Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 553050Generated: October 26, 2026

1,10-Phenanthroline → HCID 57399776, compound

https://huagongshe.com/reaction/553050

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,10-PhenanthrolineHCID 1318—
ReactantCesium carbonateHCID 10796—
Reactant3-Quinuclidinol, (+)-HCID 736411—
Reactant3,7-Dibromo-dibenzothiophene 5,5-dioxideHCID 4071898—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventTolueneHCID 1140—
ProductHCID 57399776HCID 5739977663%

Reaction Conditions

Temperature110 °C

Reaction Steps

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)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07951791B2
Source datasetuspto-grants-2011_05
ORD IDord-d7b3f6a35ebe4305b45c46fa11f232cf
Source noteuspto-grants-2011_05