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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl-8-chloro-1-ethyl-9-methoxy-4-oxo-4H-quinolizine-3-carboxylate | HCID 11185968 | — |
| Reactant | tert-butyl N-[2-(pyrrolidin-3-yl)ethyl]carbamate | HCID 21955469 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 8-[3-(N-Boc-Aminoethyl)Pyrrolidinyl]-1-Ethyl-9-Methoxy-4-Oxo-4H-Quinolizine-3-Carboxylic Acid Ethyl Ester | HCID 86589539 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06509349B1 |
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| Source dataset | uspto-grants-2003_01 |
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| ORD ID | ord-c85d9ddc9cb04eba93f66c39a505a5a1 |
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| Source note | uspto-grants-2003_01 |
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