DEGRADATION OF MECILLINAM IN AQUEOUS-SOLUTION

被引:21
作者
BALTZER, B
LUND, F
RASTRUPANDERSEN, N
机构
[1] Leo Pharmaceutical Products, Ballerup
关键词
Antibiotics—mecillinam; degradation in aqueous solution; isolation of degradation products; degradation pathways; rate constants; Hydrolysis—mecillinam in aqueous solution; degradation products; Mecillinam—degradation in aqueous solution;
D O I
10.1002/jps.2600681005
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The hydrolysis of mecillinam in aqueous solution (37°) was studied at pH 2‐10. The degradation products observed by TLC and NMR were identified and quantified. Several of these compounds were synthesized. Mecillinam and the key degradation product, (6R)‐6‐formamidopenicillanic acid, underwent reversible 6‐epimerization in basic solution. Some of the thiazolidine derivatives formed epimerized at position 2. In contrast to penicillins, the degradation pattern of mecillinam becomes more complex with increasing pH. Rate constants for some processes are given. Copyright © 1979 Wiley‐Liss, Inc., A Wiley Company
引用
收藏
页码:1207 / 1215
页数:9
相关论文
共 38 条
[1]   KINETIC-ANALYSIS OF PENICILLIN DEGRADATION IN ACIDIC MEDIA [J].
BLAHA, JM ;
KNEVEL, AM ;
KESSLER, DP ;
MINCY, JW ;
HEM, SL .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1976, 65 (08) :1165-1170
[2]   DETERMINATION OF CONFIGURATION OF 4 D-BENZYLPENICILLOATES [J].
BUSSON, R ;
CLAES, PJ ;
VANDERHAEGHE, H .
JOURNAL OF ORGANIC CHEMISTRY, 1976, 41 (15) :2556-2561
[3]   BASE-CATALYZED-HYDROLYSIS OF 6-AMINOPENICILLANIC ACID - KINETIC AND THERMODYNAMIC PRODUCTS [J].
CARROLL, RD ;
JUNG, S ;
SKLAVOUNOS, CG .
JOURNAL OF HETEROCYCLIC CHEMISTRY, 1977, 14 (03) :503-505
[4]  
Clarke H. T., 1949, CHEM PENICILLIN
[5]   PENICILLANIC ACIDS - REQUIREMENTS FOR EPIMERISATION AT C-6 [J].
CLAYTON, JP ;
NAYLER, JHC ;
SOUTHGAT.R ;
STOVE, ER .
JOURNAL OF THE CHEMICAL SOCIETY D-CHEMICAL COMMUNICATIONS, 1969, (03) :129-&
[6]  
Cook A. H., 1949, CHEM PENICILLIN, P921
[7]   DEGRADATION KINETICS OF 6-AMINOPENICILLANIC ACID [J].
DENNEN, DW .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1967, 56 (10) :1273-&
[8]  
deWolfe R. H, 1975, CHEM AMIDINES IMIDAT, P349
[9]  
EBERHARDT U, 1971, Patent No. 81111
[10]   TOTAL SYNTHESIS OF BETA-LACTAM ANTIBIOTICS .4. EPIMERIZATION OF 6(7)-AMINOPENICILLINS AND 6(7)-CEPHALOSPORINS FROM ALPHA TO BETA [J].
FIRESTONE, RA ;
MACIEJEWICZ, NS ;
RATCLIFFE, RW ;
CHRISTENSEN, BG .
JOURNAL OF ORGANIC CHEMISTRY, 1974, 39 (04) :437-440