1-(3-tert-butyl-1-(quinolin-6-yl)-1H-pyrazol-5-yl)-3-(2-fluoro-5-(2-(methylamino)pyrimidin-4-yloxy)phenyl)urea

Base Information

• Chemical Name: 1-(3-tert-butyl-1-(quinolin-6-yl)-1H-pyrazol-5-yl)-3-(2-fluoro-5-(2-(methylamino)pyrimidin-4-yloxy)phenyl)urea
• CAS No.: 1020172-28-4
• Molecular Formula: C₂₈H₂₇FN₈O₂
• Molecular Weight: 526.573
• Mol file: 1020172-28-4.mol

Synonyms:1-(3-tert-butyl-1-(quinolin-6-yl)-1H-pyrazol-5-yl)-3-(2-fluoro-5-(2-(methylamino)pyrimidin-4-yloxy)phenyl)urea

Chemical Property of 1-(3-tert-butyl-1-(quinolin-6-yl)-1H-pyrazol-5-yl)-3-(2-fluoro-5-(2-(methylamino)pyrimidin-4-yloxy)phenyl)urea

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 1-(3-tert-butyl-1-(quinolin-6-yl)-1H-pyrazol-5-yl)-3-(2-fluoro-5-(2-(methylamino)pyrimidin-4-yloxy)phenyl)urea

There total 13 articles about 1-(3-tert-butyl-1-(quinolin-6-yl)-1H-pyrazol-5-yl)-3-(2-fluoro-5-(2-(methylamino)pyrimidin-4-yloxy)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: 49.0%

4-(3-amino-4-fluorophenoxy)-N-methylpyrimidin-2-amine (1020173-91-4) + 2,2,2-trichloroethyl (3-(tert-butyl)-1-(quinolin-6-yl)-1H-pyrazol-5-yl)carbamate (1011464-72-4) → 1-(3-tert-butyl-1-(quinolin-6-yl)-1H-pyrazol-5-yl)-3-(2-fluoro-5-(2-(methylamino)pyrimidin-4-yloxy)phenyl)urea (1020172-28-4)

Guidance literature:

4-(3-amino-4-fluorophenoxy)-N-methylpyrimidin-2-amine; With trifluoroacetic acid;

2,2,2-trichloroethyl (3-(tert-butyl)-1-(quinolin-6-yl)-1H-pyrazol-5-yl)carbamate; With N-ethyl-N,N-diisopropylamine; In dimethyl sulfoxide; at 50 ℃;

Reference yield: 49.0%

2,2,2-trichloroethyl (3-(tert-butyl)-1-(quinolin-6-yl)-1H-pyrazol-5-yl)carbamate (1011464-72-4) + 4-(3-amino-4-fluorophenoxy)-N-methylpyrimidin-2-amine trifluoroacetate (1020173-92-5) → 1-(3-tert-butyl-1-(quinolin-6-yl)-1H-pyrazol-5-yl)-3-(2-fluoro-5-(2-(methylamino)pyrimidin-4-yloxy)phenyl)urea (1020172-28-4)

Guidance literature:

With N-ethyl-N,N-diisopropylamine; In dimethyl sulfoxide; at 50 ℃;

Reference yield:

5-hydroxy-2-fluoroaniline (62257-16-3) → 1-(3-tert-butyl-1-(quinolin-6-yl)-1H-pyrazol-5-yl)-3-(2-fluoro-5-(2-(methylamino)pyrimidin-4-yloxy)phenyl)urea (1020172-28-4)

Guidance literature:

Multi-step reaction with 3 steps

1.1: potassium tert-butylate / N,N-dimethyl acetamide / 50 °C

2.1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 20 °C

2.2: 40 °C

3.1: N-ethyl-N,N-diisopropylamine / dimethyl sulfoxide / 50 °C

With potassium tert-butylate; N-ethyl-N,N-diisopropylamine; 3-chloro-benzenecarboperoxoic acid; In dichloromethane; N,N-dimethyl acetamide; dimethyl sulfoxide;

upstream raw materials:

4-(3-amino-4-fluorophenoxy)-N-methylpyrimidin-2-amine

2,2,2-trichloroethyl (3-(tert-butyl)-1-(quinolin-6-yl)-1H-pyrazol-5-yl)carbamate

6-hydroxyquinoline

quinolin-6-yl triflate