4-Chloro-2-(2-fluoro-phenyl)-quinazoline

Base Information

• Chemical Name: 4-Chloro-2-(2-fluoro-phenyl)-quinazoline
• CAS No.: 610276-37-4
• Molecular Formula: C14H8ClFN2
• Molecular Weight: 258.682
• DSSTox Substance ID: DTXSID00406184
• Wikidata: Q82211088
• Mol file: 610276-37-4.mol

Synonyms:4-chloro-2-(2-fluorophenyl)quinazoline;610276-37-4;4-CHLORO-2-(2-FLUORO-PHENYL)-QUINAZOLINE;SCHEMBL4714364;DTXSID00406184;RHJMTCRHSSQQIU-UHFFFAOYSA-N;AKOS000200117;AB13020;FT-0706622;5-CHLORO-4-[(CHLOROACETYL)AMINO]-2-METHOXYBENZOICACID

Chemical Property of 4-Chloro-2-(2-fluoro-phenyl)-quinazoline

Chemical Property:

• Vapor Pressure: 0.0017mmHg at 25°C
• Refractive Index: 1.649
• Boiling Point: 303.2°C at 760 mmHg
• Flash Point: 137.1°C
• PSA: 25.78000
• Density: 1.351g/cm³
• LogP: 4.08930
• Storage Temp.: 2-8°C
• XLogP3: 4.6
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• Exact Mass: 258.0360041
• Heavy Atom Count: 18
• Complexity: 289

Purity/Quality:

97% ^*data from raw suppliers

4-Chloro-2-(2-fluorophenyl)quinazoline 98% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C2C(=C1)C(=NC(=N2)C3=CC=CC=C3F)Cl

Technology Process of 4-Chloro-2-(2-fluoro-phenyl)-quinazoline

There total 3 articles about 4-Chloro-2-(2-fluoro-phenyl)-quinazoline 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: 73.0%

2-(2-fluorophenyl)quinazolin-4(3Η)-one (138867-16-0) → 4-chloro-2-(2-fluoro-phenyl)-quinazoline (610276-37-4)

Guidance literature:

With thionyl chloride; N,N-dimethyl-formamide; In chloroform; at 0 - 80 ℃; for 4h;

Reference yield:

anthranilic acid amide (28144-70-9,88-68-6) → 4-chloro-2-(2-fluoro-phenyl)-quinazoline (610276-37-4)

Guidance literature:

Multi-step reaction with 2 steps

1: dimethyl sulfoxide / 110 °C

2: thionyl chloride; N,N-dimethyl-formamide / Reflux

With thionyl chloride; N,N-dimethyl-formamide; In dimethyl sulfoxide;

DOI:10.1021/acs.jafc.9b04733

Reference yield:

2-Fluorobenzaldehyde (446-52-6) → 4-chloro-2-(2-fluoro-phenyl)-quinazoline (610276-37-4)

Guidance literature:

Multi-step reaction with 2 steps

1: dimethyl sulfoxide / 110 °C

2: thionyl chloride; N,N-dimethyl-formamide / Reflux

With thionyl chloride; N,N-dimethyl-formamide; In dimethyl sulfoxide;

DOI:10.1021/acs.jafc.9b04733

upstream raw materials:

2-(2-fluorophenyl)quinazolin-4(3Η)-one

2-Fluorobenzaldehyde

anthranilic acid amide