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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167664Generated: November 1, 2026

N-(2-furanylmethyl) 5-nitro-2-(3-chloro-5-pyridyloxy)benzamide → N-(2-furanylmethyl) 5-amino-2-(3-chloro-5-pyridyloxy)benzamide

https://huagongshe.com/reaction/1167664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(2-furanylmethyl) 5-nitro-2-(3-chloro-5-pyridyloxy)benzamideHCID 54136240—
CatalystNickelHCID 935—
SolventMethanolHCID 887—
ProductN-(2-furanylmethyl) 5-amino-2-(3-chloro-5-pyridyloxy)benzamideHCID 5371239076%

Reaction Steps

To a 0.08M solution of N-(2-furanylmethyl) 5-nitro-2-(3-chloro-5-pyridyloxy)benzamide (3.7 g, 10 mmol, prepared in Example 35.2) in MeOH was added a 50% aqueous slurry of Raney nickel (˜6 mL). Hydrogen was then bubbled through the resulting solution for one minute. The resulting mixture was stirred at ambient temperature under one atmosphere of hydrogen for 16 hr. The crude reaction mixture was filtered through a pad of Celite® and the filter cake was washed 3× with MeOH. NOTE: Raney nickel is pyrophoric and should always be kept wet with solvent during the filtration. The Raney nickel can be quenched by adding 6M aqueous HCl. The filtrate was concentrated in the presence of benzene to azeotropically remove water. The residue was purified by chromatography (1-3% MeOH in CH2Cl2) to yield 2.6 g (76%) of N-(2-furanylmethyl) 5-amino-2-(3-chloro-5-pyridyloxy)benzamide as a pale brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06620827B2
Source datasetuspto-grants-2003_09
ORD IDord-45b400661faa458ab5dcd7d9cc7a3327
Source noteuspto-grants-2003_09