N-(4-cyanophenyl)-3-(4-(2-((4-methoxybenzyl)amino)ethoxy)phenyl)-N-methylimidazo[1,2-a]pyrazine-6-carboxamide

Base Information

• Chemical Name: N-(4-cyanophenyl)-3-(4-(2-((4-methoxybenzyl)amino)ethoxy)phenyl)-N-methylimidazo[1,2-a]pyrazine-6-carboxamide
• CAS No.: 1610671-16-3
• Molecular Formula: C₃₁H₂₈N₆O₃
• Molecular Weight: 532.602
• Mol file: 1610671-16-3.mol

Synonyms:N-(4-cyanophenyl)-3-(4-(2-((4-methoxybenzyl)amino)ethoxy)phenyl)-N-methylimidazo[1,2-a]pyrazine-6-carboxamide

Chemical Property of N-(4-cyanophenyl)-3-(4-(2-((4-methoxybenzyl)amino)ethoxy)phenyl)-N-methylimidazo[1,2-a]pyrazine-6-carboxamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of N-(4-cyanophenyl)-3-(4-(2-((4-methoxybenzyl)amino)ethoxy)phenyl)-N-methylimidazo[1,2-a]pyrazine-6-carboxamide

There total 6 articles about N-(4-cyanophenyl)-3-(4-(2-((4-methoxybenzyl)amino)ethoxy)phenyl)-N-methylimidazo[1,2-a]pyrazine-6-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:

3-(4-(2-((4-methoxybenzyl)amino)ethoxy)phenyl)imidazo[1,2-a]pyrazine-6-carbonyl chloride (1610671-14-1) + 4-cyano-N-methylaniline (4714-62-9) → N-(4-cyanophenyl)-3-(4-(2-((4-methoxybenzyl)amino)ethoxy)phenyl)-N-methylimidazo[1,2-a]pyrazine-6-carboxamide (1610671-16-3)

Guidance literature:

In dichloromethane; at 20 ℃;

Reference yield:

(4-(cyanomethoxy)phenyl)boronic acid (947533-23-5) → N-(4-cyanophenyl)-3-(4-(2-((4-methoxybenzyl)amino)ethoxy)phenyl)-N-methylimidazo[1,2-a]pyrazine-6-carboxamide (1610671-16-3)

Guidance literature:

Multi-step reaction with 5 steps

1.1: dipotassium hydrogenphosphate / tetrahydrofuran; water / 0.75 h / 150 °C / Microwave irradiation

2.1: sodium tetrahydroborate; nickel dichloride / ethanol / 0.17 h / 0 °C

3.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 12 h / 20 °C

4.1: sodium hydroxide / acetonitrile / 12 h / 20 °C

4.2: 20 °C

5.1: dichloromethane / 20 °C

With sodium tetrahydroborate; dipotassium hydrogenphosphate; N-ethyl-N,N-diisopropylamine; sodium hydroxide; nickel dichloride; In tetrahydrofuran; ethanol; dichloromethane; water; acetonitrile; 1.1: |Suzuki Coupling;

Reference yield:

methyl 3-bromoimidazo[1,2-a]pyrazine-6-carboxylate (1607830-93-2) → N-(4-cyanophenyl)-3-(4-(2-((4-methoxybenzyl)amino)ethoxy)phenyl)-N-methylimidazo[1,2-a]pyrazine-6-carboxamide (1610671-16-3)

Guidance literature:

Multi-step reaction with 5 steps

1.1: dipotassium hydrogenphosphate / tetrahydrofuran; water / 0.75 h / 150 °C / Microwave irradiation

2.1: sodium tetrahydroborate; nickel dichloride / ethanol / 0.17 h / 0 °C

3.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 12 h / 20 °C

4.1: sodium hydroxide / acetonitrile / 12 h / 20 °C

4.2: 20 °C

5.1: dichloromethane / 20 °C

With sodium tetrahydroborate; dipotassium hydrogenphosphate; N-ethyl-N,N-diisopropylamine; sodium hydroxide; nickel dichloride; In tetrahydrofuran; ethanol; dichloromethane; water; acetonitrile; 1.1: |Suzuki Coupling;

upstream raw materials:

methyl 3-bromoimidazo[1,2-a]pyrazine-6-carboxylate

(4-(cyanomethoxy)phenyl)boronic acid

methyl 3-(4-(cyanomethoxy)phenyl)imidazo[1,2-a]pyrazine-6-carboxylate

methyl 3-(4-(2-aminoethoxy)phenyl)imidazo[1,2-a]pyrazine-6-carboxylate

Downstream raw materials:

3-[4-(2-aminoethoxy)phenyl]-N-(4-cyanophenyl)-N-methylimidazo[1,2-a]pyrazine-6-carboxamide