201547-00-4

Upstream product

• 201547-50-4 4-cyanophenyl 2,3,4,6-tetra-O-acetyl-1,5-dithio-β-D-glucopyranoside 
• 36801-01-1 4-cyanobenzenethiol 
• 84039-44-1 2,3,4,6-tetra-O-acetyl-5-thio-α-D-glucopyranosyl bromide 

Downstream Products

• 201547-50-4 4-cyanophenyl 2,3,4,6-tetra-O-acetyl-1,5-dithio-β-D-glucopyranoside 
• 201547-52-6 4-cyanophenyl 2,3,4-tri-O-acetyl-6-O-methanesulfonyl-1,5-dithio-β-D-glucopyranoside 

Relevant academic research and scientific papers

Synthesis of 4-cyanophenyl 1,5-dithio-β-D-glucopyranoside and its 6-deoxy, as well as 6-deoxy-5-ene derivatives as oral antitbrombotic agents

Condensation of 5-thio-D-glucopyranose pentaacetate with 4-cyanobenzenethiol, in the presence of trim ethylsilyl triflate, gave 4-cyanophenyl 2,3,4,6-tetra-O-acetyl-1,5-dithio-α-D-glucopyranoside 7 and 3,4,6-tri-O-acetyl-2,5-anhydro-5-thio-D-mannose bis(4-cyanophenyl) dithioacetal 9 in a 2:3 ratio. The latter is probably formed from the 4-cyanophenyl 2,3,4,6-tetra-O-acetyl-1,5-dithio-β-D-glucopyranoside 6 via a transannular participation of the ring sulfur atom. When 2,3,4,6-tetra-O-acetyl-5-thio-α-D-glucopyranosyl bromide was used as donor and the reaction was carried out in the presence of potassium carbonate, 6, 7, 4-cyano-2-(2,3,4,6-tetra-O-acetyl-5-thio-α-D-glucopyranosyl)phenyl and 4-cyano-2-(2,3,4,6-tetra-O-acetyl-5-thio-β-D-glucopyranosyl)phenyl 1,5-dithio-β-D-glucopyranoside (14 and 16) were formed in a 23:4:2:1 ratio. The mechanism of formation of 14 and 16 is discussed. Condensation of 2,3,4-tri-O-acetyl-6-deoxy-5-thio-α-D-glucopyranosyl bromide with 4-cyanobenzenethiol in the presence of potassium carbonate gave 4-cyanophenyl 2,3,4-tri-O-acetyl-6-deoxy-1,5-dithio-α- and β-D-glucopyranoside (29 and 30) as well as 4-cyano-2-(2,3,4-tri-O-acetyl-6-deoxy-5-thio-α-D-glucopyranosyl)phenyl 2,3,4-tri-O-acetyl-6-deoxy- 1,5-dithio-β-D-glucopyranoside in a ratio of ~ 1:8:1. Compound 30 could be obtained in a higher overall yield using 2 as starting material and converting it via its 4-cyanophenyl 2,3,3-tri-O-acetyl-6-O-methanesulfonyl-1,5-dithio-β-D-glucopyranoside derivative into the 4-cyanophenyl 2,3,4-tri-O-acetyl-6-deoxy-6-iodo-1,5-dithio-β-D-glucopyranoside 33 which gave 30 on reduction with sodium borohydride-nickel(II) chloride. Treatment of 33 with silver acetate gave 4-cyanophenyl 2,3,4-tri-O-acetyl-6-deoxy-1,5-dithio-β-D-xylo-hex-5-enopyranoside 35. The compounds obtained on deacetylation of 6, 9, 14, 30 and 35 showed a stronger oral antithrombotic effect in rats as compared to beciparcil, used as reference.