Identification | Back Directory | [Name]
2-AMINO-3,5-DIBROMO-6-METHYLPYRAZINE | [CAS]
74290-66-7 | [Synonyms]
3,5-DIBROMO-6-METHYLPYRAZIN-2-AMINE 2-AMINO-3,5-DIBROMO-6-METHYLPYRAZINE 3,5-DIBROMO-6-METHYLPYRAZIN-2-YLAMINE 2-Pyrazinamine, 3,5-dibromo-6-methyl- | [Molecular Formula]
C5H5Br2N3 | [MDL Number]
MFCD08705764 | [MOL File]
74290-66-7.mol | [Molecular Weight]
266.92 |
Chemical Properties | Back Directory | [Melting point ]
167-168 °C | [Boiling point ]
300.2±37.0 °C(Predicted) | [density ]
2.104±0.06 g/cm3(Predicted) | [storage temp. ]
under inert gas (nitrogen or Argon) at 2–8 °C | [pka]
1.11±0.10(Predicted) |
Hazard Information | Back Directory | [Synthesis]
General procedure for the synthesis of 2-amino-3,5-dibromo-6-methylpyrazine from 2-amino-6-methylpyrazine: In a dry reaction flask, 6-methylpyrazin-2-amine (14.40 g, 132 mmol) and pyridine (26.0 g, 330 mmol) were dissolved in dichloromethane (DCM, 300 mL). A DCM solution of bromine (53.00 g, 330 mmol) was slowly added dropwise at room temperature. After the dropwise addition was completed, the reaction mixture was stirred at room temperature overnight. Upon completion of the reaction, the reaction was quenched by the addition of water (150 mL) and the mixture was transferred to a dispensing funnel for liquid-liquid partitioning. The organic phase was washed with saturated brine (100 mL), dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated in vacuum to afford 2-amino-3,5-dibromo-6-methylpyrazine as a yellow solid (34.01 g, 96% yield). Mass spectrum (ESI, cation mode) m/z: 267.9 [M + H]+. | [References]
[1] Patent: WO2018/108125, 2018, A1. Location in patent: Paragraph 00500 [2] Patent: WO2008/51493, 2008, A2. Location in patent: Page/Page column 101 [3] Patent: CN106336413, 2017, A. Location in patent: Paragraph 0357; 0358; 0359; 0340 [4] Tetrahedron, 2006, vol. 62, # 26, p. 6272 - 6288 [5] Patent: WO2008/83070, 2008, A1. Location in patent: Page/Page column 85 |
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NovoChemy Ltd.
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SynAsst Chemical.
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021-60343070 |
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