Alkylation of 2,4-(1H,3H)-Quinazolinediones with Dialkyl Carbonates Under Microwave Irradiations

被引:16
作者
Alfredo Rivero, Ignacio [1 ,2 ]
Guerrero, Leticia [1 ]
Alejandra Espinoza, Karla [3 ]
Cecilia Meza, Martha [1 ]
Ramon Rodriguez, Jesus [3 ]
机构
[1] Inst Tecnol Tijuana, Ctr Grad & Invest Quim, Tijuana 1166, Mexico
[2] Inst Nacl Invest Nucl, Dept Quim, Mexico City 52750, DF, Mexico
[3] Univ Autonoma Baja California, Fac Quim, Tijuana 22390, BC, Mexico
关键词
alkylation; quinazoline-2,4-dione; antihypertensive activity; microwaves; MULTIPLE-DRUG RESISTANCE; HETEROCYCLIC COMPOUND; TUMOR-CELLS; METABOLITES; 5-N-ACETYLARDEEMIN; FUMIQUINAZOLINES; FERMENTATION; INHIBITOR; ALKALOIDS; TAXONOMY;
D O I
10.3390/molecules14051860
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Alkylation is a very important chemical reaction which modifies the biological properties of drugs. Quinazolinedione derivatives are of considerable interest due to their wide array of pharmacological properties. We now report application of a practical alkylation procedure to several quinazolinediones, including pelanserine (5f), which shows antihypertensive properties, 1-methyl-3-(2'-phenylethyl)-1H,3H-quinazoline-2,4-dione (1ab) and 1-methyl-3-[2'-(4'-methoxyphenyl)ethyl]-1H,3H-quinazoline-2,4-dione (1ae), which had been isolated from natural sources. The alkylation was optimized using dimethyl and diethyl carbonates under microwave irradiations.
引用
收藏
页码:1860 / 1868
页数:9
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