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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 82195Generated: October 26, 2026

Ethyl bromoacetate → Ethyl (1H-pyrazolo[3,4-b]pyridin-1-yl)acetate

https://huagongshe.com/reaction/82195

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
Reactant1H-pyrazolo(3,4-b)pyridineHCID 2755850—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductEthyl (1H-pyrazolo[3,4-b]pyridin-1-yl)acetateHCID 5764279849%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 7-aza indazole (250 mg, 2.1 mmol) and ethyl bromoacetate (0.47 mL, 4.2 mmol) in DMF (8 mL) was added K2CO3 (1.16 gm, 8.4 mmol) and the resulting mixture stirred at 70° C. for 16 hours. The reaction mixture was cooled to room temperature and diluted with ethyl acetate (20 mL). The organic layer was washed with water (2×5 mL), brine (5 mL), dried over sodium sulphate, filtered and concentrated under reduced pressure. The crude material was purified using silica gel column chromatography eluting with EtOAc:hexane 10:90 to afford the title compound as an off-white solid in 49% yield, 210 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846698B2
Source datasetuspto-grants-2014_09
ORD IDord-794e1543a55d4c98b01bac4bcb6cc64f
Source noteuspto-grants-2014_09