Abstract:
Pharmaceutical compositions comprising 2-methyl-3-carboxylic acid-amido-quinoxaline-1,4-di-N-oxides of the formula
wherein: R1 is hydrogen, lower alkyl, lower alkoxy or chlorine, R2 is hydrogen, straight or branched chain alkyl or straight or branched chain alkyl substituted by hydroxy, lower alkoxy, carbalkoxy, monoalkylamino or dialkylamino, and R3 is straight or branched chain alkyl, straight or branched chain alkyl substituted by hydroxy, lower alkoxy, carbalkoxy, monoalkylamino or dialkylamino, or when R2 is hydrogen, cyclohexyl, or R2 and R3 together with the amido nitrogen atom form part of a 5- or 6- membered heterocyclic ring, IN COMBINATION WITH A PHARMACEUTICALLY ACCEPTABLE INERT CARRIER ARE USEFUL FOR THEIR ANTIBACTERIAL EFFECT. These compositions or their active compounds can be administered subcutaneously or orally to humans or animals.
R1 IS HYDROGEN, LOWER ALKYL, LOWER ALKOXY OR CHLORINE, R2 IS HYDROGEN, STRAIGHT OR BRANCHED CHAIN ALKYL OR STRAIGHT OR BRANCHED CHAIN ALKYL SUBSTITUTED BY HYDROXY LOWER ALKOXY, ACYLOXY, MONOALKYLAMINO OR DIALKYLAMINO, R3 IS HYDROGEN, STRAIGHT OR BRANCHED CHAIN ALKYL, STRAIGHT OR BRANCHED CHAIN ALKYL SUBSTITUTED BY HYDROXY, LOWER ALKOXY, ACYLOXY, MONOALKYLAMINO OR DIALKYLAMINO, OR WHEN R2 IS HYDROGEN, CYCLOHEXYL, OR R2 AND R3 TOGETHER WITH THE AMIDE NITROGEN ATOM FORM PART OF A 5- OR 6-MENBERED HETEROCYCLIC RING, AND HAL IS CHLORINE OR BROMINE,
ARE USEFUL FOR THEIR ANTIBACTERIAL EFFECT. THESE COMPOUNDS MAY BE PRODUCED, INTER ALIA, BY REACTING A 2-HALOMETHYL3-CARBOXYLIC ACID AMIDO-QUIOXALINE-1,4-DI-N-OXIDE OF THE FORMULA:
R1-,1,4-DI-O WITH THIOUREA, WHEREIN R1, R2, R3 AND HAL ARE AS ABOVE DEFINED.
Abstract:
QUINOXALINE-DI-N-OXIDES, HAVING PHARMACOLOGICAL PROPERTIES AND USABLE AS INTERMEDIATES FOR PRODUCTING PLANT PROTECTING AGENTS, PRODUCED BY REACTING IN AN ORGANIC DILUENT (E.G. AT 20-100*C.) BENZOFURAZANE-N-OXIDE (OPTIONALLY SUBSTITUTED WITH HALO, ALKYL, ALKOXY, ACYL, SUBSTITUTED ACYL, AMIDO, SUBSTITUTED AMIDO, SULFONAMIDO, AND/ OR SUBSTITUTED SULFONAMIDO)WITH A REAGENT COMPOSED OF EITHER (A) AT LEAST AN EQUIVALENT QUANTITY OF BOTH AN ORGANIC CARBONYL COMPOUND (E.G. LINERR OR CYLCLO ALIPHATIC, ARYL, OR HETEROCYCLIC CARBONYL COMPOUND) WITH IS OPTIONALLY SUBSTITUTED AND WHICH CONTAINS THE LINKAGE
-CH2-CO-
AND A PRIMARY ALIPHATIC AMINE OR AMMONIA; OR (B) AT LEAST AN EQUIVALENT QUANTITY OF THE CORRESPONDING SCHIFF''S BASE TO THE REAGENT UNDER (A).
