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| | 3-Aminopyrazine-2-carbonitrile Basic information |
| Product Name: | 3-Aminopyrazine-2-carbonitrile | | Synonyms: | BUTTPARK 29\04-92;2-aMino-3-cyanopyrazine;Pyrazinecarbonitrile, 3-amino-;3-Amino-2-pyrazinecarbonitrile;2-Pyrazinecarbonitrile, 3-amino-;3-AMINOPYRAZINE-2-CARBONITRILE ISO 9001：2015 REACH;3-Aminopyrazine-2-carbonitrile | | CAS: | 25911-65-3 | | MF: | C5H4N4 | | MW: | 120.11 | | EINECS: | | | Product Categories: | Pyrazine | | Mol File: | 25911-65-3.mol |  |
| | 3-Aminopyrazine-2-carbonitrile Chemical Properties |
| Melting point | 191.9 °C | | Boiling point | 364.8±42.0 °C(Predicted) | | density | 1.34±0.1 g/cm3(Predicted) | | storage temp. | under inert gas (nitrogen or Argon) at 2–8 °C | | pka | 1.45±0.10(Predicted) | | Appearance | Light brown to yellow Solid |
| | 3-Aminopyrazine-2-carbonitrile Usage And Synthesis |
| Uses | 3-Aminopyrazine-2-carbonitrile is a useful synthesis reagent. | | Synthesis Reference(s) | Journal of Heterocyclic Chemistry, 26, p. 817, 1989 DOI: 10.1002/jhet.5570260357 | | Synthesis | Example 3 Synthesis of 3-aminopyrazine-2-carbonitrile (Intermediate 2): Intermediate 1 (3-aminopyrazine-2-carboxamide, 3.5 g, 25 mmol) was dissolved in DMF (40 mL) at room temperature, followed by slow dropwise addition of POCl3 (4.5 mL, 49 mmol). The reaction mixture was heated at 80 °C with stirring for 15 min, after which it was cooled to room temperature. The reaction mixture was slowly poured into ice water and the pH was adjusted to neutral with 10% NaOH solution. The precipitated solid was collected by filtration and redissolved in 5% HCl solution. The acidic solution was heated at 70 °C for 30 min, followed by filtration to separate the solid product. The target compound 3-aminopyrazine-2-carbonitrile was obtained as a brown solid (1.7 g, 56% yield) after sufficient washing with water. The product was characterized by 1H NMR (500 MHz, DMSO-d6): δ 8.28 (d, J=2.4 Hz, 1H), 7.90 (d, J=2.4 Hz, 1H), 7.32 (br s, 2H). Mass spectrum (ES+): m/z 121 ([M+H]+). | | References | [1] Patent: US2007/259876, 2007, A1. Location in patent: Page/Page column 18
[2] Journal of the American Chemical Society, 1945, vol. 67, p. 1711
[3] Bioorganic and Medicinal Chemistry Letters, 2009, vol. 19, # 12, p. 3238 - 3242 |
| | 3-Aminopyrazine-2-carbonitrile Preparation Products And Raw materials |
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