Abstract:
AN IMPROVED METHOD OF PREPARING 2,3-DIHYDRO - 1HPYRIDO-(2,3-B)(1,4)THIAZIN - 2 - ONES BY REACTING AN APPROPRIATE 2-MERCAPTO - 3 - NITROPYRIDINE WITH AN APPROPRIATELY SUBSTITUTED HALOACETIC ACID MOIETY.
Abstract:
Biodegradable insecticides having the formula: where X, Y and R are different, and X and Y are selected from the group consisting of hydrogen, halo, lower alkyl and lower alkoxy, and R is selected from the group consisting of nitrogen, oxygen, sulfur and sulfone.
Abstract:
1321360 Process for preparing 2,3-dihydro-1H- pyrido[2,3-b][1,4]thiazin-2-ones ABBOTT LABORATORIES 19 April 1971 [20 Jan 1971] 25672/71 Heading C2C A process for preparing compounds of the Formula I wherein each of Rand X is hydrogen or methyl, comprises reacting a 2-mercapto-3-nitropyridine of the formula with a haloacetic acid or ester Y-CHRCOOR 2 wherein Y is bromo, chloro, fluoro, or iodo, R 2 is hydrogen, methyl and ethyl in a suitable solvent to yield a 3-nitro-pyridinyl-2-thioacetic acid or ester III and hydrogenating the compound III. Pharmaceutical compositions of the compounds I show anti-inflammatory activity.
Abstract:
Covers a method of inducing abscission of fruit by applying a chemical composition containing an effective amount of a 4-nitropyrazole as the active ingredient in an agronomically acceptable carrier. Said composition comprises in addition to said carrier an effective amount of a compound having a formula selected from the group consisting of: WHERE R, R2, R3 and R5 are selected from the group consisting of alkyl, hydrogen, halo, cycloalkyl, aryl, substituted aryl and haloalkyl; and R1 and R4 are selected from the group consisting of hydrogen, loweralkyl, aryl, substituted aryl, haloalkyl, halothioalkyl, arylthio, alkylthio, substituted arylthio, hydroxyalkyl, hydroxyhaloalkyl, alkylcarbamoyl, dialkylcarbamoyl, aryl substituted carbamoyl, substituted diarylcarbamoyl, alkylarylcarbamoyl, alkylsulfonyl, haloalkylsulfonyl, arylsulfonyl, substituted arylsulfonyl, formyl, carboalkoxy, carboaryloxy, pyranyl, thiocarbamoyl, halocarboalkoxy, aroyl, substituted aroyl, aryloxyaceto, substituted aryloxyaceto, arylthioaceto, substituted arylthioaceto, benzyl, substituted benzyl, phenacetyl, substituted phenacetyl, phosphonoalkyl, thiophosphonoalkyl, acetylanilide and metallic salts of any of the foregoing R1 and R4 groups, in an agronomically acceptable carrier. Also covers certain 4-nitropyrazoles having a formula selected from the group consisting of: WHERE R, R2, R3 and R5 are selected from the group consisting of C2-C20 alkyl, hydrogen, halo, cycloalkyl, aryl, substituted aryl, and haloalkyl; and R1 and R4 are selected from the group consisting of hydrogen lower-alkyl, aryl, haloalkyl, halothioalkyl, arylthio, alkylthio, substituted arylthio, hydroxyalkyl, hydroxyhaloalkyl, alkylcarbamoyl, dialkylcarbamoyl, aryl substituted carbamoyl, substituted diarylcarbamoyl, alkylarylcarbamoyl, alkylsulfonyl, haloalkylsulfonyl, arylsulfonyl, substituted arylsulfonyl, formyl, carboalkoxy, carboalkoxy, pyranyl, thiocarbamoyl, halocarboalkoxy, aroyl, substituted aroyl, aryloxyaceto, substituted aryloxyaceto, arylthioaceto, substituted arylthioaceto, benzyl substituted benzyl, phenacetyl, substituted phenacetyl, phosphonoalkyl, thiophosphonoalkyl, and acetylanilide with the proviso that when R5 is chloro and R3 is hydrogen, the nitrogen in the one position is substituted.
Abstract:
Biodegradable insecticides having the formula: where X, Y and R are different, and X and Y are selected from the group consisting of hydrogen, halo, lower alkyl and lower alkoxy, and R is selected from the group consisting of nitrogen, oxygen, sulfur and sulfone.