EP1280773A1

EP1280773A1 - 5-aryl-1.3.3.-trimethyl-2-methylene-indoline derivatives and salts thereof, methods for the production and use of said compounds for the temporary coloration of fibres

Info

Publication number: EP1280773A1
Application number: EP02727315A
Authority: EP
Inventors: Guido Sauter; Hans-Jürgen BRAUN; Nadia Reichlin
Original assignee: Wella GmbH
Current assignee: Procter and Gamble Deutschland GmbH
Priority date: 2001-04-19
Filing date: 2002-01-24
Publication date: 2003-02-05
Also published as: US7056348B2; DE10119204A1; US20030213071A1; WO2002085854A1; JP3856313B2; BR0205040A; JP2004519521A

Abstract

The invention relates to a method for the production of 5-Aryl-1.3.3.-trimethyl-2-methylene-indoline-derivatives of formula (I) or salts thereof of formula (Ia). Said method is characterised in that 1 mole of a 5-Aryl-2.3.3-trimethyl-3H-indole-derivative of formula (VII) is reacted with 1 50 moles of a compound of formula R1-A at a temperature of between 20 - 180 DEG C, in an apolar aprotic or polar protic or polar aprotic solution, for between 1 and 44 hours. According to said method, the novel compounds of formula (I)/(Ia) and (V) can be obtained. The invention also relates to an agent for colouring keratin fibres containing at least one compound of formula (I)/(Ia) and at least one carbonyl/amine compound and a method for the temporary coloration of keratin fibres, whereby the keratin fibres are coloured with said agent and at a later time are de-coloured by a preparation containing sulphite.

Description

5-aryl-1,3,3-trimethyl-2-methylene-indoline derivatives and their salts, process for their preparation and use of these compounds for the temporary dyeing of fibers

The present invention relates to the use of 5-aryl-1,3,3-trimethyl-2-methylene-indoline derivatives and their physiologically tolerable salts with organic or inorganic acids as a dye precursor in colorants for fibers, in particular human hair , whereby - if desired - the coloring obtained can also be gently decolorized at any later point in time. Another subject is 5-aryl-1, 3,3-trimethyl-2-methylene-indoline derivatives and a process for their preparation.

From Chemical Abstract No. 1976: 462913 of the Russian publication Khimiya Geterotsiklicheskikh Soedinenii 1976, page 497-499 is a process for the preparation of 5-phenyl-1, 3,3-trimethyl-2-methylene-indoline and 4-methoxyphenyl 1, 3,3-trimethyl-2-methylene-indoline known, which is based on the corresponding arylhydrazine derivative. Since the corresponding arylhydrazine must first be prepared for each aryl modification in this process, this process is quite complex and unsuitable for the parallel synthesis of structurally related 5-aryl-1,3,3-trimethyl-2-methylene-indoline derivatives.

The object was therefore to provide a production process for 5-aryl-1,3,3-trimethyl-2-methylene-indoline derivatives, which it enables a large number of structurally related 5-aryl-1, 3,3-trimethyl-2-methylene-indoline derivatives to be produced in good yields in a simple manner with a few reaction steps, starting from a key building block.

Surprisingly, it has now been found that 5-aryl-1,3,3-trimethyl-2-methylene is obtained by N-alkylation of 5-aryl-2,3,3-trimethyl-3H-indole derivatives of the formula (VII) -indoline derivatives of the formula (I) or their salts of the formula (Ia) can be prepared in a simple manner, the compounds of the formula (VII) having a Suzuki reaction of an indole derivative of the formula (II) or of the formula (V) Arylboronic acid derivatives of the formula (III) or by a Suzuki reaction of an indole derivative of the formula (II) with a diborone compound of the formula (IV) and an aryl halide of the formula (VI) can be obtained in good yields.

The present invention therefore relates to a process for the preparation of 5-aryl-1,3,3-trimethyl-2-methylene-indoline derivatives of the formula (I) or their salts of the formula (Ia),

(I) (la) which is characterized in that 1 mol of a 5-aryl-2,3,3-trimethyl-3H-indole derivative of the formula (VII) at a temperature of 20 to 180 ° C in an apolar aprotic or polar protic or polar aprotic solvent with 1 to 50 moles of a compound of the formula

R1-A is reacted for 1 to 44 hours;

(VII) where:

R1 is equal to a straight-chain or branched C1-C8 alkyl group, a C1 to C8 monohydroxyalkyl group, a C2-C8 polyhydroxyalkyl group, a C1-C8 alkoxy (C1-C8) alkyl group, a thio (C1- C8) alkyl group, one - (CH ₂ ) _m -X- (CH ₂ ) _n -Y- (CH ₂ ) _p R ^a group, one - (CH ₂ ) _n -XR ^a group, one - (CH ₂ ) _m -Y- (CH ₂ ) _n -X- (CH ₂ ) _p -R ^a group, one - (CH ₂ ) _m -CO- (CH ₂ ) _p -XR ^a group, one - (CH ₂ ) _P -R ^a group, a - (CH ₂ ) _m -X- (CH ₂ ) _p -CO-YR ^a group or one of the following 3 groups

wherein X and Y are independently an oxygen atom, a sulfur atom or an NR ^b group, R ^a and R ^{b are} independently a hydrogen atom, an optionally substituted aromatic carbocycle or heterocycle or a straight-chain or branched C1-C8-alkyl group; m and n are independently an integer from 1 to 6 and p is an integer from 0 to 6;

