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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 462716Generated: October 30, 2026

Water → 5-Methyl-2-oxo-1,2-dihydro-1,6-naphthyridine-3-carboxylic acid

https://huagongshe.com/reaction/462716

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSulfuric AcidHCID 1118—
ReactantAmmonium HydroxideHCID 14923—
Reactant5-methyl-2-oxo-1H-1,6-naphthyridine-3-carbonitrileHCID 5713068—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
SolventDiethyl EtherHCID 3283—
Product5-Methyl-2-oxo-1,2-dihydro-1,6-naphthyridine-3-carboxylic acidHCID 13232052—

Reaction Steps

E-6. 1,2-Dihydro-5-methyl-2-oxo-1,6-naphthyridine-3-carboxylic acid--A mixture containing 63 g of 1,2-dihydro-5-methyl-2-oxo-1,6-naphthyridine-3-carbonitrile, 100 ml of concentrated sulphuric acid and 100 ml of water was heated on a steam bath for 16 hours, after which time tlc analyses (20% methanol in ether) indicated the presence of a considerable amount of starting material. Therefore, the reaction mixture was heated in a oil bath at 135°-140° C. for 8 hours, cooled to room temperature and poured on ice (1 l. beaker, 1/3 filled). The resulting aqueous mixture was neutralized by adding aqueous ammonium hydroxide until slightly basic and was then reacidified by adding acetic acid. The resulting solid was collected, washed successively with water and methanol, and dried at 100° C. to yield 54.8 g of 1,2-dihydro-5-methyl-2-oxo-1,6-naphthyridine-3-carboxylic acid, m.p. 255°-257° C. with decomposition. Another 7.2 g of the product, m.p. 252° -255° C. was obtained from the mother liquor.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04517190
Source datasetuspto-grants-1985_05
ORD IDord-5846d8dde2564718af43c6ebd0fc4564
Source noteuspto-grants-1985_05