Identification | Back Directory | [Name]
2,4-DICHLORO-6-FLUOROQUINAZOLINE | [CAS]
134517-57-0 | [Synonyms]
4-dichloro-6-fluoroquinazoline 2,4-Dichloro-6-fluoroquinazolin Quinazoline, 2,4-dichloro-6-fluoro- 2,4-dichloro-6-fluoroquinazoline 97+% | [Molecular Formula]
C8H3Cl2FN2 | [MDL Number]
MFCD09954884 | [MOL File]
134517-57-0.mol | [Molecular Weight]
217.03 |
Chemical Properties | Back Directory | [Boiling point ]
277.3±22.0 °C(Predicted) | [density ]
1.571±0.06 g/cm3(Predicted) | [storage temp. ]
under inert gas (nitrogen or Argon) at 2-8°C | [pka]
-1.09±0.30(Predicted) | [Appearance]
White to yellow Solid |
Hazard Information | Back Directory | [Synthesis]
(Step 2) Synthesis of 2,4-dichloro-6-fluoroquinazoline: Phosphorus pentachloride (12.5 g, 60.0 mmol) was added to phosphorus trichloride (46.0 mL, 502.5 mmol), followed by the slow addition of 6-fluoroquinazoline-2,4(1H,3H)-dione (3.6 g, 20.0 mmol) under stirring. The reaction mixture was heated to reflux and stirred for 9 hours. After completion of the reaction, the mixture was cooled and the solvent was removed under vacuum. An ice-water mixture (400 mL) was added to the residue and stirring was continued for 0.5 hours. The mixture was extracted with dichloromethane (DCM, 250 mL x 3). The DCM layers were combined, dried with anhydrous sodium sulfate, filtered, and the filtrate was concentrated under vacuum. The residue was purified by silica gel column chromatography (eluent: petroleum ether/ethyl acetate, v/v=30/1) to afford the title compound 2,4-dichloro-6-fluoroquinazoline as a white solid (3.735 g, 86.0% yield). m/z MS (ESI, cationic): 216.9 [M + H]+; 1H NMR (CDCl3, 400 MHz) δ ( ppm): 8.03 (dd, J=9.2 Hz, 4.9 Hz, 1H), 7.86 (dd, J=8.1 Hz, 2.7 Hz, 1H), 7.79-7.73 (m, 1H). | [References]
[1] Patent: WO2017/12502, 2017, A1. Location in patent: Page/Page column 52 [2] Patent: WO2017/88759, 2017, A1. Location in patent: Paragraph 00214 [3] Patent: CN105949203, 2016, A. Location in patent: Paragraph 0179; 0185; 0186 [4] Bioorganic and Medicinal Chemistry, 2015, vol. 23, # 24, p. 7717 - 7727 [5] Journal of Medicinal Chemistry, 2008, vol. 51, # 24, p. 7855 - 7865 |
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