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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 536857Generated: October 30, 2026

4-Aminophenylboronic acid → 1-(4-(4-Aminophenyl)-6-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1,3,5-triazin-2-yl)piperidin-4-one

https://huagongshe.com/reaction/536857

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Aminophenylboronic acidHCID 2734615—
ReactantToluene ethanolHCID 21863594—
Reactant1-(4-(8-Oxa-3-azabicyclo[3.2.1]octan-3-yl)-6-chloro-1,3,5-triazin-2-yl)piperidin-4-oneHCID 86636519—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventSodium CarbonateHCID 10340—
Product1-(4-(4-Aminophenyl)-6-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1,3,5-triazin-2-yl)piperidin-4-oneHCID 67021932—

Reaction Steps

A suspension of 1-(4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-6-chloro-1,3,5-triazin-2-yl)piperidin-4-one (1.0 g, 3.1 mmol), 4-aminophenylboronic acid, pinacol ester (1.0 g, 4.7 mmol), and tetrakis(triphenylphosphine) palladium (0.20 g, 0.17 mmol) in aqueous 2 M sodium carbonate solution (3 mL) and 1:1 ethanol/toluene (12 mL) was irradiated in the microwave at 120° C. for 1 hour. After cooling, the biphasic mixture was extracted thrice with ethyl acetate. The extracts were washed with saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, filtered, and concentrated to dryness under reduced pressure to give the title compound as a golden yellow foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859542B2
Source datasetuspto-grants-2014_10
ORD IDord-d554b068e369475792358cc28fa8d59e
Source noteuspto-grants-2014_10