R2 is a straight chain C1-C6 alkyl group;

R2 'is a CH-R' group with R 'being hydrogen or one C1-C5 alkyl group;

R3 and R4 are, independently of one another, identical to a straight-chain or branched C1-C4-alkyl group (in particular a methyl group), a - (CH ₂ ) _n -R ^c group, a - (CH ₂ ) _m -CHR ^c -X- (CH ₂ ) _n -R ^c group, a - (CH ₂ ) _n -CO-R ^c group, a - (CH ₂ ) _n -CO-XR ^c group, a - (CH ₂ ) _n -CN group , a - (CH ₂ ) _n -CH = C (CH ₃ ) ₂ group, a - (CH ₂ ) _m -X-CHR ^c - (CH ₂ ) _n -R ^c group or a - (CH ₂ ) _n CH = CH group, where X is an oxygen atom, a sulfur atom or an NR ^b group, m and n are independently an integer from 1 to 6 and R ^c is a hydrogen atom, an optionally substituted aromatic carbocycle or Heterocycle or a straight-chain or branched C1-C6-alkyl group; with the proviso that the radicals R3 and R4, also connected via a (CH ₂ ) _n group (with n equal to an integer from 1 to 3), can form a spiro compound together with the 3H carbon; R5, R6 and R7 are independently a hydrogen atom, a straight-chain or branched C1-C4-alkyl group, a C1-C4-hydroxyalkyl group, a hydroxy group, a methoxy group, a benzyl group, a halogen atom (F, Cl, Br, J), a nitro group, a nitroso group, a cyano group, a trifluoromethyl group, a -CHO group, a -COR ^d group, a -COOH group, a -CO ₂ R ^d group, a -OCOR ^d group, a -OCH ₂ aryl group, an -SO ₂ NH ₂ group, an -NH ₂ group, an -NH ₃ ⁺ group, an -NHR ^d group, an -NH ₂ R ^{d +} group, an -N ( R ^d ) ₂ group, an -N (R ^d ) ₃ ⁺ group, an -NHCOR ^d group, an -NHCOOR ^d group, a -CH ₂ NH ₂ group, a -CH ₂ NHR ^d group , a -CH ₂ N (R ^d ) ₂ group, a -CO ₂ CF ₃ group, a -PO (OR ^d ) ₂ group, an -SO ₂ CHF ₂ group, an -SO ₂ CF ₃ - Group, an -SO ₂ R ^d group or an -SR ^d group, where R ^d is a hydrogen atom, an optionally substituted aromatic carbocycle or heterocycle or a C1-C6-alkyl group, with the proviso that the adjacent radicals R6 and R7 together with the carbon atoms of the aromatic nucleus also form a 5- or 6-membered alicyclic or aromatic Can form a ring, which may optionally contain one or more sulfur atoms, nitrogen atoms and / or oxygen atoms; and

Aryl is equal to a substituted pyrimidyl group, a cyclic radical of the formula (IX) or a heterocyclic radical of the formula (X) or (XI) or (XII).

(IX) (X) (XI) (XM)

wherein R8, R9, R10, R11, R12, R13, R14, R15, R16, R17, R18 and R19 independently of one another are equal to a hydrogen atom, a straight-chain or branched C1-C4-alkyl group, a C1-C4-hydroxyalkyl group, one Hydroxy group, a methoxy group, a benzyl group, a halogen atom (F, Cl, Br, J), a nitro group, a nitroso group, a cyano group, a trifluoromethyl group, a -CHO group, a -COR ^e group, a -COOH group , a -CO ₂ R ^e group, an -OCOR ^e group, an -OCH ₂ aryl group, an -SO ₂ NH ₂ group, an -NH ₂ group, a - (NH ₃ ) ⁺ group , a -NHR ^e group, a - (NH ₂ R ^e ) ⁺ group, a -N (R ^e ) ₂ group, a - (N (R ^β ) ₃ ) ⁺ group, one -NHCOR ^e group, an -NHCOOR ^Θ group, a -CH ₂ NH ₂ group, a -CH ₂ NHR ^e group, a -CH ₂ N (R ^e ) ₂ group, a -CO ₂ CF ₃ Group, an -PO (OR ^e ) ₂ group, an -SO ₂ CHF ₂ group, an -SO ₂ CF ₃ group, an -SO ₂ R ⁸ group or an -SR ^e group, with R ^e equal to a hydrogen atom, an optionally substituted aromatic carbocycle or heterocycle or a C1-C6 alkyl group, with the proviso that two adjacent radicals R8 to R19 together with the carbon atoms of the aromatic nucleus also form a 5- or δ-membered alicyclic or aromatic ring can form, which may optionally contain one or more sulfur atoms, nitrogen atoms and / or oxygen atoms; and

Z is sulfur, nitrogen, oxygen or an N ⁽⁺⁾ -R ^f group; Q is sulfur, nitrogen, oxygen or an NR ^f group; R ^f is hydrogen, a C ₁ -C ₆ -alkyl group, a C2-C4-hydroxyalkyl group, a phenyl group, an acetyl group or sulfonyl group; A ^" is equal to the anion of an organic or inorganic acid, preferably chloride, bromide, iodide, hydrogen sulfate, sulfate, toluenesulfonate, benzenesulfonate, monomethyl sulfate, hexafluorophosphate, perchlorate, hexafluoroantimonate, tetrafluoroborate, tetraphenylborate, formate, acetate or chloridionate Tetrafluoroboration, the Acetation and the hydrogen sulfate ion are particularly preferred.

