IP Library › Granted Patent US 11,130,768

Granted Patent B2

US 11,130,768 · App. 16/608,744 · Granted Sep 28, 2021

Bicyclic pyrazole derivatives

Inventors: Nils Griebenow (Dormagen, DE); Wei Zhuang (Monheim, DE); Daniel Kulke (Leverkusen, DE); Adeline Köhler (Langenfeld, DE); Thomas Ilg (Monheim, DE); Claudia Welz (Düsseldorf, DE); Hans-Georg Schwarz (Dorsten, DE); Ulrich Görgens (Ratingen, DE); Walter Hübsch (Wuppertal, DE); Johannes Köbberling (Neuss, DE)

Assignee: Bayer Animal Health GmbH

C07D513/04 A61P33/10

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Quick Facts

Patent No.: US 11,130,768
App. No.: 16/608,744
Granted: Sep 28, 2021
Kind: B2

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Abstract

The present invention covers bicyclic pyrazole compounds of general formula (I): in which G, A, R 1 , R 2 , R 3 , and Q are as defined herein, methods of preparing said compounds, intermediate compounds useful for preparing said compounds, pharmaceutical compositions and combinations comprising said compounds and the use of said compounds for manufacturing pharmaceutical compositions for the treatment, control and/or prevention of diseases, in particular of helminth infections, as a sole agent or in combination with other active ingredients.

Claims (267)

1. A compound of formula (I):

wherein

A is A1 or A2,

o is 0, 1, 2, 3 or 4,

R is selected from the group consisting of hydrogen, halogen, cyano, nitro, —OH, C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, C 1 -C 4 -alkoxy, C 1 -C 4 -halogenoalkoxy having 1 to 5 halogen atoms, C 3 -C 6 -cycloalkyl, —NH 2 , —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 , —S—C 1 -C 4 -alkyl, —S(O)—C 1 -C 4 -alkyl, —SO 2 —C 1 -C 4 -alkyl, —S—C 1 -C 4 -halogenoalkyl, —S(O)—C 1 -C 4 -halogenoalkyl, and —SO 2 —C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms,

X and Y are independently selected from the group consisting of CR 6 R 7 , O, S, and N—R 8 , wherein at least one of X and Y is CR 6 R 7 , or

X and Y form together a group selected from —C(O)—O—, —C(O)—NR 8 —, —S(O)—NR 8 —, —SO 2 —NR 8 —, and —SO 2 —O—,

G is S,

heterocyclyl-C 1 -C 4 -alkyl, wherein the heterocyclyl substituent is selected from the group consisting of 4- to 10-membered heterocycloalkyl, 5-membered heteroaryl, and 6-membered heteroaryl, each of which is optionally substituted by 1, 2 or 3 substituents independently selected from the group consisting of halogen, —OH, —NO 2 , cyano, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, C 1 -C 4 -alkoxy, C 1 -C 4 -halogenoalkoxy having 1 to 5 halogen atoms, —NH 2 , —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 , —S—C 1 -C 4 -alkyl, —S(O)—C 1 -C 4 -alkyl, —SO 2 —C 1 -C 4 -alkyl, —S—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, —S(O)—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, and —SO 2 —C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms,

R 2 is selected from the group consisting of hydrogen, halogen, cyano, —COOH, C 1 -C 4 -alkoxy-C(O)—, —C(O)—NH 2 , —C(O)—NH(C 1 -C 4 -alkyl), —C(O)—N(C 1 -C 4 -alkyl) 2 , —C(O)—NH(C 3 -C 6 -cycloalkyl), —C(O)—N(C 1 -C 4 -alkyl)(C 3 -C 6 -cycloalkyl), —NR 9 R 10 , —OR 11 , —SR 12 , —S(O)R 12 , —SO 2 R 12 , C 1 -C 6 -alkyl, C 3 -C 6 -cycloalkyl, C 2 -C 4 -alkenyl, C 3 -C 6 -cycloalkenyl, C 2 -C 4 -alkynyl, phenyl-C 1 -C 4 -alkyl, each of which is optionally substituted by 1, 2, 3, 4 or 5 substituents independently selected from the group consisting of halogen, —OH, —NO 2 , cyano, C 1 -C 4 -alkyl-C(O)—, C 1 -C 4 -alkoxy-C(O)—, —C(O)—NH 2 , —C(O)—NH(C 1 -C 4 -alkyl), —C(O)—N(C 1 -C 4 -alkyl) 2 , C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, C 1 -C 4 -alkoxy, —NH 2 , —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 , —NH(C 3 -C 6 -cycloalkyl), —N(C 1 -C 4 -alkyl)(C 3 -C 6 -cycloalkyl), —S—C 1 -C 4 -alkyl, —S(O)—C 1 -C 4 -alkyl, —SO 2 —C 1 -C 4 -alkyl, —S—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, —S(O)—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, and —SO 2 —C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms,

heterocyclyl-C 1 -C 4 -alkyl, wherein the heterocyclyl substituent is selected from the group consisting of 4- to 10-membered heterocycloalkyl, 5-membered heteroaryl, and 6-membered heteroaryl, each of which is optionally substituted by 1, 2 or 3 substituents independently selected from the group consisting of halogen, —OH, —NO 2 , cyano, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, C 1 -C 4 -alkoxy, C 1 -C 4 -halogenoalkoxy having 1 to 5 halogen atoms, —NH 2 , —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 , —NH(C 3 -C 6 -cycloalkyl), —N(C 1 -C 4 -alkyl)(C 3 -C 6 -cycloalkyl), —S—C 1 -C 4 -alkyl, —S(O)—C 1 -C 4 -alkyl, —SO 2 —C 1 -C 4 -alkyl, —S—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, —S(O)—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, and —SO 2 —C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms,

phenyl which is optionally substituted by 1, 2 or 3 substituents independently selected from the group consisting of halogen, cyano, nitro, —OH, C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, C 1 -C 4 -alkoxy, C 1 -C 4 -halogenoalkoxy having 1 to 5 halogen atoms, C 3 -C 6 -cycloalkyl, —NH 2 , —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 , —NH(C 3 -C 6 -cycloalkyl), —N(C 1 -C 4 -alkyl)(C 3 -C 6 -cycloalkyl), —S—C 1 -C 4 -alkyl, —S(O)—C 1 -C 4 -alkyl, —SO 2 —C 1 -C 4 -alkyl, —S—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, —S(O)—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, and —SO 2 —C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, and

a monocyclic or a bicyclic heterocycle selected from the group consisting of 4- to 10-membered heterocycloalkyl, heterospirocycloalkyl, 5-membered heteroaryl, and 6-membered heteroaryl, each of which is optionally substituted by 1, 2, 3 or 4 substituents independently selected from the group consisting of halogen, cyano, nitro, —OH, oxo, thiono, —COOH, C 1 -C 4 -alkoxy-C(O)—, —C(O)—NH 2 , —C(O)—NH(C 1 -C 4 -alkyl), —C(O)—N(C 1 -C 4 -alkyl) 2 , C 1 -C 4 -alkyl, C 1 -C 4 -alkyl-C(O)—, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, C 1 -C 4 -alkoxy, hydroxy-C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy-C 1 -C 4 -alkyl-, C 1 -C 4 -halogenoalkoxy having 1 to 5 halogen atoms, C 3 -C 6 -cycloalkyl, —NH 2 , —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 , —NH(C 3 -C 6 -cycloalkyl), —N(C 1 -C 4 -alkyl)(C 3 -C 6 -cycloalkyl), —S—C 1 -C 4 -alkyl, —S(O)—C 1 -C 4 -alkyl, —SO 2 —C 1 -C 4 -alkyl, —S—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, —S(O)—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, —SO 2 —C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, and 4- to 10-membered heterocycloalkyl,

R 3 is selected from the group consisting of hydrogen, halogen, —OH, cyano, C 1 -C 4 -alkyl, C 3 -C 6 -cycloalkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, C 1 -C 4 -alkoxy-C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy, C 1 -C 4 -alkyl-C(O)—, —NH 2 , —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 , —NH(C 3 -C 6 -cycloalkyl), —N(C 1 -C 4 -alkyl)(C 3 -C 6 -cycloalkyl), —S—C 1 -C 4 -alkyl, —S(O)—C 1 -C 4 -alkyl, and —SO 2 —C 1 -C 4 -alkyl,

R 4 is selected from the group consisting of hydrogen, —OH, C 1 -C 4 -alkyl, and C 1 -C 4 -alkoxy,

R 5 is selected from the group consisting of hydrogen, C 1 -C 4 -alkyl, and C 1 -C 4 -alkoxy,

or R 4 and R 5 form, together with the carbon atom to which they are attached, a 3- to 6-membered ring selected from the group consisting of C 3 -C 6 -cycloalkyl and 3- to 6-membered heterocycloalkyl,

R 6 is selected from the group consisting of hydrogen, —OH, fluorine, C 1 -C 4 -alkyl, and C 1 -C 4 -alkoxy,

