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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1928657Generated: October 31, 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/1928657

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 numberUS08183387B2
Source datasetuspto-grants-2012_05
ORD IDord-766cb27d95844bfc99573b9393ae67f4
Source noteuspto-grants-2012_05