N-(3-(4-(4-methoxybenzyloxy)-2-(4-methylpiperazin-1-yl)pyrimidin-5-ylthio)phenyl)acetamide

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Chemical Name:N-(3-(4-(4-methoxybenzyloxy)-2-(4-methylpiperazin-1-yl)pyrimidin-5-ylthio)phenyl)acetamide
CAS No.:1268273-96-6
Molecular Formula:C₂₅H₂₉N₅O₃S
Molecular Weight:479.603
Hs Code.:

Synonyms:N-(3-(4-(4-methoxybenzyloxy)-2-(4-methylpiperazin-1-yl)pyrimidin-5-ylthio)phenyl)acetamide

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Chemical Property of N-(3-(4-(4-methoxybenzyloxy)-2-(4-methylpiperazin-1-yl)pyrimidin-5-ylthio)phenyl)acetamide

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Technology Process of N-(3-(4-(4-methoxybenzyloxy)-2-(4-methylpiperazin-1-yl)pyrimidin-5-ylthio)phenyl)acetamide

There total 5 articles about N-(3-(4-(4-methoxybenzyloxy)-2-(4-methylpiperazin-1-yl)pyrimidin-5-ylthio)phenyl)acetamide 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: 88.0%

: 1268273-95-5
3-(4-(4-methoxybenzyloxy)-2-(4-methylpiperazin-1-yl)pyrimidin-5-ylthio)aniline

: 108-24-7
acetic anhydride

: 1268273-96-6
N-(3-(4-(4-methoxybenzyloxy)-2-(4-methylpiperazin-1-yl)pyrimidin-5-ylthio)phenyl)acetamide

Guidance literature:: 3-(4-(4-methoxybenzyloxy)-2-(4-methylpiperazin-1-yl)pyrimidin-5-ylthio)aniline; acetic anhydride; In dichloromethane; at 20 ℃; for 3h; Inert atmosphere;

With sodium carbonate; In dichloromethane;

Reference yield:

: 105-13-5
4-Methoxybenzyl alcohol

: 1268273-96-6
N-(3-(4-(4-methoxybenzyloxy)-2-(4-methylpiperazin-1-yl)pyrimidin-5-ylthio)phenyl)acetamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: potassium hydroxide / 18-crown-6 ether / toluene / 1 h / 20 °C / Inert atmosphere

2.1: N,N-dimethyl-formamide / 1.5 h / 80 °C / Inert atmosphere

3.1: trifluoroacetic acid; N-iodo-succinimide / acetonitrile / 1 h / 20 °C / Inert atmosphere

3.2: 0.03 h

4.1: potassium carbonate; copper(I) thiophene-2-carboxylate / N,N-dimethyl-formamide / 25 h / 120 °C / Inert atmosphere

5.1: dichloromethane / 3 h / 20 °C / Inert atmosphere

With N-iodo-succinimide; copper(I) thiophene-2-carboxylate; potassium carbonate; trifluoroacetic acid; potassium hydroxide; 18-crown-6 ether; In dichloromethane; N,N-dimethyl-formamide; toluene; acetonitrile;

Reference yield:

: 1268273-93-3
4-(4-methoxybenzyloxy)-2-(4-methylpiperazin-1-yl)pyrimidine

: 1268273-96-6
N-(3-(4-(4-methoxybenzyloxy)-2-(4-methylpiperazin-1-yl)pyrimidin-5-ylthio)phenyl)acetamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: trifluoroacetic acid; N-iodo-succinimide / acetonitrile / 1 h / 20 °C / Inert atmosphere

1.2: 0.03 h

2.1: potassium carbonate; copper(I) thiophene-2-carboxylate / N,N-dimethyl-formamide / 25 h / 120 °C / Inert atmosphere

3.1: dichloromethane / 3 h / 20 °C / Inert atmosphere

With N-iodo-succinimide; copper(I) thiophene-2-carboxylate; potassium carbonate; trifluoroacetic acid; In dichloromethane; N,N-dimethyl-formamide; acetonitrile;