IP Library Granted Patent US 12,435,068
Granted Patent B2
US 12,435,068 · App. 17/287,548 · Granted Oct 7, 2025

Anthelmintic compounds

Inventors: Nils Griebenow (Dormagen, DE); Walter Huebsch (Wuppertal, DE); Hans-Georg Schwarz (Dorsten, DE); Wei Zhuang (Monheim am Rhein, DE); Bernd ALig (Koenigswinter, DE); Adeline Koehler (Langenfeld, DE); Daniel Kulke (Leverkusen, DE); Iring Heisler (Duesseldorf, DE); Thomas Ilg (Monheim, DE)
Assignee: Elanco Animal Health GmbH
C07D405/14A61P33/10C07D241/42C07D249/18C07D311/58C07D311/68C07D405/12C07D409/12C07D471/04C07D495/04
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 12,435,068
App. No.
17/287,548
Granted
Oct 7, 2025
Kind
B2
Abstract

The present invention relates to novel compounds of general formula (I): with A being A1 or A 2 : and in which T, X, Y, Ro, R 1 , R 10 and R 11 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 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 (328)

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, Y are independently selected from the group consisting of CR 7 R 8 , O, S, and N—R 9 , wherein at least one of X and Y is CR 7 R 8 ,

or

X, Y form together a ring member selected from the group consisting of —C(O)—O—, —C(O)—NR 9 —, —S(O)—NR 9 —, —SO 2 —NR 9 — and —SO 2 —O—;

T is selected from the group consisting of T 1 , T 2 , T 3 , T 4 , T 5 , T 6 , T 7 , T 8a , and T 8b :

L is selected from the group consisting of O and NR 9 ;

M is selected from the group consisting of C═O and CR 7 R 8 ;

U is selected from the group consisting of CR 7 and N;

V is selected from the group consisting of CR 7 and N;

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, and —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 ;

—NR 12 R 13 ;

—OR 14 ;

—SR 15 , —S(O)R 15 , —SO 2 R 15 ;

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 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, —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 , —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;

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, 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 , —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 or C 1 -C 4 -alkyl;

R 4 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 -halogenoalkoxy having 1 to 5 halogen atoms, C 1 -C 4 -alkyl-C(O)—, —NH 2 , —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 , —S—C 1 -C 4 -alkyl, —S—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms —S(O)—C 1 -C 4 -alkyl, —SO 2 —C 1 -C 4 -alkyl;

R 5 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 , —S—C 1 -C 4 -alkyl, —S(O)—C 1 -C 4 -alkyl, —SO 2 —C 1 -C 4 -alkyl;

R 6 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 -halogenoalkoxy having 1 to 5 halogen atoms, C 1 -C 4 -alkyl-C(O)—, —NH 2 , —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 , —S—C 1 -C 4 -alkyl, —S—C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, —S(O)—C 1 -C 4 -alkyl, —SO 2 —C 1 -C 4 -alkyl;

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

R 8 is selected from the group consisting of hydrogen, —OH, halogen, C 1 -C 4 -alkyl and C 1 -C 4 -alkoxy;

or R 7 and R 8 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 9 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 10 is selected from the group consisting of hydrogen, —OH, C 1 -C 4 -alkyl and C 1 -C 4 -alkoxy;

R 11 is selected from the group consisting of hydrogen, C 1 -C 4 -alkyl and C 1 -C 4 -alkoxy;

or R 10 and R 11 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 12 and R 13 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 14 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;

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 -alky) 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 15 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, —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;

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, 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 16 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 17 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;

Q is selected from the group consisting of 6- to 10-membered aryl and 5- to 10-membered heteroaryl, each of which is substituted by 1, 2, 3, 4 or 5 substituents selected from the group consisting of halogen, SFs, cyano, —CHO, oxo, C 1 -C 4 -alkyl, C 1 -C 4 -hydroxyalkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, —OH, 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—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), —NHCO(C 1 -C 4 -halogenoalkyl) having 1 to 5 halogen atoms;

wherein when Y is O, S or N—R 9 , none of R 7 , R 8 , R 10 and R 11 is —OH, and wherein

when X is O, S or N—R 9 , none of R 7 and R 8 is —OH;

and/or a stereoisomer, tautomer, N-oxide, hydrate, solvate, and/or a salt thereof,

and/or a mixture thereof.

