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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2106771Generated: October 30, 2026

Potassium Iodide → 1,4-dihydro-1-[4-[4-(4-methoxyphenyl)-1-piperazinyl]-phenyl]-4-propyl-5H-tetrazol-5-one

https://huagongshe.com/reaction/2106771

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantCyclohexanolHCID 7966—
ReactantN,N-Bis(2-chloroethyl)-4-methoxybenzenamineHCID 15064—
ReactantSodium BicarbonateHCID 516892—
Reactant1-(4-aminophenyl)-1,4-dihydro-4-propyl-5H-tetrazol-5-one monohydrochlorideHCID 23048854—
SolventWaterHCID 962—
Product1,4-dihydro-1-[4-[4-(4-methoxyphenyl)-1-piperazinyl]-phenyl]-4-propyl-5H-tetrazol-5-oneHCID 1512548739%

Reaction Steps

A mixture of 25 parts of N,N-bis(2-chloroethyl)-4-methoxybenzenamine, 25.5 parts of 1-(4-aminophenyl)-1,4-dihydro-4-propyl-5H-tetrazol-5-one monohydrochloride, 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 crystallized from 1-butanol, yielding 15.5 parts (39%) of 1,4-dihydro-1-[4-[4-(4-methoxyphenyl)-1-piperazinyl]-phenyl]-4-propyl-5H-tetrazol-5-one; mp. 189.7 ° C. (int. 33).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04931444
Source datasetuspto-grants-1990_06
ORD IDord-42b8aece752e48ff905e522bbec02a29
Source noteuspto-grants-1990_06