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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-(Methoxycarbonyl)benzeneboronic acid | HCID 2734714 | — |
| Reactant | 5-Bromopyrazolo[3,4-b]pyridine | HCID 40427454 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,4-Dioxane--water (1/1) | HCID 21886435 | — |
| Product | methyl 3-(1H-pyrazolo[3,4-b]pyridin-5-yl)benzoate | HCID 59836056 | 65% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07452993B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-12d18f1e1f634fdbb275ddae2a90bd36 |
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| Source note | uspto-grants-2008_11 |
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