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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_fa206d5abb07311badcc825b0af7ebbd
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D295-073
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C209-365
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D295-073
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C209-36
filingDate 1997-12-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_58028cc45ac7552e04403f32a90b2fb0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_499b8c6fa93e9630559efb5932c5344c
publicationDate 1998-09-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DE-19757538-A1
titleOfInvention Process for the preparation of 4-dialkylamino-3-fluoroanilines and 2-dialkylamino-5-fluoroanilines
abstract Preparation of dialkyl-amino-fluoro-aniline derivatives of formula (I) comprises: (i) reacting an amino-chloro-fluoro-nitrobenzene derivative of formula (II) with hydrogen in the presence of a hydrogenation catalyst and optionally a solvent at 20-160 deg C and 1-150 mbar; and (ii) reacting the obtained amino-chloro-fluoro-aniline derivative of formula (III) with hydrogen, in presence of a base and a noble metal catalyst and optionally a solvent, at 50-200 deg C and 1-100 bars, with elimination of hydrogen chloride. one of A,B = NR1R2 and the other = Cl; one of A', B' = NR1R2 and the other = H; R1, R2 = 1-10C alkyl; or NR1R2 = 3-7-membered ring.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2008122555-A1
priorityDate 1997-03-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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