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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 396019Generated: October 28, 2026

t-butyl-[4-(2S)-oxiranylmethoxy-phenoxy]-diphenylsilane → 4-(4-[2-[(2S)-2-Hydroxy-3-(4-hydroxy-phenoxy)-propylamino]-ethyl}-phenylsulfanyl)-piperidine-1-carboxylic acid phenylamide

https://huagongshe.com/reaction/396019

Reaction equation

Participants

RoleNameHCIDCharge
Reactantt-butyl-[4-(2S)-oxiranylmethoxy-phenoxy]-diphenylsilaneHCID 11327180—
Reactant4-{[4-(2-Aminoethyl)phenyl]sulfanyl}-N-phenyl-1-piperidinecarboxamideHCID 18173601—
SolventDichloromethane chloroform methanolHCID 86584582—
Product4-(4-[2-[(2S)-2-Hydroxy-3-(4-hydroxy-phenoxy)-propylamino]-ethyl}-phenylsulfanyl)-piperidine-1-carboxylic acid phenylamideHCID 1014280926%

Reaction Steps

4-{[4-(2-Aminoethyl)phenyl]sulfanyl}-N-phenyl-1-piperidinecarboxamide (0.45 g, 1.27 mmol) was reacted with tert-butyl{4-[(2S)oxiranylmethoxy]phenoxy}diphenylsilane (0.512 g, 1.27 mmol) according to Procedure G (eluant: 12:3:1 dichloromethane-chloroform-methanol) to give the title compound (0.25 g, 0.33 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06605618B2
Source datasetuspto-grants-2003_08
ORD IDord-2f7e1a799e644a5bb204d9323e131cbc
Source noteuspto-grants-2003_08