http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2003342264-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_129e393582e6bdf4029baf2206522f45
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D241-04
filingDate 2003-03-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3b036025edb87044b7d1a7acd599adbe
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_01f2c97262c20e10ea31d8b78b63c352
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_50f2757db14a9773bfe74100c9b63ede
publicationDate 2003-12-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2003342264-A
titleOfInvention Method for producing 1-substituted-2-alkylpiperazines
abstract (57) Abstract: A 1-substituted-2-alkylpiperazine having high chemical purity can be produced at low cost. SOLUTION: General formula (1) (Where R 1 is an alkyl group having 1 to 6 carbon atoms, R 2 is i) a hydrogen atom, ii) a methyl group, iii) an alkoxyl group having 1 to 4 carbon atoms, iv) an aromatic ring is unsubstituted or substituted Benzyloxy group. Further, it means that the carbon atom marked with * is an asymmetric center. From 1-substituted-3-alkylpiperazines represented by By obtaining -substituted-2-alkylpiperazines and then deprotecting the 4-position, 1-substituted-2-alkylpiperazines of high chemical purity are produced at low cost.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2004115510-A
priorityDate 2002-03-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 21.