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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 70865Erstellt: 24. Oktober 2026

Trifluoroacetic acid → (R)-4-biphenyl-4-yl-3-(3-carboxy-propionylamino)-butyric acid ethyl ester

https://huagongshe.com/de/reaction/70865

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrifluoroacetic acidHCID 6422—
EduktSuccinic anhydrideHCID 7922—
Edukt(R)-ethyl 4-(biphenyl-4-yl)-3-(tert-butoxycarbonylamino)butanoateHCID 59607632—
LösungsmittelDichloromethaneHCID 6344—
Produkt(R)-4-biphenyl-4-yl-3-(3-carboxy-propionylamino)-butyric acid ethyl esterHCID 4982222350,2%

Reaktionsschritte

To a solution of (R)-4-biphenyl-4-yl-3-tert-butoxycarbonylamino-butyric acid ethyl ester (400 mg, 1.04 mmol) in DCM (10 mL) at room temperature is added TFA (2.009 mL, 26.1 mmol) and the mixture is stirred at room temperature for 1 hour. The mixture is concentrated under reduced pressure. To the obtained TFA salt in DCM (10 mL) at ice bath temperature is added succinic anhydride (125 mg, 1.25 mmol) and followed by TEA (0.363 mL, 2.61 mmol). The reaction is stirred at room temperature for 16 hours. The mixture is concentrated under reduced pressure. The obtained residue is purified by flash chromatography (silica gel, 2% to 5% EtOH/DCM) give (R)-4-biphenyl-4-yl-3-(3-carboxy-propionylamino)-butyric acid ethyl ester (200 mg). HPLC retention time=1.53 minutes (condition C); MS=384 (m+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08822534B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-d1bb9c9294a7440fa0cfad366f1f6fab
Quellennotizuspto-grants-2014_09