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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 408558Generated: October 29, 2026

Sodium Bicarbonate → 2-Methyl-5-oxo-4-{3-[6-(propan-2-yloxy)pyridin-3-yl}-1H-indazol-5-yl]-1,4,5,7-tetrahydrofuro-[3,4-b]pyridine-3-carbonitrile

https://huagongshe.com/reaction/408558

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant[6-(Propan-2-yloxy)pyridin-3-yl]boronic acidHCID 44754864—
ReactantHCID 178428406HCID 178428406—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-DioxaneHCID 31275—
Product2-Methyl-5-oxo-4-{3-[6-(propan-2-yloxy)pyridin-3-yl}-1H-indazol-5-yl]-1,4,5,7-tetrahydrofuro-[3,4-b]pyridine-3-carbonitrileHCID 4691127019.6%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a degassed solution of 120 mg (0.323 mmol) 4-(3-bromo-1H-indazol-5-yl)-2-methyl-5-oxo-1,4,5,7-tetrahydrofuro[3,4-b]pyridine-3-carbonitrile (Example 24) and 70.2 mg (0.388 mmol) [6-(propan-2-yloxy)pyridin-3-yl]boronic acid in anhydrous 1,4-dioxane (3.5 ml) were added under inert gas atmosphere 37.4 mg (0.032 mmol) tetrakis(triphenylphosphine)palladium(0) and aqueous sodium bicarbonate solution (2 M, 0.77 ml). The resulting mixture was stirred at 100° C. for 12 h. After cooling to room temperature and concentration under reduced pressure, the remaining solid was dissolved in ethyl acetate (20 ml). The solution was subsequently washed with water and brine, dried over sodium sulfate and concentrated under reduced pressure. The crude product was purified by preparative RP-HPLC (acetonitrile/water gradient, final mixture 95:5 v/v) to yield the title compound as a white solid (27 mg, 19% of th.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759341B2
Source datasetuspto-grants-2014_06
ORD IDord-b9d2cb5b011247199a4fa4f996baa603
Source noteuspto-grants-2014_06