SYNTHESES AND OPTICAL ROTATORY DISPERSION STUDIES OF (S)-5-(2'-PENTYL)BARBITURIC ACID DERIVATIVES

被引:26
作者
CARROLL, FI
MECK, R
机构
[1] Chemistry and Life Sciences Laboratory, Research Triangle Institute, Research Triangle Park
关键词
D O I
10.1021/jo01261a041
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The syntheses of several (S)-5-(2ʹ-pentyl)barbituric acid derivatives are reported and their optical properties have been investigated. Although the ultraviolet spectra of (S)-(-)-5-ethyl-5-(2ʹ-pentyl)barbituric acid (IIa) shows only one maximum under the conditions studied, optical rotatory dispersion measurements have shown two Cotton effects. Some pH dependent optical rotatory dispersion studies indicate that the lower wavelength Cotton effect is the result of a π-π* transition and the higher wavelength Cotton effect is of type n-π*. The π-π* Cotton effect is positive and the n-π* Cotton effect is negative. The ultraviolet spectrum of the monosubstituted barbituric acid, (S)-(+)-5-(2ʹ-pentyl)barbiturie acid (IIc), in acid solution showed one maximum and the optical rotatory dispersion curve in the same solvent showed a negative π-π* low wavelength and a positive n-π* high wavelength Cotton effect. These results show that the biologically active IIa has optical rotatory dispersion properties greatly different from those of the biologically inactive IIc. These results are discussed in relation to the differences in the structure of these two compounds. © 1969, American Chemical Society. All rights reserved.
引用
收藏
页码:2676 / &
相关论文
共 15 条
[1]  
Abe K., 1955, J PHARM SOC JPN, V75, P891
[2]   CORRELATIONS IN ULTRAVIOLET SPECTRA OF PURINE AND PYRIMIDINE BASES [J].
CLARK, LB ;
TINOCO, I .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1965, 87 (01) :11-&
[3]   SYNTHESIS OF (R)-5-(2'-PENTYL)BARBITURIC ACID DERIVATIVES OF HIGH OPTICAL PURITY [J].
COOK, CE ;
TALLENT, CR .
JOURNAL OF HETEROCYCLIC CHEMISTRY, 1969, 6 (02) :203-&
[4]  
Doran W. J, 1959, MED CHEM, VIV, P1
[5]  
FOX JJ, 1952, B SOC CHIM BELG, V61, P44
[6]   INTERMEDIATES FOR THE SYNTHESIS OF OPTICALLY ACTIVE METHYL-SUBSTITUTED LONG-CHAIN ACIDS .3. [J].
HOLLIDAY, IA ;
POLGAR, N .
JOURNAL OF THE CHEMICAL SOCIETY, 1957, (JUL) :2934-2936
[7]   Studies on some optically active barbituric acids [J].
Kleiderer, EC ;
Shonle, HA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1934, 56 (07) :1772-1774
[8]  
KNABE J, 1966, ARCH PHARM WEINHEIM, V299, P232
[9]  
Levene PA, 1931, J BIOL CHEM, V91, P77
[10]   OPTICAL ROTATORY DISPERSION CIRCULAR DICHROISM AND ABSORPTION STUDIES ON SOME NATURALLY OCCURRING RIBONUCLEOSIDES AND RELATED DERIVATIVES [J].
MILES, DW ;
ROBINS, RK ;
EYRING, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1967, 57 (05) :1138-&