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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 279309Generated: October 30, 2026

Ammonia → 4-Chlorobenzyl-4-[[2-(3-(4-trifluoromethylphenyl)ureido)acetylamino]methyl]piperidine

https://huagongshe.com/reaction/279309

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantPiperidineHCID 8082—
Reactant3-(Trifluoromethyl)phenyl isocyanateHCID 9483—
ReactantIsocyanateHCID 105034—
Reactant1-(4-Chlorobenzyl)-4-((glycylamino)methyl}piperidineHCID 18426155—
SolventChloroformHCID 6212—
Product4-Chlorobenzyl-4-[[2-(3-(4-trifluoromethylphenyl)ureido)acetylamino]methyl]piperidineHCID 50880178%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 1-(4-chlorobenzyl)-4-{(glycylamino)methyl}piperidine (14.8 mg, 0.05 mmol) in CHCl3 (2 mL) was treated with (piperidinomethyl)polystyrene resin (28 mg, 2.8 mmol/g), 3-(trifluoromethyl)phenyl isocyanate (1.3 equiv.) and stirred at 25° C. for 16 h. (Aminomethyl)polystyrene was added to scavenge the residual isocyanate and the reaction mixture was stirred at 25° C. for 16 h. Filtration and concentration afforded 1-(4-chlorobenzyl)-4-[{2-(3-(4-trifluoromethylphenyl)ureido)acetylamino}methyl]piperidine (19 mg, 78%) (compound No. 852): The purity was determined by RPLC/MS (92%); ESI/MS m/e 483 (M++H, C23H26ClF3N4O2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06362177B1
Source datasetuspto-grants-2002_03
ORD IDord-de47e466f4b04f9ba56ba38b666b72dc
Source noteuspto-grants-2002_03