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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1252989Generated: November 1, 2026

5-amino-3H-pyrazol-3-one → 7-(2,3-Dichlorophenyl)-1,2,4,7-tetrahydro-5-methyl-2-oxopyrazolo[1,5-a]pyrimidine-6-carboxylic acid, ethyl ester

https://huagongshe.com/reaction/1252989

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-amino-3H-pyrazol-3-oneHCID 4255556—
ReactantEthyl 2-[(2,3-dichlorophenyl)methylidene]-3-oxobutanoateHCID 54112468—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product7-(2,3-Dichlorophenyl)-1,2,4,7-tetrahydro-5-methyl-2-oxopyrazolo[1,5-a]pyrimidine-6-carboxylic acid, ethyl esterHCID 1413043138.6%

Reaction Steps

A solution of 2-[(2,3-dichlorophenyl)methylene]-3-oxobutanoic acid, ethyl ester (2.8 g; 10.0 mmole) in dimethylformamide (7 ml) was treated with 3-amino-5-pyrazolone (990 mg) and the resulting mixture was heated at 65° C.±5° for 15 hours. The reaction mixture was allowed to cool to room temperature and then diluted with ethyl acetate. The solution was washed with water, brine, and dried over anhydrous magnesium sulfate. Evaporation of the solvent provided a foam which was purified by flash chromatography (7% methanol in dichloromethane). The product was crystallized from acetonitrile-isopropyl ether to provide the title compound as a solid (1.42 g; melting point 213°-218° C.; sinters above 155° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04746656
Source datasetuspto-grants-1988_05
ORD IDord-f78e2d7279a34a54a79cf6d7d830d5ac
Source noteuspto-grants-1988_05