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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 133599Generated: October 26, 2026

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

https://huagongshe.com/reaction/133599

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 508801—

Reaction Conditions

Temperature25 °C

Reaction Steps

A (piperidinomethyl)polystyrene resin (28 mg, 2.8 mmol/g) and 3-(trifluoromethyl)phenyl isocyanate (1.3 equivalents) were added to a chloroform (2 mL) solution of 1-(4-chlorobenzyl)-4-[(glycylamino)methyl]piperidine (14.8 mg, 0.05 mmol). The resulting mixture was stirred at 25° C. for 16 hours, and an (aminomethyl)polystyrene resin was added to the obtained mixture. The resulting mixture was stirred at 25° C. for 16 hours to trap the remaining isocyanate. The obtained mixture was filtered and concentrated to thereby provide 1-(4-chlorobenzyl)-4-[[2-(3-(4-trifluoromethylphenyl)ureido) acetylamino]methyl]piperidine (Comp d. No. 852) (19 mg, 78%). 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 numberUS07390830B1
Source datasetuspto-grants-2008_06
ORD IDord-fa8d1e61e8c842c3b28f85b84cb1c0c5
Source noteuspto-grants-2008_06