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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1350908Generated: November 1, 2026

Ethanol → HCID 23599443, compound

https://huagongshe.com/reaction/1350908

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium CarbonateHCID 10340—
Reactant3-Aminophenylboronic acidHCID 92269—
ReactantHCID 952706HCID 952706—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23599443HCID 23599443—

Reaction Steps

Prepared by a method analogous to that described in Example 1 from (R)-N-(1-azabicyclo[2.2.2]oct-3-yl)(5-bromofuran-2-carboxamide) and 3-aminophenylboronic acid, using tetrakis(triphenylphosphine)palladium (0) and sodium carbonate in a mixture of tetrahydrofuran, ethanol and water. The compound was purified by flash chromatography using 5–20% 3.5M methanolic ammonia/chloroform mixtures as the eluent and then by reverse phase HPLC on a Waters Bondapak® C18 column using a gradient of acetonitrile and 0.1% aqueous trifluoroacetic acid as the eluent. The free base was prepared by basification of the product-containing fractions and extraction into chloroform followed by evaporation to gave the title compound; MS (ES+) 312 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07214688B2
Source datasetuspto-grants-2007_05
ORD IDord-71b4e3ab0f044808a1578397ca79bd66
Source noteuspto-grants-2007_05