Claims
- 1. A cationic diketopyrrolopyrrole of the general formula (I) wherein, independently of one another, Q1 and Q2 represent an optionally substituted, aromatic, isocyclic or heterocyclic group with 5 to 14 atoms in the ring, the heterocyclic group containing at least one oxygen, nitrogen or sulfur atom, and the R1 and R2 groups, independently of one another, represent hydrogen or a Y—B+A− group, with the proviso that at least one of the R1 and R2 groups is not hydrogen; B+ is an aromatic, aliphatic, alicyclic, aromatic heterocyclic or non-aromatic heterocyclic, quaternary ammonium group or a quaternary phosphonium group; Y is an optionally substituted linear or branched C1 to C6 alkylene group and A− is an anion.
- 2. The diketopyrrolopyrrole of claim 1, wherein, in formula (I), B+ represents (i) an aromatic, heterocyclic quaternary ammonium compound; (ii) a non-aromatic, heterocyclic quaternary ammonium compound; (iii) a quaternary alkylammonium compound or arylammonium compound, arylalkylammonium compound of formula NR5R6R7, in which R5, R6 and R7 independently of one another are a benzyl group, a phenyl group or a C1 to C6 alkyl group, the aforementioned alkyl groups being unsubstituted or substituted with one or more hydroxy groups or amino groups; or (iv) a quaternary phosphonium compound.
- 3. The diketopyrrolopyrrole of claims 1, wherein, in formula (I), Y represents a —CH2— group, a —CH2—CH2— group, a —CH2—CH2—CH2— group, a —CH2—CH2—CH2—CH2— group or a linear or branched C2 to C6 alkylene group, substituted with one or more alkyl groups, hydroxy groups, amino groups, acyl groups or quaternary ammonium groups.
- 4. The diketopyrrolopyrrole of claim 1, wherein, in formula (I), the anion A− is selected from iodide, chloride, bromide, sulfate, phosphate, hydrogen phosphate, oxalate, carbonate, hydrogen carbonate, formate, acetate, citrate, tartrate, malonate and pyruvate.
- 5. A process for the synthesis of diketopyrrolopyrroles of formula (I) of claim 1, for which a compound of formula (II) is reacted with the appropriate alkyl dihalide in the presence of a base in an aprotic polar solvent and the halide obtained is subsequently reacted with a tertiary amine or a tertiary phosphine wherein Q1 and Q2 are as defined as in claim 1.
- 6. The process for the synthesis of the diketopyrrolopyrroles of formula (I) of claim 1, for which a compound of the general formula (II) is reacted with cationic chain X—Y—B+A−, wherein Q1, Q2, X, —Y, B+ and A− are as defined as in claim 1.
- 7. An dye composition for dyeing keratin fibers, wherein the composition contains at least one diketopyrrolopyrrole compound of formula (I) as defined in claim 1.
- 8. The dye composition of claim 7, wherein the diketopyrrolopyrrole compound of formula (I) is selected from the group consisting of 2,5-bis-(4-trimethylammoniumbutyl)-3,6-diphenyl-pyrrolo[3,4-c]pyrrole-1,4-dione dibromide, 2,5-bis(4-trimethylammonium-butyl)-3,6-diphenyl-pyrrolo[3,4-c]pyrrole-1,4-dione dichloride, 2,5-bis(4-trimethylammonium-butyl)-3,6-bis[4-dimethylamino)phenyl]-pyrrolo[3,4-c]-1,4-dione dibromide, 2,5-bis(4-trimethylammonium-butyl)-3,6-bis[4-(dimethylamino)phenyl]-pyrrolo[3,4-c]pyrrole-1,4-dione dichloride, 2,5-bis[4-[4-(dimethylamino)pyridinium]butyl]-3,6-diphenyl-pyrrolo[3,4-c]pyrrole-1,4-dione dibromide; 2,5-bis[4-[4-(dimethylamino)pyridinium]-butyl]-3,6-diphenyl-pyrrolo-[3,4-c]pyrrole-1,4-dione dichloride; 2,5-bis[4-[N-(methylimidazolium)butyl]]-3,6-diphenyl-pyrrolo[3,4-c]pyrrole-1,4-dione dibromide and 2,5-bis[4-[N-(methylimidazolium)butyl]]-3,6-diphenyl-pyrrolo[3,4-c]pyrrole-1,4-dione dichloride.
- 9. The dye composition of claim 7, wherein the diketopyrrolopyrrole compound of formula (I) is contained in an amount of 0.01 to 10% by weight.
- 10. The dye composition of claim 7, wherein it contains additionally at least one further direct dye from the group, consisting of plant dyes, nitro dyes, azo dyes, anthraquinone dyes and triphenylmethane dyes.
- 11. A method for dyeing hair comprising applying a dye composition as defined in claim 7 to the hair in an amount sufficient for the dyeing of said hair.
Priority Claims (1)
Number |
Date |
Country |
Kind |
100 09 070 |
Feb 2000 |
DE |
|
Parent Case Info
This application is a 371 of PCT/EP01/00784 Jan. 25, 2001.
PCT Information
Filing Document |
Filing Date |
Country |
Kind |
PCT/EP01/00784 |
|
WO |
00 |
Publishing Document |
Publishing Date |
Country |
Kind |
WO01/62759 |
8/30/2001 |
WO |
A |
US Referenced Citations (1)
Number |
Name |
Date |
Kind |
5169953 |
Mizuguchi |
Dec 1992 |
A |
Foreign Referenced Citations (4)
Number |
Date |
Country |
40 11 927 |
Oct 1990 |
DE |
40 37 556 |
May 1991 |
DE |
44 35 211 |
Apr 1995 |
DE |
0 953 343 |
Nov 1999 |
EP |