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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1028972Generated: October 25, 2026

Cesium carbonate → 6-bromo-3-(2-ethylmorpholino)-N-(4-methoxybenzyl)quinolin-2-amine

https://huagongshe.com/reaction/1028972

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant2-(2-Methylpropanoyl)cyclohexan-1-oneHCID 11469301—
Reactant2-EthylmorpholineHCID 14933206—
Reactant6-bromo-3-iodo-N-(4-methoxybenzyl)quinolin-2-amineHCID 67345652—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethylformamideHCID 6228—
Product6-bromo-3-(2-ethylmorpholino)-N-(4-methoxybenzyl)quinolin-2-amineHCID 71253261—

Reaction Conditions

Temperature125 °C

Reaction Steps

A mixture of 6-bromo-3-iodo-N-(4-methoxybenzyl)quinolin-2-amine (0.30 g, 0.640 mmol, prepared as in Example 1, Step 1-2), 2-ethylmorpholine (1.105 g, 9.59 mmol), copper(I) iodide (6.09 mg, 0.032 mmol), cesium carbonate (0.417 g, 1.279 mmol), and 2-isobutyrylcyclohexanone (0.021 mL, 0.128 mmol) in DMF (3 mL) was heated at 125° C. for 10 min. Some product was observed but mostly starting material. The mixture was heated again at 125° C. for 10 min more. This process was repeated 3× until the starting material was completely consumed. The reaction was brought to RT, poured into water (20 mL) and extracted with EtOAc. The combined organics were dried over Na2SO4, filtered, concentrated, and chromatographed on silica gel using gradient 2:1 hexanes/EtOAc to afford a brown oil as 6-bromo-3-(2-ethylmorpholino)-N-(4-methoxybenzyl)quinolin-2-amine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735384B2
Source datasetuspto-grants-2014_05
ORD IDord-25fb7f4caf964db3946e1685e7ddeeb0
Source noteuspto-grants-2014_05