HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 478202Generated: October 30, 2026
Potassium Carbonate → HCID 18001243, compound
https://huagongshe.com/reaction/478202
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Piperidine, 1-(3-chloropropyl)-4-phenyl-, hydrochloride | HCID 203688 | — |
| Reactant | 3-(4-Piperidinyl)-1H-indole | HCID 702235 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18001243 | HCID 18001243 | 40% |
Reaction Steps
To a suspended solution of 4-(3-indolyl)piperidine (2.0 g, 10 mmol) and 1-(3-chloropropyl)-4-phenylpiperidine hydrochloride (3.1 g, 11.2 mmol) in DMF (60 mL) was added potassium carbonate (5.5 g, 40 mmol), and the mixture was stirred at 100° C. for 4 hours. After the precipitated salt was filtered off, the filtrate was concentrated, water (50 mL) was added to the filtrate, and the mixture was extracted with chloroform. After drying over anhydrous sodium sulfate, the chloroform layer was concentrated to afford a crude product. The crude product was purified by column chromatography on a silica gel (silica gel NH-DM 1020 produced by Fuji Silysia Chemical Ltd., eluent; chloroform) and was then recrystallized from ethyl acetate to afford a free form (1.6 g, yield: 40%) of the title compound as white crystals. After adding hydrochloric acid/methanol to a solution of the free form (1.6 g) in methanol, the mixture was concentrated and was then recrystallized from methanol/ether to afford the title compound (1.8 g) as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06642228B1 |
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| Source dataset | uspto-grants-2003_11 |
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| ORD ID | ord-0a2cf5f9c1ef416083e1abf734d75bb4 |
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| Source note | uspto-grants-2003_11 |
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