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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2073015Generated: October 30, 2026

Aniline → HCID 14390294, compound

https://huagongshe.com/reaction/2073015

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 (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 numberUS04914109
Source datasetuspto-grants-1990_04
ORD IDord-a40233d2f8da4617a8b7acad3390d533
Source noteuspto-grants-1990_04