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filingDate 2016-03-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2021-11-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1438617cfe659e3f24443ba62c107a04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_208dba8dc393b27db5ccfae095b8acc7
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publicationDate 2021-11-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2878041-T3
titleOfInvention Piperazine Carbamates and Methods to Prepare and Use Them
abstract A compound of formula (I): **(See formula)** wherein: R1 is halogen, -OR3, -CN, aryl (optionally substituted with one, two or three residues each independently selected from R4), aryloxy (optionally substituted with one, two or three residues each selected independently from R4), heteroaryl (optionally substituted with one, two or three residues each selected independently from R4), heteroaryloxy (optionally substituted with one, two or three residues selected each one independently of R4), heterocycle (optionally substituted with one, two or three residues each independently selected from R4), cycloalkyl (optionally substituted with one, two or three residues each independently selected from R4), optionally substituted C1-6 alkyl , optionally substituted C2-6 alkenyl, optionally substituted C2-6 alkynyl, -NR9R10, -NR8C(O)R9, -NR8SO2R9, -NR8C(O)OR9, -NR8C(O)NR9R10, - C(O)R9, - C(O)OR9, -C(O)NR9R10, -S(O)wR11, or -SH; R2 is -NR5R6; each R3 is independently selected from H, C1-6 alkyl, haloalkyl, and aminoalkyl; each R4 is independently selected from halogen, -OR3, -CN, nitro, optionally substituted C1-6 alkyl, optionally substituted C1-6 alkenyl, optionally substituted C1-6 alkynyl, cycloalkyl, -NR9R10, -NR8C(O)R9, - NR8SO2R9, -NR8C(O)OR9, -NR8C(O)NR9R10, -C(O)R9, -C(O)OR9, -C(O)NR9R10, -S(O)wR11, and -SH; R5 and R6, together with the nitrogen to which they are attached, form an 8-membered bridged heterocyclic ring selected from **(See formula)** in which the 8-membered bridged heterocyclic ring is optionally substituted with one or more substituents independently selected from halogen, -CN, oxo, optionally substituted C1-6 alkyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted heterocycle, optionally substituted cycloalkyl, -S(O)wR11, -OR3, -OR7, -C( O)R9, -C(O)OR9, -C(O)NR9R10, -NR9R10, -NR8C(O)R9, -NR8SO2R9, -NR8C(O)OR9, and -NR8C(O)NR9R10; R7 is alkynyl or (alkynyl)alkyl; each R8 is independently selected from H, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, and optionally substituted heterocycloalkyl; each R9 and R10 is independently selected from H, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, and optionally substituted heterocycloalkyl; or R9 and R10, together with the nitrogen to which they are attached, form an optionally substituted heterocycle optionally containing an additional O, N or S; each R11 is independently selected from optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, and optionally substituted heterocycloalkyl; and w is 0, 1 or 2; or one of its solvates, hydrates, tautomers, N-oxides, stereoisomers, or pharmaceutically acceptable salts.
priorityDate 2015-03-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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