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酮与六氟磷酸亚胺盐的环化反应:三取代吡啶的高效合成

Annulation of ketones with vinamidinium hexafluorophosphate salts: an efficient preparation of trisubstituted pyridines.

作者信息

Marcoux J F, Corley E G, Rossen K, Pye P, Wu J, Robbins M A, Davies I W, Larsen R D, Reider P J

机构信息

Department of Process Research, Merck & Co., Inc., P.O. Box 2000, Rahway, New Jersey 07065, USA.

出版信息

Org Lett. 2000 Jul 27;2(15):2339-41. doi: 10.1021/ol006097b.

Abstract

alpha-Aryl ketones react with vinamidinium hexafluorophosphate salts to give access to the corresponding 3-arylpyridines. The annulation reactions proceed in good to excellent yields with vinamidinium salts containing electron-withdrawing groups at the beta-position (R(2)). The reaction was applied to the preparation of the COX-2 specific inhibitor 5-chloro-3-(4-methylsulfonyl)phenyl-2-(2-methyl-5-pyridinyl)pyridine (1), as well as a series of analogues.

摘要

α-芳基酮与六氟磷酸亚胺盐反应可得到相应的3-芳基吡啶。环化反应对于β位(R(2))含有吸电子基团的亚胺盐,产率良好至优异。该反应应用于COX-2特异性抑制剂5-氯-3-(4-甲磺酰基)苯基-2-(2-甲基-5-吡啶基)吡啶(1)以及一系列类似物的制备。

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