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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 621995Generated: October 30, 2026

Dimethylamine → (S)-2-(4-Chlorophenyl)-N,N,alpha-trimethyl-3H-imidazo[4,5-b]pyridine-3-acetamide

https://huagongshe.com/reaction/621995

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant(S)-2-(4-chlorophenyl)-alpha-methyl-3H-imidazo[4,5-b]pyridine-3-acetic acidHCID 14390427—
SolventTetrahydrofuranHCID 8028—
Product(S)-2-(4-Chlorophenyl)-N,N,alpha-trimethyl-3H-imidazo[4,5-b]pyridine-3-acetamideHCID 1439040759%

Reaction Steps

A solution of (S)-2-(4-chlorophenyl)-α-methyl-3H-imidazo[4,5-b]pyridine-3-acetic acid (5.0 g, 0.0166 mole), 1,1'-carbonyldiimidazole (3.21 g, 0.0198 mole) and dry tetrahydrofuran (100 ml) was stirred at room temperature for 3 hours with nitrogen bubbling through it. A solution of dimethylamine (2.26 g, 0.050 mole) in tetrahydrofuran (20 ml) was added and the reaction mixture was stirred at room temperature under nitrogen overnight. The mixture was evaporated to an oil and partitioned between ethyl acetate (50 ml) and water (50 ml). The layers were separated and the aqueous layer was re-extracted with ethyl acetate. The combined organic layers were washed once with water (50 ml), twice with 5% potassium hydroxide solution (50 ml portions), and once more with water (50 ml). Drying over magnesium sulfate, treatment with charcoal, filtration and evaporation of the solvents gave a residue which upon recrystallization from hot isopropyl ether and drying under high vacuum gave 3.20 g (59%) of title compound, mp 124°-126° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04824951
Source datasetuspto-grants-1989_04
ORD IDord-d5c2dfc35cbd4abf92ba8437168106a7
Source noteuspto-grants-1989_04