| Predicate |
Object |
| assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c3f0a3a6e35bacf4186f6234590ab5c4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_905e8de029e16a0e19189751d9a5a6a1 |
| classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55 |
| classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H17-08 |
| classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H1-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H17-08 |
| filingDate |
1999-11-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate |
2003-03-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cd41ae76777314eae9f9887d8d367343
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_26ab5d28066f32210b6c0a8b1f9ef174
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9484ffbf7bba63f016b12c46a2291c76
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6bc757e2d4b55a2343758f76a1d16c2e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_82f1d541b0ede0e6f18b86d58a3350dd
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d7ca2352f1b99f655c6bf3becbb0109f |
| publicationDate |
2003-03-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber |
EP-1133511-B1 |
| titleOfInvention |
Novel intermediates, process for preparing macrolide antibiotic agent therefrom |
| abstract |
An erythromycin A 9-O-benzodithiol oxime intermediate represented by the following formula (III) useful for synthesis of clarthromycin and crystalline solvate thereof:Wherein, Y1 and Y2 are independently a hydrogen atoms or trimethylsilyl groups. And, a process for the preparation of clarithromycin using the erythromycin A 9-O-benzodithiol oxime intermediate as described in the specification. |
| priorityDate |
1998-11-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type |
http://data.epo.org/linked-data/def/patent/Publication |