(1,2,4)Triazolo(1,5-a)pyrazine

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(1,2,4)Triazolo(1,5-a)pyrazine Basic information
Product Name:(1,2,4)Triazolo(1,5-a)pyrazine
Synonyms:(1,2,4)Triazolo(1,5-a)pyrazine
CAS:399-66-6
MF:C5H4N4
MW:120.11
EINECS:
Product Categories:
Mol File:399-66-6.mol
(1,2,4)Triazolo(1,5-a)pyrazine Structure
(1,2,4)Triazolo(1,5-a)pyrazine Chemical Properties
Melting point 125-126 °C
density 1.48±0.1 g/cm3(Predicted)
storage temp. Store at room temperature
pka0.08±0.30(Predicted)
AppearanceOff-white to light brown Solid
Safety Information
MSDS Information
(1,2,4)Triazolo(1,5-a)pyrazine Usage And Synthesis
Synthesis
Methanimidamide, N-hydroxy-N'-2-pyrazinyl-

51519-20-1

(1,2,4)Triazolo(1,5-a)pyrazine

399-66-6

The general procedure for the synthesis of [1,2,4]triazolo[1,5-a]pyrazines from the compound (CAS:51519-20-1) is as follows: polyphosphoric acid (250 g) was added to (Z)-N'-hydroxy-N-(pyrazin-2-yl)carbamoylamide (25.07 g, 181 mmol), followed by immediately heating the reaction mixture to 90 °C. The reaction mixture was kept stirred at this temperature for 4 hours. After completion of the reaction, the hot reaction mixture was slowly poured into ice water and the pH was adjusted to basic with sodium bicarbonate. Subsequently, the aqueous phase was extracted with dichloromethane (1 L, followed by 3 x 0.5 L). All organic phases were combined and dried with anhydrous sodium sulfate (Na2SO4), after which the organic phase was concentrated. The crude product was purified by batch crystallization from ethanol. A final product of 18.10 g was obtained in 83% yield.

References[1] Patent: US2008/153843, 2008, A1. Location in patent: Page/Page column 68
(1,2,4)Triazolo(1,5-a)pyrazine Preparation Products And Raw materials
Raw materialsMethanimidamide, N-hydroxy-N'-2-pyrazinyl--->Sodium bicarbonate
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