(2S,3S,4S,5R,6S)-3,5-Diazido-4-benzyloxy-2-benzyloxymethyl-6-ethylsulfanyl-tetrahydro-pyran

Base Information

Chemical Name:(2S,3S,4S,5R,6S)-3,5-Diazido-4-benzyloxy-2-benzyloxymethyl-6-ethylsulfanyl-tetrahydro-pyran
CAS No.:635310-01-9
Molecular Formula:C₂₂H₂₆N₆O₃S
Molecular Weight:454.553
Hs Code.:

Synonyms:(2S,3S,4S,5R,6S)-3,5-Diazido-4-benzyloxy-2-benzyloxymethyl-6-ethylsulfanyl-tetrahydro-pyran

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Chemical Property of (2S,3S,4S,5R,6S)-3,5-Diazido-4-benzyloxy-2-benzyloxymethyl-6-ethylsulfanyl-tetrahydro-pyran

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Technology Process of (2S,3S,4S,5R,6S)-3,5-Diazido-4-benzyloxy-2-benzyloxymethyl-6-ethylsulfanyl-tetrahydro-pyran

There total 7 articles about (2S,3S,4S,5R,6S)-3,5-Diazido-4-benzyloxy-2-benzyloxymethyl-6-ethylsulfanyl-tetrahydro-pyran 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:

: 1125-88-8
benzaldehyde dimethyl acetal

: 635310-01-9
(2S,3S,4S,5R,6S)-3,5-Diazido-4-benzyloxy-2-benzyloxymethyl-6-ethylsulfanyl-tetrahydro-pyran

Guidance literature:: Multi-step reaction with 6 steps

1: p-TsOH

2: TBAI; NaH

3: 68 percent / TFA

4: 94 percent / N₂H₄*AcOH

5: 92 percent / TfN₃

With triflic azide; hydrazinium monoacetate; tetra-(n-butyl)ammonium iodide; sodium hydride; toluene-4-sulfonic acid; trifluoroacetic acid;
DOI:10.1055/s-2003-40351

Reference yield:

: 100-39-0
benzyl bromide

: 635310-01-9
(2S,3S,4S,5R,6S)-3,5-Diazido-4-benzyloxy-2-benzyloxymethyl-6-ethylsulfanyl-tetrahydro-pyran

Guidance literature:: Multi-step reaction with 5 steps

1: TBAI; NaH

2: 68 percent / TFA

3: 94 percent / N₂H₄*AcOH

4: 92 percent / TfN₃

With triflic azide; hydrazinium monoacetate; tetra-(n-butyl)ammonium iodide; sodium hydride; trifluoroacetic acid;
DOI:10.1055/s-2003-40351

Reference yield:

: 99409-33-3
ethyl 4,6-O-benzylidene-2-deoxy-2-N-phthalamido-1-thio-β-Dglucopyranoside

: 635310-01-9
(2S,3S,4S,5R,6S)-3,5-Diazido-4-benzyloxy-2-benzyloxymethyl-6-ethylsulfanyl-tetrahydro-pyran

Guidance literature:: Multi-step reaction with 5 steps

1: TBAI; NaH

2: 68 percent / TFA

3: 94 percent / N₂H₄*AcOH

4: 92 percent / TfN₃

With triflic azide; hydrazinium monoacetate; tetra-(n-butyl)ammonium iodide; sodium hydride; trifluoroacetic acid;
DOI:10.1055/s-2003-40351