1-butyl-2-(ethoxycarbonyl)-N-benzyl-N-(p-methoxybenzyl)aziridine-2-carboxamide

Base Information

• Chemical Name: 1-butyl-2-(ethoxycarbonyl)-N-benzyl-N-(p-methoxybenzyl)aziridine-2-carboxamide
• CAS No.: 145126-73-4
• Molecular Formula: C₂₅H₃₂N₂O₄
• Molecular Weight: 424.54
• Mol file: 145126-73-4.mol

Synonyms:1-butyl-2-(ethoxycarbonyl)-N-benzyl-N-(p-methoxybenzyl)aziridine-2-carboxamide

Chemical Property of 1-butyl-2-(ethoxycarbonyl)-N-benzyl-N-(p-methoxybenzyl)aziridine-2-carboxamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 1-butyl-2-(ethoxycarbonyl)-N-benzyl-N-(p-methoxybenzyl)aziridine-2-carboxamide

There total 8 articles about 1-butyl-2-(ethoxycarbonyl)-N-benzyl-N-(p-methoxybenzyl)aziridine-2-carboxamide 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: 48.0%

benzyl-(4-methoxybenzyl)amine (14429-02-8) + 1-Butyl-2-chlorocarbonyl-aziridine-2-carboxylic acid ethyl ester (156641-24-6) → 1-butyl-2-(ethoxycarbonyl)-N-benzyl-N-(p-methoxybenzyl)aziridine-2-carboxamide (145126-73-4)

Guidance literature:

With sodium hydroxide; In diethyl ether; dichloromethane; for 0.5h; Ambient temperature;

DOI:10.1021/jo00052a015

Reference yield:

diethyl α,β-dibromomethylmalonate (53084-38-1) → 1-butyl-2-(ethoxycarbonyl)-N-benzyl-N-(p-methoxybenzyl)aziridine-2-carboxamide (145126-73-4)

Guidance literature:

Multi-step reaction with 4 steps

1: 87 percent / Et₃N / acetonitrile / 5 h / Ambient temperature

2: NaOH / ethanol / Ambient temperature; overnight

3: SOCl₂ / CH₂Cl₂ / 1.5 h / -78 - -30 °C

4: 48 percent / 15percent aq. NaOH / CH₂Cl₂; diethyl ether / 0.5 h / Ambient temperature

With sodium hydroxide; thionyl chloride; triethylamine; In diethyl ether; ethanol; dichloromethane; acetonitrile;

DOI:10.1021/jo00052a015

Reference yield:

N-(4-methoxylbenzylidene)benzylamine (622-72-0) → 1-butyl-2-(ethoxycarbonyl)-N-benzyl-N-(p-methoxybenzyl)aziridine-2-carboxamide (145126-73-4)

Guidance literature:

Multi-step reaction with 2 steps

1: NaBH₄ / ethanol / 1.5 h / Ambient temperature

2: 48 percent / 15percent aq. NaOH / CH₂Cl₂; diethyl ether / 0.5 h / Ambient temperature

With sodium hydroxide; sodium tetrahydroborate; In diethyl ether; ethanol; dichloromethane;

DOI:10.1021/jo00052a015

upstream raw materials:

benzyl-(4-methoxybenzyl)amine

1-Butyl-2-chlorocarbonyl-aziridine-2-carboxylic acid ethyl ester

diethyl α,β-dibromomethylmalonate

N-(4-methoxylbenzylidene)benzylamine