ChemicalBook--->CAS DataBase List--->89466-19-3

89466-19-3

89466-19-3 Structure

89466-19-3 Structure
IdentificationBack Directory
[Name]

5-BroMo-2,3-diMethoxypyrazine
[CAS]

89466-19-3
[Synonyms]

5-BroMo-2,3-diMethoxypyrazine
Pyrazine, 5-bromo-2,3-dimethoxy-
[Molecular Formula]

C6H7BrN2O2
[MDL Number]

MFCD18205982
[MOL File]

89466-19-3.mol
[Molecular Weight]

219.04
Chemical PropertiesBack Directory
[Boiling point ]

210.5±35.0 °C(Predicted)
[density ]

1.563±0.06 g/cm3(Predicted)
[storage temp. ]

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

-2.23±0.10(Predicted)
[Appearance]

White to off-white Solid
Spectrum DetailBack Directory
[Spectrum Detail]

5-BroMo-2,3-diMethoxypyrazine(89466-19-3)1HNMR
Hazard InformationBack Directory
[Synthesis]

2,3-diMethoxypyrazine

68468-30-4

5-BroMo-2,3-diMethoxypyrazine

89466-19-3

N-Bromosuccinimide (11.88 g, 84.91 mmol) was added to a solution of 2,3-dimethoxypyrazine (8.5 g, 60.71 mmol) in N,N-dimethylformamide (85 mL) under nitrogen protection. The reaction mixture was stirred at room temperature for 48 hours. Upon completion of the reaction, the mixture was cooled to -40°C and subsequently slowly poured into a 1.0 N aqueous solution of Na2S2O3. The resulting mixture was continued to be stirred at 0°C for 30 minutes. The reaction mixture was collected as a solid product by filtration and washed with deionized water. The crude product was further purified by silica gel column chromatography with the eluent ethyl acetate/hexane (0-2% gradient) to afford 5-bromo-2,3-dimethoxypyrazine (6.0 g, 45% yield). The product was analyzed by LC-MS showing m/z of 219.0 [M + H]+ and 1H NMR (400 MHz, CDCl3) data as follows: δ 7.71 (s, 1H), 4.01 (d, J = 14.0 Hz, 6H).

[References]

[1] Patent: WO2018/47109, 2018, A1. Location in patent: Paragraph 00216
[2] Journal of Medicinal Chemistry, 2014, vol. 57, # 19, p. 8086 - 8098
[3] Patent: WO2009/20642, 2009, A1. Location in patent: Page/Page column 73-74
[4] Patent: US2010/35931, 2010, A1. Location in patent: Page/Page column 19
[5] Patent: WO2010/51236, 2010, A1. Location in patent: Page/Page column 51
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