ChemicalBook--->CAS DataBase List--->53987-60-3

53987-60-3

53987-60-3 Structure

53987-60-3 Structure
IdentificationBack 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 PropertiesBack 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
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

1,3-DIBROMOISOQUINOLINE(53987-60-3)1HNMR
Hazard InformationBack Directory
[Synthesis]

1,2,3,4-Tetrahydroisoquinoline-1,3-dione

4456-77-3

1,3-DIBROMOISOQUINOLINE

53987-60-3

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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