2. The compound of claim 1 , wherein:

A is A1 or A2,

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, Y are independently selected from the group consisting of CR 7 R 8 , O, S, and N—R 9 , wherein at least one of X and Y is CR 7 R 8 ,

or

X, Y form together a ring member selected from the group consisting of —C(O)—O—, —C(O)—NR 9 —, —S(O)—NR 9 —, —SO 2 —NR 9 —and —SO 2 —O—;

T is selected from the group consisting of T 1 , T 2 , T 3 , T 4 , T 5 , T 6 , T 7 , T 8a , and T 8b :

L is selected from the group consisting of O and NR 9 ;

M is selected from the group consisting of C═O and CR 7 R 8 ;

U is selected from the group consisting of CR 7 and N;

V is selected from the group consisting of CR 7 and N;

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, and —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 ;

—NR 12 R 13 ;

—OR 14 ;

—SR 15 , —S(O)R 15 , —SO 2 R 15 ;

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 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, —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 , —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;

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, 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 , —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 or C 1 -C 4 -alkyl;

R 4 is 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;

R 5 is 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;

R 6 is 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;

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

R 8 is selected from the group consisting of hydrogen, —OH, halogen, C 1 -C 4 -alkyl and C 1 -C 4 -alkoxy;

R 9 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 10 is selected from the group consisting of hydrogen, —OH, C 1 -C 4 -alkyl and C 1 -C 4 -alkoxy;

R 11 is selected from the group consisting of hydrogen, C 1 -C 4 -alkyl and C 1 -C 4 -alkoxy;

R 12 and R 13 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;

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 14 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;

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, 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 15 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, —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;

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, 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 16 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 17 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;

Q is selected from the group consisting of 6-membered aryl and 5- to 6-membered heteroaryl, each of which is substituted by 1, 2, 3, 4 or 5 substituents selected from the group consisting of halogen, SF 5 , cyano, —CHO, oxo, C 1 -C 4 -alkyl, C 1 -C 4 -hydroxyalkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, —OH, 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—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), —NHCO(C 1 -C 4 -halogenoalkyl) having 1 to 5 halogen atoms;

wherein when Y is O, S or N—R 9 , none of R 7 , R 8 , R 10 and R 11 is —OH, and wherein

when X is O, S or N—R 9 , none of R 7 and R 8 is —OH;

and/or a stereoisomer, tautomer, N-oxide, hydrate, solvate, and/or a salt thereof,

and/or a mixture thereof.

3. The compound of claim 1 , wherein:

A is A1 or A2;

o is 0, 1 or 2;

R is 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;

X, Y are independently selected from the group consisting of CR 7 R 8 , O, S, and N—R 9 , wherein at least one of X and Y is CR 7 R 8 ;

T is selected from the group consisting of T 1 , T 2 , T 3 , T 4 , T 5 , T 6 , T 7 , T 8a , and T 8b :

L is selected from the group consisting of O and NR 9 ;

M is selected from the group consisting of C═O and CR 7 R 8 ;

U is selected from the group consisting of CR 7 and N;

V is selected from the group consisting of CR 7 and N;

R 1 is 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 -alkoxy;

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 ;

—NR 12 R 13 ;

—OR 14 ;

—R 15 , —S(O)R 15 , —SO 2 R 15 ;

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 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, —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 , —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 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 , —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 or C 1 -C 4 -alkyl;

R 4 is 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;

R 5 is 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;

R 6 is 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;

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

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

R 9 is selected from the group consisting of hydrogen, C 1 -C 4 -alkyl;

R 10 is selected from the group consisting of hydrogen, —OH, C 1 -C 4 -alkyl and C 1 -C 4 -alkoxy;

R 11 is selected from the group consisting of hydrogen;

R 12 and R 13 are independently selected from the group consisting of hydrogen;