R 7 is selected from the group consisting of hydrogen, —OH, fluorine, C 1 -C 4 -alkyl, and C 1 -C 4 -alkoxy,

or R 6 and R 7 form, together with the carbon atom to which they are attached, a 3- to 6-membered ring selected from the group consisting of C 3 -C 6 -cycloalkyl and 3- to 6-membered heterocycloalkyl,

R 8 is selected from the group consisting of hydrogen, C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, and C 1 -C 4 -alkoxy,

R 9 and R 10 are independently selected from the group consisting of hydrogen, —OH, —NH 2 , —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 , —NH(—C(O)—C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl)(—C(O)—C 1 -C 4 -alkyl), C 1 -C 4 -alkoxy, C 1 -C 4 -alkoxy-C(O)—, C 1 -C 4 -alkyl, C 3 -C 6 -cycloalkyl, phenyl-C 1 -C 4 -alkyl, each of which is optionally substituted by 1, 2 or 3 substituents independently selected from the group consisting of halogen, —OH, cyano, —COOH, C 1 -C 4 -alkoxy-C(O)—, —C(O)—NH 2 , —C(O)—NH(C 1 -C 4 -alkyl), —C(O)—N(C 1 -C 4 -alkyl) 2 , —NH—C(O)—C 1 -C 4 -alkyl, —N(C 1 -C 4 -alkyl)(—C(O)—C 1 -C 4 -alkyl), C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, C 1 -C 4 -alkoxy, C 1 -C 4 -halogenoalkoxy having 1 to 5 halogen atoms, C 3 -C 6 -cycloalkyl, —NH 2 , —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 , —S—C 1 -C 4 -alkyl, —S(O)—C 1 -C 4 -alkyl, —SO 2 —C 1 -C 4 -alkyl, —S—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, —S(O)—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, —SO 2 —C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, and (C 1 -C 4 -alkoxy) 2 P(═O)—,

heterocyclyl-C 1 -C 4 -alkyl, wherein the heterocyclyl substituent is selected from the group consisting of 4- to 10-membered heterocycloalkyl, 5-membered heteroaryl, and 6-membered heteroaryl, each of which is optionally substituted by 1, 2 or 3 substituents independently selected from the group consisting of halogen, cyano, nitro, —OH, oxo, thiono, —COOH, C 1 -C 4 -alkoxy-C(O)—, —C(O)—NH 2 , —C(O)—NH(C 1 -C 4 -alkyl), —C(O)—N(C 1 -C 4 -alkyl) 2 , C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, C 1 -C 4 -alkoxy, hydroxy-C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkoxy having 1 to 5 halogen atoms, C 3 -C 6 -cycloalkyl, —NH 2 , —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 , —S—C 1 -C 4 -alkyl, —S(O)—C 1 -C 4 -alkyl, —SO 2 —C 1 -C 4 -alkyl, —S—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, —S(O)—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, and —SO 2 —C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms,

phenyl, benzo-C 5 -C 6 -cycloalkyl, each of which is optionally substituted by 1, 2 or 3 substituents independently selected from the group consisting of halogen, cyano, nitro, —OH, C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, C 1 -C 4 -alkoxy, C 1 -C 4 -halogenoalkoxy having 1 to 5 halogen atoms, C 3 -C 6 -cycloalkyl, —NH 2 , —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 , —S—C 1 -C 4 -alkyl, —S(O)—C 1 -C 4 -alkyl, —SO 2 —C 1 -C 4 -alkyl, —S—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, —S(O)—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, and —SO 2 —C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms,

a monocyclic or a bicyclic heterocycle selected from the group of 4- to 10-membered heterocycloalkyl, 5-membered heteroaryl, and 6-membered heteroaryl, each of which is optionally substituted by 1, 2 or 3 substituents independently selected from the group consisting of halogen, cyano, nitro, —OH, oxo, thiono, —COOH, C 1 -C 4 -alkoxy-C(O)—, —C(O)—NH 2 , —C(O)—NH(C 1 -C 4 -alkyl), —C(O)—N(C 1 -C 4 -alkyl) 2 , C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, C 1 -C 4 -alkoxy, hydroxy-C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkoxy having 1 to 5 halogen atoms, C 3 -C 6 -cycloalkyl, —NH 2 , —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 , —S—C 1 -C 4 -alkyl, —S(O)—C 1 -C 4 -alkyl, —SO 2 —C 1 -C 4 -alkyl, —S—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, —S(O)—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, and —SO 2 —C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms,

R 11 is selected from the group consisting of

—NH 2 , —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 ,

C 1 -C 4 -alkyl, C 3 -C 6 -cycloalkyl, phenyl-C 1 -C 4 -alkyl, each of which is optionally substituted by 1, 2 or 3 substituents independently selected from the group consisting of halogen, —OH, cyano, —COOH, C 1 -C 4 -alkoxy-C(O)—, —C(O)—NH 2 , —C(O)—NH(C 1 -C 4 -alkyl), —C(O)—N(C 1 -C 4 -alkyl) 2 , C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, C 1 -C 4 -alkoxy, C 1 -C 4 -halogenoalkoxy having 1 to 5 halogen atoms, C 3 -C 6 -cycloalkyl, —NH 2 , —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 , —S—C 1 -C 4 -alkyl, —S(O)—C 1 -C 4 -alkyl, —SO 2 —C 1 -C 4 -alkyl, —S—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, —S(O)—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, and —SO 2 —C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms,

phenyl, which is optionally substituted by 1, 2 or 3 substituents independently selected from the group consisting of halogen, cyano, nitro, —OH, C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, C 1 -C 4 -alkoxy, C 1 -C 4 -halogenoalkoxy having 1 to 5 halogen atoms, C 3 -C 6 -cycloalkyl, —NH 2 , —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 , —S—C 1 -C 4 -alkyl, —S(O)—C 1 -C 4 -alkyl, —SO 2 —C 1 -C 4 -alkyl, —S—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, —S(O)—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, and —SO 2 —C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, and

a monocyclic or a bicyclic heterocycle selected from the group consisting of 4- to 10-membered heterocycloalkyl, 5-membered heteroaryl, and 6-membered heteroaryl, each of which is optionally substituted by 1, 2 or 3 substituents independently selected from the group consisting of halogen, cyano, nitro, —OH, oxo, thiono, —COOH, C 1 -C 4 -alkoxy-C(O)—, —C(O)—NH 2 , —C(O)—NH(C 1 -C 4 -alkyl), —C(O)—N(C 1 -C 4 -alkyl) 2 , C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, C 1 -C 4 -alkoxy, hydroxy-C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkoxy having 1 to 5 halogen atoms, C 3 -C 6 -cycloalkyl, —NH 2 , —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 , —S—C 1 -C 4 -alkyl, —S(O)—C 1 -C 4 -alkyl, —SO 2 —C 1 -C 4 -alkyl, —S—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, —S(O)—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, and —SO 2 —C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms,

R 12 is selected from the group consisting of hydrogen,

heterocyclyl-C 1 -C 4 -alkyl, wherein the heterocyclyl substituent is selected from the group consisting of 4- to 10-membered heterocycloalkyl, 5-membered heteroaryl, and 6-membered heteroaryl, each of which is optionally substituted by 1, 2 or 3 substituents independently selected from the group consisting of halogen, cyano, nitro, —OH, oxo, thiono, —COOH, C 1 -C 4 -alkoxy-C(O)—, —C(O)—NH 2 , —C(O)—NH(C 1 -C 4 -alkyl), —C(O)—N(C 1 -C 4 -alkyl) 2 , C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, C 1 -C 4 -alkoxy, hydroxy-C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkoxy having 1 to 5 halogen atoms, C 3 -C 6 -cycloalkyl, —NH 2 , —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 , —S—C 1 -C 4 -alkyl, —S(O)—C 1 -C 4 -alkyl, —SO 2 —C 1 -C 4 -alkyl, —S—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, —S(O)—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, and —SO 2 —C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms,

