Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 46947163 | HCID 46947163 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 46947167 | HCID 46947167 | 46.1% |
Reaction Steps
Potassium carbonate (35 mg, 0.245 mmol) and iodomethane (CH3I, 21 μL, 0.330 mmol) were added to an anhydrous tetrahydrofuran (5 mL) solution having the 2-[4-(N-monomethylamino)phenyl]-6-(2-fluoroethoxy)benzothiophene (1-12, 50 mg, 0.165 mmol) prepared in Example 12 dissolved therein, and stirred at 80° C. for 12 hours. The reaction mixture was cooled to room temperature and water was added. Organic compounds were extracted with ethyl acetate and evaporated after a treatment with sodium sulfate. Purification was performed by column chromatograph to give the target compound 2-[4-(N,N-dimethylamino)phenyl]-6-(2-fluoroethoxy)benzothiophene (1-16, 24 mg, 46%). The obtained target compound 1-16 had a melting point of 183.9-195.9° C., and the following physical data;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08497260B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-5a43878dd34c4c4e9c82c5d8f11ff2bc |
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| Source note | uspto-grants-2013_07 |
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