(R)-4-((1-cyclobutylethyl)amino)-7-methyl-3-(4-(trifluoromethyl)benzyl)-3H-imidazo[4,5-c]pyridine-6-carbonitrile

Base Information

Chemical Name:(R)-4-((1-cyclobutylethyl)amino)-7-methyl-3-(4-(trifluoromethyl)benzyl)-3H-imidazo[4,5-c]pyridine-6-carbonitrile
CAS No.:1616434-21-9
Molecular Formula:C₂₂H₂₂F₃N₅
Molecular Weight:413.445
Hs Code.:

Synonyms:(R)-4-((1-cyclobutylethyl)amino)-7-methyl-3-(4-(trifluoromethyl)benzyl)-3H-imidazo[4,5-c]pyridine-6-carbonitrile

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Chemical Property of (R)-4-((1-cyclobutylethyl)amino)-7-methyl-3-(4-(trifluoromethyl)benzyl)-3H-imidazo[4,5-c]pyridine-6-carbonitrile

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Technology Process of (R)-4-((1-cyclobutylethyl)amino)-7-methyl-3-(4-(trifluoromethyl)benzyl)-3H-imidazo[4,5-c]pyridine-6-carbonitrile

There total 10 articles about (R)-4-((1-cyclobutylethyl)amino)-7-methyl-3-(4-(trifluoromethyl)benzyl)-3H-imidazo[4,5-c]pyridine-6-carbonitrile 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:

: 13061-96-6
dihydroxy-methyl-borane

: 1616434-20-8
(R)-7-bromo-4-((1-cyclobutylethyl)amino)-3-(4-(trifluoromethyl)benzyl)-3H-imidazo[4,5-c]pyridine-6-carbonitrile

: 1616434-21-9
(R)-4-((1-cyclobutylethyl)amino)-7-methyl-3-(4-(trifluoromethyl)benzyl)-3H-imidazo[4,5-c]pyridine-6-carbonitrile

Guidance literature:: With potassium phosphate; 1,1'-bis(diphenylphosphino)ferrocene-palladium(ii)dichloride-chloroform adduct; In 1,4-dioxane; water; at 120 ℃; for 0.166667h; Inert atmosphere; Microwave irradiation;

Reference yield:

: 402-49-3
4-bromomethyltrifluoromethylbenzene

: 1616434-21-9
(R)-4-((1-cyclobutylethyl)amino)-7-methyl-3-(4-(trifluoromethyl)benzyl)-3H-imidazo[4,5-c]pyridine-6-carbonitrile

Guidance literature:: Multi-step reaction with 5 steps

1.1: caesium carbonate / N,N-dimethyl acetamide / 2 h / 20 °C

2.1: potassium fluoride / N,N-dimethyl acetamide / 0.08 h / 20 °C

2.2: 120 °C

3.1: bis(η3-allyl-μ-chloropalladium(II)) / N,N-dimethyl acetamide / 120 °C / Inert atmosphere

4.1: N-Bromosuccinimide / chloroform / 1 h / 20 - 45 °C / Inert atmosphere; Sealed tube

5.1: 1,1'-bis(diphenylphosphino)ferrocene-palladium(ii)dichloride-chloroform adduct; potassium phosphate / 1,4-dioxane; water / 0.17 h / 120 °C / Inert atmosphere; Microwave irradiation

With potassium fluoride; potassium phosphate; N-Bromosuccinimide; 1,1'-bis(diphenylphosphino)ferrocene-palladium(ii)dichloride-chloroform adduct; bis(η3-allyl-μ-chloropalladium(II)); caesium carbonate; In 1,4-dioxane; chloroform; N,N-dimethyl acetamide; water;

Reference yield:

: 1616434-17-3
4,6-dichloro-3-(4-(trifluoromethyl)benzyl)-3H-imidazo[4,5-c]pyridine

: 1616434-21-9
(R)-4-((1-cyclobutylethyl)amino)-7-methyl-3-(4-(trifluoromethyl)benzyl)-3H-imidazo[4,5-c]pyridine-6-carbonitrile

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium fluoride / N,N-dimethyl acetamide / 0.08 h / 20 °C

1.2: 120 °C

2.1: bis(η3-allyl-μ-chloropalladium(II)) / N,N-dimethyl acetamide / 120 °C / Inert atmosphere

3.1: N-Bromosuccinimide / chloroform / 1 h / 20 - 45 °C / Inert atmosphere; Sealed tube

4.1: 1,1'-bis(diphenylphosphino)ferrocene-palladium(ii)dichloride-chloroform adduct; potassium phosphate / 1,4-dioxane; water / 0.17 h / 120 °C / Inert atmosphere; Microwave irradiation

With potassium fluoride; potassium phosphate; N-Bromosuccinimide; 1,1'-bis(diphenylphosphino)ferrocene-palladium(ii)dichloride-chloroform adduct; bis(η3-allyl-μ-chloropalladium(II)); In 1,4-dioxane; chloroform; N,N-dimethyl acetamide; water;