N-(3-((2-((2-methoxy-4-(4-methylpiperazin-1-yl)phenyl)amino)quinazolin-4-yl)oxy)phenyl)acrylamide

Base Information

Chemical Name:N-(3-((2-((2-methoxy-4-(4-methylpiperazin-1-yl)phenyl)amino)quinazolin-4-yl)oxy)phenyl)acrylamide
CAS No.:1313036-18-8
Molecular Formula:C₂₉H₃₀N₆O₃
Molecular Weight:510.596
Hs Code.:

Synonyms:N-(3-((2-((2-methoxy-4-(4-methylpiperazin-1-yl)phenyl)amino)quinazolin-4-yl)oxy)phenyl)acrylamide

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Chemical Property of N-(3-((2-((2-methoxy-4-(4-methylpiperazin-1-yl)phenyl)amino)quinazolin-4-yl)oxy)phenyl)acrylamide

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Technology Process of N-(3-((2-((2-methoxy-4-(4-methylpiperazin-1-yl)phenyl)amino)quinazolin-4-yl)oxy)phenyl)acrylamide

There total 9 articles about N-(3-((2-((2-methoxy-4-(4-methylpiperazin-1-yl)phenyl)amino)quinazolin-4-yl)oxy)phenyl)acrylamide 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: 84.1%

: 1313036-49-5
4-(3-aminophenoxy)-N-(2-methoxy-4-(4-methylpiperazin-1-yl)phenyl)quinazolin-2-amine

: 814-68-6,25189-84-8
acryloyl chloride

: 1313036-18-8
N-(3-((2-((2-methoxy-4-(4-methylpiperazin-1-yl)phenyl)amino)quinazolin-4-yl)oxy)phenyl)acrylamide

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 0 ℃; for 0.5h;

Reference yield:

: 109-01-3
1-methyl-piperazine

: 1313036-18-8
N-(3-((2-((2-methoxy-4-(4-methylpiperazin-1-yl)phenyl)amino)quinazolin-4-yl)oxy)phenyl)acrylamide

Guidance literature:: Multi-step reaction with 5 steps

1: potassium carbonate / N,N-dimethyl-formamide / 20 °C

2: hydrogen / palladium 10% on activated carbon / ethanol / 2 h

3: toluene-4-sulfonic acid / isopropyl alcohol / 0.5 h / 100 °C

4: hydrogen / palladium 10% on activated carbon / ethanol / 0.5 h

5: N-ethyl-N,N-diisopropylamine / dichloromethane / 0.5 h / 0 °C

With hydrogen; potassium carbonate; toluene-4-sulfonic acid; N-ethyl-N,N-diisopropylamine; palladium 10% on activated carbon; In ethanol; dichloromethane; N,N-dimethyl-formamide; isopropyl alcohol; 3: Buckwald's amination;

Reference yield:

: 86-96-4
quinazoline-2,4-diol

: 1313036-18-8
N-(3-((2-((2-methoxy-4-(4-methylpiperazin-1-yl)phenyl)amino)quinazolin-4-yl)oxy)phenyl)acrylamide

Guidance literature:: Multi-step reaction with 5 steps

1: N-ethyl-N,N-diisopropylamine; trichlorophosphate / 3 h / 110 °C

2: potassium carbonate / N,N-dimethyl-formamide / 2 h / 60 °C

3: toluene-4-sulfonic acid / isopropyl alcohol / 0.5 h / 100 °C

4: hydrogen / palladium 10% on activated carbon / ethanol / 0.5 h

5: N-ethyl-N,N-diisopropylamine / dichloromethane / 0.5 h / 0 °C

With hydrogen; potassium carbonate; toluene-4-sulfonic acid; N-ethyl-N,N-diisopropylamine; trichlorophosphate; palladium 10% on activated carbon; In ethanol; dichloromethane; N,N-dimethyl-formamide; isopropyl alcohol; 3: Buckwald's amination;