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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2351690Generated: November 1, 2026

2-Chloroaniline → HCID 14390295, compound

https://huagongshe.com/reaction/2351690

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChloroanilineHCID 7240—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant4-chlorophenyl-3H-imidazo[4,5-b]pyridine-3-acetic acidHCID 14390457—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 14390295HCID 1439029554%

Reaction Conditions

Temperature60 °C

Reaction Steps

Under a nitrogen atmosphere, oxalyl chloride (1.73 g, 0.014 mole) was added slowly to a stirred and chilled (10°-15° C.) suspension of 2-(4-chlorophenyl)-3H-imidazo[4,5-b]pyridine-3-acetic acid (3.7 g, 0.013 mole) in 50 ml of dimethylformamide. The reaction mixture was heated at 60° C. for 5 hours. The solution of the acyl chloride prepared above was added dropwise under nitrogen atmosphere to a stirred and chilled (10°-15° C.) solution of o-chloro-aniline (1.79 g, 0.014 mole), triethylamine (1.42 g, 0.014 mole), and 75 ml of dimethylformamide. After the addition, the reaction mixture was allowed to stir at room temperature overnight. The reaction mixture was poured into 200 ml of water. The crystalline solid was collected by filtration, washed with water, and dried under high vacuum overnight to give 2.76 g (54%) of crystals, mp 232°-235.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04873251
Source datasetuspto-grants-1989_10
ORD IDord-4b3e1f352d5f4a6f8b4d272f773dc8d0
Source noteuspto-grants-1989_10