4-((4-ethylpiperazin-1-yl)methyl)-N-(3-((4-methoxy-1H-pyrrolo[2,3-b]pyridin-5-ylmethyl)amino)-4-methylphenyl)-3-(trifluoromethyl)benzamide

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Chemical Name:4-((4-ethylpiperazin-1-yl)methyl)-N-(3-((4-methoxy-1H-pyrrolo[2,3-b]pyridin-5-ylmethyl)amino)-4-methylphenyl)-3-(trifluoromethyl)benzamide
CAS No.:1315329-35-1
Molecular Formula:C₃₁H₃₅F₃N₆O₂
Molecular Weight:580.653
Hs Code.:

Synonyms:4-((4-ethylpiperazin-1-yl)methyl)-N-(3-((4-methoxy-1H-pyrrolo[2,3-b]pyridin-5-ylmethyl)amino)-4-methylphenyl)-3-(trifluoromethyl)benzamide

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Chemical Property of 4-((4-ethylpiperazin-1-yl)methyl)-N-(3-((4-methoxy-1H-pyrrolo[2,3-b]pyridin-5-ylmethyl)amino)-4-methylphenyl)-3-(trifluoromethyl)benzamide

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Technology Process of 4-((4-ethylpiperazin-1-yl)methyl)-N-(3-((4-methoxy-1H-pyrrolo[2,3-b]pyridin-5-ylmethyl)amino)-4-methylphenyl)-3-(trifluoromethyl)benzamide

There total 4 articles about 4-((4-ethylpiperazin-1-yl)methyl)-N-(3-((4-methoxy-1H-pyrrolo[2,3-b]pyridin-5-ylmethyl)amino)-4-methylphenyl)-3-(trifluoromethyl)benzamide 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: 71.0%

: 1315466-65-9
4-((4-ethylpiperazin-1-yl)methyl)-N-(3-((4-methoxy-(1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrolo[2,3-b]pyridin-5-yl)methyl)amino)-4-methylphenyl)-3-(trifluoromethyl)benzamide

: 1315329-35-1
4-((4-ethylpiperazin-1-yl)methyl)-N-(3-((4-methoxy-1H-pyrrolo[2,3-b]pyridin-5-ylmethyl)amino)-4-methylphenyl)-3-(trifluoromethyl)benzamide

Guidance literature:: 4-((4-ethylpiperazin-1-yl)methyl)-N-(3-((4-methoxy-(1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrolo[2,3-b]pyridin-5-yl)methyl)amino)-4-methylphenyl)-3-(trifluoromethyl)benzamide; With trifluoroacetic acid; In dichloromethane; for 1h;

With lithium hydroxide monohydrate; In tetrahydrofuran; methanol; water; at 20 ℃; for 2h;

Reference yield:

: 958230-19-8
4-chloro-1H-pyrrolo[2,3-b]pyridine-5-carbaldehyde

: 1315329-35-1
4-((4-ethylpiperazin-1-yl)methyl)-N-(3-((4-methoxy-1H-pyrrolo[2,3-b]pyridin-5-ylmethyl)amino)-4-methylphenyl)-3-(trifluoromethyl)benzamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium hydride / tetrahydrofuran / 0 °C

1.2: 2 h / 0 - 20 °C

2.1: sodium / 8 h / 60 °C

3.1: acetic acid; sodium tris(acetoxy)borohydride / 1,4-dioxane / 20 °C

4.1: trifluoroacetic acid / dichloromethane / 1 h

4.2: 2 h / 20 °C

With sodium; sodium tris(acetoxy)borohydride; sodium hydride; acetic acid; trifluoroacetic acid; In tetrahydrofuran; 1,4-dioxane; dichloromethane;

Reference yield:

: 1315381-29-3
4-chloro-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-pyrrolo[2,3-b]pyridine-5-carbaldehyde

: 1315329-35-1
4-((4-ethylpiperazin-1-yl)methyl)-N-(3-((4-methoxy-1H-pyrrolo[2,3-b]pyridin-5-ylmethyl)amino)-4-methylphenyl)-3-(trifluoromethyl)benzamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium / 8 h / 60 °C

2.1: acetic acid; sodium tris(acetoxy)borohydride / 1,4-dioxane / 20 °C

3.1: trifluoroacetic acid / dichloromethane / 1 h

3.2: 2 h / 20 °C

With sodium; sodium tris(acetoxy)borohydride; acetic acid; trifluoroacetic acid; In 1,4-dioxane; dichloromethane;