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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 553050Erstellt: 25. Oktober 2026

1,10-Phenanthroline → HCID 57399776, Verbindung

https://huagongshe.com/reaction/553050

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 (DCI/NH3): m/z 342 (M+1)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07951791B2
Quelldatensatzuspto-grants-2011_05
ORD IDord-d7b3f6a35ebe4305b45c46fa11f232cf
Quellennotizuspto-grants-2011_05