C₂₃H₂₄F₂N₆

Base Information

Chemical Name:C₂₃H₂₄F₂N₆
CAS No.:1431984-74-5
Molecular Formula:C₂₃H₂₄F₂N₆
Molecular Weight:422.481
Hs Code.:

C<sub>23</sub>H<sub>24</sub>F<sub>2</sub>N<sub>6</sub>

Synonyms:C₂₃H₂₄F₂N₆

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Chemical Property of C₂₃H₂₄F₂N₆

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Technology Process of C₂₃H₂₄F₂N₆

There total 10 articles about C₂₃H₂₄F₂N₆ 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: 5.0%

: 1431985-43-1
C₁₈H₁₃F₂N₅

: 6306-61-2
N-(2-chloroethyl)-N-isopropylamine hydrochloride

: 1431984-75-6
C₂₃H₂₄F₂N₆

: 1431984-74-5
C₂₃H₂₄F₂N₆

Guidance literature:: With tetrabutylammomium bromide; potassium hydroxide; In 2-methyltetrahydrofuran; water; at 50 ℃;

Reference yield:

: 1431985-32-8
C₉H₆BrClN₂O

: 1431984-75-6
C₂₃H₂₄F₂N₆

: 1431984-74-5
C₂₃H₂₄F₂N₆

Guidance literature:: Multi-step reaction with 6 steps

1.1: sodium carbonate; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / water; 1,4-dioxane / 16 h / 110 °C / Inert atmosphere

2.1: sodium hydroxide; hydrogen / ethanol; water; tetrahydrofuran / 40 h / 50 °C / 750.08 Torr

3.1: hydrogenchloride / water; 1,4-dioxane / 3 h / 80 °C

3.2: pH 9

4.1: trichlorophosphate / chloroform / 3 h / Reflux

5.1: lithium hexamethyldisilazane / tetrahydrofuran / 1 h / 0 °C

5.2: 0 - 20 °C

6.1: potassium hydroxide; tetrabutylammomium bromide / water; 2-methyltetrahydrofuran / 50 °C

With hydrogenchloride; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; tetrabutylammomium bromide; hydrogen; sodium carbonate; potassium hydroxide; sodium hydroxide; lithium hexamethyldisilazane; trichlorophosphate; In tetrahydrofuran; 2-methyltetrahydrofuran; 1,4-dioxane; ethanol; chloroform; water;

Reference yield:

: 1431985-33-9
8-chloro-2-methoxy-7-(1-methyl-1H-pyrazol-4-yl)-1,5-naphthyridine

: 1431984-75-6
C₂₃H₂₄F₂N₆

: 1431984-74-5
C₂₃H₂₄F₂N₆

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium hydroxide; hydrogen / ethanol; water; tetrahydrofuran / 40 h / 50 °C / 750.08 Torr

2.1: hydrogenchloride / water; 1,4-dioxane / 3 h / 80 °C

2.2: pH 9

3.1: trichlorophosphate / chloroform / 3 h / Reflux

4.1: lithium hexamethyldisilazane / tetrahydrofuran / 1 h / 0 °C

4.2: 0 - 20 °C

5.1: potassium hydroxide; tetrabutylammomium bromide / water; 2-methyltetrahydrofuran / 50 °C

With hydrogenchloride; tetrabutylammomium bromide; hydrogen; potassium hydroxide; sodium hydroxide; lithium hexamethyldisilazane; trichlorophosphate; In tetrahydrofuran; 2-methyltetrahydrofuran; 1,4-dioxane; ethanol; chloroform; water;