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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1489063Generated: October 31, 2026

Thionyl Chloride → 6-Nitropyridine-3-carbonyl chloride

https://huagongshe.com/reaction/1489063

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 numberUS05677299
Source datasetuspto-grants-1997_10
ORD IDord-4a4c71a79da4400bb39308179a35ae18
Source noteuspto-grants-1997_10