FIELD: heterocyclic compounds.
SUBSTANCE: invention relates to heterocyclic compounds of formula I
, where represents ; m is 1, 2, 3 or 4; R3 is H, halogen, C1-C6 haloalkyl or C1-C6 alkyl; when m is not equal to 1, R3 is independently the same or different; W is a single bond; is phenyl; n is either 1, 2, 3 or 4; R1 is independently H, halogen, unsubstituted or substituted C1-C6 alkyl; where the specified substituted C1-C6 alkyl substituted by one to three halogens; and when n is not equal to 1, R1 is independently the same or different; Q is -NH-C(=O)-R1-1, -S(=O)2-N(R1-9R1-10), -N(R1-14R1-15), -NH-S(=O)2-R1-16, unsubstituted or substituted C3-C4 cycloalkyl, unsubstituted or substituted C3-C6 heterocycloalkyl, or unsubstituted or substituted 5–6-membered heteroaryl; where the specified C3-C6 heterocycloalkyl contains 1–3 heteroatoms selected from one or more of O and N; the specified 5–6-membered heteroaryl contains 1–3 heteroatoms selected from N; the said substituted C3-C4 cycloalkyl, substituted C3-C6 heterocycloalkyl, or substituted 5–6-membered heteroaryl are substituted with one or more substituents independently selected from halo, -OH, and -CN; R2 is independently ; where R2-1 and R2-2 each independently represents H, unsubstituted C1-C6 alkyl; X and Y are each independently methylene, -O-, -N(R2-3)- or ; R2-3 and R2-4 are each independently H or unsubstituted C1-C6 alkyl-O-, intermediates and methods of their preparation and use.
EFFECT: obtaining new heterocyclic compounds of formula I which have a high P2X3 antagonistic activity and good selectivity.
26 cl, 8 dwg, 9 tbl, 192 ex
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Authors
Dates
2023-07-19—Published
2019-12-27—Filed