6-(2-Trifluoromethyl-phenyl)-pyrido[2,3-d]pyrimidin-7-ylamine

Base Information

• Chemical Name: 6-(2-Trifluoromethyl-phenyl)-pyrido[2,3-d]pyrimidin-7-ylamine
• CAS No.: 76574-59-9
• Molecular Formula: C₁₄H₉F₃N₄
• Molecular Weight: 290.247
• Mol file: 76574-59-9.mol

Synonyms:6-(2-Trifluoromethyl-phenyl)-pyrido[2,3-d]pyrimidin-7-ylamine

Chemical Property of 6-(2-Trifluoromethyl-phenyl)-pyrido[2,3-d]pyrimidin-7-ylamine

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 6-(2-Trifluoromethyl-phenyl)-pyrido[2,3-d]pyrimidin-7-ylamine

There total 4 articles about 6-(2-Trifluoromethyl-phenyl)-pyrido[2,3-d]pyrimidin-7-ylamine 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: 58.0%

4-aminopyrimidine-5-carboxaldehyde (16357-83-8) + 2-(trifluoromethyl)phenylacetonitrile (3038-47-9) → 6-(2-Trifluoromethyl-phenyl)-pyrido[2,3-d]pyrimidin-7-ylamine (76574-59-9)

Guidance literature:

With sodium ethanolate; In ethanol; for 1h; Heating;

DOI:10.1021/jm00136a006

Reference yield:

4-amino-5-cyanopyrimidine (16357-69-0) → 6-(2-Trifluoromethyl-phenyl)-pyrido[2,3-d]pyrimidin-7-ylamine (76574-59-9)

Guidance literature:

Multi-step reaction with 2 steps

1: H₂, HCO₂H / Raney nickel / 3 h / 2585.7 Torr / Ambient temperature

2: 58 percent / NaOEt / ethanol / 1 h / Heating

With formic acid; hydrogen; sodium ethanolate; nickel; In ethanol;

DOI:10.1021/jm00136a006

Reference yield:

(2-(trifluoromethyl)phenyl)methanol (346-06-5) → 6-(2-Trifluoromethyl-phenyl)-pyrido[2,3-d]pyrimidin-7-ylamine (76574-59-9)

Guidance literature:

Multi-step reaction with 3 steps

1: SOCl₂ / benzene / Heating

2: ethanol; H₂O / Heating

3: 58 percent / NaOEt / ethanol / 1 h / Heating

With thionyl chloride; sodium ethanolate; In ethanol; water; benzene;

DOI:10.1021/jm00136a006

upstream raw materials:

4-aminopyrimidine-5-carboxaldehyde

2-(trifluoromethyl)phenylacetonitrile

4-amino-5-cyanopyrimidine

(2-(trifluoromethyl)phenyl)methanol