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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1864987Generated: October 25, 2026

Ethyl Acetate → 7-(2-Chloro-4-methoxyphenyl)-2-ethyl-3-nitropyrazolo[1,5-a]pyridine

https://huagongshe.com/reaction/1864987

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantBarium hydroxide, octahydrateHCID 17749109—
Reactant7-Bromo-2-ethyl-3-nitropyrazolo[1,5-a]pyridineHCID 21984481—
Reactant2-Chloro-4-methoxyphenylboric acidHCID 21984696—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Product7-(2-Chloro-4-methoxyphenyl)-2-ethyl-3-nitropyrazolo[1,5-a]pyridineHCID 2198458373.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

After dissolving 7-bromo-2-ethyl-3-nitropyrazolo[1,5-a]pyridine (100 mg) in 1,2-dimethoxyethane (6 mL) and water (1 mL), 2-chloro-4-methoxyphenylboric acid (138 mg), tetrakis(triphenylphosphine)palladium(0) complex (86 mg) and barium hydroxide octahydrate (233 mg) were added and the mixture was heated and stirred at 80° C. for 3 hours under a nitrogen stream. Water was added to the reaction mixture, extraction was performed with ethyl acetate and the extract washed with saturated aqueous sodium hydrogencarbonate and brine, in that order. After drying over anhydrous magnesium sulfate and filtration, the solvent was concentrated under reduced pressure, the residue was purified by silica gel column chromatography, and the title compound (90 mg) was obtained from the n-hexane:ethyl acetate (30:1) fraction as yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07625925B2
Source datasetuspto-grants-2009_12
ORD IDord-3577c595748149abaeeb3f032f135b28
Source noteuspto-grants-2009_12