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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891455Generated: October 30, 2026

Ethanol → HCID 23599482, compound

https://huagongshe.com/reaction/891455

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium CarbonateHCID 10340—
Reactant3-Formylphenylboronic acidHCID 2734356—
ReactantHCID 9836523HCID 9836523—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23599482HCID 23599482—

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-bromothiophene-2-carboxamide) and 3-formylphenyl boronic acid, tetrakis(triphenylphosphine)palladium (0), sodium carbonate in a mixture of tetrahydrofuran, ethanol and water. The compound was purified 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. The aqueous layer was extracted by chloroform and evaporated to gave the title compound; MS (ES+) 341 (MH+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07001914B2
Source datasetuspto-grants-2006_02
ORD IDord-837a933dbf874bf6bda2605f1a1e96a2
Source noteuspto-grants-2006_02