Abstract:
A METHOD FOR THE PREPARATION OF 4,5,6,7,-TETRAHYDROINDAZOLES OF THE FORMULA:
1-R1,3-R2,R3,R4-4,5,6,7-TETRAHYDROINDAZOLE, OR 2-R1,3-R2,
R3,R4-4,5,6,7-TETRAHYDROINDAZOLE
IN WHICH AN INDAZOLE OF THE GENERAL FORMULA: 1-R1,3-R2,R3,R4-INDAZOLE OR 2-R1,3-R2,R3,R4-INDAZOLE IS HYDROGENATED IN THE PRESENCE OF PALLADIUM, RHODIUM OR PLATINUM OR CATALYSTS CONTAINING MIXTURES OF THEM AND IN THE PRESENCE OF A STRONG ACID IN A MOLAR EQUIVALENT AT LEAST EQUAL TO THAT OF THE BASIC GROUPS.
Abstract:
COMPOUNDS THAT HAVE THE STRUCTURAL FORMULA 1-((R-)2-N-C(=NH)-S-CH2-),3-X,(Y)N-INDAZOLE . HA WHEREIN X REPRESENTS HYDROGEN OR HALOGEN, Y REPRESENTS HALOGEN OR NITRO, EACH REPRESENTS HYDROGEN OR A LOWER ALKYL GROUP, N REPRESENTS AIN INTEGER IN THE RANGE OF ZERO TO 2, AND A REPRESENTS THE ANION OF A STRONG ACID, ARE USED TO CONTROL THE GROWTH OF FUNGI. AMONG THE MOST ACTIVE OF THESE COMPOUNDS ARE 2-(5-NITROINDAZOLYL-N1METHYL)-2-THIOPSEUDOUREA HYDROCHLORIDE AND 2 - (3 - CHLORO - 6 - NITROINDAZOLY - (1 - METHYL) - 2 - THIOPSEUDOUREA HYDROCHLORIDE.
R1 IS HYDROGEN; ALKYL OF 1 TO 17 CARBON ATOMS; MONO-, DI- OR TRI-HALO-SUBSTITUTED ALKYL OF 1 TO 17 CARBON ATOMS; ALKENYL OF 2 TO 17 CARBON ATOMS; ALKOXY OF 1 TO 2 CARBON ATOMS; PHENYL; 2,4-DICHLOROPHENOXYMETHYL; OR A-(2,4-DICHLOROPHENOXY)-ETHYL; AND R2 IS DISUBSTITUTED ACYCLIC AMINO OR OPTIONALLY SUBSTITUTED MONOCYCLIC OR BICYCLIC HETEROCYCLIC AMINO;
THE COMPOUNDS ARE USEFUL AS CONTACT OR SYSTEMIC BIOCIDAL OR BIOSTATIC AGENTS, ESPECIALLY AGAINST MILDEW AND VARIOUS OTHER FUNGI.
Abstract:
INDAZOLE-3-CARBOXYLIC AMIDES OF THE GENERAL FORMULA
1-Q,3-(R1-N(-R2)-CO-),5,6-DI(CH3-O-)-1H-INDAZOLE
WHEREIN R1 AND R2 REPRESENT INDEPENDENTLY HYDROGEN, STRAIGHT CHAINED OR BRANCHED ALKYL OF UP TO 16 CARBON ATOMS, CYCLOALKYL, NAPHTHYL, PHENYL OR ARALKYL GROUP, WHERE THE PHENYL AND ARALKYL GROUPS MAY BE SUBSTITUTED WITH ONE OR TWO LOWER ALKYL, ALKOXY, TRIFLUOROMETHYL OR HALO SUBSTITUENT, FURTHER R1 AND R2 MAY FORM TOGETHER WITH THE ADJACENT NITROGEN ATOM AND OPTIONALLY WITH A FURTHER NITROGEN ATOM A 5 OR 6 MEMBERED HETEROCYCLIC RADICAL, Q REPRESENTS HYDROGEN, ALKALI METAL OR AN ACYL GROUP OF 1 TO 4 CARBON ATOMS HAVE BEEN PREPARED. THE NEW COMPOUNDS POSSESS VALUABLE PHARMACOLOGICAL ACTIVITIES, FIRST ALL THEY ARE POTENT ANTI-INFLAMMATORY AND ANALGESIC AGENTS.
Abstract:
R1 IS SELECTED FROM THE GROUP CONSISTING OF HYDROGEN AND (LOWER)ALKYL; R2 IS SELECTED FROM THE GROUP CONSISTING OF HYDROXY, AMINO AND (LOWER) ALKOXY; N IS A WHOLE INTEGER OF 1 OR 2. THE COMPOUNDS ARE ACTIVE AS INHIBITORS OF MYCOBACTERIUM TUBERCULOSIS.
Abstract:
1,3-Disubstituted-5,6-dihydrothiopyrano(2,3-c) pyrazoles are synthesized from the new 3-((1,3-disubstituted-5pyrazolyl)thio)propionic acids described. The new fused-ring compounds have excellent anti-inflammatory activity; they relieve edemas and are also useful as antipyretics and analgesics.
Abstract:
4 - HYDROXY-1-SUBSTITUTED-1H-THIENO(2,3-C)-PYRAZOLE-5CARBOXYLIC ACID DERIVATIVES USEFUL AS ANTIAMEBIC AGENTS ARE DISCLOSED, AS WELL AS METHODS OF SYNTHESIS OF THESE COMPOUNDS.
Abstract:
A SERIES OF INDAZOLYLPHENYLUREAS AND INDAZOLYLPHENYLTHIOUREAS, USEFUL FOR PREVENTING AND SUPPRESSING COCCIDIOSIS IN POULTRY, ARE PREPARED BY THE CONDENSATION OF AN AMINOINDAZOLE AND A PHENYLISOCYANATE OR A PHENYLISOTHIOCYANATE.