64262-08-4Relevant articles and documents
Displacement Reactions of 2,3-Dichloro-6-nitroquinoxaline: Synthesis of s-Triazoloquinoxaline
Nagarajan, K.,Parthasarathy, P. C.,Shenoy, S. J.,Anandan, L.
, p. 739 - 740 (2007/10/02)
2,3-Dichloro-6-nitroquinoxaline (1) undergoes displacement reactions with 1-methylpiperazine in the hot to give the bis-derivative (2) and at 30 deg C selectively at position-2 to afford the mono-derivative (3).Structure-proof for the latter involves transformation of 3 through hydrazine derivative (4) to the triazoloquinoxaline (5) and its 1-phenyl derivative (6) and comparison of the chemical shifts of protons at C-9 in the pair.
Antiamebic amidines and sulfonamides of 5- and 6-amino-2,3-bis(4-alkyl-1-piperazinyl)quinoxalines
Fabio,Lang Jr.,Lin,Tomcufcik
, p. 201 - 206 (2007/10/02)
A series of amidines and sulfonamides of 5- and 6-amino-2,3-bis(4-alkyl-1-piperazinyl)quinoxalines was synthesized and tested against cecal and hepatic forms of Entamoeba histolytica infections in rats and hamsters, respectively. Four compounds (5, 6, 8,
2,3-Bis(4-alkyl-1-piperazinyl)quinoxalines
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, (2008/06/13)
This disclosure describes compounds of the class of 5- or 6-substituted 2,3-bis(4-alkyl-1-piperazinyl)quinoxalines useful for ameliorating cecal and hepatic amebic infestations in warm-blooded animals.