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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 430524Generated: October 31, 2026

Acetic Anhydride → HCID 22172743, compound

https://huagongshe.com/reaction/430524

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant3-Aminoisonicotinic acidHCID 459531—
CatalystSulfuric AcidHCID 1118—
ProductHCID 22172743HCID 2217274349%

Reaction Steps

A mixture of 3-aminopyridine-4-carboxylic acid (3.38 g, 24.5 mmol), acetic anhydride (15 mL), and sulfuric acid (3 drops) was refluxed 4 hours. The reaction was cooled and carefully quenched with solid sodium bicarbonate. The mixture was filtered through Celite® (trademark). The filtrate was extracted with ethyl acetate. This organic phase was washed with brine, dried over magnesium sulfate and concentrated to give 2-methyl-3-oxa-1,7-diaza-naphthalen-4-one (1.95 g, 49%) as a brown crystalline material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06323208B1
Source datasetuspto-grants-2001_11
ORD IDord-86bf5efe66fe41f2a754c102aded1fc9
Source noteuspto-grants-2001_11