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

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Chemical Name:1-((1-(3-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methyl)-3-(6-((2-hydroxyethylamino)methyl)pyridin-3-yl)urea
CAS No.:1419600-99-9
Molecular Formula:C₂₀H₂₀ClF₃N₆O₂
Molecular Weight:468.866
Hs Code.:

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

There total 13 articles about 1-((1-(3-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methyl)-3-(6-((2-hydroxyethylamino)methyl)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: 56.0%

: 1419604-31-1
tert-butyl (5-(3-((1-(3-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methyl)ureido)pyridin-2-yl)methyl(2-methoxyethyl)carbamate

: 1419600-99-9
1-((1-(3-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methyl)-3-(6-((2-hydroxyethylamino)methyl)pyridin-3-yl)urea

Guidance literature:: With boron tribromide; In dichloromethane; at -78 ℃; for 3h;

Reference yield:

: 14763-20-3
3-chlorophenyl hydrazine

: 1419600-99-9
1-((1-(3-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methyl)-3-(6-((2-hydroxyethylamino)methyl)pyridin-3-yl)urea

Guidance literature:: Multi-step reaction with 6 steps

1: ethanol / 3 h / Reflux

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

3: 1-methyl-pyrrolidin-2-one / 2 h / 200 °C

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

5: triethylamine / dichloromethane / 16 h / 23 °C

6: boron tribromide / dichloromethane / 3 h / -78 °C

With ammonia; hydrogen; boron tribromide; triethylamine; potassium iodide; isopentyl nitrite; In 1-methyl-pyrrolidin-2-one; methanol; ethanol; dichloromethane; acetonitrile;

Reference yield:

: 55338-73-3
5-amino-2-cyanopyridine

: 1419600-99-9
1-((1-(3-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methyl)-3-(6-((2-hydroxyethylamino)methyl)pyridin-3-yl)urea

Guidance literature:: Multi-step reaction with 8 steps

1: sodium hydride / N,N-dimethyl-formamide / 3 h / 0 - 23 °C

2: diisobutylaluminium hydride / tetrahydrofuran; toluene / 3 h / -78 °C

3: sodium tris(acetoxy)borohydride; acetic acid / tetrahydrofuran / 3 h / 0 - 23 °C

4: sulfuric acid / 3 h / 50 °C

5: pyridine / acetone / 1 h / 0 - 23 °C

6: triethylamine / dichloromethane / 1 h / 0 - 23 °C

7: triethylamine / dichloromethane / 16 h / 23 °C

8: boron tribromide / dichloromethane / 3 h / -78 °C

With pyridine; sulfuric acid; boron tribromide; sodium tris(acetoxy)borohydride; sodium hydride; diisobutylaluminium hydride; acetic acid; triethylamine; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; acetone; toluene;