Identification | Back Directory | [Name]
5,8-DibroMoiMidazo[1,2-a]pyrazine | [CAS]
957344-74-0 | [Synonyms]
5,8-DibroMoiMidazo[1,2-a]pyrazine 5-bromoimidazo[1,2-a]pyrazin-8-amine Imidazo[1,2-a]pyrazine, 5,8-dibromo- | [Molecular Formula]
C6H3Br2N3 | [MDL Number]
MFCD13193554 | [MOL File]
957344-74-0.mol | [Molecular Weight]
276.92 |
Chemical Properties | Back Directory | [density ]
2.35±0.1 g/cm3(Predicted) | [storage temp. ]
under inert gas (nitrogen or Argon) at 2-8°C | [pka]
-0.30±0.30(Predicted) | [Appearance]
Light brown to light yellow Solid |
Hazard Information | Back Directory | [Synthesis]
General procedure for the synthesis of 5,8-dibromoimidazo[1,2-a]pyrazines from 2,5-dibromo-3-aminopyrazines and bromoacetaldehyde diethyl acetal: 3,6-dibromopyrazin-2-ylamine (4.0 g, 15.80 mmol) and bromoacetaldehyde diethyl acetal (3.7 mL, 24.00 mmol) were dissolved in a mixture of tetrahydrofuran (5.3 mL) and distilled water (53 mL ) in a solvent mixture. The reaction mixture was stirred at 120 °C for 4 hours. Upon completion of the reaction, the reaction solution was neutralized by addition of saturated aqueous sodium bicarbonate. The resulting solid was collected by filtration, washed with distilled water and dried to give 5,8-dibromoimidazo[1,2-a]pyrazine (2.75 g). | [References]
[1] Patent: US2009/286798, 2009, A1. Location in patent: Page/Page column 27 [2] Bioorganic and Medicinal Chemistry Letters, 2012, vol. 22, # 6, p. 2266 - 2270 [3] Patent: KR2015/113801, 2015, A. Location in patent: Paragraph 0127-0130 |
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