1429012-29-2Relevant academic research and scientific papers
Discovery of thienopyrimidine-based inhibitors of the human farnesyl pyrophosphate synthase - Parallel synthesis of analogs via a trimethylsilyl ylidene intermediate
Leung, Chun-Yuen,Langille, Adrienne M.,Mancuso, John,Tsantrizos, Youla S.
, p. 2229 - 2240 (2013/05/22)
Thienopyrimidine-based bisphosphonates were identified as a new class of nitrogen-containing bisphosphonate (N-BP) inhibitors of the human farnesyl pyrophosphate synthase (hFPPS). Analogs were prepared via cyclization of 2-(1-(trimethylsilyl)ethylidene)malononitrile to 2-amino-4-(trimethylsilyl) thiophene-3-carbonitrile in the presence of elemental sulfur. Direct ipso-iododesilylation of this intermediate led to selective iodination at C β of the sulfur atom in high efficiency. The synthetic protocols developed were used in the parallel synthesis of structurally diverse thieno[2,3-d]pyrimidin-4-amine-based bisphosphonate inhibitors of hFPPS.
