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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2373214Generated: October 31, 2026

2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → HCID 11710689, compound

https://huagongshe.com/reaction/2373214

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
Reactant1-Ethyl-1H-pyrazol-5-amineHCID 337310—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 69183199HCID 69183199—
Solventtert-ButanolHCID 6386—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11710689HCID 11710689—

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of tert-butyl -2-(methoxymethyl)-3-(5-methyl-3-pyridyl)acrylate (1.26 g) and 5-amino-1-ethylpyrazole (481 mg) in tert-BuOH (14 ml) was heated at 90° C. for 3 hours. After cooling the mixture was dissolved in THF (14 ml). To this was added 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (982 mg) and the mixture was stirred at room temperature for 1 hour. The reaction mixture was poured into saturated aqueous NaHCO3 and extracted with EtOAc. The organic layer was washed with brine, dried over anhydrous MgSO4 and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel eluting with a mixture of EtOAc and n-hexane (1:1) to give tert-butyl 1-ethyl-6-(methoxymethyl)-4-(5-methyl-3-pyridyl)-1H-pyrazolo[3,4-b]pyridine-5-carboxylate (1.23 g) as a colorless crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07459451B2
Source datasetuspto-grants-2008_12
ORD IDord-387b61e85c874762ac618a2ae2c55ca7
Source noteuspto-grants-2008_12