1-{4-[3-(4-fluorophenyl)-6-phenyl-imidazo[1,2-a]pyrimidin-7-yl]phenyl}cyclobutylamine

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Chemical Name:1-{4-[3-(4-fluorophenyl)-6-phenyl-imidazo[1,2-a]pyrimidin-7-yl]phenyl}cyclobutylamine
CAS No.:1355240-23-1
Molecular Formula:C₂₈H₂₃FN₄
Molecular Weight:434.516
Hs Code.:

Synonyms:1-{4-[3-(4-fluorophenyl)-6-phenyl-imidazo[1,2-a]pyrimidin-7-yl]phenyl}cyclobutylamine

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Chemical Property of 1-{4-[3-(4-fluorophenyl)-6-phenyl-imidazo[1,2-a]pyrimidin-7-yl]phenyl}cyclobutylamine

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Technology Process of 1-{4-[3-(4-fluorophenyl)-6-phenyl-imidazo[1,2-a]pyrimidin-7-yl]phenyl}cyclobutylamine

There total 11 articles about 1-{4-[3-(4-fluorophenyl)-6-phenyl-imidazo[1,2-a]pyrimidin-7-yl]phenyl}cyclobutylamine 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:

: 1355240-85-5
(1-{4-[3-(4-fluorophenyl)-6-phenyl-imidazo[1,2-a]pyrimidin-7-yl]phenyl}cyclobutyl)carbamic acid tert-butyl ester

: 1355240-23-1
1-{4-[3-(4-fluorophenyl)-6-phenyl-imidazo[1,2-a]pyrimidin-7-yl]phenyl}cyclobutylamine

Guidance literature:: (1-{4-[3-(4-fluorophenyl)-6-phenyl-imidazo[1,2-a]pyrimidin-7-yl]phenyl}cyclobutyl)carbamic acid tert-butyl ester; With hydrogenchloride; In 1,4-dioxane; at 20 ℃; for 3h;

With ammonia; In methanol;

Reference yield:

: 83-13-6
diethyl 2-phenylmalonate

: 1355240-23-1
1-{4-[3-(4-fluorophenyl)-6-phenyl-imidazo[1,2-a]pyrimidin-7-yl]phenyl}cyclobutylamine

Guidance literature:: Multi-step reaction with 7 steps

1: 1,8-diazabicyclo[5.4.0]undec-7-ene / N,N-dimethyl-formamide / 15 h / 100 °C

2: trichlorophosphate; N,N-dimethyl-aniline / 2.5 h / 100 °C

3: zinc; ammonium chloride / ethanol; water; tetrahydrofuran / 20 °C

4: sodium carbonate / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / 1,4-dioxane; water / 18 h / 105 °C / Inert atmosphere

5: N-Bromosuccinimide / chloroform / 2.5 h / Reflux

6: sodium carbonate / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / 1,4-dioxane; water / 0.75 h / 105 °C / microwave irradiation

7: hydrogenchloride / 1,4-dioxane / 3 h / 20 °C

With hydrogenchloride; N-Bromosuccinimide; sodium carbonate; ammonium chloride; N,N-dimethyl-aniline; 1,8-diazabicyclo[5.4.0]undec-7-ene; zinc; trichlorophosphate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In tetrahydrofuran; 1,4-dioxane; ethanol; chloroform; water; N,N-dimethyl-formamide;

Reference yield:

: 1032350-06-3
tert-butyl (1-(4-bromophenyl)cyclobutyl)carbamate

: 1355240-23-1
1-{4-[3-(4-fluorophenyl)-6-phenyl-imidazo[1,2-a]pyrimidin-7-yl]phenyl}cyclobutylamine

Guidance literature:: Multi-step reaction with 5 steps

1: potassium acetate / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / tetrahydrofuran / Reflux

2: sodium carbonate / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / 1,4-dioxane; water / 18 h / 105 °C / Inert atmosphere

3: N-Bromosuccinimide / chloroform / 2.5 h / Reflux

4: sodium carbonate / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / 1,4-dioxane; water / 0.75 h / 105 °C / microwave irradiation

5: hydrogenchloride / 1,4-dioxane / 3 h / 20 °C

With hydrogenchloride; N-Bromosuccinimide; potassium acetate; sodium carbonate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In tetrahydrofuran; 1,4-dioxane; chloroform; water;