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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2362695Generated: October 31, 2026

Bicarbonate Ion → 1-(5-(5-fluoro-1-tosyl-2-(3,4,5-trimethoxyphenyl)-1H-pyrrolo[2,3-b]pyridin-4-yl)thiazol-2-yl)cyclobutanol

https://huagongshe.com/reaction/2362695

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBicarbonate IonHCID 769—
Reactant3,4,5-Trimethoxybenzeneboronic acidHCID 2734390—
Reactant1-(5-(5-fluoro-2-iodo-1-tosyl-1H-pyrrolo[2,3-b]pyridin-4-yl)thiazol-2-yl)cyclobutanolHCID 67003482—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
Product1-(5-(5-fluoro-1-tosyl-2-(3,4,5-trimethoxyphenyl)-1H-pyrrolo[2,3-b]pyridin-4-yl)thiazol-2-yl)cyclobutanolHCID 67003483—

Reaction Conditions

Temperature70 °C

Reaction Steps

To a stirred ambient solution of 1-(5-(5-fluoro-2-iodo-1-tosyl-1H-pyrrolo[2,3-b]pyridin-4-yl)thiazol-2-yl)cyclobutanol (Example 59A) (200 mg, 0.351 mmol) and 3,4,5-trimethoxy phenylboronic acid (112 mg, 0.527 mmol) in N,N-dimethylformamide (2630 μl) was added saturated aqueous bicarbonate solution (880 μl) followed by bis(triphenylphosphine)palladium dichloride (17.26 mg, 0.025 mmol). The mixture was heated to 70° C. for 4 hours and was quenched by the addition of water and dichloromethane. The layers were separated, and the aqueous layer was extracted with additional dichloromethane. The combined organics were dried with anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to give crude product. The residue was purified by flash chromatography on silica gel, eluting with a gradient of 0 to 100% ethyl acetate in hexane, to give the title compound. MS ESI(+) m/z 610.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691810B2
Source datasetuspto-grants-2014_04
ORD IDord-a85e1aa70a3646d1a659f055d00baf23
Source noteuspto-grants-2014_04