CH674849A5 - - Google Patents

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Info

Publication number: CH674849A5
Authority: CH; Switzerland
Prior art keywords: hydrogen; formula; 4alkyl; compounds; substituted
Prior art date: 1987-01-14

Application number

CH94/88A

Other languages

German (de)

English (en)

Inventor

Paul Dr Doswald

Werner Dr Koch

Original Assignee

Sandoz 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.)

1987-01-14

Filing date

1988-01-12

Publication date

1990-07-31

1988-01-12 Application filed by Sandoz Ag filed Critical Sandoz Ag

1990-07-31 Publication of CH674849A5 publication Critical patent/CH674849A5/de

Links

150000001875 compounds Chemical class 0.000 claims abstract description 38
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 28
239000001257 hydrogen Substances 0.000 claims abstract description 28
238000004043 dyeing Methods 0.000 claims abstract description 20
150000002431 hydrogen Chemical group 0.000 claims abstract description 19
150000003839 salts Chemical class 0.000 claims abstract description 17
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims abstract description 12
239000000203 mixture Substances 0.000 claims abstract description 8
239000000758 substrate Substances 0.000 claims abstract description 8
229910052736 halogen Inorganic materials 0.000 claims abstract description 7
150000002367 halogens Chemical group 0.000 claims abstract description 7
125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 7
125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims abstract description 6
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract description 6
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims abstract description 5
229910004727 OSO3H Inorganic materials 0.000 claims abstract description 4
229910006069 SO3H Inorganic materials 0.000 claims abstract description 4
125000000751 azo group Chemical group [*]N=N[*] 0.000 claims abstract description 4
125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 4
238000000034 method Methods 0.000 claims description 16
239000002253 acid Substances 0.000 claims description 11
229910052801 chlorine Inorganic materials 0.000 claims description 10
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 10
239000000460 chlorine Substances 0.000 claims description 9
125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims description 9
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 6
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 6
239000004753 textile Substances 0.000 claims description 5
125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims description 4
125000001309 chloro group Chemical group Cl* 0.000 claims description 4
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
GOYNRDSJTYLXBU-UHFFFAOYSA-N 5-chloro-2,4,6-trifluoropyrimidine Chemical compound FC1=NC(F)=C(Cl)C(F)=N1 GOYNRDSJTYLXBU-UHFFFAOYSA-N 0.000 claims description 3
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
238000002360 preparation method Methods 0.000 claims description 3
LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims 1
239000000975 dye Substances 0.000 abstract description 20
229920000742 Cotton Polymers 0.000 abstract description 17
-1 sulpho group Chemical group 0.000 abstract description 5
125000001624 naphthyl group Chemical group 0.000 abstract 1
239000000243 solution Substances 0.000 description 13
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 8
150000001768 cations Chemical class 0.000 description 8
JFGQHAHJWJBOPD-UHFFFAOYSA-N 3-hydroxy-n-phenylnaphthalene-2-carboxamide Chemical compound OC1=CC2=CC=CC=C2C=C1C(=O)NC1=CC=CC=C1 JFGQHAHJWJBOPD-UHFFFAOYSA-N 0.000 description 6
125000004432 carbon atom Chemical group C* 0.000 description 6
230000001590 oxidative effect Effects 0.000 description 6
239000000463 material Substances 0.000 description 5
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
239000000985 reactive dye Substances 0.000 description 4
125000000217 alkyl group Chemical group 0.000 description 3
238000006243 chemical reaction Methods 0.000 description 3
239000005457 ice water Substances 0.000 description 3
IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 3
229910000029 sodium carbonate Inorganic materials 0.000 description 3
239000007858 starting material Substances 0.000 description 3
JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical group C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 2
UYBWIEGTWASWSR-UHFFFAOYSA-N 1,3-diaminopropan-2-ol Chemical compound NCC(O)CN UYBWIEGTWASWSR-UHFFFAOYSA-N 0.000 description 2
RUFPHBVGCFYCNW-UHFFFAOYSA-N 1-naphthylamine Chemical compound C1=CC=C2C(N)=CC=CC2=C1 RUFPHBVGCFYCNW-UHFFFAOYSA-N 0.000 description 2
GFPQSWFFPRQEHH-UHFFFAOYSA-N 7-aminonaphthalene-1,3,6-trisulfonic acid Chemical compound C1=C(S(O)(=O)=O)C=C2C=C(S(O)(=O)=O)C(N)=CC2=C1S(O)(=O)=O GFPQSWFFPRQEHH-UHFFFAOYSA-N 0.000 description 2
