ethyl (5-(5-((tert-butoxycarbonyl)((2S)-2-((tert-butoxycarbonyl)amino)-3-(4-(trifluoromethyl)phenyl)propyl)amino)-1,3,4-thiadiazol-2-yl)-2-nitrophenyl)acetate

Base Information

• Chemical Name: ethyl (5-(5-((tert-butoxycarbonyl)((2S)-2-((tert-butoxycarbonyl)amino)-3-(4-(trifluoromethyl)phenyl)propyl)amino)-1,3,4-thiadiazol-2-yl)-2-nitrophenyl)acetate
• CAS No.: 1104069-92-2
• Molecular Formula: C₃₂H₃₈F₃N₅O₈S
• Molecular Weight: 709.744

Synonyms:ethyl (5-(5-((tert-butoxycarbonyl)((2S)-2-((tert-butoxycarbonyl)amino)-3-(4-(trifluoromethyl)phenyl)propyl)amino)-1,3,4-thiadiazol-2-yl)-2-nitrophenyl)acetate

Chemical Property of ethyl (5-(5-((tert-butoxycarbonyl)((2S)-2-((tert-butoxycarbonyl)amino)-3-(4-(trifluoromethyl)phenyl)propyl)amino)-1,3,4-thiadiazol-2-yl)-2-nitrophenyl)acetate

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Technology Process of ethyl (5-(5-((tert-butoxycarbonyl)((2S)-2-((tert-butoxycarbonyl)amino)-3-(4-(trifluoromethyl)phenyl)propyl)amino)-1,3,4-thiadiazol-2-yl)-2-nitrophenyl)acetate

There total 1 articles about ethyl (5-(5-((tert-butoxycarbonyl)((2S)-2-((tert-butoxycarbonyl)amino)-3-(4-(trifluoromethyl)phenyl)propyl)amino)-1,3,4-thiadiazol-2-yl)-2-nitrophenyl)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:

diethyl 2-(5-(5-((S)-2-(tert-butoxycarbonylamino)-3-(4-(trifluoromethyl)phenyl)propyl-boc-amino)-1 ,3,4-thiadiazol-2-yl)-2-nitrophenyl)malonate (1104069-89-7) → ethyl (5-(5-((tert-butoxycarbonyl)((2S)-2-((tert-butoxycarbonyl)amino)-3-(4-(trifluoromethyl)phenyl)propyl)amino)-1,3,4-thiadiazol-2-yl)-2-nitrophenyl)acetate (1104069-92-2)

Guidance literature:

With water; lithium chloride; In dimethyl sulfoxide; at 100 ℃;

Reference yield: 12.0%

ethyl (5-(5-((tert-butoxycarbonyl)((2S)-2-((tert-butoxycarbonyl)amino)-3-(4-(trifluoromethyl)phenyl)propyl)amino)-1,3,4-thiadiazol-2-yl)-2-nitrophenyl)acetate (1104069-92-2) → tert-butyl (S)-1-(5-(2-oxoindolin-5-yl)-1,3,4-thiadiazol-2-ylamino)-3-(4-(trifluoromethyl)phenyl)propan-2-ylcarbamate (1104069-95-5)

Guidance literature:

With iron; acetic acid; at 100 ℃; for 1h;

upstream raw materials:

diethyl 2-(5-(5-((S)-2-(tert-butoxycarbonylamino)-3-(4-(trifluoromethyl)phenyl)propyl-boc-amino)-1 ,3,4-thiadiazol-2-yl)-2-nitrophenyl)malonate

Downstream raw materials:

tert-butyl (S)-1-(5-(2-oxoindolin-5-yl)-1,3,4-thiadiazol-2-ylamino)-3-(4-(trifluoromethyl)phenyl)propan-2-ylcarbamate

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