(+/-)-tert-Butyl 3-[3-({[4-(aminomethyl)phenyl] (cyclopentyl)acetyl}amino)-2-methyl-phenyl]propanoate

Base Information

Chemical Name:(+/-)-tert-Butyl 3-[3-({[4-(aminomethyl)phenyl] (cyclopentyl)acetyl}amino)-2-methyl-phenyl]propanoate
CAS No.:1192040-43-9
Molecular Formula:C₂₈H₃₈N₂O₃
Molecular Weight:450.621
Hs Code.:

Synonyms:(+/-)-tert-Butyl 3-[3-({[4-(aminomethyl)phenyl] (cyclopentyl)acetyl}amino)-2-methyl-phenyl]propanoate

Suppliers and Price of (+/-)-tert-Butyl 3-[3-({[4-(aminomethyl)phenyl] (cyclopentyl)acetyl}amino)-2-methyl-phenyl]propanoate

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 3-[3-({[4-(aminomethyl)phenyl] (cyclopentyl)acetyl}amino)-2-methyl-phenyl]propanoate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (+/-)-tert-Butyl 3-[3-({[4-(aminomethyl)phenyl] (cyclopentyl)acetyl}amino)-2-methyl-phenyl]propanoate

There total 8 articles about (+/-)-tert-Butyl 3-[3-({[4-(aminomethyl)phenyl] (cyclopentyl)acetyl}amino)-2-methyl-phenyl]propanoate 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: 68.0%

: 1192040-42-8
tert-butyl (+/-)-3-(3-(2-cyclopentyl-2-(4-((1,3-dioxoisoindolin-2-yl)methyl)phenyl)acetamido)-2-methylphenyl)propanoate

: 1192040-43-9
(+/-)-tert-Butyl 3-[3-({[4-(aminomethyl)phenyl] (cyclopentyl)acetyl}amino)-2-methyl-phenyl]propanoate

Guidance literature:: With hydrazine hydrate; In ethanol; Reflux;

Reference yield:

: 1663-39-4,25232-27-3
tert-Butyl acrylate

: 1192040-43-9
(+/-)-tert-Butyl 3-[3-({[4-(aminomethyl)phenyl] (cyclopentyl)acetyl}amino)-2-methyl-phenyl]propanoate

Guidance literature:: Multi-step reaction with 4 steps

1: triethylamine / palladium diacetate; tris-(o-tolyl)phosphine / N,N-dimethyl-formamide / 36 h / 125 °C / Inert atmosphere

2: hydrogen / palladium 10% on activated carbon / ethanol / 18 h / 20 °C

3: pyridine; N-[(6-chlorobenzotriazol-1-yl)oxy-(dimethylamino)methylene]-dimethyl-ammonium tetrafluoroborate / N,N-dimethyl-formamide / 0.5 h / 20 °C

4: hydrazine hydrate / ethanol / Reflux

With pyridine; N-[(6-chlorobenzotriazol-1-yl)oxy-(dimethylamino)methylene]-dimethyl-ammonium tetrafluoroborate; hydrogen; hydrazine hydrate; triethylamine; palladium 10% on activated carbon; palladium diacetate; tris-(o-tolyl)phosphine; In ethanol; N,N-dimethyl-formamide;

Reference yield:

2-bromo-6-nitrotoluene: 55289-35-5
2-bromo-6-nitrotoluene

: 1192040-43-9
(+/-)-tert-Butyl 3-[3-({[4-(aminomethyl)phenyl] (cyclopentyl)acetyl}amino)-2-methyl-phenyl]propanoate

Guidance literature:: Multi-step reaction with 4 steps

1: triethylamine / palladium diacetate; tris-(o-tolyl)phosphine / N,N-dimethyl-formamide / 36 h / 125 °C / Inert atmosphere

2: hydrogen / palladium 10% on activated carbon / ethanol / 18 h / 20 °C

3: pyridine; N-[(6-chlorobenzotriazol-1-yl)oxy-(dimethylamino)methylene]-dimethyl-ammonium tetrafluoroborate / N,N-dimethyl-formamide / 0.5 h / 20 °C

4: hydrazine hydrate / ethanol / Reflux

With pyridine; N-[(6-chlorobenzotriazol-1-yl)oxy-(dimethylamino)methylene]-dimethyl-ammonium tetrafluoroborate; hydrogen; hydrazine hydrate; triethylamine; palladium 10% on activated carbon; palladium diacetate; tris-(o-tolyl)phosphine; In ethanol; N,N-dimethyl-formamide;