Q is selected from the group consisting of 6- or 10-membered aryl and 5- to 10-membered heteroaryl, each of which is optionally substituted by 1, 2, 3, 4 or 5 substituents selected from the group consisting of halogen, SF 5 , cyano, —CHO, nitro, oxo, C 1 -C 4 -alkyl, C 1 -C 4 -hydroxyalkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, hydroxy, C 1 -C 4 -alkoxy, C 3 -C 6 -cycloalkyl-C 1 -C 4 -alkoxy, cyano-C 1 -C 4 -alkoxy, C 1 -C 4 -halogenoalkoxy having 1 to 5 halogen atoms, —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 , —NH(C 3 -C 6 -cycloalkyl), —N(C 1 -C 4 -alkyl)(C 3 -C 6 -cycloalkyl), —NH—SO 2 —(C 1 -C 4 -alkyl), —N(SO 2 —[C 1 -C 4 -alkyl])(C 1 -C 4 -alkyl), (C 1 -C 4 -alkoxyimino)-C 1 -C 4 -alkyl, 4- to 6-membered heterocyclyl, which is optionally substituted with 1 or 2 substituents selected from the group consisting of fluorine, chlorine, bromine, methyl and cyano, —CH 2 —O—(C 1 -C 4 -alkyl), —CH 2 —NH(C 1 -C 4 -alkyl), —CH 2 —N(C 1 -C 4 -alkyl) 2 , methyl substituted with a 4- to 6-membered heterocyclyl which itself is optionally substituted with 1 or 2 substituents selected from the group consisting of fluorine, chlorine, bromine, methyl and cyano, —CH 2 —S—(C 1 -C 4 -alkyl), —CH 2 —S(O)—(C 1 -C 4 -alkyl), —CH 2 —SO 2 —(C 1 -C 4 -alkyl), —S(O)—(C 1 -C 4 -alkyl), —SO 2 —(C 1 -C 4 -alkyl), —S—(C 1 -C 4 -halogenoalkyl) having 1 to 5 halogen atoms, —S(O)—(C 1 -C 4 -halogenoalkyl) having 1 to 5 halogen atoms, —SO 2 —(C 1 -C 4 -halogenoalkyl) having 1 to 5 halogen atoms, —CONH(C 1 -C 4 -alkyl), —CONH(C 3 -C 6 -cycloalkyl), —NHCO(C 1 -C 4 -alkyl), —NHCO(C 3 -C 6 -cycloalkyl), and —NHCO(C 1 -C 4 -halogenoalkyl) having 1 to 5 halogen atoms,

wherein when Y is O, S or N—R 8 , none of R 4 , R 5 , R 6 and R 7 is —OH, and wherein when X is O, S or N—R 8 , none of R 6 and R 7 is —OH,

or a stereoisomer, a tautomer, an N-oxide, a hydrate, a solvate, or a salt thereof, or a mixture of any of the foregoing.

2. The compound according to claim 1 , wherein:

A is A1 or A2,

o is 0, 1, 2, 3 or 4,

X and Y are independently selected from the group consisting of CR 6 R 7 , O, S, and N—R 8 , wherein at least one of X and Y is CR 6 R 7 , or

X and Y form together a group selected from —C(O)—O—, —C(O)—NR 8 —, —S(O)—NR 8 —, —SO 2 —NR 8 —, and —SO 2 —O—,

G is S,

R 1 is selected from the group consisting of hydrogen, cyano, —CHO, —OH, C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, C 1 -C 4 -alkoxy, C 1 -C 4 -halogenoalkoxy having 1 to 5 halogen atoms, C 3 -C 6 -cycloalkyl, C 3 -C 6 -halogenocycloalkyl having 1 to 5 halogen atoms, C 3 -C 4 -alkenyl, C 3 -C 4 -alkynyl, C 1 -C 4 -alkoxy-C 1 -C 4 -alkyl, C 3 -C 6 -cycloalkyl-C 1 -C 3 -alkyl, cyano-C 1 -C 4 -alkyl, —NH—C 1 -C 4 -alkyl, —N(C 1 -C 4 -alkyl) 2 , NH 2 —C 1 -C 4 -alkyl-, C 1 -C 4 -alkyl-NH—C 1 -C 4 -alkyl-, (C 1 -C 4 -alkyl) 2 N—C 1 -C 4 -alkyl-, C 1 -C 4 -alkyl-C(O)—, C 1 -C 4 -halogenoalkyl-C(O)— having 1 to 5 halogen atoms, C 1 -C 4 -alkoxy-C(O)—, benzyloxy-C(O)—, C 1 -C 4 -alkoxy-C 1 -C 4 -alkyl-C(O)—, —SO 2 —C 1 -C 4 -alkyl, —SO 2 —C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, phenyl-C 1 -C 4 -alkyl, optionally substituted by 1, 2, 3, 4 or 5 substituents independently selected from the group consisting of halogen, —OH, —NO 2 , cyano, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, C 1 -C 4 -alkoxy, C 1 -C 4 -halogenoalkoxy having 1 to 5 halogen atoms, —NH 2 , —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 , —S—C 1 -C 4 -alkyl, —S(O)—C 1 -C 4 -alkyl, —SO 2 —C 1 -C 4 -alkyl, —S—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, —S(O)—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, and —SO 2 —C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, heterocyclyl-C 1 -C 4 -alkyl, wherein the heterocyclyl substituent is selected from the group consisting of 4- to 10-membered heterocycloalkyl, 5-membered heteroaryl, and 6-membered heteroaryl, each of which is optionally substituted by 1, 2 or 3 substituents independently selected from the group consisting of halogen, —OH, —NO 2 , cyano, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, C 1 -C 4 -alkoxy, C 1 -C 4 -halogenoalkoxy having 1 to 5 halogen atoms, —NH 2 , —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 , —S—C 1 -C 4 -alkyl, —S(O)—C 1 -C 4 -alkyl, —SO 2 —C 1 -C 4 -alkyl, —S—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, —S(O)—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, and —SO 2 —C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms,

R 2 is selected from the group consisting of

hydrogen, halogen, cyano, —COOH, C 1 -C 4 -alkoxy-C(O)—, —C(O)—NH 2 , —C(O)—NH(C 1 -C 4 -alkyl), —C(O)—N(C 1 -C 4 -alkyl) 2 , —C(O)—NH(C 3 -C 6 -cycloalkyl), —C(O)—N(C 1 -C 4 -alkyl)(C 3 -C 6 -cycloalkyl), —NR 9 R 10 , —OR 11 , —SR 12 , —S(O)R 12 , —SO 2 R 12 , C 1 -C 6 -alkyl, C 3 -C 6 -cycloalkyl, C 2 -C 4 -alkenyl, C 3 -C 6 -cycloalkenyl, C 2 -C 4 -alkynyl, phenyl-C 1 -C 4 -alkyl, each of which is optionally substituted by 1, 2, 3, 4 or 5 substituents independently selected from the group consisting of halogen, —OH, —NO 2 , cyano, C 1 -C 4 -alkyl-C(O)—, C 1 -C 4 -alkoxy-C(O)—, —C(O)—NH 2 , —C(O)—NH(C 1 -C 4 -alkyl), —C(O)—N(C 1 -C 4 -alkyl) 2 , C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, C 1 -C 4 -alkoxy, —NH 2 , —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 , —NH(C 3 -C 6 -cycloalkyl), —N(C 1 -C 4 -alkyl)(C 3 -C 6 -cycloalkyl), —S—C 1 -C 4 -alkyl, —S(O)—C 1 -C 4 -alkyl, —SO 2 —C 1 -C 4 -alkyl, —S—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, —S(O)—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, and —SO 2 —C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms,

heterocyclyl-C 1 -C 4 -alkyl, wherein the heterocyclyl substituent is selected from the group consisting of 4- to 10-membered heterocycloalkyl, 5-membered heteroaryl, and 6-membered heteroaryl, each of which is optionally substituted by 1, 2 or 3 substituents independently selected from the group consisting of halogen, —OH, —NO 2 , cyano, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, C 1 -C 4 -alkoxy, C 1 -C 4 -halogenoalkoxy having 1 to 5 halogen atoms, —NH 2 , —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 , —NH(C 3 -C 6 -cycloalkyl), —N(C 1 -C 4 -alkyl)(C 3 -C 6 -cycloalkyl), —S—C 1 -C 4 -alkyl, —S(O)—C 1 -C 4 -alkyl, —SO 2 —C 1 -C 4 -alkyl, —S—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, —S(O)—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, and —SO 2 —C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms,

R 3 is selected from the group consisting of hydrogen, halogen, —OH, cyano, C 1 -C 4 -alkyl, C 3 -C 6 -cycloalkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, C 1 -C 4 -alkoxy-C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy, C 1 -C 4 -alkyl-C(O)—, —NH 2 , —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 , —NH(C 3 -C 6 -cycloalkyl), —N(C 1 -C 4 -alkyl)(C 3 -C 6 -cycloalkyl), —S—C 1 -C 4 -alkyl, and —S(O)—C 1 -C 4 -alkyl, —SO 2 —C 1 -C 4 -alkyl,

R 4 is selected from the group consisting of hydrogen, —OH, C 1 -C 4 -alkyl, and C 1 -C 4 -alkoxy,

R 5 is selected from the group consisting of hydrogen, C 1 -C 4 -alkyl, and C 1 -C 4 -alkoxy,

R 6 is selected from the group consisting of hydrogen, —OH, fluorine, C 1 -C 4 -alkyl, and C 1 -C 4 -alkoxy,

R 7 is selected from the group consisting of hydrogen, —OH, fluorine, C 1 -C 4 -alkyl, and C 1 -C 4 -alkoxy,

R 8 is selected from the group consisting of hydrogen, C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, and C 1 -C 4 -alkoxy,

R 9 and R 10 are independently selected from the group consisting of

hydrogen, —OH, —NH 2 , —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 , —NH(—C(O)—C 1 -C 4 -alkyl),

