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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1181550Generated: November 2, 2026

Phosphorus oxychloride → N-(5-bromo-2-pyridinyl)-(2-nitro)-5fluorophenylcarboxamide

https://huagongshe.com/reaction/1181550

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
Reactant2-Amino-5-bromopyridineHCID 70622—
Reactant5-Fluoro-2-nitrobenzoic acidHCID 2737420—
SolventPyridineHCID 1049—
ProductN-(5-bromo-2-pyridinyl)-(2-nitro)-5fluorophenylcarboxamideHCID 2259629868.1%

Reaction Steps

A solution of 5-fluoro-2-nitrobenzoic acid (10.0 g, 54 mmol, 1.0 equiv), 2-amino-5-bromopyridine (12.2 g, 1.3 equiv), in 80 mL of pyridine was treated with phosphorous oxychloride (25.3 g, 3.0 equiv) for 30 min. 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 volatile was evaporated, and the product was triturated with diethyl ether to give N-(5-bromo-2-pyridinyl)-(2-nitro)-5-fluorophenylcarboxamide (12.5 g, 68%). MS found for C12H7BrFN3O3 (M+H)+: 340, 342.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07285565B2
Source datasetuspto-grants-2007_10
ORD IDord-61336bab5a244af49ec9de3064386834
Source noteuspto-grants-2007_10