http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-10927116-B2
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_966a6c1f382ec9bcb5e3839dfd73e5b8 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-4985 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P31-22 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D487-04 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-04 |
filingDate | 2018-08-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate | 2021-02-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b3e8d9d751290ce1f000096b74febc48 |
publicationDate | 2021-02-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | US-10927116-B2 |
titleOfInvention | Process for the preparation of 4-phenyl-5-alkoxycarbonyl-2-thiazol-2-yl-1,4-dihydropyrimidin-6-yl]methyl]-3-oxo-5,6,8,8a-tetrahydro-1H-imidazo[1,5-a]pyrazin-2-yl]-carboxylic acid |
abstract | The present invention relates to a process for synthesizing a compound of formula (I), n n n n n n n n n n R 1 is phenyl, which is unsubstituted or substituted with one, two or three substituents independently selected from halogen and C 1-6 alkyl; R 2 is C 1-6 alkyl; R 3 is —C x H 2x —; x is 1, 2, 3, 4, 5, 6 or 7; or pharmaceutically acceptable salt or diastereomer thereof, which is useful for prophylaxis and treatment of a viral disease in a patient relating to hepatitis B infection or a disease caused by hepatitis B infection. |
priorityDate | 2016-02-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 388.