http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-100271907-B1

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filingDate 1993-02-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2000-11-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f90d99ed0c27fbb574adc8b5c74b3ac1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_57f0d7d2321366be107b03ec0135696b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2302fc9fcdc384fe475291c394e97e63
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7c708b05e694da30b6ebc8a92b6126ef
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_16a010aa60abc053820bdf1f4c844f38
publicationDate 2000-11-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-100271907-B1
titleOfInvention Method for producing sulfamide
abstract The method for producing sulfamide according to the present invention comprises the step of reacting an oxycarbonylsulfamide compound and an alcohol in the presence of an azodicarboxylic acid derivative and a trivalent phosphorus compound.n n n In one embodiment of the present invention, the sulfamide is represented by the following general formula (I), the alcohol is represented by the following general formula (II), and the oxycarbonyl sulfamide compound is represented by the following structural formula (III) Method for producing a sulfamide, characterized in that.n n n R 3 NHSO 2 NR 1 R 2 (I)n n n [Wherein R 1 and R 2 are each independently selected from hydrogen, alkyl, cycloalkyl, alkenyl, alkynyl, aralkyl, aryl, heterocyclic group and alkyl group substituted with these heterocyclic groups; ; R 3 is a group selected from alkyl, alkenyl, alkynyl, aralkyl, heterocyclic group, alkyl substituted with heterocyclic group and pyrrolidinyl methyl (the heterocyclic groups described above are pyranosyl, furanosyl, pipepe Lidinyl, pyrrolidinyl, azetidinone ring, cefem ring, penem ring and carbapenem ring);n n n R 3 OH (II)n n n Provided that R 3 is as defined above;n n n R 4 OOC-NHSO 2 NR 1 R 2 (III)n n n Wherein R 1 and R 2 are as defined above and R 4 is a carboxy protecting group.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-100305217-B1
priorityDate 1992-02-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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