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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 221639Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/221639

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTert-butyldimethyl(4-(oxiran-2-ylmethoxy)phenoxy)silaneHCID 19385012—
Edukt1-(5-Methylthieno[2,3-d]pyrimidin-4-yl)piperidin-4-amineHCID 69042395—
Produkt4-(2-Hydroxy-3-(1-(5-methylthieno[2,3-d]pyrimidin-4-yl)piperidin-4-ylamino)propoxy)phenolHCID 2493648811%

Reaktionsschritte

Synthesis followed SP6 (3 h), using 150 μmol tert-butyldimethyl(4-(oxiran-2-ylmethoxy)phenoxy)silane and 1-(5-methylthieno[2,3-d]pyrimidin-4-yl)piperidin-4-amine to give O-silylated intermediate upon purification by prep. HPLC (reversed phase) with 11% yield. Product was obtained by deprotection according to SP7 and purification by prep. HPLC (reversed phase) with 76% yield.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08207174B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-27cfaed441b647929fcf043d52e6a63c
Quellennotizuspto-grants-2012_06