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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 133618Generated: October 26, 2026

Acetonitrile → 4-[[N-(2-amino-5-chlorobenzoyl) glycyl]aminomethyl]-1-[4-(trifluoromethylthio)benzyl]piperidine

https://huagongshe.com/reaction/133618

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
Reactant1-(Chloromethyl)-4-((trifluoromethyl)sulfanyl)benzeneHCID 2783164—
Reactant4-[{N-(2-amino5-chlorobenzoyl)glycyl}aminomethyl]piperidineHCID 18426216—
SolventChloroformHCID 6212—
Product4-[[N-(2-amino-5-chlorobenzoyl) glycyl]aminomethyl]-1-[4-(trifluoromethylthio)benzyl]piperidineHCID 18426244—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 4-[[N-(2-amino-5-chlorobenzoyl)glycyl]aminomethyl]piperidine (16.2 mg, 0.050 mmol) with 4-(trifluoromethylthio)benzyl chloride (20.3 mg, 0.075 mmol), acetonitrile (1.0 mL) and chloroform (0.56 mL) was stirred at 60° C. for 15 hours, cooled, then loaded onto a VarianM SCX column and washed with methanol (15 mL). The obtained crude product was eluted with a 2 M methanol solution of NH3 (5 mL) and concentrated to thereby afford 4-[[N-(2-amino-5-chlorobenzoyl) glycyl]aminomethyl]-1-[4-(trifluoromethylthio)benzyl]piperidine (Compd. No. 1616) (21.9 mg, 85%). The purity was determined by RPLC/MS (96%). ESI/MS m/e 545.2 (M++H, C23H26ClF3N4O2S).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07390830B1
Source datasetuspto-grants-2008_06
ORD IDord-47fa41e0e7224472bd79c61d99bc0139
Source noteuspto-grants-2008_06