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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 396086Generated: October 30, 2026

n-[4-({4-[4-(2-{[(2s)-3-(4-{[Tert-butyl(diphenyl)silyl]oxy}phenoxy)-2-hydroxypropyl]amino}ethyl)anilino]-1-piperidinyl}sulfonyl)phenyl]-n'-hexylurea → 1-Hexyl-3-{4-[4-(4-[2-[(2S)-2-hydroxy-3-(4-hydroxy-phenoxy)-propylamino]-ethyl}-phenylamino)-piperidine-1-sulfonyl]-phenyl]-urea

https://huagongshe.com/reaction/396086

Reaction equation

Participants

RoleNameHCIDCharge
Reactantn-[4-({4-[4-(2-{[(2s)-3-(4-{[Tert-butyl(diphenyl)silyl]oxy}phenoxy)-2-hydroxypropyl]amino}ethyl)anilino]-1-piperidinyl}sulfonyl)phenyl]-n'-hexylureaHCID 88089230—
SolventChloroform methanolHCID 21584188—
Product1-Hexyl-3-{4-[4-(4-[2-[(2S)-2-hydroxy-3-(4-hydroxy-phenoxy)-propylamino]-ethyl}-phenylamino)-piperidine-1-sulfonyl]-phenyl]-ureaHCID 69985394—

Reaction Steps

N-[4-({4-[4-(2-{[(2S)-3-(4-{[tert-Butyl(diphenyl)silyl]oxy}phenoxy)-2-hydroxy-propyl]amino}ethyl)anilino]-1-piperidinyl}sulfonyl)phenyl]-N′-hexylurea (0.18 g, 0.199 mmol) was reacted according to Procedure H (eluant: 5:1 chloroform-methanol) to give the title compound as the hydrochloride salt (0.1 g, 0.142 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06605618B2
Source datasetuspto-grants-2003_08
ORD IDord-bc3c83d3c5b9452887a63ef42a98ef6b
Source noteuspto-grants-2003_08