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

Base Information

Chemical Name:(1-{4-[3-(4-methanesulfonyl-phenyl)-6-phenyl-imidazo[1,2-a]pyrimidin-7-yl]phenyl}cyclobutyl)carbamic acid tert-butyl ester
CAS No.:1355240-89-9
Molecular Formula:C₃₄H₃₄N₄O₄S
Molecular Weight:594.734
Hs Code.:

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

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Chemical Property of (1-{4-[3-(4-methanesulfonyl-phenyl)-6-phenyl-imidazo[1,2-a]pyrimidin-7-yl]phenyl}cyclobutyl)carbamic acid tert-butyl ester

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Technology Process of (1-{4-[3-(4-methanesulfonyl-phenyl)-6-phenyl-imidazo[1,2-a]pyrimidin-7-yl]phenyl}cyclobutyl)carbamic acid tert-butyl ester

There total 10 articles about (1-{4-[3-(4-methanesulfonyl-phenyl)-6-phenyl-imidazo[1,2-a]pyrimidin-7-yl]phenyl}cyclobutyl)carbamic acid tert-butyl ester 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:

: 1247897-89-7
{1-[4-(3-bromo-6-phenyl-imidazo[1,2-a]pyrimidin-7-yl)phenyl]cyclobutyl}carbamic acid tert-butyl ester

: 149104-88-1
4-methanesulphonylphenylboronic acid

: 1355240-89-9
(1-{4-[3-(4-methanesulfonyl-phenyl)-6-phenyl-imidazo[1,2-a]pyrimidin-7-yl]phenyl}cyclobutyl)carbamic acid tert-butyl ester

Guidance literature:: With sodium carbonate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In 1,4-dioxane; water; at 105 ℃; for 18h; microwave irradiation; sealed vial;

Reference yield:

: 502506-57-2
6-phenylimidazo[1,2-a]pyrimidine-5,7-diol

: 1355240-89-9
(1-{4-[3-(4-methanesulfonyl-phenyl)-6-phenyl-imidazo[1,2-a]pyrimidin-7-yl]phenyl}cyclobutyl)carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 5 steps

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

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

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

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

5: sodium carbonate / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / 1,4-dioxane; water / 18 h / 105 °C / microwave irradiation; sealed vial

With N-Bromosuccinimide; sodium carbonate; ammonium chloride; N,N-dimethyl-aniline; zinc; trichlorophosphate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In tetrahydrofuran; 1,4-dioxane; ethanol; chloroform; water;

Reference yield:

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

: 1355240-89-9
(1-{4-[3-(4-methanesulfonyl-phenyl)-6-phenyl-imidazo[1,2-a]pyrimidin-7-yl]phenyl}cyclobutyl)carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 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 / 18 h / 105 °C / microwave irradiation; sealed vial

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