methyl 3-azido-2,3-dideoxy-6-O-p-tolylsulfonyl-β-D-arabino-hexopyranoside

Base Information

Chemical Name:methyl 3-azido-2,3-dideoxy-6-O-p-tolylsulfonyl-β-D-arabino-hexopyranoside
CAS No.:825632-25-5
Molecular Formula:C₁₄H₁₉N₃O₆S
Molecular Weight:357.387
Hs Code.:

Synonyms:methyl 3-azido-2,3-dideoxy-6-O-p-tolylsulfonyl-β-D-arabino-hexopyranoside

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of methyl 3-azido-2,3-dideoxy-6-O-p-tolylsulfonyl-β-D-arabino-hexopyranoside

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Technology Process of methyl 3-azido-2,3-dideoxy-6-O-p-tolylsulfonyl-β-D-arabino-hexopyranoside

There total 1 articles about methyl 3-azido-2,3-dideoxy-6-O-p-tolylsulfonyl-β-D-arabino-hexopyranoside 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: 77.0%

: 98-59-9
p-toluenesulfonyl chloride

: 116724-59-5
methyl 3-azido-2,3-dideoxy-β-D-arabino-hexopyranoside

: 825632-25-5
methyl 3-azido-2,3-dideoxy-6-O-p-tolylsulfonyl-β-D-arabino-hexopyranoside

: methyl 3-azido-2,3-dideoxy-4,6-di-O-p-tolylsulfonyl-β-D-arabino-hexopyranoside

Guidance literature:: With pyridine; In dichloromethane; at 20 ℃;
DOI:10.1081/CAR-200040117

Reference yield: 92.0%

: 825632-25-5
methyl 3-azido-2,3-dideoxy-6-O-p-tolylsulfonyl-β-D-arabino-hexopyranoside

: 108-24-7
acetic anhydride

: 825632-30-2
methyl 4-O-acetyl-3-azido-2,3-dideoxy-6-O-p-tolylsulfonyl-β-D-arabino-hexopyranoside

Guidance literature:: With pyridine; for 0.5h;
DOI:10.1081/CAR-200040117

Reference yield:

: 825632-25-5
methyl 3-azido-2,3-dideoxy-6-O-p-tolylsulfonyl-β-D-arabino-hexopyranoside

: 825632-40-4
(2S,3R,5R)-2-acetoxy-3-azido-5-hydroxycyclohexanone

Guidance literature:: Multi-step reaction with 4 steps

1: 92 percent / pyridine / 0.5 h

2: 42 percent / NaI / acetone / 48 h / Heating

3: 72 percent / AgF; pyridine / 48 h

4: 85 percent / H₂SO₄ / 0.25 h / Heating

With pyridine; sulfuric acid; silver fluoride; sodium iodide; In acetone; 4: Ferrier carbocyclization;
DOI:10.1081/CAR-200040117