4-tert-butyl-N-(5-(4-formyl)phenyl-6-(2-((5-methylthio-2-pyrimidinyl)oxy)ethoxy)-4-pyrimidinyl)benzenesulfonamide

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Chemical Name:4-tert-butyl-N-(5-(4-formyl)phenyl-6-(2-((5-methylthio-2-pyrimidinyl)oxy)ethoxy)-4-pyrimidinyl)benzenesulfonamide
CAS No.:169679-65-6
Molecular Formula:C₂₈H₂₉N₅O₅S₂
Molecular Weight:579.701
Hs Code.:

Synonyms:4-tert-butyl-N-(5-(4-formyl)phenyl-6-(2-((5-methylthio-2-pyrimidinyl)oxy)ethoxy)-4-pyrimidinyl)benzenesulfonamide

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Chemical Property of 4-tert-butyl-N-(5-(4-formyl)phenyl-6-(2-((5-methylthio-2-pyrimidinyl)oxy)ethoxy)-4-pyrimidinyl)benzenesulfonamide

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Technology Process of 4-tert-butyl-N-(5-(4-formyl)phenyl-6-(2-((5-methylthio-2-pyrimidinyl)oxy)ethoxy)-4-pyrimidinyl)benzenesulfonamide

There total 3 articles about 4-tert-butyl-N-(5-(4-formyl)phenyl-6-(2-((5-methylthio-2-pyrimidinyl)oxy)ethoxy)-4-pyrimidinyl)benzenesulfonamide 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: 70.0%

: 169678-58-4
4-tert-butyl-N-(5-(4-diethoxymethyl)phenyl-6-(2-((5-methylthio-2-pyrimidinyl)oxy)ethoxy)-4-pyrimidinyl)benzenesulfonamide

: 169679-65-6
4-tert-butyl-N-(5-(4-formyl)phenyl-6-(2-((5-methylthio-2-pyrimidinyl)oxy)ethoxy)-4-pyrimidinyl)benzenesulfonamide

Guidance literature:: With toluene-4-sulfonic acid; In tetrahydrofuran; at 20 ℃; for 1h;
DOI:10.1021/jm000538f

Reference yield:

: 4-tributylstannylbenzaldehyde diethyl acetal

: 169679-65-6
4-tert-butyl-N-(5-(4-formyl)phenyl-6-(2-((5-methylthio-2-pyrimidinyl)oxy)ethoxy)-4-pyrimidinyl)benzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: 37 percent / CuBr; 2,6-di-tert-butylcresol; PPh₃ / PdCl₂(PPh₃)2 / dioxane / 4 h / Heating

2: 70 percent / aq. TsOH / tetrahydrofuran / 1 h / 20 °C

With 2,4-di-t-butyl-3-methyl phenol; toluene-4-sulfonic acid; triphenylphosphine; copper(I) bromide; bis-triphenylphosphine-palladium(II) chloride; In tetrahydrofuran; 1,4-dioxane;
DOI:10.1021/jm000538f

Reference yield:

: 169677-21-8
N-{5-bromo-6-[2-(5-methylthiopyrimidin-2-yloxy)ethoxy]-pyrimidin-4-yl}-4-tert-butylbenzenesulfonamide

: 169679-65-6
4-tert-butyl-N-(5-(4-formyl)phenyl-6-(2-((5-methylthio-2-pyrimidinyl)oxy)ethoxy)-4-pyrimidinyl)benzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: 37 percent / CuBr; 2,6-di-tert-butylcresol; PPh₃ / PdCl₂(PPh₃)2 / dioxane / 4 h / Heating

2: 70 percent / aq. TsOH / tetrahydrofuran / 1 h / 20 °C

With 2,4-di-t-butyl-3-methyl phenol; toluene-4-sulfonic acid; triphenylphosphine; copper(I) bromide; bis-triphenylphosphine-palladium(II) chloride; In tetrahydrofuran; 1,4-dioxane;
DOI:10.1021/jm000538f