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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464387Generated: October 29, 2026

Pyridine → HCID 54717980, compound

https://huagongshe.com/reaction/464387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 54710916HCID 54710916—
SolventWaterHCID 962—
ProductHCID 54717980HCID 54717980—

Reaction Steps

A mixture of 2 parts of N-(4-aminophenyl)-1,2-dihydro-4-hydroxy-1-methyl-2-oxo-quinoline-3-carboxamide, 5 parts of pyridine, and 10 parts of acetic anhydride is left overnight at room temperature. Water is added and the precipitate is filtered off and washed with 2M aqueous hydrochloric acid, water, methanol and ethylether to give N-(4-acetylaminophenyl)-1,2-dihydro-4-hydroxy-1-methyl-2-oxo-quinoline-3-carboxamide (1). M. p. 231°-4° C. (The same compound as 1:41.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04547511
Source datasetuspto-grants-1985_10
ORD IDord-d9f1d685c68c49019154bec93cb2d70c
Source noteuspto-grants-1985_10