http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2003012613-A
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_25cabd848a625c278d0f654e54a2f0c0 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C209-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C211-23 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00 |
filingDate | 2001-07-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0ca23d84718aab236b13ba33b3e1f5b4 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_86fd852c64f7599a438db9be820e55f8 |
publicationDate | 2003-01-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | JP-2003012613-A |
titleOfInvention | Method for producing propargylamine derivative |
abstract | (57) [Summary] (Corrected) [PROBLEMS] To provide a method for producing a propargylamine derivative which is an intermediate of a phenylalkanoic acid amide derivative having excellent bactericidal activity. SOLUTION: General formula 1 (R 1, R 2 are independently hydrogen, or represents a C 1 -C 6 alkyl group, R 1 and R 2 combine to form a cyclopentyl group with bonded carbon, or a cyclohexyl group together, R 3 Represents a C 1 -C 6 alkyl group. A) reacting the ester derivative with ammonia in the presence of a monovalent copper catalyst and a phase transfer catalyst or in the presence of a monovalent copper catalyst and a reducing agent; (Wherein R 1 and R 2 are the same as described above). |
isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6958419-B2 |
priorityDate | 2001-07-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 101.