FIELD: chemistry.
SUBSTANCE: invention relates to compounds of formula I , where A is -(C=O); L201 is absent; M is absent or is selected from O or NR1; where R1 is selected, during each appearance thereof, from hydrogen; L101 is selected from -C1-C8 alkylene, -C2-C8 alkenylene or C1-C8 alkylene-O; or -C1-C8 alkylene, -C2-C8 alkenylene or C1-C8 alkylene-O, each of which is independently substituted with 1, 2 or 3 substitutes selected from C1-C8 alkyl or halogen, or two hydrogen atoms per carbon atom of -C1-C8 alkylene, -C2-C8 alkenylene or C1-C8 alkylene-O can be substituted with substitutes, where two substitutes, taken together, form a C3-C12 cycloalkyl ring; Z101 is phenyl; phenyl substituted with 1, 2 or 3 halogens; or thienyl; W101 is absent; X and Y, taken together with carbon atoms with which they are bonded, form a phenyl ring; R is -C1-C8 alkyl; R' is -C1-C8 alkyl, -C2-C8 alkenyl or CHQ1Q2; Q1 and Q2 each is independently F, Cl or Br; G is selected from -OH or -NHS(O)2-R2; R2 is - C3-C12 cycloalkyl; m is 1; m' is 1; and s is 1. The invention also relates to a pharmaceutical composition which inhibits serine protease activity, particularly activity of hepatitis C virus (HCV) NS3-NS4A protease, based on said compounds.
EFFECT: obtaining novel compounds and a pharmaceutical composition based on said compounds, which can be used in medicine for treating hepatitis C.
19 cl, 4 dwg, 3 tbl, 1588 ex
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Authors
Dates
2013-09-20—Published
2008-11-14—Filed