1-(4-cyanophenyl)-3-(4-(6-((3-(trifluoromethyl)phenyl)amino)pyrimidin-4-yl)phenyl)urea

Base Information

• Chemical Name: 1-(4-cyanophenyl)-3-(4-(6-((3-(trifluoromethyl)phenyl)amino)pyrimidin-4-yl)phenyl)urea
• CAS No.: 1376770-24-9
• Molecular Formula: C₂₅H₁₇F₃N₆O
• Molecular Weight: 474.445

Synonyms:1-(4-cyanophenyl)-3-(4-(6-((3-(trifluoromethyl)phenyl)amino)pyrimidin-4-yl)phenyl)urea

Chemical Property of 1-(4-cyanophenyl)-3-(4-(6-((3-(trifluoromethyl)phenyl)amino)pyrimidin-4-yl)phenyl)urea

Chemical Property:

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Technology Process of 1-(4-cyanophenyl)-3-(4-(6-((3-(trifluoromethyl)phenyl)amino)pyrimidin-4-yl)phenyl)urea

There total 4 articles about 1-(4-cyanophenyl)-3-(4-(6-((3-(trifluoromethyl)phenyl)amino)pyrimidin-4-yl)phenyl)urea 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: 79.0%

6-(4-aminophenyl)-N-(3-(trifluoromethyl)phenyl)pyrimidin-4-amine (1376770-17-0) + p-cyanophenyl isocyanate (40465-45-0) → 1-(4-cyanophenyl)-3-(4-(6-((3-(trifluoromethyl)phenyl)amino)pyrimidin-4-yl)phenyl)urea (1376770-24-9)

Guidance literature:

In tetrahydrofuran; at 20 ℃;

DOI:10.1016/j.bmcl.2012.03.092

Reference yield:

4-chloro-6-(4-nitrophenyl)pyrimidine (954221-91-1) → 1-(4-cyanophenyl)-3-(4-(6-((3-(trifluoromethyl)phenyl)amino)pyrimidin-4-yl)phenyl)urea (1376770-24-9)

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: tetrahydrofuran / 20 °C

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

DOI:10.1016/j.bmcl.2012.03.092

Reference yield:

3-trifluoromethylaniline (98-16-8) → 1-(4-cyanophenyl)-3-(4-(6-((3-(trifluoromethyl)phenyl)amino)pyrimidin-4-yl)phenyl)urea (1376770-24-9)

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: tetrahydrofuran / 20 °C

With hydrogenchloride; tin(ll) chloride; In tetrahydrofuran; 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

p-cyanophenyl isocyanate

3-trifluoromethylaniline

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