HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 987579Generated: October 30, 2026
Dimethyl Sulfoxide → 6-Methoxy-8-[2-(3-naphthalen-2-yl-8-azabicyclo[3.2.1]oct-2-en-8-yl)-ethoxy]-quinoline
https://huagongshe.com/reaction/987579
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 6-Methoxyquinolin-8-ol | HCID 18009170 | — |
| Reactant | 8-(2-Chloroethyl)-3-(2-naphthyl)-8-azabicyclo[3.2.1]oct-2-ene | HCID 18009181 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-Methoxy-8-[2-(3-naphthalen-2-yl-8-azabicyclo[3.2.1]oct-2-en-8-yl)-ethoxy]-quinoline | HCID 10296755 | 38% |
Reaction Steps
8-(2-Chloroethyl)-3-(2-naphthyl)-8-azabicyclo[3.2.1]oct-2-ene (0.50 g, 1.70 mmol), 0.39 g (2.20 mmol) 6-methoxyquinolin-8-ol, 0.08 g (2.00 mmol) NaH (60% dispersion in mineral oil) and 3 mL DMSO are stirred at 50 C for 16 h. The reaction mixture is poured into 100 mL of H2O and extracted with 3×50 mL EtOAc. The combined organics are washed with 3×100 mL H2O, 1×100 mL brine, dried over MgSO4, filtered, and the volatiles are evaporated. The crude product is subjected to flash chromatography on SiO2 gel, eluting with EtOAc and then 40/1 EtOAc/2M NH3 in MeOH, to produce an off-white solid. This solid is treated with 0.06 g (0.67 mmol) (CO2H)2 in 4 mL of absolute EtOH to give 0.33 g (0.13 mmol, a 38% yield) of the oxalate salt of the title compound as a white solid. mp: 100-103° C.; MS (ES) m/z 437 (MH)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06632824B2 |
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| Source dataset | uspto-grants-2003_10 |
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| ORD ID | ord-81263b350d7f4000a7d2492b05504210 |
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| Source note | uspto-grants-2003_10 |
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