4-Benzyloxycarbonylamino-3-[((S)-1-carbamoyl-2-methyl-propyl)-methoxymethyl-sulfamoyl]-butyric acid tert-butyl ester

Base Information

Chemical Name:4-Benzyloxycarbonylamino-3-[((S)-1-carbamoyl-2-methyl-propyl)-methoxymethyl-sulfamoyl]-butyric acid tert-butyl ester
CAS No.:189292-59-9
Molecular Formula:C₂₃H₃₇N₃O₈S
Molecular Weight:515.628
Hs Code.:

Synonyms:4-Benzyloxycarbonylamino-3-[((S)-1-carbamoyl-2-methyl-propyl)-methoxymethyl-sulfamoyl]-butyric acid tert-butyl ester

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Chemical Property of 4-Benzyloxycarbonylamino-3-[((S)-1-carbamoyl-2-methyl-propyl)-methoxymethyl-sulfamoyl]-butyric acid tert-butyl ester

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Technology Process of 4-Benzyloxycarbonylamino-3-[((S)-1-carbamoyl-2-methyl-propyl)-methoxymethyl-sulfamoyl]-butyric acid tert-butyl ester

There total 6 articles about 4-Benzyloxycarbonylamino-3-[((S)-1-carbamoyl-2-methyl-propyl)-methoxymethyl-sulfamoyl]-butyric acid tert-butyl ester 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: 58.0%

: 5292-43-3
bromoacetic acid tert-butyl ester

: 189292-57-7
{2-[((S)-1-Carbamoyl-2-methyl-propyl)-methoxymethyl-sulfamoyl]-ethyl}-carbamic acid benzyl ester

: 189292-59-9
4-Benzyloxycarbonylamino-3-[((S)-1-carbamoyl-2-methyl-propyl)-methoxymethyl-sulfamoyl]-butyric acid tert-butyl ester

Guidance literature:: With lithium diisopropyl amide; In tetrahydrofuran; at -78 ℃;
DOI:10.1016/S0960-894X(97)00090-5

Reference yield:

: 4540-60-7,20108-78-5
L-valinamide

: 189292-59-9
4-Benzyloxycarbonylamino-3-[((S)-1-carbamoyl-2-methyl-propyl)-methoxymethyl-sulfamoyl]-butyric acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 29 percent / triethylamine; CH₂Cl₂

2: 58 percent / NaH / diethyl ether; tetrahydrofuran

3: 58 percent / LDA / tetrahydrofuran / -78 °C

With sodium hydride; lithium diisopropyl amide; In tetrahydrofuran; diethyl ether; dichloromethane; triethylamine;
DOI:10.1016/S0960-894X(97)00090-5

Reference yield:

: 52530-50-4
benzyl (2-(chlorosulfonyl)ethyl)carbamate

: 189292-59-9
4-Benzyloxycarbonylamino-3-[((S)-1-carbamoyl-2-methyl-propyl)-methoxymethyl-sulfamoyl]-butyric acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 29 percent / triethylamine; CH₂Cl₂

2: 58 percent / NaH / diethyl ether; tetrahydrofuran

3: 58 percent / LDA / tetrahydrofuran / -78 °C

With sodium hydride; lithium diisopropyl amide; In tetrahydrofuran; diethyl ether; dichloromethane; triethylamine;
DOI:10.1016/S0960-894X(97)00090-5