FIELD: pharmaceuticals.
SUBSTANCE: invention relates to a compound of formula (I) or a pharmaceutically acceptable salt thereof, a pharmaceutical composition and a drug based on it for the treatment of a disease in which Nav 1.7 (SCN9A) is involved, selected from neuropathic pain, nociceptive pain, inflammatory pain, small fiber neuropathy, erythromelalgia, paroxysmal extreme pain disorder, dysuria or multiple sclerosis, as well as a method of treating such diseases using it. In general formula (I), R1a, R1c and R1d are hydrogen, R1b is C6 aryl, C6 aryloxy or 6-membered heteroaryloxy, wherein the aryl and aryl group in aryloxy and the heteroaryl group in heteroaryloxy may be independently substituted with 1–2 substituents independently selected from the group consisting of halogen, C1-4 alkyl optionally substituted with 1–3 substituents independently selected from Substituent Group A, and C1-4 alkoxy optionally substituted with 1–3 substituents independently selected from Substituent Group A; R4 is hydrogen, m=0 or 1, L is CR7 R8, R7 and R8 are hydrogen; or R2 and R3 are methyl or together with the carbon atom to which they are attached form a group of formula (II) with -OR4 ; in formula (II), e and f are 1, R4 is as defined above, V is an oxygen atom, R5a, R5b, R5c and R5d are hydrogen, Substituent Group A is independently halogen, and any 1–6 atoms of hydrogen in the compound of formula (I) may be replaced by deuterium atoms.
EFFECT: obtaining a deuterized benzimidazole compound.
11 cl, 5 ex
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Authors
Dates
2023-09-27—Published
2018-03-14—Filed