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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2067925Generated: October 31, 2026

3-Nitropyridin-2-ylamine → 2-Bromo-3-nitropyridine

https://huagongshe.com/reaction/2067925

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Nitropyridin-2-ylamineHCID 77887—
Reactant2,3-DibromopyridineHCID 817102—
SolventHydrogen BromideHCID 260—
Product2-Bromo-3-nitropyridineHCID 555054—

Reaction Steps

Bouillon et al in Tetrahedron, 2002, 58, 17, 3323-3328 reported a three-step process for the preparation of 2,3-dibromopyridine from 2-amino-3-nitropyridine. The process involves diazotization of 2-amino-3-nitropyridine followed by addition of CuBr in 47% HBr to obtain 2-bromo-3-nitropyridine. The 2-bromo-3-nitropyridine so obtained is reduced with Fe and acetic acid to 3-amino-2-bromopyridine and subsequent diazotization to give 2,3-dibromopyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293918B2
Source datasetuspto-grants-2012_10
ORD IDord-7b0313d5e5e14bca9d9eb20cacab75c0
Source noteuspto-grants-2012_10