5-[2-(5-bromo-2-trifluoromethoxyphenylamino)pyrimidin-4-yl]-1-methyl-1H-pyrrole-3-carboxylic acid amide

Base Information

Chemical Name:5-[2-(5-bromo-2-trifluoromethoxyphenylamino)pyrimidin-4-yl]-1-methyl-1H-pyrrole-3-carboxylic acid amide
CAS No.:1137467-79-8
Molecular Formula:C₁₇H₁₃BrF₃N₅O₂
Molecular Weight:456.222
Hs Code.:

Synonyms:5-[2-(5-bromo-2-trifluoromethoxyphenylamino)pyrimidin-4-yl]-1-methyl-1H-pyrrole-3-carboxylic acid amide

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Chemical Property of 5-[2-(5-bromo-2-trifluoromethoxyphenylamino)pyrimidin-4-yl]-1-methyl-1H-pyrrole-3-carboxylic acid amide

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Technology Process of 5-[2-(5-bromo-2-trifluoromethoxyphenylamino)pyrimidin-4-yl]-1-methyl-1H-pyrrole-3-carboxylic acid amide

There total 6 articles about 5-[2-(5-bromo-2-trifluoromethoxyphenylamino)pyrimidin-4-yl]-1-methyl-1H-pyrrole-3-carboxylic acid amide 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: 82.0%

: sodium 5-[2-(5-bromo-2-trifluoromethoxyphenylamino)pyrimidin-4-yl]-1-methyl-1H-pyrrole-3-carboxylate

: 1137467-79-8
5-[2-(5-bromo-2-trifluoromethoxyphenylamino)pyrimidin-4-yl]-1-methyl-1H-pyrrole-3-carboxylic acid amide

Guidance literature:: With ammonium 1H-1,2,3-benzotriazol-1-ate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In dichloromethane; N,N-dimethyl-formamide; at 20 ℃;

Reference yield:

: 1137467-70-9
5-[2-(5-bromo-2-trifluoromethoxyphenylamino)pyrimidin-4-yl]-1-methyl-1H-pyrrole-3-carboxylic acid

: 1137467-79-8
5-[2-(5-bromo-2-trifluoromethoxyphenylamino)pyrimidin-4-yl]-1-methyl-1H-pyrrole-3-carboxylic acid amide

Guidance literature:: With N-hydroxybenzotriazole ammonium salt; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In dichloromethane; N,N-dimethyl-formamide; at 20 ℃; for 24h;
DOI:10.1016/j.bmcl.2011.11.065

Reference yield:

: 1137468-07-5
5-(2-amino-pyrimidin-4-yl)-1H-pyrrole-3-carboxylic acid ethyl ester

: 1137467-79-8
5-[2-(5-bromo-2-trifluoromethoxyphenylamino)pyrimidin-4-yl]-1-methyl-1H-pyrrole-3-carboxylic acid amide

Guidance literature:: Multi-step reaction with 5 steps

1: sodium hydride / tetrahydrofuran; dimethyl sulfoxide / 12 h / 20 °C

2: copper(l) iodide; cesium iodide; isopentyl nitrite / 1,2-dimethoxyethane / 6 h / 70 °C

3: palladium diacetate; potassium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl / N,N-dimethyl-formamide / 6 h / 80 °C

4: potassium hydroxide / ethanol / 3 h / 80 °C

5: N-hydroxybenzotriazole ammonium salt; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine / dichloromethane; N,N-dimethyl-formamide / 24 h / 20 °C

With copper(l) iodide; N-hydroxybenzotriazole ammonium salt; palladium diacetate; sodium hydride; potassium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; potassium hydroxide; cesium iodide; isopentyl nitrite; In tetrahydrofuran; 1,2-dimethoxyethane; ethanol; dichloromethane; dimethyl sulfoxide; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2011.11.065