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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 621948Generated: October 31, 2026

2-Chloroaniline → HCID 14390295, compound

https://huagongshe.com/reaction/621948

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-chloroaniline (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 ater, 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 numberUS04824951
Source datasetuspto-grants-1989_04
ORD IDord-5c8c82ab4d2e4b68a195b1095f30ee65
Source noteuspto-grants-1989_04