New efficient approach for the synthesis of 2-alkyl(aryl) substituted 4H-pyrido[1,2-a]pyrimidin-4-ones

被引:20
作者
Bonacorso, HG [1 ]
Righi, FJ [1 ]
Rodrigues, IR [1 ]
Cechinel, CA [1 ]
Costa, MB [1 ]
Wastowski, AD [1 ]
Martins, MAP [1 ]
Zanatta, N [1 ]
机构
[1] Univ Fed Santa Maria, Dept Quim, NUQUIMHE, BR-97105900 Santa Maria, RS, Brazil
关键词
D O I
10.1002/jhet.5570430136
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A new, efficient and easy route for the preparation of a series of 2-alkyl(aryl) substituted 4-oxo-4H-pyrido[1,2-a]pyrimidines, where alkyl = CH3; aryl = C6H5,4-FC6H4,4-ClC6H4,4-BrC6H4, 4-CH3C6H4, 4-OCH3- C6H4, 4-NO2C6H4 in 45 - 80 % yield from the reaction of beta-alkoxyvinyl trichloromethyl ketones with 2-aminopyridine under mild conditions, is then reported.
引用
收藏
页码:229 / 233
页数:5
相关论文
共 40 条
[1]   NEW SYNTHESES OF HETEROCYCLIC COMPOUNDS .12. THE CONDENSATION OF ETHYL BETA-AMINOCROTONATE WITH SOME CYCLIC AMIDINES [J].
ANTAKI, H ;
PETROW, V .
JOURNAL OF THE CHEMICAL SOCIETY, 1951, (FEB) :551-555
[2]   ORAL ANTIALLERGIC ACTIVITY IN ASCARIS HYPERSENSITIVE DOGS - A STUDY OF KNOWN ANTIHISTAMINES AND OF THE NEW COMPOUNDS RAMASTINE (R-57-959) AND LEVOCABASTINE (R-50-547) [J].
AWOUTERS, F ;
VERMEIRE, J ;
SMEYERS, F ;
VERMOTE, P ;
VANBEEK, R ;
NIEMEGEERS, CJE .
DRUG DEVELOPMENT RESEARCH, 1986, 8 (1-4) :95-102
[3]   Synthesis of some N-[1-alkyl(aryl)3-oxo-4,4,4-trichloro(trifluoro)-1-buten-1-yl]-o-aminophenols and o-phenylenediamines as potential anticancer agents [J].
Bonacorso, HG ;
Wentz, AP ;
Bittencourt, SRT ;
Marques, LML ;
Zanatta, N ;
Martins, MAP .
SYNTHETIC COMMUNICATIONS, 2002, 32 (03) :335-341
[4]   β-Alkoxyvinyl trichloromethyl ketones as N-heterocyclic acylating agent.: A new access to 5H-thiazolo[3,2-a]pyrimidin-5-ones [J].
Bonacorso, HG ;
Lourega, RV ;
Wastowski, AD ;
Flores, AFC ;
Zanatta, N ;
Martins, MAP .
TETRAHEDRON LETTERS, 2002, 43 (51) :9315-9318
[5]  
Bonacorso HG, 2002, SYNTHESIS-STUTTGART, P1037
[6]   Trifluoroacetylation of unsymmetrical ketone acetals. A convenient route to obtain alkyl side chain trifluoromethylated heterocycles [J].
Bonacorso, HG ;
Martins, MAP ;
Bittencourt, SRT ;
Lourega, RV ;
Zanatta, N ;
Flores, AFC .
JOURNAL OF FLUORINE CHEMISTRY, 1999, 99 (02) :177-182
[7]  
Bonacorso HG, 2000, SYNTHESIS-STUTTGART, P1431
[8]   Haloacetylated enol ethers.: 13.: Synthesis of N-[1-aryl(alkyl)-3-oxo-4,4,4-trichloro-1-buten-1-yl]-o-phenylenediamines and 2-trichloromethyl-4-aryl-3H-1,5-benzodiazepines [J].
Bonacorso, HG ;
Bittencourt, SRT ;
Wastowski, AD ;
Wentz, AP ;
Zanatta, N ;
Martins, MAP .
JOURNAL OF HETEROCYCLIC CHEMISTRY, 1999, 36 (01) :45-48
[9]   SYNTHESIS OF 4(1H)-QUINOLONES BY THERMOLYSIS OF ARYLAMINOMETHYLENE MELDRUM ACID-DERIVATIVES [J].
CASSIS, R ;
TAPIA, R ;
VALDERRAMA, JA .
SYNTHETIC COMMUNICATIONS, 1985, 15 (02) :125-133
[10]  
COLLA A, 1991, SYNTHESIS-STUTTGART, P483