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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701702Generated: October 30, 2026

3-Nitro-N-(pyridin-4-yl)pyridin-2-amine → HCID 12445535, compound

https://huagongshe.com/reaction/1701702

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Nitro-N-(pyridin-4-yl)pyridin-2-amineHCID 12445392—
ReactantHCID 178418361HCID 178418361—
SolventEthanolHCID 702—
ProductHCID 12445535HCID 12445535—

Reaction Steps

A solution of 16.5 g of 2-(4-pyridylamino)-3-nitro-pyridine in 400 ml of 95% ethanol containing 1.6 g of 10% palladized carbon was hydrogenated at 30°-40° C. at atmospheric pressure until 5.8 liters of hydrogen were absorbed and the mixture was filtered to remove the catalyst. The filtrate was evaporated to dryness and the residue was taken up in petroleum ether. The mixture was filtered to obtain 13.5 g (95% yield) of raw product melting at 202°-204° C. which was crystallized from 95% ethanol to obtain 2-(4-pyridylamino)-3-amino-pyridine in the form of a pale yellow, crystalline powder melting at 203°-205° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04195088
Source datasetuspto-grants-1980_03
ORD IDord-dc5289a80a244ddf826de2a0350af6b0
Source noteuspto-grants-1980_03