摘要:
THE PRESENT INVENTEION PERTAINS TO NEW, PHARMACOLOGICALLY VALUABLE BASICALLY SUBSTITUTED 1,2,3-BENZOTRIAZINE-4(3H)-ONE DERIVATIVES HAVING EXCELLENT CORONARY DILATOR PROPERTIES AND WHICH HAVE THE STRUCTURAL FORMULA
WHEREIN R'' IS A RADICAL SELECTED FROM THE GROUP CONSISTING OF N,N - DI - LOWER-ALKYLAMINO, N-LOWER-ALKYL-N-ALLYLAMINO, N-LOWER-ALKYL-N-(METHOXY-LOWER-ALKYL)-AMINO, N-LOWER-ALKYL-N-(DIETHYLAMINO-LOWER-ALKYL)-AMINO AND N-LOWER-ALKYL-N-BENZYL-AMINO,LOWER ALKYL MEANING ALKYL HAVING 1 TO 4 CARBON ATOMS, SAID RADICAL BEING BOUND VIA IS NITROGEN ATOM, R1 IS A LOIWER ALKOXY GROUP HAVING 1-4 CARBON ATOMS WHICH MAY BE IN THE 6,7 OR 6,7,8-POSITION, R2 IS AN ALKOXY GROUP HAVING 1-4 CARBON ATOMS, M IS AN INTEGER SELECTED FROM 1,2 AND 3, AND N IS AN INTEGER SELECTED FROM THE GROUP CONSISTING OF 2 AND 3 AND PHARMACEUTICALLY ACCEPTABLE ACID ADDITION SALTS THEREOF.
摘要:
THE PRESNET INVENTION PERTAINS TO NEW, PHARMACOLOGICALLY VALUABLE BASICALLY SUBSTITUTED 1,2,3-BENZOTHIAZINE4(3H)-ONE DERIVATIVES HAVING EXCELLENT CORONARY DILATOR PROERTIES AND WHICH HAVE THE STRUCTURAL FORMULA
WHEREIN R'' IS A N-METHYL-N-CYCLOALKYLAMINO RADICAL, CYCLOALKYL HAVING 3-6 CARBON ATOMS, SAID RADICAL BEING BOUND VIA ITS NITROGEN ATOM; R1 IS A LOWER ALKOXY GROUP HAVING 1-4 CARBON ATOMS WHICH MAY BE IN THE 6,7 OR 6,7,8-POSITION; R2 IS AN ALKOXY GROUP HAVING 1-4 CARBON ATOMS; M IS AN INTEGER SELECTED FROM 1, 2 AND 3; AND N IS AN INTEGER SELECTED FROM THE GROUP CONSISTING OF 2 AND 3 AND PHARMACEUTICALLY ACCEPTABLE ACID ADDITION SALTS THEREOF.
摘要:
Alkylthio-, alkylsulfinyl- and alkylsulfonyl-substituted S-((4oxo-1,2,3-benzotriazin-3(4H)-yl)methyl) phosphorothioates and phosphorodithioates of the formula
AND METHODS EMPLOYING AND COMPOSITIONS COMPRISING THESE SUBSTITUTED PHOSPHOROTHIOATES AND SUBSTITUTED PHOSPHORODITHIOATES FOR CONTROLLING PARASITES, ESPECIALLY ARTHROPOD PESTS SUCH AS INSECTS AND ARACHNIDS. In the above and succeeding formulas in the present specification and claims, Z represents oxygen or sulfur; R represents loweralkylthio, loweralkylsulfinyl or loweralkylsulfonyl; and each R'' independently represents loweralkyl.
摘要:
DISCLOSED ARE COMPOUNDS OF THE CLASS OF 4-OXO-1,2,3BENZOTRIAZINE-3-PROPIONIC ACIDS AND ESTERS THEREOF, E.G. 6CHLORO-4-OXO-1,2,3-BENZOTRIAZINE-3-B-PROPIONIC ACID ETHYL ESTER. THE COMPOUNDS HAVE PHARMACOLOGICAL ACTIVITY IN ANIMALS, E.G. ANTI-INFLAMMATORY ACTIVITY. THE COMPOUNDS MAY BE PREPARED, FOR EXAMPLE, BY ADDITION TO THE CORRESPONDING 3-UNSUBSTITUTED COMPOUNDS AND BY REACTION OF AN ANTHRANIL AMIDE WITH SODIUM NITRITE AND A STRONG INORGANIC ACID, E.G. SULFURIC ACID. THE ACID FORMS ARE PREFERABLY PREPARED FROM THE ESTERS IN A KNOWN MANNER.
摘要:
THE PRESENT INVENTION PERTAINS TO NEW, PHARMACOLOGICALLY VALUABLE BASICALLY SUBSTITUTED 1,2,3-BENZOTRIAZINE4(3H)-ONE DERIVATIVES HAVING EXCELLENT CORONARY DILATORY PROPERTIES AND WHICH HAVE THE STRUCTURAL FORMULA
WHEREIN R'' IS A RADICAL SELECTED FROM THE GROUP CONSISTING OF N-METHYLPIPERAZINO, N-PHENYPIPERAZINO AND N-TRIMETHOXYBENZOXYETHYLPIPERAZINO, SAID RADICAL BEING BOUND VIA A NITROGEN ATOM; R1 IS A LOWER ALKOXY GROUP HAVING 1-4 CARBON ATOMS WHICH MAY BE IN THE 6,7 OR 6,7,8-POSITION; R2 IS AN ALKOXY HAVING 1-4 CARBON ATOMS; M IS AN INTEGER SELECTED FORM 1,2 AND 3; AND N IS AN INTEGER SELECTED FROM THE GROUP CONSISTING OF 2 AND 3 AND PHARMACEUTICALLY ACCEPTABLE ACID ADDITION SALTS THEREOF.
摘要:
5-IMINO-1,2,4-TRIAZINES, I.E. 3-(ALKYLMERCAPTO, ALKYLAMINO AND DIALKYLAMINO)-4-(ALKYL AND AMINO)-5-IMINO-6-(OPTIONALLY CHLORO SUBSTITUTED)-PHENYL-1,2,4-TRIAZINES, WHICH POSSESS HERBICIDAL PROPERTIES, AND WHICH MAY BE PRODUCED BY CONVENTIONAL METHODS.