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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1412312Erstellt: 27. Oktober 2026

Tetrahydrofuran → HCID 178438685, Verbindung

https://huagongshe.com/reaction/1412312

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetrahydrofuranHCID 8028—
EduktSodium cyanoborohydrideHCID 5003444—
Edukt4'-({5-oxo-7-propyl-4-[(3a'R,6a'S)-tetrahydro-3a'H-spiro[cyclohexane-1,2'-cyclopenta[d][1,3]dioxol]-4-yl]-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl}methyl)biphenyl-2-carbonitrileHCID 67009097—
LösungsmittelEthyl AcetateHCID 8857—
ProduktHCID 178438685HCID 17843868572%

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

A mixture of 4′-({5-oxo-7-propyl-4-[(3a′R,6a′S)-tetrahydro-3a′H-spiro[cyclohexane-1,2′-cyclopenta[d][1,3]dioxol]-4-yl]-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl}methyl)biphenyl-2-carbonitrile (1.2 g), sodium cyanoborohydride (0.65 g), boron trifluoride-diethyl ether complex (1.3 mL) and tetrahydrofuran (30 mL) was stirred at 70° C. for 16 hr. The reaction mixture was diluted with ethyl acetate, washed with water and then 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 colorless solid (0.82 g, 72%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08921379B2
Quelldatensatzuspto-grants-2014_12
ORD IDord-4bed93575bba40bea63536c9f2fa673b
Quellennotizuspto-grants-2014_12