C₂₈H₂₆N₄O

Base Information

Chemical Name:C₂₈H₂₆N₄O
CAS No.:1447816-26-3
Molecular Formula:C₂₈H₂₆N₄O
Molecular Weight:434.541
Hs Code.:

C<sub>28</sub>H<sub>26</sub>N<sub>4</sub>O

Synonyms:C₂₈H₂₆N₄O

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Chemical Property of C₂₈H₂₆N₄O

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Technology Process of C₂₈H₂₆N₄O

There total 3 articles about C₂₈H₂₆N₄O 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: 82.0%

: 1447816-00-3
C₂₈H₂₄N₄O

: 1447816-26-3
C₂₈H₂₆N₄O

Guidance literature:: With quinoline; rosenmund catalyst; hydrogen; In methanol; at 20 ℃; for 5h;
DOI:10.1021/ja4066656

Reference yield:

: 1447816-50-3
1-benzyl-3,3-di(prop-2-yn-1-yl)indolin-2-one

: 1447816-26-3
C₂₈H₂₆N₄O

Guidance literature:: Multi-step reaction with 2 steps

1.1: copper(l) chloride; (S,S)-2,6-bis(4-phenyl-2-oxazolinyl)pyridine / 0.5 h / 0 °C

1.2: 96 h / 0 °C

2.1: hydrogen; rosenmund catalyst; quinoline / methanol / 5 h / 20 °C

With quinoline; rosenmund catalyst; hydrogen; copper(l) chloride; (S,S)-2,6-bis(4-phenyl-2-oxazolinyl)pyridine; In methanol;
DOI:10.1021/ja4066656

Reference yield:

: 7135-32-2
1-benzylindolin-2-one

: 1447816-26-3
C₂₈H₂₆N₄O

Guidance literature:: Multi-step reaction with 3 steps

1.1: tetra(n-butyl)ammonium hydrogensulfate; potassium carbonate / acetonitrile / 6 h / 70 °C

2.1: copper(l) chloride; (S,S)-2,6-bis(4-phenyl-2-oxazolinyl)pyridine / 0.5 h / 0 °C

2.2: 96 h / 0 °C

3.1: hydrogen; rosenmund catalyst; quinoline / methanol / 5 h / 20 °C

With quinoline; rosenmund catalyst; hydrogen; tetra(n-butyl)ammonium hydrogensulfate; potassium carbonate; copper(l) chloride; (S,S)-2,6-bis(4-phenyl-2-oxazolinyl)pyridine; In methanol; acetonitrile;
DOI:10.1021/ja4066656