4-{(2S,3R)-2-({[(3R,3AS,6AR)-Hexahydrofuro[2,3-b]furan-3-yloxy]carbonyl)amino)-4-[(1,3-benzodioxol-5-ylsulfonyl)(isobutyl)amino]-3-hydroxybutyl}phenyl 4-nitrophenyl carbonate

Base Information

• Chemical Name: 4-{(2S,3R)-2-({[(3R,3AS,6AR)-Hexahydrofuro[2,3-b]furan-3-yloxy]carbonyl)amino)-4-[(1,3-benzodioxol-5-ylsulfonyl)(isobutyl)amino]-3-hydroxybutyl}phenyl 4-nitrophenyl carbonate
• CAS No.: 313681-24-2
• Molecular Formula: C₃₅H₃₉N₃O₁₄S
• Molecular Weight: 757.772

Synonyms:4-{(2S,3R)-2-({[(3R,3AS,6AR)-Hexahydrofuro[2,3-b]furan-3-yloxy]carbonyl)amino)-4-[(1,3-benzodioxol-5-ylsulfonyl)(isobutyl)amino]-3-hydroxybutyl}phenyl 4-nitrophenyl carbonate

Chemical Property of 4-{(2S,3R)-2-({[(3R,3AS,6AR)-Hexahydrofuro[2,3-b]furan-3-yloxy]carbonyl)amino)-4-[(1,3-benzodioxol-5-ylsulfonyl)(isobutyl)amino]-3-hydroxybutyl}phenyl 4-nitrophenyl carbonate

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Technology Process of 4-{(2S,3R)-2-({[(3R,3AS,6AR)-Hexahydrofuro[2,3-b]furan-3-yloxy]carbonyl)amino)-4-[(1,3-benzodioxol-5-ylsulfonyl)(isobutyl)amino]-3-hydroxybutyl}phenyl 4-nitrophenyl carbonate

There total 1 articles about 4-{(2S,3R)-2-({[(3R,3AS,6AR)-Hexahydrofuro[2,3-b]furan-3-yloxy]carbonyl)amino)-4-[(1,3-benzodioxol-5-ylsulfonyl)(isobutyl)amino]-3-hydroxybutyl}phenyl 4-nitrophenyl carbonate 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: 79.0%

(3R,3AS,6AR)-hexahydrofuro[2,3-b]furan-3-yl (1S,2R)-3-[(1,3-benzodioxol-5-ylsulfonyl)(isobutyl)amino]-2-hydroxy-1-(4-hydroxybenzyl)propylcarbamate (313679-57-1) + 4-Nitrophenyl chloroformate (7693-46-1) → 4-{(2S,3R)-2-({[(3R,3AS,6AR)-Hexahydrofuro[2,3-b]furan-3-yloxy]carbonyl)amino)-4-[(1,3-benzodioxol-5-ylsulfonyl)(isobutyl)amino]-3-hydroxybutyl}phenyl 4-nitrophenyl carbonate (313681-24-2)

Guidance literature:

With pyridine; In dichloromethane; at 20 ℃; for 1h;

Reference yield:

N-[2-(aminoethyl)]imidazole (5739-10-6) + 4-{(2S,3R)-2-({[(3R,3AS,6AR)-Hexahydrofuro[2,3-b]furan-3-yloxy]carbonyl)amino)-4-[(1,3-benzodioxol-5-ylsulfonyl)(isobutyl)amino]-3-hydroxybutyl}phenyl 4-nitrophenyl carbonate (313681-24-2) → (3R,3AS,6AR)-Hexahydrofuro[2,3-b]furan-3-yl (1S,2R)-3-[(1,3-benzodioxol-5-ylsulfonyl)(isobutyl)amino]-2-hydroxy-1-{4-[({[2-(1H-imidazol-1-yl)ethyl]amino}carbonyl)oxy]benzyl}propylcarbamate (313681-27-5)

Guidance literature:

In 1,4-dioxane; at 20 ℃; for 0.5h;

Reference yield:

4-{(2S,3R)-2-({[(3R,3AS,6AR)-Hexahydrofuro[2,3-b]furan-3-yloxy]carbonyl)amino)-4-[(1,3-benzodioxol-5-ylsulfonyl)(isobutyl)amino]-3-hydroxybutyl}phenyl 4-nitrophenyl carbonate (313681-24-2) + dimethyl amine (124-40-3) → (3R,3AS,6AR)-Hexahydrofuro[2,3-b]furan-3-yl (1S,2R)-3-[(1,3-benzodioxol-5-ylsulfonyl)(isobutyl)amino]-1-(4-{[(dimethylamino)carbonyl]oxy}benzyl)-2-hydroxypropylcarbamate (313681-25-3)

Guidance literature:

In tetrahydrofuran; at 20 ℃; for 0.5h;

upstream raw materials:

(3R,3AS,6AR)-hexahydrofuro[2,3-b]furan-3-yl (1S,2R)-3-[(1,3-benzodioxol-5-ylsulfonyl)(isobutyl)amino]-2-hydroxy-1-(4-hydroxybenzyl)propylcarbamate

4-Nitrophenyl chloroformate

Downstream raw materials:

(3R,3AS,6AR)-Hexahydrofuro[2,3-b]furan-3-yl (1S,2R)-3-[(1,3-benzodioxol-5-ylsulfonyl)(isobutyl)amino]-1-(4-{[(dimethylamino)carbonyl]oxy}benzyl)-2-hydroxypropylcarbamate

(3R,3AS,6AR)-Hexahydrofuro[2,3-b]furan-3-yl (1S,2R)-3-[(1,3-benzodioxol-5-ylsulfonyl)(isobutyl)amino]-2-hydroxy-1-{4-[({[2-(1H-imidazol-1-yl)ethyl]amino}carbonyl)oxy]benzyl}propylcarbamate

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