N-(2-hydroxyethyl)-4-(trifluoromethyl)-2-[2-[3-(trifluoromethyl)benzyl]-2H-indazol-4-yl]-1,3-thiazole-5-carboxamide

Base Information

Chemical Name:N-(2-hydroxyethyl)-4-(trifluoromethyl)-2-[2-[3-(trifluoromethyl)benzyl]-2H-indazol-4-yl]-1,3-thiazole-5-carboxamide
CAS No.:1313197-73-7
Molecular Formula:C₂₂H₁₆F₆N₄O₂S
Molecular Weight:514.451
Hs Code.:

Synonyms:N-(2-hydroxyethyl)-4-(trifluoromethyl)-2-[2-[3-(trifluoromethyl)benzyl]-2H-indazol-4-yl]-1,3-thiazole-5-carboxamide

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Chemical Property of N-(2-hydroxyethyl)-4-(trifluoromethyl)-2-[2-[3-(trifluoromethyl)benzyl]-2H-indazol-4-yl]-1,3-thiazole-5-carboxamide

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Technology Process of N-(2-hydroxyethyl)-4-(trifluoromethyl)-2-[2-[3-(trifluoromethyl)benzyl]-2H-indazol-4-yl]-1,3-thiazole-5-carboxamide

There total 6 articles about N-(2-hydroxyethyl)-4-(trifluoromethyl)-2-[2-[3-(trifluoromethyl)benzyl]-2H-indazol-4-yl]-1,3-thiazole-5-carboxamide 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:

: 186407-74-9
4-bromoindazole

: 1313197-73-7
N-(2-hydroxyethyl)-4-(trifluoromethyl)-2-[2-[3-(trifluoromethyl)benzyl]-2H-indazol-4-yl]-1,3-thiazole-5-carboxamide

Guidance literature:: Multi-step reaction with 5 steps

1: N,N-dimethyl-formamide / 20 h / 50 °C

2: potassium acetate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / N,N-dimethyl-formamide / 14 h / 85 °C

3: sodium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,2-dimethoxyethane; water / Inert atmosphere; Reflux

4: sodium hydroxide; water / tetrahydrofuran; methanol / 7 h / 10 - 35 °C

5: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide / 10 - 35 °C

With water; potassium acetate; sodium carbonate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; sodium hydroxide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In tetrahydrofuran; methanol; 1,2-dimethoxyethane; water; N,N-dimethyl-formamide;

Reference yield:

: 1313197-75-9
4-(trifluoromethyl)-2-[2-[3-(trifluoromethyl)benzyl]-2H-indazol-4-yl]-1,3-thiazole-5-carboxylic acid

: 141-43-5
ethanolamine

: 1313197-73-7
N-(2-hydroxyethyl)-4-(trifluoromethyl)-2-[2-[3-(trifluoromethyl)benzyl]-2H-indazol-4-yl]-1,3-thiazole-5-carboxamide

Guidance literature:: With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In N,N-dimethyl-formamide; at 10 - 35 ℃;

Reference yield:

: 402-23-3
1-bromomethyl-3-trifluoromethylbenzene

: 1313197-73-7
N-(2-hydroxyethyl)-4-(trifluoromethyl)-2-[2-[3-(trifluoromethyl)benzyl]-2H-indazol-4-yl]-1,3-thiazole-5-carboxamide

Guidance literature:: Multi-step reaction with 5 steps

1: N,N-dimethyl-formamide / 20 h / 50 °C

2: potassium acetate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / N,N-dimethyl-formamide / 14 h / 85 °C

3: sodium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,2-dimethoxyethane; water / Inert atmosphere; Reflux

4: sodium hydroxide; water / tetrahydrofuran; methanol / 7 h / 10 - 35 °C

5: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide / 10 - 35 °C

With water; potassium acetate; sodium carbonate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; sodium hydroxide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In tetrahydrofuran; methanol; 1,2-dimethoxyethane; water; N,N-dimethyl-formamide;