2,4,6-Trichloroquinazoline

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2,4,6-Trichloroquinazoline manufacturers

2,4,6-Trichloroquinazoline Basic information
Uses
Product Name:2,4,6-Trichloroquinazoline
Synonyms:2,4,6-TRICHLOROQUINOXALINE;2,4,6-Trichloroquinazoline 98%;2,4,6-trichlroquinazoline;Quinazoline, 2,4,6-trichloro-;2,4,6-Trichloroquinazoline
CAS:20028-68-6
MF:C8H3Cl3N2
MW:233.48
EINECS:
Product Categories:
Mol File:20028-68-6.mol
2,4,6-Trichloroquinazoline Structure
2,4,6-Trichloroquinazoline Chemical Properties
Melting point 131 °C
Boiling point 230-240 °C(Press: 15 Torr)
density 1.600±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
pka-1.15±0.30(Predicted)
AppearanceWhite to light yellow Solid
Safety Information
Hazard Codes T,Xi
Risk Statements 25-37/38-41
Safety Statements 26-36
HS Code 2933998090
MSDS Information
2,4,6-Trichloroquinazoline Usage And Synthesis
Uses2,4,6-Trichloroquinazoline is a heterocyclic organic compound that can be used as a pharmaceutical intermediate.
Synthesis
6-Chloroquinazoline-2,4(1H,3H)-dione

1640-60-4

2,4,6-TRICHLOROQUINAZOLINE

20028-68-6

Part C: Preparation of 2,4,6-trichloroquinazoline. 6-Chloro-2,4-quinazoline dione (3.27 g, 1.0 equiv) was suspended in 30 mL of phosphoryl chloride and 1.5 mL of N,N-dimethylaniline was added as a catalyst. The reaction mixture was heated to reflux and held for 4.5 hours. Upon completion of the reaction, the mixture was cooled to room temperature and then slowly poured into a pre-cooled (0°C) mixture of solvents (300 mL of diethyl ether with 300 mL of water). The organic layer was separated, washed with saturated sodium chloride solution and dried over anhydrous magnesium sulfate. After filtration, the solvent was removed by concentration under reduced pressure to give 3.54 g of brown to yellow solid product in 91% yield. The structure of the product was confirmed by 1H NMR (DMSO-d6, 300 MHz): δ 8.325 (m, 1H), 8.20 (m, 1H), 8.085 (m, 1H).

References[1] Patent: US5187168, 1993, A
[2] Bioorganic and Medicinal Chemistry, 2015, vol. 23, # 24, p. 7717 - 7727
[3] Bioorganic and Medicinal Chemistry, 2003, vol. 11, # 11, p. 2439 - 2444
[4] Patent: WO2010/78449, 2010, A2. Location in patent: Page/Page column 235-236
[5] Scientia Sinica (English Edition), 1958, vol. 7, p. 617,628
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