2-(N-benzyloxycarbonyl)-aminoethyl (2-azido-4,6-O-benzylidene-2-deoxy-β-D-mannopyranosyl-(1->4)-2,3,4-tri-O-benzyl-β-D-glucopyranoside

Base Information

Chemical Name:2-(N-benzyloxycarbonyl)-aminoethyl (2-azido-4,6-O-benzylidene-2-deoxy-β-D-mannopyranosyl-(1->4)-2,3,4-tri-O-benzyl-β-D-glucopyranoside
CAS No.:499126-48-6
Molecular Formula:C₅₀H₅₄N₄O₁₂
Molecular Weight:902.998
Hs Code.:

Synonyms:2-(N-benzyloxycarbonyl)-aminoethyl (2-azido-4,6-O-benzylidene-2-deoxy-β-D-mannopyranosyl-(1->4)-2,3,4-tri-O-benzyl-β-D-glucopyranoside

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Chemical Property of 2-(N-benzyloxycarbonyl)-aminoethyl (2-azido-4,6-O-benzylidene-2-deoxy-β-D-mannopyranosyl-(1->4)-2,3,4-tri-O-benzyl-β-D-glucopyranoside

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Technology Process of 2-(N-benzyloxycarbonyl)-aminoethyl (2-azido-4,6-O-benzylidene-2-deoxy-β-D-mannopyranosyl-(1->4)-2,3,4-tri-O-benzyl-β-D-glucopyranoside

There total 14 articles about 2-(N-benzyloxycarbonyl)-aminoethyl (2-azido-4,6-O-benzylidene-2-deoxy-β-D-mannopyranosyl-(1->4)-2,3,4-tri-O-benzyl-β-D-glucopyranoside 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: 82.0%

: 499126-47-5
2-(N-benzyloxycarbonyl)-aminoethyl (3-O-allyl-2-azido-4,6-O-benzylidene-2-deoxy-β-D-mannopyranosyl-(1->4)-2,3,4-tri-O-benzyl-β-D-glucopyranoside

: 499126-48-6
2-(N-benzyloxycarbonyl)-aminoethyl (2-azido-4,6-O-benzylidene-2-deoxy-β-D-mannopyranosyl-(1->4)-2,3,4-tri-O-benzyl-β-D-glucopyranoside

Guidance literature:: 2-(N-benzyloxycarbonyl)-aminoethyl (3-O-allyl-2-azido-4,6-O-benzylidene-2-deoxy-β-D-mannopyranosyl-(1->4)-2,3,4-tri-O-benzyl-β-D-glucopyranoside; With hydrogen; palladium on activated charcoal; (1,5-cyclooctadiene)bis(methyldiphenylphosphine) iridium hexafluorophosphate; In tetrahydrofuran; for 20h;

With N-iodo-succinimide; water; for 0.5h;
DOI:10.1016/S0008-6215(02)00263-X

Reference yield:

: 1125-88-8
benzaldehyde dimethyl acetal

: 499126-48-6
2-(N-benzyloxycarbonyl)-aminoethyl (2-azido-4,6-O-benzylidene-2-deoxy-β-D-mannopyranosyl-(1->4)-2,3,4-tri-O-benzyl-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 10 steps

1.1: 70 percent / p-TsOH / dimethylformamide / 24 h / 50 °C

2.1: 79 percent / NaH / dimethylformamide / 20 °C

3.1: PPh₃ / CH₂Cl₂ / 20 °C

3.2: water / 20 h / Heating

4.1: 80 percent / pyridine / 1.5 h / 0 °C

5.1: 99 percent / NaCNBH₃; HCl / tetrahydrofuran; diethyl ether / 4.5 h / 20 °C

6.1: 84 percent / NIS; TfOH / CH₂Cl₂ / 1 h / -30 °C

7.1: NaOMe / methanol; CH₂Cl₂ / 3 h / 20 °C / pH 12

8.1: pyridine / CH₂Cl₂ / 20 h / 0 °C

9.1: 0.85 g / NaN₃ / dimethylformamide / 3 h / 70 °C

10.1: H₂ / Pd/C; [bis(methyldiphenylphosphine)](1,5-cyclooctadiene)Ir(I)PF₆ / tetrahydrofuran / 20 h

10.2: 82 percent / NIS; water / 0.5 h

With pyridine; hydrogenchloride; N-iodo-succinimide; sodium azide; trifluorormethanesulfonic acid; hydrogen; sodium methylate; sodium hydride; sodium cyanoborohydride; toluene-4-sulfonic acid; triphenylphosphine; palladium on activated charcoal; (1,5-cyclooctadiene)bis(methyldiphenylphosphine) iridium hexafluorophosphate; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/S0008-6215(02)00263-X

Reference yield:

: 20701-61-5,56119-28-9,131564-36-8,142924-31-0,151123-92-1,141899-53-8
ethyl 4,6-O-benzylidene-1-thio-β-D-glucopyranoside

: 499126-48-6
2-(N-benzyloxycarbonyl)-aminoethyl (2-azido-4,6-O-benzylidene-2-deoxy-β-D-mannopyranosyl-(1->4)-2,3,4-tri-O-benzyl-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 7 steps

1.1: Bu₂SnO / methanol / 1 h / Heating

1.2: 67 percent / CsF / dimethylformamide / 20 °C

2.1: 97 percent / pyridine / 1 h / 20 °C

3.1: 84 percent / NIS; TfOH / CH₂Cl₂ / 1 h / -30 °C

4.1: NaOMe / methanol; CH₂Cl₂ / 3 h / 20 °C / pH 12

5.1: pyridine / CH₂Cl₂ / 20 h / 0 °C

6.1: 0.85 g / NaN₃ / dimethylformamide / 3 h / 70 °C

7.1: H₂ / Pd/C; [bis(methyldiphenylphosphine)](1,5-cyclooctadiene)Ir(I)PF₆ / tetrahydrofuran / 20 h

7.2: 82 percent / NIS; water / 0.5 h

With pyridine; N-iodo-succinimide; sodium azide; trifluorormethanesulfonic acid; hydrogen; sodium methylate; di(n-butyl)tin oxide; palladium on activated charcoal; (1,5-cyclooctadiene)bis(methyldiphenylphosphine) iridium hexafluorophosphate; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/S0008-6215(02)00263-X