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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2351714Generated: November 3, 2026

Dipropylamine → 2-(3,4-Dichlorophenyl)-N,N-dipropyl-3H-imidazo[4,5-b]pyridine-3-acetamide hydrate

https://huagongshe.com/reaction/2351714

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDipropylamineHCID 8902—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant2-(3,4-dichlorophenyl)3H-imidazo[4,5-b]pyridine-3-acetic acidHCID 15617193—
SolventTetrahydrofuranHCID 8028—
Product2-(3,4-Dichlorophenyl)-N,N-dipropyl-3H-imidazo[4,5-b]pyridine-3-acetamide hydrateHCID 1439032781.6%

Reaction Steps

Under nitrogen bubbling, a mixture of 2-(3,4-dichlorophenyl)-3H-imidazo [4,5-b]pyridine-3-acetic acid (3.5 g, 0.011 mole) and 1,1'-carbonyldiimidazole (1.95 g, 0.011 mole) in 120 ml of tetrahydrofuran was stirred at room temperature for 31/2 hrs. Then, under nitrogen atmosphere, dipropylamine (2.43 g, 0.024 mole) was added at room temperature and the reaction mixture was heated at reflux for 6 hrs. The reaction mixture was filtered, and the filtrate was evaporated to dryness. The residue was treated with water and refrigerated. The solid was collected by filtration, washed with water, and dried under high vacuum at 50°-60° C. overnight. The solid was recrystallized from isopropyl alcohol-water, collected, washed with water, and dried under high vacuum at 50°-60° C. overnight. Two crops gave 1.9 g (43%) of crystals, mp 122°-123° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04873251
Source datasetuspto-grants-1989_10
ORD IDord-2fc182fe407843588e240ea3a83e1d24
Source noteuspto-grants-1989_10