HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 992288Generated: November 1, 2026
Triethylamine → (S)-N-(1-Benzylpyrrolidin-3-yl)-1-adamantanecarboxamide
https://huagongshe.com/reaction/992288
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Adamantanecarbonyl chloride | HCID 98915 | — |
| Reactant | (3S)-(+)-1-Benzyl-3-aminopyrrolidine | HCID 1519353 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (S)-N-(1-Benzylpyrrolidin-3-yl)-1-adamantanecarboxamide | HCID 9884297 | 77.1% |
Reaction Steps
(S)-3-Amino-1-benzylpyrrolidine (10 g) and triethylamine (24 ml) were dissolved in DMF (100 ml). Under ice-cooling, 1-adamantanecarbonyl chloride (12.4 g) was added thereto, and the mixture was stirred overnight at room temperature. The solvent was evaporated under reduced pressure. To the obtained residue was added ethyl acetate 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-benzylpyrrolidin-3-yl)-1-adamantanecarboxamide (14.8 g), melting point 130-132° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06468998B1 |
|---|
| Source dataset | uspto-grants-2002_10 |
|---|
| ORD ID | ord-f50cc3d55cf34034827cb4f2a2a80aee |
|---|
| Source note | uspto-grants-2002_10 |
|---|