Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 216759Erstellt: 25. Oktober 2026

Dabco → HCID 178424198, Verbindung

https://huagongshe.com/reaction/216759

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDabcoHCID 9237—
EduktSodium hydrideHCID 24758—
Edukt6-ChloropurineHCID 5359277—
Edukt(8-Methyl-2-o-tolylquinolin-3-yl)methanolHCID 57707986—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelDimethyl SulfoxideHCID 679—
LösungsmittelSodium chloride; waterHCID 57417360—
ProduktHCID 178424198HCID 178424198—

Reaktionsschritte

Prepared according to procedure L A mixture of 6-chloropurine (110 mg, 0.71 mmol) and 1,4-diazabicyclo[2.2.2]octane (160 mg, 1.43 mmol) in DMSO (0.7 mL) was stirred at rt for 4 h and was then added via cannula to a mixture of (8-methyl-2-o-tolylquinolin-3-yl)methanol (94 mg, 0.36 mmol) and sodium hydride, 60% dispersion in mineral oil (57 mg, 1.43 mmol) in DMSO (1 mL) that had been stirred at rt for 15 min prior to the addition. The mixture was stirred at rt for 3.5 h, neutralized by the addition of glacial acetic acid, diluted with brine (15 mL), and extracted with EtOAc (3×15 mL). The combined organic layers were dried (MgSO4) and concentrated under reduced pressure. The resulting yellow oil was dissolved in CH2Cl2, evaporated onto silica gel (deactivated with 2M NH3 in MeOH), and purified by flash chromatography (Biotage® Si 25+M) eluting with 2 M NH3 in MeOH/CH2Cl2 (5%) to provide a white solid [PI3δ IC50=27 nM]. MS (APCI+) m/z=282.3 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08193199B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-76503cf13c79468a84ad45caee737755
Quellennotizuspto-grants-2012_06