http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2008001663-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_13378daf1ea3e93deba77c21f881e972 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C209-68 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C211-52 |
| filingDate | 2006-06-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c16e51cf50c1a258110b403ff0656152 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_405e6d4f745dba8f4eccfc5ac1d55bed http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_85f6be725925d671ee0bd1da18b79bcc http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cfb801f563cc52b7954c3a1156734a30 |
| publicationDate | 2008-01-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-2008001663-A |
| titleOfInvention | Method for producing 2-chloroaniline compound |
| abstract | PROBLEM TO BE SOLVED: To provide a method capable of producing a 2-chloroaniline compound useful as an intermediate for synthesis of a pharmaceutical product safely, easily and in a high yield. SOLUTION: General formula (1): (In the formula, R represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms.) The 3-chloro-4-aminobenzenesulfonic acid compound represented by the above formula is heated in the presence of water without adding an acid. General formula (2) characterized by: (In formula, R shows the same group as R in General formula (1).) The manufacturing method of the 2-chloro aniline compound represented. [Selection figure] None |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-110015963-A |
| priorityDate | 2006-06-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 34.