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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 572849Generated: October 29, 2026

Potassium Carbonate → HCID 66835664, compound

https://huagongshe.com/reaction/572849

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Dicyclohexylphosphino-2',6'-diisopropoxybiphenylHCID 16217985—
ReactantPotassium (3-tert-butoxy-3-oxopropyl)(trifluoro)borate(1-)HCID 49761675—
ReactantHCID 66835733HCID 66835733—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 66835664HCID 66835664—

Reaction Conditions

Temperature120 °C

Reaction Steps

A screw-cap tube is charged with 2-[(3-bromophenyl)(1-methylpiperidin-4-yloxy)methyl]benzothiazole (208 mg), palladium(II) acetate (3 mg), RuPhos® (12 mg), potassium 3-trifluoroboratopropionate tert-butyl ester (118 mg), potassium carbonate (207 mg), water (2.5 mL) and toluene (2.5 mL). The tube is evacuated, filled with argon and sealed. After stirring at 120° C. overnight, the mixture is diluted with ethyl acetate and water and the aqueous phase is extracted with ethyl acetate. The pooled organic extracts are dried over magnesium sulfate and concentrated under reduced pressure. The residue is purified by chromatography (gradient dichloromethane/methanol from 100/0 to 95/5) to afford 3-{3-[benzothiazol-2-yl(1-methylpiperidin-4-yloxy)methyl]phenyl}propionic acid tert-butyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029357B2
Source datasetuspto-grants-2015_05
ORD IDord-d95913f7b4f1458ab1e576033e534949
Source noteuspto-grants-2015_05