The N-alkylation of the compounds of the formula (VII) is preferably carried out at a temperature of 40 to 120 ° C., a reaction temperature of 40 to 85 ° C. being particularly preferred. The reaction time is preferably 4 to 24 hours and in particular 4 to 8 hours.

The reaction is preferably carried out in an apolar aprotic or polar protic solvent, such as benzene, toluene, alcohols such as methanol or ethanol, halogenated hydrocarbons such as trichloromethane or dichloromethane, acetonitrile and 3-methoxypropionitrile, with benzene, toluene, methanol, ethanol, dichloromethane and Trichloromethane are particularly preferred.

The compound of formula (VII) and the compound of formula R1-A are preferably used in a molar ratio of 1: 1.1 to 1:10 and in particular in a molar ratio of 1: 1.1 to 1: 2. The aforementioned reaction can optionally be carried out with the aid of ultrasound or in an autoclave or a bomb tube under excess pressure (0.1 to 50 bar, preferably 1 to 20 bar, in particular 1 to 5 bar).

The 5-aryl-2,3,3-trimethyl-3H-indole derivatives of the formula (VII) can be obtained by a Suzuki reaction in a simple manner either by reacting a 5-halogeno-2,3,3-trimethyl-3H-indole Derivatives of the formula (II) with an arylboronic acid derivative of the formula (III) or by reacting a 5-halogeno-2,3,3-trimethyl-3H-indole derivative of the formula (II) with a diborone compound of the formula (IV) and an arylhalogen compound of formula (VI) can be prepared.

The Suzuki reaction takes place at 20 to 180 ° C., preferably 40 to 120 ° C. and in particular 60 to 100 ° C., in an apolar aprotic solvent or a polar aprotic solvent, for example nitriles, Ether compounds or aromatic hydrocarbons, preferably benzene, toluene, tetrahydrofuran, dioxane, 1, 2-dimethoxyethane, acetonitirl and 3-methoxypropionitrile, and in particular toluene, tetrahydrofuran and 1, 2-dimethoxyethane, with or without the addition of water, with the addition of a suitable catalyst (for example a Pd catalyst in an amount of 0.001 to 0.5 mol, in particular 0.05 to 0.12 mol with 1 mol of educt) and / or a suitable organic or inorganic base, such as sodium hydroxide, potassium hydroxide , Potassium carbonate and potassium acetate, with potassium carbonate and potassium acetate being particularly preferred. The reaction medium is oxygen-free, the reaction preferably being carried out under an inert gas, for example under argon or nitrogen. The reaction time is about 1 to 24 hours, a reaction time of 1 to 8 hours and in particular 2 to 6 hours being preferred.

The synthesis process for the compounds of the formulas (I) / (Ia), including the preparation of the starting compounds of the formula (VII), is summarized in Scheme 1 below. In scheme 1 below, the residual groups R1 to R7, aryl and A have the meaning given above, while R20 and R21 independently of one another are equal to a hydrogen atom or a straight-chain or branched C1-C4-alkyl group; R22 is a straight-chain or branched C1-C4-alkyl group, where x is 0 or 1 and Hai is an iodine atom, bromine atom or chlorine atom or a CF ₃ -SO ₂ -O group, the bromine atom and the chlorine atom being preferred, and R23 and R'23 are independently the same Are hydrogen or a C, -C ₆ alkyl group, or R23 and R'23 together with the group -OBO- form a ring of formula (VIII).

Scheme 1:

The starting compounds of the formulas (II), (III), (IV) and (VI) are known from the literature, the compounds of the formulas (IM), (IV) and (VI) are also commercially available. The compounds of the formula (II) can be obtained, for example, using standard synthetic methods known from the literature, as described, for example, in the dissertation by Andreas Leiminer, University of Regensburg (1995); DE-OS 1 949 716 or US Pat. No. 3,865,837 can be produced. In addition, further substituents, such as a nitrofunction, can be introduced via electrophilic substitution reactions on the aromatic nucleus known from the literature. In this context, in particular, that of DJ. Gale, JFK Wilshire in J. Soc. Dyers Color; 1974, pages 97-100 synthetic methods described. Subsequent treatment by means of reducing agents or oxidizing agents or with the aid of suitable protective group addition reactions or protective group elimination reactions can optionally be re-functionalized, as a result of which further compounds of the general formulas (II) can be obtained.

