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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1031182Generated: October 31, 2026

Toluene → 2-[2-[4-[Bis(4-fluorophenyl)methyl]-1-piperidinyl]ethyl]-3,4-dihydro-1,4-dimethyl-1H-[1,3,5]-triazepino[3,2-a]benzimidazol-5(2H)-one

https://huagongshe.com/reaction/1031182

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactant4-[Bis(4-fluorophenyl)methyl]piperidineHCID 13250544—
Reactant2-(2-Chloroethyl)-3,4-dihydro-1,4-dimethyl-1H-[1,3,5]triazepino[3,2-a]benzimidazol-5(2H)-oneHCID 19819759—
SolventTriethylamineHCID 8471—
Product2-[2-[4-[Bis(4-fluorophenyl)methyl]-1-piperidinyl]ethyl]-3,4-dihydro-1,4-dimethyl-1H-[1,3,5]-triazepino[3,2-a]benzimidazol-5(2H)-oneHCID 19819778—

Reaction Steps

To a solution of 50 mL of toluene containing 4.0 g (0.04 mol) of triethylamine was added 3.0 g (0.01 mol) of 2-(2-chloroethyl)-3,4-dihydro-1,4-dimethyl-1H-[1,3,5]triazepino[3,2-a]benzimidazol-5(2H)-one and 4.0 g (0.014 mol) of 4-[bis(4-fluorophenyl)methyl]piperidine. The mixture was heated to reflux for 3 days after which time 1.0 g (0.003 mL) of 4-[bis(4-fluorophenyl)methyl]piperidine and 1.0 g (0.01 mol) of triethylamine was added. Heating under reflux was continued for 24 hr. The solvent was removed by rotary evaporation and the residue dissolved in 100 mL of CH2Cl2. The organic phase was washed with 2×100 mL of 1N NaOH, dried over Na2SO4, filtered, and concentrated by rotary evaporation. The residue was subjected to preparative HPLC using silica gel as the stationary phase and eluting with ethanol. Combination of like fractions afforded 3.1 g (57%) of analytically pure material as a glass.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05109013
Source datasetuspto-grants-1992_04
ORD IDord-0d6fba876235442b8f3d154f78a4b27c
Source noteuspto-grants-1992_04