Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2373239Generated: October 30, 2026

2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → HCID 86602416, compound

https://huagongshe.com/reaction/2373239

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 86602399HCID 86602399—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 86602416HCID 8660241677.9%

Reaction Conditions

Temperature140 °C

Reaction Steps

A mixture of ethyl (2Z)-2-benzoyl-3-(6-chloro-3-pyridyl)acrylate (2.018 g) and 5-amino-1-ethylpyrazole (710 mg) in N-methylpyrrolidone (15 ml) was heated at 140° C. for 3.5 hours. Another 5-amino-1-ethylpyrazole (200 mg) was added and the mixture was heated at 140° C. for 2 hours. After cooling, 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (1.45 g) was added 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 saturated aqueous NaHCO3 (×4), 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 (1:7) to give ethyl 4-(6-chloro-3-pyridyl)-1-ethyl-6-phenyl-1H-pyrazolo[3,4-b]pyridine-5-carboxylate (2.024 g) as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07459451B2
Source datasetuspto-grants-2008_12
ORD IDord-d70aaa0318be41179bf465703211b383
Source noteuspto-grants-2008_12