The Suzuki reaction can take place in analogy to processes known from the literature; for example that of S.L. Buchwald et al. in the "Journal of the American Chemical Society" 1999, 121, pages 9550-9561. In this context, reference should also be made to "The Strem Chemiker: Recent Progress in the Suzuki Reactions of Aryl Chlorides" by S.L. Buchwald and J.M. Fox; Vol. XVIII, No.1; May, 2000, pages 1-33, as well as the literature citations mentioned there.

The compounds of the formulas (I) and (Ia) are outstandingly suitable as dye precursors in the non-oxidative system for dyeing keratin fibers. The present invention therefore furthermore relates to an agent for dyeing keratin fibers, for example wool, silk or hair, in particular human hair, which is characterized in that it (a) comprises at least one compound of the formulas (I) and / or (la) and (b) contains at least one carbonyl compound and / or imine compound.

Although the compounds of the formula (I) and (Ia) are particularly suitable for use in dyeing keratin fibers, it is in principle also possible to dye other natural or synthetic fibers, for example cotton or nylon 66, with these compounds.

Suitable compounds of the formulas (I) and (Ia) can in particular be the following compounds and their salts: 5- (2,4-dimethoxyphenyl) -1, 3,3-trimethyl-2-methylene-indoline, 5- ( 1,3-benzodioxol-5-yl) -1,3,3-trimethyl-2-methylene-indoline, 5- (2- (trifluoromethyl) phenyl) -1,3,3-trimethyl-2-methylene- indoline, 5- (phenyl) -1, 3,3-trimethyl-2-methylene-indoline, 5- (p-tolyl) -1, 3,3-trimethyl-2-methylene-indoline, 5- (naphthalene-1 -yl) -1, 3,3-trimethyl-2-methylene-indoline, 5- (4-methylsulfanylphenyl) -1, 3,3-trimethyl-2-methylene-indoline, 5- (4-hydroxyphenyl) - 1,3,3-trimethyl-2-methylene-indoline, 5- (naphthalen-2-yl) -1,3,3-trimethyl-2-methylene-indoline, 5- (2-hydroxy-naphthalen-6-yl ) -1,3,3-trimethyl-2-methylene-indoline, 5- (anthracen-9-yl) -1,3,3-trimethyl-2-methylene-indoline, 5- (3,5-dimethylphenyl ) -1,3,3-trimethyl-2-methylene-indoline, 5- (acenaphthen-5-yl) -1,3,3-trimethyl-2-methylene-indoline, 5- (4-methoxy-2-methyl -phenyl) -1,3,3-trimethyl-2-methylene-indoline, 5- (biphenyl-4-yl) -1,3,3-tr imethyl-2-methylene-indoline, 5- (benzo [b] thiophene-3-yl) -1-ethyl-, 3,3-dimethyl-2-methylene-indoline, 1-ethyl-3- (1-ethyl- 3,3-dimethyl-2-methylene-2,3-dihydro-1 H-indol-5-yl) pyridinium tetrafluoroborate, 5- (furan-3-yl) -1- ethyl-3,3-dimethyl-2-methylene-indoline, 5- (thiophene-3-yl) -1, 3,3-trimethyl-2-methylene-indoline, 5- (thiophene-2-yl) -1- ethyl-3,3-dimethyl-2-methylene indoline and 1- ^(1, ^_3,> ^{^{3-trimethyl-2,}} _{-methylene-2)} ^3,2, ^3, ^{-tetrahydro-1,} - / - [5,5 '] biindolyl-1-yl) ethanone; where the 5- (2,4-dimethoxyphenyl) -1, 2,3,3-tetramethyl-3H-indol-1 -ium-tetrafluoroborate, 5- (1,3-benzodioxol-5-yl) -1, 2, 3,3-tetramethyl-3H-indole-1-tetrafluoroborate, 1, 2,3,3-tetramethyl-5- (-2-trifluoromethyl) phenyl) -3H-indole-1-iumium tetrafluoroborate, 1, 2 , 3,3-tetramethyl-5- (thiophene-3-yl) -3H-indolium iodide, 5-phenyl-1, 2,2,3-tetramethyl-1 (3H) -indolium tetrafluoroborate, 1, 2, 3,3-tetramethyl-5-p-tolyl-3H-indolium tetrafluoroborate, 1, 2,3,3-tetramethyl-5-naphthalene-1 -yl-3H-indolium tetrafluoroborate, 1-ethyl-2,3, 3-trimethyl-5- (4-methylsulfanyl-phenyl) -3H-indolium tetrafluoroborate, 1-ethyl-5- (4-hydroxy-phenyl) -2,3,3-trimethyl-3H-indolium tetrafluoroborate, 1- Ethyl-2,3,3-trimethyl-5-naphthalene-2-yl-3H-indolium tetrafluoroborate, 1-ethyl-5- (6-hydroxy-naphthalene-2-yl) -2,3,3-trimethyl- 3H-indolium tetrafluoroborate, 5-anthracen-9-yl-1-ethyl-2,3,3-trimethyl-3H-indolium tetrafluoroborate, 5- (3,5-dimethyl-phenyl) -1-ethyl-2, 3,3-trimethyl-3H-indolium tetrafluoroborate, 5-benzo [b] thiophene-3 -yl-1-ethyl-2,3,3-trimethyl-3H-indolium tetrafluoroborate, 5-acenaphthen-5-yl-1-ethyl-2,3,3-trimethyl-3H-indolium tetrafluoroborate, 1-ethyl -5- (4-methoxy-2-methylphenyl) -2,3,3-trimethyl-3H-indolium tetrafluoroborate, 5-biphenyl-4-yl-1-ethyl-2,3,3-trimethyl-3H indolium tetrafluoroborate, 5-benzo [b] thiophene-3-yl-1-ethyl-2,3,3-trimethyl-3H-indolium tetrafluoroborate, 1-ethyl-5- (1-ethyl-3-pyridiniumyl) -2,3,3-trimethyl-3H-indolium