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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1634803Generated: November 1, 2026

t-butyl(diphenyl)silyl 3-chloro-4-[(2S)oxiranylmethoxy]phenyl ether → 1-[4-(4-{[(2S)-3-(2-Chloro-4-hydroxy-phenoxy)-2-hydroxy-propylamino]-methyl}-piperidine-1-sulfonyl}-phenyl]-3-(2,5-difluoro-benzyl)-urea

https://huagongshe.com/reaction/1634803

Reaction equation

Participants

RoleNameHCIDCharge
Reactantt-butyl(diphenyl)silyl 3-chloro-4-[(2S)oxiranylmethoxy]phenyl etherHCID 23381354—
ReactantN-(4-{[4-(aminomethyl)-1-piperidinyl]sulfonyl}phenyl)-N'-(2,5-difluorobenzyl)urea formateHCID 69999063—
Product1-[4-(4-{[(2S)-3-(2-Chloro-4-hydroxy-phenoxy)-2-hydroxy-propylamino]-methyl}-piperidine-1-sulfonyl}-phenyl]-3-(2,5-difluoro-benzyl)-ureaHCID 1014607119.7%

Reaction Steps

N-(4-{[4-(aminomethyl)-1-piperidinyl]sulfonyl}phenyl)-N′-(2,5-difluorobenzyl)urea formate (0.827 g, 1.72 mmol) was reacted with t-butyl(diphenyl)silyl 3-chloro-4-[(2S)oxiranylmethoxy]phenyl ether (0.516 9,1.17 mmol) according to example 37 to give the title compound (0.15 g, 0.23 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06506901B2
Source datasetuspto-grants-2003_01
ORD IDord-69df0de30f1f4ceda22eea21c050127f
Source noteuspto-grants-2003_01