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical class [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical class C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
229910001413 alkali metal ion Inorganic materials 0.000 description 2
125000002947 alkylene group Chemical group 0.000 description 2
239000007844 bleaching agent Substances 0.000 description 2
238000006482 condensation reaction Methods 0.000 description 2
MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 description 2
150000004985 diamines Chemical class 0.000 description 2
125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 2
WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Chemical compound Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 description 2
238000002955 isolation Methods 0.000 description 2
229910052757 nitrogen Inorganic materials 0.000 description 2
239000011541 reaction mixture Substances 0.000 description 2
238000005185 salting out Methods 0.000 description 2
229910052708 sodium Inorganic materials 0.000 description 2
239000011734 sodium Chemical class 0.000 description 2
239000011780 sodium chloride Substances 0.000 description 2
LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
239000000725 suspension Substances 0.000 description 2
ZNXSFVXZQBETRJ-UHFFFAOYSA-N (3-aminophenyl)urea Chemical compound NC(=O)NC1=CC=CC(N)=C1 ZNXSFVXZQBETRJ-UHFFFAOYSA-N 0.000 description 1
125000006273 (C1-C3) alkyl group Chemical group 0.000 description 1
IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
229920003043 Cellulose fiber Polymers 0.000 description 1
WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical class [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
239000004952 Polyamide Substances 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical class [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
229920000297 Rayon Polymers 0.000 description 1
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
125000003545 alkoxy group Chemical group 0.000 description 1
239000003945 anionic surfactant Substances 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
229910052794 bromium Inorganic materials 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
238000005119 centrifugation Methods 0.000 description 1
239000003086 colorant Substances 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
239000003599 detergent Substances 0.000 description 1
239000012954 diazonium Substances 0.000 description 1
150000001989 diazonium salts Chemical class 0.000 description 1
238000001035 drying Methods 0.000 description 1
238000000605 extraction Methods 0.000 description 1
239000004744 fabric Substances 0.000 description 1
239000002657 fibrous material Substances 0.000 description 1
125000000623 heterocyclic group Chemical group 0.000 description 1
QWPPOHNGKGFGJK-UHFFFAOYSA-N hypochlorous acid Chemical compound ClO QWPPOHNGKGFGJK-UHFFFAOYSA-N 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
239000010985 leather Substances 0.000 description 1
229910052744 lithium Inorganic materials 0.000 description 1
NYGZLYXAPMMJTE-UHFFFAOYSA-M metanil yellow Chemical group [Na+].[O-]S(=O)(=O)C1=CC=CC(N=NC=2C=CC(NC=3C=CC=CC=3)=CC=2)=C1 NYGZLYXAPMMJTE-UHFFFAOYSA-M 0.000 description 1
239000010446 mirabilite Substances 0.000 description 1
125000004433 nitrogen atom Chemical group N* 0.000 description 1
239000001048 orange dye Substances 0.000 description 1
150000002978 peroxides Chemical class 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000011591 potassium Chemical class 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 1
239000004627 regenerated cellulose Substances 0.000 description 1
239000013535 sea water Substances 0.000 description 1
239000000661 sodium alginate Substances 0.000 description 1
235000010413 sodium alginate Nutrition 0.000 description 1
229940005550 sodium alginate Drugs 0.000 description 1
235000010288 sodium nitrite Nutrition 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
RSIJVJUOQBWMIM-UHFFFAOYSA-L sodium sulfate decahydrate Chemical compound O.O.O.O.O.O.O.O.O.O.[Na+].[Na+].[O-]S([O-])(=O)=O RSIJVJUOQBWMIM-UHFFFAOYSA-L 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
125000000547 substituted alkyl group Chemical group 0.000 description 1
QEMXHQIAXOOASZ-UHFFFAOYSA-N tetramethylammonium Chemical compound C[N+](C)(C)C QEMXHQIAXOOASZ-UHFFFAOYSA-N 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
GSEJCLTVZPLZKY-UHFFFAOYSA-O triethanolammonium Chemical compound OCC[NH+](CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-O 0.000 description 1
ZMANZCXQSJIPKH-UHFFFAOYSA-O triethylammonium ion Chemical compound CC[NH+](CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-O 0.000 description 1
GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 1
238000005406 washing Methods 0.000 description 1

