6-methoxy-2-(4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-3-(4-((tetrahydro-2H-pyran-2-yl)oxy)phenyl)chroman-4-one

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Chemical Name:6-methoxy-2-(4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-3-(4-((tetrahydro-2H-pyran-2-yl)oxy)phenyl)chroman-4-one
CAS No.:1444006-85-2
Molecular Formula:C₃₅H₄₁NO₆
Molecular Weight:571.714
Hs Code.:

Synonyms:6-methoxy-2-(4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-3-(4-((tetrahydro-2H-pyran-2-yl)oxy)phenyl)chroman-4-one

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Chemical Property of 6-methoxy-2-(4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-3-(4-((tetrahydro-2H-pyran-2-yl)oxy)phenyl)chroman-4-one

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Technology Process of 6-methoxy-2-(4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-3-(4-((tetrahydro-2H-pyran-2-yl)oxy)phenyl)chroman-4-one

There total 5 articles about 6-methoxy-2-(4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-3-(4-((tetrahydro-2H-pyran-2-yl)oxy)phenyl)chroman-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:

: 36603-49-3
4-(tetrahydropyran-2'-yloxy)-1-bromobenzene

: 1443993-02-9
6-methoxy-2-(4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)chroman-4-one

: 1444006-85-2
6-methoxy-2-(4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-3-(4-((tetrahydro-2H-pyran-2-yl)oxy)phenyl)chroman-4-one

Guidance literature:: With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; potassium hydrogencarbonate; tri tert-butylphosphoniumtetrafluoroborate; In 1,4-dioxane; water; at 110 ℃; for 7h;

Reference yield:

: (+)-(R)-2-methylbutane-1,4-diyl dimethanesulfonate

: 1444006-85-2
6-methoxy-2-(4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-3-(4-((tetrahydro-2H-pyran-2-yl)oxy)phenyl)chroman-4-one

Guidance literature:: Multi-step reaction with 4 steps

1: 24 h / 20 °C

2: copper(l) iodide; caesium carbonate / m-xylene / 140 °C / Inert atmosphere

3: pyrrolidine / methanol / 48 h / 50 °C

4: potassium hydrogencarbonate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; tri tert-butylphosphoniumtetrafluoroborate / water; 1,4-dioxane / 7 h / 110 °C

With pyrrolidine; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; copper(l) iodide; potassium hydrogencarbonate; caesium carbonate; tri tert-butylphosphoniumtetrafluoroborate; In 1,4-dioxane; methanol; water; m-xylene;

Reference yield:

: 2938-98-9,70423-38-0,101978-85-2,22644-28-6
(R)-2-methylbutane-1,4-diol

: 1444006-85-2
6-methoxy-2-(4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-3-(4-((tetrahydro-2H-pyran-2-yl)oxy)phenyl)chroman-4-one

Guidance literature:: Multi-step reaction with 5 steps

1: triethylamine / dichloromethane / 1 h / -20 - -15 °C

2: 24 h / 20 °C

3: copper(l) iodide; caesium carbonate / m-xylene / 140 °C / Inert atmosphere

4: pyrrolidine / methanol / 48 h / 50 °C

5: potassium hydrogencarbonate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; tri tert-butylphosphoniumtetrafluoroborate / water; 1,4-dioxane / 7 h / 110 °C

With pyrrolidine; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; copper(l) iodide; potassium hydrogencarbonate; caesium carbonate; triethylamine; tri tert-butylphosphoniumtetrafluoroborate; In 1,4-dioxane; methanol; dichloromethane; water; m-xylene;