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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 1-(4-Fluorophenyl)-1,3,8-triazaspiro(4.5)decan-4-one | HCID 93915 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | N-(2-chloroethyl)-1-methyl-1H-pyrrole-2-carboxamide | HCID 21428944 | — |
| Solvent | Methyl Isobutyl Ketone | HCID 7909 | — |
| Product | N-{2-[1-(4-fluorophenyl)-4-oxo-1,3,8-triazaspiro[4,5]dec-8-yl] ethyl}-1-methyl-1H-pyrrole-2-carboxamide hydrochloride | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04031226 |
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| Source dataset | uspto-grants-1977_06 |
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| ORD ID | ord-c1348b2e1ee04e47ae2e36bdcb9ca14b |
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| Source note | uspto-grants-1977_06 |
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