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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1896728Generated: October 27, 2026

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

https://huagongshe.com/reaction/1896728

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 numberUS08518977B2
Source datasetuspto-grants-2013_08
ORD IDord-c0ee46460f684fe5855b940d3edcbc87
Source noteuspto-grants-2013_08