HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 478203Generated: October 30, 2026
Potassium Carbonate → 1-(1-(3-(4-Indol-3-ylpiperidyl)propyl)-3-piperidyl)-4-methoxybenzene Hydrochloride
https://huagongshe.com/reaction/478203
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-(4-Piperidinyl)-1H-indole | HCID 702235 | — |
| Reactant | 1-(3-Chloropropyl)-3-(4-methoxyphenyl)piperidine hydrochloride | HCID 18001209 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-(1-(3-(4-Indol-3-ylpiperidyl)propyl)-3-piperidyl)-4-methoxybenzene Hydrochloride | HCID 18001260 | 98.3% |
Reaction Steps
To a suspended solution of 4-(3-indolyl)piperidine (48 mg, 0.24 mmol) and 1-(3-chloropropyl)-3-(4-methoxyphenyl)piperidine hydrochloride (61 mg, 0.2 mmol) in acetonitrile (13 mL) was added potassium carbonate (111 mg, 0.8 mmol), and the resulting mixture was refluxed for 12 hours. After the precipitated salt was filtered off, the filtrate was concentrated, and the resulting crude product was purified by column chromatography on a silica gel (eluent; chloroform:ammonia-saturated chloroform=10:1→3:1→1:2) to afford a free form (92 mg) of the title compound as a colorless viscous oil. After adding hydrochloric acid/methanol to a solution of the free form in methanol, the mixture was concentrated and was then freeze-dried to afford the title compound (81 mg, yield: 80%) as a white amorphous solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06642228B1 |
|---|
| Source dataset | uspto-grants-2003_11 |
|---|
| ORD ID | ord-48c1da86bfff4693b205fa9e7154138b |
|---|
| Source note | uspto-grants-2003_11 |
|---|