C₃₂H₂₅N₃O₂

Base Information

Chemical Name:C₃₂H₂₅N₃O₂
CAS No.:1332324-39-6
Molecular Formula:C₃₂H₂₅N₃O₂
Molecular Weight:483.569
Hs Code.:

C<sub>32</sub>H<sub>25</sub>N<sub>3</sub>O<sub>2</sub>

Synonyms:C₃₂H₂₅N₃O₂

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Chemical Property of C₃₂H₂₅N₃O₂

Chemical Property:

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Technology Process of C₃₂H₂₅N₃O₂

There total 5 articles about C₃₂H₂₅N₃O₂ 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:

: 1332324-25-0
4-methyl-2-oxo-5-phenyl-1,2-dihydro-pyridine-3-carbaldehyde

: 62-53-3
aniline

: 1332324-39-6
C₃₂H₂₅N₃O₂

Guidance literature:: With benzylidene phenylamine; acetic acid; In methanol; acetonitrile; at 20 ℃; for 0.5h;
DOI:10.1021/ol202080x

Reference yield:

: 1332324-22-7
3,5-dibromo-2-methoxy-4-methyl-pyridine

: 1332324-39-6
C₃₂H₂₅N₃O₂

Guidance literature:: Multi-step reaction with 4 steps

1.1: n-butyllithium / diethyl ether; hexane / 0.25 h / -70 °C / Inert atmosphere

1.2: 0.5 h / -70 °C / Inert atmosphere

2.1: potassium fluoride; palladium diacetate / methanol; PEG-400 / 1.5 h / 20 °C

3.1: hydrogen bromide; acetic acid / water / 40 °C / Inert atmosphere

4.1: benzylidene phenylamine; acetic acid / methanol; acetonitrile / 0.5 h / 20 °C

With potassium fluoride; n-butyllithium; hydrogen bromide; palladium diacetate; benzylidene phenylamine; acetic acid; In methanol; PEG-400; diethyl ether; hexane; water; acetonitrile; 2.1: Suzuki coupling;
DOI:10.1021/ol202080x

Reference yield:

: 100848-70-2
2-methoxy-4-methyl-pyridine

: 1332324-39-6
C₃₂H₂₅N₃O₂

Guidance literature:: Multi-step reaction with 5 steps

1.1: bromine; sodium acetate; acetic acid / 80 °C / Inert atmosphere

2.1: n-butyllithium / diethyl ether; hexane / 0.25 h / -70 °C / Inert atmosphere

2.2: 0.5 h / -70 °C / Inert atmosphere

3.1: potassium fluoride; palladium diacetate / methanol; PEG-400 / 1.5 h / 20 °C

4.1: hydrogen bromide; acetic acid / water / 40 °C / Inert atmosphere

5.1: benzylidene phenylamine; acetic acid / methanol; acetonitrile / 0.5 h / 20 °C

With potassium fluoride; n-butyllithium; hydrogen bromide; bromine; sodium acetate; palladium diacetate; benzylidene phenylamine; acetic acid; In methanol; PEG-400; diethyl ether; hexane; water; acetonitrile; 3.1: Suzuki coupling;
DOI:10.1021/ol202080x