6-(((R)-1-cyclobutylethyl)amino)-7-((trans-4-(trifluoromethyl)cyclohexyl)methyl)-7H-purine-2-carbonitrile

Base Information

Chemical Name:6-(((R)-1-cyclobutylethyl)amino)-7-((trans-4-(trifluoromethyl)cyclohexyl)methyl)-7H-purine-2-carbonitrile
CAS No.:1621225-45-3
Molecular Formula:C₂₀H₂₅F₃N₆
Molecular Weight:406.454
Hs Code.:

Synonyms:6-(((R)-1-cyclobutylethyl)amino)-7-((trans-4-(trifluoromethyl)cyclohexyl)methyl)-7H-purine-2-carbonitrile

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Chemical Property of 6-(((R)-1-cyclobutylethyl)amino)-7-((trans-4-(trifluoromethyl)cyclohexyl)methyl)-7H-purine-2-carbonitrile

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Technology Process of 6-(((R)-1-cyclobutylethyl)amino)-7-((trans-4-(trifluoromethyl)cyclohexyl)methyl)-7H-purine-2-carbonitrile

There total 6 articles about 6-(((R)-1-cyclobutylethyl)amino)-7-((trans-4-(trifluoromethyl)cyclohexyl)methyl)-7H-purine-2-carbonitrile 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:

: 557-21-1
zinc(II) cyanide

: 1621225-44-2
2-chloro-N-((R)-1-cyclobutylethyl)-7-((trans-4-(trifluoromethyl)cyclohexyl)methyl)-7H-purin-6-amine

: 1621225-45-3
6-(((R)-1-cyclobutylethyl)amino)-7-((trans-4-(trifluoromethyl)cyclohexyl)methyl)-7H-purine-2-carbonitrile

Guidance literature:: With tetrakis(triphenylphosphine) palladium⁽⁰⁾; In N,N-dimethyl acetamide; at 120 ℃; for 12h; Sealed tube; Inert atmosphere;

Reference yield:

: 133261-33-3
trans-4-trifluoro-methyl-cyclohexanecarboxylic acid

: 1621225-45-3
6-(((R)-1-cyclobutylethyl)amino)-7-((trans-4-(trifluoromethyl)cyclohexyl)methyl)-7H-purine-2-carbonitrile

Guidance literature:: Multi-step reaction with 6 steps

1: diborane / tetrahydrofuran / 0 - 20 °C

2: carbon tetrabromide; triphenylphosphine / dichloromethane / 0 - 20 °C

3: sodium carbonate / N,N-dimethyl-formamide / 100 °C

4: trichlorophosphate; 1,8-diazabicyclo[5.4.0]undec-7-ene / 2 h / 60 - 120 °C

5: N-ethyl-N,N-diisopropylamine / ethanol / 12 h / Reflux

6: tetrakis(triphenylphosphine) palladium⁽⁰⁾ / N,N-dimethyl acetamide / 12 h / 120 °C / Sealed tube; Inert atmosphere

With tetrakis(triphenylphosphine) palladium⁽⁰⁾; carbon tetrabromide; sodium carbonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; N-ethyl-N,N-diisopropylamine; triphenylphosphine; diborane; trichlorophosphate; In tetrahydrofuran; ethanol; dichloromethane; N,N-dimethyl acetamide; N,N-dimethyl-formamide;

Reference yield:

: 1621225-43-1
3-methyl-7-((trans-4-(trifluoromethyl)cyclohexyl)methyl)-1H-purine-2,6(3H,7H)-dione

: 1621225-45-3
6-(((R)-1-cyclobutylethyl)amino)-7-((trans-4-(trifluoromethyl)cyclohexyl)methyl)-7H-purine-2-carbonitrile

Guidance literature:: Multi-step reaction with 3 steps

1: trichlorophosphate; 1,8-diazabicyclo[5.4.0]undec-7-ene / 2 h / 60 - 120 °C

2: N-ethyl-N,N-diisopropylamine / ethanol / 12 h / Reflux

3: tetrakis(triphenylphosphine) palladium⁽⁰⁾ / N,N-dimethyl acetamide / 12 h / 120 °C / Sealed tube; Inert atmosphere

With tetrakis(triphenylphosphine) palladium⁽⁰⁾; 1,8-diazabicyclo[5.4.0]undec-7-ene; N-ethyl-N,N-diisopropylamine; trichlorophosphate; In ethanol; N,N-dimethyl acetamide;