Development of a concise scaleable synthesis of 2-chloro-5-(pyridin-2-yl) pyrimidine via a Negishi cross-coupling

C Pérez-Balado, A Willemsens…

Index: Perez-Balado, Carlos; Willemsens, Albert; Ormerod, Dominic; Aelterman, Wim; Mertens, Narda Organic Process Research and Development, 2007 , vol. 11, # 2 p. 237 - 240

Full Text: HTML

Citation Number: 24

Abstract

A practical and scaleable synthesis of 2-chloro-5-(pyridin-2-yl) pyrimidine, an intermediate in the synthesis of a selective PDE-V inhibitor, was developed. A Negishi cross-coupling between the in situ prepared 2-pyridylzinc chloride and 5-iodo-2-chloropyrimidine catalyzed by Pd (PPh3) 4 afforded the product in one step. Development of a convenient purification did away with the necessity of chromatography, allowing the preparation of the product on ...

Related Articles:

Convenient One??Pot Synthesis of Sulfonamides from Thiols using Trichloroisocyanuric Acid

[Bonk, Jason D.; Amos, David T.; Olson, Sarah J. Synthetic Communications, 2007 , vol. 37, # 12 p. 2039 - 2050]

The synthesis of substituted pyridylpyrimidine fungicides using palladium-catalysed cross-coupling reactions

[Hargreaves, Stephanie L.; Pilkington, Brian L.; Russell, Sally E.; Worthington, Paul A. Tetrahedron Letters, 2000 , vol. 41, # 10 p. 1653 - 1656]

Trialkylalanes in Palladium-Catalyzed C-Alkylations of

[Acta Chemica Scandinavica, , vol. 51, # 3 p. 302 - 306]

Trialkylalanes in Palladium-Catalyzed C-Alkylations of

[Acta Chemica Scandinavica, , vol. 51, # 3 p. 302 - 306]

More Articles...