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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 215760Generated: October 26, 2026

Cesium carbonate → 1-(4-{3-[(2R)-2-methylpyrrolidin-1-yl]propoxy}phenyl)-1H-pyrazole-4-carboxylic acid ethyl ester

https://huagongshe.com/reaction/215760

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactantethyl 1H-pyrazole-4-carboxylateHCID 142179—
Reactanttrans-N,N'-dimethyl-1,2-cyclohexanediamineHCID 2733821—
Reactant(2R)-1-[3-(4-iodophenoxy)propyl]-2-methylpyrrolidineHCID 57675747—
CatalystCopper iodideHCID 83717—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product1-(4-{3-[(2R)-2-methylpyrrolidin-1-yl]propoxy}phenyl)-1H-pyrazole-4-carboxylic acid ethyl esterHCID 59541721—

Reaction Steps

A suspension of (2R)-1-[3-(4-iodophenoxy)propyl]-2-methylpyrrolidine obtained in Example 1-(2) (1.60 g), 1H-pyrazole-4-carboxylic acid ethyl ester (0.779 g), (rac-trans-N,N′-dimethylcyclohexane-1,2-diamine (0.263 g), copper iodide (0.088 g) and cesium carbonate (3.02 g) in N,N-dimethylformamide (2.5 mL) was stirred at 120° C. for 4 hours. The reaction mixture was cooled to room temperature, diluted with water and extracted with ethyl acetate. The organic layer was concentrated under reduced pressure, and the resulting residue was purified by silica gel column chromatography (eluting solvent: n-hexane:ethyl acetate=3:1) to give the titled compound (1.11 g) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193176B2
Source datasetuspto-grants-2012_06
ORD IDord-c9d47b40d81d441994cbb5e8f2d4a1eb
Source noteuspto-grants-2012_06