methyl 3-O-(2,4-di-O-benzyl-3-O-[2,3,4-tri-O-benzyl-α-L-mannopyranosyl]-α-L-rhamnopyranosyl)-4,6-O-benzylidene-2-deoxy-2-(N-α-fluorenylmethoxycarbonyl-glycinyl)-amido-β-D-glucopyranoside

Base Information

Chemical Name:methyl 3-O-(2,4-di-O-benzyl-3-O-[2,3,4-tri-O-benzyl-α-L-mannopyranosyl]-α-L-rhamnopyranosyl)-4,6-O-benzylidene-2-deoxy-2-(N-α-fluorenylmethoxycarbonyl-glycinyl)-amido-β-D-glucopyranoside
CAS No.:864874-18-0
Molecular Formula:C₇₈H₈₂N₂O₁₇
Molecular Weight:1319.51
Hs Code.:

methyl 3-O-(2,4-di-O-benzyl-3-O-[2,3,4-tri-O-benzyl-α-L-mannopyranosyl]-α-L-rhamnopyranosyl)-4,6-O-benzylidene-2-deoxy-2-(N-α-fluorenylmethoxycarbonyl-glycinyl)-amido-β-D-glucopyranoside

Synonyms:methyl 3-O-(2,4-di-O-benzyl-3-O-[2,3,4-tri-O-benzyl-α-L-mannopyranosyl]-α-L-rhamnopyranosyl)-4,6-O-benzylidene-2-deoxy-2-(N-α-fluorenylmethoxycarbonyl-glycinyl)-amido-β-D-glucopyranoside

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Chemical Property of methyl 3-O-(2,4-di-O-benzyl-3-O-[2,3,4-tri-O-benzyl-α-L-mannopyranosyl]-α-L-rhamnopyranosyl)-4,6-O-benzylidene-2-deoxy-2-(N-α-fluorenylmethoxycarbonyl-glycinyl)-amido-β-D-glucopyranoside

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Technology Process of methyl 3-O-(2,4-di-O-benzyl-3-O-[2,3,4-tri-O-benzyl-α-L-mannopyranosyl]-α-L-rhamnopyranosyl)-4,6-O-benzylidene-2-deoxy-2-(N-α-fluorenylmethoxycarbonyl-glycinyl)-amido-β-D-glucopyranoside

There total 1 articles about methyl 3-O-(2,4-di-O-benzyl-3-O-[2,3,4-tri-O-benzyl-α-L-mannopyranosyl]-α-L-rhamnopyranosyl)-4,6-O-benzylidene-2-deoxy-2-(N-α-fluorenylmethoxycarbonyl-glycinyl)-amido-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:

: 864874-16-8
methyl 2-amino-3-O-(2,4-di-O-benzyl-3-O-[2,3,4-tri-O-benzyl-6-O-tert-butyl-diphenylsilyl-α-L-mannopyranosyl]-α-L-rhamnopyranosyl)-4,6-O-benzylidene-2-deoxy-β-D-glucopyranoside

: 864874-18-0
methyl 3-O-(2,4-di-O-benzyl-3-O-[2,3,4-tri-O-benzyl-α-L-mannopyranosyl]-α-L-rhamnopyranosyl)-4,6-O-benzylidene-2-deoxy-2-(N-α-fluorenylmethoxycarbonyl-glycinyl)-amido-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 86 percent / TBAF / tetrahydrofuran / 15 h / 60 °C

2: 86 percent / TBTU; HOBt; N-ethylmorpholine / dimethylformamide / 18 h / 20 °C

With N-ethylmorpholine;; tetrabutyl ammonium fluoride; benzotriazol-1-ol; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1039/b416105j

Reference yield: 43.0%

: 864874-18-0
methyl 3-O-(2,4-di-O-benzyl-3-O-[2,3,4-tri-O-benzyl-α-L-mannopyranosyl]-α-L-rhamnopyranosyl)-4,6-O-benzylidene-2-deoxy-2-(N-α-fluorenylmethoxycarbonyl-glycinyl)-amido-β-D-glucopyranoside

: 864874-20-4
methyl 3-O-(2,4-di-O-benzyl-3-O-[2,3,4-tri-O-benzyl-α-L-mannopyranosyluronic acid]-α-L-rhamnopyranosyl)-4,6-O-benzylidene-2-deoxy-2-(N-α-fluorenylmethoxycarbonyl-glycinyl)-amido-β-D-glucopyranoside

Guidance literature:: With 2,2,6,6-tetramethyl-piperidine-N-oxyl; tetrabutyl-ammonium chloride; potassium bromide; sodium hypochlorite; sodium chloride; In dichloromethane; sodium hydrogencarbonate;
DOI:10.1039/b416105j

Reference yield:

: 864874-18-0
methyl 3-O-(2,4-di-O-benzyl-3-O-[2,3,4-tri-O-benzyl-α-L-mannopyranosyl]-α-L-rhamnopyranosyl)-4,6-O-benzylidene-2-deoxy-2-(N-α-fluorenylmethoxycarbonyl-glycinyl)-amido-β-D-glucopyranoside

: 864874-22-6
methyl 2-(2-aminoacetamido)-3-O-(2,4-di-O-benzyl-3-O-[2,3,4-tri-O-benzyl-α-L-mannopyranosyluronic acid]-α-L-rhamnopyranosyl)-4,6-O-benzylidene-2-deoxy-β-D-glucopyranoside lactam

Guidance literature:: Multi-step reaction with 3 steps

1: 43 percent / TEMPO; KBr; Bu₄NCl / NaOCl; NaCl / CH₂Cl₂; aq. NaHCO₃

2: piperidine / dimethylformamide / 1 h / 20 °C

3: 19 mg / TBTU; HOBt; N-ethylmorpholine / dimethylformamide / 24 h / 20 °C

With piperidine; N-ethylmorpholine;; 2,2,6,6-tetramethyl-piperidine-N-oxyl; tetrabutyl-ammonium chloride; benzotriazol-1-ol; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; potassium bromide; sodium hypochlorite; sodium chloride; In dichloromethane; sodium hydrogencarbonate; N,N-dimethyl-formamide;
DOI:10.1039/b416105j