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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571981Generated: October 28, 2026

Pyridine → phenyl 1H-pyrazolo[3,4-b]pyridin-5-ylcarbamate

https://huagongshe.com/reaction/571981

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetonitrileHCID 6342—
ReactantPhenyl chloroformateHCID 15891—
Reactant1-Methyl-3,5-dinitro-1H-pyridin-2-oneHCID 3621236—
Productphenyl 1H-pyrazolo[3,4-b]pyridin-5-ylcarbamateHCID 86676322—

Reaction Steps

1H-Pyrazolo[3,4-b]pyridin-5-amine (B) (212 mg, 1.58 mmol) was dissolved in acetonitrile. To the reaction mixture was added pyridine (0.15 mL, 1.896 mmol) and phenyl chloroformate (0.2 mL, 1.659 mmol) and stirred at room temperature for 30 min under N2. TLC showed complete consumption of starting material. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic part was washed with water and brine. The organic layer was dried over MgSO4 and concentrated under reduced pressure. The crude was purified by column chromatography to give phenyl 1H-pyrazolo[3,4-b]pyridin-5-ylcarbamate (C). (285 mg, 71%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029378B2
Source datasetuspto-grants-2015_05
ORD IDord-deeb550db3d74083a74d75ce34b3fe80
Source noteuspto-grants-2015_05