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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2420315Generated: October 26, 2026

Sodium Carbonate → 8-[3-(1,3-dihydro-3-methyl-2-oxo-2H-benzimidazol-1-yl)propyl]-1-phenyl-1,3,8-triazaspiro[4,5]-decan-4-one

https://huagongshe.com/reaction/2420315

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant1-Phenyl-1,3,8-triazaspiro(4.5)decan-4-oneHCID 70556—
Reactant1,3-dihydro-1-(3-iodopropyl)-3-methyl-2H-benzimidazol-2-oneHCID 21989977—
SolventDimethylformamideHCID 6228—
Product8-[3-(1,3-dihydro-3-methyl-2-oxo-2H-benzimidazol-1-yl)propyl]-1-phenyl-1,3,8-triazaspiro[4,5]-decan-4-oneHCID 20385616—

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 5 parts of 1,3-dihydro-1-(3-iodopropyl)-3-methyl-2H-benzimidazol-2-one, 3.4 parts of 1-phenyl-1,3,8-triazaspiro[4,5]decan-4-one. 2.65 parts of sodium carbonate and 22.5 parts of N,N-dimethylformamide is stirred and heated for 2 hours at 70° C. The reaction mixture is cooled and poured onto water, whereupon an oily precipitate is formed. The supernatant aqueous phase is decanted and the residual oil is dissoved in trichloromethane. The solution is dried, filtered and evaporated. The residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and 5% of methanol as eluent. The pure fractions are collected and the eluent is evaporated, yielding 1 part of 8-[3-(1,3-dihydro-3-methyl-2-oxo-2H-benzimidazol-1-yl)propyl]-1-phenyl-1,3,8-triazaspiro[4,5]-decan-4-one; mp. 164.4° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04110333
Source datasetuspto-grants-1978_08
ORD IDord-3607ddd8f3424dadba6f8857bc2200cc
Source noteuspto-grants-1978_08