(2S,3S,4R)-4-{[(2S,3S,4R)-4-Azido-3-(tert-butyl-diphenyl-silanyloxy)-tetrahydro-furan-2-carbonyl]-amino}-3-(tert-butyl-diphenyl-silanyloxy)-tetrahydro-furan-2-carboxylic acid

Base Information

Chemical Name:(2S,3S,4R)-4-{[(2S,3S,4R)-4-Azido-3-(tert-butyl-diphenyl-silanyloxy)-tetrahydro-furan-2-carbonyl]-amino}-3-(tert-butyl-diphenyl-silanyloxy)-tetrahydro-furan-2-carboxylic acid
CAS No.:909723-66-6
Molecular Formula:C₄₂H₅₀N₄O₇Si₂
Molecular Weight:779.053
Hs Code.:

(2S,3S,4R)-4-{[(2S,3S,4R)-4-Azido-3-(tert-butyl-diphenyl-silanyloxy)-tetrahydro-furan-2-carbonyl]-amino}-3-(tert-butyl-diphenyl-silanyloxy)-tetrahydro-furan-2-carboxylic acid

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Chemical Property of (2S,3S,4R)-4-{[(2S,3S,4R)-4-Azido-3-(tert-butyl-diphenyl-silanyloxy)-tetrahydro-furan-2-carbonyl]-amino}-3-(tert-butyl-diphenyl-silanyloxy)-tetrahydro-furan-2-carboxylic acid

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Technology Process of (2S,3S,4R)-4-{[(2S,3S,4R)-4-Azido-3-(tert-butyl-diphenyl-silanyloxy)-tetrahydro-furan-2-carbonyl]-amino}-3-(tert-butyl-diphenyl-silanyloxy)-tetrahydro-furan-2-carboxylic acid

There total 4 articles about (2S,3S,4R)-4-{[(2S,3S,4R)-4-Azido-3-(tert-butyl-diphenyl-silanyloxy)-tetrahydro-furan-2-carbonyl]-amino}-3-(tert-butyl-diphenyl-silanyloxy)-tetrahydro-furan-2-carboxylic acid 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:

: 605668-26-6
isopropyl 2,5-anhydro-4-azido-3-O-tert-butyldiphenylsilyl-4-deoxy-L-ribonate

: 909723-66-6
(2S,3S,4R)-4-{[(2S,3S,4R)-4-Azido-3-(tert-butyl-diphenyl-silanyloxy)-tetrahydro-furan-2-carbonyl]-amino}-3-(tert-butyl-diphenyl-silanyloxy)-tetrahydro-furan-2-carboxylic acid

Guidance literature:: Multi-step reaction with 3 steps

1: H₂ / Pd/C / propan-2-ol / 13 h / 20 °C

2: 0.58 g / DIPEA; TBTU / dimethylformamide / 23 h / 20 °C

3: KOH; H₂O / methanol / 20 h / 20 °C

With potassium hydroxide; water; hydrogen; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine; palladium on activated charcoal; In methanol; N,N-dimethyl-formamide; isopropyl alcohol;
DOI:10.1016/j.tet.2006.05.067

Reference yield:

: 857499-51-5
isopropyl 4-amino-2,5-anhydro-3-O-tert-butyldiphenylsilyl-4-N-(2,5-anhydro-4-azido-3-O-tert-butyldiphenylsilyl-4-deoxy-L-ribonyl)-4-deoxy-L-ribonate

: 909723-66-6
(2S,3S,4R)-4-{[(2S,3S,4R)-4-Azido-3-(tert-butyl-diphenyl-silanyloxy)-tetrahydro-furan-2-carbonyl]-amino}-3-(tert-butyl-diphenyl-silanyloxy)-tetrahydro-furan-2-carboxylic acid

Guidance literature:: With potassium hydroxide; water; In methanol; at 20 ℃; for 20h;
DOI:10.1016/j.tet.2006.05.067

Reference yield:

: 909723-62-2
(2S,3S,4R)-4-Amino-3-(tert-butyl-diphenyl-silanyloxy)-tetrahydro-furan-2-carboxylic acid isopropyl ester

: 909723-66-6
(2S,3S,4R)-4-{[(2S,3S,4R)-4-Azido-3-(tert-butyl-diphenyl-silanyloxy)-tetrahydro-furan-2-carbonyl]-amino}-3-(tert-butyl-diphenyl-silanyloxy)-tetrahydro-furan-2-carboxylic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 0.58 g / DIPEA; TBTU / dimethylformamide / 23 h / 20 °C

2: KOH; H₂O / methanol / 20 h / 20 °C

With potassium hydroxide; water; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine; In methanol; N,N-dimethyl-formamide;
DOI:10.1016/j.tet.2006.05.067