N-tert-butyl-3-((4-(4-(3-(cyclopropylmethyl)ureido)benzoyl)piperazin-1-yl)methyl)benzamide 2,2,2-trifluoroacetate

Base Information

Chemical Name:N-tert-butyl-3-((4-(4-(3-(cyclopropylmethyl)ureido)benzoyl)piperazin-1-yl)methyl)benzamide 2,2,2-trifluoroacetate
CAS No.:1124211-89-7
Molecular Formula:C₂HF₃O₂*C₂₈H₃₇N₅O₃
Molecular Weight:605.657
Hs Code.:

Synonyms:N-tert-butyl-3-((4-(4-(3-(cyclopropylmethyl)ureido)benzoyl)piperazin-1-yl)methyl)benzamide 2,2,2-trifluoroacetate

Suppliers and Price of N-tert-butyl-3-((4-(4-(3-(cyclopropylmethyl)ureido)benzoyl)piperazin-1-yl)methyl)benzamide 2,2,2-trifluoroacetate

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 N-tert-butyl-3-((4-(4-(3-(cyclopropylmethyl)ureido)benzoyl)piperazin-1-yl)methyl)benzamide 2,2,2-trifluoroacetate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of N-tert-butyl-3-((4-(4-(3-(cyclopropylmethyl)ureido)benzoyl)piperazin-1-yl)methyl)benzamide 2,2,2-trifluoroacetate

There total 8 articles about N-tert-butyl-3-((4-(4-(3-(cyclopropylmethyl)ureido)benzoyl)piperazin-1-yl)methyl)benzamide 2,2,2-trifluoroacetate 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:

: 1124211-98-8
3-((4-(4-aminobenzoyl)piperazin-1-yl)methyl)-N-tert-butylbenzamide

: 7693-46-1
4-Nitrophenyl chloroformate

: 2516-47-4
cyclopropanemethylamine

: 1124211-89-7
N-tert-butyl-3-((4-(4-(3-(cyclopropylmethyl)ureido)benzoyl)piperazin-1-yl)methyl)benzamide 2,2,2-trifluoroacetate

Guidance literature:: 3-((4-(4-aminobenzoyl)piperazin-1-yl)methyl)-N-tert-butylbenzamide; 4-Nitrophenyl chloroformate; In dichloromethane; at -78 - 20 ℃; for 2.5h;

cyclopropanemethylamine; In dichloromethane; at 20 ℃; for 18h;

Reference yield:

: 1124211-98-8
3-((4-(4-aminobenzoyl)piperazin-1-yl)methyl)-N-tert-butylbenzamide

: 7693-46-1
4-Nitrophenyl chloroformate

: 76-05-1
trifluoroacetic acid

: 2516-47-4
cyclopropanemethylamine

: 1124211-89-7
N-tert-butyl-3-((4-(4-(3-(cyclopropylmethyl)ureido)benzoyl)piperazin-1-yl)methyl)benzamide 2,2,2-trifluoroacetate

Guidance literature:: 3-((4-(4-aminobenzoyl)piperazin-1-yl)methyl)-N-tert-butylbenzamide; 4-Nitrophenyl chloroformate; In dichloromethane; at -78 - 20 ℃;

cyclopropanemethylamine; In dichloromethane; at 20 ℃; for 18h;

trifluoroacetic acid; In water; acetonitrile;

Reference yield:

: 1094362-66-9
N-tert-butyl-3-(chloromethyl)benzamide

: 1124211-89-7
N-tert-butyl-3-((4-(4-(3-(cyclopropylmethyl)ureido)benzoyl)piperazin-1-yl)methyl)benzamide 2,2,2-trifluoroacetate

Guidance literature:: Multi-step reaction with 5 steps

1.1: N-ethyl-N,N-diisopropylamine / dimethyl sulfoxide / 20 °C / Inert atmosphere

2.1: hydrogenchloride / ethanol / 4 h / 20 °C

3.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 0 °C / Inert atmosphere

3.2: Cooling with ice

4.1: hydrogen / Raney 2800 nickel / methanol; water / 1.02 h / 20 °C / 760.05 Torr / Sealed flask

5.1: dichloromethane / -78 - 20 °C

5.2: 18 h / 20 °C

With hydrogenchloride; hydrogen; N-ethyl-N,N-diisopropylamine; Raney 2800 nickel; In methanol; ethanol; dichloromethane; water; dimethyl sulfoxide;