N-[4-chloro-2-[1-[3-fluoro-5-(trifluoromethyl)-2-pyridyl]pyrazole-4-carbonyl]phenyl]-3-(piperazin-1-ylmethyl)benzamide

Base Information

• Chemical Name: N-[4-chloro-2-[1-[3-fluoro-5-(trifluoromethyl)-2-pyridyl]pyrazole-4-carbonyl]phenyl]-3-(piperazin-1-ylmethyl)benzamide
• CAS No.: 1441144-43-9
• Molecular Formula: C₂₈H₂₃ClF₄N₆O₂
• Molecular Weight: 586.976
• Mol file: 1441144-43-9.mol

Synonyms:N-[4-chloro-2-[1-[3-fluoro-5-(trifluoromethyl)-2-pyridyl]pyrazole-4-carbonyl]phenyl]-3-(piperazin-1-ylmethyl)benzamide

Chemical Property of N-[4-chloro-2-[1-[3-fluoro-5-(trifluoromethyl)-2-pyridyl]pyrazole-4-carbonyl]phenyl]-3-(piperazin-1-ylmethyl)benzamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of N-[4-chloro-2-[1-[3-fluoro-5-(trifluoromethyl)-2-pyridyl]pyrazole-4-carbonyl]phenyl]-3-(piperazin-1-ylmethyl)benzamide

There total 6 articles about N-[4-chloro-2-[1-[3-fluoro-5-(trifluoromethyl)-2-pyridyl]pyrazole-4-carbonyl]phenyl]-3-(piperazin-1-ylmethyl)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:

N-[4-chloro-2-[1-[3-fluoro-5-(trifluoromethyl)-2-pyridyl]pyrazole-4-carbonyl]phenyl]-3-(piperazin-1-ylmethyl)benzamide (1450819-70-1) → N-[4-chloro-2-[1-[3-fluoro-5-(trifluoromethyl)-2-pyridyl]pyrazole-4-carbonyl]phenyl]-3-(piperazin-1-ylmethyl)benzamide (1441144-43-9)

Guidance literature:

With trifluoroacetic acid; In dichloromethane; at 20 ℃; for 0.5h;

Reference yield:

(5-chloro-2-nitro-phenyl)-(1-tritylpyrazol-4-yl)methanone (152493-32-8) → N-[4-chloro-2-[1-[3-fluoro-5-(trifluoromethyl)-2-pyridyl]pyrazole-4-carbonyl]phenyl]-3-(piperazin-1-ylmethyl)benzamide (1441144-43-9)

Guidance literature:

Multi-step reaction with 6 steps

1: iron; acetic acid / ethanol; water / 1 h / 60 °C

2: N-ethyl-N,N-diisopropylamine / dichloromethane / 5 h / 20 °C

3: trifluoroacetic acid / water / 2 h / 60 °C

4: potassium carbonate / acetonitrile / 60 °C

5: trans-N,N'-dimethyl-1,2-cyclohexyldiamine; copper(l) iodide; potassium carbonate / isopropyl alcohol / 1 h / 120 °C / Microwave irradiation

6: trifluoroacetic acid / dichloromethane / 0.5 h / 20 °C

With trans-N,N'-dimethyl-1,2-cyclohexyldiamine; copper(l) iodide; iron; potassium carbonate; acetic acid; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; In ethanol; dichloromethane; water; isopropyl alcohol; acetonitrile;

Reference yield:

3-(chloromethyl)-N-[4-chloro-2-(1-tritylpyrazole-4-carbonyl)phenyl]benzamide (1441142-15-9) → N-[4-chloro-2-[1-[3-fluoro-5-(trifluoromethyl)-2-pyridyl]pyrazole-4-carbonyl]phenyl]-3-(piperazin-1-ylmethyl)benzamide (1441144-43-9)

Guidance literature:

Multi-step reaction with 4 steps

1: trifluoroacetic acid / water / 2 h / 60 °C

2: potassium carbonate / acetonitrile / 60 °C

3: trans-N,N'-dimethyl-1,2-cyclohexyldiamine; copper(l) iodide; potassium carbonate / isopropyl alcohol / 1 h / 120 °C / Microwave irradiation

4: trifluoroacetic acid / dichloromethane / 0.5 h / 20 °C

With trans-N,N'-dimethyl-1,2-cyclohexyldiamine; copper(l) iodide; potassium carbonate; trifluoroacetic acid; In dichloromethane; water; isopropyl alcohol; acetonitrile;

upstream raw materials:

N-[4-chloro-2-[1-[3-fluoro-5-(trifluoromethyl)-2-pyridyl]pyrazole-4-carbonyl]phenyl]-3-(piperazin-1-ylmethyl)benzamide

(5-chloro-2-nitro-phenyl)-(1-tritylpyrazol-4-yl)methanone

(2-amino-5-chloro-phenyl)-(1-tritylpyrazol-4-yl)methanone

3-(chloromethyl)-N-[4-chloro-2-(1-tritylpyrazole-4-carbonyl)phenyl]benzamide