N-tert-butyl-3-((4-(4-(3-isoxazol-3-ylureido)benzoyl)piperazin-1-yl)methyl)benzamide

Base Information

Chemical Name:N-tert-butyl-3-((4-(4-(3-isoxazol-3-ylureido)benzoyl)piperazin-1-yl)methyl)benzamide
CAS No.:1124212-08-3
Molecular Formula:C₂₇H₃₂N₆O₄
Molecular Weight:504.589
Hs Code.:

Synonyms:N-tert-butyl-3-((4-(4-(3-isoxazol-3-ylureido)benzoyl)piperazin-1-yl)methyl)benzamide

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Chemical Property of N-tert-butyl-3-((4-(4-(3-isoxazol-3-ylureido)benzoyl)piperazin-1-yl)methyl)benzamide

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Technology Process of N-tert-butyl-3-((4-(4-(3-isoxazol-3-ylureido)benzoyl)piperazin-1-yl)methyl)benzamide

There total 7 articles about N-tert-butyl-3-((4-(4-(3-isoxazol-3-ylureido)benzoyl)piperazin-1-yl)methyl)benzamide 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:

: 1750-42-1
3-aminoisoxazole

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

: 7693-46-1
4-Nitrophenyl chloroformate

: 1124212-08-3
N-tert-butyl-3-((4-(4-(3-isoxazol-3-ylureido)benzoyl)piperazin-1-yl)methyl)benzamide

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

3-aminoisoxazole; In dichloromethane; at 20 ℃;

Reference yield:

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

: 1124212-08-3
N-tert-butyl-3-((4-(4-(3-isoxazol-3-ylureido)benzoyl)piperazin-1-yl)methyl)benzamide

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 / 20 °C

5.2: 20 °C

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

Reference yield:

: 1124211-96-6
N-tert-butyl-3-((4-(4-nitrobenzoyl)piperazin-1-yl)methyl)benzamide

: 1124212-08-3
N-tert-butyl-3-((4-(4-(3-isoxazol-3-ylureido)benzoyl)piperazin-1-yl)methyl)benzamide

Guidance literature:: Multi-step reaction with 2 steps

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

2.1: dichloromethane / 20 °C

2.2: 20 °C

With hydrogen; Raney 2800 nickel; In methanol; dichloromethane; water;