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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1774950Generated: November 2, 2026

4-Methyl-5-nitro-2,3'-bipyridine → 4-Methyl-6-(pyridin-3-yl)pyridin-3-amine

https://huagongshe.com/reaction/1774950

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methyl-5-nitro-2,3'-bipyridineHCID 46316008—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product4-Methyl-6-(pyridin-3-yl)pyridin-3-amineHCID 4631525682.1%

Reaction Steps

A mixture of 4-methyl-5-nitro-2,3′-bipyridine (215 g, 1 mol), Pd/C (10 g, 10%) and MeOH (1000 mL) was stirred at room temperature for 16 h under 10 atm of hydrogen. After reaction, the mixture was filtered. The filtrate was evaporated at reduced pressure to afford 4-methyl-2,3′-bipyridin-5-amine as a yellow solid (152 g, 82%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260425B2
Source datasetuspto-grants-2016_02
ORD IDord-e0ac3da9f5c349a2bf79d375b9dcf18f
Source noteuspto-grants-2016_02