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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1635094Generated: October 26, 2026

Triethylamine → 8-[3-(N-Boc-Aminoethyl)Pyrrolidinyl]-1-Ethyl-9-Methoxy-4-Oxo-4H-Quinolizine-3-Carboxylic Acid Ethyl Ester

https://huagongshe.com/reaction/1635094

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl-8-chloro-1-ethyl-9-methoxy-4-oxo-4H-quinolizine-3-carboxylateHCID 11185968—
Reactanttert-butyl N-[2-(pyrrolidin-3-yl)ethyl]carbamateHCID 21955469—
SolventAcetonitrileHCID 6342—
Product8-[3-(N-Boc-Aminoethyl)Pyrrolidinyl]-1-Ethyl-9-Methoxy-4-Oxo-4H-Quinolizine-3-Carboxylic Acid Ethyl EsterHCID 86589539—

Reaction Conditions

Temperature40 °C

Reaction Steps

Ethyl-8-chloro-1-ethyl-9-methoxy-4-oxo-4H-quinolizine-3-carboxylate (Precursor A) (0.151 g) and triethylamine (0.5 ml) are dissolved in acetonitrile (6 ml). To this solution 3-(N-boc-aminoethyl)pyrrolidine (Precursor D) (0.215 g) is added and the solution stirred at 40° C. for 18 hours. The solvent is evaporated and the residue dissolved in dichloromethane, washed with 1N hydrochloric acid and dried over sodium sulfate. The desired product is obtained by evaporation of the solvent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06509349B1
Source datasetuspto-grants-2003_01
ORD IDord-c85d9ddc9cb04eba93f66c39a505a5a1
Source noteuspto-grants-2003_01