Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1465733Generated: October 30, 2026

Cesium carbonate → tert-Butyl 4-(6-cyanoquinolin-2-yl)-3-oxopiperazine-1-carboxylate

https://huagongshe.com/reaction/1465733

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
ReactantTert-butyl 3-oxopiperazine-1-carboxylateHCID 3157178—
Reactant2-Chloroquinoline-6-carbonitrileHCID 11252468—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Producttert-Butyl 4-(6-cyanoquinolin-2-yl)-3-oxopiperazine-1-carboxylateHCID 131732662—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a 25 mL flask was added a stir bar, 2-chloroquinoline-6-carbonitrile (0.015 g, 0.79 mmol), Pd2 dba3 (0.072 g, 0.08 mmol), Xantphos (0.09 g, 0.16 mmol), cesium carbonate (0.36 g, 1.13 mmol) and tert-Butyl 3-oxopiperazine-1-carboxylate (0.31 g, 1.6 mmol). The resulting mixture was degassed and purged with N2 (3×). To the flask was added 1,4-dioxane (10 mL). The reaction mixture was then refluxed at 100° C. overnight. Analysis of the reaction mixture by LC indicated that reaction had gone to completion. The solution was concentrated in vacuo and the resulting crude was dissolved in EtOAc and washed with brine, dried over Na2SO4, filtered and concentrated in vacuo. The crude residue was purified by silica gel column chromatography (10% MeOH in DCM) to provide the title product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999991B2
Source datasetuspto-grants-2015_04
ORD IDord-39f5ec5f0ff042449979f97d353b15d4
Source noteuspto-grants-2015_04