4-bromo-N-(4-(6-((3-(trifluoromethyl)phenyl)amino)pyrimidin-4-yl)phenyl)benzenesulfonamide

Base Information

• Chemical Name: 4-bromo-N-(4-(6-((3-(trifluoromethyl)phenyl)amino)pyrimidin-4-yl)phenyl)benzenesulfonamide
• CAS No.: 1376770-32-9
• Molecular Formula: C₂₃H₁₆BrF₃N₄O₂S
• Molecular Weight: 549.371

Synonyms:4-bromo-N-(4-(6-((3-(trifluoromethyl)phenyl)amino)pyrimidin-4-yl)phenyl)benzenesulfonamide

Chemical Property of 4-bromo-N-(4-(6-((3-(trifluoromethyl)phenyl)amino)pyrimidin-4-yl)phenyl)benzenesulfonamide

Chemical Property:

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Technology Process of 4-bromo-N-(4-(6-((3-(trifluoromethyl)phenyl)amino)pyrimidin-4-yl)phenyl)benzenesulfonamide

There total 5 articles about 4-bromo-N-(4-(6-((3-(trifluoromethyl)phenyl)amino)pyrimidin-4-yl)phenyl)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: 80.0%

6-(4-aminophenyl)-N-(3-(trifluoromethyl)phenyl)pyrimidin-4-amine (1376770-17-0) + 4-bromobenzenesulfonyl chloride (98-58-8) → 4-bromo-N-(4-(6-((3-(trifluoromethyl)phenyl)amino)pyrimidin-4-yl)phenyl)benzenesulfonamide (1376770-32-9)

Guidance literature:

With triethylamine; In dichloromethane; at 20 ℃;

DOI:10.1016/j.bmcl.2012.03.092

Reference yield:

4-chloro-6-(4-nitrophenyl)pyrimidine (954221-91-1) → 4-bromo-N-(4-(6-((3-(trifluoromethyl)phenyl)amino)pyrimidin-4-yl)phenyl)benzenesulfonamide (1376770-32-9)

Guidance literature:

Multi-step reaction with 3 steps

1: hydrogenchloride / water; isopropyl alcohol / 0.33 h / 100 °C / Microwave irradiation

2: tin(ll) chloride / ethyl acetate / 12 h / 20 °C

3: triethylamine / dichloromethane / 20 °C

With hydrogenchloride; triethylamine; tin(ll) chloride; In dichloromethane; water; ethyl acetate; isopropyl alcohol;

DOI:10.1016/j.bmcl.2012.03.092

Reference yield:

3-trifluoromethylaniline (98-16-8) → 4-bromo-N-(4-(6-((3-(trifluoromethyl)phenyl)amino)pyrimidin-4-yl)phenyl)benzenesulfonamide (1376770-32-9)

Guidance literature:

Multi-step reaction with 3 steps

1: hydrogenchloride / water; isopropyl alcohol / 0.33 h / 100 °C / Microwave irradiation

2: tin(ll) chloride / ethyl acetate / 12 h / 20 °C

3: triethylamine / dichloromethane / 20 °C

With hydrogenchloride; triethylamine; tin(ll) chloride; In dichloromethane; water; ethyl acetate; isopropyl alcohol;

DOI:10.1016/j.bmcl.2012.03.092

upstream raw materials:

4-chloro-6-(4-nitrophenyl)pyrimidine

6-(4-aminophenyl)-N-(3-(trifluoromethyl)phenyl)pyrimidin-4-amine

4-bromobenzenesulfonyl chloride

3-trifluoromethylaniline

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