ChemicalBook--->CAS DataBase List--->54013-07-9

54013-07-9

54013-07-9 Structure

54013-07-9 Structure
IdentificationBack Directory
[Name]

2-AMINO-5-METHOXYPYRAZINE
[CAS]

54013-07-9
[Synonyms]

5-Methoxy-2-pyrazinamine
2-AMINO-5-METHOXYPYRAZINE
2-Pyrazinamine, 5-methoxy-
5-Methoxy-pyrazin-2-ylaMine
[Molecular Formula]

C5H7N3O
[MDL Number]

MFCD09909647
[MOL File]

54013-07-9.mol
[Molecular Weight]

125.13
Chemical PropertiesBack Directory
[Melting point ]

110-111℃
[Boiling point ]

258.7±35.0℃ (760 Torr)
[density ]

1.224±0.06 g/cm3 (20 ºC 760 Torr)
[Fp ]

110.3±25.9℃
[storage temp. ]

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

2.74±0.10(Predicted)
[Appearance]

Light yellow to brown 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
[HS Code ]

2933998090
Spectrum DetailBack Directory
[Spectrum Detail]

2-AMINO-5-METHOXYPYRAZINE(54013-07-9)1HNMR
Hazard InformationBack Directory
[Synthesis]

Sodium Methoxide

124-41-4

2-Amino-5-chloropyrazine

33332-29-5

2-AMINO-5-METHOXYPYRAZINE

54013-07-9

GENERAL METHOD: 5-Chloropyrazin-2-amine (0.2 g, 1.54 mmol) was dissolved in methanol (3 mL), and copper powder (0.13 g, 2.07 mmol) and a methanolic solution of sodium methanolate (0.38 mL, 1.75 mmol) were added sequentially. The reaction mixture was placed in a sealed tube and the reaction was stirred at 150 °C for 24 hours. After completion of the reaction, the reaction mixture was filtered through diatomaceous earth and the filtrate was concentrated under vacuum to obtain the crude product. The crude product was purified by silica gel column chromatography (100-200 mesh, methanol: dichloromethane, 2-3%) to afford the target compound 2-amino-5-methoxypyrazine (0.13 g, 67% yield).LC-MS (ES+) analysis showed m/z 126 ([M+H]+) with a retention time of 1.06 min (Method 1).

[References]

[1] Patent: WO2013/68458, 2013, A1. Location in patent: Page/Page column 45
[2] Patent: US2014/315885, 2014, A1. Location in patent: Paragraph 0242
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