{(2R,3R,4R,5S)-4-Benzyloxy-2-benzyloxymethyl-5-[(1R,2R,3S,5R,6S)-3,5-diazido-2-((2R,3R,4R,5R,6R)-3-azido-6-azidomethyl-4,5-bis-benzyloxy-tetrahydro-pyran-2-yloxy)-6-benzyloxy-cyclohexyloxy]-tetrahydro-furan-3-yloxy}-acetaldehyde

Base Information

Chemical Name:{(2R,3R,4R,5S)-4-Benzyloxy-2-benzyloxymethyl-5-[(1R,2R,3S,5R,6S)-3,5-diazido-2-((2R,3R,4R,5R,6R)-3-azido-6-azidomethyl-4,5-bis-benzyloxy-tetrahydro-pyran-2-yloxy)-6-benzyloxy-cyclohexyloxy]-tetrahydro-furan-3-yloxy}-acetaldehyde
CAS No.:205192-01-4
Molecular Formula:C₅₄H₅₈N₁₂O₁₁
Molecular Weight:1051.13
Hs Code.:

{(2R,3R,4R,5S)-4-Benzyloxy-2-benzyloxymethyl-5-[(1R,2R,3S,5R,6S)-3,5-diazido-2-((2R,3R,4R,5R,6R)-3-azido-6-azidomethyl-4,5-bis-benzyloxy-tetrahydro-pyran-2-yloxy)-6-benzyloxy-cyclohexyloxy]-tetrahydro-furan-3-yloxy}-acetaldehyde

Synonyms:{(2R,3R,4R,5S)-4-Benzyloxy-2-benzyloxymethyl-5-[(1R,2R,3S,5R,6S)-3,5-diazido-2-((2R,3R,4R,5R,6R)-3-azido-6-azidomethyl-4,5-bis-benzyloxy-tetrahydro-pyran-2-yloxy)-6-benzyloxy-cyclohexyloxy]-tetrahydro-furan-3-yloxy}-acetaldehyde

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Chemical Property of {(2R,3R,4R,5S)-4-Benzyloxy-2-benzyloxymethyl-5-[(1R,2R,3S,5R,6S)-3,5-diazido-2-((2R,3R,4R,5R,6R)-3-azido-6-azidomethyl-4,5-bis-benzyloxy-tetrahydro-pyran-2-yloxy)-6-benzyloxy-cyclohexyloxy]-tetrahydro-furan-3-yloxy}-acetaldehyde

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Technology Process of {(2R,3R,4R,5S)-4-Benzyloxy-2-benzyloxymethyl-5-[(1R,2R,3S,5R,6S)-3,5-diazido-2-((2R,3R,4R,5R,6R)-3-azido-6-azidomethyl-4,5-bis-benzyloxy-tetrahydro-pyran-2-yloxy)-6-benzyloxy-cyclohexyloxy]-tetrahydro-furan-3-yloxy}-acetaldehyde

There total 6 articles about {(2R,3R,4R,5S)-4-Benzyloxy-2-benzyloxymethyl-5-[(1R,2R,3S,5R,6S)-3,5-diazido-2-((2R,3R,4R,5R,6R)-3-azido-6-azidomethyl-4,5-bis-benzyloxy-tetrahydro-pyran-2-yloxy)-6-benzyloxy-cyclohexyloxy]-tetrahydro-furan-3-yloxy}-acetaldehyde 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:

: 100-39-0
benzyl bromide

: 205192-01-4
{(2R,3R,4R,5S)-4-Benzyloxy-2-benzyloxymethyl-5-[(1R,2R,3S,5R,6S)-3,5-diazido-2-((2R,3R,4R,5R,6R)-3-azido-6-azidomethyl-4,5-bis-benzyloxy-tetrahydro-pyran-2-yloxy)-6-benzyloxy-cyclohexyloxy]-tetrahydro-furan-3-yloxy}-acetaldehyde

Guidance literature:: Multi-step reaction with 2 steps

1: 84 percent / NaH / dimethylformamide / 1 h

2: 1.) O₃, 2.) DMS / 1.) CH₂Cl₂, -78 deg C, 2.) CH₂Cl₂, RT, 2 d

With 2,3-dimercapto-succinic acid; sodium hydride; ozone; In N,N-dimethyl-formamide;
DOI:10.1021/ja972599h

Reference yield:

: 182554-04-7
1,3,2′,6′-tetraazido-6,3′,4′-tri-O-acetylneamine

: 205192-01-4
{(2R,3R,4R,5S)-4-Benzyloxy-2-benzyloxymethyl-5-[(1R,2R,3S,5R,6S)-3,5-diazido-2-((2R,3R,4R,5R,6R)-3-azido-6-azidomethyl-4,5-bis-benzyloxy-tetrahydro-pyran-2-yloxy)-6-benzyloxy-cyclohexyloxy]-tetrahydro-furan-3-yloxy}-acetaldehyde

Guidance literature:: Multi-step reaction with 4 steps

1: 63 percent / BF₃*OEt₂ / CH₂Cl₂ / 4.5 h

2: 93 percent / aq. LiOH / methanol; dioxane / Ambient temperature

3: 84 percent / NaH / dimethylformamide / 1 h

4: 1.) O₃, 2.) DMS / 1.) CH₂Cl₂, -78 deg C, 2.) CH₂Cl₂, RT, 2 d

With lithium hydroxide; 2,3-dimercapto-succinic acid; boron trifluoride diethyl etherate; sodium hydride; ozone; In 1,4-dioxane; methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/ja972599h

Reference yield:

: 205191-99-7
(2R,3S,4R,5R,6R)-6-[(1R,2R,3S,4R,6S)-2-((2S,3R,4S,5R)-4-Allyloxy-5-benzyloxymethyl-3-hydroxy-tetrahydro-furan-2-yloxy)-4,6-diazido-3-hydroxy-cyclohexyloxy]-5-azido-2-azidomethyl-tetrahydro-pyran-3,4-diol

: 205192-01-4
{(2R,3R,4R,5S)-4-Benzyloxy-2-benzyloxymethyl-5-[(1R,2R,3S,5R,6S)-3,5-diazido-2-((2R,3R,4R,5R,6R)-3-azido-6-azidomethyl-4,5-bis-benzyloxy-tetrahydro-pyran-2-yloxy)-6-benzyloxy-cyclohexyloxy]-tetrahydro-furan-3-yloxy}-acetaldehyde

Guidance literature:: Multi-step reaction with 2 steps

1: 84 percent / NaH / dimethylformamide / 1 h

2: 1.) O₃, 2.) DMS / 1.) CH₂Cl₂, -78 deg C, 2.) CH₂Cl₂, RT, 2 d

With 2,3-dimercapto-succinic acid; sodium hydride; ozone; In N,N-dimethyl-formamide;
DOI:10.1021/ja972599h