Identification | Back Directory | [Name]
1,3-DIBROMOISOQUINOLINE | [CAS]
53987-60-3 | [Synonyms]
1,3-DIBROMOISOQUINOLINE 1,3-Dibromoisoquineline Isoquinoline, 1,3-dibromo- 1,3-DIBROMOISOQUINOLINE ISO 9001:2015 REACH | [Molecular Formula]
C9H5Br2N | [MDL Number]
MFCD00234474 | [MOL File]
53987-60-3.mol | [Molecular Weight]
286.95 |
Chemical Properties | Back Directory | [Boiling point ]
370.9±22.0 °C(Predicted) | [density ]
1.923±0.06 g/cm3(Predicted) | [storage temp. ]
under inert gas (nitrogen or Argon) at 2-8°C | [pka]
-1.49±0.50(Predicted) | [Appearance]
White to yellow Solid |
Hazard Information | Back Directory | [Synthesis]
General procedure for the synthesis of 1,3-dibromoisoquinoline from 1,3-[2H,4H]-isoquinolinedione: A mixture of 1,3-[2H,4H]-isoquinolinedione (20a, 0.65 g, 4.02 mmol), phosphorus tribromide (1.51 mL, 16.05 mmol) and phosphorus tribromide (1.04 g, 3.61 mmol) was reacted at 180°C The reaction was stirred for 2 hours. Upon completion of the reaction, the mixture was cooled to room temperature, slowly poured into ice water and the pH was adjusted to 8-9 with aqueous 2 N potassium hydroxide. subsequently, the aqueous layer was extracted with toluene and the organic layer was filtered through a neutral alumina column. Finally, the filtrate was evaporated to give the title compound 1,3-dibromoisoquinoline (0.58 g, 56% yield) as a white solid.LRMS (m/z): 286/288/290 (M + 1)+.1H NMR (400 MHz, chloroform-d) δ ppm: 7.67-7.76 (m, 3H), 7.84 (s, 1H), 8.24 (d, J = 8.40 Hz, 1H). | [References]
[1] Patent: US6340759, 2002, B1. Location in patent: Example 28 [2] Patent: WO2012/41476, 2012, A1. Location in patent: Page/Page column 56-57 [3] Patent: EP2441755, 2012, A1. Location in patent: Paragraph 0172 [4] Bioorganic and Medicinal Chemistry, 2015, vol. 23, # 17, p. 5891 - 5908 |
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