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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 396052Generated: October 29, 2026

Tert-butyl-(4-oxiranylmethoxy-phenoxy)-diphenylsilane → 4-(4-[2-[(2S)-2-Hydroxy-3-(4-hydroxy-phenoxy)-propylamino]-ethoxy}-phenylamino)-piperidine-1-carboxylic acid octylamide

https://huagongshe.com/reaction/396052

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl-(4-oxiranylmethoxy-phenoxy)-diphenylsilaneHCID 12045564—
Reactant4-[4-(2-Aminoethoxy)anilino]-N-octyl-1-piperidinecarboxamide formateHCID 69987684—
SolventChloroform methanolHCID 21584188—
Product4-(4-[2-[(2S)-2-Hydroxy-3-(4-hydroxy-phenoxy)-propylamino]-ethoxy}-phenylamino)-piperidine-1-carboxylic acid octylamideHCID 1023120741.2%

Reaction Steps

4-[4-(2-Aminoethoxy)anilino]-N-octyl-1-piperidinecarboxamide formate (0.40 g, 0.916 mmol) was reacted with tert-butyl-(4-oxiranylmethoxy-phenoxy)-diphenyl-silane (0.37 g, 0.916 mmol) according to Procedure G (eluant: 20:1 chloroform-methanol) to give the title compound (0.30 g, 0.377 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06605618B2
Source datasetuspto-grants-2003_08
ORD IDord-1c26f994b5274f94a3b036a24617e690
Source noteuspto-grants-2003_08