Synthesis and Characterization of 2 methylindolizino[1,2 b]quinolin 9(11H) one
Синтез и характеристика 2‑метилиндолизино[1,2-b]хинолин-9(11H)-она
2025-01-01
SCID: 54.1/umtsb7xw
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2-methylindolizino[1,2-b]quinolin-9(11H)-one2-pyridone starting materialcamptothecin analogscharacterization by FT-IR, LC-MS, 1H NMRtetracyclic (ABCD) ring core synthesis
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Abstract (AI)
Camptothecin is a natural quinoline alkaloid, initially extracted from the bark of the Chinese tree Camptotheca acuminata, which acts as a powerful anti-cancer agent by inhibiting DNA topoisomerase I. Number of Camptothecin analogs synthesized by researchers to find potent anticancer drug. Camptothecin drug having Quinoline and 2-pyrodone moiety in their structure have biological activity and their derivatives are used in number of drugs. In present work a Tetracyclic (ABCD) ring core of camptothecin was synthesized by simple method using simple starting material like aniline derivatives and 2-pyridone in six steps. The intermediates were confirmed and characterized by FT-IR, LC-MS and 1HNMR.
Key Findings
1
A tetracyclic (ABCD) ring core of camptothecin was synthesized from aniline derivatives and 2-pyridone in six steps.
2
Intermediates from the six-step synthesis were characterized by FT-IR, LC-MS, and 1H NMR.
3
The synthetic route uses simple starting materials and a described straightforward method to access the camptothecin core.
4
The target scaffold synthesized is 2-methylindolizino[1,2-b]quinolin-9(11H)-one (a camptothecin tetracyclic core analog).
Research Object
Tetracyclic 2-methylindolizino[1,2-b]quinolin-9(11H)-one core (synthesized camptothecin-like tetracyclic ABCD ring system)
Research Subject
Synthesis and structural characterization (via FT-IR, LC-MS, 1H NMR) of the camptothecin-like tetracyclic core derived from aniline derivatives and 2-pyridone in a six-step route
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2025-01-01
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