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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2351689Generated: October 31, 2026

Aniline → HCID 14390294, compound

https://huagongshe.com/reaction/2351689

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant2-(3-Chlorophenyl)-3H-imidazo[4,5-b]pyridine-3-acetic acidHCID 14390454—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 14390294HCID 1439029437.3%

Reaction Steps

Under a nitrogen atmosphere, oxalyl chloride (4.6 g, 0.037 mole was added dropwise (slowly) to a stirred and chilled (10°-15° C.) solution of 2-(3-chlorophenyl)-3H-imidazo[4,5-b]pyridine-3-acetic acid (10.0 g, 0.035 mole) in anhydrous dimethylformamide (b 100 ml). The reaction mixture was heated at 55°-60° C. for 5 hours, cooled to room temperature, and added dropwise to a stirred and chilled (10°-15° C.) solution of aniline (3.5 g, 0.038 mole) and triethylamine (7.6 g, 0.076 mole) in anhydrous dimethylformamide (75 ml). The reaction was stirred at room temperature overnight, poured into water (500 ml), allowed to precipitate, and filtered. The filter cake was twice suspended in potassium bicarbonate solution (250 ml) and filtered. The filter cake was washed with water, air dried, and recrystallized from ethanol, giving 4.74 g (37%) of off-white needles, mp 211°-212° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04873251
Source datasetuspto-grants-1989_10
ORD IDord-5441b03392614e3e90ce0f6f9943ebf2
Source noteuspto-grants-1989_10