2-(2-aminopyrimidin-4-yl)-4-(2-trifluoromethylphenyl)thiazole-5-carboxamide

Base Information

Chemical Name:2-(2-aminopyrimidin-4-yl)-4-(2-trifluoromethylphenyl)thiazole-5-carboxamide
CAS No.:1612886-98-2
Molecular Formula:C₁₅H₁₀F₃N₅OS
Molecular Weight:365.339
Hs Code.:

Synonyms:2-(2-aminopyrimidin-4-yl)-4-(2-trifluoromethylphenyl)thiazole-5-carboxamide

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Chemical Property of 2-(2-aminopyrimidin-4-yl)-4-(2-trifluoromethylphenyl)thiazole-5-carboxamide

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Technology Process of 2-(2-aminopyrimidin-4-yl)-4-(2-trifluoromethylphenyl)thiazole-5-carboxamide

There total 6 articles about 2-(2-aminopyrimidin-4-yl)-4-(2-trifluoromethylphenyl)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: 37.0%

: 1612887-11-2
2-(2-aminopyrimidin-4-yl)-4-(2-trifluoromethylphenyl)thiazole-5-carboxylic acid

: 1612886-98-2
2-(2-aminopyrimidin-4-yl)-4-(2-trifluoromethylphenyl)thiazole-5-carboxamide

Guidance literature:: 2-(2-aminopyrimidin-4-yl)-4-(2-trifluoromethylphenyl)thiazole-5-carboxylic acid; With N-ethyl-N,N-diisopropylamine; HATU; In N,N-dimethyl-formamide; at 20 ℃; for 0.5h;

With ammonia; In 1,4-dioxane; N,N-dimethyl-formamide; at 20 ℃; for 2h;
DOI:10.1016/j.ejmech.2014.04.013

Reference yield:

: 36314-98-4
2-aminopyrimidine-4-carbonitrile

: 1612886-98-2
2-(2-aminopyrimidin-4-yl)-4-(2-trifluoromethylphenyl)thiazole-5-carboxamide

Guidance literature:: Multi-step reaction with 6 steps

1.1: diammonium sulfide; triethylamine; pyridine / 2 h / 52 °C

2.1: pyridine / ethanol / 16 h / Reflux

3.1: pyridine / dichloromethane / 2 h / 0 °C

4.1: trans-bis(triphenylphosphine)palladium dichloride; sodium carbonate monohydrate / water; 1,4-dioxane / 1.5 h / 60 °C

5.1: water; lithium hydroxide monohydrate / tetrahydrofuran / 14 h / 20 °C / Reflux

6.1: HATU; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 0.5 h / 20 °C

6.2: 2 h / 20 °C

With pyridine; diammonium sulfide; trans-bis(triphenylphosphine)palladium dichloride; sodium carbonate monohydrate; lithium hydroxide monohydrate; water; triethylamine; N-ethyl-N,N-diisopropylamine; HATU; In tetrahydrofuran; 1,4-dioxane; ethanol; dichloromethane; water; N,N-dimethyl-formamide; 4.1: |Suzuki Coupling;
DOI:10.1016/j.ejmech.2014.04.013

Reference yield:

: 1612886-90-4
ethyl 2-(2-aminopyrimidin-4-yl)-4-(2-trifluoromethylphenyl)thiazole-5-carboxylate

: 1612886-98-2
2-(2-aminopyrimidin-4-yl)-4-(2-trifluoromethylphenyl)thiazole-5-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: water; lithium hydroxide monohydrate / tetrahydrofuran / 14 h / 20 °C / Reflux

2.1: HATU; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 0.5 h / 20 °C

2.2: 2 h / 20 °C

With lithium hydroxide monohydrate; water; N-ethyl-N,N-diisopropylamine; HATU; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1016/j.ejmech.2014.04.013