Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 390714Erstellt: 24. Oktober 2026

Cesium carbonate → HCID 87447416, Verbindung

https://huagongshe.com/de/reaction/390714

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCesium carbonateHCID 10796—
Edukt5-Chloro-1,10-phenanthrolineHCID 77865—
Edukt5-Bromo-2-(trifluoromethyl)pyridineHCID 2761197—
EduktWater ammonium hydroxideHCID 86589665—
EduktN-1,3-thiazol-2-ylpyrrolidine-1-carboxamideHCID 86631924—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
ProduktHCID 87447416HCID 87447416—

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

In a 4 mL vial charged with a stir bar, N-1,3-thiazol-2-ylpyrrolidine-1-carboxamide (46 mg, 0.23 mmol, Example 32A) was added, followed by copper(I) trifluoromethanesulfonate benzene complex (30 mg, 0.05 mmol), 5-chloro-1,10-phenanthroline (23 mg, 0.09 mmol) and cesium carbonate (100 mg, 0.3 mmol). A loose cap with septum was placed on the vial and the vial was placed under vacuum in a vacuum oven for 30 minutes. The solid mixture was purged with nitrogen gas a couple of times. Then 5-bromo-2-(trifluoromethyl)pyridine (68 mg, 0.3 mmol) dissolved in 1-methyl-2-pyrrolidinone (1.0 mL) was added to the solid mixture. The vial was capped and placed on a heater/stirrer and heated to 120° C. overnight. Then a 1 mL solution of concentrated ammonium hydroxide/water (1:2) was added. The reaction was filtered and concentrated to dryness. The residue was purified by reverse phase HPLC (C18, gradient 10-95% acetonitrile/water/0.1% trifluoroacetic acid) to provide the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08383657B2
Quelldatensatzuspto-grants-2013_02
ORD IDord-56378088470641529a5f4944003f1830
Quellennotizuspto-grants-2013_02