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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1952356Generated: November 3, 2026

2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → Methyl [1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazolo[3,4-b]pyridin-3-yl]acetate

https://huagongshe.com/reaction/1952356

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
Reactant3,4-dihydro-2H-pyranHCID 8080—
ReactantHCID 178499647HCID 178499647—
SolventAcetonitrileHCID 6342—
ProductMethyl [1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazolo[3,4-b]pyridin-3-yl]acetateHCID 59529754—

Reaction Conditions

Temperature75 °C

Reaction Steps

To a solution of methyl 1H-pyrazolo[3,4-b]pyridin-3-ylacetate (84 mg, 0.439 mmol) in acetonitrile (3 mL) was added DHP (37 mg, 0.439 mmol) and DDQ (10 mg, 0.044 mmol). This mixture was heated to 75° C. for 20 minutes. After this time, additional DHP (37 μL, 0.44 mmol) was added and the reaction mixture heated to 85° C. for 1.5 hours. The reaction mixture was partitioned between water (10 mL) and ethyl acetate (2×20 mL). The combined organic extracts were washed with brine, dried over MgSO4, filtered and evaporated in vacuo. This residue was purified by chromatography using RediSep column (12 g) and eluting with gradient of 0-20% EtOAc/CH2Cl2. The desired fractions were combined and the solvent evaporated in vacuo to give the title compound. LRMS (M+1): 276.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404856B2
Source datasetuspto-grants-2013_03
ORD IDord-2195b8d89fb34522bc7ebaf36583a4b3
Source noteuspto-grants-2013_03