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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2106762Generated: October 31, 2026

Potassium Iodide → 2,4-dihydro-2-[4-[4-(4-methoxyphenyl)-1-piperazinyl]phenyl]-5-methyl-4-propyl-3H-1,2,4-triazol-3-one

https://huagongshe.com/reaction/2106762

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantCyclohexanolHCID 7966—
ReactantN,N-Bis(2-chloroethyl)-4-methoxybenzenamineHCID 15064—
ReactantSodium BicarbonateHCID 516892—
Reactant2-(4-aminophenyl)-2,4-dihydro-5-methyl-4-propyl-3H-1,2,4-triazol-3-oneHCID 15125477—
SolventWaterHCID 962—
Product2,4-dihydro-2-[4-[4-(4-methoxyphenyl)-1-piperazinyl]phenyl]-5-methyl-4-propyl-3H-1,2,4-triazol-3-oneHCID 1512547844%

Reaction Steps

A mixture of 25 parts of N,N-bis(2-chloroethyl)-4-methoxybenzenamine, 23.2 parts of 2-(4-aminophenyl)-2,4-dihydro-5-methyl-4-propyl-3H-1,2,4-triazol-3-one, 2 parts of potassium iodide and 200 parts of cyclohexanol was stirred and refluxed for 5 hours using a water-separator. The reaction mixture was cooled and neutralized with a sodium hydrogen carbonate solution. The product was filtered off and dissolved in trichloromethane. The solution was filtered over silica gel and the solvent was evaporated. The residue was crystallized from 1-butanol, yielding 18 parts (44%) of 2,4-dihydro-2-[4-[4-(4-methoxyphenyl)-1-piperazinyl]phenyl]-5-methyl-4-propyl-3H-1,2,4-triazol-3-one; mp. 202.2° C. (int. 22).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04931444
Source datasetuspto-grants-1990_06
ORD IDord-78d1efba909f42949bb2bf0793bd8dec
Source noteuspto-grants-1990_06