ditetrafluoroborate, 1-ethyl-5- furan-3-yl-2,3,3-trimethyl-3H-indolium tetrafluoroborate, 1-ethyl-2,3,3- trimethyl-5- (2-thienyl) -3H-indolium tetrafluoroborate and ^{1'-acetyl-1-ethyl-2,3,3-trimethyl-2,} ^{3-dihydro-3H,} 1Η- ^[5.5] biindolyl-1-ium tetrafluoroborate are particularly preferred. Suitable carbonyl compounds and imine compounds which can be mentioned in particular are: 4-hydroxy-3-methoxybenzaldehyde (vanillin), 3-hydroxy-4-methoxybenzaldehyde (isovanillin), 3,4-dihydroxybenzaldehyde, 4-hydroxybenzaldehyde, 3, 5-dimethoxy-4-hydroxybenzaldehyde, 4-dimethylaminobenzaldehyde, 4-methyl-5-imidazole-carboxaldehyde, 4-dimethylamino-cinnamaldehyde, 4-hydroxy-2-methoxy-benzaldehyde, 3,5-dimethyl-4-hydroxybenzaldehyde, 4-dimethylamino-2-methoxybenzaldehyde, 2-hydroxybenzaldehyde, 4-hydroxy-1-naphthaldehyde, 4-methoxy-1-naphthaldehyde, 4-dimethylamino-1-naphthaldehyde, 4'-hydroxy-biphenyl-1-carbaldehyde, 2-hydroxy -3-methoxybenzaldehyde, 2,4-dihydroxybenzaldehyde, 3,4-dihydroxybenzaldehyde, 2,5-dihydroxybenzaldehyde, 2,3,4-trihydroxybenzaldehyde, 3,4,5-trihydroxybenzaldehyde, 2,4,6-trihydroxybenzaldehyde , 2,4-dimethoxybenzaldehyde, 2,3-dimethoxybenzaldehyde, 2,5-dimethoxybenzaldehyde, 3,5-dimethoxybenzaldehyde, 3,4-dimethoxybenzaldehyde, indole-3-carbaldehyde, benzene-1,4-dicarbaldehyde . 4-ethoxybenzaldehyde, 2-methyl-1,4-naphthoquinone, 4-carboxybenzaldehyde, 4-hydroxy-3-methoxycinnamaldehyde, 3,5-dimethoxy-4-hydroxycinnamaldehyde, 3-methoxy-4- (1-pyrrolidinyl ) -benzaldehyde, 4-diethylamino-3-methoxybenzaldehyde, 1, 2-phthalaldehyde, pyrrole-2-aldehyde, thiophene-2-aldehyde, thiophene-3-aldehyde, chromone-3-carboxaldehyde, 6-methyl-4-oxo 1 (4H) -benzopyran-3-carbaldehyde, N-methylpyrrole-2-aldehyde, 5-methyl-furfural, 6-hydroxychromene-3-carboxaldehyde, 6-methylindole-3-carboxaldehyde, 4-dibutylamino-benzaldehyde, N -Ethylcarbazol-3-aldehyde, 4-diethylamino-2-hydroxybenzaldehyde, 3,4-dimethoxy-5-hydroxybenzaldehyde, 5- (4- (diethylamino) phenyl) -2,4-pentadienal, 2,3-thiophene- dicarboxaldehyde, 2,5-thiophene dicarboxaldehyde, 2-methoxy-1-naphthaldehyde, 3-ethoxy-4-hydroxybenzaldehyde, 2-nitrobenzaldehyde, 3-nitro- benzaldehyde and 4-nitrobenzaldehyde, 4 - (((2-hydroxyethyl) imino) methyl) -2-methoxyphenol, 5 - (((2-hydroxyethyl) imino) methyl) -2-methoxyphenol, 2,6-dimethoxy-4- (((2-hydroxyethyl) imino) methyl) phenol, 4 - (((2-hydroxyethyl) imino) methyl) phenol, 1, 2-dihydroxy-4 - (((2-hydroxyethyl) imino) - methyl) benzene, N, N-dimethyl-4 - (((2-hydroxyethyl) imino) methyl) aniline, 1, 2-dihydroxy-3 - (((2-hydroxyethyl) imino) methyl) benzene, 4 - ((( 3-hydroxypropyl) imino) methyl) phenol, 2,6-dimethoxy-4 - (((3-hydroxypropyl) irino) - methyl) phenol, 4 - (((2,3-dihydroxypropyl) imino) methyl) phenol , 2,6-Dimethoxy-4 - (((2,3-dihydroxypropyl) imino) methyl) phenol, 2 - [(4-hydroxybenzylidene) amino] propane-1,3-diol, 2 - [( 4-Hydroxy-3,5-dimethoxy-benzylidene) amino] propane-1,3-diol, 4 - (((2-hydroxy-2-phenylethyl) imino) methyl) phenol, 2,6-dimethoxy -4 - (((1-phenyl-2-hydroxyethyl) imino) methyl) phenol, 4 - (((2-hydroxyphenyl) imino) methyl) phenol, 2,6-dimethoxy-4 - (((2-hydroxyphenyl ) imino) methyl) phenol, 5-guanidino-2- [(4-hydroxy-benzylidene) amino] pentane acid, 2 - [(4-dimethylamino-naphthalene-1-ylmethylene) amino] ethanol, 5-guanidino-2 - [(4-hydroxy-3,5-dimethoxybenzylidene) amino] pentanoic acid, 2- [(4-Hydroxy-3,5-dimethoxybenzylidene) amino] -3- (3 / - / - imidazol-4-yl) propanoic acid, 2 - [(4-hydroxybenzylidene) amino] -3 - (3 - -imidazol-4-yl) propanoic acid, 2 - [(4-hydroxy-3,5-dimethoxybenzylidene) amino] -3- (1 / - / - indol-3-yl) propanoic acid , 2 - [(4-Hydroxy-benzylidene) amino] -3- (1fy-indol-3-yl) propanoic acid, 2 - (((2-hydroxyethyl) imino) methyl) phenol, 1, 2-dihydroxy- 3 - (((2-hydroxyethyl) imino) methyl) benzene, 1, 2,3-trihydroxy-4 - (((2-hydroxyethyl) imino) methyl) benzene, 1, 2,3,4-tetrahydroxy- 5 - (((2-hydroxyethyl) imino) methyl) benzene and 1, 2,4-trihydroxy-4 - (((2-hydroxyethyl) imino) methyl) benzene. The carbonyl compounds can also be prepared in situ by enzymatic oxidation of corresponding aryl alcohols and benzyl alcohols using one or more suitable oxidation enzymes.

