These compounds can be used as rorg inhibitors and for the treatment of rorg vector diseases. Claim 1: a compound calculated according to formula (1),Or acceptable salt in the same product, where a1-a1-a1 8308son n n or CR1,Proud,CRI 3,CR¹⁴,respectively, with the proviso that no more than two of the four positions A can simultaneously be N； R¹ is C₂₋₆ alkyl,C₃₋₆ cycloalkyl,C₃₋₆ cycloalkyl-C₁₋₃ alkyl,(di) C₃₋₆amino cycloalkyl or (di) (C₃₋₆-C₁₋₃ alkylcycloalkyl) -amino, with all the carbon atoms of the alkyl groups optionally substituted with one or more F and all the carbon atoms of the cycloalkyl groups optionally substituted with one or more F or methyl； R² and R³ are independently H, F, methyl, ethyl, hydroxy, methoxy or R² and R³ together is carbonyl, all alkyl groups, if present, being optionally substituted with one or more F； R⁴ is H or C₁₋₆ alkyl；R es H hidroxietilo metoxietilo alquilo Caryl C₆₋₁₀,C₆₋₁₀ aryl-C alquilo alkyl,a. Heterosexuality；C₁₋₉-C₁₋₃ alkyl heteroaryl,C₃₋₆ cycloalkyl,C₃₋₆ cycloalkyl-C₁₋₃ alkyl,e. Heterosexual c8322quil c83318325 or heterosexual c832283318c8325；a. All optional groups are changed to one or more f, Cl, c83231 / 8322；e. Alcoxi c83218d3183222 or cyanogen； the sulfuryl group containing R1 is represented by r831181；R8322 or r8313；the remainder R⁶-R¹⁴ are independently H, halogen, amino, C₁₋₃ alkoxy,(Di) alquil C -amino o alquilo Ca. All optional rental units are 1 or more f； R1 8309es h, c832131 rental unit；C₃₋₆ cycloalkyl,C₃₋₆ cycloalkyl-C₁₋₃ alkyl,aryl C₆₋₁₀,C₆₋₁₀ aryl-C alquilo alkyl,a. Heterosexuality；C₁₋₉-C₁₋₃ alkyl heteroaryl,e. Heterosexual c8322quil c83318325 or heterosexual c832283318c8325；a. All optional groups are changed to one or more f, Cl, c83231 / 8322；C₁₋₂ or cyano alkoxy； and R¹⁶ is C₁₋₆ alkyl,C₃₋₆ cycloalkyl,C₃₋₆ cycloalkyl-C₁₋₃ alkyl,aryl C₆₋₁₀,C₆₋₁₀ aryl-C alquilo alkyl,a. Heterosexuality；C₁₋₉-C₁₋₃ alkyl heteroaryl,e. Heterosexual c8322quil c83318325 or heterosexual c832283318c8325；a. All optional groups are
