5-hydroxy-2-phenyl-7-(3-(4-(3-((1,2,3,4-tetrahydroacridin-9-yl)amino)propyl)piperazin-1-yl)propoxy)-4H-chromen-4-one

Base Information

Chemical Name:5-hydroxy-2-phenyl-7-(3-(4-(3-((1,2,3,4-tetrahydroacridin-9-yl)amino)propyl)piperazin-1-yl)propoxy)-4H-chromen-4-one
CAS No.:1489102-99-9
Molecular Formula:C₃₈H₄₂N₄O₄
Molecular Weight:618.776
Hs Code.:

Synonyms:5-hydroxy-2-phenyl-7-(3-(4-(3-((1,2,3,4-tetrahydroacridin-9-yl)amino)propyl)piperazin-1-yl)propoxy)-4H-chromen-4-one

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Chemical Property of 5-hydroxy-2-phenyl-7-(3-(4-(3-((1,2,3,4-tetrahydroacridin-9-yl)amino)propyl)piperazin-1-yl)propoxy)-4H-chromen-4-one

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Technology Process of 5-hydroxy-2-phenyl-7-(3-(4-(3-((1,2,3,4-tetrahydroacridin-9-yl)amino)propyl)piperazin-1-yl)propoxy)-4H-chromen-4-one

There total 9 articles about 5-hydroxy-2-phenyl-7-(3-(4-(3-((1,2,3,4-tetrahydroacridin-9-yl)amino)propyl)piperazin-1-yl)propoxy)-4H-chromen-4-one 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: 45.0%

: 873302-14-8
7-(3-bromopropoxy)-5-hydroxy-2-phenyl-4H-chromen-4-one

: 1489102-49-9
N-(3-(piperazin-1-yl)propyl)-1,2,3,4-tetrahydroacridin-9-amine

: 1489102-99-9
5-hydroxy-2-phenyl-7-(3-(4-(3-((1,2,3,4-tetrahydroacridin-9-yl)amino)propyl)piperazin-1-yl)propoxy)-4H-chromen-4-one

Guidance literature:: With potassium carbonate; In acetonitrile; for 8h; Reflux;
DOI:10.1016/j.ejmech.2013.09.024

Reference yield:

: 480-66-0,67471-34-5
2,4,6-trihydroxyacetophenone

: 1489102-99-9
5-hydroxy-2-phenyl-7-(3-(4-(3-((1,2,3,4-tetrahydroacridin-9-yl)amino)propyl)piperazin-1-yl)propoxy)-4H-chromen-4-one

Guidance literature:: Multi-step reaction with 3 steps

1.1: lithium hexamethyldisilazane / tetrahydrofuran / 3.25 h / -78 °C / Inert atmosphere

1.2: 5.17 h / -78 - 20 °C / Inert atmosphere

2.1: potassium carbonate / acetone / 4 h / Reflux

3.1: potassium carbonate / acetonitrile / 8 h / Reflux

With potassium carbonate; lithium hexamethyldisilazane; In tetrahydrofuran; acetone; acetonitrile;
DOI:10.1016/j.ejmech.2013.09.024

Reference yield:

: 98-88-4
benzoyl chloride

: 1489102-99-9
5-hydroxy-2-phenyl-7-(3-(4-(3-((1,2,3,4-tetrahydroacridin-9-yl)amino)propyl)piperazin-1-yl)propoxy)-4H-chromen-4-one

Guidance literature:: Multi-step reaction with 3 steps

1.1: lithium hexamethyldisilazane / tetrahydrofuran / 3.25 h / -78 °C / Inert atmosphere

1.2: 5.17 h / -78 - 20 °C / Inert atmosphere

2.1: potassium carbonate / acetone / 4 h / Reflux

3.1: potassium carbonate / acetonitrile / 8 h / Reflux

With potassium carbonate; lithium hexamethyldisilazane; In tetrahydrofuran; acetone; acetonitrile;
DOI:10.1016/j.ejmech.2013.09.024