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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1863035Generated: October 31, 2026

Potassium Iodide → HCID 86736638, compound

https://huagongshe.com/reaction/1863035

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium CarbonateHCID 10340—
Reactant1-(2-Chloroethyl)-4-ethyl-1,4-dihydro-5H-tetrazol-5-oneHCID 3017906—
ReactantMethyl 4-(phenylpropanylamino)piperidine-4-carboxylate hydrochlorideHCID 12298180—
SolventWaterHCID 962—
SolventMethyl Isobutyl KetoneHCID 7909—
ProductHCID 86736638HCID 8673663813%

Reaction Steps

A mixture of 3.6 parts of 1-(2-chloroethyl)-4-ethyl-1,4-dihydro-5H-tetrazol-5-one, 6.4 parts of methyl 4-[N-(1-oxopropyl)N-phenylamino]-4-piperidinecarboxylate hydrochloride, 4 parts of sodium carbonate, 0.1 parts of potassium iodide and 240 parts of 4-methyl-2-pentanone is stirred and refluxed overnight with water-separator. The reaction mixture is cooled and poured onto water. The organic phase is separated, dried, filtered and evaporated. The residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (97:3 by volume) as eluent. The pure fractions are collected and the eluent is evaporated. The residue is converted into the ethanedioate salt in 2-propanone. The salt is filtered off and dried, yielding 1.5 parts (13%) of methyl 1-[2-(4-ethyl-4,5-dihydro-5-oxo-1H-tetrazol-1-yl)ethyl]-4-[(1-oxopropyl)phenylamino]-4-piperidinecarboxylate ethanedioate (2:3); mp. 158.9° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04167574
Source datasetuspto-grants-1979_09
ORD IDord-bbfd417353a14755bf12fac04c2ec573
Source noteuspto-grants-1979_09