4-tert-butyl-N-[6-chloro-5-(o-methoxyphenoxy)-2-methylsulfanyl-pyrimidin-4-yl]-benzenesulfonamide

Base Information

• Chemical Name: 4-tert-butyl-N-[6-chloro-5-(o-methoxyphenoxy)-2-methylsulfanyl-pyrimidin-4-yl]-benzenesulfonamide
• CAS No.: 184779-25-7
• Molecular Formula: C₂₂H₂₄ClN₃O₄S₂
• Molecular Weight: 494.035
• Mol file: 184779-25-7.mol

Synonyms:4-tert-butyl-N-[6-chloro-5-(o-methoxyphenoxy)-2-methylsulfanyl-pyrimidin-4-yl]-benzenesulfonamide

Chemical Property of 4-tert-butyl-N-[6-chloro-5-(o-methoxyphenoxy)-2-methylsulfanyl-pyrimidin-4-yl]-benzenesulfonamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 4-tert-butyl-N-[6-chloro-5-(o-methoxyphenoxy)-2-methylsulfanyl-pyrimidin-4-yl]-benzenesulfonamide

There total 5 articles about 4-tert-butyl-N-[6-chloro-5-(o-methoxyphenoxy)-2-methylsulfanyl-pyrimidin-4-yl]-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:

tert.-butylphenylsulfonamide potassium salt + 4,6-dichloro-5-(2-methoxy-phenoxy)-2-methylsulfanyl-pyrimidine (179401-12-8) → 4-tert-butyl-N-[6-chloro-5-(o-methoxyphenoxy)-2-methylsulfanyl-pyrimidin-4-yl]-benzenesulfonamide (184779-25-7)

Guidance literature:

In dimethyl sulfoxide;

Reference yield:

4-tert-butylbenzenesulphonamide (6292-59-7) + 4,6-dichloro-5-(2-methoxy-phenoxy)-2-methylsulfanyl-pyrimidine (179401-12-8) → 4-tert-butyl-N-[6-chloro-5-(o-methoxyphenoxy)-2-methylsulfanyl-pyrimidin-4-yl]-benzenesulfonamide (184779-25-7)

Guidance literature:

With potassium carbonate; In dimethyl sulfoxide; at 80 ℃;

DOI:10.1016/S0960-894X(01)00682-5

Reference yield:

2-(2-Methoxyphenoxy)propanedioic acid diethyl ester (20730-58-9) → 4-tert-butyl-N-[6-chloro-5-(o-methoxyphenoxy)-2-methylsulfanyl-pyrimidin-4-yl]-benzenesulfonamide (184779-25-7)

Guidance literature:

Multi-step reaction with 3 steps

1.1: NaOMe / methanol / 16 h / 20 °C

1.2: 90 percent / aq. K₂CO₃ / 3 h / 20 °C

2.1: POCl₃; PhNMe₂ / Heating

3.1: K₂CO₃ / dimethylsulfoxide / 80 °C

With sodium methylate; potassium carbonate; N,N-dimethyl-aniline; trichlorophosphate; In methanol; dimethyl sulfoxide;

DOI:10.1016/S0960-894X(01)00682-5

upstream raw materials:

4-tert-butylbenzenesulphonamide

4,6-dichloro-5-(2-methoxy-phenoxy)-2-methylsulfanyl-pyrimidine

2-(2-Methoxyphenoxy)propanedioic acid diethyl ester

4,6-dihydroxy-5-(2-methoxyphenoxy)-2-methylthiopyrimidine

Downstream raw materials:

N-{6-[2-(5-bromopyrimidin-2-yloxy)ethoxy]-5-(2-methoxy-phenoxy)-2-methylsulfonylpyrimidin-4-yl}-4-tert-butylbenzenesulfonamide

N-{6-[2-(5-bromopyrimidin-2-yloxy)ethoxy]-5-(2-methoxyphenoxy)-2-methylthiopyrimidin-4-yl}-4-tert-butylbenzene-sulfonamide

4-tert-butyl-N-[6-(2-hydroxyethoxy)-5-(2-methoxyphenoxy)-2-methylthiopyrimidin-4-yl]-benzenesulfonamide