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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1797264Erstellt: 24. Oktober 2026

Triethylamine → HCID 68575706, Verbindung

https://huagongshe.com/de/reaction/1797264

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Edukt(E)-3-(5-cyano-2-methoxy-phenyl)-acrylic acidHCID 11458357—
EduktHCID 68576481HCID 68576481—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 68575706HCID 68575706—

Reaktionsschritte

A solution of (E)-3-(5-cyano-2-methoxy-phenyl)-acrylic acid (0.916 g, 4.51 mmol), triethylamine (1.257 ml, 9.02 mmol) and 2-(1H-benzotriazol-1-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate (1.44 g, 4.51 mmol) in DCM (10 ml) is treated with (R)-3-amino-4-[4-(4-fluoro-phenoxy)-piperidin-1-yl]-butyric acid benzyl ester. The reaction mixture is stirred at ambient temperature for 2 hours, then is washed with water, dried over MgSO4 and evaporated. The crude product is purified by flash silica chromatography (elution with 2:1 ethylacetate:hexane) to afford (R)-3-[(E)-3-(5-cyano-2-methoxy-phenyl)-acryloylamino]-4-[4-(4-fluoro-phenoxy)-piperidin-1-yl]-butyric acid benzyl ester. [MH]+ 572.1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07034042B2
Quelldatensatzuspto-grants-2006_04
ORD IDord-f2098ee258b54dee8f28f07d97d8407b
Quellennotizuspto-grants-2006_04