FIELD: chemistry.
SUBSTANCE: present invention relates to compounds of formula
, where Q denotes C1-6alkyl substituted with a heterocycle, selected from oxazolidine, morpholinyl or hexahydrooxazepine; where each of the said heterocycles can be optionally substituted with one or two C1-6alkyls; each Alk independently denotes C1-6alkanediyl; R1 denotes pyridyl, pyrazinyl, pyridazinyl, pyrimidiniyl or pyrrolyl, where each of the said heterocycles may be optionally substituted with 1, 2 or 3 substitutes, independently selected from hydroxy, C1-6alkyl hydroxy C1-6alkyl; R2 denotes hydrogen; R3 denotes hydroxy C1-6alkyl; R4 denotes hydrogen or C1-6alkyl; R5 denotes hydrogen or C1-6alkyl; and Het denotes pyridyl, pyrazinyl, pyridazinyl, pyrimidinyl or pyrrolyl. The present invention also relates to a method of producing compounds of formula (I).
EFFECT: obtained compositions, as well as compositions based on said compounds, can inhibit respiratory syncytial virus (RSV) replication.
11 cl, 12 ex, 2 tbl
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Authors
Dates
2011-05-27—Published
2006-06-20—Filed