Estimation of impurity profiles of drugs and related materials .16. Identification of the side-products of the ethinylation step in the synthesis of contraceptive gestogens

被引:18
作者
Horvath, P [1 ]
Balogh, G [1 ]
Brlik, J [1 ]
Csehi, A [1 ]
Dravecz, F [1 ]
Halmos, Z [1 ]
Lauko, A [1 ]
Renyei, M [1 ]
Varga, K [1 ]
Gorog, S [1 ]
机构
[1] GEDEON RICHTER CHEM WORKS LTD,CHEM WORKS,H-1475 BUDAPEST,HUNGARY
关键词
norgestrel; impurities in norgestrel; impurity profiling; chromatography; (TLC; GLC; HPLC); spectroscopy; (UV; NMR; MS; GC/MS); 3,17 alpha-diethinyl-13-ethyl-3,5-gonadiene-17-ol; 17; alpha-ethinyl-13-ethyl-4-gonen-17-ol;
D O I
10.1016/S0731-7085(96)02008-0
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A new apolar impurity (3,17 alpha-diethinyl-13-ethyl-3,5-gonadiene-17-ol, IIb) was detected and identified in norgestrel with the aid of thin-layer and high-performance chromatography and spectroscopic techniques. IIb is the product of the acid-catalysed dehydration of an overethinylated side product (Ib) of the ethinylation step in the synthesis of norgestrel. IIb can be determined by thin-layer densitometry and high-performance liquid chromatography. Another impurity (17 alpha-ethinyl-13-ethyl-4-gonene-17-ol, IV), originating from a side product of the Birch reduction step in the synthesis of norgestrel was also detected and identified. The spot of IV overlaps with that of IIb in the TLC system of USP XXIII but can be separated and quantificated by more selective TLC systems and by gas chromatograpy. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:1343 / 1349
页数:7
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