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ES416264A1 - Procedure for dying or stamping organic materials with azoic developing colorants. (Machine-translation by Google Translate, not legally binding) - Google Patents

Procedure for dying or stamping organic materials with azoic developing colorants. (Machine-translation by Google Translate, not legally binding)

Info

Publication number
ES416264A1
ES416264A1 ES416264A ES416264A ES416264A1 ES 416264 A1 ES416264 A1 ES 416264A1 ES 416264 A ES416264 A ES 416264A ES 416264 A ES416264 A ES 416264A ES 416264 A1 ES416264 A1 ES 416264A1
Authority
ES
Spain
Prior art keywords
group
formula
radical
see formula
optionally substituted
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
ES416264A
Other languages
Spanish (es)
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Novartis AG
Original Assignee
Ciba Geigy AG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from DE2231245A external-priority patent/DE2231245C3/en
Application filed by Ciba Geigy AG filed Critical Ciba Geigy AG
Publication of ES416264A1 publication Critical patent/ES416264A1/en
Expired legal-status Critical Current

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  • Pyridine Compounds (AREA)

Abstract

Procedure for dyeing or printing organic materials with developmental azo dyes, in which diazo salts and coupling components are brought onto the organic material to be dyed or stamped successively or simultaneously and are coupled together, characterized in that as components For coupling the diazo components, in the dye-forming reaction in the same organic material to be stained, at least one of the following formulas is selected: **(See formula)** in which R1 means hydrogen, an optionally substituted alkyl group, a fibroreactive acylaminoalkyl group, an optionally substituted aryl radical, a heterocyclic radical, an alkylene radical, which links the radical of the formula (1) with another heterocyclic radical of the same class, an optionally N-monosubstituted or N-disubstituted amino group, R2 means hydrogen, an optionally substituted alkyl group, cycloalkyl, cyano, nitro, nitroso, H2N, an acylamino group that eventually shows monoreactive groups, an alkylcarbonyl, arylcarbonyl or sulfonyl group, an aminosulfonyl group, an alkoxycarbonyl radical or aryloxycarbonyl, an aminocarbonyl group, a halogen atom, a sulfoalkyl group, an acylaminomethyl group, in which the acyl radical corresponds to the formula -CO-RX, where R is an alkyl ene group and X a halogen atom, a quaternized amino group or a sulfo group, or a group of the formulas **(See formula)** in which the two groups -C0- or -SO2- are linked in a neighboring position to a 6-membered aromatic ring, the sulfo or carboxyl group, a quaternized amino group or a group of the formula **(See formula)** in which the hydrogen atom is part of a 5- or 6-membered ring, which may still contain other heteroatoms, such as nitrogen or oxygen atoms, R3 signifies hydrogen, an optionally substituted alkyl group, an optionally substituted aryl radical, a heterocyclic radical, the cyano group, an alkoxycarbonyl or aryloxycarbonyl radical, an aminocarbonyl group, an alkoxycarbonylmethyl or aryloxycarbonylmethyl radical, a cyanomethyl group, a group of acylomethyl, an aminocarbonyl group, the carboxyl group or the hydroxymethyl group, or those of formula (2) **(See formula)** in which R2 and R3 have the meanings indicated in the explanation of formula (1) and X means a group - (CH2), where n is 2 or 3 or a radical of the formula **(See formula)** and of the formula (3) **(See formula)** in which R1 has the significance indicated in the explanation of formula (I), and R2 and R3 together with the carbon atoms of the pyridone ring, to which they are attached, form a 5- or 6-membered ring, for example composed of the formulas **(See formula)** in which R1 has the significance indicated in the explanation of formula (I), and H indicates on the ring the fully hydrogenated state of the respective ring, as well as those of formula (4) **(See formula)** in which X means the hydroxyl or amino group e Y means a hydrogen or halogen atom. (Machine-translation by Google Translate, not legally binding)
ES416264A 1972-06-26 1973-06-25 Procedure for dying or stamping organic materials with azoic developing colorants. (Machine-translation by Google Translate, not legally binding) Expired ES416264A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE2231245A DE2231245C3 (en) 1972-06-26 1972-06-26 Process for dyeing and printing cellulose, linen, wool, silk, polyamides or leather with development mono- or disazo dyes
CH781773A CH564121A (en) 1972-06-26 1973-05-29

Publications (1)

Publication Number Publication Date
ES416264A1 true ES416264A1 (en) 1976-06-01

Family

ID=25702272

Family Applications (1)

Application Number Title Priority Date Filing Date
ES416264A Expired ES416264A1 (en) 1972-06-26 1973-06-25 Procedure for dying or stamping organic materials with azoic developing colorants. (Machine-translation by Google Translate, not legally binding)

Country Status (2)

Country Link
ES (1) ES416264A1 (en)
IT (1) IT985786B (en)

Also Published As

Publication number Publication date
IT985786B (en) 1974-12-20

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