(3-{2-[(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]-ethylamino}-propyl)-carbamic acid benzyl ester

Base Information Edit

Chemical Name:(3-{2-[(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]-ethylamino}-propyl)-carbamic acid benzyl ester
CAS No.:236115-83-6
Molecular Formula:C₄₆H₅₄N₁₄O₈
Molecular Weight:931.024
Hs Code.:
Mol file:236115-83-6.mol

(3-{2-[(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]-ethylamino}-propyl)-carbamic acid benzyl ester

Synonyms:(3-{2-[(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]-ethylamino}-propyl)-carbamic acid benzyl ester

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Chemical Property of (3-{2-[(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]-ethylamino}-propyl)-carbamic acid benzyl ester Edit

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Technology Process of (3-{2-[(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]-ethylamino}-propyl)-carbamic acid benzyl ester

There total 3 articles about (3-{2-[(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]-ethylamino}-propyl)-carbamic acid benzyl ester 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:

: 236115-80-3
1,3,2',6'-tetraazido-6,3',4'-tri-O-benzyl neamine

: 236115-83-6
(3-{2-[(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]-ethylamino}-propyl)-carbamic acid benzyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 99 percent / NaH, tetrabutylammonium iodide / dimethylformamide / 2 h / Ambient temperature

2: 1.) O₃, 2.) Me₂S / 1.) CH₂Cl₂, MeOH, -78 deg C, 20 s, 2.) CH₂Cl₂, MeOH, RT, 1 h

3: NaCNBH₃ / methanol; acetic acid / 2 h / Ambient temperature

With dimethylsulfide; tetra-(n-butyl)ammonium iodide; sodium hydride; sodium cyanoborohydride; ozone; In methanol; acetic acid; N,N-dimethyl-formamide;
DOI:10.1021/ja9910356

Reference yield:

: 236115-81-4
5-O-allyl-1,3,2',6'-tetraazido-6,3',4'-tri-O-benzyl neamine

: 236115-83-6
(3-{2-[(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]-ethylamino}-propyl)-carbamic acid benzyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) O₃, 2.) Me₂S / 1.) CH₂Cl₂, MeOH, -78 deg C, 20 s, 2.) CH₂Cl₂, MeOH, RT, 1 h

2: NaCNBH₃ / methanol; acetic acid / 2 h / Ambient temperature

With dimethylsulfide; sodium cyanoborohydride; ozone; In methanol; acetic acid;
DOI:10.1021/ja9910356