Synthesis of isotopically labelled SGLT inhibitors and their metabolites

被引:14
作者
Derdau, Volker [1 ]
Fey, Thorsten [1 ]
Atzrodt, Jens [1 ]
机构
[1] Sanofi Aventis Deutschland GmbH, Isotope Chem & Metabolite Synth, D-65926 Frankfurt, Germany
关键词
MASS-BALANCE; DRUG; DEPROTECTION; SAFETY;
D O I
10.1016/j.tet.2009.12.003
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Isotopically labelled analogues of two structurally very similar SGLT inhibitors AVE2268 (1a) and AVE8887 (1b) have been synthesized by various routes. The radioactive labelled [C-14]-AVE2268 was prepared in five steps including a Friedel-Crafts acylation as the key step for the C-14-label introduction. For [C-14]-AVE8887 the same synthetic approach was not successful and therefore an alternative thiophene metallation/Weinreb amide sequence was developed. This pathway was also applied to obtain stable isotopically labelled analogues of both AVE2268 and AVE8887. Finally, the synthesis of two metabolites, sulfate 12 and glucuronide 13 were achieved by applying interesting protecting group and oxidation strategies. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1472 / 1482
页数:11
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