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filingDate 2002-11-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2004-09-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_900fca5c20d4824242ea8432dc711fb3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a02101dd61cec52a2e627f38e7fb6c04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9f39ce09610430bfa7d1c4115eaf6d47
publicationDate 2004-09-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-6790955-B2
titleOfInvention Processes for the preparation of aminophenylsulfonyl-ureas and intermediate products for the processes
abstract The invention relates to the preparation of compounds (I)in which A=H or acyl and R<1>, R<2>, R<3>, R, n, X, Y and Z are as defined in claim 1 by halogenation and rearrangement of compounds (II) (optionally salt) to give compounds (III)a) ammonolysis of (III) to (IV), reduction of the nitro group and reaction with carbamate (salts) (VI) of the formula Ar-OCO-N(M)-Het, where Ar=phenyl, M=H or cation and Het=heterocycle from formula (I), to give compounds (I) (A=H), orb) ammonolysis of (III) to (IV), reaction with carbamate (salt) (VI) and reduction of resulting compounds (VII) at the NO2 group to give compounds (I) (A=H), orc) reaction of (III) with cyanates and amines (VII) of the formula HNR<3>-Het and reduction of the resulting compound (VII) at the NO2 group to give compounds (I) (A=H) and optional acylation if A is to be other than H. Compounds of the formulae (I) (A=H), (III), (IV), (V), (VI) (M=cation) and (VII) are novel.
priorityDate 1995-11-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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