Abstract:
Title compds. (I; R1 = C1-4 alkyl; R2,R3 = H, oxalic acid, C1-4 alkoxy, halogen, CF3, C1-4 alkyl, carboalkoxy, CN), useful as anthelimintics, were prepd. Thus, O-phenylene diamines(II) were condensed with HN:C(SCH3)NHCO2R1 at pH1-6,NCNHCO2R' at pH 1-6, R1OC (;O)N;C Cl2 at -10-40≦̸C in the presence of base, and R4S(R5S)C:N CO2R1(R4,R5 = same or not C1-4 alkyl, C3-5 alkenyl, cyclohexyl) to give I.
Abstract:
Benzimidazole derivatives of the formula
wherein R1 is alkyl or cycloalkyl and R2 is alkyl, haloalkyl, cycloalkyl or optionally substituted phenyl, benzyl or naphthyl, are valuable fungicides and anthelmintics.
Abstract translation:式N的苯并咪唑衍生物N ANGLE ANGLE -NH-COOCH 3 N | O = C-NH-SO 2 -N-SO 2 -R 2 | R 1其中R 1是烷基或环烷基,R 2是烷基,卤代烷基,环烷基或任选取代的苯基,苄基或 萘基,是有价值的杀真菌剂和驱虫剂。
Abstract:
The invention describes novel 2-carbalkoxy-amino-benzimidazolyl5(6)-amino-phenyl ether of the formula (I)
wherein R1 is alkyl having 1 to 4 carbon atoms, R2, in each case independently from one another, represents hydrogen, alkyl having 1 to 4 carbon atoms, hydroxyl, alkoxy having 1 to 4 carbon atoms, halogen or trifluoromethyl, n represents the integers 0, 1 or 2 and X represents oxygen or sulfur, the salts of such compounds with physiologically tolerable salts and their preparation. These compounds are chemotherapeutics and act particularly against helminths in humans and animals.
WHEREIN R1 is alkyl, R2 is alkyl, cyclo-alkyl, benzyl or phenyl, SR2 being in 2- or 3-position, R3 is hydrogen, alkyl, aliphatic saturated alkanoyl, chlorine, bromine, cyano, methoxy, ethoxy, phenoxy, phenylthio or benzoyl, and R4 is hydrogen, chlorine or methyl are valuable fungicides and anthelminthics.
Abstract:
AND TO A PROCESS FOR PREPARING THESE COMPOUNDS. The products of the invention are useful as pesticides, especially as fungicides on the plant system and as antiparasites.
The invention relates to bis-triazinobenzimidazoles of the formula
Abstract:
4-Methylene-2-quinolones of formula (I) and their tautomers of formula (Ia) and their isomers, salts and prodrugs are new: n = 0-4; R1 = halo, CF3, OCF3, OH, alkyl, cycloalkyl, alkoxy, alkoxyalkoxy, alkylthio, alkylsulphinyl, alkylsulphonyl, NO2, NH2, azido, alkylamino, dialkylamino, piperidino, morpholino, pyrrolidino, acyl, acyloxy, acylamino, CONH2, COOH, alkoxycarbonyl, SO3H, SO2NH2, Ar, OAr, COOAr, SAr, SOAr, SO2Ar, SO3Ar, OSO2Ar, SO2NHAr, NHSO2Ar, COAr, Ar', etc.; Ar,Ar' = phenyl and heteroaryl resp., etc.; X = O, S, Se, NR2 or NOR2; R2 = H; alkyl opt. substd. by halogen, CN, NH2, OH, etc.;R5, R6 = COOH or gps. as defined for R2; or R5+R6 forms a 3-8C carbocyclic ring; R3,R4 = alkyl, alkenyl, cycloalkyl or cycloalkenyl,etc.; or R3+R4 = a 3-8C carbocyclic ring; or R3+R4 = CZ1Z2 gp., where Z1 and Z2 are as defined for R3 and R4 as above; provided that X is not O when R1=R2=R5=R6=H and R3=R4=Me or R3+R4= (CH2)4.
Abstract:
Quinoxaline derivs. of formula (I) and tautomers of formula (Ia), and their salts and prodrugs are new: R1 = F, Cl,OH or 1-3C alkoxy; R2 = 1-4C alkyl (opt. substd. by OH, 1-4C alkoxy or 1-4C alkylthio); R3 = 1-6C alkoxy-carbonyl or 2-6C alkenyloxy carbonyl; X = 0, S or Se; n = 0-2.
Abstract:
4-Methylene-2-quinolones of formula (I) and their tautomers of formula (Ia) and their isomers, salts and prodrugs are new: n = 0-4; R1 = halo, CF3, OCF3, OH, alkyl, cycloalkyl, alkoxy, alkoxyalkoxy, alkylthio, alkylsulphinyl, alkylsulphonyl, NO2, NH2, azido, alkylamino, dialkylamino, piperidino, morpholino, pyrrolidino, acyl, acyloxy, acylamino, CONH2, COOH, alkoxycarbonyl, SO3H, SO2NH2, Ar, OAr, COOAr, SAr, SOAr, SO2Ar, SO3Ar, OSO2Ar, SO2NHAr, NHSO2Ar, COAr, Ar', etc.; Ar,Ar' = phenyl and heteroaryl resp., etc.; X = O, S, Se, NR2 or NOR2; R2 = H; alkyl opt. substd. by halogen, CN, NH2, OH, etc.;R5, R6 = COOH or gps. as defined for R2; or R5+R6 forms a 3-8C carbocyclic ring; R3,R4 = alkyl, alkenyl, cycloalkyl or cycloalkenyl,etc.; or R3+R4 = a 3-8C carbocyclic ring; or R3+R4 = CZ1Z2 gp., where Z1 and Z2 are as defined for R3 and R4 as above; provided that X is not O when R1=R2=R5=R6=H and R3=R4=Me or R3+R4= (CH2)4.
Abstract:
Compounds of the formula I, (I) and also their tautomeric forms of the formula Ia, (Ia) in which the substituents R1 to R6 and X have said meanings, exhibit antiviral activity.
Abstract:
4-Methylene-2-quinolones of formula (I) and their tautomers of formula (Ia) and their isomers, salts and prodrugs are new: n = 0-4; R1 = halo, CF3, OCF3, OH, alkyl, cycloalkyl, alkoxy, alkoxyalkoxy, alkylthio, alkylsulphinyl, alkylsulphonyl, NO2, NH2, azido, alkylamino, dialkylamino, piperidino, morpholino, pyrrolidino, acyl, acyloxy, acylamino, CONH2, COOH, alkoxycarbonyl, SO3H, SO2NH2, Ar, OAr, COOAr, SAr, SOAr, SO2Ar, SO3Ar, OSO2Ar, SO2NHAr, NHSO2Ar, COAr, Ar', etc.; Ar,Ar' = phenyl and heteroaryl resp., etc.; X = O, S, Se, NR2 or NOR2; R2 = H; alkyl opt. substd. by halogen, CN, NH2, OH, etc.;R5, R6 = COOH or gps. as defined for R2; or R5+R6 forms a 3-8C carbocyclic ring; R3,R4 = alkyl, alkenyl, cycloalkyl or cycloalkenyl,etc.; or R3+R4 = a 3-8C carbocyclic ring; or R3+R4 = CZ1Z2 gp., where Z1 and Z2 are as defined for R3 and R4 as above; provided that X is not O when R1=R2=R5=R6=H and R3=R4=Me or R3+R4= (CH2)4.