2-{4-[4-fluoro-3-(1-methyl-1H-imidazol-4-yl)phenyl]-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-pyrazol-3-yl}-6-methylpyridine

Base Information

Chemical Name:2-{4-[4-fluoro-3-(1-methyl-1H-imidazol-4-yl)phenyl]-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-pyrazol-3-yl}-6-methylpyridine
CAS No.:879488-09-2
Molecular Formula:C₂₅H₃₀FN₅OSi
Molecular Weight:463.63
Hs Code.:

Synonyms:2-{4-[4-fluoro-3-(1-methyl-1H-imidazol-4-yl)phenyl]-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-pyrazol-3-yl}-6-methylpyridine

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Chemical Property of 2-{4-[4-fluoro-3-(1-methyl-1H-imidazol-4-yl)phenyl]-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-pyrazol-3-yl}-6-methylpyridine

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Technology Process of 2-{4-[4-fluoro-3-(1-methyl-1H-imidazol-4-yl)phenyl]-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-pyrazol-3-yl}-6-methylpyridine

There total 6 articles about 2-{4-[4-fluoro-3-(1-methyl-1H-imidazol-4-yl)phenyl]-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-pyrazol-3-yl}-6-methylpyridine 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: 53.0%

: 879487-60-2
2-(4-[4-Fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-pyrazol-3-yl)-6-methylpyridine

: 71759-87-0
4-iodo-1-methyl-1H-imidazole

: 879488-09-2
2-{4-[4-fluoro-3-(1-methyl-1H-imidazol-4-yl)phenyl]-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-pyrazol-3-yl}-6-methylpyridine

Guidance literature:: With potassium phosphate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In 1,2-dimethoxyethane; water; for 4h; Heating / reflux;

Reference yield:

: 1122-72-1
6-methyl-2-pyridinecarboxaldehyde

: 879488-09-2
2-{4-[4-fluoro-3-(1-methyl-1H-imidazol-4-yl)phenyl]-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-pyrazol-3-yl}-6-methylpyridine

Guidance literature:: Multi-step reaction with 6 steps

1.1: isopropyl alcohol / 1 h / 20 °C

2.1: caesium carbonate / tetrahydrofuran; isopropyl alcohol / 2 h / 20 °C

2.2: 1 h / 20 °C

3.1: N,N-dimethyl-formamide / 2 h / 20 - 90 °C

3.2: 3 h / 20 °C

4.1: sodium hydride / tetrahydrofuran / 0.33 h / 0 - 20 °C

4.2: 3 h / 20 °C

5.1: potassium acetate / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / N,N-dimethyl-formamide / 8 h / 100 °C

6.1: potassium phosphate / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / 1,2-dimethoxyethane; water / 4 h / Heating / reflux

With potassium phosphate; potassium acetate; sodium hydride; caesium carbonate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In tetrahydrofuran; 1,2-dimethoxyethane; water; N,N-dimethyl-formamide; isopropyl alcohol;

Reference yield:

: 1282894-23-8
2-(3-bromo-4-fluorophenyl)-1-(6-methylpyridin-2-yl)ethanone

: 879488-09-2
2-{4-[4-fluoro-3-(1-methyl-1H-imidazol-4-yl)phenyl]-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-pyrazol-3-yl}-6-methylpyridine

Guidance literature:: Multi-step reaction with 4 steps

1.1: N,N-dimethyl-formamide / 2 h / 20 - 90 °C

1.2: 3 h / 20 °C

2.1: sodium hydride / tetrahydrofuran / 0.33 h / 0 - 20 °C

2.2: 3 h / 20 °C

3.1: potassium acetate / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / N,N-dimethyl-formamide / 8 h / 100 °C

4.1: potassium phosphate / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / 1,2-dimethoxyethane; water / 4 h / Heating / reflux

With potassium phosphate; potassium acetate; sodium hydride; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In tetrahydrofuran; 1,2-dimethoxyethane; water; N,N-dimethyl-formamide;