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    • 22. 发明专利
    • DE19541985A1
    • 1997-05-15
    • DE19541985
    • 1995-11-10
    • DYSTAR TEXTILFARBEN GMBH & CO
    • SCHUMACHER CHRISTIAN DRHERD KARL-JOSEF DR
    • C07D498/04C09B19/02C09B62/002C09B62/04C09B62/20C09B62/503D06P1/38D06P1/39D06P3/10D06P3/06D06P3/66D06P3/62
    • A method of preparing acylated 3,10-diamino-tri-pheno-dioxazine of formula (I) comprises: (i) reducing a diamino-tri-pheno-dioxazine of formula (V) to a leuco compound of formula (III); (ii) reacting (IV) with a reactive derivative based on the Z1 and/or Z2 group; and (iii) re-oxidising the resultant leuco compound of formula (IV) to (I). R1, R2 = H or 1-4 C alkyl, which may be mono- or di-substituted by hydroxy, 1-4 C alkoxy, sulpho or sulphato; X1, X2 = halogen, H, 1-6 C alkyl, phenyl, phenoxy or 1-4 C alkoxy; E = sulpho, carboxy, 1-4 C alkylsulphonyl, SO2Y, -SO2NR3R4 or -CONR3R4; Y = vinyl or CH2CH2V; V = OH or a labile (thio)sulphato, phosphato or halogen group; R3, R4 = H, phenyl or 1-4 C alkyl, which may be substituted by OH, carboxy, sulpho or sulphato or SO2Y; or NR3R4 is a 5- or 6-membered heterocycle, optionally with 1-3 more heteroatoms of N, O and S in the ring; V1, V2 = H, sulpho, methoxy, methyl or halogen; and Z1, Z2 = acyl, unsubstituted, alkylated or arylated aminocarbonyl, sulphonyl or N-heteroaryl. T = H, Z1 or Z2. Also claimed are: (i) acylated 3,10-diamino-tri-pheno-dioxazine-disulphonic acids and salts (IA-IF) of formula (I) with specified substituents; and (ii) intermediate leuco compounds (III) and (IV) formed in the preparation of (I).
    • 24. 发明专利
    • AT248207T
    • 2003-09-15
    • AT99121806
    • 1999-11-04
    • DYSTAR TEXTILFARBEN GMBH & CO
    • SCHUMACHER CHRISTIAN DREDEN BIRGIT
    • C09B62/085C09B62/09C09B62/245C09B62/325C09B62/51C09B62/513C09B67/22D06P3/10D06P3/66
    • Dyestuff mixtures of at least one dye of formula (Ia) or (Ib) and at least one dye of formula (IIa), (IIb) or (IIc) are used for yellow dyeing of OH- and carbonamide group-containing materials, especially fibers. Dyestuff mixtures comprise one or more dyes of formula (Ia) and/or (Ib) and one or more dyes of formula (IIa) and/or (IIb) and/or (IIc) in a molar ratio (Ia) and/or (Ib) to (IIa) and/or (IIb) and/or (IIc) of 70:30 to 30:70. M = H or alkali metal; D = a residue of the benzene or naphthalene series; Y = vinyl or ethyl which is substituted in the beta -position by a substituent which is eliminated under alkaline conditions; R = amino or 1-4 C alkyl or 1-4 C alkyl substituted by carboxy, sulfo, phosphato, OH or -SO2Y ; Y = as for Y : R = H, 1-4 C alkyl, 1-4 C alkoxy or sulfo; m = 1, 2 or 3; Z = a fiber-reactive residue selected from halopyrimidine, dichloroquinoxaline or optionally ether- or amino group-substituted halotriazine series, where the halotriazine residue may also be bonded to a group of formula -SO2-Y which is bonded to the amino group bound to the triazine residue via a bridging member; Y = as for Y ; Zo = a bivalent group of formula (III); Hal = Cl or F; W = phenylene, alkylene, phenylene-alkylene-phenylene or phenylene-phenylene or a residue of general formula phenylene-G-phenylene, in which the phenylene residues are optionally substituted by 1 or 2 substituents selected from OMe, OEt, Me, Et, sulfo or carboxy, the alkyl residues have 1-6 C and may be substituted by sulfo or carboxy and/or may be interrupted by 1 or 2 heteroatoms, and the alkylene residues have 2-4 C; G = -O-, -NH-, -CO- or -NH-CO-NH; R = Me or carboxy; R = H, halogen, 1-4 C alkyl or 1-4 C alkoxy; p, q = 0 ,1 or 2; and (p+q) = 1, 2 or 3. If p = 0 or q = 0 then M = H. In (IIa) the group -NH-Z may be bound to benzene ring A or benzene ring B. In (IIb) one amino group of the bridging member -NH-Zo-NH- is bound to benzene ring A of one monoazo residue and the other amino group to benzene ring B of the other monoazo residue, or the two amino groups may both be bound to A or to B. R , R , R = H, sulfo, 1-4 C alkyl or 1-4 C alkoxy; R = Me or carboxy; n = 1 or 2; and B = H when n = 1, or when n = 2, Bo = a direct covalent bond, alkylene, alkenylene or alkylene-phenylene-alkylene, in which the phenylene residues are optionally substituted with 1 or 2 substituents selected from OMe, OEt, Me, Et, sulfo and carboxy, the alkylene groups have 1-6 C and may be substituted by sulfo or carboxy and/or interrupted by 1 or 2 hetero groups and the alkenylene residues have 2-4 C, or is a residue as described above for Zo.
    • 27. 发明专利
    • DE19542547A1
    • 1997-05-22
    • DE19542547
    • 1995-11-15
    • DYSTAR TEXTILFARBEN GMBH & CO
    • RUSS WERNER DRSCHUMACHER CHRISTIAN DRREDDIG WOLFRAM DR
    • C09B62/51C09B62/026C09B62/08C09B62/24C09B62/40C09B62/44C09B62/507C09B62/002C09B43/136C09B43/16D06P1/38D06P3/10D06P3/66
    • Fibre reactive azo dyes of formula (I) are claimed, where D is a residue of diazo component of the benzene- or naphthalene series; K is a coupling component of formula (II); M is H or alkali metal, a = 0 or 1, b = 0 or 1 and the bond marked with * is connected to the azo group; R is H or optionally substituted 1-6C alkyl; R is H or optionally substituted 1-6C alkyl; Y is bonded to the amino residue -NR - or -NR - and is a residue of formula (III); R is H, optionally substituted 1-4C alkyl or optionally substituted phenyl; A is amino, cyanamino, 1-4C alkoxy, phenoxy, the residue of a heterocyclic compound in which the ring contains a N atom and optionally another hetero atom, alkylamino in which the alkyl has 1-4C and may be substituted by substituents selected from sulpho, carboxy, Me, Et and OEt, dialkylamino with 1-4 alkyl residues which may be substituted by substituents selected from sulpho, carboxy, Me, Et and OEt, or a phenylamino group which is optionally substituted in the phenyl residue; c = 0 or 1; G is an optionally substituted phenylene; B is a 1-6C alkylene or ethylene-oxy-ethylene; X is beta -hydroxyethyl, vinyl or ethyl that is substituted in the beta -position by a substituent that can be eliminated by alkali; and Z is bound to the amino residue -NR - or -NR - and is a heterocyclic fibre- reactive residue which is different to Y.