(3aS,5R,6aR)-3-oxohexahydro-2H-cyclopenta[b]furan-5-yl (2S,3R)-3-hydroxy-4-(4-(hydroxymethyl)-N-isobutylphenylsulfonamido)-1-phenylbutan-2-yl-carbamate

Base Information

Chemical Name:(3aS,5R,6aR)-3-oxohexahydro-2H-cyclopenta[b]furan-5-yl (2S,3R)-3-hydroxy-4-(4-(hydroxymethyl)-N-isobutylphenylsulfonamido)-1-phenylbutan-2-yl-carbamate
CAS No.:1321531-37-6
Molecular Formula:C₂₉H₃₈N₂O₈S
Molecular Weight:574.695
Hs Code.:

(3aS,5R,6aR)-3-oxohexahydro-2H-cyclopenta[b]furan-5-yl (2S,3R)-3-hydroxy-4-(4-(hydroxymethyl)-N-isobutylphenylsulfonamido)-1-phenylbutan-2-yl-carbamate

Synonyms:(3aS,5R,6aR)-3-oxohexahydro-2H-cyclopenta[b]furan-5-yl (2S,3R)-3-hydroxy-4-(4-(hydroxymethyl)-N-isobutylphenylsulfonamido)-1-phenylbutan-2-yl-carbamate

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Chemical Property of (3aS,5R,6aR)-3-oxohexahydro-2H-cyclopenta[b]furan-5-yl (2S,3R)-3-hydroxy-4-(4-(hydroxymethyl)-N-isobutylphenylsulfonamido)-1-phenylbutan-2-yl-carbamate

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Technology Process of (3aS,5R,6aR)-3-oxohexahydro-2H-cyclopenta[b]furan-5-yl (2S,3R)-3-hydroxy-4-(4-(hydroxymethyl)-N-isobutylphenylsulfonamido)-1-phenylbutan-2-yl-carbamate

There total 4 articles about (3aS,5R,6aR)-3-oxohexahydro-2H-cyclopenta[b]furan-5-yl (2S,3R)-3-hydroxy-4-(4-(hydroxymethyl)-N-isobutylphenylsulfonamido)-1-phenylbutan-2-yl-carbamate 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: 49.0%

: 1037666-14-0
C₂₁H₃₀N₂O₄S

: 1321531-30-9
(3aS,5R,6aR)-3-oxohexahydro-2H-cyclopenta[b]furan-5-yl(4-nitrophenyl)carbonate

: 1321531-37-6
(3aS,5R,6aR)-3-oxohexahydro-2H-cyclopenta[b]furan-5-yl (2S,3R)-3-hydroxy-4-(4-(hydroxymethyl)-N-isobutylphenylsulfonamido)-1-phenylbutan-2-yl-carbamate

Guidance literature:: C₂₁H₃₀N₂O₄S; With pyridine; trifluoroacetic acid; In dichloromethane; at 20 ℃; for 2h; Inert atmosphere;

(3aS,5R,6aR)-3-oxohexahydro-2H-cyclopenta[b]furan-5-yl(4-nitrophenyl)carbonate; With triethylamine; In acetonitrile; at 0 ℃; for 36h; Inert atmosphere;
DOI:10.1021/jm200649p

Reference yield:

: 1079393-55-7
(3aS,5R,6aR)-5-(tert-butyldimethyl-silanyloxy)-tetrahydro-2H-cyclopenta[b]furan-3-one

: 1321531-37-6
(3aS,5R,6aR)-3-oxohexahydro-2H-cyclopenta[b]furan-5-yl (2S,3R)-3-hydroxy-4-(4-(hydroxymethyl)-N-isobutylphenylsulfonamido)-1-phenylbutan-2-yl-carbamate

Guidance literature:: Multi-step reaction with 3 steps

1.1: pyridine; pyridine hydrogenfluoride / acetonitrile / 4 h / 0 °C / Inert atmosphere

2.1: pyridine / dichloromethane / 0 - 20 °C / Inert atmosphere

3.1: pyridine; trifluoroacetic acid / dichloromethane / 2 h / 20 °C / Inert atmosphere

3.2: 36 h / 0 °C / Inert atmosphere

With pyridine; pyridine hydrogenfluoride; trifluoroacetic acid; In dichloromethane; acetonitrile;
DOI:10.1021/jm200649p

Reference yield:

: 1321531-05-8
(3aS,5R,6aR)-5-hydroxytetrahydro-2H-cyclopenta[b]furan-3(3aH)-one

: 1321531-37-6
(3aS,5R,6aR)-3-oxohexahydro-2H-cyclopenta[b]furan-5-yl (2S,3R)-3-hydroxy-4-(4-(hydroxymethyl)-N-isobutylphenylsulfonamido)-1-phenylbutan-2-yl-carbamate

Guidance literature:: Multi-step reaction with 2 steps

1.1: pyridine / dichloromethane / 0 - 20 °C / Inert atmosphere

2.1: pyridine; trifluoroacetic acid / dichloromethane / 2 h / 20 °C / Inert atmosphere

2.2: 36 h / 0 °C / Inert atmosphere

With pyridine; trifluoroacetic acid; In dichloromethane;
DOI:10.1021/jm200649p