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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2286558Generated: October 30, 2026

Potassium Iodide → 1-(4-methoxyphenyl)-4-[4-(1H-pyrazol-1-yl)phenyl]piperazine

https://huagongshe.com/reaction/2286558

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantN,N-Bis(2-chloroethyl)-4-methoxybenzenamineHCID 15064—
ReactantSodium BicarbonateHCID 516892—
Reactant4-(1H-Pyrazol-1-yl)anilineHCID 594274—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Product1-(4-methoxyphenyl)-4-[4-(1H-pyrazol-1-yl)phenyl]piperazineHCID 12877031—

Reaction Steps

A mixture of 12.5 parts of N,N-bis(2-chloroethyl)-4-methoxybenzenamine, 8 parts of 4-(1H-pyrazol-1-yl)benzenamine, 2 parts of potassium iodide, 80 parts of 2-propanone and 100 parts of water is stirred and refluxed for 24 hours. The reaction mixture is cooled. The precipitated product is filtered off (the filtrate is set aside), washed with water and with 2-propanone, yielding a first crude fraction of 6 parts. The filtrate (see above) is neutralized with a sodium hydrogen carbonate solution and extracted with trichloromethane. The extract is dried, filtered and evaporated. The residue is triturated in 2-propanol. The product is filtered off and washed with methanol, yielding a second crude fraction of 2 parts. The combined crude crops (resp. 6 and 2 parts) are crystallized from 1-butanol, yielding 7.1 parts of 1-(4-methoxyphenyl)-4-[4-(1H-pyrazol-1-yl)-phenyl]piperazine; mp. 207.7° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04267179
Source datasetuspto-grants-1981_05
ORD IDord-8f7ad85df39c4f27a91e72b6cfea9815
Source noteuspto-grants-1981_05