Classifications

- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/38—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using reactive dyes
- D06P1/382—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using reactive dyes reactive group directly attached to heterocyclic group
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B62/00—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves
- C09B62/02—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group directly attached to a heterocyclic ring
- C09B62/022—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group directly attached to a heterocyclic ring the heterocyclic ring being alternatively specified
- C09B62/026—Azo dyes
- C09B62/028—Monoazo dyes

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Engineering & Computer Science (AREA)
Textile Engineering (AREA)
Coloring (AREA)

CH94/88A 1987-01-14 1988-01-12 CH674849A5 (it)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE3700846		1987-01-14

Publications (1)

Publication Number	Publication Date
CH674849A5 true CH674849A5 (it)	1990-07-31

Family

ID=6318796

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH94/88A CH674849A5 (it)	1987-01-14	1988-01-12

Country Status (6)

Country	Link
JP (1)	JPS63182373A (it)
CH (1)	CH674849A5 (it)
FR (1)	FR2609468B1 (it)
GB (1)	GB2200131B (it)
IT (1)	IT1219792B (it)
OA (1)	OA08706A (it)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5227477A (en) *	1988-06-14	1993-07-13	Sandoz Ltd.	Dyes having one or two 2,4- or 4,6-dichloro-5-cyanopyrimidyl groups linked through bridging radicals containing at least two nitrogen atoms to chloro-1,3,5-triazinyl groups
US5274083A (en) *	1989-05-03	1993-12-28	Bayer Aktiengesellschaft	Polyfunctional fibre-reactive dyestuffs
DE59108710D1 (de) *	1990-09-25	1997-06-26	Ciba Geigy Ag	Reaktivfarbstoffe, Verfahren zu deren Herstellung und deren Verwendung
DE59206979D1 (de) *	1991-05-15	1996-10-02	Bayer Ag	Reaktivfarbstoffe
BR9303266A (pt) *	1992-08-14	1994-03-08	Sandoz Ag	Compostos e seus sais ou misturas de fais compostos ou sais,processos para sua preparacao,e processo para tingimento ou estampagem de um substrato organico
BR9303283A (pt) *	1992-08-14	1994-03-08	Sandoz Ag	Compostos e seus sais,ou uma mistura de tais compostos ou sais;processo para sua preparacao,e processo para tingimento ou estampagem de um substrato organico
JP3657627B2 (ja) *	1992-10-12	2005-06-08	クラリアントファイナンス（ビーブイアイ）リミティド	繊維反応性アゾ染料化合物およびその製造法

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2607028A1 (de) *	1976-02-20	1977-08-25	Bayer Ag	Reaktivfarbstoffe
DE2706417A1 (de) *	1976-02-27	1977-09-01	Sandoz Ag	Monoazoverbindungen enthaltend einen pyrimidinrest
EP0097119A3 (de) *	1982-06-11	1984-09-05	Ciba-Geigy Ag	Reaktivfarbstoffe, deren Herstellung und Verwendung

1988
- 1988-01-06 FR FR888800076A patent/FR2609468B1/fr not_active Expired
- 1988-01-12 GB GB8800618A patent/GB2200131B/en not_active Expired - Lifetime
- 1988-01-12 CH CH94/88A patent/CH674849A5/de not_active IP Right Cessation
- 1988-01-12 OA OA59261A patent/OA08706A/xx unknown
- 1988-01-13 JP JP63003915A patent/JPS63182373A/ja active Pending
- 1988-01-13 IT IT47523/88A patent/IT1219792B/it active

Also Published As

Publication number	Publication date
IT8847523A0 (it)	1988-01-13
FR2609468A1 (fr)	1988-07-15
OA08706A (fr)	1989-03-31
GB2200131A (en)	1988-07-27
JPS63182373A (ja)	1988-07-27
GB2200131B (en)	1991-01-09
IT1219792B (it)	1990-05-24
FR2609468B1 (fr)	1989-07-13
GB8800618D0 (en)	1988-02-10

Legal Events

Date	Code	Title	Description
1995-09-29	PL	Patent ceased
2024-10-31	PL	Patent ceased

Publication	Publication Date	Title
DE3930738B4 (de)	2004-07-29	Phthalocyanin-Reaktivfarbstoffe, ihre Herstellung und ihre Verwendung
DE3918653C2 (de)	2003-01-16	Chromophore Verbindung mit heterocyclischem Reaktivrest
AT395981B (de)	1993-04-26	Faserreaktive phthalocyanin-azoverbindungen
CH674849A5 (it)	1990-07-31
CH688935A5 (de)	1998-06-15	Aluminium-Phthalocyanin-Reaktivfarbstoffe.
DE4304242A1 (de)	1994-08-18	Phthalocyanin-Reaktivfarbstoffe
AT389306B (de)	1989-11-27	Faserreaktive monoazos-triazin-derivat
CH666298A5 (de)	1988-07-15	Faserreaktive monoazoverbindungen.
DE2944624C2 (it)	1987-07-02
CH685705A5 (de)	1995-09-15	Faserreaktive Disazofarbstoffe.
DE19515251B4 (de)	2006-05-04	Faserreaktive Disazofarbstoffe
DE4327006B4 (de)	2006-04-20	Faserreaktive Monoazofarbstoffe
DE4334185B4 (de)	2006-04-20	Faserreaktive Azofarbstoffe
CH679400A5 (it)	1992-02-14
DE3835724A1 (de)	1990-04-26	Faserreaktive metallisierte monoazoverbindungen
DE4327005B4 (de)	2006-02-09	Faserreaktive Disazofarbstoffe
DE3800093A1 (de)	1988-07-28	Faserreaktive monoazoverbindungen
DE4331386B4 (de)	2006-02-16	Faserreaktive Monoazofarbstoffe
CH671769A5 (it)	1989-09-29
CH685762A5 (de)	1995-09-29	Faserreaktive Monoazofarbstoffe.
DE3923483A1 (de)	1991-01-24	Faserreaktive disazofarbstoffe
CH685704A5 (de)	1995-09-15	Faserreaktive Monoazofarbstoffe.
DE4241924A1 (it)	1993-06-24
CH680796A5 (it)	1992-11-13
DE3835659A1 (de)	1990-04-26	Faserreaktive disazoverbindungen