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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1281499Generated: October 31, 2026

t-butyl(diphenyl)silyl 3-chloro-4-[(2S)oxiranylmethoxy]phenyl ether → 4-[4-(2-{[(2S)-3-(2-Chloro-4-hydroxyphenoxy)-2-hydroxypropyl]amino}ethyl)anilino]-N-octyl-1-piperidinecarboxamide

https://huagongshe.com/reaction/1281499

Reaction equation

Participants

RoleNameHCIDCharge
Reactantt-butyl(diphenyl)silyl 3-chloro-4-[(2S)oxiranylmethoxy]phenyl etherHCID 23381354—
Reactant4-[4-(2-Aminoethyl)anilino]-N-octyl-1-piperidinecarboxamide formateHCID 69987252—
SolventChloroform methanolHCID 21584188—
Product4-[4-(2-{[(2S)-3-(2-Chloro-4-hydroxyphenoxy)-2-hydroxypropyl]amino}ethyl)anilino]-N-octyl-1-piperidinecarboxamideHCID 1023176617%

Reaction Steps

4-[4-(2-Aminoethyl)anilino]-N-octyl-1-piperidinecarboxamide formate (0.57 g, 1.35 mmol) was reacted with tert-butyl(diphenyl)silyl 3-chloro-4-[(2S)oxiranyl-methoxy]phenyl ether (0.59 g, 1.35 mmol) according to Procedure G (eluant: 20:1 chloroform-methanol) to give the title compound (0.185 g, 0.23 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06451814B1
Source datasetuspto-grants-2002_09
ORD IDord-64fb9257f293400f938e5d1b13a511a0
Source noteuspto-grants-2002_09