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, —OH, oxo, 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;

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, C 1 -C 4 -halogenoalkoxy 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, —OH, oxo, 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;

R 14 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, C 3 -C 6 -cycloalkyl;

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, —OH, oxo, 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;

R 15 is selected from the group consisting of

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, C 1 -C 4 -halogenoalkoxy 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, 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;

R 16 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 17 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;

Q is selected from the group consisting of 6-membered aryl and 5- to 6-membered heteroaryl, each of which is substituted by 1, 2, 3, 4 or 5 substituents selected from the group consisting of halogen, cyano, C 1 -C 4 -alkyl, C 1 -C 4 -hydroxyalkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms, —OH, 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 , 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;

wherein when Y is O, S or N—R 9 , none of R 7 , R 8 , R 10 and R 11 is —OH, and wherein

when X is O, S or N—R 9 , none of R 7 and R 8 is —OH;

and/or a stereoisomer, tautomer, N-oxide, hydrate, solvate, and/or a salt thereof,

and/or a mixture thereof.

4. The compound of claim 1 , wherein:

A is A1 or A2;

is 0 or 1;

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

X is selected from the group consisting of CR 7 R 8 , O, S, and N—R 9 ,

Y is CR 7 R 8 ;

T is selected from the group consisting of T 1 , T 2 , T 3 , T 4 , T 5 , T 6 , T 7 , T 8a , and T 8b :

L is selected from the group consisting of O and NR 9 ;

M is selected from the group consisting of C═O and CR 7 R 8 ;

U is selected from the group consisting of CR 7 and N;

V is selected from the group consisting of CR 7 and N;

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

R 2 is selected from the group consisting of

hydrogen, halogen;

—NR 12 R 13 ;

—OR 14 ;

—R 15 , —S(O)R 15 , —SO 2 R 15 ;

C 1 -C 6 -alkyl or C 3 -C 6 -cycloalkyl, 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 -alkyl;

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, 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 -alkoxy-C 1 -C 4 -alkyl-, C 1 -C 4 -halogenoalkoxy having 1 to 5 halogen atoms;

R 3 is selected from the group consisting of hydrogen, halogen or C 1 -C 4 -alkyl;

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

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

R 6 is selected from the group consisting of hydrogen, halogen, C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms;

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

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

R 9 is selected from the group consisting of hydrogen, C 1 -C 4 -alkyl;

R 10 is selected from the group consisting of hydrogen, C 1 -C 4 -alkyl;

R 11 is selected from the group consisting of hydrogen;

R 12 and R 13 are independently selected from the group consisting of hydrogen;

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, C 3 -C 6 -cycloalkyl;

heterocyclyl-C 1 -C 4 -alkyl, wherein the heterocyclyl substituent is selected from the group consisting of 4- to 10-membered heterocycloalkyl, which is optionally substituted by 1, 2 or 3 substituents independently selected from the group consisting of halogen, 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;

phenyl, which is optionally substituted by 1, 2 or 3 substituents independently selected from the group consisting of halogen, 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;

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, 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;

R 14 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, 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;

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, 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;

R 15 is selected from the group consisting of

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, 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;

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, 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;

R 16 is selected from the group consisting of hydrogen, C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms;

R 17 is selected from the group consisting of hydrogen, C 1 -C 4 -alkyl, C 1 -C 4 -halogenoalkyl having 1 to 5 halogen atoms;

Q is selected from the group consisting of 6-membered aryl and 5- to 6-membered heteroaryl, each of which is substituted by 1, 2, 3, 4 or 5 substituents selected from the group consisting of halogen, 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;

wherein when Y is O, S or N—R 9 , none of R 7 , R 8 , R 10 and R 11 is —OH, and wherein

when X is O, S or N—R 9 , none of R 7 and R 8 is —OH;

and/or a stereoisomer, tautomer, N-oxide, hydrate, solvate, and/or a salt thereof,

and/or a mixture thereof.

