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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 229109Erstellt: 25. Oktober 2026

Methyl Acetate → (r)-2-(3-{3-[[3-(Trifluoromethyl)-4-fluoro-benzyl](2,2-diphenylethyl)amino]-1-methyl-propoxy}-phenyl)acetic acid hydrochloride salt

https://huagongshe.com/reaction/229109

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl AcetateHCID 6584—
Edukt4-Fluoro-3-(trifluoromethyl)benzaldehydeHCID 522269—
Edukt2-Chloro-3-(trifluoromethyl)benzaldehydeHCID 2736672—
EduktEther hydrochlorideHCID 10953452—
Edukt(R)-2-(3-{3-[(2,2-diphenylethyl)amino]-1-methyl-propoxy}phenyl)acetic acidHCID 68864815—
LösungsmittelDiethyl EtherHCID 3283—
Produkt(r)-2-(3-{3-[[3-(Trifluoromethyl)-4-fluoro-benzyl](2,2-diphenylethyl)amino]-1-methyl-propoxy}-phenyl)acetic acid hydrochloride saltHCID 68864196—

Reaktionsschritte

Following the procedure of Example 7(d) except (R)-2-(3-{3-[(2,2-diphenylethyl)amino]-1-methyl-propoxy}-phenyl)acetic acid and 3-(trifluoromethyl)-4-fluoro-benzaldehyde were used instead of (R)-2-(3-{3-(2,2-diphenylethyl)amino]-3-methyl-propoxy}phenyl)acetic acid methyl ester and 2-chloro-3-trifluoromethylbenzaldehyde in step (d) the corresponding carboxylic acid was obtained. The crude product was purified by preparative HPLC (TMC CombiPrep PDS, 75×30 mm, 25 mL/min, acetonitrile: H2O, UV detection at 254 nm) to afford the free base. The resulting amine/carboxylic acid was dissolved in Et2O (diethylether) and acidified with 1.0 M HCl/Et2O. The reaction mixture was concentrated in vacuo and dried under reduced pressure to give the title compound as a white solid, 95 mg (88%). MS (ESI) 580.6 (M+H+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07560586B2
Quelldatensatzuspto-grants-2009_07
ORD IDord-04f1056c8c994635b795ee80ded4a5ce
Quellennotizuspto-grants-2009_07