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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1688861Erstellt: 26. Oktober 2026

N,N-Diethylaniline → 4'-{[4-(1,4-Dioxaspiro[4.5]dec-8-yl)-2-methyl-5-oxo-7-propyl-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl]methyl}-2'-methylbiphenyl-2-carbonitrile

https://huagongshe.com/reaction/1688861

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN,N-DiethylanilineHCID 7061—
Edukt1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
EduktEthyl 2-[(2'-cyano-2-methylbiphenyl-4-yl)methyl]-3-oxohexanoateHCID 67010208—
EduktHCID 178434680HCID 178434680—
LösungsmittelHydrochloric AcidHCID 313—
Produkt4'-{[4-(1,4-Dioxaspiro[4.5]dec-8-yl)-2-methyl-5-oxo-7-propyl-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl]methyl}-2'-methylbiphenyl-2-carbonitrileHCID 6701027553,2%

Reaktionsbedingungen

Temperatur180 °C

Reaktionsschritte

A mixture of ethyl 2-[(2′-cyano-2-methylbiphenyl-4-yl)methyl]-3-oxohexanoate (3.00 g), N-(1,4-dioxaspiro[4.5]dec-8-yl)-3-methyl-1H-1,2,4-triazol-5-amine (1.00 g), 1,8-diazabicyclo[5.4.0]undec-7-ene (0.3 mL) and N,N-diethylaniline (10 mL) was stirred at 180° C. overnight, allowed to cool and poured into 1 M hydrochloric acid (50 mL), and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography to give the title compound as a brown oil (1.20 g, 53%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08148383B2
Quelldatensatzuspto-grants-2012_04
ORD IDord-dcec214da8f94e259c14cbe9cdb76d8e
Quellennotizuspto-grants-2012_04