Mathias Stephan Respondek;Laura Quaranta;Clemens Lamberth;Sarah Sulzer-Mosse
发明人:
Sarah Sulzer-Mosse,Clemens Lamberth,Laura Quaranta,Mathias Stephan Respondek
申请号：
US13390023
公开号：
US08367844B2
申请日:
2010.08.06
申请国别(地区):
US
年份:
2013
代理人:
摘要：
The present invention relates to heterocyclic compounds of formula I which have microbiocidal activity, in particular fungicidal activity as well as methods of using the compounds of formula (I) to control microbes: wherein A is x-C(R10R11)—C(═O)—, x-C(R12R13)—C(═S)—, x-O—C(═O)—, x-O—C(═S)—, x-N(R14)—C(═O)—, x-N(R15)—C(═S)—, x-C(R16R17)—SO2— or X—N═C(R30)—, in each case x indicates the bond that is connected to R1； T is CR18 or N； Y1, Y2, Y3, and Y4 are independently CR19 or N； Q is O or S； n is 1 or 2； p is 1 or 2, providing that when n is 2, p is 1. R1 is phenyl, pyridyl, imidazolyl, or pyrazolyl； wherein the phenyl, pyridyl, imidazolyl and pyrazolyl are each optionally substituted by 1 to 3 substituents independently selected from C1-C4 alkyl, C1-C4 haloalkyl, halogen, cyano, hydroxy and amino； R2, R3, R4, R5, R6, R7, R10, R11, R12, R13, R16, R17, R18, R19 and R30 each independently are hydrogen, halogen, cyano, C1-C4alkyl, or C1-C4haloalkyl； R8, R14 and R15 each independently are hydrogen or C1-C4alkyl； and R9 is phenyl, benzyl or group (a): wherein the phenyl, benzyl and group (a) are each optionally substituted with 1 to 3 substituents independently selected from C1-C4 alkyl, C1-C4 haloalkyl, halogen, cyano, hydroxy and amino； or a salt or a N-oxide thereof.
