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

Base Information

• Chemical Name: 4-tert-butyl-N-(5-(4-diethoxymethyl)phenyl-6-(2-((5-methylthio-2-pyrimidinyl)oxy)ethoxy)-4-pyrimidinyl)benzenesulfonamide
• CAS No.: 169678-58-4
• Molecular Formula: C₃₂H₃₉N₅O₆S₂
• Molecular Weight: 653.824
• Mol file: 169678-58-4.mol

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

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

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

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

There total 1 articles about 4-tert-butyl-N-(5-(4-diethoxymethyl)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: 37.0%

4-tributylstannylbenzaldehyde diethyl acetal + N-{5-bromo-6-[2-(5-methylthiopyrimidin-2-yloxy)ethoxy]-pyrimidin-4-yl}-4-tert-butylbenzenesulfonamide (169677-21-8) → 4-tert-butyl-N-(5-(4-diethoxymethyl)phenyl-6-(2-((5-methylthio-2-pyrimidinyl)oxy)ethoxy)-4-pyrimidinyl)benzenesulfonamide (169678-58-4)

Guidance literature:

With 2,4-di-t-butyl-3-methyl phenol; triphenylphosphine; copper(I) bromide; bis-triphenylphosphine-palladium(II) chloride; In 1,4-dioxane; for 4h; Heating;

DOI:10.1021/jm000538f

Reference yield: 70.0%

4-tert-butyl-N-(5-(4-diethoxymethyl)phenyl-6-(2-((5-methylthio-2-pyrimidinyl)oxy)ethoxy)-4-pyrimidinyl)benzenesulfonamide (169678-58-4) → 4-tert-butyl-N-(5-(4-formyl)phenyl-6-(2-((5-methylthio-2-pyrimidinyl)oxy)ethoxy)-4-pyrimidinyl)benzenesulfonamide (169679-65-6)

Guidance literature:

With toluene-4-sulfonic acid; In tetrahydrofuran; at 20 ℃; for 1h;

DOI:10.1021/jm000538f

Reference yield:

4-tert-butyl-N-(5-(4-diethoxymethyl)phenyl-6-(2-((5-methylthio-2-pyrimidinyl)oxy)ethoxy)-4-pyrimidinyl)benzenesulfonamide (169678-58-4) → 4-tert-butyl-N-{5-(4-hydroxymethyl-phenyl)-6-[2-(5-methylsulfanyl-pyrimidin-2-yloxy)-ethoxy]-pyrimidin-4-yl}-benzenesulfonamide

Guidance literature:

Multi-step reaction with 2 steps

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

2: 66 percent / NaBH₄ / tetrahydrofuran; propan-2-ol / 0.25 h / 0 °C

With sodium tetrahydroborate; toluene-4-sulfonic acid; In tetrahydrofuran; isopropyl alcohol;

DOI:10.1021/jm000538f

upstream raw materials:

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

Downstream raw materials:

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