C 1 -C 4 -alkoxy,

C 1 -C 4 -alkyl, C 3 -C 6 -cycloalkyl, phenyl-C 1 -C 4 -alkyl, each of which is optionally substituted by 1, 2 or 3 substituents independently selected from the group consisting of halogen, —OH, cyano, —COOH, C 1 -C 4 -alkoxy-C(O)—, —C(O)—NH 2 , —C(O)—NH(C 1 -C 4 -alkyl), —C(O)—N(C 1 -C 4 -alkyl) 2 , —NH—C(O)—C 1 -C 4 -alkyl, —N(C 1 -C 4 -alkyl)-(—C(O)—C 1 -C 4 -alkyl), C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, C 1 -C 4 -alkoxy, C 1 -C 4 -halogenoalkoxy having 1 to 5 halogen atoms, C 3 -C 6 -cycloalkyl, —NH 2 , —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 , —S—C 1 -C 4 -alkyl, —S(O)—C 1 -C 4 -alkyl, —SO 2 —C 1 -C 4 -alkyl, —S—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, —S(O)—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, —SO 2 —C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, and (C 1 -C 4 -alkoxy) 2 P(═O)—,

heterocyclyl-C 1 -C 4 -alkyl, wherein the heterocyclyl substituent is selected from the group consisting of 4- to 10-membered heterocycloalkyl, 5-membered heteroaryl, and 6-membered heteroaryl, each of which is optionally substituted by 1, 2 or 3 substituents independently selected from the group consisting of halogen, cyano, nitro, —OH, oxo, thiono, —COOH, C 1 -C 4 -alkoxy-C(O)—, —C(O)—NH 2 , —C(O)—NH(C 1 -C 4 -alkyl), —C(O)—N(C 1 -C 4 -alkyl) 2 , C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, C 1 -C 4 -alkoxy, hydroxy-C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkoxy having 1 to 5 halogen atoms, C 3 -C 6 -cycloalkyl, —NH 2 , —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 , —S—C 1 -C 4 -alkyl, —S(O)—C 1 -C 4 -alkyl, —SO 2 —C 1 -C 4 -alkyl, —S—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, —S(O)—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, and —SO 2 —C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms,

R 11 is selected from the group consisting of

—NH 2 , —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 ,

heterocyclyl-C 1 -C 4 -alkyl, wherein the heterocyclyl substitutent is selected from the group consisting of 4- to 10-membered heterocycloalkyl, 5-membered heteroaryl, and 6-membered heteroaryl, each of which is optionally substituted by 1, 2 or 3 substituents independently selected from the group consisting of halogen, cyano, nitro, —OH, oxo, thiono, —COOH, C 1 -C 4 -alkoxy-C(O)—, —C(O)—NH 2 , —C(O)—NH(C 1 -C 4 -alkyl), —C(O)—N(C 1 -C 4 -alkyl) 2 , C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, C 1 -C 4 -alkoxy, hydroxy-C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkoxy having 1 to 5 halogen atoms, C 3 -C 6 -cycloalkyl, —NH 2 , —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 , —S—C 1 -C 4 -alkyl, —S(O)—C 1 -C 4 -alkyl, —SO 2 —C 1 -C 4 -alkyl, —S—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, —S(O)—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, and —SO 2 —C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, phenyl, which is optionally substituted by 1, 2 or 3 substituents independently selected from the group consisting of halogen, cyano, nitro, —OH, C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, C 1 -C 4 -alkoxy, C 1 -C 4 -halogenoalkoxy having 1 to 5 halogen atoms, C 3 -C 6 -cycloalkyl, —NH 2 , —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 , —S—C 1 -C 4 -alkyl, —S(O)—C 1 -C 4 -alkyl, —SO 2 —C 1 -C 4 -alkyl, —S—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, —S(O)—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, and —SO 2 —C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, and

a monocyclic or a bicyclic heterocycle selected from the group consisting of 4- to 10-membered heterocycloalkyl, 5-membered heteroaryl and 6-membered heteroaryl, each of which is optionally substituted by 1, 2 or 3 substituents independently selected from the group consisting of halogen, cyano, nitro, —OH, oxo, thiono, —COOH, C 1 -C 4 -alkoxy-C(O)—, —C(O)—NH 2 , —C(O)—NH(C 1 -C 4 -alkyl), —C(O)—N(C 1 -C 4 -alkyl) 2 , C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, C 1 -C 4 -alkoxy, hydroxy-C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkoxy having 1 to 5 halogen atoms, C 3 -C 6 -cycloalkyl, —NH 2 , —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 , —S—C 1 -C 4 -alkyl, —S(O)—C 1 -C 4 -alkyl, —SO 2 —C 1 -C 4 -alkyl, —S—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, —S(O)—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, and —SO 2 —C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms,

R 12 is selected from the group consisting of

Hydrogen,

heterocyclyl-C 1 -C 4 -alkyl, wherein the heterocyclyl substituent is selected from the group consisting of 4- to 10-membered heterocycloalkyl, 5-membered heteroaryl, and 6-membered heteroaryl, each of which is optionally substituted by 1, 2 or 3 substituents independently selected from the group consisting of halogen, cyano, nitro, —OH, oxo, thiono, —COOH, C 1 -C 4 -alkoxy-C(O)—, —C(O)—NH 2 , —C(O)—NH(C 1 -C 4 -alkyl), —C(O)—N(C 1 -C 4 -alkyl) 2 , C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, C 1 -C 4 -alkoxy, hydroxy-C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkoxy having 1 to 5 halogen atoms, C 3 -C 6 -cycloalkyl, —NH 2 , —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 , —S—C 1 -C 4 -alkyl, —S(O)—C 1 -C 4 -alkyl, —SO 2 —C 1 -C 4 -alkyl, —S—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, —S(O)—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, and —SO 2 —C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms,

Q is a phenyl ring of formula (Q1)

wherein

Z 1 , Z 2 , Z 3 , Z 4 , and Z 5 are independently selected from the group consisting of hydrogen, halogen, SF 5 , cyano, —CHO, nitro, C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, hydroxy, C 1 -C 4 -alkoxy, C 3 -C 6 -cycloalkyl-C 1 -C 4 -alkoxy, cyano-C 1 -C 4 -alkoxy, C 1 -C 4 -halogenoalkoxy having 1 to 5 halogen atoms, —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 , —NH(C 3 -C 6 -cycloalkyl), —N(C 1 -C 4 -alkyl)(C 3 -C 6 -cycloalkyl), —NH—SO 2 —(C 1 -C 4 -alkyl), —N(SO 2 —[C 1 -C 4 -alkyl])(C 1 -C 4 -alkyl), (C 1 -C 4 -alkoxyimino)-C 1 -C 4 -alkyl, 4- to 6-membered heterocyclyl, which is optionally substituted with 1 or 2 substituents selected from the group consisting of fluorine, chlorine, bromine, methyl, and cyano, —CH 2 —O—(C 1 -C 4 -alkyl), —CH 2 —NH(C 1 -C 4 -alkyl), —CH 2 —N(C 1 -C 4 -alkyl) 2 , methyl substituted with a 4- to 6-membered heterocyclyl which itself is optionally substituted with 1 or 2 substituents selected from the group consisting of fluorine, chlorine, bromine, methyl and cyano, —CH 2 —S—(C 1 -C 4 -alkyl), —CH 2 —S(O)—(C 1 -C 4 -alkyl), —CH 2 —SO 2 —(C 1 -C 4 -alkyl), —S—(C 1 -C 4 -alkyl), —S(O)—(C 1 -C 4 -alkyl), —SO 2 —(C 1 -C 4 -alkyl), —S—(C 1 -C 4 -halogenoalkyl) having 1 to 5 halogen atoms, —S(O)—(C 1 -C 4 -halogenoalkyl) having 1 to 5 halogen atoms, —SO 2 —(C 1 -C 4 -halogenoalkyl) having 1 to 5 halogen atoms, —CONH(C 1 -C 4 -alkyl), —CONH(C 3 -C 6 -cycloalkyl), —NHCO(C 1 -C 4 -alkyl), —NHCO(C 3 -C 6 -cycloalkyl), and —NHCO(C 1 -C 4 -halogenoalkyl) having 1 to 5 halogen atoms, or

Z 1 and Z 2 form, together with the carbon atoms that they are connected to, a 5- or 6-membered saturated or partially saturated heterocyclic ring, a 5-membered heteroaryl, or a 6-membered heteroaryl, each of which may be optionally substituted with one or two substitutents selected from the group consisting of methyl, fluorine, and oxo, and

