http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1074028-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_634538388f2dd27ea0a8bc2a2032c517
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09B1-207
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09B1-325
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B1-32
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B1-20
filingDate 1965-11-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1967-06-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-1074028-A
titleOfInvention Dyestuffs of the amino-anthraquinone series
abstract The invention comprises anthraquinone compounds of the formula <FORM:1074028/C4-C5/1> and their quaternary derivatives of the formula <FORM:1074028/C4-C5/2> wherein R1 is an aryl radical of the benzene or naphthalene series containing at least one halogen substituent in a position ortho to the amino group; R2 is a 1,4-phenylene radical or a C2-C4 alkylene radical; R3 and R4 are alkyl radicals or, together with the N atom to which they are attached, form a heterocyclic ring; R5 is alkyl, hydroxyalkyl, cycloalkyl or aralkyl; and A\sK is an inorganic or organic anion. They may be obtained by condensing a diamine of formula <FORM:1074028/C4-C5/3> with a 1-(o-haloarylamino) anthraquinone derivative of the formula <FORM:1074028/C4-C5/4> wherein X is a replaceable substituent, e.g. halogen, NO2 or lower alkoxy, in the presence of a condensing agent and a weak acid-binding agent in an inert organic diluent, and if desired, converting the anthraquinone base formed to the quaternary ammonium dyestuff by treating with a quaternizing agent in the presence of a solvent. Several anthraquinones of the first formula above are specified. An example is given for the preparation of 1-(21 - bromo - 41 - methylanilino) - 4 -(31-dimethylaminopropylamino) anthraquinone and the quaternary ammonium compound obtained by treatment with dimethyl sulphate. The dyes are useful for dyeing acrylic fibres greenish-blue shades and in conjunction with CI Basic Yellow 11 to give a green shade. The corresponding unhalogenated dyestuff trimethyl - (3 - [41 - p - toluidino - 11 -anthraquinonyl]aminopropyl) ammonium methyl sulphate is obtained by a similar method from 1 - p - toluidino - 4 - bromoanthraquinone and dyes acrylic fibres reddish-blue shades.ALSO:Polyacrylonitrile textiles are dyed with anthraquinone dyes of the formula: <FORM:1074028/D1-D2/1> where R1 is an aryl radical of the benzene or naphthalene series containing at least one halogen substituent in an o-position to the amino group; R2 is a 1,4-phenylene radical or a C2-C4 alkylene radical; R3 and R4 are alkyl radicals or together with the N atom form a heterocyclic ring; R5 is alkyl, hydroxyalkyl, cycloalkyl or aralkyl; and A is an inorganic or organic anion. The dyes are preferably applied from mildly acidic aqueous dyebaths which may contain a surface active agent. In an Example the dye is previously mixed with dextrin and pulverised. Other dyes may be present such as CI basic yellow 11.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2019223015-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4123222-A
priorityDate 1964-12-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 35.