145575-50-4Relevant academic research and scientific papers
Synthesis of C-Glycosyltetrazoles Related to 3-Deoxy-D-arabino-heptulosonic Acid 7-Phosphate (DHAP); Potential Inhibitors of Early Steps in the Shikimate Pathway
Buchanan, J. Grant,Clelland, Andrew P. W.,Johnson, Trevor,Rennie, Robert A. C.,Wightman, Richard H.
, p. 2593 - 2602 (2007/10/02)
Treatment of 3,4,5,7-tetra-O-acetyl-2,6-anhydro-D-glycero-D-galacto-heptononitrile 16 with diazabicycloundecene (DBU) formed 4,5,7-tri-O-acetyl-2,6-anhydro-3-deoxy-D-arabino-hept-2-enononitrile 22, which on treatment with ammonium azide gave the corresponding unsaturated tetrazole 23.Stereoselective catalytic reduction of 23 and subsequent deacetylation produced 5-(2-deoxy-β-D-arabino-hexopyranosyl)tetrazole 24, which was converted in two steps into its 6-phosphate 10.Reaction of 4,5,7-tri-O-acetyl-2,6-anhydro-3-deoxy-D-manno-heptononitrile 27 with ammonium azide, followed by deacetylation, gave 5-(2-deoxy-α-D-arabino-hexopyranosyl)tetrazole 29 (81percent overall), which was converted into its 6-phosphate 11.When 4,5,7-tri-O-acetyl-2,6-anhydro-2-bromo-3-deoxy-D-gluco-heptononitrile 31 was treated with methanol and 2,6-lutidine, methyl 3,4,6-tri-O-acetyl-1-cyano-2-deoxy-β-D-arabino-hexopyranoside 34 was obtained (40percent) together with the α-anomer 35 (11percent).Cycloaddition of 34 with azide ion, followed by sequential treatment with base and with acid, gave 2-deoxy-1-tetrazol-5-yl-α-D-arabino-hexopyranose 12 (54percent overall).Treatment of 1,3,4,6-tetra-O-acetyl-2-deoxy-α-D-lyxo-hexopyranose 38 with trimethylsilyl cyanide and boron trifluoride in nitromethane gave 4,5,7-tri-O-acetyl-2,6-anhydro-3-deoxy-D-talo-heptononitrile 40 (53percent), together with the D-galacto-epimer 39 (17percent).Cycloaddition of 39 and 40 with azide ion and subsequent deprotection gave 5-(2-deoxy-β-D-lyxo-hexopyranosyl)tetrazole 13 and the α-D-lyxo-isomer 14 respectively in good yields.Reaction of nitrile 40 with N-bromosuccinimide formed 4,5,7-tri-O-acetyl-2,6-anhydro-2-bromo-3-deoxy-D-galacto-heptononitrile 43 (63percent), which with methanol and 2,6-lutidine was converted into the methyl β-D-glycoside 44.Cycloaddition of 44 with azide ion, deacetylation, and hydrolysis led to 2-deoxy-1-tetrazol-5-yl-α-D-lyxo-hexopyranose 15.None of the C-glycosyltetrazoles were strong inhibitors of dehydroquinate synthase from E.coli.
