4-CHLORO-2-PHENYLQUINAZOLINE Chemical Properties

Melting point:

124-126 °C(lit.)

Boiling point:

383.11°C (rough estimate)

Density 

1.285

refractive index 

1.5749 (estimate)

storage temp. 

under inert gas (nitrogen or Argon) at 2–8 °C

form 

Crystalline Powder

pka

0.67±0.30(Predicted)

color 

Slightly yellow to yellow

InChIKey

OBHKONRNYCDRKM-UHFFFAOYSA-N

CAS DataBase Reference

6484-25-9(CAS DataBase Reference)

Safety Information

Hazard Codes 

Xi

Risk Statements 

36/37/38

Safety Statements 

37/39-26

WGK Germany 

3

HS Code 

29339980

MSDS

• Language:English Provider:SigmaAldrich
• Language:English Provider:ACROS

4-CHLORO-2-PHENYLQUINAZOLINE Usage And Synthesis

Chemical Properties

slightly yellow to yellow crystalline powder

Uses

Reactant involved in the synthesis of biologically active molecules including:

• Nitrotriazole amines or nitroimidazole amines for use as antitrypanosomal activity and mammalian cytotoxicity
• Quinazoline-containing piperazinylpyrimidine derivatives with antitumor activity
• Quinazoline substituted cyclopentane as HCV NS3/4A protease inhibitors
• Quinazolines with antibacterial and antitumor activity
• Aurora inhibitor MK-0457

Reactant involved in Suzuki-Miyaura cross-coupling and catalyst-free / base-free water promoted nucleophilic aromatic substitution

Uses

4-Chloro-2-phenylquinazoline can be involved in the synthesis of biologically active molecules including: Nitrotriazole amines or nitroimidazole amines for use as antitrypanosomal activity and mammalian cytotoxicity.

Synthesis Reference(s)

Journal of the American Chemical Society, 68, p. 1299, 1946 DOI: 10.1021/ja01211a055

Synthesis

General procedure for the synthesis of 4-chloro-2-phenylquinazoline from 4-hydroxy-2-phenylquinazoline: 4-hydroxy-2-phenylquinazoline (10 mmol) was mixed with phosphorochloridic acid (10 mL) and the reaction was stirred under reflux conditions for 9 hours. After completion of the reaction, the solvent was removed by distillation under reduced pressure. Ice water was added to the residue and neutralized with ammonium hydroxide until a precipitate was formed, followed by filtration to collect the precipitate. The product 4-chloro-2-phenylquinazoline (7) was purified by recrystallization from ethanol to give a brown solid in 68% yield. The structure of the product was determined by 1H NMR (500 MHz, DMSO-d6) δ 8.19-8.12 (m, 3H), 7.90-7.85 (m, 2H), 7.67-7.62 (m, 1H), 7.61-7.55 (m, 3H) and 13C NMR (126 MHz, DMSO-d6) δ 161.80, 153.93, 146.17, 135.15, 132.29, 131.09, 128.78, 128.50, 127.31, 126.21, 125.70, 120.75 for confirmation.

References

[1] Medicinal Chemistry Research, 2012, vol. 21, # 7, p. 1199 - 1206
[2] Acta Chimica Hungarica, 1983, vol. 113, # 3, p. 247 - 256
[3] Organic Letters, 2016, vol. 18, # 9, p. 2150 - 2153
[4] Bioorganic and Medicinal Chemistry, 2011, vol. 19, # 6, p. 1987 - 1998
[5] Bioorganic and Medicinal Chemistry, 2013, vol. 21, # 24, p. 7858 - 7873

4-CHLORO-2-PHENYLQUINAZOLINE(6484-25-9)Related Product Information

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• AURORA 19333