1L-N¹-benzyloxycarbonyl-O⁶-(2-benzyloxycarbonylamino-O⁴,O⁶-cyclohexane-1,1-diyl-α-D-ribo-2,3-dideoxy-hexopyranosyl)-N³,O⁴-carbonyl-2-deoxy-streptamine

Base Information

• Chemical Name: 1L-N¹-benzyloxycarbonyl-O⁶-(2-benzyloxycarbonylamino-O⁴,O⁶-cyclohexane-1,1-diyl-α-D-ribo-2,3-dideoxy-hexopyranosyl)-N³,O⁴-carbonyl-2-deoxy-streptamine
• CAS No.: 63604-34-2
• Molecular Formula: C₃₅H₄₃N₃O₁₁
• Molecular Weight: 681.74

Synonyms:

Chemical Property of 1L-N¹-benzyloxycarbonyl-O⁶-(2-benzyloxycarbonylamino-O⁴,O⁶-cyclohexane-1,1-diyl-α-D-ribo-2,3-dideoxy-hexopyranosyl)-N³,O⁴-carbonyl-2-deoxy-streptamine

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 1L-N¹-benzyloxycarbonyl-O⁶-(2-benzyloxycarbonylamino-O⁴,O⁶-cyclohexane-1,1-diyl-α-D-ribo-2,3-dideoxy-hexopyranosyl)-N³,O⁴-carbonyl-2-deoxy-streptamine

There total 1 articles about 1L-N¹-benzyloxycarbonyl-O⁶-(2-benzyloxycarbonylamino-O⁴,O⁶-cyclohexane-1,1-diyl-α-D-ribo-2,3-dideoxy-hexopyranosyl)-N³,O⁴-carbonyl-2-deoxy-streptamine 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:

→ 1L-N1-benzyloxycarbonyl-O6-(2-benzyloxycarbonylamino-O4,O6-cyclohexane-1,1-diyl-α-D-ribo-2,3-dideoxy-hexopyranosyl)-N3,O4-carbonyl-2-deoxy-streptamine (63604-34-2)

Guidance literature:

Deoxyparomamin 1 1.NaH,DMF 2.1,1-Dimethoxycyclohexan;

DOI:10.1246/bcsj.50.972

Reference yield:

1L-N1-benzyloxycarbonyl-O6-(2-benzyloxycarbonylamino-O4,O6-cyclohexane-1,1-diyl-α-D-ribo-2,3-dideoxy-hexopyranosyl)-N3,O4-carbonyl-2-deoxy-streptamine (63604-34-2) → 1L-N1-benzyloxycarbonyl-O6-(2-benzyloxycarbonylamino-α-D-ribo-2,3-dideoxy-hexopyranosyl)-O5-[O2,O3-bis-(4-nitro-benzoyl)-O5-(toluene-4-sulfonyl)-β-D-xylofuranosyl]-N3,O4-carbonyl-2-deoxy-streptamine (68537-55-3)

Guidance literature:

Multi-step reaction with 2 steps

1: (i) HCl, CH₂Cl₂, (ii) /BRN= 1068056/, Drierite, Hg(CN)2, (iii) Py, CHCl₃

2: AcOH / dioxane

With acetic acid; In 1,4-dioxane;

DOI:10.7164/antibiotics.31.863

Reference yield:

1L-N1-benzyloxycarbonyl-O6-(2-benzyloxycarbonylamino-O4,O6-cyclohexane-1,1-diyl-α-D-ribo-2,3-dideoxy-hexopyranosyl)-N3,O4-carbonyl-2-deoxy-streptamine (63604-34-2) → 1L-N1-benzyloxycarbonyl-O6-[2-benzyloxycarbonylamino-O6-(toluene-4-sulfonyl)-α-D-ribo-2,3-dideoxy-hexopyranosyl]-O5-[O2,O3-bis-(4-nitro-benzoyl)-O5-(toluene-4-sulfonyl)-β-D-xylofuranosyl]-N3,O4-carbonyl-2-deoxy-streptamine (68537-56-4)

Guidance literature:

Multi-step reaction with 3 steps

1: (i) HCl, CH₂Cl₂, (ii) /BRN= 1068056/, Drierite, Hg(CN)2, (iii) Py, CHCl₃

2: AcOH / dioxane

3: Py / -10 °C

With pyridine; acetic acid; In 1,4-dioxane;

DOI:10.7164/antibiotics.31.863

Downstream raw materials:

1L-N¹-benzyloxycarbonyl-O⁶-(2-benzyloxycarbonylamino-O⁴,O⁶-cyclohexane-1,1-diyl-α-D-ribo-2,3-dideoxy-hexopyranosyl)-O⁵-[O²,O⁵-bis-(4-nitro-benzoyl)-β-D-erythro-3-deoxy-pentofuranosyl]-N³,O⁴-carbonyl-2-deoxy-streptamine

1L-N¹-benzyloxycarbonyl-O⁶-(2-benzyloxycarbonylamino-O⁴,O⁶-cyclohexane-1,1-diyl-α-D-ribo-2,3-dideoxy-hexopyranosyl)-O⁵-[O²,O³-bis-(4-nitro-benzoyl)-O⁵-(toluene-4-sulfonyl)-β-D-xylofuranosyl]-N³,O⁴-carbonyl-2-deoxy-streptamine

1L-N¹-benzyloxycarbonyl-O⁶-(2-benzyloxycarbonylamino-α-D-ribo-2,3-dideoxy-hexopyranosyl)-O⁵-[O²,O³-bis-(4-nitro-benzoyl)-O⁵-(toluene-4-sulfonyl)-β-D-xylofuranosyl]-N³,O⁴-carbonyl-2-deoxy-streptamine

1L-N¹-benzyloxycarbonyl-O⁶-[2-benzyloxycarbonylamino-O⁶-(toluene-4-sulfonyl)-α-D-ribo-2,3-dideoxy-hexopyranosyl]-O⁵-[O²,O³-bis-(4-nitro-benzoyl)-O⁵-(toluene-4-sulfonyl)-β-D-xylofuranosyl]-N³,O⁴-carbonyl-2-deoxy-streptamine

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