Ethyl 6-(4-(3-((6-(bis(tert-butoxycarbonyl)amino)pyridin-3-yl)methyl)ureido)-2-methylbutan-2-yl)-2-(phenylamino)nicotinate

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Chemical Name:Ethyl 6-(4-(3-((6-(bis(tert-butoxycarbonyl)amino)pyridin-3-yl)methyl)ureido)-2-methylbutan-2-yl)-2-(phenylamino)nicotinate
CAS No.:1246609-94-8
Molecular Formula:C₃₆H₄₈N₆O₇
Molecular Weight:676.813
Hs Code.:

Synonyms:Ethyl 6-(4-(3-((6-(bis(tert-butoxycarbonyl)amino)pyridin-3-yl)methyl)ureido)-2-methylbutan-2-yl)-2-(phenylamino)nicotinate

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Chemical Property of Ethyl 6-(4-(3-((6-(bis(tert-butoxycarbonyl)amino)pyridin-3-yl)methyl)ureido)-2-methylbutan-2-yl)-2-(phenylamino)nicotinate

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Technology Process of Ethyl 6-(4-(3-((6-(bis(tert-butoxycarbonyl)amino)pyridin-3-yl)methyl)ureido)-2-methylbutan-2-yl)-2-(phenylamino)nicotinate

There total 5 articles about Ethyl 6-(4-(3-((6-(bis(tert-butoxycarbonyl)amino)pyridin-3-yl)methyl)ureido)-2-methylbutan-2-yl)-2-(phenylamino)nicotinate 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:

: 1027511-51-8
di(tert-butyl) [5-(aminomethyl)pyridin-2-yl]imidodicarbonate

: C₂₄H₂₈N₄O₆

: 1246609-94-8
Ethyl 6-(4-(3-((6-(bis(tert-butoxycarbonyl)amino)pyridin-3-yl)methyl)ureido)-2-methylbutan-2-yl)-2-(phenylamino)nicotinate

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

Reference yield:

: 153039-16-8
tert-butyl 3,3-dimethyl-2-oxo-pyrrolidine-1-carboxylate

: 1246609-94-8
Ethyl 6-(4-(3-((6-(bis(tert-butoxycarbonyl)amino)pyridin-3-yl)methyl)ureido)-2-methylbutan-2-yl)-2-(phenylamino)nicotinate

Guidance literature:: Multi-step reaction with 5 steps

1.1: tetrahydrofuran / 0.5 h / -70 - -45 °C

1.2: 18 °C

2.1: ethanol / 72 h / Reflux

3.1: hydrogenchloride / dichloromethane; 1,4-dioxane / 12 h / 20 °C

4.1: dmap; triethylamine / tetrahydrofuran / 0.08 h / 20 °C

5.1: dmap; triethylamine / tetrahydrofuran / 12 h / 20 °C

With hydrogenchloride; dmap; triethylamine; In tetrahydrofuran; 1,4-dioxane; ethanol; dichloromethane; 2.1: Bohlman-Rahtz Reaction;

Reference yield:

: 1246609-90-4
tert-Butyl 3,3-dimethyl-4-oxohex-5-ynylcarbamate

: 1246609-94-8
Ethyl 6-(4-(3-((6-(bis(tert-butoxycarbonyl)amino)pyridin-3-yl)methyl)ureido)-2-methylbutan-2-yl)-2-(phenylamino)nicotinate

Guidance literature:: Multi-step reaction with 4 steps

1: ethanol / 72 h / Reflux

2: hydrogenchloride / dichloromethane; 1,4-dioxane / 12 h / 20 °C

3: dmap; triethylamine / tetrahydrofuran / 0.08 h / 20 °C

4: dmap; triethylamine / tetrahydrofuran / 12 h / 20 °C

With hydrogenchloride; dmap; triethylamine; In tetrahydrofuran; 1,4-dioxane; ethanol; dichloromethane; 1: Bohlman-Rahtz Reaction;