5. The compound of claim 1 , wherein:

Q is a substituted phenyl ring of formula (Q1)

in which:

Z 1 , Z 2 , Z 3 , Z 4 , and Z 5 are independently selected from the group consisting of hydrogen, halogen, SFs, cyano, —CHO, —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—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), —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 substituents 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, SF 5 , cyano, CHO, 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—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 or 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), —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 substituents 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, 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—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 or 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), —NHCO(C 1 -C 4 -halogenoalkyl) having 1 to 5 halogen atoms, or

Q is a pyridine ring of formula (Q2)

in which:

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, C 1 -C 4 -hydroxyalkyl, NH 2 , —NH(C 1 -C 4 -alkyl), —N(C 1 -C 4 -alkyl) 2 , —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, —SO 2 —(C 1 -C 4 -halogenoalkyl) having 1 to 5 halogen atoms, or

Q is a pyrimidine ring of formula (Q3)

in which:

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 , or

Q is a pyridine ring of formula (Q4)

in which:

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

Q is a pyridine ring of formula (Q5)

in which:

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 , or

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

in which:

G 1 -G 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 G 1 -G 4 is O, not more than one of G 1 -G 4 is S, not more than one of G 1 -G 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, 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, C 1 -C 4 -alkoxy-C 1 -C 4 -alkyl, or

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

in which:

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, C 1 -C 4 -halogenoalkoxy having 1 to 5 halogen atoms,

and/or a stereoisomer, tautomer, N-oxide, hydrate, solvate, and/or a salt thereof,

and/or a mixture thereof.

6. The compound of claim 1 , wherein:

A is selected from the group consisting of

T is selected from the group consisting of T 1 , T 2 , T 3 , T 4 , T 5 , T 6 , T 7 , T 8a , and T 8b :

L is selected from the group consisting of O and NR 9 ;

M is selected from the group consisting of C═O and CR 7 R 8 ;

U is selected from the group consisting of CR 7 and N;

V is selected from the group consisting of CR 7 and N;

R 1 is selected from the group consisting of hydrogen or methyl;

R 2 is selected from the group consisting of

hydrogen, chlorine, fluorine, bromine;

—NR 12 R 13 ;

—OR 14 ;

methyl, ethyl, propyl, isopropyl, cyclopropyl, cyclohexyl, each of which is optionally substituted by 1 of 2 substituents independently selected from the group consisting of fluorine, chlorine, cyano, methyl, ethyl, propyl, and isopropyl;

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, tetrahydropyrane, 1,2-oxazolidine, 1,2-oxazine, morpholine, thiomorpholine, 3,4-dihydroisoquinoline, 2,3-dihydro-indole, 1,3-dihydro-isoindole, 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, —OH, methyl, trifluoromethyl, methoxymethyl, trifluoromethoxymethyl;

R 3 is selected from the group consisting of hydrogen, chlorine or methyl;

R 4 is selected from the group consisting of hydrogen, fluorine, chlorine, methyl, methoxy, trifluoromethyl, trifluoromethoxy;

R 5 is selected from the group consisting of hydrogen, fluorine, chlorine, methyl, trifluoromethyl;

R 6 is selected from the group consisting of hydrogen, fluorine, chlorine, methyl, methoxy, trifluoromethyl, trifluoromethoxy;

R 12 and R 13 are independently selected from the group consisting of

hydrogen and methyl;

R 14 is methyl;

R 16 is selected from the group consisting of hydrogen, methyl, ethyl, propyl, isopropyl, trifluoromethyl;

R 17 is selected from the group consisting of hydrogen, methyl, ethyl, propyl, isopropyl, trifluoromethyl;

Q is a phenyl ring of formula (Q1)

wherein:

Z 1 to Z 5 are independently selected from the group consisting of hydrogen, fluorine, chlorine, methyl and trifluoromethyl;

or

Q is a pyridine ring of formula (Q2)

wherein:

Z 6 to Z 9 are independently selected from the group consisting of hydrogen, fluorine, chlorine, methyl and trifluoromethyl;

and/or a stereoisomer, tautomer, N-oxide, hydrate, solvate, and/or a salt thereof,

and/or a mixture thereof.

