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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 221636Generated: October 25, 2026

Tert-butyldimethyl(4-(oxiran-2-ylmethoxy)phenoxy)silane → 4-(2-Hydroxy-3-(1-(5-phenylthieno[2,3-d]pyrimidin-4-yl)piperidin-4-ylamino)propoxy)phenol

https://huagongshe.com/reaction/221636

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyldimethyl(4-(oxiran-2-ylmethoxy)phenoxy)silaneHCID 19385012—
Reactant1-(5-Phenylthieno[2,3-d]pyrimidin-4-yl)piperidin-4-amineHCID 69041562—
Product4-(2-Hydroxy-3-(1-(5-phenylthieno[2,3-d]pyrimidin-4-yl)piperidin-4-ylamino)propoxy)phenolHCID 2493648921%

Reaction Steps

Synthesis followed SP6 (3 h), using 220 μmol tert-butyldimethyl(4-(oxiran-2-ylmethoxy)phenoxy)silane and 1-(5-phenylthieno[2,3-d]pyrimidin-4-yl)piperidin-4-amine to give O-silylated intermediate upon purification by prep. HPLC (reversed phase) with 21% yield. Product was obtained by deprotection according to SP7 and purification by prep. HPLC (reversed phase) with 70% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207174B2
Source datasetuspto-grants-2012_06
ORD IDord-db3e060e84df466588edd70edd129e8c
Source noteuspto-grants-2012_06