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Solid-phase synthesis of libraries generated from a 4-phenyl-2-carboxy-piperazine Scaffold

Nilsson, Jonas W. (author)
Linköpings universitet,Organisk Kemi,Tekniska högskolan
Thorstensson, Fredrik (author)
Linköpings universitet,Organisk Kemi,Tekniska högskolan
Kvarnström, Ingemar (author)
Linköpings universitet,Organisk Kemi,Tekniska högskolan
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Oprea, Tudor (author)
Department of Organic Chemistry, Arrhenius Laboratory, Stockholm University, Stockholm, Sweden
Samuelsson, Bertil (author)
Department of Organic Chemistry, Arrhenius Laboratory, Stockholm University, Stockholm, Sweden
Nilsson, Ingemar (author)
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 (creator_code:org_t)
2001-09-06
2001
English.
In: Journal of Combinatorial Chemistry. - : American Chemical Society (ACS). - 2156-8952 .- 1520-4766 .- 1520-4774. ; 3:6, s. 546-553
  • Journal article (peer-reviewed)
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  • Strategies for finding novel structures of therapeutical interest are discussed. The rationale for the selection of the two scaffolds N4-(m-aminophenyl)-piperazine-2-carboxylic acid E and N4-(o-aminophenyl)-piperazine-2-carboxylic F is described. The synthesis of the appropriate precursors to scaffold E and F and their use in solid-phase chemistry are described. A 160-member library was produced combining these novel piperazine scaffolds with eight sulfonyl chlorides/acid chlorides and 10 amines. The compound library prepared was analyzed using LC-MS, showing the expected base peak in all wells at an average purity of 82%.

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