Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 219907Erstellt: 25. Oktober 2026

Trichloroacetonitrile → Methyl 2-fluoro-4-{5-[2'-(trifluoromethyl)biphenyl-4-yl]-1,2,4-oxadiazol-3-yl}benzoate

https://huagongshe.com/reaction/219907

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrichloroacetonitrileHCID 11011—
EduktTriphenylphosphineHCID 11776—
EduktDiisopropylethylamineHCID 81531—
Edukt2'-Trifluoromethyl (1,1'-biphenyl)-4-carboxylic acidHCID 2782714—
EduktMethyl 4-[amino(hydroxyimino)methyl]-2-fluorobenzoateHCID 76644654—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktMethyl 2-fluoro-4-{5-[2'-(trifluoromethyl)biphenyl-4-yl]-1,2,4-oxadiazol-3-yl}benzoateHCID 6752907870%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

In a microwave vial were added 4-(2-trifluoromethylphenyl)benzoic acid (Fluorochem, 53.2 mg; 0.20 mmol; 1 eq.), triphenylphosphine polymer bound (375 mg; 0.60 mmol; 3 eq.) and trichloroacetonitrile (30 μl; 0.30 mmol; 1.50 eq.). Anhydrous THF (2 mL) was added and the reaction vessel was sealed and heated to 100° C. for 5 min in the microwave. After cooling, the reaction vessel was uncapped and without filtering, Intermediate 1 (46.7 mg; 0.22 mmol; 1.10 eq.) in anhydrous THF (2 mL) was added to the solution along with DIEA (69 μl; 0.40 mmol; 2 eq.). The reaction was capped and heated at 150° C. for 15 min. After cooling, the reaction vessel was uncapped again and the resin was filtered, the filtrate passed through an NH2 SPE column (2 g) and washed by additional THF (2×2 mL). Solvents were evaporated, affording the title compound as a brown solid (61.9 mg; 70%). It was used in the next step without further purification. LC/MS (Method A): 443.3 (M+H)+. HPLC (Method A), Rt 5.98 min (Purity: 87.9%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08202865B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-cf38cb242a1d4de1b3521303a53bc788
Quellennotizuspto-grants-2012_06