4-((5-methyl-4-(1-methyl-1H-4-pyrazolyl)pyrimidin-2-yl)amino)-N-(2-methyl-5-(morpholinylmethyl)phenyl)benzamide

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Chemical Name:4-((5-methyl-4-(1-methyl-1H-4-pyrazolyl)pyrimidin-2-yl)amino)-N-(2-methyl-5-(morpholinylmethyl)phenyl)benzamide
CAS No.:1550177-63-3
Molecular Formula:C₂₈H₃₁N₇O₂
Molecular Weight:497.6
Hs Code.:

Synonyms:4-((5-methyl-4-(1-methyl-1H-4-pyrazolyl)pyrimidin-2-yl)amino)-N-(2-methyl-5-(morpholinylmethyl)phenyl)benzamide

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Chemical Property of 4-((5-methyl-4-(1-methyl-1H-4-pyrazolyl)pyrimidin-2-yl)amino)-N-(2-methyl-5-(morpholinylmethyl)phenyl)benzamide

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Technology Process of 4-((5-methyl-4-(1-methyl-1H-4-pyrazolyl)pyrimidin-2-yl)amino)-N-(2-methyl-5-(morpholinylmethyl)phenyl)benzamide

There total 6 articles about 4-((5-methyl-4-(1-methyl-1H-4-pyrazolyl)pyrimidin-2-yl)amino)-N-(2-methyl-5-(morpholinylmethyl)phenyl)benzamide 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: 64.1%

: 110-91-8,99108-56-2
morpholine

: 1550180-02-3
N-(5-(chloromethyl)-2-methylphenyl)-4-((5-methyl-4-(1-methyl-1H-4-pyrazolyl)pyrimidin-2-yl)amino)benzamide

: 1550177-63-3
4-((5-methyl-4-(1-methyl-1H-4-pyrazolyl)pyrimidin-2-yl)amino)-N-(2-methyl-5-(morpholinylmethyl)phenyl)benzamide

Guidance literature:: With potassium carbonate; potassium iodide; In acetonitrile; at 85 ℃; for 12h; Inert atmosphere;

Reference yield:

: methyl 4-((5-methyl-4-(1-methyl-1H-pyrazol-4-yl)pyrimidin-2-yl)amino)benzoate

: 1550177-63-3
4-((5-methyl-4-(1-methyl-1H-4-pyrazolyl)pyrimidin-2-yl)amino)-N-(2-methyl-5-(morpholinylmethyl)phenyl)benzamide

Guidance literature:: Multi-step reaction with 4 steps

1: sodium hydroxide; water / methanol / Reflux

2: 2-( 1H-7-azabenzotniazol-1-yl)-1,1,3,3-tetrarmethyluroniumhexafluorophosphate methanaminium; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 85 °C

3: thionyl chloride / dichloromethane / 2 h / 20 °C

4: potassium carbonate / N,N-dimethyl-formamide / 20 °C

With thionyl chloride; 2-( 1H-7-azabenzotniazol-1-yl)-1,1,3,3-tetrarmethyluroniumhexafluorophosphate methanaminium; water; potassium carbonate; N-ethyl-N,N-diisopropylamine; sodium hydroxide; In methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2013.12.050

Reference yield:

: 1550179-90-2
N-(5-(hydroxymethyl)-2-methylphenyl)-4-((5-methyl-4-(1-methyl-1H-pyrazol-4-yl)pyrimidin-2-yl)amino)benzamide

: 1550177-63-3
4-((5-methyl-4-(1-methyl-1H-4-pyrazolyl)pyrimidin-2-yl)amino)-N-(2-methyl-5-(morpholinylmethyl)phenyl)benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: thionyl chloride / dichloromethane / 2 h / 20 °C

2: potassium carbonate / N,N-dimethyl-formamide / 20 °C

With thionyl chloride; potassium carbonate; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2013.12.050