7. The compound of claim 1 , wherein:

Q is a phenyl ring of formula (Q1)

wherein:

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

Z 2 and Z 4 are independently selected from the group consisting of hydrogen, fluorine, chlorine and trifluoromethyl;

or

Q is a pyridine ring of formula (Q2)

wherein:

Z 6 to Z 9 are independently selected from the group consisting of hydrogen, fluorine and chlorine; and/or a stereoisomer, tautomer, N-oxide, hydrate, solvate, and/or a salt thereof, and/or a mixture thereof.

8. The compound of claim 1 , wherein:

A is selected from the group consisting of

and/or a stereoisomer, tautomer, N-oxide, hydrate, solvate, and/or a salt thereof,

and/or a mixture thereof.

9. The compound of claim 1 , wherein:

A is selected from the group consisting of

T is selected from the group consisting of T 1 , T 2 , T 3 , T 4 , T 5 , T 6 , T 7 , T 8a , and T 8b :

L is selected from the group consisting of O and NR 9 ;

M is selected from the group consisting of C═O and CR 7 R 8 ;

U is selected from the group consisting of CR 7 and N;

V is selected from the group consisting of CR 7 and N;

R 1 is hydrogen;

R 2 is selected from the group consisting of hydrogen, chlorine, —NR 12 R 13 , —OR 14 ; methyl, isopropyl, and morpholine;

R 3 is hydrogen or methyl;

R 4 is hydrogen or fluorine;

R 5 is hydrogen or methyl;

R 6 is hydrogen or fluorine;

R 12 and R 13 are independently selected from the group consisting of hydrogen and methyl;

R 14 is methyl;

R 16 is methyl or isopropyl;

R 17 is methyl;

Q is a phenyl ring of formula (Q1)

wherein:

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

Z 2 and Z 4 are independently selected from the group consisting of hydrogen, fluorine, chlorine and trifluoromethyl;

or

Q is a pyridine ring of formula (Q2)

wherein:

Z 6 to Z 9 are independently selected from the group consisting of hydrogen and chlorine;

and/or a stereoisomer, tautomer, N-oxide, hydrate, solvate, and/or a salt thereof,

and/or a mixture thereof.

10. The compound of claim 1 , wherein:

A is selected from the group consisting of

and/or a stereoisomer, tautomer, N-oxide, hydrate, solvate, and/or a salt thereof,

and/or a mixture thereof.

11. A method of preparing a compound of claim 1 , said method comprising allowing an intermediate compound of formula Int-I-T1, Int-I-T2, Int-I-T3, Int-I-T4, Int-I-T5, Int-I-T6, Int-I-T7, Int-I-T8a, or Int-I-T8b:

wherein L, M, U, V, A, R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 16 and R 17 are as defined for the compound of claim 1 , and wherein Hal is halogen,

to react with a compound of formula 1H

Q-B(OR) 2   1H,

wherein Q is as defined for the compound of claim 1 , and

wherein each R may be individually H or Me or both R are pinacolate,

thereby giving a compound of formula (I):

wherein T, L, M, U, V, A, R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , and Q are as defined in claim 1 ,

or

allowing an intermediate compound of formula Int-II-T1, Int-II-T2, Int-II-T3, Int-II-T4, Int-II-T5, Int-II-T6, Int-II-T7, Int-II-T8a, or Int-II-T8b:

to react with a compound of formula 1V:

thereby giving a compound of formula (I):

12. A pharmaceutical composition comprising a compound of claim 1 and one or more pharmaceutically acceptable excipients.

13. A method for controlling helminth infection in humans and/or animals comprising administering an anthelminthically effective amount of at least one compound of claim 1 or a pharmaceutical composition thereof to a human or an animal in need thereof.