Abstract:
2-METHYL-3-CARBOXYLIC ACID-AMIDO-QUINOXALINE - 1,4-DIN-OXIDES OF THE FORMULA:
1,4-DI(O=),2-CH3,3-(R2-N(-R3)-OC-),R1-QUINOXALINE
WHEREIN: R1 IS HYDROGEN, LOWER ALKYL, LOWER ALKOXY OR CHLORINE, R2 IS HYDROGEN, STRAIGHT OR BRANCHED CHAIN ALKYL OR STRAIGHT OR BRANCHED CHAIN ALKYL SUBSTITUTED BY HYDROXY, LOWER ALKOXY, CARBALKOXY, MONOALKYLAMINO OR DIALKYLAMINO, AND R3 IS HYDROGEN, STRAIGHT OR BRANCHED CHAIN ALKYL, STRAIGHT OR BRANCHED CHAIN ALKYL SUBSTITUTED BY HYDROXY, LOWER ALKOXY, CARBALKOXY, MONOALKYLAMINO OR DIALKYLAMINO, OR WHEN R2 IS IS HYDROGEN, CYCLOHEXYL, OR R2 AND R3 TOGETHER WITH THE AMIDE NITROGEN ATOM FORM PART OF A 5OR 6-MEMBERED HETEROCYCLIC RING, ARE USEFUL FOR THEIR ANTIBACTERIAL EFFECT. THESE COMPOUNDS MAY BE PRODUCED, INTER ALIA, BY REACTING A BENZOFUROXAN OF THE FORMULA:
Abstract:
The invention disclosed herein relates to the stabilization of natural and synthetic diene polymers with cresol derivatives such a 2-tert. butyl-4-methyl-6-cyclopentyl-phenol, and 2-ter. butyl4-methyl-6-indanyl phenol.
R REPRESENTS AN ALKYL RADICAL OPTIONALLY SUBSTITUTED BY CHLORINE, A CYCLOALKYL RADICAL, AN ARYL RADICAL OPTIONALLY SUBSTITUTED BY AT LEAST ONE ALKYL GROUP AND/OR CHLORINE ATOM, AN ARALKYL RADICAL OR A DIALKYLAMINO GROUP, R1 REPRESENTS AN ARYL RADICAL OPTIONALLY SUBSTITUTED BY AT LEAST ONE ALKYL GROUP AND/OR CHLORINE ATOM, AND X REPRESENTS CHLORINE OR FLORINE ARE USED AS VULCANIZATION RETARDERS INNATURAL AND/OR SYNTHETIC RUBBER MIXTURES. ONE OF THESE VULCANIZATION RETARDERS OF THE AFOREMENTIONED GENERAL FORMULA IS NPHENYL - N -(TRICHLOROMETHYLSULPHENYL) - METHYLSULPHONAMIDE.
Abstract:
AS STABILIZERS AND FURTEHERMORE TO STABILIZED POLYURETHANES BEING STABILIZED WITH A SYNERGISTIC MIXUTRE CONSISTING OF A) AN ANISOLE AND B) A 2-(2''-HYDROXYPHENYL)-BENZOTRIAZOLE.
2-((2-(CH3-O-)PHENYL)-CH2-),6-(TERT ALKYL-)PHENOL
THE INVENTION RELATES TO STABILIZED POLYURETHANES, ESPECAILLY PLYURETHANE ELASTOMER THREADS AND FOILS, AGAINST DEGARADTATION AND DISCLORATIN CAUSED BY THE ACTION OF LIGHT OR UV RADIATION, OXYGEN, SUBSTANCES PRESENT IN THE ATMOSPHERE, SUCH AS NITROGEN OXIDES, AND HEAT BY THE ADDITION OF ALKOXY SUBSTITUTED, STERICALLY HINDERED PHENOLS WHICH HAVE A 2-(2''-HYDROXY-3''-TERTIARY ALKYL BENZYL)-ANISOLE UNIT:
Abstract:
(CYCLOHEXEN-(3)-YLIDENE-METHYL)-HYDROCARBON ETHERS AND THIOETHER AND THEIR CORRESPONDING 2,5-ENDOMETHYLENE DERIVATIVES, PREPARATION THEREOF AND THEIR USE AS ANTI-OZONANTS.
Abstract:
Pharmaceutical compositions are provided for controlling bacterial infections caused by gram-positive and gram-negative bacteria containing a 3-carboxylic acid amido-quinoxaline-1,4-diN-oxide as active ingredient, as exemplified by 2-acetoxymethyl3-carboxylic acid ethylamidoquinoxaline-di-N-oxide and its congeners. The dosage ranges from 5 mg/kg to 150 mg/kg daily orally or parenterally.