tert-Butyl 4-{[4-({6-[(2-{4-[(biphenyl-2-ylcarbamoyl)oxy]piperidin-1-yl}ethyl)(methyl)amino]-6-oxohexyl}amino)phenyl]carbonyl}piperazine-1-carboxylate

Base Information

Chemical Name:tert-Butyl 4-{[4-({6-[(2-{4-[(biphenyl-2-ylcarbamoyl)oxy]piperidin-1-yl}ethyl)(methyl)amino]-6-oxohexyl}amino)phenyl]carbonyl}piperazine-1-carboxylate
CAS No.:1246248-75-8
Molecular Formula:C₄₃H₅₈N₆O₆
Molecular Weight:754.97
Hs Code.:

tert-Butyl 4-{[4-({6-[(2-{4-[(biphenyl-2-ylcarbamoyl)oxy]piperidin-1-yl}ethyl)(methyl)amino]-6-oxohexyl}amino)phenyl]carbonyl}piperazine-1-carboxylate

Synonyms:tert-Butyl 4-{[4-({6-[(2-{4-[(biphenyl-2-ylcarbamoyl)oxy]piperidin-1-yl}ethyl)(methyl)amino]-6-oxohexyl}amino)phenyl]carbonyl}piperazine-1-carboxylate

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Chemical Property of tert-Butyl 4-{[4-({6-[(2-{4-[(biphenyl-2-ylcarbamoyl)oxy]piperidin-1-yl}ethyl)(methyl)amino]-6-oxohexyl}amino)phenyl]carbonyl}piperazine-1-carboxylate

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Technology Process of tert-Butyl 4-{[4-({6-[(2-{4-[(biphenyl-2-ylcarbamoyl)oxy]piperidin-1-yl}ethyl)(methyl)amino]-6-oxohexyl}amino)phenyl]carbonyl}piperazine-1-carboxylate

There total 4 articles about tert-Butyl 4-{[4-({6-[(2-{4-[(biphenyl-2-ylcarbamoyl)oxy]piperidin-1-yl}ethyl)(methyl)amino]-6-oxohexyl}amino)phenyl]carbonyl}piperazine-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:

: 1246247-06-2
4-({6-[(2-{4-[(biphenyl-2-ylcarbamoyl)oxy]piperidin-1-yl}ethyl)(methyl)amino]-6-oxohexyl}amino)benzoic acid

: 57260-71-6
1-t-Butoxycarbonylpiperazine

: 1246248-75-8
tert-Butyl 4-{[4-({6-[(2-{4-[(biphenyl-2-ylcarbamoyl)oxy]piperidin-1-yl}ethyl)(methyl)amino]-6-oxohexyl}amino)phenyl]carbonyl}piperazine-1-carboxylate

Guidance literature:: With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In dichloromethane; at 20 ℃; for 17h;

Reference yield:

: 25542-62-5
6-bromo-hexanoic acid ethyl ester

: 1246248-75-8
tert-Butyl 4-{[4-({6-[(2-{4-[(biphenyl-2-ylcarbamoyl)oxy]piperidin-1-yl}ethyl)(methyl)amino]-6-oxohexyl}amino)phenyl]carbonyl}piperazine-1-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1.1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 72 h / 50 °C

1.2: 96 h / 50 °C

2.1: sodium hydroxide; water / ethanol / 3.5 h / 20 °C

2.3: 1 h / 20 °C

3.1: hydrogenchloride / 1,4-dioxane / 15 h / 20 °C

4.1: triethylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 17 h / 20 °C

With hydrogenchloride; water; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; N-ethyl-N,N-diisopropylamine; sodium hydroxide; In 1,4-dioxane; ethanol; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 1246247-04-0
tert-Butyl 4-[(6-ethoxy-6-oxohexyl)amino]benzoate

: 1246248-75-8
tert-Butyl 4-{[4-({6-[(2-{4-[(biphenyl-2-ylcarbamoyl)oxy]piperidin-1-yl}ethyl)(methyl)amino]-6-oxohexyl}amino)phenyl]carbonyl}piperazine-1-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium hydroxide; water / ethanol / 3.5 h / 20 °C

1.3: 1 h / 20 °C

2.1: hydrogenchloride / 1,4-dioxane / 15 h / 20 °C

3.1: triethylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 17 h / 20 °C

With hydrogenchloride; water; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; sodium hydroxide; In 1,4-dioxane; ethanol; dichloromethane;