Suitable aryl alcohols and benzyl alcohols include, for example, the following compounds: benzyl alcohol, 4-hydroxy-benzyl alcohol, 4-hydroxy-3-methoxy-benzyl alcohol (vanillyl alcohol), 3-hydroxy-4-methoxy-benzyl alcohol (isovanillyl- alcohol), 3,5-dimethoxy-4-hydroxy-benzyl alcohol, 3,4-dihydroxy-benzyl alcohol, 2-hydroxy-3-methoxy-benzyl alcohol, 4-ethoxy-benzyl alcohol, 4-carboxybenzyl alcohol, 2,5-dihydroxy -benzyl alcohol, 2,4-dihydroxy-benzyl alcohol, 2-hydroxy-benzyl alcohol, 3,5-dimethoxy-4-hydroxy-benzyl alcohol, 4-hydroxy-2-methoxy-benzyl alcohol, 2,4-dimethoxy-benzyl alcohol, 2,3 -Dimethoxy-benzyl alcohol, 2,5-dimethoxy-benzyl alcohol, 3,5-dimethoxy-benzyl alcohol, 3,4-methylenedioxy-benzyl alcohol, 3,4-dimethoxy-benzyl alcohol, 3-ethoxy-4-hydroxy-benzyl alcohol, 3.5 -Dimethyl-4-hydroxy-benzyl alcohol, 3,4-dimethoxy-5-hydroxy-benzyl alcohol, 3,4,5-trimethoxy-benzyl alcohol, 2,4,6-trihydroxy-benzyl alcohol, 3,4,5-trihydroxy-benzyl - alcohol, 2,3,4-trihydroxy-benzyl alcohol, 3,5-di tert-butyl-4-hydroxy-benzyl alcohol, 2-nitro-benzyl alcohol, 3-nitro-benzyl alcohol, 4-nitro-benzyl alcohol, 2-amino-benzyl alcohol, 3-amino-benzyl alcohol, 3-amino-4-methyl-benzyl alcohol , 3,5-diamino-benzyl alcohol, 4-amino-benzyl alcohol, 4-dimethylamino-benzyl alcohol, 4-diethylamino-2-hydroxy-benzyl alcohol, 4-diethylamino-3-methoxy-benzyl alcohol, 4-dimethylamino-2-methoxy-benzyl alcohol , 4-dibutylamino-benzyl alcohol, 3-methoxy-4- (1-pyrrolidinyl) benzyl alcohol, (4-methoxy-naphthalen-1-yl) methanol, (4-dimethylamino-naphthalene-1-yl) methanol, 2- (hydroxymethyl) -1-naphtol, 1-naphthalene-methanol, 2-naphthalene-methanol, (2-methoxy-naphtaline-1-yl) -methanol, 4-hydroxymethyl-naphthalene-1-ol, 4'-hydroxymethyl-biphenyl-4-ol, (4-hydroxymethyl-phenyl) -methanol, 4- (3-hydroxypropenyl) -2-methoxy-phenol, 4 - (3-Hydroxy-propenyl) -2,6-dimethoxy-phenol, 3- (4-dimethylamino-phenyl) -prop-2-en-1-ol, 5- (4- (diethylamino-phenyl) penta- 2,4-dien-1-ol, thiophene-2-yl-methanol, (5-hydroxymethyl-thiophene-2-yl) -methanol, thiophene-3-yl-methanol, (1 - -pyrrol-2-yl) -methanol, (1-methyl-1 - pyrrol-2-yl) -methanol, 5-methyl-furan-2-yl) -methanol, (1H-indol-3-yl) -methanol and (6-methyl- 1H-indol-3-yl) -methanol.

