5-O-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)-1-N-tert-butoxycarbonyl-6,3',4'-tri-O-acetyl-3,2',6'-triazidoneamine

Base Information

Chemical Name:5-O-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)-1-N-tert-butoxycarbonyl-6,3',4'-tri-O-acetyl-3,2',6'-triazidoneamine
CAS No.:942420-68-0
Molecular Formula:C₃₄H₄₈N₁₀O₁₈
Molecular Weight:884.811
Hs Code.:

Synonyms:5-O-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)-1-N-tert-butoxycarbonyl-6,3',4'-tri-O-acetyl-3,2',6'-triazidoneamine

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Chemical Property of 5-O-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)-1-N-tert-butoxycarbonyl-6,3',4'-tri-O-acetyl-3,2',6'-triazidoneamine

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Technology Process of 5-O-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)-1-N-tert-butoxycarbonyl-6,3',4'-tri-O-acetyl-3,2',6'-triazidoneamine

There total 3 articles about 5-O-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)-1-N-tert-butoxycarbonyl-6,3',4'-tri-O-acetyl-3,2',6'-triazidoneamine 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: 31.0%

: 942420-67-9
5-O-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)-6,3',4'-tri-O-acetyl-1,3,2',6'-tetraazidoneamine

: 58632-95-4
2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrile

: 942420-68-0
5-O-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)-1-N-tert-butoxycarbonyl-6,3',4'-tri-O-acetyl-3,2',6'-triazidoneamine

Guidance literature:: With trimethylphosphane; In toluene; at -78 - 10 ℃;
DOI:10.1021/jo062588j

Reference yield:

: 52544-88-4
phenyl 2,3,5-tri-O-acetyl-1-thio-β-D-ribofuranoside

: 942420-68-0
5-O-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)-1-N-tert-butoxycarbonyl-6,3',4'-tri-O-acetyl-3,2',6'-triazidoneamine

Guidance literature:: Multi-step reaction with 2 steps

1: 37 percent / N-iodosuccinimide; trimethylsilyl triflate; 4 Angstroem molecular sieves / CH₂Cl₂ / -50 - 20 °C

2: 31 percent / Me₃P / toluene / -78 - 10 °C

With N-iodo-succinimide; trimethylsilyl trifluoromethanesulfonate; 4 A molecular sieve; trimethylphosphane; In dichloromethane; toluene; 2: Staudinger reaction;
DOI:10.1021/jo062588j

Reference yield:

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

: 942420-68-0
5-O-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)-1-N-tert-butoxycarbonyl-6,3',4'-tri-O-acetyl-3,2',6'-triazidoneamine

Guidance literature:: Multi-step reaction with 2 steps

1: 37 percent / N-iodosuccinimide; trimethylsilyl triflate; 4 Angstroem molecular sieves / CH₂Cl₂ / -50 - 20 °C

2: 31 percent / Me₃P / toluene / -78 - 10 °C

With N-iodo-succinimide; trimethylsilyl trifluoromethanesulfonate; 4 A molecular sieve; trimethylphosphane; In dichloromethane; toluene; 2: Staudinger reaction;
DOI:10.1021/jo062588j