(R)-N-(N-(benzyloxycarbonyl)sulfamoyl)-N-(O-benzylhydroxy)-β-phenylalanine

Base Information

Chemical Name:(R)-N-(N-(benzyloxycarbonyl)sulfamoyl)-N-(O-benzylhydroxy)-β-phenylalanine
CAS No.:719296-35-2
Molecular Formula:C₂₅H₂₆N₂O₇S
Molecular Weight:498.557
Hs Code.:

Synonyms:(R)-N-(N-(benzyloxycarbonyl)sulfamoyl)-N-(O-benzylhydroxy)-β-phenylalanine

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Chemical Property of (R)-N-(N-(benzyloxycarbonyl)sulfamoyl)-N-(O-benzylhydroxy)-β-phenylalanine

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Technology Process of (R)-N-(N-(benzyloxycarbonyl)sulfamoyl)-N-(O-benzylhydroxy)-β-phenylalanine

There total 4 articles about (R)-N-(N-(benzyloxycarbonyl)sulfamoyl)-N-(O-benzylhydroxy)-β-phenylalanine 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: 93.0%

: 478182-58-0
(R)-2-benzyl-3-(N-benzyloxy-N-(N-benzyloxycarbonyl)sulfamoyl)aminopropanoic acid methyl ester

: 719296-35-2
(R)-N-(N-(benzyloxycarbonyl)sulfamoyl)-N-(O-benzylhydroxy)-β-phenylalanine

Guidance literature:: With lithium hydroxide; In methanol; water; at 20 ℃; for 2h;
DOI:10.1016/j.bmc.2004.02.012

Reference yield:

: 89979-13-5
benzyl N-chlorosulfonylcarbamate

: 719296-35-2
(R)-N-(N-(benzyloxycarbonyl)sulfamoyl)-N-(O-benzylhydroxy)-β-phenylalanine

Guidance literature:: Multi-step reaction with 2 steps

1: 0.53 g / triethylamine / CH₂Cl₂ / 6 h / 20 °C

2: 93 percent / lithium hydroxide / methanol; H₂O / 2 h / 20 °C

With lithium hydroxide; triethylamine; In methanol; dichloromethane; water;
DOI:10.1016/j.bmc.2004.02.012

Reference yield:

: 100-51-6,185532-71-2
benzyl alcohol

: 719296-35-2
(R)-N-(N-(benzyloxycarbonyl)sulfamoyl)-N-(O-benzylhydroxy)-β-phenylalanine

Guidance literature:: Multi-step reaction with 3 steps

1: CH₂Cl₂ / 0.5 h / 0 °C

2: 0.53 g / triethylamine / CH₂Cl₂ / 6 h / 20 °C

3: 93 percent / lithium hydroxide / methanol; H₂O / 2 h / 20 °C

With lithium hydroxide; triethylamine; In methanol; dichloromethane; water;
DOI:10.1016/j.bmc.2004.02.012