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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1281494Generated: November 1, 2026

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

https://huagongshe.com/reaction/1281494

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl-(4-oxiranylmethoxy-phenoxy)-diphenylsilaneHCID 12045564—
Reactant4-[4-(2-Aminoethyl)anilino]-N-methyl-1-piperidinecarboxamide formateHCID 69987376—
Product4(4-{2-[(2S)-2-Hydroxy-3-(4-hydroxy-phenoxy)-propylamino]-ethyl}-phenylamino)-piperidine-1-carboxylic acid methylamideHCID 1027515716.7%

Reaction Steps

4-[4-(2-Aminoethyl)anilino]-N-methyl-1-piperidinecarboxamide formate (0.322 g, 1.0 mmol) was reacted with tert-butyl-(4-oxiranylmethoxy-phenoxy)-diphenyl-silane (0.364 g, 0.90 mmol) according to Procedure G to give the title compound (eluant: 20:1 chloroform-methanol) (0.1 g, 0.15 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06451814B1
Source datasetuspto-grants-2002_09
ORD IDord-757de68760bf4f77a0c46a1e60fb74e0
Source noteuspto-grants-2002_09