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

Base Information

Chemical Name:N-(5-(hydroxymethyl)-2-methylphenyl)-4-((5-methyl-4-(1-methyl-1H-pyrazol-4-yl)pyrimidin-2-yl)amino)benzamide
CAS No.:1550179-90-2
Molecular Formula:C₂₄H₂₄N₆O₂
Molecular Weight:428.494
Hs Code.:

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

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Chemical Property of N-(5-(hydroxymethyl)-2-methylphenyl)-4-((5-methyl-4-(1-methyl-1H-pyrazol-4-yl)pyrimidin-2-yl)amino)benzamide

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Technology Process of N-(5-(hydroxymethyl)-2-methylphenyl)-4-((5-methyl-4-(1-methyl-1H-pyrazol-4-yl)pyrimidin-2-yl)amino)benzamide

There total 4 articles about N-(5-(hydroxymethyl)-2-methylphenyl)-4-((5-methyl-4-(1-methyl-1H-pyrazol-4-yl)pyrimidin-2-yl)amino)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: 34.0%

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

: 81863-45-8
3-(hydroxymethyl)-6-methylaniline

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

Guidance literature:: With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In N,N-dimethyl-formamide; at 20 ℃; for 12h; Inert atmosphere;

Reference yield:

: 1780-31-0
2,6-dichloro-5-methylpyrimidine

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

Guidance literature:: Multi-step reaction with 4 steps

1: bis-triphenylphosphine-palladium(II) chloride; triethylamine / N,N-dimethyl-formamide; water / 80 °C

2: palladium diacetate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; caesium carbonate / 1,4-dioxane / 3 h / 170 °C / Microwave irradiation

3: sodium hydroxide; water / methanol / Reflux

4: 2-( 1H-7-azabenzotniazol-1-yl)-1,1,3,3-tetrarmethyluroniumhexafluorophosphate methanaminium; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 85 °C

With bis-triphenylphosphine-palladium(II) chloride; 2-( 1H-7-azabenzotniazol-1-yl)-1,1,3,3-tetrarmethyluroniumhexafluorophosphate methanaminium; water; palladium diacetate; caesium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; triethylamine; N-ethyl-N,N-diisopropylamine; sodium hydroxide; In 1,4-dioxane; methanol; water; N,N-dimethyl-formamide; 1: |Suzuki Coupling / 2: |Buchwald-Hartwig Coupling;
DOI:10.1016/j.bmcl.2013.12.050

Reference yield:

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

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

Guidance literature:: Multi-step reaction with 2 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

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