1-(3-chloro-4-fluorophenyl)-3-(3-(methyl(2-methyl-6-(4-methylpiperazin-1-yl)pyrimidin-4-yl)amino)phenyl)urea

Base Information

Chemical Name:1-(3-chloro-4-fluorophenyl)-3-(3-(methyl(2-methyl-6-(4-methylpiperazin-1-yl)pyrimidin-4-yl)amino)phenyl)urea
CAS No.:1402747-35-6
Molecular Formula:C₂₄H₂₇ClFN₇O
Molecular Weight:483.976
Hs Code.:

Synonyms:1-(3-chloro-4-fluorophenyl)-3-(3-(methyl(2-methyl-6-(4-methylpiperazin-1-yl)pyrimidin-4-yl)amino)phenyl)urea

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Chemical Property of 1-(3-chloro-4-fluorophenyl)-3-(3-(methyl(2-methyl-6-(4-methylpiperazin-1-yl)pyrimidin-4-yl)amino)phenyl)urea

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Technology Process of 1-(3-chloro-4-fluorophenyl)-3-(3-(methyl(2-methyl-6-(4-methylpiperazin-1-yl)pyrimidin-4-yl)amino)phenyl)urea

There total 6 articles about 1-(3-chloro-4-fluorophenyl)-3-(3-(methyl(2-methyl-6-(4-methylpiperazin-1-yl)pyrimidin-4-yl)amino)phenyl)urea 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: 23.0%

: 367-21-5
3-chloro-4-fluorophenylamine

: 3-(methyl(2-methyl-6-(4-methylpiperazin-1-yl)pyrimidin-4-yl)amino)phenyl carbamate 4-nitrophenyl hydrochloride

: 1402747-35-6
1-(3-chloro-4-fluorophenyl)-3-(3-(methyl(2-methyl-6-(4-methylpiperazin-1-yl)pyrimidin-4-yl)amino)phenyl)urea

Guidance literature:: With triethylamine; In N,N-dimethyl-formamide; at 40 ℃; for 9h;

Reference yield:

: 99-09-2
3-nitro-aniline

: 1402747-35-6
1-(3-chloro-4-fluorophenyl)-3-(3-(methyl(2-methyl-6-(4-methylpiperazin-1-yl)pyrimidin-4-yl)amino)phenyl)urea

Guidance literature:: Multi-step reaction with 6 steps

1: hydrogenchloride / acetone; water / 2 h / Reflux

2: potassium carbonate / N,N-dimethyl-formamide

3: dimethyl sulfoxide / 0.33 h / 40 °C / Inert atmosphere

4: iron; ammonium chloride; hydrogenchloride / water; ethanol; tetrahydrofuran / 2 h / Reflux

5: dichloromethane / 2.5 h / 0 - 20 °C

6: triethylamine / N,N-dimethyl-formamide / 9 h / 40 °C

With hydrogenchloride; iron; potassium carbonate; ammonium chloride; triethylamine; In tetrahydrofuran; ethanol; dichloromethane; water; dimethyl sulfoxide; N,N-dimethyl-formamide; acetone;

Reference yield:

: 1402747-90-3
N,2-dimethyl-6-(4-methylpiperazin-1-yl)-N-(3-nitrophenyl)pyrimidin-4-amine

: 1402747-35-6
1-(3-chloro-4-fluorophenyl)-3-(3-(methyl(2-methyl-6-(4-methylpiperazin-1-yl)pyrimidin-4-yl)amino)phenyl)urea

Guidance literature:: Multi-step reaction with 3 steps

1: iron; ammonium chloride; hydrogenchloride / water; ethanol; tetrahydrofuran / 2 h / Reflux

2: dichloromethane / 2.5 h / 0 - 20 °C

3: triethylamine / N,N-dimethyl-formamide / 9 h / 40 °C

With hydrogenchloride; iron; ammonium chloride; triethylamine; In tetrahydrofuran; ethanol; dichloromethane; water; N,N-dimethyl-formamide;