5-butyl-N-((1-methyl-1H-imidazol-5-yl)methyl)-1-(5-methyl-4-phenoxypyrimidin-2-yl)-1H-pyrazole-4-carboxamide

Base Information

• Chemical Name: 5-butyl-N-((1-methyl-1H-imidazol-5-yl)methyl)-1-(5-methyl-4-phenoxypyrimidin-2-yl)-1H-pyrazole-4-carboxamide
• CAS No.: 1019253-57-6
• Molecular Formula: C₂₄H₂₇N₇O₂
• Molecular Weight: 445.524
• Mol file: 1019253-57-6.mol

Synonyms:5-butyl-N-((1-methyl-1H-imidazol-5-yl)methyl)-1-(5-methyl-4-phenoxypyrimidin-2-yl)-1H-pyrazole-4-carboxamide

Chemical Property of 5-butyl-N-((1-methyl-1H-imidazol-5-yl)methyl)-1-(5-methyl-4-phenoxypyrimidin-2-yl)-1H-pyrazole-4-carboxamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 5-butyl-N-((1-methyl-1H-imidazol-5-yl)methyl)-1-(5-methyl-4-phenoxypyrimidin-2-yl)-1H-pyrazole-4-carboxamide

There total 9 articles about 5-butyl-N-((1-methyl-1H-imidazol-5-yl)methyl)-1-(5-methyl-4-phenoxypyrimidin-2-yl)-1H-pyrazole-4-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:

5-butyl-1-(4-chloro-5-methylpyrimidin-2-yl)-N-((1-methyl-1H-imidazol-5-yl)methyl)-1H-pyrazole-4-carboxamide (1019253-53-2) + phenol (108-95-2,27073-41-2) → 5-butyl-N-((1-methyl-1H-imidazol-5-yl)methyl)-1-(5-methyl-4-phenoxypyrimidin-2-yl)-1H-pyrazole-4-carboxamide (1019253-57-6)

Guidance literature:

With sodium hydride; In N,N-dimethyl-formamide;

Reference yield:

C19H30N4O3Si (1019258-13-9) → 5-butyl-N-((1-methyl-1H-imidazol-5-yl)methyl)-1-(5-methyl-4-phenoxypyrimidin-2-yl)-1H-pyrazole-4-carboxamide (1019253-57-6)

Guidance literature:

Multi-step reaction with 5 steps

1.1: tetrabutyl ammonium fluoride / tetrahydrofuran; acetonitrile / 20 °C

2.1: methanol; lithium hydroxide; water / 50 °C

2.2: pH 3

3.1: trichlorophosphate / 2 h / 100 °C

4.1: 0.5 h / 20 °C

5.1: sodium hydride / N,N-dimethyl-formamide

With methanol; lithium hydroxide; tetrabutyl ammonium fluoride; water; sodium hydride; trichlorophosphate; In tetrahydrofuran; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

2-chloro-5-methyl-4-(2-trimethylsilanylethoxy)pyrimidine (204636-94-2) → 5-butyl-N-((1-methyl-1H-imidazol-5-yl)methyl)-1-(5-methyl-4-phenoxypyrimidin-2-yl)-1H-pyrazole-4-carboxamide (1019253-57-6)

Guidance literature:

Multi-step reaction with 7 steps

1.1: pyridine; hydrazine / 1 h / 100 °C

2.1: acetic acid / 2 h / 90 °C

3.1: tetrabutyl ammonium fluoride / tetrahydrofuran; acetonitrile / 20 °C

4.1: methanol; lithium hydroxide; water / 50 °C

4.2: pH 3

5.1: trichlorophosphate / 2 h / 100 °C

6.1: 0.5 h / 20 °C

7.1: sodium hydride / N,N-dimethyl-formamide

With pyridine; methanol; lithium hydroxide; tetrabutyl ammonium fluoride; water; sodium hydride; acetic acid; hydrazine; trichlorophosphate; In tetrahydrofuran; N,N-dimethyl-formamide; acetonitrile;

upstream raw materials:

5-butyl-1-(4-chloro-5-methylpyrimidin-2-yl)-N-((1-methyl-1H-imidazol-5-yl)methyl)-1H-pyrazole-4-carboxamide

phenol

1‐methyl‐5‐aminomethylimidazole

2,6-dichloro-5-methylpyrimidine