3-(5-bromo-2-isopropoxyphenyl)-2-((4-(2-(4-chlorophenoxy)ethanoyl)piperazin-1-yl)methyl)quinazolin-4(3H)-one

Base Information

• Chemical Name: 3-(5-bromo-2-isopropoxyphenyl)-2-((4-(2-(4-chlorophenoxy)ethanoyl)piperazin-1-yl)methyl)quinazolin-4(3H)-one
• CAS No.: 1538593-67-7
• Molecular Formula: C₃₀H₃₀BrClN₄O₄
• Molecular Weight: 625.95
• Mol file: 1538593-67-7.mol

Synonyms:3-(5-bromo-2-isopropoxyphenyl)-2-((4-(2-(4-chlorophenoxy)ethanoyl)piperazin-1-yl)methyl)quinazolin-4(3H)-one

Chemical Property of 3-(5-bromo-2-isopropoxyphenyl)-2-((4-(2-(4-chlorophenoxy)ethanoyl)piperazin-1-yl)methyl)quinazolin-4(3H)-one

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 3-(5-bromo-2-isopropoxyphenyl)-2-((4-(2-(4-chlorophenoxy)ethanoyl)piperazin-1-yl)methyl)quinazolin-4(3H)-one

There total 3 articles about 3-(5-bromo-2-isopropoxyphenyl)-2-((4-(2-(4-chlorophenoxy)ethanoyl)piperazin-1-yl)methyl)quinazolin-4(3H)-one 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:

C22H25BrN4O2 + 4-chlorophenyloxyacetyl chloride (4122-68-3) → 3-(5-bromo-2-isopropoxyphenyl)-2-((4-(2-(4-chlorophenoxy)ethanoyl)piperazin-1-yl)methyl)quinazolin-4(3H)-one (1538593-67-7)

Guidance literature:

With dmap; N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃; for 3h; Inert atmosphere;

DOI:10.1016/j.bmcl.2015.07.018

Reference yield:

C18H16BrClN2O2 → 3-(5-bromo-2-isopropoxyphenyl)-2-((4-(2-(4-chlorophenoxy)ethanoyl)piperazin-1-yl)methyl)quinazolin-4(3H)-one (1538593-67-7)

Guidance literature:

Multi-step reaction with 2 steps

1: tetrahydrofuran / 12 h / 20 °C / Inert atmosphere

2: N-ethyl-N,N-diisopropylamine; dmap / dichloromethane / 3 h / 20 °C / Inert atmosphere

With dmap; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane;

DOI:10.1016/j.bmcl.2015.07.018

Reference yield:

4-bromo-2-nitro-1-(propan-2-yloxy)benzene (383869-57-6) → 3-(5-bromo-2-isopropoxyphenyl)-2-((4-(2-(4-chlorophenoxy)ethanoyl)piperazin-1-yl)methyl)quinazolin-4(3H)-one (1538593-67-7)

Guidance literature:

Multi-step reaction with 4 steps

1: hydrogenchloride; tin(ll) chloride / tetrahydrofuran; water / 1.5 h / 50 °C / Inert atmosphere

2: N-ethyl-N,N-diisopropylamine; phosphorus trichloride / 1,4-dioxane / 7 h / 70 °C / Inert atmosphere

3: tetrahydrofuran / 12 h / 20 °C / Inert atmosphere

4: N-ethyl-N,N-diisopropylamine; dmap / dichloromethane / 3 h / 20 °C / Inert atmosphere

With hydrogenchloride; dmap; N-ethyl-N,N-diisopropylamine; tin(ll) chloride; phosphorus trichloride; In tetrahydrofuran; 1,4-dioxane; dichloromethane; water;

DOI:10.1016/j.bmcl.2015.07.018

upstream raw materials:

4-bromo-2-nitro-1-(propan-2-yloxy)benzene

4-chlorophenyloxyacetyl chloride

Downstream raw materials:

2-((4-(2-(4-chlorophenoxy)ethanoyl)piperazin-1-yl)methyl)-3-(2-isopropoxy-5-(piperazin-1-ylmethyl)phenyl)qiuinazolin-4(3H)-one

3-(2-((4-(2-(4-chlorophenoxy)ethanoyl)piperazin-1-yl)methyl)-4-oxoquinazolin-3(4H)-yl)-4-isopropoxybenzaldehyde

2-((4-(2-(4-chlorophenoxy)ethanoyl)piperazin-1-yl)methyl)-3-(2-isopropoxy-5-vinylphenyl)quinazolin-4(3H)-one