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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2260529Generated: October 26, 2026

Glyoxal → 8-(4-Fluorophenyl)-7-(pyridin-4-yl)pyrazolo[1,5-b][1,2,4]triazine

https://huagongshe.com/reaction/2260529

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlyoxalHCID 7860—
ReactantSodium BicarbonateHCID 516892—
ReactantO-(2,4,6-Trimethylbenzenesulfonyl)hydroxylamineHCID 11830845—
ReactantHCID 178509114HCID 178509114—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product8-(4-Fluorophenyl)-7-(pyridin-4-yl)pyrazolo[1,5-b][1,2,4]triazineHCID 19957270—

Reaction Steps

To a solution of 5-amino-4-(4-fluorophenyl)-3-(pyridin-4-yl)pyrazole (1.674 g) in ethanol (33 ml) was added O-mesitylsulfonylhydroxylamine (2.362 g). The mixture was stirred at ambient temperature for 30 minutes and to the mixture was added a solution of glyoxal in water (40%, 955 mg). The mixture was refluxed for 4 hours and cooled. The reaction mixture was poured into an aqueous saturated sodium bicarbonate solution and the separated oil was extracted with dichloromethane. The extract was washed with brine, dried and concentrated in vacuo. The residue was purified by column chromatography on silica gel and the obtained oil was crystallized from ethanol to give 8-(4-fluorophenyl)-7-(pyridin-4-yl)pyrazolo[1,5-b][1,2,4]triazine (63 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05478827
Source datasetuspto-grants-1995_12
ORD IDord-db30fbb3b61947f2831d9e3117a44962
Source noteuspto-grants-1995_12