HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2356390Generated: November 3, 2026
Potassium Iodide → 2-Ethyl-6-fluoro-3-{1-[3-(4-fluorophenylsulfanyl)-propyl]-piperidin-4-YL}-1-phenyl-1H-indole
https://huagongshe.com/reaction/2356390
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Benzene, 1-[(3-bromopropyl)thio]-4-fluoro- | HCID 14575314 | — |
| Reactant | 2-Ethyl-6-fluoro-1-phenyl-3-piperidin-4-YL-1H-indole | HCID 58748000 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Ethyl-6-fluoro-3-{1-[3-(4-fluorophenylsulfanyl)-propyl]-piperidin-4-YL}-1-phenyl-1H-indole | HCID 11952524 | 64% |
Reaction Steps
A mixture of 2-ethyl-6-fluoro-1-phenyl-3-piperidin-4-yl-1H-indole (70 mg, TFA salt), 1-(3-Bromo-propylsulfanyl)-4-fluoro-benzene (44 mg), potassium iodide (5 mg) and potassium carbonate (55 mg) in DMF (3 ml) is heated at 80° C. for 3 h, and allowed to cool to r.t. overnight. Ethyl acetate (50 ml) and water (25 ml) are added and the organic phase is washed with water, dried and concentrated in vacuo. The crude product is purified by flash chromatography (98:2 CH2Cl2:MeOH) to give 50 mg pure product (64%) as brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07759365B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-f02b3860461d421696049fe42406db5c |
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| Source note | uspto-grants-2010_07 |
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