1,3,6-tri-O-benzoyl-2-deoxy-4-O-<(imidazol-1yl)thiocarbonyl>-β-D-arabino-hexopyranose

Base Information

Chemical Name:1,3,6-tri-O-benzoyl-2-deoxy-4-O-<(imidazol-1yl)thiocarbonyl>-β-D-arabino-hexopyranose
CAS No.:108274-13-1
Molecular Formula:C₃₁H₂₆N₂O₈S
Molecular Weight:586.622
Hs Code.:

Synonyms:1,3,6-tri-O-benzoyl-2-deoxy-4-O-<(imidazol-1yl)thiocarbonyl>-β-D-arabino-hexopyranose

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Chemical Property of 1,3,6-tri-O-benzoyl-2-deoxy-4-O-<(imidazol-1yl)thiocarbonyl>-β-D-arabino-hexopyranose

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Technology Process of 1,3,6-tri-O-benzoyl-2-deoxy-4-O-<(imidazol-1yl)thiocarbonyl>-β-D-arabino-hexopyranose

There total 1 articles about 1,3,6-tri-O-benzoyl-2-deoxy-4-O-<(imidazol-1yl)thiocarbonyl>-β-D-arabino-hexopyranose which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 97.0%

: 108274-11-9
1,3,6-tri-O-benzoyl-2-deoxy-β-D-arabino-hexopyranose

: 6160-65-2
1,1'-Thiocarbonyldiimidazole

: 108274-13-1
1,3,6-tri-O-benzoyl-2-deoxy-4-O-<(imidazol-1yl)thiocarbonyl>-β-D-arabino-hexopyranose

Guidance literature:: In 1,2-dimethoxyethane; for 7h; Heating;
DOI:10.1016/S0008-6215(00)90275-1

Reference yield: 76.0%

: 108274-13-1
1,3,6-tri-O-benzoyl-2-deoxy-4-O-<(imidazol-1yl)thiocarbonyl>-β-D-arabino-hexopyranose

: 108274-14-2
1,3,6-tri-O-benzoyl-2,4-dideoxy-β-D-threo-hexopyranose

Guidance literature:: With azobisisobutyronitrile; tri-n-butyl-tin hydride; In benzene; for 2h; Heating;
DOI:10.1016/S0008-6215(00)90275-1

Reference yield:

: 108274-13-1
1,3,6-tri-O-benzoyl-2-deoxy-4-O-<(imidazol-1yl)thiocarbonyl>-β-D-arabino-hexopyranose

: 108274-15-3,108274-17-5
3,6-di-O-benzoyl-2,4-dideoxy-D-threo-hexopyranose

Guidance literature:: Multi-step reaction with 2 steps

1: 76 percent / n-Bu3SnH, α,α'-azobisisobutyronitrile / benzene / 2 h / Heating

2: 74 percent / ammonia / tetrahydrofuran; methanol / 48 h / 0 °C

With azobisisobutyronitrile; ammonia; tri-n-butyl-tin hydride; In tetrahydrofuran; methanol; benzene;
DOI:10.1016/S0008-6215(00)90275-1