ChemicalBook--->CAS DataBase List--->19838-08-5

19838-08-5

19838-08-5 Structure

19838-08-5 Structure
IdentificationBack Directory
[Name]

2-Amino-3-methylpyrazine
[CAS]

19838-08-5
[Synonyms]

(S)-HEXAHYDROPYRRO...
3-methylpyrazin-2-amine
3-Methyl-2-pyrazinamine
2-Pyrazinamine,3-methyl-
2-AMINO-3-METHYLPYRAZINE
2-Methyl-3-aMinopyrazine
3-METHYLPYRAZIN-2-YLAMINE
3-Methylpyrazin-2-amine 97%
2-Amino-3-methylpyrazine,95%
[Molecular Formula]

C5H7N3
[MDL Number]

MFCD08705770
[MOL File]

19838-08-5.mol
[Molecular Weight]

109.13
Chemical PropertiesBack Directory
[Melting point ]

165-167 °C
[Boiling point ]

194.6°C (rough estimate)
[density ]

1.1118 (rough estimate)
[refractive index ]

1.5340 (estimate)
[storage temp. ]

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

Solid
[pka]

3.56±0.10(Predicted)
[Appearance]

White to yellow Solid
[InChI]

InChI=1S/C5H7N3/c1-4-5(6)8-3-2-7-4/h2-3H,1H3,(H2,6,8)
[InChIKey]

VQPHZDDLWFHRHR-UHFFFAOYSA-N
[SMILES]

C1(N)=NC=CN=C1C
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P280a-P304+P340-P305+P351+P338-P405-P501a
[HS Code ]

2933998090
Spectrum DetailBack Directory
[Spectrum Detail]

2-Amino-3-methylpyrazine(19838-08-5)1HNMR
Hazard InformationBack Directory
[Pharmaceutical Applications]

2-Amino-3-methylpyrazine is utilized in medicinal chemistry as a scaffold for developing bioactive molecules, such as kinases and potential antiviral agents.
[Synthesis]

2-CHLORO-3-METHYLPYRAZINE

95-58-9

2-Amino-3-methylpyrazine

19838-08-5

The general procedure for the synthesis of 2-amino-3-methylpyrazine from 2-chloro-3-methylpyrazine was as follows: a mixture of 2-chloro-3-methylpyrazine (7 g, 54.69 mmol) and 25% ammonia (100 mL) was placed in a sealed tube, heated to 160 °C and reacted for 24 hours. After completion of the reaction, the mixture was cooled to room temperature and extracted with ethyl acetate (3 x 200 mL). The organic phases were combined, dried over anhydrous sodium sulfate, and subsequently concentrated under reduced pressure to give 2.18 g (89% yield) of 3-methylpyrazin-2-amine as a yellow solid. m/z 110 ([M+H]+) by LCMS.

[References]

[1] Patent: WO2009/29625, 2009, A1. Location in patent: Page/Page column 67
[2] Patent: WO2005/120513, 2005, A1. Location in patent: Page/Page column 15; 16
[3] Patent: WO2006/131003, 2006, A1. Location in patent: Page/Page column 17
[4] Synthesis, 1994, # 9, p. 931 - 934
[5] Patent: WO2010/83617, 2010, A1. Location in patent: Page/Page column 62
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