http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-434568-A1

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_5c24684033fba97d1ad845ce453a57e3
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D307-52
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C301-00
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-52
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-38
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C303-40
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-14
filingDate 1975-02-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1976-12-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-434568-A1
titleOfInvention PROCEDURE FOR THE PREPARATION OF SULFAMOILANTRA-NILIC ACIDS.
abstract Process for the preparation of sulfamoylantranilic acids of the general formula i ** (see formula) ** Wherein ph means a phenyl radical optionally substituted with 1-2 halogen atoms, alkyl groups or etherified hydroxy groups and r means aralcohyl, heteroaralkyl or cycloalkohilalcoyl radicals which in the aliphatic portion may be unsaturated, interrupted by oxygen or sulfur and/or in the aromatic portion they can be substituted with halogen atoms, alkyl or alkoxy radicals, characterized in that carboxylic acids of the general formula iv are reacted ** (see formula) ** At temperatures above 120ยบ c, with at least one molar equivalent of an amine of the general formula r-nh2, wherein r has the above meanings. (Machine-translation by Google Translate, not legally binding)
priorityDate 1974-02-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

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Total number of triples: 25.