14. The method of claim 11 , wherein Hal is selected from the group consisting of chlorine, bromine, and iodine.

Assignments (3)
CHANGE OF NAME Recorded Nov 4, 2024
From: BAYER ANIMAL HEALTH GMBH
To: ELANCO ANIMAL HEALTH GMBH
Reel/Frame 069300/0663 →
CORRECTIVE ASSIGNMENT TO CORRECT THE APPLICANT ADDRESS PREVIOUSLY RECORDED ON REEL 056414 FRAME 0782. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Jul 28, 2021
From: GRIEBENOW, NILS; HUEBSCH, WALTER; SCHWARZ, HANS-GEORG; ZHUANG, WEI; ALIG, BERND; KOEHLER, ADELINE; KULKE, DANIEL; HEISLER, IRING; ILG, THOMAS
To: BAYER ANIMAL HEALTH GMBH
Reel/Frame 057521/0331 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 2, 2021
From: GRIEBENOW, NILS; HUEBSCH, WALTER; SCHWARZ, HANS-GEORG; ZHUANG, WEI; ALIG, BERND; KOEHLER, ADELINE; KULKE, DANIEL; HEISLER, IRING; ILG, THOMAS
To: BAYER ANIMAL HEALTH GMBH
Reel/Frame 056414/0782 →
Priority Claims (1)
EP 18202419 · Oct 24, 2018 · regional
Continuity (1)
Related Publication 20210380566A1 · Dec 9, 2021
References Cited (111)
US 10604525B2 · Koehler et al. · 2020 [cited by applicant]
US 10889573B2 · Hübsch · 2021 [cited by examiner]
US 10934301B2 · Goergens et al. · 2021 [cited by applicant]
US 11001590B2 · Schwarz et al. · 2021 [cited by applicant]
US 11254661B2 · Griebenow et al. · 2022 [cited by applicant]
US 11505545B2 · Hübsch · 2022 [cited by examiner]
US 20070129359A1 · Huwe et al. · 2007 [cited by applicant]
US 20080242695A1 · Morgan et al. · 2008 [cited by applicant]
US 20110034441A1 · Hood · 2011 [cited by examiner]
US 20140235612A1 · Chappie et al. · 2014 [cited by applicant]
US 20140275503A1 · Giampietro et al. · 2014 [cited by applicant]
US 20190071447A1 · Kohler et al. · 2019 [cited by applicant]
US 20200024264A1 · Hubsch et al. · 2020 [cited by applicant]
US 20200239482A1 · Gorgens et al. · 2020 [cited by applicant]
US 20200299299A1 · Schwarz et al. · 2020 [cited by applicant]
US 20200377486A1 · Griebenow et al. · 2020 [cited by applicant]
US 20210115026A1 · Huebsch et al. · 2021 [cited by applicant]
US 20210380566A1 · Griebenow et al. · 2021 [cited by applicant]
CL 2018002920A1 · 2019 [cited by applicant]
CL 2019001292A1 · 2019 [cited by applicant]
CL 2020000301A1 · 2020 [cited by applicant]
CL 2020002919A1 · 2021 [cited by applicant]
CL 2021000646A1 · 2021 [cited by applicant]
CL 2021000994A1 · 2021 [cited by applicant]
CL 2021001057A1 · 2021 [cited by applicant]
CL 2021001040A1 · 2021 [cited by applicant]
CL 2021001025A1 · 2021 [cited by applicant]
CN 101337937A · 2009 [cited by applicant]
CN 101337940A · 2009 [cited by applicant]
CN 101715774A · 2010 [cited by applicant]
CN 103109816A · 2013 [cited by applicant]
CN 103232431A · 2013 [cited by applicant]
CN 103265527A · 2013 [cited by applicant]
CN 103524422A · 2014 [cited by applicant]
CN 104884453A · 2015 [cited by applicant]
CN 106536518A · 2017 [cited by applicant]
DE 3639877A1 · 1988 [cited by applicant]
EP 2647626A1 · 2013 [cited by applicant]
JP 2010018586A · 2010 [cited by applicant]
RU 2543374C2 · 2015 [cited by applicant]
WO 0232856A2 · 2002 [cited by applicant]
WO 2002070509A2 · 2002 [cited by applicant]
WO 03106457A1 · 2003 [cited by applicant]
WO 2004099160A1 · 2004 [cited by applicant]
