N-(2,6-dimethylphenyl)-4-((7-methyl-4-(4-(trifluoromethoxy)phenyl)-7H-pyrrolo[2,3-d]pyrimidin-2-yl)amino)benzamide

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Chemical Name:N-(2,6-dimethylphenyl)-4-((7-methyl-4-(4-(trifluoromethoxy)phenyl)-7H-pyrrolo[2,3-d]pyrimidin-2-yl)amino)benzamide
CAS No.:1620147-17-2
Molecular Formula:C₂₉H₂₄F₃N₅O₂
Molecular Weight:531.537
Hs Code.:

Synonyms:N-(2,6-dimethylphenyl)-4-((7-methyl-4-(4-(trifluoromethoxy)phenyl)-7H-pyrrolo[2,3-d]pyrimidin-2-yl)amino)benzamide

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Chemical Property of N-(2,6-dimethylphenyl)-4-((7-methyl-4-(4-(trifluoromethoxy)phenyl)-7H-pyrrolo[2,3-d]pyrimidin-2-yl)amino)benzamide

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Technology Process of N-(2,6-dimethylphenyl)-4-((7-methyl-4-(4-(trifluoromethoxy)phenyl)-7H-pyrrolo[2,3-d]pyrimidin-2-yl)amino)benzamide

There total 10 articles about N-(2,6-dimethylphenyl)-4-((7-methyl-4-(4-(trifluoromethoxy)phenyl)-7H-pyrrolo[2,3-d]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: 69.0%

: 1620147-16-1
N-(2,6-dimethylphenyl)-4-((4-(4-(trifluoromethoxy)phenyl)-7H-pyrrolo[2,3-d]pyrimidin-2-yl)amino)benzamide

: 74-88-4
methyl iodide

: 1620147-17-2
N-(2,6-dimethylphenyl)-4-((7-methyl-4-(4-(trifluoromethoxy)phenyl)-7H-pyrrolo[2,3-d]pyrimidin-2-yl)amino)benzamide

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 90 ℃; for 1h;

Reference yield:

: 90213-66-4
2,4-dichloro-7H-pyrrolo[2,3-d]pyrimidine

: 1620147-17-2
N-(2,6-dimethylphenyl)-4-((7-methyl-4-(4-(trifluoromethoxy)phenyl)-7H-pyrrolo[2,3-d]pyrimidin-2-yl)amino)benzamide

Guidance literature:: Multi-step reaction with 5 steps

1: triethylamine; bis-triphenylphosphine-palladium(II) chloride / N,N-dimethyl-formamide; water / 4 h / 80 °C

2: sodium hydroxide / acetone / 3 h / 20 °C

3: palladium diacetate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; caesium carbonate / 1,4-dioxane / 4 h / 150 °C / Microwave irradiation

4: sodium hydroxide / methanol / 1 h / Reflux

5: potassium carbonate / N,N-dimethyl-formamide / 6 h / 20 °C

With bis-triphenylphosphine-palladium(II) chloride; palladium diacetate; potassium carbonate; caesium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; triethylamine; sodium hydroxide; In 1,4-dioxane; methanol; water; N,N-dimethyl-formamide; acetone; 1: |Suzuki Coupling;
DOI:10.1016/j.bmcl.2014.05.066

Reference yield:

: 1620147-13-8
2-chloro-4-(4-(trifluoromethoxy)phenyl)-7H-pyrrolo[2,3-d]pyrimidine

: 1620147-17-2
N-(2,6-dimethylphenyl)-4-((7-methyl-4-(4-(trifluoromethoxy)phenyl)-7H-pyrrolo[2,3-d]pyrimidin-2-yl)amino)benzamide

Guidance literature:: Multi-step reaction with 4 steps

1: sodium hydroxide / acetone / 3 h / 20 °C

2: palladium diacetate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; caesium carbonate / 1,4-dioxane / 4 h / 150 °C / Microwave irradiation

3: sodium hydroxide / methanol / 1 h / Reflux

4: potassium carbonate / N,N-dimethyl-formamide / 6 h / 20 °C

With palladium diacetate; potassium carbonate; caesium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; sodium hydroxide; In 1,4-dioxane; methanol; N,N-dimethyl-formamide; acetone;
DOI:10.1016/j.bmcl.2014.05.066