Z 3 , r, and Z 5 are independently selected from the group consisting of hydrogen, halogen, SF 5 , cyano, CHO, nitro, C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, hydroxy, C 1 -C 4 -alkoxy, C 3 -C 6 -cycloalkyl-C 1 -C 4 -alkoxy, cyano-C 1 -C 4 -alkoxy, C 1 -C 4 -alkoxy-C(O)—, C 1 -C 4 -halogenoalkoxy having 1 to 5 halogen atoms, —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 , —NH(C 3 -C 6 -cycloalkyl), —N(C 1 -C 4 -alkyl)(C 3 -C 6 -cycloalkyl), —NH—SO 2 —(C 1 -C 4 -alkyl), —N(SO 2 —[C 1 -C 4 -alkyl])(C 1 -C 4 -alkyl), (C 1 -C 4 -alkoxyimino)-C 1 -C 4 -alkyl, 4- to 6-membered heterocycloalkyl which is optionally substituted with 1 or 2 substituents selected from the group consisting of fluorine, methyl, and cyano, —CH 2 —O—(C 1 -C 4 -alkyl), —CH 2 —NH(C 1 -C 4 -alkyl), —CH 2 —N(C 1 -C 4 -alkyl) 2 , methyl substituted with a 4- to 6-membered heterocycloalkyl which itself is optionally substituted with 1 or 2 substituents selected from the group consisting of fluorine, methyl or cyano, —CH 2 —S—(C 1 -C 4 -alkyl), —CH 2 —S(O)—(C 1 -C 4 -alkyl), —CH 2 —SO 2 —(C 1 -C 4 -alkyl), —S—(C 1 -C 4 -alkyl), —S(O)—(C 1 -C 4 -alkyl), —SO 2 —(C 1 -C 4 -alkyl), —S—(C 1 -C 4 -halogenoalkyl) having 1 to 5 halogen atoms, —S(O)—(C 1 -C 4 -halogenoalkyl) having 1 to 5 halogen atoms, —SO 2 —(C 1 -C 4 -halogenoalkyl) having 1 to 5 halogen atoms, —CONH(C 1 -C 4 -alkyl), —CONH(C 3 -C 6 -cycloalkyl), —NHCO(C 1 -C 4 -alkyl), —NHCO(C 3 -C 6 -cycloalkyl), and —NHCO(C 1 -C 4 -halogenoalkyl) having 1 to 5 halogen atoms, or

Z 2 and Z 3 form, together with the carbon atoms that they are connected to, a 5- or 6-membered saturated or partially saturated heterocyclic ring, a 5-membered heteroaryl, or a 6-membered heteroaryl, each of which may be optionally substituted with one or two substitutents selected from the group consisting of methyl, fluorine, and oxo, and

Z 1 , Z 4 , and Z 5 are independently selected from the group consisting of hydrogen, halogen, SF 5 , cyano, CHO, nitro, C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, hydroxy, C 1 -C 4 -alkoxy, C 3 -C 6 -cycloalkyl-C 1 -C 4 -alkoxy, cyano-C 1 -C 4 -alkoxy, C 1 -C 4 -halogenoalkoxy having 1 to 5 halogen atoms, —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 , —NH(C 3 -C 6 -cycloalkyl), —N(C 1 -C 4 -alkyl)(C 3 -C 6 -cycloalkyl), —NH—SO 2 —(C 1 -C 4 -alkyl), —N(SO 2 —[C 1 -C 4 -alkyl])(C 1 -C 4 -alkyl), (C 1 -C 4 -alkoxyimino)-C 1 -C 4 -alkyl, 4- to 6-membered heterocycloalkyl which is optionally substituted with 1 or 2 substituents selected from the group consisting of fluorine, methyl, and cyano, —CH 2 —O—(C 1 -C 4 -alkyl), —CH 2 —NH(C 1 -C 4 -alkyl), —CH 2 —N(C 1 -C 4 -alkyl) 2 , methyl substituted with a 4- to 6-membered heterocycloalkyl which itself is optionally substituted with 1 or 2 substituents selected from the group consisting of fluorine, methyl, and cyano, —CH 2 —S—(C 1 -C 4 -alkyl), —CH 2 —S(O)—(C 1 -C 4 -alkyl), —CH 2 —SO 2 —(C 1 -C 4 -alkyl), —S—(C 1 -C 4 -alkyl), —S(O)—(C 1 -C 4 -alkyl), —SO 2 —(C 1 -C 4 -alkyl), —S—(C 1 -C 4 -halogenoalkyl) having 1 to 5 halogen atoms, —S(O)—(C 1 -C 4 -halogenoalkyl) having 1 to 5 halogen atoms, —SO 2 —(C 1 -C 4 -halogenoalkyl) having 1 to 5 halogen atoms, —CONH(C 1 -C 4 -alkyl), —CONH(C 3 -C 6 -cycloalkyl), —NHCO(C 1 -C 4 -alkyl), —NHCO(C 3 -C 6 -cycloalkyl), and —NHCO(C 1 -C 4 -halogenoalkyl) having 1 to 5 halogen atoms, or

Q is a pyridine ring of formula (Q2)

wherein

Z 6 , Z 7 , Z 8 and Z 9 are independently selected from the group consisting of hydrogen, halogen, cyano, C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, C 1 -C 4 -alkoxy, C 1 -C 4 -halogenoalkoxy having 1 to 5 halogen atoms, —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 , —NH(C 3 -C 6 -cycloalkyl), and —N(C 1 -C 4 -alkyl)(C 3 -C 6 -cycloalkyl), or

Q is a pyrimidine ring of formula (Q3)

wherein

Z 10 , Z 11 and Z 12 are independently selected from the group consisting of hydrogen, halogen, cyano, C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, C 1 -C 4 -alkoxy, C 1 -C 4 -halogenoalkoxy having 1 to 5 halogen atoms, —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 , —NH(C 3 -C 6 -cycloalkyl), and —N(C 1 -C 4 -alkyl)(C 3 -C 6 -cycloalkyl), or

Q is a pyridine ring of formula (Q4)

wherein

Z 13 , Z 14 , Z 15 and Z 16 are independently selected from the group consisting of hydrogen halogen, cyano, C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, C 1 -C 4 -alkoxy, C 1 -C 4 -halogenoalkoxy having 1 to 5 halogen atoms, C 1 -C 4 -hydroxyalkyl, NH 2 , —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 , —NH(C 3 -C 6 -cycloalkyl), —N(C 1 -C 4 -alkyl)(C 3 -C 6 -cycloalkyl), —NH—CO—C 1 -C 4 -alkyl, and monocyclic heterocycles selected from the group of 4- to 7-membered heterocycloalkyl or 5-membered heteroaryls having at least one nitrogen atom via which the heteroaryl ring is connected to the pyridine ring, each of which is optionally substituted with 1, 2 or 3 substituents independently selected from the group consisting of halogen, cyano, nitro, —OH, oxo, thiono, C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, C 1 -C 4 -alkoxy, C 1 -C 4 -halogenoalkoxy having 1 to 5 halogen atoms, C 3 -C 6 -cycloalkyl, —NH 2 , —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 , —S—C 1 -C 4 -alkyl, —S(O)—C 1 -C 4 -alkyl, —SO 2 —C 1 -C 4 -alkyl, —S—(C 1 -C 4 -halogenoalkyl) having 1 to 5 halogen atoms, —S(O)—(C 1 -C 4 -halogenoalkyl) having 1 to 5 halogen atoms, and —SO 2 —(C 1 -C 4 -halogenoalkyl) having 1 to 5 halogen atoms, or

Q is a pyridine ring of formula (Q5)

wherein

Z 17 , Z 18 , Z 19 and Z 20 are independently selected from the group consisting of hydrogen, halogen, cyano, C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, C 1 -C 4 -alkoxy, C 1 -C 4 -halogenoalkoxy having 1 to 5 halogen atoms, —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 , —NH(C 3 -C 6 -cycloalkyl), and —N(C 1 -C 4 -alkyl)(C 3 -C 6 -cycloalkyl), or

Q is a 5-membered aromatic heterocycle of formula (Q6)

wherein

T 1 -T 4 are independently selected from the group consisting of N, O, S, C-Z 21 , and N—Z 22 , wherein not more than one of T 1 -T 4 is O, not more than one of T 1 -T 4 is S, not more than one of T 1 -T 4 is N—Z 22 , and wherein

each Z 21 is independently selected from the group consisting of hydrogen, halogen, cyano, C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, C 1 -C 4 -alkoxy, and C 1 -C 4 -halogenoalkoxy having 1 to 5 halogen atoms, and

each Z 22 is independently selected from the group consisting of hydrogen, C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, C 1 -C 4 -alkyl-C 3 -C 6 -cycloalkyl, and C 1 -C 4 -alkoxy-C 1 -C 4 -alkyl, or

Q is a 5-membered aromatic heterocycle of formula (Q7)

wherein

U 1 -U 4 are independently selected from the group consisting of N and C—Z 23 , wherein not more than three of U 1 -U 4 are N, and wherein

each Z 23 is independently selected from the group consisting of hydrogen, halogen, cyano, C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, C 1 -C 4 -alkoxy, and C 1 -C 4 -halogenoalkoxy having 1 to 5 halogen atoms,

wherein when Y is O, S or N—R 8 , none of R 4 , R 5 , R 6 and R 7 is —OH, and wherein when X is O, S or N—R 8 , none of R 6 and R 7 is —OH,

or a stereoisomer, a tautomer, an N-oxide, a hydrate, a solvate, or a salt thereof, or a mixture of any of the foregoing.

