931-18-0Relevant articles and documents
1, 3-dipolar cycloaddition reactions of benzonitrile oxide to 2(1II)-pyrazinone and its n- and o-methyl derivatives
Corsaro, Antonino,Chiacchio, Ugo,Pistara, Venerando,Perrini, Giancarlo
, p. 69 - 80 (2007/10/03)
2(1H)-Pyrazinone, which is in equilibrium with 2-pyrazinol, reacts with benzonitrile oxide (BNO) affording the N-adducl with a 67% yield, while 2-methoxypyrazine gives two methoxypyrazinones (ca. 3%) and a biscycloadduct together with its degradation product, which derive from the two unisolable monocycloadducts to the C=N4 double bond. Af-Methylpyrazinone gives only the degradation product (3.4%) of the initial monocycloadduct of BNO to C=N4: double bond.
Synthesis of Derivatives of Pyrazinopyridimidin-4-ones
Dennin, F.,Blondeau, D.,Sliwa, H.
, p. 1639 - 1643 (2007/10/02)
3-Alkoxy-2-aminopyrazines have been condensed with ethyl ethoxymethylenemalonate and isopropylidene methoxymethylenemalonate to afford 9-alkoxypyrazinopyrimidin-4-ones substituted in the first case by an ethoxycarbonyl group at 3 position.