N-(3-((2-chloro-6-fluorophenyl)ethynyl)-5-(5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl)pyridin-2-yl)-2,2,2-trifluoroacetamide

Base Information

Chemical Name:N-(3-((2-chloro-6-fluorophenyl)ethynyl)-5-(5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl)pyridin-2-yl)-2,2,2-trifluoroacetamide
CAS No.:1612287-75-8
Molecular Formula:C₂₀H₁₀ClF₇N₄O
Molecular Weight:490.767
Hs Code.:

Synonyms:N-(3-((2-chloro-6-fluorophenyl)ethynyl)-5-(5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl)pyridin-2-yl)-2,2,2-trifluoroacetamide

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Chemical Property of N-(3-((2-chloro-6-fluorophenyl)ethynyl)-5-(5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl)pyridin-2-yl)-2,2,2-trifluoroacetamide

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Technology Process of N-(3-((2-chloro-6-fluorophenyl)ethynyl)-5-(5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl)pyridin-2-yl)-2,2,2-trifluoroacetamide

There total 8 articles about N-(3-((2-chloro-6-fluorophenyl)ethynyl)-5-(5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl)pyridin-2-yl)-2,2,2-trifluoroacetamide 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: 100.0%

: 1612287-74-7
3-((2-chloro-6-fluorophenyl)ethynyl)-5-(5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl)pyridin-2-amine

: 407-25-0
trifluoroacetic anhydride

: 1612287-75-8
N-(3-((2-chloro-6-fluorophenyl)ethynyl)-5-(5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl)pyridin-2-yl)-2,2,2-trifluoroacetamide

Guidance literature:: In 1,4-dioxane; at 20 ℃; for 1h;

Reference yield:

: 10010-93-2
5-methyl-3-trifluoromethyl-1H-pyrazole

: 1612287-75-8
N-(3-((2-chloro-6-fluorophenyl)ethynyl)-5-(5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl)pyridin-2-yl)-2,2,2-trifluoroacetamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium phosphate; cis-N,N'-dimethyl-1,2-diaminocyclohexane; copper(l) iodide / 1,4-dioxane / 130 °C / Schlenk technique; Inert atmosphere

2.1: N-Bromosuccinimide / acetonitrile / 3 h / 20 °C

3.1: triethylamine / N,N-dimethyl-formamide / 0.17 h / Inert atmosphere; Microwave irradiation

3.2: 0.5 h / 120 °C

4.1: 1,4-dioxane / 1 h / 20 °C

With potassium phosphate; N-Bromosuccinimide; copper(l) iodide; triethylamine; cis-N,N'-dimethyl-1,2-diaminocyclohexane; In 1,4-dioxane; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 1072-97-5
5-bromo-2-pyridylamine

: 1612287-75-8
N-(3-((2-chloro-6-fluorophenyl)ethynyl)-5-(5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl)pyridin-2-yl)-2,2,2-trifluoroacetamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium phosphate; cis-N,N'-dimethyl-1,2-diaminocyclohexane; copper(l) iodide / 1,4-dioxane / 130 °C / Schlenk technique; Inert atmosphere

2.1: N-Bromosuccinimide / acetonitrile / 3 h / 20 °C

3.1: triethylamine / N,N-dimethyl-formamide / 0.17 h / Inert atmosphere; Microwave irradiation

3.2: 0.5 h / 120 °C

4.1: 1,4-dioxane / 1 h / 20 °C

With potassium phosphate; N-Bromosuccinimide; copper(l) iodide; triethylamine; cis-N,N'-dimethyl-1,2-diaminocyclohexane; In 1,4-dioxane; N,N-dimethyl-formamide; acetonitrile;