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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1356466Generated: November 1, 2026

1-Pyrrolidineethanamine → HCID 18508358, compound

https://huagongshe.com/reaction/1356466

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PyrrolidineethanamineHCID 1344—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantHCID 17817484HCID 17817484—
SolventAcetonitrileHCID 6342—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
SolventPotassium CarbonateHCID 11430—
ProductHCID 18508358HCID 1850835868.4%

Reaction Steps

To a solution of 1-(2-aminoethyl)pyrrolidine (230 mg) in acetonitrile (5 ml)/THF (10 ml) were added 1-(4-biphenylylmethyl)-1,6-dihydro-6-oxo-3-pyridinecarboxylic acid (500 mg), WSC (380 mg), HOBt (260 mg), and triethylamine (0.7 ml) at room temperature. After stirring at room temperature for 12 hr, the reaction mixture was diluted with 5% aqueous potassium carbonate and extracted with ethyl acetate. The organic layer was washed with water and saturated aqueous sodium chloride sequentially, dried, and the solvent was removed in vacuo. The residue was purified by alumina column chromatography (eluent; THF) and recrystallized from ethyl acetate/diisopropylether to obtain the titled compound (450 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06586475B1
Source datasetuspto-grants-2003_07
ORD IDord-0b42fd7ba82548959beee945c9136e05
Source noteuspto-grants-2003_07