4-methoxyphenyl 3-O-acetyl-6-azido-2,4-diacetamido-2,4,6-trideoxy-β-D-mannopyranoside

Base Information

Chemical Name:4-methoxyphenyl 3-O-acetyl-6-azido-2,4-diacetamido-2,4,6-trideoxy-β-D-mannopyranoside
CAS No.:1593082-63-3
Molecular Formula:C₁₉H₂₅N₅O₇
Molecular Weight:435.437
Hs Code.:

Synonyms:4-methoxyphenyl 3-O-acetyl-6-azido-2,4-diacetamido-2,4,6-trideoxy-β-D-mannopyranoside

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Chemical Property of 4-methoxyphenyl 3-O-acetyl-6-azido-2,4-diacetamido-2,4,6-trideoxy-β-D-mannopyranoside

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Technology Process of 4-methoxyphenyl 3-O-acetyl-6-azido-2,4-diacetamido-2,4,6-trideoxy-β-D-mannopyranoside

There total 11 articles about 4-methoxyphenyl 3-O-acetyl-6-azido-2,4-diacetamido-2,4,6-trideoxy-β-D-mannopyranoside 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: 90.0%

: 1593082-55-3
4-methoxyphenyl 6-azido-2,4-diacetamido-2,4,6-trideoxy-β-D-mannopyranoside

: 108-24-7
acetic anhydride

: 1593082-63-3
4-methoxyphenyl 3-O-acetyl-6-azido-2,4-diacetamido-2,4,6-trideoxy-β-D-mannopyranoside

Guidance literature:: With pyridine; In dichloromethane; at 20 ℃; for 5h;
DOI:10.1002/anie.201309072

Reference yield:

: 1593082-59-7
C₂₉H₂₄F₆O₁₃S₂

: 1593082-63-3
4-methoxyphenyl 3-O-acetyl-6-azido-2,4-diacetamido-2,4,6-trideoxy-β-D-mannopyranoside

Guidance literature:: Multi-step reaction with 7 steps

1: tetrabutylammoniun azide / toluene / 3 h / 65 - 100 °C

2: sodium methylate / methanol / 1 h / 20 °C

3: hydrogen; 10 wt% Pd(OH)2 on carbon / methanol / 1.5 h / 30 °C

4: methanol / 1 h / 20 °C

5: pyridine / dichloromethane / 0.5 h / 0 °C

6: sodium azide / N,N-dimethyl-formamide / 15 h / 80 °C

7: pyridine / dichloromethane / 5 h / 20 °C

With pyridine; sodium azide; 10 wt% Pd(OH)2 on carbon; hydrogen; sodium methylate; tetrabutylammoniun azide; In methanol; dichloromethane; N,N-dimethyl-formamide; toluene;
DOI:10.1002/anie.201309072

Reference yield:

: 3150-20-7,6032-32-2,28541-75-5,85481-53-4,89731-58-8,109121-56-4,121468-39-1,12167-34-9
4-methoxyphenyl β-D-galactopyranoside

: 1593082-63-3
4-methoxyphenyl 3-O-acetyl-6-azido-2,4-diacetamido-2,4,6-trideoxy-β-D-mannopyranoside

Guidance literature:: Multi-step reaction with 9 steps

1: 2-Aminoethoxydiphenylborane; N-ethyl-N,N-diisopropylamine / acetonitrile / 1 h / 20 °C

2: pyridine / dichloromethane / 1.5 h / 0 °C

3: tetrabutylammoniun azide / toluene / 3 h / 65 - 100 °C

4: sodium methylate / methanol / 1 h / 20 °C

5: hydrogen; 10 wt% Pd(OH)2 on carbon / methanol / 1.5 h / 30 °C

6: methanol / 1 h / 20 °C

7: pyridine / dichloromethane / 0.5 h / 0 °C

8: sodium azide / N,N-dimethyl-formamide / 15 h / 80 °C

9: pyridine / dichloromethane / 5 h / 20 °C

With pyridine; sodium azide; 10 wt% Pd(OH)2 on carbon; 2-Aminoethoxydiphenylborane; hydrogen; sodium methylate; tetrabutylammoniun azide; N-ethyl-N,N-diisopropylamine; In methanol; dichloromethane; N,N-dimethyl-formamide; toluene; acetonitrile;
DOI:10.1002/anie.201309072