In principle, any enzyme which can catalyze the oxidation of the alcohol to an aldehyde or ketone can be used as the "oxidation enzyme". Examples of such enzymes, without being limited to them, are: alcohol dehydrogenases (EC Classification 1.1.1.-), alcohol oxidases (EC Classification 1.1.2.- and 1.1.3.- and 1.1.99.-), Flavin oxidases (EC Classification 1.2.-), laccases (EC Classification 1.4 .--), peroxidases (EC Classification 1.11.1.-), hydroxylases and monooxygenases (EC Classification 1.13.12.- and 1.13.99.-), whereby Enzymes optimized (for example genetically modified) for the oxidation of the alcohols used are particularly preferred.

The enzyme is preferably used in an amount of 5-100 units per millimole of substrate (alcohol), where one unit of enzyme activity indicates the amount of enzyme required to catalyze the oxidation of 1 micromole of alcohol per minute. The compounds of the formulas (I) and / or (Ia) are kept separate from the carbonyl compounds / imine compounds until shortly before use. The colorant according to the invention therefore generally consists of two components, namely a colorant (A1) which contains the compounds of the formula (I) and / or (la) and, where appropriate, substantive dyes, and a further colorant (A2) which comprises the carbonyl compound / Contains imine compound and optionally direct dyes. These two components are mixed into a ready-to-use dye immediately before use and then applied to the fiber to be dyed. Of course, it is also possible for one or both components to consist of several individual components which are mixed together before use. However, a two-component kit consisting of an agent of component (A1) and an agent of component (A2) is particularly preferred.

The compounds of the formulas (I) and / or (Ia) and the carbonyl compounds / imine compound in the respective color carrier composition (component (A1) or component (A2)) are in each case preferably in a total amount of about 0.02 to 20 percent by weight 0.2 to 10 percent by weight, wherein in the ready-to-use colorant obtained by mixing components (A1) and (A2), the compounds of the formulas (I) and / or (Ia) and the carbonyl compound / imine compound each in a total amount of about 0.01 to 10 percent by weight, preferably 0.1 to 5 percent by weight, are included.

Furthermore, the colorant according to the invention can optionally additionally contain customary, physiologically acceptable, direct Contain dyes from the group of acidic or basic dyes, nitro dyes, azo dyes, quinone dyes and triphenylmethane dyes.

The substantive dyes can be used in component (A1) and / or component (A2) in a total amount of about 0.02 to 20 percent by weight, preferably 0.2 to 10 percent by weight, the total amount of substantive dyes in the ready-to-use colorants obtained by mixing components (A1) and (A2) is about 0.01 to 10 percent by weight, preferably 0.1 to 5 percent by weight.

The preparation form for the ready-to-use colorant and components (A1) and (A2) can be, for example, a solution, in particular an aqueous or aqueous-alcoholic solution. Other suitable forms of preparation are a cream, a gel, a foam or an emulsion. Their composition represents a mixture of the compounds of the formulas (I) and / or (Ia) and / or the carbonyl compounds / imine compounds with the additives customary for such preparations.

Customary additives used in colorants in solutions, creams, emulsions, gels or foams are, for example, solvents such as water, lower aliphatic alcohols, for example ethanol, n-propanol and isopropanol or glycols such as glycerol and 1,2-propanediol, and also wetting agents or emulsifiers the classes of anionic, cationic, amphoteric or nonionic surface-active substances such as fatty alcohol sulfates, oxethylated Fatty alcohol sulfates, alkylsulfonates, alkylbenzenesulfonates, alkyltrimethylammonium ammonium salts, alkylbetaines, oxyethylated fatty alcohols, oxyethylated nonylphenols, fatty acid alkanolamides, ethoxylated fatty alcohols, oxyethylated nonylphenols, fatty acid alkanolamides, ethoxylated fatty acid ester, also thickeners such as higher fatty alcohols, starch or cellulose derivatives, perfumes, hair pretreatment agents, conditioners, hair-swelling agents, preservatives , petroleum jelly, paraffin oil and fatty acids as well as care products such as cationic resins, lanolin derivatives, cholesterol, pantothenic acid and betaine. The constituents mentioned are used in the amounts customary for such purposes, for example the wetting agents and emulsifiers in concentrations of about 0.5 to 30 percent by weight (based on the colorant), the thickeners in an amount of about 0.1 to 30 percent by weight ( based on the colorant) and the care substances in a concentration of about 0.1 to 5 percent by weight (based on the colorant).

