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

Base Information

Chemical Name:tert-butyl {[6-(3-amino-3-oxopropyl)-4-(4-methylphenyl)-2-(2-methylpropyl)quinolin-3-yl]methyl}carbamate
CAS No.:660450-71-5
Molecular Formula:C₂₉H₃₇N₃O₃
Molecular Weight:475.631
Hs Code.:

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

Suppliers and Price of tert-butyl {[6-(3-amino-3-oxopropyl)-4-(4-methylphenyl)-2-(2-methylpropyl)quinolin-3-yl]methyl}carbamate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

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

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

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

There total 16 articles about tert-butyl {[6-(3-amino-3-oxopropyl)-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: 81.0%

: 660449-19-4
tert-butyl ({6-[(1E)-3-amino-3-oxoprop-1-en-1-yl]-4-(4-methylphenyl)-2-(2-methylpropyl)quinolin-3-yl}methyl)carbamate

: 660450-71-5
tert-butyl {[6-(3-amino-3-oxopropyl)-4-(4-methylphenyl)-2-(2-methylpropyl)quinolin-3-yl]methyl}carbamate

Guidance literature:: With hydrogen; 5%-palladium/activated carbon; In tetrahydrofuran; ethanol; at 20 ℃; for 12h;

Reference yield:

: C₂₁H₂₄N₂O

: 660450-71-5
tert-butyl {[6-(3-amino-3-oxopropyl)-4-(4-methylphenyl)-2-(2-methylpropyl)quinolin-3-yl]methyl}carbamate

Guidance literature:: Multi-step reaction with 6 steps

1.1: tetrahydrofuran / 96 h / 20 °C

2.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.5 h / 0 °C

3.1: bis-triphenylphosphine-palladium(II) chloride; triethylamine / N,N-dimethyl-formamide / 20 h / 70 °C / Inert atmosphere

4.1: sodium hydroxide / ethanol; water / 4 h / 60 °C

4.2: 20 °C

5.1: N-hydroxybenzotriazole ammonium salt; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 17 h / 20 °C

6.1: palladium 10% on activated carbon; hydrogen / tetrahydrofuran; ethanol / 3.5 h / 20 °C / 760.05 Torr

With bis-triphenylphosphine-palladium(II) chloride; N-hydroxybenzotriazole ammonium salt; palladium 10% on activated carbon; hydrogen; sodium hydride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; sodium hydroxide; In tetrahydrofuran; ethanol; water; N,N-dimethyl-formamide; mineral oil; 3.1: Heck reaction;
DOI:10.1016/j.bmc.2011.06.032

Reference yield:

: 660449-03-6
6-hydroxy-4-(4-methylphenyl)-2-(2-methylpropyl)quinoline-3-carbonitrile

: 660450-71-5
tert-butyl {[6-(3-amino-3-oxopropyl)-4-(4-methylphenyl)-2-(2-methylpropyl)quinolin-3-yl]methyl}carbamate

Guidance literature:: Multi-step reaction with 7 steps

1.1: ammonia; hydrogen / tetrahydrofuran; methanol; water / 8 h / 90 °C / 3750.38 Torr

2.1: tetrahydrofuran / 96 h / 20 °C

3.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.5 h / 0 °C

4.1: bis-triphenylphosphine-palladium(II) chloride; triethylamine / N,N-dimethyl-formamide / 20 h / 70 °C / Inert atmosphere

5.1: sodium hydroxide / ethanol; water / 4 h / 60 °C

5.2: 20 °C

6.1: N-hydroxybenzotriazole ammonium salt; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 17 h / 20 °C

7.1: palladium 10% on activated carbon; hydrogen / tetrahydrofuran; ethanol / 3.5 h / 20 °C / 760.05 Torr

With bis-triphenylphosphine-palladium(II) chloride; N-hydroxybenzotriazole ammonium salt; palladium 10% on activated carbon; ammonia; hydrogen; sodium hydride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; sodium hydroxide; In tetrahydrofuran; methanol; ethanol; water; N,N-dimethyl-formamide; mineral oil; 4.1: Heck reaction;
DOI:10.1016/j.bmc.2011.06.032