ChemicalBook--->CAS DataBase List--->39576-82-4

39576-82-4

39576-82-4 Structure

39576-82-4 Structure
IdentificationBack Directory
[Name]

2,4-DICHLORO-6-METHYLQUINAZOLINE
[CAS]

39576-82-4
[Synonyms]

EOS-60385
2,4-DICHLORO-6-METHYLQUINAZOLINE
6-Methyl-2,4-dichloroquinazoline
Quinazoline, 2,4-dichloro-6-methyl-
2,4-Dichloro-6-methylquinazoline,97%
2,4-Dichloro-6-methylquinazoline 97%
[Molecular Formula]

C9H6Cl2N2
[MDL Number]

MFCD10697888
[MOL File]

39576-82-4.mol
[Molecular Weight]

213.07
Chemical PropertiesBack Directory
[Boiling point ]

292.4±33.0 °C(Predicted)
[density ]

1.418±0.06 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[form ]

Solid
[pka]

-0.30±0.30(Predicted)
[Appearance]

White to off-white Solid
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P280a-P304+P340-P305+P351+P338-P405-P501a
[HS Code ]

2933992000
Spectrum DetailBack Directory
[Spectrum Detail]

2,4-DICHLORO-6-METHYLQUINAZOLINE(39576-82-4)1HNMR
Hazard InformationBack Directory
[Synthesis]

2,4(1H,3H)-Quinazolinedione, 6-methyl-

62484-16-6

2,4-DICHLORO-6-METHYLQUINAZOLINE

39576-82-4

6-Methylquinazoline-2,4(1H,3H)-dione (550 mg, 3.12 mmol) was used as a starting material, which was dissolved in POCl3 (4.0 mL), followed by the addition of N,N'-diethylaniline (0.5 mL). The reaction mixture was heated to 135 °C and the reaction was stirred at this temperature for 3 hours. Upon completion of the reaction, the mixture was cooled to room temperature and carefully poured into ice water. The precipitated solid was collected by filtration and dried to afford 2,4-dichloro-6-methylquinazoline (590 mg, 89% yield), which could be used in subsequent steps without further purification.

[References]

[1] Bioorganic and Medicinal Chemistry Letters, 2012, vol. 22, # 1, p. 461 - 467
[2] Bioorganic and Medicinal Chemistry, 2009, vol. 17, # 1, p. 119 - 132
[3] Patent: WO2004/87680, 2004, A1. Location in patent: Page 162
[4] ACS Medicinal Chemistry Letters, 2015, vol. 6, # 3, p. 308 - 312
[5] Patent: WO2008/16666, 2008, A2. Location in patent: Page/Page column 49
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