Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2073034Generated: October 31, 2026

N-Methylaniline → HCID 14390323, compound

https://huagongshe.com/reaction/2073034

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethylanilineHCID 7515—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant4-chlorophenyl-3H-imidazo[4,5-b]pyridine-3-acetic acidHCID 14390457—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 14390323HCID 1439032345.8%

Reaction Conditions

Temperature60 °C

Reaction Steps

Under nitrogen atmosphere, oxalyl chloride (2.21 g, 0.0174 mole) was added slowly dropwise to a stirred and chilled (~10° C.) suspension of 2-(4-chlorophenyl)-3H-imidazo[4,5-b]pyridine-3-acetic acid (5.0 g, 0.0174 mole) in 75 ml of dimethylformamide. After the addition was complete, the reaction was heated at 60° C. for 5 hrs. This acylchloride solution was added dropwise to a stirred and cooled (~10° C.) solution of N-methylaniline (2.02 g, 0.019 mole), triethylamine (1.88 g, 0.019 mole), and 74 ml of dimethylformamide. The reaction was stirred at room temperature overnight. The reaction mixture was poured into 200 ml of water and diluted with water until the cloud point. The mixture was seeded and refrigerated overnight. The solid was collected by filtration and dried under high vacuum. The solid was suspended in dilute sodium bicarbonate, collected by filtration, washed with water, and dried under high vacuum at 50° C. The solid was recrystallized from isopropyl alcohol-water, collected by filtration, washed with water, and dried under high vacuum first at 56° C., then at 98° C. for 2 days to give 3.0 g (45.7%) of crystals, mp 170°-171° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04914109
Source datasetuspto-grants-1990_04
ORD IDord-04767d87949a4716804717d1328853ad
Source noteuspto-grants-1990_04