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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2411238Generated: October 31, 2026

Tetrahydrofuran → HCID 71251889, compound

https://huagongshe.com/reaction/2411238

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantMethylboronic AcidHCID 139377—
ReactantPotassium FluorideHCID 522689—
ReactantHCID 66524905HCID 66524905—
Catalystpalladium(II) acetateHCID 167845—
Catalyst2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
SolventWaterHCID 962—
ProductHCID 71251889HCID 71251889108.7%

Reaction Steps

Under a nitrogen stream, to a mixture of 4-(5-bromo-3-cyanopyridin-2-yl)piperazine-1-carboxylic acid tert-butyl ester (1.52 g) described in Preparation Example 105, methylboronic acid (0.50 g), palladium(II) acetate (46 mg), 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl (0.17 g) and potassium fluoride (0.96 g) was added tetrahydrofuran (40 mL), and the mixture was stirred with heating under reflux for 8 hr. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and the solvent was evaporated. The obtained residue was purified by silica gel column chromatography (hexane:ethyl acetate) to give the title compound (1.36 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08816079B2
Source datasetuspto-grants-2014_08
ORD IDord-5db5ff3d587c408d8997ed0186d503fa
Source noteuspto-grants-2014_08