3. The compound according to claim 1 , wherein:

A is A1 or A2,

o is 0, 1 or 2,

R is selected from the group consisting of hydrogen, halogen, C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy, cyano, and C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms,

X and Y are independently selected from the group consisting of CR 6 R 7 , O, S, and N—R 8 , wherein at least one of X and Y is CR 6 R 7 ,

G is S,

R 1 is selected from the group consisting of hydrogen, C 1 -C 4 -alkyl, C 3 -C 6 -cycloalkyl, C 3 -C 4 -alkenyl, C 3 -C 4 -alkynyl, C 1 -C 4 -alkoxy-C 1 -C 4 -alkyl, C 3 -C 6 -cycloalkyl-C 1 -C 3 -alkyl, and cyano-C 1 -C 4 -alkyl,

R 2 is selected from the group consisting of

hydrogen, halogen, cyano, —COOH, C 1 -C 4 -alkoxy-C(O)—, —C(O)—NH 2 , —C(O)—NH(C 1 -C 4 -alkyl), —C(O)—N(C 1 -C 4 -alkyl) 2 , —C(O)—NH(C 3 -C 6 -cycloalkyl), —C(O)—N(C 1 -C 4 -alkyl)(C 3 -C 6 -cycloalkyl), —NR 9 R 10 , —OR 11 , —SR 12 , —S(O)R 12 , —SO 2 R 12 , C 1 -C 4 -alkyl, C 3 -C 6 -cycloalkyl, C 2 -C 4 -alkenyl, C 3 -C 6 -cycloalkenyl, C 2 -C 4 -alkynyl or phenyl-C 1 -C 4 -alkyl, each of which is optionally substituted by 1, 2, 3, 4 or 5 substituents independently selected from the group consisting of halogen, —OH, cyano, C 1 -C 4 -alkoxy-C(O)—, —C(O)—NH 2 , —C(O)—NH(C 1 -C 4 -alkyl), —C(O)—N(C 1 -C 4 -alkyl) 2 , C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, C 1 -C 4 -alkoxy, —NH 2 , —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 , —NH(C 3 -C 6 -cycloalkyl), —N(C 1 -C 4 -alkyl)(C 3 -C 6 -cycloalkyl), —S—C 1 -C 4 -alkyl, —S(O)—C 1 -C 4 -alkyl, —SO 2 —C 1 -C 4 -alkyl, —S—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, —S(O)—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, and —SO 2 —C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, and

a monocyclic or a bicyclic heterocycle selected from the group consisting of 4- to 10-membered heterocycloalkyl, heterospirocycloalkyl, 5-membered heteroaryl, and 6-membered heteroaryl, each of which is optionally substituted by 1, 2, 3 or 4 substituents independently selected from the group consisting of halogen, cyano, —OH, oxo, —COOH, C 1 -C 4 -alkoxy-C(O)—, —C(O)—NH 2 , —C(O)—NH(C 1 -C 4 -alkyl), —C(O)—N(C 1 -C 4 -alkyl) 2 , C 1 -C 4 -alkyl, C 1 -C 4 -alkyl-C(O)—, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, C 1 -C 4 -alkoxy, hydroxy-C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy-C 1 -C 4 -alkyl-, C 1 -C 4 -halogenoalkoxy having 1 to 5 halogen atoms, C 3 -C 6 -cycloalkyl, —NH 2 , —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 , —NH(C 3 -C 6 -cycloalkyl), —N(C 1 -C 4 -alkyl)(C 3 -C 6 -cycloalkyl), and 4- to 10-membered heterocycloalkyl,

R 4 is selected from the group consisting of hydrogen, —OH, C 1 -C 4 -alkyl, and C 1 -C 4 -alkoxy,

R 5 is hydrogen,

R 6 is selected from the group consisting of hydrogen and C 1 -C 4 -alkyl,

R 7 is selected from the group consisting of hydrogen and C 1 -C 4 -alkyl,

R 8 is selected from the group consisting of hydrogen and C 1 -C 4 -alkyl,

R 9 and R 10 are independently selected from the group consisting of

hydrogen, —NH(—C(O)—C 1 -C 4 -alkyl), C 1 -C 4 -alkoxy,

C 1 -C 4 -alkyl, C 3 -C 6 -cycloalkyl, phenyl-C 1 -C 4 -alkyl, each of which is optionally substituted by 1, 2 or 3 substituents independently selected from the group consisting of halogen, —OH, cyano, —COOH, C 1 -C 4 -alkoxy-C(O)—, —C(O)—NH 2 , —C(O)—NH(C 1 -C 4 -alkyl), —C(O)—N(C 1 -C 4 -alkyl) 2 , —NH—C(O)—C 1 -C 4 -alkyl, —N(C 1 -C 4 -alkyl)-(—C(O)—C 1 -C 4 -alkyl), C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, C 1 -C 4 -alkoxy, C 1 -C 4 -halogenoalkoxy having 1 to 5 halogen atoms, C 3 -C 6 -cycloalkyl, —NH 2 , —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 , —S—C 1 -C 4 -alkyl, —S(O)—C 1 -C 4 -alkyl, —SO 2 —C 1 -C 4 -alkyl, —S—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, —S(O)—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, —SO 2 —C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, and (C 1 -C 4 -alkoxy) 2 P(═O)—,

phenyl, benzo-C 5 -C 6 -cycloalkyl, each of which is optionally substituted by 1, 2 or 3 substituents independently selected from the group consisting of halogen, cyano, C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, C 1 -C 4 -alkoxy, and C 1 -C 4 -halogenoalkoxy having 1 to 5 halogen atoms, and

R 11 is selected from the group consisting of

C 1 -C 4 -alkyl, C 3 -C 6 -cycloalkyl, phenyl-C 1 -C 4 -alkyl, each of which is optionally substituted by 1, 2 or 3 substituents independently selected from the group consisting of halogen, —OH, cyano, C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, C 1 -C 4 -alkoxy, C 1 -C 4 -halogenoalkoxy having 1 to 5 halogen atoms, and C 3 -C 6 -cycloalkyl, and

R 12 is selected from the group consisting of

hydrogen,

C 1 -C 4 -alkyl, phenyl-C 1 -C 4 -alkyl, each of which is optionally substituted by 1, 2 or 3 substituents independently selected from the group consisting of halogen, —OH, cyano, C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, C 1 -C 4 -alkoxy, and C 1 -C 4 -halogenoalkoxy having 1 to 5 halogen atoms,

Q is a phenyl ring of formula (Q1)

wherein

Z 1 , Z 2 , Z 3 , Z 4 , and Z 5 are independently selected from the group consisting of hydrogen, halogen, cyano, C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, hydroxy, C 1 -C 4 -alkoxy, C 1 -C 4 -halogenoalkoxy having 1 to 5 halogen atoms, —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 , —NH(C 3 -C 6 -cycloalkyl), —N(C 1 -C 4 -alkyl)(C 3 -C 6 -cycloalkyl), 4- to 6-membered heterocyclyl, which is optionally substituted with 1 or 2 substituents selected from the group consisting of fluorine, chlorine, bromine, methyl, and cyano, —S—(C 1 -C 4 -alkyl), —S(O)—(C 1 -C 4 -alkyl), and —SO 2 —(C 1 -C 4 -alkyl), or

Z 1 and Z 2 form, together with the carbon atoms that they are connected to, a 5- or 6-membered heterocycloalkyl, a 5-membered heteroaryl, or a 6-membered heteroaryl, each of which may be optionally substituted with one or two substitutents selected from the group consisting of methyl, fluorine, and oxo, and

Z 3 , Z 4 , and Z 5 are independently selected from the group consisting of hydrogen, halogen, cyano, C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, C 1 -C 4 -alkoxy, C 1 -C 4 -alkoxy-C(O)—, and C 1 -C 4 -halogenoalkoxy having 1 to 5 halogen atoms, or

Z 1 , Z 4 , and Z 5 are independently selected from the group consisting of hydrogen, halogen, cyano, C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, C 1 -C 4 -alkoxy, and C 1 -C 4 -halogenoalkoxy having 1 to 5 halogen atoms,

wherein when Y is O, S or N—R 8 , R 4 is not —OH,

or a stereoisomer, a tautomer, an N-oxide, a hydrate, a solvate, or a salt thereof, or a mixture of any of the foregoing.

