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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2109870Generated: October 30, 2026

N-(4-fluorobenzyl)-3-nitro-2-pyridinamine → HCID 677108, compound

https://huagongshe.com/reaction/2109870

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(4-fluorobenzyl)-3-nitro-2-pyridinamineHCID 3647990—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 677108HCID 677108—

Reaction Steps

A mixture of 2-(4-fluorobenzylamino)-3-nitropyridine (1.0 g, 4.05 mmol) and 10% Pd/C (0.3 g) in methanol (50 mL) was stirred under an atmosphere of hydrogen (1 atm) at room temperature for 5 hours. The product mixture was filtered through a pad of Celite, and concentrated under vacuum. The residual methanol was removed by co-evaporation with benzene. The resultant N2-(4-Fluorobenzyl)pyridine-2,3-diamine was used in the following step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07517532B2
Source datasetuspto-grants-2009_04
ORD IDord-ede2666f14cc488595d856e3f767f11b
Source noteuspto-grants-2009_04