methyl (5-benzyloxyacetamido-7,8,9-tri-O-acetyl-5-N,4-O-carbonyl-2-thioadamantyl-3,5-dideoxy-D-glycero-β-D-galactonon-2-ulopyranoside)onate

Base Information

Chemical Name:methyl (5-benzyloxyacetamido-7,8,9-tri-O-acetyl-5-N,4-O-carbonyl-2-thioadamantyl-3,5-dideoxy-D-glycero-β-D-galactonon-2-ulopyranoside)onate
CAS No.:1453169-33-9
Molecular Formula:C₃₆H₄₅NO₁₃S
Molecular Weight:731.818
Hs Code.:

Synonyms:methyl (5-benzyloxyacetamido-7,8,9-tri-O-acetyl-5-N,4-O-carbonyl-2-thioadamantyl-3,5-dideoxy-D-glycero-β-D-galactonon-2-ulopyranoside)onate

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Chemical Property of methyl (5-benzyloxyacetamido-7,8,9-tri-O-acetyl-5-N,4-O-carbonyl-2-thioadamantyl-3,5-dideoxy-D-glycero-β-D-galactonon-2-ulopyranoside)onate

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Technology Process of methyl (5-benzyloxyacetamido-7,8,9-tri-O-acetyl-5-N,4-O-carbonyl-2-thioadamantyl-3,5-dideoxy-D-glycero-β-D-galactonon-2-ulopyranoside)onate

There total 1 articles about methyl (5-benzyloxyacetamido-7,8,9-tri-O-acetyl-5-N,4-O-carbonyl-2-thioadamantyl-3,5-dideoxy-D-glycero-β-D-galactonon-2-ulopyranoside)onate 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: 85.0%

: methyl (7,8,9-tri-O-acetyl-5-N,4-O-carbonyl-2-thioadamantyl-3,5-dideoxy-D-glycero-β-D-galactonon-2-ulopyranoside)onate

: 19810-31-2
Benzyloxyacetyl chloride

: 1453169-33-9
methyl (5-benzyloxyacetamido-7,8,9-tri-O-acetyl-5-N,4-O-carbonyl-2-thioadamantyl-3,5-dideoxy-D-glycero-β-D-galactonon-2-ulopyranoside)onate

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 0 - 20 ℃; for 16h; Inert atmosphere;
DOI:10.1002/ejoc.201300664

Reference yield: 76.0%

: 1453169-33-9
methyl (5-benzyloxyacetamido-7,8,9-tri-O-acetyl-5-N,4-O-carbonyl-2-thioadamantyl-3,5-dideoxy-D-glycero-β-D-galactonon-2-ulopyranoside)onate

: 4064-06-6
1,2:3,4-di-O-isopropylidene-α-D-galactopyranose

: 1453169-37-3
methyl (5-benzyloxyacetamido-7,8,9-tri-O-acetyl-5-N,4-O-carbonyl-3,5-dideoxy-D-glycero-α-D-galacto-non-2-ulopyranosyl)onate-(2→6)-1,2-3,4-diisopropyl-α-D-galactopyranoside

Guidance literature:: With N-iodo-succinimide; trifluorormethanesulfonic acid; In dichloromethane; acetonitrile; at -78 ℃; for 0.333333h; diastereoselective reaction; Inert atmosphere; Molecular sieve;
DOI:10.1002/ejoc.201300664

Reference yield: 73.0%

: 1453169-33-9
methyl (5-benzyloxyacetamido-7,8,9-tri-O-acetyl-5-N,4-O-carbonyl-2-thioadamantyl-3,5-dideoxy-D-glycero-β-D-galactonon-2-ulopyranoside)onate

: 1453169-36-2
N-benzyloxycarbonyl-5-aminopentyl 3,4-di-O-acetyl-2-deoxy-(2,2,2-trichloroethyloxycarbonyl)-amino-β-D-glucosamine

: 1453169-40-8
methyl (5-benzyloxyacetamido-7,8,9-tri-O-acetyl-5-N,4-O-carbonyl-3,5-dideoxy-D-glycero-α-D-galacto-non-2-ulopyranosyl)onate-(2→6)-N-benzyloxycarbonyl-5-aminopentyl 3,4-di-O-acetyl-6-O-tert-butyldimethylsilyl-2-deoxy-(2,2,2-trichloroethyloxycarbonyl)amino-β-D-glucosamine

Guidance literature:: With N-iodo-succinimide; trifluorormethanesulfonic acid; In dichloromethane; acetonitrile; at -78 ℃; for 0.333333h; diastereoselective reaction; Inert atmosphere; Molecular sieve;
DOI:10.1002/ejoc.201300664