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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 272017Generated: October 26, 2026

Sodium Bicarbonate → methyl 3-(1H-pyrazolo[3,4-b]pyridin-5-yl)benzoate

https://huagongshe.com/reaction/272017

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant3-(Methoxycarbonyl)benzeneboronic acidHCID 2734714—
Reactant5-Bromopyrazolo[3,4-b]pyridineHCID 40427454—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-Dioxane--water (1/1)HCID 21886435—
Productmethyl 3-(1H-pyrazolo[3,4-b]pyridin-5-yl)benzoateHCID 5983605665%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 5-bromo-1H-pyrazolo[3,4-b]pyridine (2.00 g, 10.10 mmol), 3-(methoxycarbonyl)phenylboronic acid (2.20 g, 12.12 mmol), sodium bicarbonate (2.2 g, 6.00 mmol), and tetrakis(triphenylphosphine)palladium(0) (0.250 g, 0.202 mmol) in dioxane/water (40 mL/10 mL) was stirred at 110° C. for 15 hours. The mixture was then poured into ice water and extracted with ethyl acetate (3×). The organic layers were combined, dried over sodium sulfate, filtered and concentrated to dryness. Silica gel chromatography of the crude product afforded methyl 3-(1H-pyrazolo[3,4-b]pyridin-5-yl)benzoate (8) (1.65 g, 65% yield) as yellow solids. MS: m/z 254.0 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07452993B2
Source datasetuspto-grants-2008_11
ORD IDord-12d18f1e1f634fdbb275ddae2a90bd36
Source noteuspto-grants-2008_11