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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Adamantanecarbonyl chlorideHCID 98915—
Reactant(3S)-(+)-1-Benzyl-3-aminopyrrolidineHCID 1519353—
SolventDimethylformamideHCID 6228—
Product(S)-N-(1-Benzylpyrrolidin-3-yl)-1-adamantanecarboxamideHCID 988429777.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06468998B1
Source datasetuspto-grants-2002_10
ORD IDord-f50cc3d55cf34034827cb4f2a2a80aee
Source noteuspto-grants-2002_10