1-((1-(3-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methyl)-3-(6-(2-(methylsulfonyl)ethyl)pyridin-3-yl)urea

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Chemical Name:1-((1-(3-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methyl)-3-(6-(2-(methylsulfonyl)ethyl)pyridin-3-yl)urea
CAS No.:1419597-47-9
Molecular Formula:C₂₀H₁₉ClF₃N₅O₃S
Molecular Weight:501.917
Hs Code.:

Synonyms:1-((1-(3-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methyl)-3-(6-(2-(methylsulfonyl)ethyl)pyridin-3-yl)urea

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Chemical Property of 1-((1-(3-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methyl)-3-(6-(2-(methylsulfonyl)ethyl)pyridin-3-yl)urea

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Technology Process of 1-((1-(3-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methyl)-3-(6-(2-(methylsulfonyl)ethyl)pyridin-3-yl)urea

There total 10 articles about 1-((1-(3-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methyl)-3-(6-(2-(methylsulfonyl)ethyl)pyridin-3-yl)urea 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: 46.0%

: 1146222-03-8
6-(2-(methylsulfonyl)ethyl)pyridin-3-amine

: 1360686-94-7
phenyl (1-(3-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methylcarbamate

: 1419597-47-9
1-((1-(3-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methyl)-3-(6-(2-(methylsulfonyl)ethyl)pyridin-3-yl)urea

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; at 150 ℃; for 1h; under 5250.53 Torr; Microwave irradiation;

Reference yield:

: 14763-20-3
3-chlorophenyl hydrazine

: 1419597-47-9
1-((1-(3-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methyl)-3-(6-(2-(methylsulfonyl)ethyl)pyridin-3-yl)urea

Guidance literature:: Multi-step reaction with 6 steps

1: ethanol / 5 h / Reflux

2: N-chloro-succinimide / N,N-dimethyl-formamide / 3.25 h / 23 °C

3: triethylamine / toluene / 20 h / 80 °C

4: hydrogen; ammonia / methanol / 80 °C / 7500.75 Torr

5: triethylamine / dichloromethane / 23 °C

6: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 1 h / 150 °C / 5250.53 Torr / Microwave irradiation

With N-chloro-succinimide; ammonia; hydrogen; triethylamine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; methanol; ethanol; dichloromethane; N,N-dimethyl-formamide; toluene;

Reference yield:

: 108-42-9
3-chloro-aniline

: 1419597-47-9
1-((1-(3-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methyl)-3-(6-(2-(methylsulfonyl)ethyl)pyridin-3-yl)urea

Guidance literature:: Multi-step reaction with 7 steps

1.1: hydrogenchloride / water / 0.17 h / -5 - 0 °C

1.2: 5 h / -5 - 0 °C

2.1: ethanol / 3 h / Reflux

3.1: potassium iodide; isopentyl nitrite / acetonitrile / 20 h / 0 - 1000 °C

4.1: 1-methyl-pyrrolidin-2-one / 2 h / 200 °C

5.1: hydrogen; ammonia / methanol / 80 °C / 7500.75 Torr

6.1: triethylamine / dichloromethane / 23 °C

7.1: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 1 h / 150 °C / 5250.53 Torr / Microwave irradiation

With hydrogenchloride; ammonia; hydrogen; triethylamine; N-ethyl-N,N-diisopropylamine; potassium iodide; isopentyl nitrite; In tetrahydrofuran; 1-methyl-pyrrolidin-2-one; methanol; ethanol; dichloromethane; water; acetonitrile;