WO 2005012283A1 · 2005 [cited by applicant]
WO 2006003494A2 · 2006 [cited by applicant]
WO 2006043635A1 · 2006 [cited by applicant]
WO 2007040280A1 · 2007 [cited by applicant]
WO 2007040282A1 · 2007 [cited by applicant]
WO 2007092403A1 · 2007 [cited by applicant]
WO 2009100250A1 · 2009 [cited by applicant]
WO 2009155388A1 · 2009 [cited by applicant]
WO 2010051926A2 · 2010 [cited by applicant]
WO 2010052161A2 · 2010 [cited by applicant]
WO 2010066780A1 · 2010 [cited by applicant]
WO 2011085575A1 · 2011 [cited by applicant]
WO 2011105506A1 · 2011 [cited by applicant]
WO 2011151146A1 · 2011 [cited by applicant]
WO 2012087861A1 · 2012 [cited by applicant]
WO 2012106472A1 · 2012 [cited by applicant]
WO 2012112363A1 · 2012 [cited by applicant]
WO 2013050317A1 · 2013 [cited by applicant]
WO 2013162715A2 · 2013 [cited by applicant]
WO 2013162716A2 · 2013 [cited by applicant]
WO 2014081697A2 · 2014 [cited by applicant]
WO 2014187846A1 · 2014 [cited by applicant]
WO 2015058021A1 · 2015 [cited by applicant]
WO 2015058028A1 · 2015 [cited by applicant]
WO 2015179414A1 · 2015 [cited by applicant]
WO 2016005276A1 · 2016 [cited by applicant]
WO 2016123392A2 · 2016 [cited by applicant]
WO 2016133011A1 · 2016 [cited by applicant]
WO 2017143041A1 · 2017 [cited by applicant]
WO 2017178416A1 · 2017 [cited by applicant]
WO WO2018087036A1 · 2018 [cited by examiner]
WO 2019025341A1 · 2019 [cited by applicant]
WO 2020014068A1 · 2020 [cited by applicant]
WO 2020061150A1 · 2020 [cited by applicant]
WO 2020083733A1 · 2020 [cited by applicant]
WO 2020084492A1 · 2020 [cited by applicant]
WO 2020085219A1 · 2020 [cited by applicant]
WO 2020086844A1 · 2020 [cited by applicant]
WO 2019222112A1 · 2020 [cited by applicant]
CAS Registry entry for Registry No. 1351352-38-9. (Year: 2011). [cited by examiner]
Babulreddy et al. Synthesis, Characterization and Antimicrobial Screening of New Class of 1-Substituted-N-(1,2,3,4-Tetrahydronaphthalen-1-yl)-1hbenzo[ D][1,2,3]Triazole-5-Caboxamide Derivatives (Heteroletters, 2(3), 253… [cited by examiner]
CAS Registry No. 1383704-53-7. (Year: 2012). [cited by examiner]
Wojnarowska et al., “On the kinetics of tautomerism in drugs:New application of broadband dielectricspectroscopy”, J. Chem. Phys. (2010), vol. 133, No. 9, 094507. [cited by applicant]
Kier et al., “Bioisosterism: Quantitation of Structure and Property Eff ects”, Chemistry & Biodiversity (2004), vol. 1, Issue 1, pp. 138-151. [cited by applicant]
Babulreddy et al., “Synthesis, Characterization and Antimicrobial Screening of New Class of 1-Substituted-N-(1,2,3,4-Tetrahydronapthalen-1-YL)-1Hbenzo[D][1,2,3]Triazole-5-Caboxamide Derivatives”, Heterocyclic Letters, 2… [cited by applicant]
International Search Report of International Patent Application No. PCT/EP2019/078835 dated May 8, 2020. [cited by applicant]
European Search Report of International Patent Application No. PCT/EP2019/078835 dated Mar. 26, 2019. [cited by applicant]
Uray, G. et al., “Diphenylethanediamine derivatives as chiral selectors”, Journal of Chromatography A, Apr. 1994, pp. 41-53, vol. 666, No. 1-2, 22, Elsevier, Amsterdam, NL. [cited by applicant]
