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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 404467Generated: October 29, 2026

4-Aminophenylboronic acid → Tert-butyl 4-(4-(4-aminophenyl)-6-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1,3,5-triazin-2-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/404467

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Aminophenylboronic acidHCID 2734615—
ReactantToluene ethanolHCID 21863594—
ReactantTert-butyl 4-(4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-6-chloro-1,3,5-triazin-2-yl)piperazine-1-carboxylateHCID 86636518—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventSodium CarbonateHCID 10340—
ProductTert-butyl 4-(4-(4-aminophenyl)-6-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1,3,5-triazin-2-yl)piperazine-1-carboxylateHCID 67021837—

Reaction Steps

A suspension of tert-butyl 4-(4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-6-chloro-1,3,5-triazin-2-yl)piperazine-1-carboxylate (1.0 g, 2.4 mmol), 4-aminophenylboronic acid, pinacol ester (0.69 g, 3.2 mmol), and tetrakis(triphenylphosphine) palladium (0.28 g, 0.24 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08748421B2
Source datasetuspto-grants-2014_06
ORD IDord-46dafe0b1b554e30bb09a0d3bc687e54
Source noteuspto-grants-2014_06