C₂₆H₂₃N₅

Base Information

Chemical Name:C₂₆H₂₃N₅
CAS No.:1187313-01-4
Molecular Formula:C₂₆H₂₃N₅
Molecular Weight:405.502
Hs Code.:

C<sub>26</sub>H<sub>23</sub>N<sub>5</sub>

Synonyms:C₂₆H₂₃N₅

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Chemical Property of C₂₆H₂₃N₅

Chemical Property:

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Technology Process of C₂₆H₂₃N₅

There total 13 articles about C₂₆H₂₃N₅ 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:

: 1187313-20-7
C₃₁H₃₁N₅O₂

: 1187313-01-4
C₂₆H₂₃N₅

Guidance literature:: With hydrogenchloride; methanol; In dichloromethane; at 0 - 20 ℃;

Reference yield:

: 6281-32-9
4-quinolylmethanol

: 1187313-01-4
C₂₆H₂₃N₅

Guidance literature:: Multi-step reaction with 8 steps

1.1: thionyl chloride / dichloromethane / 2.33 h / 0 - 20 °C

1.2: pH > 7 / Saturated solution

2.1: N,N-dimethyl-formamide / 20 - 80 °C

3.1: 6 h / 120 °C

4.1: hydrazine monohydrobromide / ethanol; water / 5 h / 110 °C

4.2: Saturated solution

5.1: acetic acid / ethanol / 5 h / 50 °C

6.1: potassium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,4-dioxane; water / 150 °C / Inert atmosphere; Microwave irradiation

7.1: hydrogen / platinum(IV) oxide; 5%-palladium/activated carbon / methanol; dichloromethane

8.1: hydrogenchloride; methanol / dichloromethane / 0 - 20 °C

With hydrogenchloride; methanol; thionyl chloride; hydrazine monohydrobromide; hydrogen; potassium carbonate; acetic acid; platinum(IV) oxide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; 5%-palladium/activated carbon; In 1,4-dioxane; methanol; ethanol; dichloromethane; water; N,N-dimethyl-formamide;

Reference yield:

: 4363-93-3
quinoline-4-carboxaldehyde

: 1187313-01-4
C₂₆H₂₃N₅

Guidance literature:: Multi-step reaction with 9 steps

1.1: methanol; sodium tetrahydroborate / 1.33 h / 0 - 20 °C

2.1: thionyl chloride / dichloromethane / 2.33 h / 0 - 20 °C

2.2: pH > 7 / Saturated solution

3.1: N,N-dimethyl-formamide / 20 - 80 °C

4.1: 6 h / 120 °C

5.1: hydrazine monohydrobromide / ethanol; water / 5 h / 110 °C

5.2: Saturated solution

6.1: acetic acid / ethanol / 5 h / 50 °C

7.1: potassium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,4-dioxane; water / 150 °C / Inert atmosphere; Microwave irradiation

8.1: hydrogen / platinum(IV) oxide; 5%-palladium/activated carbon / methanol; dichloromethane

9.1: hydrogenchloride; methanol / dichloromethane / 0 - 20 °C

With hydrogenchloride; methanol; sodium tetrahydroborate; thionyl chloride; hydrazine monohydrobromide; hydrogen; potassium carbonate; acetic acid; platinum(IV) oxide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; 5%-palladium/activated carbon; In 1,4-dioxane; methanol; ethanol; dichloromethane; water; N,N-dimethyl-formamide;