HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 992282Generated: October 31, 2026
Potassium Carbonate → (S)-N-(1-(2-(4-cyanophenyl)ethyl)pyrrolidin-3-yl)-1-adamantanecarboxamide
https://huagongshe.com/reaction/992282
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 22033501 | HCID 22033501 | — |
| Reactant | (S)-N-(pyrrolidin-3-yl)-1-adamantanecarboxamide | HCID 49760538 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (S)-N-(1-(2-(4-cyanophenyl)ethyl)pyrrolidin-3-yl)-1-adamantanecarboxamide | HCID 9907753 | 73.2% |
Reaction Steps
(S)-N-(Pyrrolidin-3-yl)-1-adamantanecarboxamide (1.0 g) and 2-(4-cyanophenyl)ethyl p-toluenesulfonate (1.2 g) were dissolved in acetonitrile, and potassium carbonate was added thereto. The mixture was stirred under heating at 70° C. for 5 hours. After the completion of the reaction, the solvent was evaporated under reduced pressure. Ethyl acetate was added to the obtained residue and the mixture was washed with saturated brine. The solvent was evaporated under reduced pressure, and the obtained residue was subjected to silica gel column chromatography (chloroform:methanol=30:1). The obtained eluate was concentrated and IPE was added to the obtained residue. The precipitated crystals were collected by filtration to give (S)-N-(1-(2-(4-cyanophenyl)ethyl)pyrrolidin-3-yl)-1-adamantanecarboxamide (1.1 g), melting point 104-105° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06468998B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-6aa3ed44ee8e49d99c01d0e9d9726089 |
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| Source note | uspto-grants-2002_10 |
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