ethyl (2R,3S)-2-(tert-butyloxycarbonyl-amino)-3-hydroxy-4-(tri-O-benzyl-α-L-fucopyranosyl)-butanoate

Base Information

Chemical Name:ethyl (2R,3S)-2-(tert-butyloxycarbonyl-amino)-3-hydroxy-4-(tri-O-benzyl-α-L-fucopyranosyl)-butanoate
CAS No.:236744-32-4
Molecular Formula:C₃₈H₄₉NO₉
Molecular Weight:663.808
Hs Code.:

Synonyms:ethyl (2R,3S)-2-(tert-butyloxycarbonyl-amino)-3-hydroxy-4-(tri-O-benzyl-α-L-fucopyranosyl)-butanoate

Suppliers and Price of ethyl (2R,3S)-2-(tert-butyloxycarbonyl-amino)-3-hydroxy-4-(tri-O-benzyl-α-L-fucopyranosyl)-butanoate

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of ethyl (2R,3S)-2-(tert-butyloxycarbonyl-amino)-3-hydroxy-4-(tri-O-benzyl-α-L-fucopyranosyl)-butanoate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of ethyl (2R,3S)-2-(tert-butyloxycarbonyl-amino)-3-hydroxy-4-(tri-O-benzyl-α-L-fucopyranosyl)-butanoate

There total 3 articles about ethyl (2R,3S)-2-(tert-butyloxycarbonyl-amino)-3-hydroxy-4-(tri-O-benzyl-α-L-fucopyranosyl)-butanoate 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: 85.0%

: 24424-99-5
di-tert-butyl dicarbonate

: 236744-31-3
ethyl (2R,3S)-2-azido-3-hydroxy-4-(tri-O-benzyl-α-L-fucopyranosyl)-butanoate

: 236744-32-4
ethyl (2R,3S)-2-(tert-butyloxycarbonyl-amino)-3-hydroxy-4-(tri-O-benzyl-α-L-fucopyranosyl)-butanoate

Guidance literature:: With hydrogen; palladium on activated charcoal; In ethyl acetate; for 18h; Ambient temperature;
DOI:10.1016/S0968-0896(98)00245-4

Reference yield:

: ethyl (2R,3S)-2,3-dihydroxy-4-(tri-O-benzyl-α-L-fucopyranosyl)-butanoate

: 236744-32-4
ethyl (2R,3S)-2-(tert-butyloxycarbonyl-amino)-3-hydroxy-4-(tri-O-benzyl-α-L-fucopyranosyl)-butanoate

Guidance literature:: Multi-step reaction with 3 steps

1: 88 percent / pyridine / 25 h / 4 °C

2: 88 percent / NaN₃ / dimethylformamide / 21 h / 50 °C

3: 85 percent / H₂ / Pd/C / ethyl acetate / 18 h / Ambient temperature

With sodium azide; hydrogen; palladium on activated charcoal; In pyridine; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1016/S0968-0896(98)00245-4

Reference yield:

: 236744-30-2
ethyl (2R,3S)-3-hydroxy-2-(4-nitrobenzenesulfonyloxy)-4-(tri-O-benzyl-α-L-fucopyranosyl)-butanoate

: 236744-32-4
ethyl (2R,3S)-2-(tert-butyloxycarbonyl-amino)-3-hydroxy-4-(tri-O-benzyl-α-L-fucopyranosyl)-butanoate

Guidance literature:: Multi-step reaction with 2 steps

1: 88 percent / NaN₃ / dimethylformamide / 21 h / 50 °C

2: 85 percent / H₂ / Pd/C / ethyl acetate / 18 h / Ambient temperature

With sodium azide; hydrogen; palladium on activated charcoal; In ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1016/S0968-0896(98)00245-4