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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1157533Erstellt: 25. Oktober 2026

3-(1,3-Oxazol-5-yl)aniline → 2,2,2-Trifluoro-N-{3-[3-(2-{[3-(1,3-oxazol-5-yl)phenyl]amino}-4-pyrimidinyl)pyrazolo[1,5-a]pyridin-2-yl]phenyl}acetamide hydrochloride

https://huagongshe.com/reaction/1157533

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-(1,3-Oxazol-5-yl)anilineHCID 2739289—
EduktN-{3-[3-(2-chloro-4-pyrimidinyl)pyrazolo[1,5-a]pyridin-2-yl]phenyl}-2,2,2-trifluoroacetamideHCID 59513717—
KatalysatorHydrochloric AcidHCID 313—
LösungsmittelIsopropanolHCID 3776—
Produkt2,2,2-Trifluoro-N-{3-[3-(2-{[3-(1,3-oxazol-5-yl)phenyl]amino}-4-pyrimidinyl)pyrazolo[1,5-a]pyridin-2-yl]phenyl}acetamide hydrochlorideHCID 8663108398%

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

To a mixture of N-{3-[3-(2-chloro-4-pyrimidinyl)pyrazolo[1,5-a]pyridin-2-yl]phenyl}-2,2,2-trifluoroacetamide (0.5 g, 1.2 mmol) in i-PrOH (4 mL) was added 5-(3-aminophenyl)oxazole (0.25 g, 1.56 mmol) and 2 drops of conc. HCl. The reaction was heated in a microwave to 120° C. for 40 min. and allowed to cool to rt. The resulting solid was filtered off, washed with i-PrOH and dried to give the title compound as a tan solid (0.68 g) in 98% yield. ES-LC/MS m/z=542 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07807673B2
Quelldatensatzuspto-grants-2010_10
ORD IDord-5b708d425ea04c8ebe9c87a4f038f71c
Quellennotizuspto-grants-2010_10