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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1440252Generated: November 1, 2026

Thionyl Chloride → 6-Nitropyridine-3-carbonyl chloride

https://huagongshe.com/reaction/1440252

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant6-Nitronicotinic acidHCID 298629—
Product6-Nitropyridine-3-carbonyl chlorideHCID 45081634—

Reaction Steps

To 6-nitronicotinic acid (3.5 g) is added thionyl chloride (50 ml), and the mixture is refluxed for three hours, and evaporated to remove thionyl chloride to give 6-nitronicotinoyl chloride, which is added with stirring to a solution of 7-chloro-5-oxo-2,3,4,5-tetrahydro-1H-benzazepine (3.4 g) in pyridine (50 ml) under ice-cooling. The mixture is stirred at room temperature overnight. To the reaction mixture is added water, and the mixture is extracted with ethyl acetate. The extract is washed successively with 0.1N aqueous hydrochloric acid and water, and dried over magnesium sulfate. The resultant is evaporated under reduced pressure to remove the solvent, and the residue is purified by silica gel column chromatography to give 7-chloro-5-oxo-1-(6-nitronicotinoyl)-2,3,4,5-tetrahydro-1H-benzazepine (4.9 g) as colorless amorphous.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05498609
Source datasetuspto-grants-1996_03
ORD IDord-5e2fba5081f3468999881cc8eeacb410
Source noteuspto-grants-1996_03