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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 130475Generated: October 30, 2026

5-Methyl-2-furanboronic Acid → N-[5-(cis-3,5-Dimethyl-1-piperazinyl)-2-(methyloxy)phenyl]-2-fluoro-4-(5-methyl-2-furanyl)benzenesulfonamide

https://huagongshe.com/reaction/130475

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Methyl-2-furanboronic AcidHCID 2734372—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant4-Bromo-N-[5-(cis-3,5-dimethyl-1-piperazinyl)-2-(methyloxy)phenyl]-2-fluorobenzenesulfonamideHCID 59007083—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductN-[5-(cis-3,5-Dimethyl-1-piperazinyl)-2-(methyloxy)phenyl]-2-fluoro-4-(5-methyl-2-furanyl)benzenesulfonamideHCID 24803515—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a mixture of 4-bromo-N-[5-(cis-3,5-dimethyl-1-piperazinyl)-2-(methyloxy)phenyl]-2-fluorobenzenesulfonamide (E103) (200 mg, 0.42 mmol) and (5-methyl-2-furanyl)boronic acid (106 mg, 0.84 mmol) in DME (3 ml) was added potassium tert-butoxide (430 mg, 3.8 mmol) and tetrakis(triphenylphosphine)palladium(0) (20 mg, 0.017 mmol) in water (1 ml) and the resulting mixture stirred in a microwave (set at high absorbance) at 100° C. for 30 minutes. The solvent was evaporated in vacuo and residue purified using an SCX column followed by mass directed autoprep HPLC (with addition of 0.1 ml of 10% citric acid in water to the DMSO/MeCN sample to help dissolution) to afford the title compound (E309). MS (ES+) m/e 474 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07381728B2
Source datasetuspto-grants-2008_06
ORD IDord-10fdb4f385b845bf99114b2a987c3e4e
Source noteuspto-grants-2008_06