4. The compound according to claim 1 , wherein:

A is A1 or A2,

o is 0 or 1,

R is selected from the group consisting of hydrogen, halogen, C 1 -C 4 -alkyl, and C 1 -C 4 -alkoxy,

X is selected from the group consisting of CR 6 R 7 , O, S, and N—R 8 ,

Y is CR 6 R 7 ,

G is S,

R 1 is hydrogen or C 1 -C 4 -alkyl,

R 2 is selected from the group consisting of

hydrogen, halogen, —NR 9 R 10 , —OR 11 , —SR 12 , —S(O)R 12 , —SO 2 R 12 , C 1 -C 4 alkyl, C 3 -C 6 -cycloalkyl, C 2 -C 4 -alkenyl or C 3 -C 6 -cycloalkenyl, each of which is optionally substituted by 1, 2, 3, 4 or 5 substituents independently selected from the group consisting of halogen, cyano, C 1 -C 4 -alkoxy-C(O)—, and —C(O)—NH 2 , and a monocyclic or a bicyclic heterocycle selected from the group consisting of 4- to 10-membered heterocycloalkyl, heterospirocycloalkyl, 5-membered heteroaryl, and 6-membered heteroaryl, each of which is optionally substituted by 1, 2, 3 or 4 substituents independently selected from the group consisting of halogen, —OH, oxo, —COOH, C 1 -C 4 -alkoxy-C(O)—, —C(O)—NH 2 , C 1 -C 4 -alkyl, C 1 -C 4 -alkyl-C(O)—, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, hydroxy-C 1 -C 4 -alkyl-, C 1 -C 4 -alkoxy-C 1 -C 4 -alkyl-, —NH 2 , —N(C 1 -C 4 -alkyl) 2 , —NH(C 3 -C 6 -cycloalkyl), —N(C 1 -C 4 -alkyl)(C 3 -C 6 -cycloalkyl), and 4- to 10-membered heterocycloalkyl,

R 3 is selected from the group consisting of hydrogen, halogen, —OH, cyano, C 1 -C 4 -alkyl, C 3 -C 6 -cycloalkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, C 1 -C 4 -alkoxy-C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy, C 1 -C 4 -alkyl-C(O)—, —NH 2 , —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 , —NH(C 3 -C 6 -cycloalkyl), —N(C 1 -C 4 -alkyl)(C 3 -C 6 -cycloalkyl)-S—C 1 -C 4 -alkyl, —S(O)—C 1 -C 4 -alkyl, and —SO 2 —C 1 -C 4 -alkyl,

R 4 is selected from the group consisting of hydrogen, —OH, and C 1 -C 4 -alkyl,

R 5 is hydrogen,

R 6 is selected from the group consisting of hydrogen and C 1 -C 4 -alkyl,

R 7 is selected from the group consisting of hydrogen and C 1 -C 4 -alkyl,

R 8 is selected from the group consisting of hydrogen and C 1 -C 4 -alkyl,

R 9 and R 10 are independently selected from the group consisting of

hydrogen, —NH(—C(O)—C 1 -C 4 -alkyl), C 1 -C 4 -alkoxy,

a monocyclic or a bicyclic heterocycle selected from the group of 4- to 10-membered heterocycloalkyl, 5-membered heteroaryl, and 6-membered heteroaryl each of which is optionally substituted by 1, 2 or 3 substituents independently selected from the group consisting of halogen, —OH, oxo, cyano, C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, C 1 -C 4 -alkoxy, and C 1 -C 4 -halogenoalkoxy having 1 to 5 halogen atoms,

R 11 is selected from the group consisting of

R 12 is selected from the group consisting of

hydrogen,

C 1 -C 4 -alkyl, which is optionally substituted by 1, 2 or 3 substituents independently selected from the group consisting of —OH and —COOH, and a 6-membered heteroaryl,

Q is a phenyl ring of formula (Q1)

wherein

Z 1 is selected from the group consisting of hydrogen, halogen, C 1 -C 4 -alkyl, and C 1 -C 4 -alkoxy,

Z 2 is selected from the group consisting of hydrogen, halogen, —OH, C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy, —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 , —NH(C 3 -C 6 -cycloalkyl), —N(C 1 -C 4 -alkyl)(C 3 -C 6 -cycloalkyl), C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, C 1 -C 4 -halogenoalkoxy having 1 to 5 halogen atoms, —S—(C 1 -C 4 -alkyl), and a 4- to 6-membered heterocycloalkyl, and

Z 3 is selected from the group consisting of hydrogen, halogen, C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy, —NH(C 1 -C 4 -alkyl), and —N(C 1 -C 4 -alkyl) 2 ,

Z 4 is selected from the group consisting of hydrogen, halogen, C 1 -C 4 -alkyl, and C 1 -C 4 -alkoxy,

Z 5 is selected from the group consisting of hydrogen, halogen, C 1 -C 4 -alkyl, and C 1 -C 4 -alkoxy,

or a stereoisomer, a tautomer, an N-oxide, a hydrate, a solvate, or a salt thereof, or a mixture of any of the foregoing.

5. The compound according to claim 1 , wherein:

A is selected from the group consisting of

G is S,

R 1 is hydrogen or methyl,

R 2 is selected from the group consisting of hydrogen, chlorine, fluorine, —NR 9 R 10 , —OR 11 , —SR 12 , —S(O)R 12 , —SO 2 R 12 , methyl, ethyl, propyl, isopropyl, cyclopropyl, cyclohexyl, propenyl, cyclopentenyl, cyclohexenyl, each of which is optionally substituted by 1 or 2 substituents independently selected from the group consisting of cyano, ethoxy-C(O)—, and —C(O)—NH 2 ; and

a monocyclic or a bicyclic heterocycle selected from the group consisting of azetidine, pyrrolidine, pyrazolidine, imidazolidine, 1,2,4-triazolidine, piperidine, piperazine, tetrahydropyridine, dihydro-2H-pyrane, 1,2-oxazolidine, 1,2-oxazine, morpholine, thiomorpholine, 3,4-dihydroisoquinoline, 2,3-dihydro-indole, 1,3-dihydro-isoindoel, 3,9-dioxa-7-azabicyclo[3.3.1]nonane, 6-oxa-3-azabicyclo[3.1.1]heptane, 8-oxa-3-azabicyclo[3.2.1]octane, imidazole, pyrazole, 1,2,4-triazole, 1,2,3-triazole, 4-oxa-7-azaspiro[2.5]octane, each of which is optionally substituted by 1, 2, 3 or 4 substituents independently selected from the group consisting of fluorine, chlorine, cyano, —OH, oxo, —COOH, methoxy-C(O)—, ethoxy-C(O)—, tert-butoxy-C(O)—, —C(O)—NH 2 , methyl, methyl-C(O)—, trifluoromethyl, hydroxymethyl-, methoxymethyl-, —NH 2 , —NMe 2 , and pyrrolidine,

R 3 is selected from the group consisting of hydrogen, fluorine, chlorine, cyano, methyl, methoxy, and trifluoromethyl,

R 8 is selected from the group consisting of hydrogen and methyl,

R 9 and R 19 are independently selected from the group consisting of

hydrogen, —NH(—C(O)-methyl), methoxy,

methyl, ethyl, propyl, isopropyl, butyl, isobutyl, cyclopropyl, cyclobutyl, benzyl, 1-phenylethyl, each of which is optionally substituted by 1, 2 or 3 substituents independently selected from the group consisting of fluorine, —OH, —COOH, methoxy-C(O)—, ethoxy-C(O)—, tert-butoxy-C(O)—, —C(O)—NH 2 , —C(O)—NMe 2 , —NH—C(O)-methyl, methyl, methoxy, cyclopropyl, —NH 2 , NMe 2 , S-methyl, S(O)-methyl, SO 2 -methyl, and (EtO) 2 P(═O)—,

heterocyclyl-methyl, heterocyclyl-ethyl, wherein the heterocyclyl substituent is selected from the group consisting of pyrrolidine, morpholine, pyrazole, 1,2,4-oxadiazole, pyridine, each of which is optionally substituted by 1 substituent independently selected from the group consisting of fluorine, chlorine, —OH, oxo, and methyl, phenyl,

2,3-dihydro-1H-indene, and

a monocyclic or a bicyclic heterocycle selected from the group of oxetane, thietane, pyrrolidine, morpholine, tetrahydropyrane, pyridine, and pyrazole, each of which is optionally substituted by 1 or 2 substituents independently selected from the group consisting of fluorine, chlorine, —OH, oxo, and methyl;

R 11 is selected from the group consisting of

methyl, ethyl, isopropyl, butyl, cyclopentyl, benzyl, each of which is optionally substituted by 1 or 2 substituents independently selected from the group consisting of fluorine, —OH, methyl, methoxy, and cyclopentyl; and

a monocyclic or a bicyclic heterocycle selected from the group consisting of pyrrolidin and tetrahydropyran,

R 12 is selected from the group consisting of

methyl, ethyl, each of which is optionally substituted by 1 substituent independently selected from the group consisting of —OH and —COOH; and

pyridine,

Q is a phenyl ring of formula (Q1)

wherein

Z 1 is selected from the group consisting of hydrogen, fluorine, chlorine, methyl, and methoxy,

Z 2 is selected from the group consisting of hydrogen, fluorine, chlorine, —OH, methyl, ethyl, methoxy, ethoxy, —NH(CH 3 ), —N(CH 3 ) 2 , trifluoromethyl, and trifluoromethoxy,

Z 3 is selected from the group consisting of hydrogen, fluorine, chlorine, methyl, methoxy, —NH(CH 3 ), and —N(CH 3 ) 2 ,

Z 4 is selected from the group consisting of hydrogen, fluorine, chlorine, methyl, and methoxy,

Z 5 is selected from the group consisting of hydrogen, fluorine, chlorine methyl, and methoxy,

or a stereoisomer, a tautomer, an N-oxide, a hydrate, a solvate, or a salt thereof, or a mixture of any of the foregoing.

