tert-butyl 2-((5-(((benzyloxycarbonyl)((S)-3,3-dimethylbutan-2-yl)amino)methyl)-2-(4-(difluoromethyl)-benzamido)-1H-benzo[d]imidazol-1-yl)methyl)pyrrolidine-1-carboxylate

Base Information

Chemical Name:tert-butyl 2-((5-(((benzyloxycarbonyl)((S)-3,3-dimethylbutan-2-yl)amino)methyl)-2-(4-(difluoromethyl)-benzamido)-1H-benzo[d]imidazol-1-yl)methyl)pyrrolidine-1-carboxylate
CAS No.:1575819-90-7
Molecular Formula:C₄₀H₄₉F₂N₅O₅
Molecular Weight:717.856
Hs Code.:

tert-butyl 2-((5-(((benzyloxycarbonyl)((S)-3,3-dimethylbutan-2-yl)amino)methyl)-2-(4-(difluoromethyl)-benzamido)-1H-benzo[d]imidazol-1-yl)methyl)pyrrolidine-1-carboxylate

Synonyms:tert-butyl 2-((5-(((benzyloxycarbonyl)((S)-3,3-dimethylbutan-2-yl)amino)methyl)-2-(4-(difluoromethyl)-benzamido)-1H-benzo[d]imidazol-1-yl)methyl)pyrrolidine-1-carboxylate

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Chemical Property of tert-butyl 2-((5-(((benzyloxycarbonyl)((S)-3,3-dimethylbutan-2-yl)amino)methyl)-2-(4-(difluoromethyl)-benzamido)-1H-benzo[d]imidazol-1-yl)methyl)pyrrolidine-1-carboxylate

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Technology Process of tert-butyl 2-((5-(((benzyloxycarbonyl)((S)-3,3-dimethylbutan-2-yl)amino)methyl)-2-(4-(difluoromethyl)-benzamido)-1H-benzo[d]imidazol-1-yl)methyl)pyrrolidine-1-carboxylate

There total 6 articles about tert-butyl 2-((5-(((benzyloxycarbonyl)((S)-3,3-dimethylbutan-2-yl)amino)methyl)-2-(4-(difluoromethyl)-benzamido)-1H-benzo[d]imidazol-1-yl)methyl)pyrrolidine-1-carboxylate 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:

: 42564-51-2
4-fluoro-3-nitrobenzaldehyde

: 1575819-90-7
tert-butyl 2-((5-(((benzyloxycarbonyl)((S)-3,3-dimethylbutan-2-yl)amino)methyl)-2-(4-(difluoromethyl)-benzamido)-1H-benzo[d]imidazol-1-yl)methyl)pyrrolidine-1-carboxylate

Guidance literature:: Multi-step reaction with 6 steps

1: N-ethyl-N,N-diisopropylamine / acetonitrile / 16 h / 20 °C

2: acetic acid; sodium tris(acetoxy)borohydride / 1,2-dichloro-ethane / 6 h / 20 °C / Inert atmosphere

3: sodium hydroxide / 1,4-dioxane; water / 3 h / 10 - 20 °C

4: zinc; ammonium chloride / methanol / 2 h / 50 °C

5: ethanol / 16 h / 20 °C / Inert atmosphere

6: HATU; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 12 h / 0 - 20 °C / Inert atmosphere

With sodium tris(acetoxy)borohydride; ammonium chloride; acetic acid; N-ethyl-N,N-diisopropylamine; HATU; sodium hydroxide; zinc; In 1,4-dioxane; methanol; ethanol; water; 1,2-dichloro-ethane; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 1575819-57-6
tert-butyl 2-((4-formyl-2-nitrophenylamino)methyl)pyrrolidine-1-carboxylate

: 1575819-90-7
tert-butyl 2-((5-(((benzyloxycarbonyl)((S)-3,3-dimethylbutan-2-yl)amino)methyl)-2-(4-(difluoromethyl)-benzamido)-1H-benzo[d]imidazol-1-yl)methyl)pyrrolidine-1-carboxylate

Guidance literature:: Multi-step reaction with 5 steps

1: acetic acid; sodium tris(acetoxy)borohydride / 1,2-dichloro-ethane / 6 h / 20 °C / Inert atmosphere

2: sodium hydroxide / 1,4-dioxane; water / 3 h / 10 - 20 °C

3: zinc; ammonium chloride / methanol / 2 h / 50 °C

4: ethanol / 16 h / 20 °C / Inert atmosphere

5: HATU; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 12 h / 0 - 20 °C / Inert atmosphere

With sodium tris(acetoxy)borohydride; ammonium chloride; acetic acid; N-ethyl-N,N-diisopropylamine; HATU; sodium hydroxide; zinc; In 1,4-dioxane; methanol; ethanol; water; 1,2-dichloro-ethane; N,N-dimethyl-formamide;

Reference yield:

: 1575819-58-7
tert-butyl 2-((4-(((S)-3,3-dimethylbutan-2-ylamino)methyl)-2-nitrophenylamino)methyl)-pyrrolidine-1-carboxylate

: 1575819-90-7
tert-butyl 2-((5-(((benzyloxycarbonyl)((S)-3,3-dimethylbutan-2-yl)amino)methyl)-2-(4-(difluoromethyl)-benzamido)-1H-benzo[d]imidazol-1-yl)methyl)pyrrolidine-1-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1: sodium hydroxide / 1,4-dioxane; water / 3 h / 10 - 20 °C

2: zinc; ammonium chloride / methanol / 2 h / 50 °C

3: ethanol / 16 h / 20 °C / Inert atmosphere

4: HATU; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 12 h / 0 - 20 °C / Inert atmosphere

With ammonium chloride; N-ethyl-N,N-diisopropylamine; HATU; sodium hydroxide; zinc; In 1,4-dioxane; methanol; ethanol; water; N,N-dimethyl-formamide;