http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CH-626324-A5
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_a717ea5b2ac78ac329ab3a9659d834d2 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C233-00 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C237-44 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C231-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C231-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C233-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C231-12 |
| filingDate | 1975-09-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6c692f0aebdcb8f637c4dce57c31fcb7 |
| publicationDate | 1981-11-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CH-626324-A5 |
| titleOfInvention | Process for the preparation of 2-methoxy- and 2-ethoxy-6-aminobenzamide |
| abstract | 2-Methoxy- or 2-ethoxy-6-aminobenzamide is obtained from 2,6-dinitrobenzoyl halide. The latter is treated in solution with gaseous NH3, and 2,6-dinitrobenzamide is formed. Reaction with methanol or ethanol in the presence of alkali metal (which is in the form of alkanolate) results in 2-methoxy- or 2-ethoxy-6-nitrobenzamide which is finally reduced to the title compound. It is used mainly for the preparation of lower alkyl 2'-carbamoyl-3'-methoxy(ethoxy)oxanilates which are antiallergics. |
| priorityDate | 1974-10-02-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 112.