http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20010060172-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c999fee6428152a996011d506925c2d7
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C231-02
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C231-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D211-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C237-22
filingDate 2000-10-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f89ff6f195827782adb51495a278a046
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9a9b34e53faaa7bce5f6aa2a55d2ef72
publicationDate 2001-07-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20010060172-A
titleOfInvention Process for production of N-acyl amino acid amide
abstract The present invention dehydrates condensation of N-acyl amino acids with amines and / or ammonia, preferably primary amines, secondary amines and / or ammonia in high yields for a short time in the presence of boron compounds as catalysts and coexistence of alcohols as co-solvents Provided is a method for preparing an N-acyl amino acid amide, including reacting.n n n Hilotropic dehydration media such as hydrocarbon compounds may be used in the reaction.
priorityDate 1999-10-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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