phenyl 3-O-acetyl-2-azido-4-O-benzyl-6-O-tert-butyl-diphenylsilyl-2-deoxy-1-thio-α-D-galactopyranoside

Base Information

Chemical Name:phenyl 3-O-acetyl-2-azido-4-O-benzyl-6-O-tert-butyl-diphenylsilyl-2-deoxy-1-thio-α-D-galactopyranoside
CAS No.:1356031-07-6
Molecular Formula:C₃₇H₄₁N₃O₅SSi
Molecular Weight:667.901
Hs Code.:

Synonyms:phenyl 3-O-acetyl-2-azido-4-O-benzyl-6-O-tert-butyl-diphenylsilyl-2-deoxy-1-thio-α-D-galactopyranoside

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Chemical Property of phenyl 3-O-acetyl-2-azido-4-O-benzyl-6-O-tert-butyl-diphenylsilyl-2-deoxy-1-thio-α-D-galactopyranoside

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Technology Process of phenyl 3-O-acetyl-2-azido-4-O-benzyl-6-O-tert-butyl-diphenylsilyl-2-deoxy-1-thio-α-D-galactopyranoside

There total 5 articles about phenyl 3-O-acetyl-2-azido-4-O-benzyl-6-O-tert-butyl-diphenylsilyl-2-deoxy-1-thio-α-D-galactopyranoside 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: 92.0%

: 1356031-06-5
phenyl 3-O-acetyl-2-azido-4-O-benzyl-2-deoxy-1-thio-α-D-galactopyranoside

: 58479-61-1
tert-butylchlorodiphenylsilane

: 1356031-07-6
phenyl 3-O-acetyl-2-azido-4-O-benzyl-6-O-tert-butyl-diphenylsilyl-2-deoxy-1-thio-α-D-galactopyranoside

Guidance literature:: With 1H-imidazole; In dichloromethane; at 20 ℃; for 1h;
DOI:10.1016/j.tet.2011.11.088

Reference yield:

: 1260181-56-3
phenyl 3-O-acetyl-2-azido-4,6-O-benzylidene-2-deoxy-1-thio-α-D-galactopyranoside

: 1356031-07-6
phenyl 3-O-acetyl-2-azido-4-O-benzyl-6-O-tert-butyl-diphenylsilyl-2-deoxy-1-thio-α-D-galactopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: borane-THF; di-n-butylboryl trifluoromethanesulfonate / tetrahydrofuran; dichloromethane / 1 h / 0 °C

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

With 1H-imidazole; borane-THF; di-n-butylboryl trifluoromethanesulfonate; In tetrahydrofuran; dichloromethane;
DOI:10.1016/j.tet.2011.11.088

Reference yield:

: 197663-12-0
phenyl 3,4,6-tri-O-acetyl-2-azido-2-deoxy-1-thiol-D-galactopyranoside

: 1356031-07-6
phenyl 3-O-acetyl-2-azido-4-O-benzyl-6-O-tert-butyl-diphenylsilyl-2-deoxy-1-thio-α-D-galactopyranoside

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium methylate / methanol / 1 h

1.2: IR₁₂₀ H⁺

2.1: toluene-4-sulfonic acid / N,N-dimethyl-formamide / 40 °C

3.1: pyridine / 2 h

4.1: borane-THF; di-n-butylboryl trifluoromethanesulfonate / tetrahydrofuran; dichloromethane / 1 h / 0 °C

5.1: 1H-imidazole / dichloromethane / 1 h / 20 °C

With pyridine; 1H-imidazole; borane-THF; di-n-butylboryl trifluoromethanesulfonate; sodium methylate; toluene-4-sulfonic acid; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.tet.2011.11.088