共 24 条
Original loading and Suzuki conditions for the solid-phase synthesis of biphenyltetrazoles.: Application to the first solid-phase synthesis of irbesartan
被引:13
作者:

Cousaert, Nicolas
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h-index: 0
机构: INSERM, Biostruct & Drug Discovery U761, F-59006 Lille, France

Willand, Nicolas
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h-index: 0
机构: INSERM, Biostruct & Drug Discovery U761, F-59006 Lille, France

Gesquiere, Jean-Claude
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h-index: 0
机构: INSERM, Biostruct & Drug Discovery U761, F-59006 Lille, France

Tartar, Andre
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h-index: 0
机构: INSERM, Biostruct & Drug Discovery U761, F-59006 Lille, France

Deprez, Benoit
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h-index: 0
机构: INSERM, Biostruct & Drug Discovery U761, F-59006 Lille, France

Deprez-Poulain, Rebecca
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机构: INSERM, Biostruct & Drug Discovery U761, F-59006 Lille, France
机构:
[1] INSERM, Biostruct & Drug Discovery U761, F-59006 Lille, France
[2] Univ Lille, Fac Pharm, F-59006 Lille, France
[3] Inst Pasteur, IFR 142, F-59021 Lille, France
关键词:
tetrazoles;
solid-phase;
irbesartan;
zinc triflate;
D O I:
10.1016/j.tetlet.2008.02.147
中图分类号:
O62 [有机化学];
学科分类号:
070303 ;
081704 ;
摘要:
Biphenyltetrazoles are recognized privileged structures. Among them, the therapeutically important class of sartans displays antagonistic activity on ATI receptors. We have developed a method for anchoring tetrazole derivatives via the heterocycle on a hydroxylated resin using zinc triflate. New Suzuki-Miyaura cross-coupling conditions are developed for the quantitative formation of the phenylphenyl bond. Our straightforward synthesis scheme, starting from the conserved phenyltetrazole moiety and ending with the appending of the structurally variable moiety, is well suited to the preparation of sartans and their analogues at a laboratory scale. We thus describe here the first solid phase synthesis of irbesartan, a marketed ATI antagonist. (c) 2008 Elsevier Ltd. All rights reserved.
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页码:2743 / 2747
页数:5
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