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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 564729Generated: October 31, 2026

Sodium hydride → 2-Acetyl-7-methoxyfuro[2,3-c]pyridine4-carboxylic acid (3,5-dichloropyridin-4-yl)amide

https://huagongshe.com/reaction/564729

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant4-Amino-3,5-dichloropyridineHCID 89888—
Reactant2-Acetyl-7-methoxyfuro[2,3-c]pyridine-4-carboxylic acid 4-nitrophenyl esterHCID 54165983—
SolventDimethylformamideHCID 6228—
Product2-Acetyl-7-methoxyfuro[2,3-c]pyridine4-carboxylic acid (3,5-dichloropyridin-4-yl)amideHCID 979999411.2%

Reaction Steps

A solution of 4-amino-3,5-dichloropyridine (57 mg) in dry N,N-dimethylformamide (10 ml) was stirred at room temperature under an atmosphere of dry nitrogen. Sodium hydride (21 mg) was added and stirring continued for 45 minutes. 2-Acetyl-7-methoxyfuro[2,3-c]pyridine-4-carboxylic acid 4-nitrophenyl ester (100 mg) was added and the resulting mixture stirred overnight. The solvent was removed in vacuo, the residue taken up in water (100 ml) and extracted with ethyl acetate (3×100 ml). The combined organic extracts were washed with water (100 ml) then brine (50 ml), dried over magnesium sulfate, filtered and the solvent removed in vacuo. Purification by column chromatography on silica eluting with 50% hexane in ethyl acetate gave the title compound (12 mg) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06169090A
Source datasetuspto-grants-2001_01
ORD IDord-d43e9da2ff5742ddbcfef6d11021c5b8
Source noteuspto-grants-2001_01