Anticoccidials. VI. An improved synthesis of 1,6-dihydro-6-oxo-2-pyrazinecarboxylic acid 4-oxide and some related derivatives and determination of anticoccidial activity.
- 1 January 1981
- journal article
- research article
- Published by Pharmaceutical Society of Japan in CHEMICAL & PHARMACEUTICAL BULLETIN
- Vol. 29 (1) , 88-97
- https://doi.org/10.1248/cpb.29.88
Abstract
1,6-Dihydro-6-oxo-2-pyrazinecarboxylic acid 4-oxide (1) was synthesized by 2 different methods. The first is a hydrolysis of methyl 6-chloro-2-pyrazinecarboxylate 4-oxide, which was in turn obtained from methyl 6-chloro-2-pyrazinecarboxylate by reaction with m-chloroperbenzoic acid. The 2nd is an oxidation of 6-hydroxymethyl- 2(1H)-pyrazinone 4-oxide with nickel peroxide. Compound 1 was converted to amine salts, esters and amides. 6-Methoxy, 6-mercapto and 1-alkyl derivatives were also prepared. The compounds prepared were tested for anticoccidial activity in chickens against Eimeria tenella and marked activity was seen with compound 1 and amine salts of 1. The activity of 1 was counteracted by the simultaneous administration of an equal weight of orotic acid or adenine.This publication has 5 references indexed in Scilit:
- Anticoccidials. V. Synthesis and anticoccidial activity of 2(1H)-pyrazinone 4-oxide derivatives.CHEMICAL & PHARMACEUTICAL BULLETIN, 1980
- Anticoccidials. IV. A convenient synthesis of 2(1H)-pyrazinone 4-oxide derivatives.CHEMICAL & PHARMACEUTICAL BULLETIN, 1980
- Anticoccidials. VII. Synthesis of 4,5-dihydro-5-oxo-2-pyrazinecarboxylic acid 1-oxides.CHEMICAL & PHARMACEUTICAL BULLETIN, 1980
- Anticoccidials. I. Syntheses and anticoccidial activity of 2-amino-5-aryl-1,3,4-oxadiazoles, 5-alkoxy-3-aryl-1H-1,2,4-triazoles, and 3-aryl-.DELTA.2-1,2,4-triazolin-5-ones.CHEMICAL & PHARMACEUTICAL BULLETIN, 1976
- Orotidylic Acid Decarboxylase: Inhibition Studies with Azauridine 5′-PhosphateJournal of Biological Chemistry, 1960