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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 215779Generated: October 30, 2026

Cesium carbonate → [1-(3-fluoro-4-{3-[(2R)-2-methylpyrrolidin-1-yl]propoxy}phenyl)-1H-pyrazol-4-yl](morpholin-4-yl)methanone

https://huagongshe.com/reaction/215779

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactanttrans-N,N'-dimethyl-1,2-cyclohexanediamineHCID 2733821—
ReactantMorpholino(1H-pyrazol-4-yl)methanoneHCID 20784942—
Reactant(2R)-1-[3-(4-bromo-2-fluorophenoxy)propyl]-2-methylpyrrolidineHCID 59541739—
CatalystCopper iodideHCID 83717—
SolventDimethylformamideHCID 6228—
Product[1-(3-fluoro-4-{3-[(2R)-2-methylpyrrolidin-1-yl]propoxy}phenyl)-1H-pyrazol-4-yl](morpholin-4-yl)methanoneHCID 4261035236%

Reaction Conditions

Temperature130 °C

Reaction Steps

To a solution of (2R)-1-[3-(4-bromo-2-fluorophenoxy)propyl]-2-methylpyrrolidine obtained in Example 62-(2) (0.72 g) and morpholin-4-yl(1H-pyrazol-4-yl)methanone (0.45 g) in N,N-dimethylformamide (3 mL), cesium carbonate (1.6 g), copper iodide (0.1 g) and (1R,2R)—N,N′-dimethylcyclohexane-1,2-diamine (0.36 mL) were added and the mixture was heated to 130° C., at which it was stirred for 6 hours. The reaction mixture was cooled to room temperature and filtered to remove insoluble materials, and the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluting solvent: chloroform:methanol=11:1 to 3:1) and NH-type silica gel column chromatography (eluting solvent: chloroform:methanol=10:0 to 100:1) to give the titled compound (0.34 g, 36%) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193176B2
Source datasetuspto-grants-2012_06
ORD IDord-5f0905fb1bc64c18979ca8b10503e879
Source noteuspto-grants-2012_06