HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 5-Methoxy-3-{2-[4-(4-toluyl)piperdyl]ethyl}indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-(2-bromoethyl)-5-methoxy-1H-indole | HCID 11107868 | — |
| Reactant | 4-(4-Methylphenyl)piperidine hydrochloride | HCID 20351543 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-Methoxy-3-{2-[4-(4-toluyl)piperdyl]ethyl}indole | HCID 20318885 | — |
Reaction Steps
A solution of 8.8 g of 3-(2-bromoethyl)-5-methoxy indole in 100 ml of dimethylformamide is added to a stirring mixture of 4-(4-toluyl)piperidine hydrochloride [Example 5(a)] and 10.1 g of potassium carbonate in 400 ml of dimethylformamide and the reaction mixture is stirred at ambient temperature for 80 hours and then at 50° C. for 10 additional hours. It is cooled to ambient temperature, filtered, and 2 liters of water are added dropwise to produce a precipitate. The precipitate is triturated with ether and eluted with a 5% methanol in benzene solution through a silica gel column. The precipitate is recrystallized from an ethanol-water mixture to give off-white crystals, mp 131°-133° C., 5-methoxy-3-{2-[4-(4-toluyl)piperidyl]ethyl}indole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04101663 |
| Source dataset | uspto-grants-1978_07 |
| ORD ID | ord-f956e1b010bc4193ab4c4a9b26ebe8c7 |
| Source note | uspto-grants-1978_07 |