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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 489850Generated: October 30, 2026

Potassium Iodide → 5-Amino-1-(4-fluorophenyl)-4-[3-{3-(morpholin-4-yl)propylamino}benzoyl]pyrazole

https://huagongshe.com/reaction/489850

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantMorpholineHCID 8083—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Amino-4-[3-(3-chloropropylamino)benzoyl]-1-(4-fluorophenyl)pyrazoleHCID 22262803—
SolventAcetonitrileHCID 6342—
SolventSodium chloride; waterHCID 57417360—
Product5-Amino-1-(4-fluorophenyl)-4-[3-{3-(morpholin-4-yl)propylamino}benzoyl]pyrazoleHCID 9888541—

Reaction Steps

A mixture of 5-amino-4-[3-(3-chloropropylamino)benzoyl]-1-(4-fluorophenyl)pyrazole (0.05 g, 0.13 mmol), morpholine (0.1 ml, 1.1 mmol), potassium carbonate (0.1 g) and potassium iodide (0.1 g) in acetonitrile (3 ml) was heated at reflux. After 2 days, the reaction mixture was poured into brine and the product was extracted into ethyl acetate. The organic layer was separated, washed with brine, dried over sodium sulfate and concentrated in vacuo. The residue was purified by flash chromatography (elution gradient: 3% MeOH/CH2Cl2) to give 5-amino-1-(4-fluorophenyl)-4-[3-{3-(morpholin-4-yl)propylamino}benzoyl]pyrazole as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06979693B2
Source datasetuspto-grants-2005_12
ORD IDord-f304f173c11640889aba222ce35e80c7
Source noteuspto-grants-2005_12