http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CZ-2004923-A3

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_61073c1e31fd071ce34b222022390b02
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B11-24
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D411-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D311-82
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B11-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D327-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B11-26
filingDate 2004-09-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f2654243cb7f6038726293bf5d925193
publicationDate 2006-04-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CZ-2004923-A3
titleOfInvention Chemoselective method of monoaminomethylation of sulfophthalein and sulfofluorescein derivatives
abstract Aminomethylated sulfophthalenes and sulfofluoresceins are prepared by treating N-alkoxymethylamine, N-aryloxymethylamine, 1-N-benztriazolylmethylamine, N-imidazolylmethylamine, N-1,2,3-triazolylamine, N-1,2,3-triazolylamine, imidyloxymethylamine. acyloxymethylamine, iminomethylamine, aminomethylamine, and methylene ammonium salts to the starting sulfophthaleins of formula I wherein at least one substituent of the group R @ 2, R @ 2, R @ 3, R @ 6, R @ 6, R @ 6. or R.sup.7.n. hydrogen, to the starting sulfofluoresceins of formula (II) wherein at least one substituent of the group R @ 2, R @ 2, R @ 3, R @ 4, R @ 4, R @ 4, R @ 4, R @ 4, R @ 4, R @ 4, R @ 4. and R.sup.5.n. hydrogen, in the environment of protic or aprotic polar solvents at temperatures ranging from 25 to 300 degC. The aminomethylation by this method is highly chemoselective and regioselective.
priorityDate 2004-09-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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