| abstract |
5-Phenylpyrimidines of formula (I), where the substituents and the indices have the following meanings: R1, R2 = H, alkyl, haloalkyl, cycloalkyl, halocycloalkyl, alkenyl, haloalkenyl, alkinyl or haloalkinyl, where R1 and R 2 together with the nitrogen atom to which they are bonded may form a saturate d or unsaturated ring, interrupted by an ether, thio, sulphoxy or sulphonyl group and which can be substituted by one to four groups Ra and/or Rb, R3 = H, halo, cyano, alkyl, haloalkyl, alkoxy, haloalkoxy or alkenyloxy, R4 = H, hal o, cyano, hydroxy, mercapto, azido, alkyl, alkenyl, alkinyl, haloalkyl, alkoxy, alkenyloxy, alkinyloxy, haloalkoxy, alkylthio, alkenylthio, alkinylthio, haloalkylthio, -ON=CRaRb, -CRc=NORa, -NRcN=CRaRb, -NRaRb, -NRcNRaRb, -NORa, - NRcC (=NRc') NRaRb, -NRcC (=0) NRaRb, -NRaC (=0) Rc, -NRaC (=NORc)Rc', -OC (=0) Rc, -C (=NORc) NRaRb, -CRc (=NNRaRb), -C (=0) NRaRb or -C (=0) Rc, wher e Ra,Rb,Rc are as defined in the description, X = halo, alkyl, alkoxy or haloalkyl and m = a whole number from 1 to 5. The invention further relates to methods for production of the above compounds, agents containing the same an d use thereof for the treatment of noxious mycoses. |