N-(4-chloro-2-(4-(3,3,3-trifluoropropyl)piperazin-1-yl)phenyl)-2,3-difluoro-4-((2-(4-(hydroxymethyl)piperidin-1-yl)acetamido)methyl)benzamide

Base Information

Chemical Name:N-(4-chloro-2-(4-(3,3,3-trifluoropropyl)piperazin-1-yl)phenyl)-2,3-difluoro-4-((2-(4-(hydroxymethyl)piperidin-1-yl)acetamido)methyl)benzamide
CAS No.:1436424-53-1
Molecular Formula:C₂₉H₃₅ClF₅N₅O₃
Molecular Weight:632.074
Hs Code.:

Synonyms:N-(4-chloro-2-(4-(3,3,3-trifluoropropyl)piperazin-1-yl)phenyl)-2,3-difluoro-4-((2-(4-(hydroxymethyl)piperidin-1-yl)acetamido)methyl)benzamide

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Chemical Property of N-(4-chloro-2-(4-(3,3,3-trifluoropropyl)piperazin-1-yl)phenyl)-2,3-difluoro-4-((2-(4-(hydroxymethyl)piperidin-1-yl)acetamido)methyl)benzamide

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Technology Process of N-(4-chloro-2-(4-(3,3,3-trifluoropropyl)piperazin-1-yl)phenyl)-2,3-difluoro-4-((2-(4-(hydroxymethyl)piperidin-1-yl)acetamido)methyl)benzamide

There total 14 articles about N-(4-chloro-2-(4-(3,3,3-trifluoropropyl)piperazin-1-yl)phenyl)-2,3-difluoro-4-((2-(4-(hydroxymethyl)piperidin-1-yl)acetamido)methyl)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:

: 6457-49-4
4-piperidinemethanol

: C₂₃H₂₃Cl₂F₅N₄O₂

: 1436424-53-1
N-(4-chloro-2-(4-(3,3,3-trifluoropropyl)piperazin-1-yl)phenyl)-2,3-difluoro-4-((2-(4-(hydroxymethyl)piperidin-1-yl)acetamido)methyl)benzamide

Guidance literature:: In N,N-dimethyl-formamide; at 80 ℃; for 1h;

Reference yield:

: 1436426-21-9
4-chloro-2-(4-(3,3,3-trifluoropropyl)piperazin-1-yl)aniline

: 1436424-53-1
N-(4-chloro-2-(4-(3,3,3-trifluoropropyl)piperazin-1-yl)phenyl)-2,3-difluoro-4-((2-(4-(hydroxymethyl)piperidin-1-yl)acetamido)methyl)benzamide

Guidance literature:: Multi-step reaction with 4 steps

1: HATU; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 12 h / 20 °C

2: hydrogenchloride / 1,4-dioxane / 12 h

3: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 0.25 h / 20 °C

4: N,N-dimethyl-formamide / 1 h / 80 °C

With hydrogenchloride; N-ethyl-N,N-diisopropylamine; HATU; In 1,4-dioxane; N,N-dimethyl-formamide;

Reference yield:

: 700-37-8
4-chloro-2-fluoro-nitrobenzene

: 1436424-53-1
N-(4-chloro-2-(4-(3,3,3-trifluoropropyl)piperazin-1-yl)phenyl)-2,3-difluoro-4-((2-(4-(hydroxymethyl)piperidin-1-yl)acetamido)methyl)benzamide

Guidance literature:: Multi-step reaction with 7 steps

1: isopropyl alcohol / 20 °C / Cooling with ice

2: N-ethyl-N,N-diisopropylamine / tetrahydrofuran; methanol / Reflux

3: ethanol; tin(ll) chloride / 1 h / 80 °C / Cooling with ice

4: HATU; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 12 h / 20 °C

5: hydrogenchloride / 1,4-dioxane / 12 h

6: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 0.25 h / 20 °C

7: N,N-dimethyl-formamide / 1 h / 80 °C

With hydrogenchloride; ethanol; N-ethyl-N,N-diisopropylamine; HATU; tin(ll) chloride; In tetrahydrofuran; 1,4-dioxane; methanol; N,N-dimethyl-formamide; isopropyl alcohol;