2-{5-[(7-{3-[ethyl(2-hydroxyethyl)amino]propoxy}quinazolin-4-yl)amino]-1H-pyrazol-3-yl}-N-(3-fluorophenyl)acetamide

Base Information

• Chemical Name: 2-{5-[(7-{3-[ethyl(2-hydroxyethyl)amino]propoxy}quinazolin-4-yl)amino]-1H-pyrazol-3-yl}-N-(3-fluorophenyl)acetamide
• CAS No.: 1218904-24-5
• Molecular Formula: C₂₆H₃₀FN₇O₃
• Molecular Weight: 507.568
• Mol file: 1218904-24-5.mol

Synonyms:

Chemical Property of 2-{5-[(7-{3-[ethyl(2-hydroxyethyl)amino]propoxy}quinazolin-4-yl)amino]-1H-pyrazol-3-yl}-N-(3-fluorophenyl)acetamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 2-{5-[(7-{3-[ethyl(2-hydroxyethyl)amino]propoxy}quinazolin-4-yl)amino]-1H-pyrazol-3-yl}-N-(3-fluorophenyl)acetamide

There total 8 articles about 2-{5-[(7-{3-[ethyl(2-hydroxyethyl)amino]propoxy}quinazolin-4-yl)amino]-1H-pyrazol-3-yl}-N-(3-fluorophenyl)acetamide 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:

4-chloro-7-hydroxyquinazoline (849345-42-2) → 2-{5-[(7-{3-[ethyl(2-hydroxyethyl)amino]propoxy}quinazolin-4-yl)amino]-1H-pyrazol-3-yl}-N-(3-fluorophenyl)acetamide (1218904-24-5,722544-51-6)

Guidance literature:

Multi-step reaction with 5 steps

1: copper(I) oxide; ammonia / 200 °C / 60006 Torr

2: sulfuric acid / Heating

3: tetra(n-butyl)ammonium hydrogensulfate; sodium hydroxide / water

4: tetra(n-butyl)ammonium hydrogensulfate; sodium hydroxide / water

5: tetra(n-butyl)ammonium hydrogensulfate; sodium hydroxide / water

With copper(I) oxide; sulfuric acid; ammonia; tetra(n-butyl)ammonium hydrogensulfate; sodium hydroxide; In water;

Reference yield:

meta-fluoroaniline (372-19-0) + 2-{5-[(7-{3-[ethyl(2-hydroxyethyl)amino]propoxy}quinazolin-4-yl)amino]-1H-pyrazole-3-yl}acetyl chloride → 2-{5-[(7-{3-[ethyl(2-hydroxyethyl)amino]propoxy}quinazolin-4-yl)amino]-1H-pyrazol-3-yl}-N-(3-fluorophenyl)acetamide (1218904-24-5,722544-51-6)

Guidance literature:

With tetra(n-butyl)ammonium hydrogensulfate; sodium hydroxide; In water;

Reference yield:

ethylpropylamine (20193-20-8) → 2-{5-[(7-{3-[ethyl(2-hydroxyethyl)amino]propoxy}quinazolin-4-yl)amino]-1H-pyrazol-3-yl}-N-(3-fluorophenyl)acetamide (1218904-24-5,722544-51-6)

Guidance literature:

Multi-step reaction with 6 steps

1: chlorine; tetrachloromethane / 25 °C / Irradiation

2: sodium hydroxide / water / 25 °C / Irradiation

3: sulfuric acid / Heating

4: tetra(n-butyl)ammonium hydrogensulfate; sodium hydroxide / water

5: tetra(n-butyl)ammonium hydrogensulfate; sodium hydroxide / water

6: tetra(n-butyl)ammonium hydrogensulfate; sodium hydroxide / water

With tetrachloromethane; sulfuric acid; tetra(n-butyl)ammonium hydrogensulfate; chlorine; sodium hydroxide; In water;

upstream raw materials:

4-amino-7-hydroxyquinazoline

ethylpropylamine

meta-fluoroaniline

3-ethylamino-propan-1-ol