phenyl 2-azido-2-deoxy-3,4-di-O-acetyl-6-O-triisopropylsilyl-1-thio-α/β-D-glucopyranoside

Base Information

Chemical Name:phenyl 2-azido-2-deoxy-3,4-di-O-acetyl-6-O-triisopropylsilyl-1-thio-α/β-D-glucopyranoside
CAS No.:1445797-14-7
Molecular Formula:C₂₅H₃₉N₃O₆SSi
Molecular Weight:537.753
Hs Code.:

Synonyms:phenyl 2-azido-2-deoxy-3,4-di-O-acetyl-6-O-triisopropylsilyl-1-thio-α/β-D-glucopyranoside

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Chemical Property of phenyl 2-azido-2-deoxy-3,4-di-O-acetyl-6-O-triisopropylsilyl-1-thio-α/β-D-glucopyranoside

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Technology Process of phenyl 2-azido-2-deoxy-3,4-di-O-acetyl-6-O-triisopropylsilyl-1-thio-α/β-D-glucopyranoside

There total 4 articles about phenyl 2-azido-2-deoxy-3,4-di-O-acetyl-6-O-triisopropylsilyl-1-thio-α/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: 97.0%

: C₂₁H₃₅N₃O₄SSi

: 108-24-7
acetic anhydride

: 1445797-14-7
phenyl 2-azido-2-deoxy-3,4-di-O-acetyl-6-O-triisopropylsilyl-1-thio-α/β-D-glucopyranoside

Guidance literature:: With pyridine;

Reference yield:

: 183875-22-1
phenyl 2-azido-2-deoxy-3,4,6-tri-O-acetyl-1-thio-α/β-D-glucopyranoside

: 1445797-14-7
phenyl 2-azido-2-deoxy-3,4-di-O-acetyl-6-O-triisopropylsilyl-1-thio-α/β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: sodium methylate / methanol / 1 h

2: 1H-imidazole / dichloromethane / 1 h / 20 °C

3: pyridine

With pyridine; 1H-imidazole; sodium methylate; In methanol; dichloromethane;

Reference yield:

: 171032-74-9
1,3,4,6-tetra-O-acetyl-2-azido-2-deoxy-D-glucopyranose

: 1445797-14-7
phenyl 2-azido-2-deoxy-3,4-di-O-acetyl-6-O-triisopropylsilyl-1-thio-α/β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 4 steps

1: boron trifluoride diethyl etherate / dichloromethane / 72 h / 20 °C / Cooling with ice

2: sodium methylate / methanol / 1 h

3: 1H-imidazole / dichloromethane / 1 h / 20 °C

4: pyridine

With pyridine; 1H-imidazole; boron trifluoride diethyl etherate; sodium methylate; In methanol; dichloromethane;