tert-butyl {5-[({4-[3-(2-cyclohexylethoxy)benzoyl]piperazin-1-yl}carbonyl)amino]pyridin-3-yl}carbamate

Base Information

Chemical Name:tert-butyl {5-[({4-[3-(2-cyclohexylethoxy)benzoyl]piperazin-1-yl}carbonyl)amino]pyridin-3-yl}carbamate
CAS No.:1008775-39-0
Molecular Formula:C₃₀H₄₁N₅O₅
Molecular Weight:551.686
Hs Code.:

Synonyms:tert-butyl {5-[({4-[3-(2-cyclohexylethoxy)benzoyl]piperazin-1-yl}carbonyl)amino]pyridin-3-yl}carbamate

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Chemical Property of tert-butyl {5-[({4-[3-(2-cyclohexylethoxy)benzoyl]piperazin-1-yl}carbonyl)amino]pyridin-3-yl}carbamate

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Technology Process of tert-butyl {5-[({4-[3-(2-cyclohexylethoxy)benzoyl]piperazin-1-yl}carbonyl)amino]pyridin-3-yl}carbamate

There total 3 articles about tert-butyl {5-[({4-[3-(2-cyclohexylethoxy)benzoyl]piperazin-1-yl}carbonyl)amino]pyridin-3-yl}carbamate 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:

: 1008774-26-2
1-[3-(2-cyclohexylethoxy)benzoyl]piperazine hydrochloride

: C₁₁H₁₃N₃O₃

: 1008775-39-0
tert-butyl {5-[({4-[3-(2-cyclohexylethoxy)benzoyl]piperazin-1-yl}carbonyl)amino]pyridin-3-yl}carbamate

Guidance literature:: With triethylamine; In tetrahydrofuran; toluene; at 20 ℃; for 15h;

Reference yield:

: C₁₁H₁₃N₅O₃

: 1008775-39-0
tert-butyl {5-[({4-[3-(2-cyclohexylethoxy)benzoyl]piperazin-1-yl}carbonyl)amino]pyridin-3-yl}carbamate

Guidance literature:: Multi-step reaction with 2 steps

1: toluene / 3 h / 110 °C

2: triethylamine / tetrahydrofuran; toluene / 15 h / 20 °C

With triethylamine; In tetrahydrofuran; toluene;

Reference yield:

: 337904-92-4
5-[(tert-butoxycarbonyl)amino]nicotinic acid

: 1008775-39-0
tert-butyl {5-[({4-[3-(2-cyclohexylethoxy)benzoyl]piperazin-1-yl}carbonyl)amino]pyridin-3-yl}carbamate

Guidance literature:: Multi-step reaction with 3 steps

1: diphenyl phosphoryl azide; triethylamine / toluene / 1 h

2: toluene / 3 h / 110 °C

3: triethylamine / tetrahydrofuran; toluene / 15 h / 20 °C

With diphenyl phosphoryl azide; triethylamine; In tetrahydrofuran; toluene;