6. The compound according to claim 1 , wherein:

A is selected from the group consisting of

G is S,

R 1 is hydrogen or methyl,

R 2 is selected from the group consisting of hydrogen, chlorine, fluorine, —NH 2 , —NH(CH 3 ), —N(CH 3 ) 2 , methoxy, ethoxy, methyl, ethyl, propyl, isopropyl, cyclopropyl, trifluoromethyl, and trifluoromethoxy,

R 3 is selected from the group consisting of hydrogen, chlorine, fluorine, methyl, methoxy, and trifluoromethyl,

Q is a phenyl ring of formula (Q1)

wherein

Z 1 is selected from the group consisting of hydrogen, fluorine, chlorine, methyl, and methoxy,

Z 2 is selected from the group consisting of hydrogen, fluorine, chlorine, —OH, methyl, ethyl, methoxy, ethoxy, —NH(CH 3 ), —N(CH 3 ) 2 , trifluoromethyl, and trifluoromethoxy,

Z 3 is selected from the group consisting of hydrogen, fluorine, chlorine, methyl, methoxy, —NH(CH 3 ), and —N(CH 3 ) 2 ,

Z 4 is selected from the group consisting of hydrogen, fluorine, chlorine, methyl, and methoxy,

Z 5 is selected from the group consisting of hydrogen, fluorine, chlorine, methyl, and methoxy,

or a stereoisomer, a tautomer, an N-oxide, a hydrate, a solvate, or a salt thereof, or a mixture of any of the foregoing.

7. A compound of formula (II):

wherein

A is selected from the group consisting of

R 1 is hydrogen or methyl,

R 2 is selected from the group consisting of hydrogen, chlorine, fluorine, methoxy, methyl, ethyl, propyl, isopropyl, trifluoromethyl, and trifluoromethoxy,

R 3 is selected from the group consisting of hydrogen, chlorine, fluorine, methyl, methoxy, and trifluoromethyl,

Q is a phenyl ring of formula (Q1)

wherein

Z 1 is selected from the group consisting of hydrogen and halogen,

Z 2 is selected from the group consisting of hydrogen, halogen, —N(C 1 -C 4 -alkyl) 2 , —C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, and C 1 -C 4 -halogenoalkoxy having 1 to 5 halogen atoms,

Z 3 is selected from the group consisting of hydrogen and halogen,

Z 4 is selected from the group consisting of hydrogen and halogen,

Z 5 is selected from the group consisting of hydrogen and halogen,

or a stereoisomer, a tautomer, an N-oxide, a hydrate, a solvate, or a salt thereof, or a mixture of any of the foregoing.

8. The compound according to claim 7 , wherein

A is selected from the group consisting of

R 1 is hydrogen,

R 2 is isopropyl,

R 3 is methyl,

Q is a phenyl ring of formula (Q1)

wherein

Z 1 , Z 3 , Z 4 and Z 5 are independently selected from the group consisting of hydrogen, fluorine, and chlorine, and

Z 2 is selected from the group consisting of hydrogen, fluorine, chlorine, —N(CH 3 ) 2 , trifluoromethyl, and trifluoromethoxy,

or a stereoisomer, a tautomer, an N-oxide, a hydrate, a solvate, or a salt thereof, or a mixture of any of the foregoing.

9. A pharmaceutical composition comprising a compound of formula (I) according to claim 1 , or a stereoisomer, a tautomer, an N-oxide, a hydrate, a solvate, or a salt thereof, or a mixture of any of the foregoing, and one or more pharmaceutically acceptable excipients.

10. A method for controlling helminth infections in humans and/or animals comprising administering an anthelminthically effective amount of at least one compound of formula (I) according to claim 1 , or a stereoisomer, a tautomer, an N-oxide, a hydrate, a solvate, or a salt thereof, or a mixture of any of the foregoing, to a human or an animal in need thereof.

11. A pharmaceutical composition comprising a compound of formula (II) according to claim 7 , or a stereoisomer, a tautomer, an N-oxide, a hydrate, a solvate, or a salt thereof, or a mixture of any of the foregoing, and one or more pharmaceutically acceptable excipients.

12. A method for controlling helminth infections in humans and/or animals comprising administering an anthelminthically effective amount of at least one compound of formula (II) according to claim 7 , or a stereoisomer, a tautomer, an N-oxide, a hydrate, a solvate, or a salt thereof, or a mixture of any of the foregoing, to a human or an animal in need thereof.

13. A compound of formula (I)

wherein

(a) G is S, R 1 is H, R 2 is isopropyl, R 3 is methyl, Q is 3,5-dichlorophenyl, and A is (4S)-3,4-dihydro-2H-chromen-4-yl,

(b) G is S, R 1 is H, R 2 is isopropyl, R 3 is methyl, Q is 2,3-dichlorophenyl, and A is (4S)-3,4-dihydro-2H-chromen-4-yl,

(c) G is S, R 1 is H, R 2 is isopropyl, R 3 is methyl, Q is 2-fluoro-3-(trifluoromethyl)-phenyl, and A is (4S)-3,4-dihydro-2H-chromen-4-yl,

(d) G is S, R 1 is H, R 2 is isopropyl, R 3 is methyl, Q is 2-fluoro-3-(trifluoromethoxy)-phenyl, and A is (4S)-3,4-dihydro-2H-chromen-4-yl,

(e) G is S, R 1 is H, R 2 is isopropyl, R 3 is methyl, Q is 3,5-dichloro-4-fluorophenyl, and A is (4S)-3,4-dihydro-2H-chromen-4-yl,

(f) G is S, R 1 is H, R 2 is isopropyl, R 3 is methyl, Q is 2,4-difluoro-3-(dimethylamino)-phenyl, and A is (4S)-3,4-dihydro-2H-chromen-4-yl,

(g) G is S, R 1 is H, R 2 is isopropyl, R 3 is methyl, Q is 3,4-dichlorophenyl, and A is (4S)-3,4-dihydro-2H-chromen-4-yl,

(h) G is S, R 1 is H, R 2 is isopropyl, R 3 is methyl, Q is 3,4-difluorophenyl, and A is (4S)-3,4-dihydro-2H-chromen-4-yl,

(i) G is S, R 1 is H, R 2 is isopropyl, R 3 is methyl, Q is 2,3,4-trifluorophenyl, and A is (4S)-3,4-dihydro-2H-chromen-4-yl,

(j) G is S, R 1 is H, R 2 is isopropyl, R 3 is methyl, Q is 2,6-dichlorophenyl, and A is (4S)-3,4-dihydro-2H-chromen-4-yl,

(k) G is S, R 1 is H, R 2 is isopropyl, R 3 is methyl, Q is 2-chloro-3-(trifluoromethyl)-phenyl, and A is (4S)-3,4-dihydro-2H-chromen-4-yl,

(l) G is S, R 1 is H, R 2 is isopropyl, R 3 is methyl, Q is 2,3,5-trifluorophenyl, and A is (4S)-3,4-dihydro-2H-chromen-4-yl,

(m) G is S, R 1 is H, R 2 is isopropyl, R 3 is methyl, Q is 2-fluoro-3-(dimethylamino)-phenyl, and A is (4S)-3,4-dihydro-2H-chromen-4-yl,

(n) G is S, R 1 is H, R 2 is isopropyl, R 3 is methyl, Q is 3,5-dichloro-4-fluorophenyl, and A is (1S)-2,3-dihydro-1H-inden-1-yl, and

(o) G is S, R 1 is H, R 2 is isopropyl, R 3 is methyl, Q is 2,3-dichlorophenyl, and A is (1S)-2,3-dihydro-1H-inden-1-yl.

Assignments (2)

CHANGE OF NAME Recorded Feb 8, 2024

From: BAYER ANIMAL HEALTH GMBH

To: ELANCO ANIMAL HEALTH GMBH

Reel/Frame 066525/0898 →

ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 15, 2019

From: GRIEBENOW, NILS; ZHUANG, WEI; KULKE, DANIEL; KÖHLER, ADELINE; ILG, THOMAS; WELZ, CLAUDIA; SCHWARZ, HANS-GEORG; GÖRGENS, ULRICH; HÜBSCH, WALTER; KÖBBERLING, JOHANNES

To: BAYER ANIMAL HEALTH GMBH

Reel/Frame 051018/0610 →