Thexyldimethylsilyl 4-C-(2,6-anhydro-4,5,7-tri-O-benzyl-3-deoxy-D-talo-hept-2-enit-1-yl)-2-acetamido-3,6-di-O-benzyl-2,4-dideoxy-β-D-glucopyranoside

Base Information

Chemical Name:Thexyldimethylsilyl 4-C-(2,6-anhydro-4,5,7-tri-O-benzyl-3-deoxy-D-talo-hept-2-enit-1-yl)-2-acetamido-3,6-di-O-benzyl-2,4-dideoxy-β-D-glucopyranoside
CAS No.:174175-64-5
Molecular Formula:C₅₈H₇₃NO₁₀Si
Molecular Weight:972.304
Hs Code.:

Thexyldimethylsilyl 4-C-(2,6-anhydro-4,5,7-tri-O-benzyl-3-deoxy-D-talo-hept-2-enit-1-yl)-2-acetamido-3,6-di-O-benzyl-2,4-dideoxy-β-D-glucopyranoside

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Chemical Property of Thexyldimethylsilyl 4-C-(2,6-anhydro-4,5,7-tri-O-benzyl-3-deoxy-D-talo-hept-2-enit-1-yl)-2-acetamido-3,6-di-O-benzyl-2,4-dideoxy-β-D-glucopyranoside

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Technology Process of Thexyldimethylsilyl 4-C-(2,6-anhydro-4,5,7-tri-O-benzyl-3-deoxy-D-talo-hept-2-enit-1-yl)-2-acetamido-3,6-di-O-benzyl-2,4-dideoxy-β-D-glucopyranoside

There total 21 articles about Thexyldimethylsilyl 4-C-(2,6-anhydro-4,5,7-tri-O-benzyl-3-deoxy-D-talo-hept-2-enit-1-yl)-2-acetamido-3,6-di-O-benzyl-2,4-dideoxy-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:

: 157488-88-5
thexyldimethylsilyl 2-azido-2-deoxy-β-D-glucopyranoside

: 174175-64-5
Thexyldimethylsilyl 4-C-(2,6-anhydro-4,5,7-tri-O-benzyl-3-deoxy-D-talo-hept-2-enit-1-yl)-2-acetamido-3,6-di-O-benzyl-2,4-dideoxy-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 11 steps

1: 95 percent / p-TsOH / acetonitrile / 1 h

2: 93 percent / NaH / dimethylformamide / 2 h / -15 °C

3: 86 percent / NaCNBH₃, HCl / diethyl ether; tetrahydrofuran

4: pyridine / CH₂Cl₂ / 0.5 h / Ambient temperature

5: acetonitrile / 1 h / 35 °C

6: 36 percent / 1 M DIBALH / toluene; CH₂Cl₂ / 1.) -70 deg C, 2 h, 2.) -70 deg C to r.t., 4 h

7: 64 percent / Et₃N / 18 h / 60 °C

8: 56 percent / LDA / tetrahydrofuran; hexane / 1.) THF, hexane, -100 deg C, 30 min, 2.) HMPA, THF, 1 h

9: Raney nickel W II / tetrahydrofuran / 7 h

10: pyridine / Ambient temperature

11: 1 M NaOMe / methanol / 2 h / Ambient temperature

With pyridine; hydrogenchloride; Raney nickel W II; sodium methylate; sodium hydride; diisobutylaluminium hydride; sodium cyanoborohydride; toluene-4-sulfonic acid; triethylamine; lithium diisopropyl amide; In tetrahydrofuran; methanol; diethyl ether; hexane; dichloromethane; N,N-dimethyl-formamide; toluene; acetonitrile;

Reference yield:

: 1125-88-8
benzaldehyde dimethyl acetal

: 174175-64-5
Thexyldimethylsilyl 4-C-(2,6-anhydro-4,5,7-tri-O-benzyl-3-deoxy-D-talo-hept-2-enit-1-yl)-2-acetamido-3,6-di-O-benzyl-2,4-dideoxy-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 11 steps

1: 95 percent / p-TsOH / acetonitrile / 1 h

2: 93 percent / NaH / dimethylformamide / 2 h / -15 °C

3: 86 percent / NaCNBH₃, HCl / diethyl ether; tetrahydrofuran

4: pyridine / CH₂Cl₂ / 0.5 h / Ambient temperature

5: acetonitrile / 1 h / 35 °C

6: 36 percent / 1 M DIBALH / toluene; CH₂Cl₂ / 1.) -70 deg C, 2 h, 2.) -70 deg C to r.t., 4 h

7: 64 percent / Et₃N / 18 h / 60 °C

8: 56 percent / LDA / tetrahydrofuran; hexane / 1.) THF, hexane, -100 deg C, 30 min, 2.) HMPA, THF, 1 h

9: Raney nickel W II / tetrahydrofuran / 7 h

10: pyridine / Ambient temperature

11: 1 M NaOMe / methanol / 2 h / Ambient temperature

With pyridine; hydrogenchloride; Raney nickel W II; sodium methylate; sodium hydride; diisobutylaluminium hydride; sodium cyanoborohydride; toluene-4-sulfonic acid; triethylamine; lithium diisopropyl amide; In tetrahydrofuran; methanol; diethyl ether; hexane; dichloromethane; N,N-dimethyl-formamide; toluene; acetonitrile;

Reference yield:

: Thexyldimethylsilyl 2-azido-4,6-O-benzylidene-2-deoxy-β-D-glucopyranoside

: 174175-64-5
Thexyldimethylsilyl 4-C-(2,6-anhydro-4,5,7-tri-O-benzyl-3-deoxy-D-talo-hept-2-enit-1-yl)-2-acetamido-3,6-di-O-benzyl-2,4-dideoxy-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 10 steps

1: 93 percent / NaH / dimethylformamide / 2 h / -15 °C

2: 86 percent / NaCNBH₃, HCl / diethyl ether; tetrahydrofuran

3: pyridine / CH₂Cl₂ / 0.5 h / Ambient temperature

4: acetonitrile / 1 h / 35 °C

5: 36 percent / 1 M DIBALH / toluene; CH₂Cl₂ / 1.) -70 deg C, 2 h, 2.) -70 deg C to r.t., 4 h

6: 64 percent / Et₃N / 18 h / 60 °C

7: 56 percent / LDA / tetrahydrofuran; hexane / 1.) THF, hexane, -100 deg C, 30 min, 2.) HMPA, THF, 1 h

8: Raney nickel W II / tetrahydrofuran / 7 h

9: pyridine / Ambient temperature

10: 1 M NaOMe / methanol / 2 h / Ambient temperature

With pyridine; hydrogenchloride; Raney nickel W II; sodium methylate; sodium hydride; diisobutylaluminium hydride; sodium cyanoborohydride; triethylamine; lithium diisopropyl amide; In tetrahydrofuran; methanol; diethyl ether; hexane; dichloromethane; N,N-dimethyl-formamide; toluene; acetonitrile;