Reactions between isopropyl-alkylamines and 2,3-dichloro-1,4-naphthoquinone and 2,3-dichloro-1,4-naphthoquinone/acetaidehyde

被引:0
作者
Kallmayer, HJ [1 ]
Thierfelder, B [1 ]
机构
[1] Univ Saarland, Fachrichtung Pharmazeut Chem, D-66041 Saarbrucken, Germany
来源
PHARMAZIE | 2003年 / 58卷 / 02期
关键词
D O I
暂无
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Isopropyl-alkylamines 2 react with 2,3-dichloro-1,4-naphthoquinone (1) to give red 2-chloro-3-isopropyl-alkylamino-1,4-naphthoquinones 3 and with 2,3-dichloro-1,4-naphthoquinone/acet-aldehyde to give blue 2-chloro-3-isopropylalkylamino-vinyl-1,4-naphthoquinones 7. It is evident that the formation of 7 is preferred sterically to the formation of 3. The reaction between 2, 1 and acetaldehyde give also red aminoquinones 3 and blue green 2-chloro-3-(4-isopropylalkylamino-buta-1,3-dienyl)-1,4-naphthoquinone like 11.
引用
收藏
页码:104 / 107
页数:4
相关论文
共 8 条
[1]   SPECTROPHOTOMETRIC ANALYSIS OF PRIMARY ALIPHATIC-AMINES WITH DICHLONE [J].
ABOUOUF, AA ;
TAHA, AM ;
SAIDHOM, MB .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1973, 62 (10) :1700-1702
[2]  
ALNABARI M, 2000, SYNTHESIS, V1087
[3]  
BEDAIR MM, 1992, SCI PHARM, V60, P235
[4]   AMINE OXIDATION .5. DEHYDROGENATION OF DIETHYLAMINE IN THE PRESENCE OF 2,3-DICHLORONAPHTHAQUINONE [J].
HENBEST, HB ;
SLADE, P .
JOURNAL OF THE CHEMICAL SOCIETY, 1960, (APR) :1558-1560
[5]   QUINONE-AMINE REACTIONS .5. COLOR PRODUCTS OF QUINHYDRONE-DESIPRAMINE REACTION [J].
KALLMAYER, HJ ;
TAPPE, C .
ARCHIV DER PHARMAZIE, 1981, 314 (10) :884-888
[6]  
Kallmayer HJ, 2002, PHARMAZIE, V57, P530
[7]  
ULRICH H, 1977, METHOD ORGAN CHEM, V7, P456
[8]  
ULRICH H, 1977, METHODEN ORGANISCHEN, V7, P450