Maddirala, Amarendar Reddy et al., “Synthesis of 3-Substituted 2-Indolinones by a Multicomponent Coupling Isocyanide-Dependent Microwave-Assisted Intramolecular Transamidation Process”, European Journal of Organic Chemi… [cited by applicant]
Azizoglu, Murat et al., “A series of novel [beta]-hydroxyamide based catalysts for borane-mediated enantioselective reductions of prochiral ketone”, Tetrahedron: Asymmetry, Pergamon Press Ltd, Jun. 10, 2016, pp. 614-622… [cited by applicant]
Ashwood, Valerie A. et al., “Synthesis and Antihypertensive Activity of 4-(Substituted-carbonylamino)-2H-1-benzopyrans”, Journal of Medicinal Chemistry, American Chemical Society, Jan. 1, 1990, pp. 2667-2672, vol. 33, N… [cited by applicant]
Folkes, Adrian et al., “Design, Synthesis and In Vitro Evaluation of Potent, Novel, Small Molecule Inhibitors of Plasminogen Activator Inhibitor-1”, Bioorganic & Medicinal Chemistry Letters, May 2002, pp. 1063-1066, vol… [cited by applicant]
Naumchuk et al., “Study of inhibitory activity of imidazolone derivatives and their non-cyclic precursors in relation to human SC2 protein kinase”, Ukrainica Bioorganica Acta 1, 2015, pp. 32-38, vol. 13(1)—(machine tran… [cited by applicant]
C. L. Perrin et al., “Secondary Deuterium Isotope Effects on the Acidity of Carboxylic Acids and Phenols”, J. Am. Chem. Soc., vol. 129, 2007 (Abstract), pp. 4490. [cited by applicant]
C. MacBean, “The Pesticide Manual”, 2012, British Crop Protection Council (First page). [cited by applicant]
T.W. Greenep.G.M. Wuts: “Protective Groups in Organic Synthesis”, 1999, Wiley. [cited by applicant]
Pure Appl Chem, vol. 45, 1976, pp. 11-30. [cited by applicant]
S. M. Berge et al.: “Pharmaceutical Salts”, J. Pharm. Sci., vol. 66, 1977, pp. 1-19. [cited by applicant]
B. Testa et al., Int. J. Pharm., vol. 19, No. 3, 1984, pp. 271. [cited by applicant]
F. Schneider et al., “Enhanced plasma concentration by selective deuteration of rofecoxib in rats”, Arzneim. Forsch. / Drug. Res., vol. 56, 2006, pp. 295. [cited by applicant]
F. Maltais et al., “In vitro and in vivo isotope effects with hepatitis C protease inhibitors: enhanced plasma exposure of deuterated telaprevir versus telaprevir in rats”, J. Med. Chem., vol. 52, 2009, pp. 7993. [cited by applicant]
Mehlhorn et al., “Encyclopedic Reference of Parasitology”, 4th edition (ISBN 978-3-662-43978-4), 2016. [cited by applicant]
C. J. Wenthur et al., “Discovery of (R)-(2-Fluoro-4-((-4-methoxyphenyl)ethynyl)phenyl) (3-Hydroxypiperidin-1-yl) methanone (ML337), An mGlu3 Selective and CNS Penetrant Negative Allosteric Modulator (Nam)”, J. Med. Chem… [cited by applicant]
C. L. Perrin et al., “Stereochemistry of β-deuterium isotope effects on amine basicity”, J. Am. Chem. Soc., vol. 127, 2005, pp. 9641. [cited by applicant]
KJR Rosman et al., “Isotopic Compositions of the Elements 1997”, Pure Appl. Chem., vol. 70, No. 1, 1998, pp. 217-235. [cited by applicant]
A. M. Sharma et al., “Nevirapine bioactivation and covalent binding in the skin”, Chem. Res. Toxicol., vol. 26, 2013, pp. 410. [cited by applicant]
A. E. Mutlib et al., “The species-dependent metabolism of efavirenz produces a nephrotoxic glutathione conjugate in rats”, Toxicol. Appl. Pharmacol., vol. 169, 2000, pp. 102. [cited by applicant]