(R)-ethyl 2-(N-(4-((tert-butoxycarbonyl)amino)-1-phenylbutan-2-yl)-2-(trifluoromethoxy)phenylsulfonamido)acetate

Base Information

Chemical Name:(R)-ethyl 2-(N-(4-((tert-butoxycarbonyl)amino)-1-phenylbutan-2-yl)-2-(trifluoromethoxy)phenylsulfonamido)acetate
CAS No.:1433993-01-1
Molecular Formula:C₂₆H₃₃F₃N₂O₇S
Molecular Weight:574.618
Hs Code.:

Synonyms:(R)-ethyl 2-(N-(4-((tert-butoxycarbonyl)amino)-1-phenylbutan-2-yl)-2-(trifluoromethoxy)phenylsulfonamido)acetate

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Chemical Property of (R)-ethyl 2-(N-(4-((tert-butoxycarbonyl)amino)-1-phenylbutan-2-yl)-2-(trifluoromethoxy)phenylsulfonamido)acetate

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Technology Process of (R)-ethyl 2-(N-(4-((tert-butoxycarbonyl)amino)-1-phenylbutan-2-yl)-2-(trifluoromethoxy)phenylsulfonamido)acetate

There total 4 articles about (R)-ethyl 2-(N-(4-((tert-butoxycarbonyl)amino)-1-phenylbutan-2-yl)-2-(trifluoromethoxy)phenylsulfonamido)acetate 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:

: 24424-99-5
di-tert-butyl dicarbonate

: 1433993-00-0
(R)-ethyl 2-(N-(4-amino-1-phenylbutan-2-yl)-2-(trifluoromethoxy)phenylsulfonamido)acetate trifluoroacetate

: 1433993-01-1
(R)-ethyl 2-(N-(4-((tert-butoxycarbonyl)amino)-1-phenylbutan-2-yl)-2-(trifluoromethoxy)phenylsulfonamido)acetate

Guidance literature:: With dmap; triethylamine; In dichloromethane; at 20 ℃; for 12h;

Reference yield:

: 1433992-98-3
(R)-ethyl 2-(N-(1-cyano-3-phenylpropan-2-yl)-2-(trifluoromethoxy)phenylsulfonamido)acetate

: 1433993-01-1
(R)-ethyl 2-(N-(4-((tert-butoxycarbonyl)amino)-1-phenylbutan-2-yl)-2-(trifluoromethoxy)phenylsulfonamido)acetate

Guidance literature:: Multi-step reaction with 2 steps

1: platinum on activated charcoal; platinum(IV) oxide; hydrogen / methanol / 12 h / 2482.38 Torr

2: dmap; triethylamine / dichloromethane / 12 h / 20 °C

With dmap; platinum(IV) oxide; platinum on activated charcoal; hydrogen; triethylamine; In methanol; dichloromethane;

Reference yield:

: 1433992-96-1
(R)-N-(1-cyano-3-phenylpropan-2-yl)-2-(trifluoromethoxy)benzenesulfonamide

: 1433993-01-1
(R)-ethyl 2-(N-(4-((tert-butoxycarbonyl)amino)-1-phenylbutan-2-yl)-2-(trifluoromethoxy)phenylsulfonamido)acetate

Guidance literature:: Multi-step reaction with 3 steps

1: potassium carbonate / N,N-dimethyl-formamide / 12 h / 20 °C

2: platinum on activated charcoal; platinum(IV) oxide; hydrogen / methanol / 12 h / 2482.38 Torr

3: dmap; triethylamine / dichloromethane / 12 h / 20 °C

With dmap; platinum(IV) oxide; platinum on activated charcoal; hydrogen; potassium carbonate; triethylamine; In methanol; dichloromethane; N,N-dimethyl-formamide;