(S)-1-(4-chloro-3-(trifluoromethyl)phenyl)-3-(3-(1-(2-(2-hydroxypropylamino)pyrimidin-4-yl)-1H-imidazol-2-yl)phenyl)urea

Base Information

• Chemical Name: (S)-1-(4-chloro-3-(trifluoromethyl)phenyl)-3-(3-(1-(2-(2-hydroxypropylamino)pyrimidin-4-yl)-1H-imidazol-2-yl)phenyl)urea
• CAS No.: 1220701-38-1
• Molecular Formula: C₂₄H₂₁ClF₃N₇O₂
• Molecular Weight: 531.925
• Mol file: 1220701-38-1.mol

Synonyms:(S)-1-(4-chloro-3-(trifluoromethyl)phenyl)-3-(3-(1-(2-(2-hydroxypropylamino)pyrimidin-4-yl)-1H-imidazol-2-yl)phenyl)urea

Chemical Property of (S)-1-(4-chloro-3-(trifluoromethyl)phenyl)-3-(3-(1-(2-(2-hydroxypropylamino)pyrimidin-4-yl)-1H-imidazol-2-yl)phenyl)urea

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (S)-1-(4-chloro-3-(trifluoromethyl)phenyl)-3-(3-(1-(2-(2-hydroxypropylamino)pyrimidin-4-yl)-1H-imidazol-2-yl)phenyl)urea

There total 6 articles about (S)-1-(4-chloro-3-(trifluoromethyl)phenyl)-3-(3-(1-(2-(2-hydroxypropylamino)pyrimidin-4-yl)-1H-imidazol-2-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: 59.4%

(S)-1-(4-(2-(3-aminophenyl)-1H-imidazol-1-yl)pyrimidin-2-ylamino)propan-2-ol (1220701-20-1) + 4-chloro-3-(trifluoromethyl)phenyl isocyanate (327-78-6) → (S)-1-(4-chloro-3-(trifluoromethyl)phenyl)-3-(3-(1-(2-(2-hydroxypropylamino)pyrimidin-4-yl)-1H-imidazol-2-yl)phenyl)urea (1220701-38-1)

Guidance literature:

In tetrahydrofuran; at 20 ℃; for 12h;

Reference yield:

2‐(3‐nitrophenyl)‐1H‐imidazole (13682-18-3) → (S)-1-(4-chloro-3-(trifluoromethyl)phenyl)-3-(3-(1-(2-(2-hydroxypropylamino)pyrimidin-4-yl)-1H-imidazol-2-yl)phenyl)urea (1220701-38-1)

Guidance literature:

Multi-step reaction with 5 steps

1: potassium phosphate / palladium diacetate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl / toluene / 3 h / 130 °C

2: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 8 h / 20 °C

3: tetrahydrofuran / 8 h / 60 °C

4: hydrogen / palladium 10% on activated carbon / methanol / 6 h / 20 °C

5: tetrahydrofuran / 12 h / 20 °C

With potassium phosphate; hydrogen; 3-chloro-benzenecarboperoxoic acid; palladium 10% on activated carbon; palladium diacetate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; In tetrahydrofuran; methanol; dichloromethane; toluene;

Reference yield:

2-(methylsulfonyl)-4-(2-(3-nitrophenyl)-1H-imidazol-1-yl)pyrimidine (1220701-16-5) → (S)-1-(4-chloro-3-(trifluoromethyl)phenyl)-3-(3-(1-(2-(2-hydroxypropylamino)pyrimidin-4-yl)-1H-imidazol-2-yl)phenyl)urea (1220701-38-1)

Guidance literature:

Multi-step reaction with 3 steps

1: tetrahydrofuran / 8 h / 60 °C

2: hydrogen / palladium 10% on activated carbon / methanol / 6 h / 20 °C

3: tetrahydrofuran / 12 h / 20 °C

With hydrogen; palladium 10% on activated carbon; In tetrahydrofuran; methanol;

upstream raw materials:

(S)-1-(4-(2-(3-aminophenyl)-1H-imidazol-1-yl)pyrimidin-2-ylamino)propan-2-ol

4-chloro-3-(trifluoromethyl)phenyl isocyanate

2‐(3‐nitrophenyl)‐1H‐imidazole

3-nitrobenzonitrile