4-((4-((4-(tert-butyl)phenyl)chloromethyl)-5-methylpyrimidin-2-yl)amino)benzonitrile

Base Information

Chemical Name:4-((4-((4-(tert-butyl)phenyl)chloromethyl)-5-methylpyrimidin-2-yl)amino)benzonitrile
CAS No.:1610953-73-5
Molecular Formula:C₂₃H₂₃ClN₄
Molecular Weight:390.915
Hs Code.:

Synonyms:4-((4-((4-(tert-butyl)phenyl)chloromethyl)-5-methylpyrimidin-2-yl)amino)benzonitrile

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Chemical Property of 4-((4-((4-(tert-butyl)phenyl)chloromethyl)-5-methylpyrimidin-2-yl)amino)benzonitrile

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Technology Process of 4-((4-((4-(tert-butyl)phenyl)chloromethyl)-5-methylpyrimidin-2-yl)amino)benzonitrile

There total 7 articles about 4-((4-((4-(tert-butyl)phenyl)chloromethyl)-5-methylpyrimidin-2-yl)amino)benzonitrile 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: 62.0%

: 1610953-79-1
C₂₃H₂₄N₄O

: 1610953-73-5
4-((4-((4-(tert-butyl)phenyl)chloromethyl)-5-methylpyrimidin-2-yl)amino)benzonitrile

Guidance literature:: With thionyl chloride; In dichloromethane; at -20 - 20 ℃; for 2h;
DOI:10.1016/j.bmc.2014.03.020

Reference yield:

: 636-26-0
5-methyl-2-thiouracil

: 1610953-73-5
4-((4-((4-(tert-butyl)phenyl)chloromethyl)-5-methylpyrimidin-2-yl)amino)benzonitrile

Guidance literature:: Multi-step reaction with 7 steps

1: sodium hydroxide / water / 24 h / 20 °C

2: 8 h / 180 - 190 °C

3: trichlorophosphate / 0.5 h / Reflux

4: sodium hydride / N,N-dimethyl-formamide; mineral oil / -20 - 20 °C / Inert atmosphere

5: air / 20 °C

6: potassium borohydride / methanol / 2 h / -20 - 20 °C

7: thionyl chloride / dichloromethane / 2 h / -20 - 20 °C

With thionyl chloride; potassium borohydride; sodium hydride; sodium hydroxide; trichlorophosphate; In methanol; dichloromethane; water; N,N-dimethyl-formamide; mineral oil;
DOI:10.1016/j.bmc.2014.03.020

Reference yield:

: 20651-30-3
2-(methylthio)-5-methylpyrimidin-4(1H)-one

: 1610953-73-5
4-((4-((4-(tert-butyl)phenyl)chloromethyl)-5-methylpyrimidin-2-yl)amino)benzonitrile

Guidance literature:: Multi-step reaction with 6 steps

1: 8 h / 180 - 190 °C

2: trichlorophosphate / 0.5 h / Reflux

3: sodium hydride / N,N-dimethyl-formamide; mineral oil / -20 - 20 °C / Inert atmosphere

4: air / 20 °C

5: potassium borohydride / methanol / 2 h / -20 - 20 °C

6: thionyl chloride / dichloromethane / 2 h / -20 - 20 °C

With thionyl chloride; potassium borohydride; sodium hydride; trichlorophosphate; In methanol; dichloromethane; N,N-dimethyl-formamide; mineral oil;
DOI:10.1016/j.bmc.2014.03.020