| Predicate |
Object |
| assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_dbdfa36b677f4ef61245ca725011e221 |
| classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-52 |
| classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-84
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J29-072
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D498-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J23-755
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-65 |
| filingDate |
2000-03-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d0f11792a846e23d5881051ed33370a2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6078724eb0f620dce779a2d4ef0f6365 |
| publicationDate |
2001-10-02-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber |
JP-2001270866-A |
| titleOfInvention |
Method for synthesizing heterocyclic compounds |
| abstract |
(57) [Summary] [Problem] Complex 6 useful as an intermediate material for synthesis of pharmaceuticals, etc. Method for synthesizing a 6-membered ring compound, particularly a 6-membered heterocyclic compound having a substituent at the 3-position, by a simpler route than via picoline and in a higher yield than the conventional method using oxazole as a raw material I will provide a. SOLUTION: The reaction is carried out at a reaction temperature of 120 ° C. to 300 ° C. under pressure or normal pressure using unsubstituted oxazole as a raw material. |
| priorityDate |
2000-03-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type |
http://data.epo.org/linked-data/def/patent/Publication |