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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-04
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filingDate 1998-04-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2000-10-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2000513013-A
titleOfInvention Pyrrolopyrrolones derivatives
abstract (57) Abstract: The present invention relates to a therapeutically effective bicyclic compound, a method for producing the compound, a pharmaceutical composition containing the compound, particularly a viral infection, and more specifically, a virus encoding a serine protease enzyme. In particular the use of this compound in the treatment and prevention of infections caused by viruses of the herpes family. Thus, according to one aspect of the present invention, the present inventors have found that R represents a substituted or unsubstituted C 1-3 alkyl; wherein R 1 is an optionally substituted C 1-3 alkyl. A heteroaryl having 1 to 4 heteroatoms or a fused heteroaryl, R 5 CO, R 5 NHCO, R 5 CS or R 5 NHCS, wherein R 5 is substituted or unsubstituted; H, C 1-6 alkyl, C 1-6 alkenyl, cycloalkyl or fused cycloalkyl, heteroaryl or fused heteroaryl containing 1-4 heteroatoms, aryl or fused aryl, or aryl C 1 -3 alkyl) represents; R 2 is R 6 -X- or R 3 CO (where, R 3 is may not be substituted may be substituted, and, optionally, one or more hetero original May contain a (A), (B), (C), (D), (E), (F), it represents the (G) or an (H)); R 4 is R 6 -X R 6 represents an optionally substituted heterocyclic or fused heterocyclic ring having 1 to 4 heteroatoms, a heteroaryl or fused heteroaryl having 1 to 4 heteroatoms, C 3 -10 cycloalkyl or fused cycloalkyl, aryl, or fused aryl; and, X is C = O, NHC = O, C (= O) C = O, CH = CHCO, CH 2 CO, CH 2 or SO 2 And a salt and a solvate thereof.
priorityDate 1997-04-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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