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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 347860Erstellt: 26. Oktober 2026

1,2-Diaminocyclohexane → N4-(2-Ethylpyrazolo[1,5-a]pyridin-3-yl)tetrahydro-2H-4-pyrancarboxamide

https://huagongshe.com/reaction/347860

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-DiaminocyclohexaneHCID 4610—
EduktPotassium Phosphate, TribasicHCID 62657—
EduktOxane-4-carboxamideHCID 13197203—
Edukt2-Ethyl-3-iodopyrazolo[1,5-a]pyridineHCID 16114933—
KatalysatorCopper iodideHCID 83717—
LösungsmittelO-XyleneHCID 7237—
ProduktN4-(2-Ethylpyrazolo[1,5-a]pyridin-3-yl)tetrahydro-2H-4-pyrancarboxamideHCID 2108412179,6%

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

A mixture of 2-ethyl-3-iodopyrazolo[1,5-a]pyridine (350 g, 1.29 mol), tetrahydro-2H-4-pyrancarboxamide (249 g, 1.93 mol), copper iodide (49.0 g, 258 mmol), tripotassium phosphate (hydrate) (546 g, 2.57 mol), 1,2-cyclohexanediamine (mixture of cis and trans) (58.7 g, 514 mmol) and xylene (3500 mL) was stirred while heating at an external temperature of 120° C. (oil bath). The reaction mixture was heated and stirred for 6 hours, and then heating was terminated and upon reaching an internal temperature of 61.5° C., hot water (58° C., 3500 mL) was added to the reaction mixture and stirring was continued overnight. After adding 28% aqueous ammonia (1050 mL) to the reaction mixture and stirring for 1 hour, the precipitate was filtered out and washed with water (1750 mL) and ethyl acetate (1050 mL) and then dried under aeration at 60° C. overnight to afford 280 g of the title compound (major conformer:minor conformer=6:1) (79.6% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07176216B2
Quelldatensatzuspto-grants-2007_02
ORD IDord-cf5d113fca9e4aa98ce6238b4f679279
Quellennotizuspto-grants-2007_02