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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437663Generated: October 29, 2026

Potassium Iodide → N-{2-[1-(4-fluorophenyl)-4-oxo-1,3,8-triazaspiro[4,5]dec-8-yl] ethyl}-1-methyl-1H-pyrrole-2-carboxamide hydrochloride

https://huagongshe.com/reaction/437663

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant1-(4-Fluorophenyl)-1,3,8-triazaspiro(4.5)decan-4-oneHCID 93915—
ReactantSodium BicarbonateHCID 516892—
ReactantN-(2-chloroethyl)-1-methyl-1H-pyrrole-2-carboxamideHCID 21428944—
SolventMethyl Isobutyl KetoneHCID 7909—
ProductN-{2-[1-(4-fluorophenyl)-4-oxo-1,3,8-triazaspiro[4,5]dec-8-yl] ethyl}-1-methyl-1H-pyrrole-2-carboxamide hydrochlorideHCID 68118485—

Reaction Steps

A mixture of 3.75 parts of N-(2-chloroethyl)-1-methyl-1H-pyrrole-2-carboxamide, 5 parts of 1-(4-fluorophenyl)-1,3,8-triazaspiro[4,5]decan-4-one, 1.7 parts of sodium hydrogen carbonate, 0.1 parts of potassium iodide and 160 parts of 4-methyl-2-pentanone is stirred and refluxed for 48 hours. The reaction mixture is cooled and the solvent is evaporated. The residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions are collected and the eluent is evaporated. The residue is converted into the hydrochloride salt in 2-propanol and 2,2'-oxybispropane. The salt is filtered off and crystallized from methanol, yielding 0.8 parts of N-{2-[1-(4-fluorophenyl)-4-oxo-1,3,8-triazaspiro[4,5]dec-8-yl] ethyl} -1-methyl-1H-pyrrole-2-carboxamide hydrochloride; mp. 273.4° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04031226
Source datasetuspto-grants-1977_06
ORD IDord-c1348b2e1ee04e47ae2e36bdcb9ca14b
Source noteuspto-grants-1977_06