Abstract
Tetrahydropyridazino-1,4-oxazinoisoquinoline derivatives with multidrug Resist. (MDR) modulating activity were designed and synthesized. A key step for cyclization of 1,4-oxazine ring was developed using K2CO3 and CH3CN in one-pot. Among prepared compounds, 2-(4-fluorobenzyl)-9,10-dimethoxy-12-methyl-6,7,11b,12-tetrahydropyridazino[4', 5',5,6] [1,4]oxazine-[3,4,-a]isoquinolin-1(2H)-one (1f) exhibited significant MDR reversing activity and low toxicity, which might be as potential MDR agent.
Original language | English (US) |
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Pages (from-to) | 75-85 |
Number of pages | 11 |
Journal | Heterocycles |
Volume | 63 |
Issue number | 1 |
DOIs | |
State | Published - Jan 1 2004 |
ASJC Scopus subject areas
- Analytical Chemistry
- Pharmacology
- Organic Chemistry