4(3H)-Quinazolinone, 3-(4-hydroxyphenyl)-2-phenyl-

Base Information

• Chemical Name: 4(3H)-Quinazolinone, 3-(4-hydroxyphenyl)-2-phenyl-
• CAS No.: 37856-23-8
• Molecular Formula: C20H14N2O2
• Molecular Weight: 314.343
• DSSTox Substance ID: DTXSID10351777
• Wikidata: Q82128479
• ChEMBL ID: CHEMBL1723451
• Mol file: 37856-23-8.mol

Synonyms:37856-23-8;3-(4-hydroxyphenyl)-2-phenylquinazolin-4(3H)-one;4(3H)-Quinazolinone, 3-(4-hydroxyphenyl)-2-phenyl-;ChemDiv2_003720;Oprea1_386536;MLS000716317;CHEMBL1723451;DTXSID10351777;HMS1379J02;HMS2643F20;STK835539;AKOS000548890;IDI1_002435;SMR000277834;EU-0007686;SR-01000458651;SR-01000458651-1;3-(4-hydroxyphenyl)-2-phenyl-3,4-dihydroquinazolin-4-one

Chemical Property of 4(3H)-Quinazolinone, 3-(4-hydroxyphenyl)-2-phenyl-

Chemical Property:

• PSA: 55.12000
• LogP: 3.75830
• XLogP3: 3.4
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 314.105527694
• Heavy Atom Count: 24
• Complexity: 490

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)C2=NC3=CC=CC=C3C(=O)N2C4=CC=C(C=C4)O

Technology Process of 4(3H)-Quinazolinone, 3-(4-hydroxyphenyl)-2-phenyl-

There total 6 articles about 4(3H)-Quinazolinone, 3-(4-hydroxyphenyl)-2-phenyl- 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: 91.0%

2-phenyl-4H-3,1-benzoxazin-4-one (1022-46-4) + 4-amino-phenol (123-30-8) → 2-phenyl-3-(4-hydroxyphenyl)-4-oxo(3H)-quinazoline (37856-23-8)

Guidance literature:

With pyridine; for 6h; Reflux;

DOI:10.3390/molecules25204780

Reference yield:

benzoyl chloride (98-88-4) → 2-phenyl-3-(4-hydroxyphenyl)-4-oxo(3H)-quinazoline (37856-23-8)

Guidance literature:

Multi-step reaction with 3 steps

1: pyridine / 6 h / 20 °C

2: acetic anhydride / 2 h / Reflux

3: potassium acetate / acetic acid / 16 h

With potassium acetate; acetic anhydride; In pyridine; acetic acid;

DOI:10.1016/j.bmcl.2015.12.037

Reference yield:

anthranilic acid (118-92-3,159201-01-1,50816-84-7,80206-34-4,104809-47-4) → 2-phenyl-3-(4-hydroxyphenyl)-4-oxo(3H)-quinazoline (37856-23-8)

Guidance literature:

Multi-step reaction with 3 steps

1: pyridine / 6 h / 20 °C

2: acetic anhydride / 2 h / Reflux

3: potassium acetate / acetic acid / 16 h

With potassium acetate; acetic anhydride; In pyridine; acetic acid;

DOI:10.1016/j.bmcl.2015.12.037

upstream raw materials:

2-phenyl-4H-3,1-benzoxazin-4-one

4-amino-phenol

4-nitro-phenol

orthobenzoic acid trimethyl ester

Downstream raw materials:

Ethyl-<4-(4-oxo-2-phenyl-3(4H)-quinazolinyl)phenoxy>acetate

1-(3-Chloro-phenyl)-3-{2-[4-(4-oxo-2-phenyl-4H-quinazolin-3-yl)-phenoxy]-acetyl}-urea

1-{2-[4-(4-Oxo-2-phenyl-4H-quinazolin-3-yl)-phenoxy]-acetyl}-3-phenyl-urea

1-{2-[4-(4-Oxo-2-phenyl-4H-quinazolin-3-yl)-phenoxy]-acetyl}-3-p-tolyl-urea