(3S,3aR,5R,6aR)-3-hydroxyhexahydro-2H-cyclopenta[b]-furan-5-yl [(2S,3R)-3-hydroxy-4-(N-isobutyl-4-methoxyphenylsulfonamido)-1-phenylbutan-2-yl]carbamate

Base Information

Chemical Name:(3S,3aR,5R,6aR)-3-hydroxyhexahydro-2H-cyclopenta[b]-furan-5-yl [(2S,3R)-3-hydroxy-4-(N-isobutyl-4-methoxyphenylsulfonamido)-1-phenylbutan-2-yl]carbamate
CAS No.:1321531-14-9
Molecular Formula:C₂₉H₄₀N₂O₈S
Molecular Weight:576.711
Hs Code.:

(3S,3aR,5R,6aR)-3-hydroxyhexahydro-2H-cyclopenta[b]-furan-5-yl [(2S,3R)-3-hydroxy-4-(N-isobutyl-4-methoxyphenylsulfonamido)-1-phenylbutan-2-yl]carbamate

Synonyms:(3S,3aR,5R,6aR)-3-hydroxyhexahydro-2H-cyclopenta[b]-furan-5-yl [(2S,3R)-3-hydroxy-4-(N-isobutyl-4-methoxyphenylsulfonamido)-1-phenylbutan-2-yl]carbamate

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Chemical Property of (3S,3aR,5R,6aR)-3-hydroxyhexahydro-2H-cyclopenta[b]-furan-5-yl [(2S,3R)-3-hydroxy-4-(N-isobutyl-4-methoxyphenylsulfonamido)-1-phenylbutan-2-yl]carbamate

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Technology Process of (3S,3aR,5R,6aR)-3-hydroxyhexahydro-2H-cyclopenta[b]-furan-5-yl [(2S,3R)-3-hydroxy-4-(N-isobutyl-4-methoxyphenylsulfonamido)-1-phenylbutan-2-yl]carbamate

There total 5 articles about (3S,3aR,5R,6aR)-3-hydroxyhexahydro-2H-cyclopenta[b]-furan-5-yl [(2S,3R)-3-hydroxy-4-(N-isobutyl-4-methoxyphenylsulfonamido)-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: 80.0%

: 1321531-13-8
(3aS,5R,6aR)-3-oxohexahydro-2H-cyclopenta[b]furan-5-yl [(2S,3R)-3-hydroxy-4-(N-isobutyl-4-methoxyphenylsulfonamido)-1-phenylbutan-2-yl]carbamate

: 1321531-14-9
(3S,3aR,5R,6aR)-3-hydroxyhexahydro-2H-cyclopenta[b]-furan-5-yl [(2S,3R)-3-hydroxy-4-(N-isobutyl-4-methoxyphenylsulfonamido)-1-phenylbutan-2-yl]carbamate

Guidance literature:: With sodium tetrahydroborate; In ethanol; at -25 ℃; for 0.5h; 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

: 1321531-14-9
(3S,3aR,5R,6aR)-3-hydroxyhexahydro-2H-cyclopenta[b]-furan-5-yl [(2S,3R)-3-hydroxy-4-(N-isobutyl-4-methoxyphenylsulfonamido)-1-phenylbutan-2-yl]carbamate

Guidance literature:: Multi-step reaction with 4 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

4.1: sodium tetrahydroborate / ethanol / 0.5 h / -25 °C / Inert atmosphere

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

Reference yield:

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

: 1321531-14-9
(3S,3aR,5R,6aR)-3-hydroxyhexahydro-2H-cyclopenta[b]-furan-5-yl [(2S,3R)-3-hydroxy-4-(N-isobutyl-4-methoxyphenylsulfonamido)-1-phenylbutan-2-yl]carbamate

Guidance literature:: Multi-step reaction with 2 steps

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

1.2: 36 h / 0 °C / Inert atmosphere

2.1: sodium tetrahydroborate / ethanol / 0.5 h / -25 °C / Inert atmosphere

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