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

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Chemical Name:N-(3-(2-(4-methylpiperazin-1-yl)-4-(pyridin-3-ylmethoxy)pyrimidin-5-ylthio)phenyl)acetamide
CAS No.:1268274-11-8
Molecular Formula:C₂₃H₂₆N₆O₂S
Molecular Weight:450.564
Hs Code.:

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

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

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

There total 6 articles about N-(3-(2-(4-methylpiperazin-1-yl)-4-(pyridin-3-ylmethoxy)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: 83.0%

: 100-55-0
3-hydroxymethylpyridin

: 1268273-98-8
N-(3-(4-chloro-2-(4-methylpiperazin-1-yl)pyrimidin-5-ylthio)phenyl)acetamide

: 1268274-11-8
N-(3-(2-(4-methylpiperazin-1-yl)-4-(pyridin-3-ylmethoxy)pyrimidin-5-ylthio)phenyl)acetamide

Guidance literature:: 3-hydroxymethylpyridin; With sodium hydride; In N,N-dimethyl-formamide; at 20 ℃; for 0.166667h; Inert atmosphere;

N-(3-(4-chloro-2-(4-methylpiperazin-1-yl)pyrimidin-5-ylthio)phenyl)acetamide; In N,N-dimethyl-formamide; at 80 ℃; for 1.5h;

Reference yield:

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

: 1268274-11-8
N-(3-(2-(4-methylpiperazin-1-yl)-4-(pyridin-3-ylmethoxy)pyrimidin-5-ylthio)phenyl)acetamide

Guidance literature:: Multi-step reaction with 6 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

4.1: trifluoroacetic acid / dichloromethane / 4.08 h / 20 °C / Inert atmosphere

5.1: trichlorophosphate / 2 h / 65 °C / Inert atmosphere

5.2: pH ~ 9

6.1: sodium hydride / N,N-dimethyl-formamide / 0.17 h / 20 °C / Inert atmosphere

6.2: 1.5 h / 80 °C

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

Reference yield:

: 1268273-94-4
5-iodo-4-(4-methoxybenzyloxy)-2-(4-methylpiperazin-1-yl)pyrimidine

: 1268274-11-8
N-(3-(2-(4-methylpiperazin-1-yl)-4-(pyridin-3-ylmethoxy)pyrimidin-5-ylthio)phenyl)acetamide

Guidance literature:: Multi-step reaction with 5 steps

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

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

3.1: trifluoroacetic acid / dichloromethane / 4.08 h / 20 °C / Inert atmosphere

4.1: trichlorophosphate / 2 h / 65 °C / Inert atmosphere

4.2: pH ~ 9

5.1: sodium hydride / N,N-dimethyl-formamide / 0.17 h / 20 °C / Inert atmosphere

5.2: 1.5 h / 80 °C

With copper(I) thiophene-2-carboxylate; sodium hydride; potassium carbonate; trifluoroacetic acid; trichlorophosphate; In dichloromethane; N,N-dimethyl-formamide;