(R)-N-(2-((tert-butyldiphenylsilyl)oxy)ethyl)-N-ethyl-4-(phenylthio)-3-((4-sulfamoyl-2-((trifluoromethyl)sulfonyl)phenyl)amino)butanamide

Base Information

Chemical Name:(R)-N-(2-((tert-butyldiphenylsilyl)oxy)ethyl)-N-ethyl-4-(phenylthio)-3-((4-sulfamoyl-2-((trifluoromethyl)sulfonyl)phenyl)amino)butanamide
CAS No.:1357575-19-9
Molecular Formula:C₃₇H₄₄F₃N₃O₆S₃Si
Molecular Weight:808.052
Hs Code.:

Synonyms:(R)-N-(2-((tert-butyldiphenylsilyl)oxy)ethyl)-N-ethyl-4-(phenylthio)-3-((4-sulfamoyl-2-((trifluoromethyl)sulfonyl)phenyl)amino)butanamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (R)-N-(2-((tert-butyldiphenylsilyl)oxy)ethyl)-N-ethyl-4-(phenylthio)-3-((4-sulfamoyl-2-((trifluoromethyl)sulfonyl)phenyl)amino)butanamide

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Technology Process of (R)-N-(2-((tert-butyldiphenylsilyl)oxy)ethyl)-N-ethyl-4-(phenylthio)-3-((4-sulfamoyl-2-((trifluoromethyl)sulfonyl)phenyl)amino)butanamide

There total 7 articles about (R)-N-(2-((tert-butyldiphenylsilyl)oxy)ethyl)-N-ethyl-4-(phenylthio)-3-((4-sulfamoyl-2-((trifluoromethyl)sulfonyl)phenyl)amino)butanamide 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: 91.0%

: 1357575-18-8
2-((tert-butyldiphenylsilyl)oxy)-N-ethylethanamine

: 1357575-05-3
(R)-4-(phenylthio)-3-((4-sulfamoyl-2-((trifluoromethyl)sulfonyl)phenyl)amino)butanoic acid

: 1357575-19-9
(R)-N-(2-((tert-butyldiphenylsilyl)oxy)ethyl)-N-ethyl-4-(phenylthio)-3-((4-sulfamoyl-2-((trifluoromethyl)sulfonyl)phenyl)amino)butanamide

Guidance literature:: With diethyl 4-oxobenzo[d][1,2,3]triazin-3(4H)-yl phosphate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; at 18 - 25 ℃; for 3h;

Reference yield:

: 58479-61-1
tert-butylchlorodiphenylsilane

: 1357575-19-9
(R)-N-(2-((tert-butyldiphenylsilyl)oxy)ethyl)-N-ethyl-4-(phenylthio)-3-((4-sulfamoyl-2-((trifluoromethyl)sulfonyl)phenyl)amino)butanamide

Guidance literature:: Multi-step reaction with 2 steps

1: 1H-imidazole / dichloromethane / 18 - 25 °C

2: N-ethyl-N,N-diisopropylamine; diethyl 4-oxobenzo[d][1,2,3]triazin-3(4H)-yl phosphate / tetrahydrofuran / 3 h / 18 - 25 °C

With 1H-imidazole; diethyl 4-oxobenzo[d][1,2,3]triazin-3(4H)-yl phosphate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane;

Reference yield:

: 1027345-08-9
4-fluoro-3-[(trifluoromethyl)sulfonyl]benzenesulfonamide

: 1357575-19-9
(R)-N-(2-((tert-butyldiphenylsilyl)oxy)ethyl)-N-ethyl-4-(phenylthio)-3-((4-sulfamoyl-2-((trifluoromethyl)sulfonyl)phenyl)amino)butanamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 1.5 h / 50 °C

2.1: water; lithium hydroxide / tetrahydrofuran; methanol / 3 h / 18 - 25 °C

2.2: 0 °C

3.1: N-ethyl-N,N-diisopropylamine; diethyl 4-oxobenzo[d][1,2,3]triazin-3(4H)-yl phosphate / tetrahydrofuran / 3 h / 18 - 25 °C

With diethyl 4-oxobenzo[d][1,2,3]triazin-3(4H)-yl phosphate; water; N-ethyl-N,N-diisopropylamine; lithium hydroxide; In tetrahydrofuran; methanol; N,N-dimethyl-formamide;