HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 553050Generated: October 26, 2026
1,10-Phenanthroline → HCID 57399776, compound
https://huagongshe.com/reaction/553050
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,10-Phenanthroline | HCID 1318 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 3-Quinuclidinol, (+)- | HCID 736411 | — |
| Reactant | 3,7-Dibromo-dibenzothiophene 5,5-dioxide | HCID 4071898 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 57399776 | HCID 57399776 | 63% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07951791B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-d7b3f6a35ebe4305b45c46fa11f232cf |
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| Source note | uspto-grants-2011_05 |
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