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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2410257Generated: November 4, 2026

Potassium Carbonate → Tetraisopropyl (2-(5-(3,5-dimethylisoxazol-4-yl)pyridin-3-yl)-1-fluoroethane-1,1-diyl)bis(phosphonate)

https://huagongshe.com/reaction/2410257

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3,5-Dimethylisoxazole-4-boronic acidHCID 2734346—
ReactantTetraisopropyl(2-(5-bromopyridin-3-yl)-1-fluoroethane-1,1-diyl)bis(phosphonate)HCID 86691496—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductTetraisopropyl (2-(5-(3,5-dimethylisoxazol-4-yl)pyridin-3-yl)-1-fluoroethane-1,1-diyl)bis(phosphonate)HCID 8669149747%

Reaction Conditions

Temperature80 °C

Reaction Steps

A sample of tetraisopropyl (2-(5-bromopyridin-3-yl)-1-fluoroethane-1,1-diyl)bis(phosphonate) (85 mg; 0.16 mmol), Pd(Ph3)4 (36.9 mg; 0.032 mmol) and (3,5-dimethylisoxazol-4-yl)boronic acid (34 mg; 0.24 mmol) are added in a vial, the vial is capped with a septum and added DME (4 mL) is added. The mixture is immediately flushed with argon, potassium carbonate solution (2.5 eq.) is added and flushed again with argon. The reaction mixture is stirred at 80° C. for 36 h under argon. The mixture is cooled, diluted with EtOAc and filtered through Celite™, the Celite™ is rinsed 3× with EtOAc/MeOH (1:1). The combined filtrate is concentrated under vacuum and deposited on silica gel. Purification by column chromatography on silica gel (pre washed with 1% NEt3 in hexanes) using a solvent gradient from hexanes to EtOAc, and then to 50% MeOH in EtOAc lead to the isolation of the product as a brown oil (41 mg; 47% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08816082B2
Source datasetuspto-grants-2014_08
ORD IDord-31cf19ce63bd4e5e9d8c6a232515eb9b
Source noteuspto-grants-2014_08