tert-butyl {[6-((2-[(tert-butoxycarbonyl)amino]ethyl)amino)-4-(4-methylphenyl)-2-(2-methylpropyl)quinolin-3-yl]methyl}carbamate

Base Information

Chemical Name:tert-butyl {[6-((2-[(tert-butoxycarbonyl)amino]ethyl)amino)-4-(4-methylphenyl)-2-(2-methylpropyl)quinolin-3-yl]methyl}carbamate
CAS No.:660451-36-5
Molecular Formula:C₃₃H₄₆N₄O₄
Molecular Weight:562.753
Hs Code.:

Synonyms:tert-butyl {[6-((2-[(tert-butoxycarbonyl)amino]ethyl)amino)-4-(4-methylphenyl)-2-(2-methylpropyl)quinolin-3-yl]methyl}carbamate

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Chemical Property of tert-butyl {[6-((2-[(tert-butoxycarbonyl)amino]ethyl)amino)-4-(4-methylphenyl)-2-(2-methylpropyl)quinolin-3-yl]methyl}carbamate

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Technology Process of tert-butyl {[6-((2-[(tert-butoxycarbonyl)amino]ethyl)amino)-4-(4-methylphenyl)-2-(2-methylpropyl)quinolin-3-yl]methyl}carbamate

There total 12 articles about tert-butyl {[6-((2-[(tert-butoxycarbonyl)amino]ethyl)amino)-4-(4-methylphenyl)-2-(2-methylpropyl)quinolin-3-yl]methyl}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:

: 24424-99-5
di-tert-butyl dicarbonate

: C₂₈H₃₈N₄O₂

: 660451-36-5
tert-butyl {[6-((2-[(tert-butoxycarbonyl)amino]ethyl)amino)-4-(4-methylphenyl)-2-(2-methylpropyl)quinolin-3-yl]methyl}carbamate

Guidance literature:: In tetrahydrofuran; at 20 ℃; for 0.5h;
DOI:10.1016/j.bmc.2011.06.032

Reference yield:

: 304854-54-4
2-amino-5-bromo-N-methoxy-N-methyl-benzamide

: 660451-36-5
tert-butyl {[6-((2-[(tert-butoxycarbonyl)amino]ethyl)amino)-4-(4-methylphenyl)-2-(2-methylpropyl)quinolin-3-yl]methyl}carbamate

Guidance literature:: Multi-step reaction with 6 steps

1: tetrahydrofuran; diethyl ether / 0 °C

2: methanesulfonic acid / toluene / 6 h / Reflux

3: palladium diacetate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; sodium t-butanolate / toluene / 1 h / 90 °C / Inert atmosphere

4: tetrahydrofuran / 1 h / 20 °C

5: ammonia; hydrogen / tetrahydrofuran; methanol; water / 6 h / 20 °C / 3750.38 Torr

6: tetrahydrofuran / 0.5 h / 20 °C

With methanesulfonic acid; ammonia; hydrogen; palladium diacetate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; sodium t-butanolate; In tetrahydrofuran; methanol; diethyl ether; water; toluene; 2: Friedlaender synthesis;
DOI:10.1016/j.bmc.2011.06.032

Reference yield:

: 660451-32-1
6-bromo-4-(4-methylphenyl)-2-(2-methylpropyl)quinoline-3-carbonitrile

: 660451-36-5
tert-butyl {[6-((2-[(tert-butoxycarbonyl)amino]ethyl)amino)-4-(4-methylphenyl)-2-(2-methylpropyl)quinolin-3-yl]methyl}carbamate

Guidance literature:: Multi-step reaction with 4 steps

1: palladium diacetate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; sodium t-butanolate / toluene / 1 h / 90 °C / Inert atmosphere

2: tetrahydrofuran / 1 h / 20 °C

3: ammonia; hydrogen / tetrahydrofuran; methanol; water / 6 h / 20 °C / 3750.38 Torr

4: tetrahydrofuran / 0.5 h / 20 °C

With ammonia; hydrogen; palladium diacetate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; sodium t-butanolate; In tetrahydrofuran; methanol; water; toluene;
DOI:10.1016/j.bmc.2011.06.032