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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 237410Generated: October 30, 2026

Sodium Bicarbonate → HCID 44547092, compound

https://huagongshe.com/reaction/237410

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant(6-Fluoropyridin-3-yl)boronic acidHCID 2783397—
ReactantHCID 178428407HCID 178428407—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 44547092HCID 4454709249.3%

Reaction Conditions

Temperature140 °C

Reaction Steps

To a degassed solution of 125 mg (0.315 mmol) 8-(3-bromo-1H-indazol-5-yl)-6-methyl-1,3,4,8-tetrahydropyrido[2,1-c][1,4]oxazine-7,9-dicarbonitrile (Example 12A) and 53.3 mg (0.379 mmol) (6-fluoropyridin-3-yl)boronic acid in anhydrous 1,4-dioxane (2.2 ml) were added under inert gas atmosphere 36.5 mg (0.032 mmol) tetrakis(triphenylphosphine)palladium(0) and aqueous sodium bicarbonate solution (2 M, 0.56 ml). The resulting mixture was stirred at 140° C. for 70 min under microwave conditions. 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 with 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 (64 mg, 49% of th.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642595B2
Source datasetuspto-grants-2014_02
ORD IDord-f545e3c29a40467e9b8d6408d3a29c2d
Source noteuspto-grants-2014_02