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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 469709Erstellt: 24. Oktober 2026

Hydrochloric Acid → 1-(3-Chloro-5-trifluoromethyl-pyridin-2-yl)-pyrrolidine-2-carboxylic acid (5-tert-butyl-isoxazol-3-yl)-amide

https://huagongshe.com/de/reaction/469709

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktTriethylamineHCID 8471—
Edukt3-Chloro-2-fluoro-5-(trifluoromethyl)pyridineHCID 1268075—
EduktHCID 67455816HCID 67455816—
LösungsmittelEthanolHCID 702—
Produkt1-(3-Chloro-5-trifluoromethyl-pyridin-2-yl)-pyrrolidine-2-carboxylic acid (5-tert-butyl-isoxazol-3-yl)-amideHCID 67458346—

Reaktionsbedingungen

Temperatur175 °C

Reaktionsschritte

A microwave reaction vessel is charged with (S)-pyrrolidine-2-carboxylic acid (5-tert-butyl-isoxazol-3-yl)-amide; hydrochloride, 3-chloro-2-fluoro-5-trifluoromethylpyridine, triethylamine and ethanol. The mixture is heated in a microwave reactor at 175° C. for 1 h, maintaining the watts at 60 to keep the reactor from shutting down. The reaction is cooled to room temperature and concentrated in vacuo to afford an oil which is purified by reverse phase preparative HPLC. Product fractions are combined and concentrated in vacuo to afford title compound (64.4 mg). ESI m/z 417 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08629157B2
Quelldatensatzuspto-grants-2014_01
ORD IDord-7db17c660c714c0eab8397d3ea7c2c51
Quellennotizuspto-grants-2014_01