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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2073090Generated: October 31, 2026

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

https://huagongshe.com/reaction/2073090

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
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,alpha-dimethyl-3H-imidazo[4,5-b]pyridine-3-acetamideHCID 1439042028%

Reaction Steps

A solution of (S)-2-(4-chlorophenyl)-α-methyl-3H-imidazo [4,5-b]pyridine-3-acetic acid (3.0 g, 0.00995 mole), 1,1'-carbonyldiimidazole (1.61 g, 0.00995 mole) and dry tetrahydrofuran (60 ml) was stirred at room temperature for 1.75 hours with a stream of nitrogen bubbling through it. A solution of methylamine in tetrahydrofuran (20 ml of a 3.03M solution, 0.060 mole) was added and the reaction mixture was stirred at room temperature overnight under nitrogen. The solvents were removed under reduced pressure and the resulting solid was triturated in water, 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. Upon cooling to room temperature, solid precipitated which was collected by filtration and dried under high vacuum at 50° C. overnight to give 0.86 g (28%) of title compound, mp 218°-220° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04914109
Source datasetuspto-grants-1990_04
ORD IDord-0e9876ee45e7450e88fd5b52755522c4
Source noteuspto-grants-1990_04