166—
Reactant4-chlorophenyl-3H-imidazo[4,5-b]pyridine-3-acetic acidHCID 14390457—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-(4-Chlorophenyl)-N-[4-(dimethylamino)phenyl]-3H-imidazo[4,5-b]pyridine-3-acetamideHCID 1439032412.7%

Reaction Conditions

Temperature60 °C

Reaction Steps

Under a nitrogen atmosphere, oxlyl chloride (2.21 g, 0.0174 mole) was added slowly dropwise to a stirred and cooled (0°-10° C.) suspension of 2-(4-chlorophenyl)-3H-imidazo[4,5-b]pyridine-3-acetic acid (5.0 g, 0.0174 mole) in 50 ml of dimethylformamide. After the addition was complete, the reaction solution was heated at 60° C. for 5 hrs. This acylchloride solution was added dropwise to a stirred and cooled (<10° C.) suspension of N,N-dimethyl-1,4-phenylenediamine dihydrochloride (3.64 g, 0.0174 mole),triethylamine (5.27 g, 0.052 mole), and 75 ml of dimethylformamide. The reaction mixture was stirred at room temperature overnight. The reaction mixture was poured into 1800 ml of water and refrigerated overnight. The solid was collected by filtration and dried. The solid was recrystallized twice from isopropyl alcohol, collected by filtration, washed with water, and dried under high vacuum at 98° C. overnight to give 0.9 g (12.7%) of crystals, mp 245°-246.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04873251
Source datasetuspto-grants-1989_10
ORD IDord-717acc8be5f94a57a577634741df146b
Source noteuspto-grants-1989_10