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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1633247Generated: October 30, 2026

Phenylhydrazine → HCID 178515215, compound

https://huagongshe.com/reaction/1633247

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylhydrazineHCID 7516—
ReactantOxalyl chlorideHCID 65578—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 178469573HCID 178469573—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 178515215HCID 178515215—

Reaction Steps

To a slurry of 1.5 g of ethyl 4-hydroxy-1,5-naphthyridine-3-carboxylate (prepared according to J. Inorg. Nucl. Chem., (1966) 28, 2439) in 17 ml of dimethylformamide is added 0.907 g of oxalyl chloride in 2 ml of methylene chloride while maintaining the reaction temperature between -25° and -30°. The mixture is stirred at -25° for 35 minutes. A solution of 0.995 g of diisopropylethylamine and 0.833 g of phenylhydrazine in 4 ml of methylene chloride is added to the mixture in 8 minutes at -30° to -25°. The mixture is then stirred for 30 minutes at -25°, 20 minutes at 0° and 40 minutes at 23°. The resultant dark purple solution is poured into 60 ml of water. Dark precipitate is collected, washed with water and crystallized from methanol to yield 2-phenyl-pyrazolo[4,3-c] [1,5]naphthyridin-3(5H)-one, m.p. 314°-316°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04479955
Source datasetuspto-grants-1984_10
ORD IDord-4054b2332f69434db1d2e76cc3c223ea
Source noteuspto-grants-1984_10