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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1478824Generated: November 1, 2026

Methyl iodide → 4-Amino-2-(2-fluorophenyl)-1,5-dimethyl-1H-pyrazol-3(2H)-one

https://huagongshe.com/reaction/1478824

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(2-Fluorophenyl)-5-methyl-2,3-dihydro-1H-pyrazol-3-oneHCID 66021677—
Reactant2-(2-Fluorophenyl)-1,5-dimethyl-1H-pyrazol-3(2H)-oneHCID 68678524—
SolventTetrahydrofuranHCID 8028—
Product4-Amino-2-(2-fluorophenyl)-1,5-dimethyl-1H-pyrazol-3(2H)-oneHCID 43163661—

Reaction Conditions

Temperature65 °C

Reaction Steps

2-(2-Fluorophenyl)-1,5-dimethyl-1H-pyrazol-3(2H)-one To a solution of 2-(2-fluorophenyl)-5-methyl-1H-pyrazol-3(2H)-one (500 g, 2602 mmol) in THF (2500 ml) heated to 58° C. was added iodomethane (163 ml) dropwise over 15 mins and the mixture was stirred at 65° C. for 30 mins. K2CO3 (198 g) was added over 20 mins and stirred for 16 hrs. Further iodomethane (16.3 ml) was added and stirring continued for 1 hr. The resulting mixture was cooled to 0° C., filtered and washed with THF (50 ml). The filtrate was evaporated to dryness and purified by column chromatography, eluting with EtOAc/Heptane to give the title compound as a red solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403833B2
Source datasetuspto-grants-2016_08
ORD IDord-b001874160e04ab09e881f8b5dec3c80
Source noteuspto-grants-2016_08