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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1793802Generated: November 1, 2026

Phosphorus oxychloride → N-(5-chloropyridin-2-yl)-5-fluoro-2-nitrobenzamide

https://huagongshe.com/reaction/1793802

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
Reactant2-Amino-5-chloropyridineHCID 66174—
Reactant5-Fluoro-2-nitrobenzoic acidHCID 2737420—
SolventPyridineHCID 1049—
ProductN-(5-chloropyridin-2-yl)-5-fluoro-2-nitrobenzamideHCID 2190625772%

Reaction Steps

A solution of 5-fluoro-2-nitrobenzoic acid (10.0 g, 54 mmol, 1.0 equiv.), 2-amino-5-chloropyridine (9.02 g, 1.3 equiv.), in 80 mL of pyridine was treated with phosphorous oxychloride (25.3 g, 3.0 equiv.) for 30 minutes. The volatile was evaporated and the residue was redissolved into EtOAc, washed with 1N HCl, saturated aqueous NaHCO3 and saturated aqueous NaCl. The organic layer was dried over Na2SO4, filtered, and evaporated. The product was triturated with diethyl ether to give N-(5-chloro-2-pyridinyl)-(2-nitro)-5-fluorophenylcarboxamide (11.5 g, 72%). MS found for C12H7ClFN3O'(M+H)+: 296, (M+2+H): 298.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07022695B2
Source datasetuspto-grants-2006_04
ORD IDord-14264308875c496eb5454edb75c702cc
Source noteuspto-grants-2006_04