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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 902984Erstellt: 25. Oktober 2026

1,10-Phenanthroline → HCID 57399776, Verbindung

https://huagongshe.com/reaction/902984

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,10-PhenanthrolineHCID 1318—
EduktCesium carbonateHCID 10796—
Edukt3-Quinuclidinol, (+)-HCID 736411—
Edukt3,7-Dibromo-dibenzothiophene 5,5-dioxideHCID 4071898—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
LösungsmittelTolueneHCID 1140—
ProduktHCID 57399776HCID 5739977663%

Reaktionsbedingungen

Temperatur110 °C

Reaktionsschritte

A mixture of 3,7-dibromodibenzothiophene-5,5-dioxide (0.60 g, 1.75 mmol; see J. Med. Chem. 1978, 21, 1084), (S)-(−)-quinuclidin-3-ol (280 mg, 2.2 mmol; Acros), copper(I) iodide (33 mg, 0.17 mmol; Aldrich), 1,10-phenanthroline (63 mg, 0.35 mol; Aldrich) and powdered cesium carbonate (0.86 g, 2.64 mmol; Aldrich) in toluene (2 mL) was heated to 110° C. with vigorous stirring for 30 h. After cooling to room temperature, the reaction mixture was filtered through diatomaceous earth, rinsing with ethyl acetate and dichloromethane, and the residue purified by flash chromatography (80 g silica gel, 1:10:89 NH4OH-MeOH-CH2Cl2) to afford the title compound (0.37 g, 1.08 mmol; 63% yield): MS (DCl/NH3): m/z 342 (M+1)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07365193B2
Quelldatensatzuspto-grants-2008_04
ORD IDord-17aef5b2e9104056a4f08525966d6bbd
Quellennotizuspto-grants-2008_04