(3-((4-(2-(5-amino-8-methylbenzo[f][1,7]naphthyridin-2-yl)ethyl)-3-methylphenoxy)methyl)phenyl)phosphonic acid

Base Information

Chemical Name:(3-((4-(2-(5-amino-8-methylbenzo[f][1,7]naphthyridin-2-yl)ethyl)-3-methylphenoxy)methyl)phenyl)phosphonic acid
CAS No.:1258595-25-3
Molecular Formula:C₂₉H₂₈N₃O₄P
Molecular Weight:513.533
Hs Code.:

Synonyms:(3-((4-(2-(5-amino-8-methylbenzo[f][1,7]naphthyridin-2-yl)ethyl)-3-methylphenoxy)methyl)phenyl)phosphonic acid

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Chemical Property of (3-((4-(2-(5-amino-8-methylbenzo[f][1,7]naphthyridin-2-yl)ethyl)-3-methylphenoxy)methyl)phenyl)phosphonic acid

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Technology Process of (3-((4-(2-(5-amino-8-methylbenzo[f][1,7]naphthyridin-2-yl)ethyl)-3-methylphenoxy)methyl)phenyl)phosphonic acid

There total 12 articles about (3-((4-(2-(5-amino-8-methylbenzo[f][1,7]naphthyridin-2-yl)ethyl)-3-methylphenoxy)methyl)phenyl)phosphonic acid 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: 10.0%

: 1269415-36-2
2-(4-(3-iodobenzyloxy)-2-methylphenethyl)-8-methylbenzo[f][1,7]naphthyridin-5-amine

: 1258595-25-3
(3-((4-(2-(5-amino-8-methylbenzo[f][1,7]naphthyridin-2-yl)ethyl)-3-methylphenoxy)methyl)phenyl)phosphonic acid

Guidance literature:: 2-(4-(3-iodobenzyloxy)-2-methylphenethyl)-8-methylbenzo[f][1,7]naphthyridin-5-amine; With palladium diacetate; for 90h;

With trimethylsilyl bromide; In dichloromethane; at 0 - 20 ℃; for 2h;

With water; In dimethyl sulfoxide; pH=9;
DOI:10.1021/acs.jmedchem.6b00489

Reference yield:

: 85331-33-5
2-Cyano-3,5-dichloropyridine

: 1258595-25-3
(3-((4-(2-(5-amino-8-methylbenzo[f][1,7]naphthyridin-2-yl)ethyl)-3-methylphenoxy)methyl)phenyl)phosphonic acid

Guidance literature:: Multi-step reaction with 7 steps

1.1: triethylamine / copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride / N,N-dimethyl-formamide / 60 °C / Inert atmosphere

2.1: potassium phosphate / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane / butan-1-ol; water / 100 °C / Inert atmosphere

3.1: hydrogen / palladium 10% on activated carbon / dichloromethane; ethanol / 20 °C

4.1: boron tribromide / dichloromethane / 0.5 h / Cooling with ice water

5.1: caesium carbonate / N,N-dimethyl-formamide / 0.5 h / 22 °C

5.2: 18 h / 55 °C

6.1: palladium diacetate / 90 °C

7.1: trimethylsilyl bromide / dichloromethane / 2 h / 0 - 20 °C

With potassium phosphate; trimethylsilyl bromide; hydrogen; boron tribromide; caesium carbonate; triethylamine; dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane; bis-triphenylphosphine-palladium(II) chloride; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; copper(l) iodide; palladium 10% on activated carbon; palladium diacetate; In ethanol; dichloromethane; water; N,N-dimethyl-formamide; butan-1-ol;

Reference yield:

: C₃₃H₃₆N₃O₄P

: 1258595-25-3
(3-((4-(2-(5-amino-8-methylbenzo[f][1,7]naphthyridin-2-yl)ethyl)-3-methylphenoxy)methyl)phenyl)phosphonic acid

Guidance literature:: C₃₃H₃₆N₃O₄P; With trimethylsilyl bromide; In dichloromethane; at 0 - 20 ℃; for 2h;

With methanol; In dichloromethane;