C₂₄H₂₈N₆O

Base Information

Chemical Name:C₂₄H₂₈N₆O
CAS No.:1346245-89-3
Molecular Formula:C₂₄H₂₈N₆O
Molecular Weight:416.526
Hs Code.:

C<sub>24</sub>H<sub>28</sub>N<sub>6</sub>O

Synonyms:C₂₄H₂₈N₆O

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Chemical Property of C₂₄H₂₈N₆O

Chemical Property:

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Technology Process of C₂₄H₂₈N₆O

There total 8 articles about C₂₄H₂₈N₆O 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:

: 1346245-88-2
C₂₀H₁₇N₅O₂

: 109-89-7
diethylamine

: 1346245-89-3
C₂₄H₂₈N₆O

Guidance literature:: With hydrogen; palladium 10% on activated carbon; In tetrahydrofuran; thiophene; methanol; di-isopropyl ether; at 50 ℃; under 57003.8 Torr; Inert atmosphere;

Reference yield:

: 82031-32-1
7-bromo-1H-quinoxalin-2-one

: 1346245-89-3
C₂₄H₂₈N₆O

Guidance literature:: Multi-step reaction with 5 steps

1.1: trichlorophosphate / 2 h / 100 °C

1.2: Cooling with ice

2.1: sodium carbonate / triphenylphosphine; palladium diacetate / 1,2-dimethoxyethane; water / 4 h / Reflux

3.1: caesium carbonate / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; XPhos / water; tert-butyl alcohol / 1 h / 105 °C / Inert atmosphere; microwave irradiation

4.1: manganese(IV) oxide / tetrahydrofuran / 18 h / 20 °C

5.1: hydrogen / palladium 10% on activated carbon / di-isopropyl ether; thiophene; tetrahydrofuran; methanol / 50 °C / 57003.8 Torr / Inert atmosphere

With manganese(IV) oxide; hydrogen; sodium carbonate; caesium carbonate; trichlorophosphate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; palladium 10% on activated carbon; palladium diacetate; triphenylphosphine; XPhos; In tetrahydrofuran; thiophene; methanol; 1,2-dimethoxyethane; di-isopropyl ether; water; tert-butyl alcohol;

Reference yield:

: 89891-65-6
7-bromo-2-chloroquinoxaline

: 1346245-89-3
C₂₄H₂₈N₆O

Guidance literature:: Multi-step reaction with 4 steps

1: sodium carbonate / triphenylphosphine; palladium diacetate / 1,2-dimethoxyethane; water / 4 h / Reflux

2: caesium carbonate / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; XPhos / water; tert-butyl alcohol / 1 h / 105 °C / Inert atmosphere; microwave irradiation

3: manganese(IV) oxide / tetrahydrofuran / 18 h / 20 °C

4: hydrogen / palladium 10% on activated carbon / di-isopropyl ether; thiophene; tetrahydrofuran; methanol / 50 °C / 57003.8 Torr / Inert atmosphere

With manganese(IV) oxide; hydrogen; sodium carbonate; caesium carbonate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; palladium 10% on activated carbon; palladium diacetate; triphenylphosphine; XPhos; In tetrahydrofuran; thiophene; methanol; 1,2-dimethoxyethane; di-isopropyl ether; water; tert-butyl alcohol;