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methyl 2-azido-4,6-O-benzylidene-2-deoxy-3-O-(2-naphthylmethyl)-β-D-galactopyranosyl-(1→4)-2,3-O-isopropylidene-1-α-L-rhamnopyranoside

Base Information
  • Chemical Name:methyl 2-azido-4,6-O-benzylidene-2-deoxy-3-O-(2-naphthylmethyl)-β-D-galactopyranosyl-(1→4)-2,3-O-isopropylidene-1-α-L-rhamnopyranoside
  • CAS No.:1380218-22-3
  • Molecular Formula:C34H39N3O9
  • Molecular Weight:633.698
  • Hs Code.:
methyl 2-azido-4,6-O-benzylidene-2-deoxy-3-O-(2-naphthylmethyl)-β-D-galactopyranosyl-(1→4)-2,3-O-isopropylidene-1-α-L-rhamnopyranoside

Synonyms:methyl 2-azido-4,6-O-benzylidene-2-deoxy-3-O-(2-naphthylmethyl)-β-D-galactopyranosyl-(1→4)-2,3-O-isopropylidene-1-α-L-rhamnopyranoside

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Chemical Property of methyl 2-azido-4,6-O-benzylidene-2-deoxy-3-O-(2-naphthylmethyl)-β-D-galactopyranosyl-(1→4)-2,3-O-isopropylidene-1-α-L-rhamnopyranoside
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Technology Process of methyl 2-azido-4,6-O-benzylidene-2-deoxy-3-O-(2-naphthylmethyl)-β-D-galactopyranosyl-(1→4)-2,3-O-isopropylidene-1-α-L-rhamnopyranoside

There total 5 articles about methyl 2-azido-4,6-O-benzylidene-2-deoxy-3-O-(2-naphthylmethyl)-β-D-galactopyranosyl-(1→4)-2,3-O-isopropylidene-1-α-L-rhamnopyranoside 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:
Guidance literature:
With N-iodo-succinimide; trimethylsilyl trifluoromethanesulfonate; In dichloromethane; acetonitrile; propiononitrile; at -70 - -60 ℃; optical yield given as %de; diastereoselective reaction; Molecular sieve; Inert atmosphere;
DOI:10.1002/ejoc.201200173
Guidance literature:
Multi-step reaction with 3 steps
1: toluene-4-sulfonic acid / acetonitrile / 0.5 h / 20 °C
2: sodium hydride / N,N-dimethyl-formamide; mineral oil / 1 h / 0 - 20 °C
3: N-iodo-succinimide; trimethylsilyl trifluoromethanesulfonate / dichloromethane; acetonitrile; propiononitrile / -70 - -60 °C / Molecular sieve; Inert atmosphere
With N-iodo-succinimide; trimethylsilyl trifluoromethanesulfonate; sodium hydride; toluene-4-sulfonic acid; In dichloromethane; N,N-dimethyl-formamide; acetonitrile; propiononitrile; mineral oil;
DOI:10.1002/ejoc.201200173
Guidance literature:
Multi-step reaction with 5 steps
1: boron trifluoride diethyl etherate / dichloromethane / 0.92 h / 20 °C / Sonication
2: methanol; sodium / dichloromethane / 1 h / 20 °C
3: toluene-4-sulfonic acid / acetonitrile / 0.5 h / 20 °C
4: sodium hydride / N,N-dimethyl-formamide; mineral oil / 1 h / 0 - 20 °C
5: N-iodo-succinimide; trimethylsilyl trifluoromethanesulfonate / dichloromethane; acetonitrile; propiononitrile / -70 - -60 °C / Molecular sieve; Inert atmosphere
With methanol; N-iodo-succinimide; trimethylsilyl trifluoromethanesulfonate; boron trifluoride diethyl etherate; sodium; sodium hydride; toluene-4-sulfonic acid; In dichloromethane; N,N-dimethyl-formamide; acetonitrile; propiononitrile; mineral oil;
DOI:10.1002/ejoc.201200173
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