http://rdf.ncbi.nlm.nih.gov/pubchem/patent/PL-181213-B1

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_35a08bb718da0b231f9f5d570466c0ab
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C311-59
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C311-15
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C235-60
filingDate 1996-03-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7ae41602ec8e61cde41ec4fa97bfb21f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3eb3ca7234db162de25f8abaefcd019a
publicationDate 2001-06-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber PL-181213-B1
titleOfInvention Preparation method 1- {4- [2- (2-methoxy-5-chlorobenzamido) -ethyl] -benzenesulfonyl) -3-cyclohexylurea
abstract Production method 1- {4- [2- (2-methoxy-5-chlorobenzamido) -ethyl] -benz.eno-n-sulfonyl} -3-cyclohexylurea by condensation of 4- [2- (2-meloxy-5-chlorohenzamido) -ethyl] -benzenesulfonamide,nobtained by the reaction 4- (2-aminoethyl) -n-benzenesulfonamide and 2-methoxy-5-chlorobenzoic acid chloride, with isocyanatencyclohexyl, characterized in that 4- [2- (2-methoxy-5-chlorobenzamido) -ethyl] -n-benzenesulfonamide, prepared by the reaction of 4- (2-aminoethyl) -benzenesulfonamidenwith 2-methoxy-5-chlorobenzoic acid chloride, in water, at a temperature ton60 ° C, with alkali metal bicarbonate or carbonate, is subjected to condensationnwith cyclohexyl isocyanate in a boiling mixture of acetone and water, in the presence ofnalkali metal hydroxide.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-107879955-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-107879955-B
priorityDate 1996-03-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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