The pH of the ready-to-use colorant is generally about 3 to 11, preferably about 6 to 11, with a pH of 6.5 to 8.5 being particularly preferred. The pH of the ready-to-use colorant is obtained when the component (A1) containing the compounds of the formula (I) and / or (la) is mixed with the carbonyl-containing / imine-containing component (A2) as a function of the pH of the components (A1 ) and (A2) and the mixing ratio of these two components. If necessary, after mixing components (A1) and (A2), the pH of the ready-to-use coloring agent can be adjusted to the desired value by adding an alkalizing agent or an acid. Alkalizing agents such as, for example, alkanolamines, alkylamines, alkali metal hydroxides or ammonium hydroxide and alkali metal carbonates or ammonium carbonates or acids such as, for example, lactic acid, acetic acid, tartaric acid, phosphoric acid, hydrochloric acid can be used to adjust the pH of the ready-to-use agent and of component (A1) or (A2) , Citric acid, ascorbic acid and boric acid can be used.

The ready-to-use colorant is obtained immediately before use by mixing component (A1) containing the compounds of the formulas (I) and / or (la) with component (A2) containing the carbonyl compound / imine compound (optionally with the addition of an alkalizing agent or an acid ) produced and then applied to the fiber. Depending on the desired depth of color, this mixture is allowed to act for 5 to 60 minutes, preferably 15 to 30 minutes, at a temperature of 20 to 50 degrees Celsius, in particular at 30 to 40 degrees Celsius. The fiber is then rinsed with water and, if necessary, washed with a shampoo.

The colorant according to the invention enables a gentle, uniform and permanent coloring of the fibers, in particular keratin fibers, such as hair, over a wide range of colors, and depending on the compound of formula (I) / (Ia) used, excellent blue colorations can also be achieved. Surprisingly, the dyeings obtained in this way can be completely and gently removed again at any time using reducing agents. Another object of the present invention is therefore a process for dyeing and later decolorizing keratin fibers, such as wool, silk or hair and in particular human hair, in which the fiber is dyed with a dyeing agent (A) according to the invention and at any later point in time the coloring is removed again with a decolorizing agent (B), component (B) containing at least one sulfite, for example an ammonium sulfite, alkali sulfite or alkaline earth sulfite, in particular sodium sulfite or ammonium sulfite, as the decolorizing agent.

The total amount of sulfites in component (B) is about 0.1 to 10 percent by weight, preferably about 2 to 5 percent by weight.

The agent for decolorizing the fibers dyed with the colorant (A) (hereinafter referred to as "decolorizing agent") can be in the form of an aqueous or aqueous-alcoholic solution, as a gel, cream, emulsion or foam, the decolorizing agent both in the form of a one-component preparation and also In addition to the powder form to protect against dust formation, the decolorizing agent can also be made up as a tablet - also effervescent tablet - or granules. This is then used before use with cold or warm water, optionally with the addition of one or more of the following It is also possible that these auxiliaries (if they are in solid form) are already contained in the decolorizing powder or decolorizing granulate or the effervescent tablet. If necessary, the dust formation can be avoided by wetting the powder with oils or waxes be changed. The decolorizing agent can contain additional auxiliaries, such as, for example, solvents such as water, lower aliphatic alcohols, for example ethanol, n-propanol and isopropanol, glycol ethers or glycols such as glycerol and in particular 1,2-propanediol, and also wetting agents or emulsifiers from the classes of the anionic, cationic , amphoteric or nonionic surface-active substances such as fatty alcohol sulfates, ethoxylated fatty alcohol sulfates, alkyl sulfonates, alkylbenzenesulfonates, alkyltrimethylammonium salts, alkylbetaines, oxyethylated fatty alcohols, oxyethylated nonylphenols, fatty acid alkanolamides, oxyethylated fatty alcohols, fatty acid alkoxylamides, higher ethoxylated fatty alcohols, oxyethylated ethoxylated alcohols, oxyethylated ethoxylates, furthermore , Perfumes, hair pretreatment agents, conditioners, hair swelling agents, preservatives, petroleum jelly, paraffin oil and fatty acids as well as care substances such as cationic resins, lanolin derivatives, choles terin, pantothenic acid and betaine.

The pH of the decolorizing agent is about 3 to 8, in particular about 4 to 7. If necessary, the desired pH can be adjusted by adding suitable acids, for example α-hydroxycarboxylic acids such as lactic acid, tartaric acid, citric acid or malic acid, phosphoric acid, acetic acid, glycolic acid, salicylic acid , Glutathione or gluconic acid lactone, or else alkalizing agents such as alkanolamines, alkylamines, alkali hydroxides, ammonium hydroxide, alkali carbonates, ammonium carbonates or alkali phosphates. The exposure time of the decolorizing agent is 5 to 60 minutes, in particular 15 to 30 minutes, depending on the color and temperature to be decolorized (about 20 to 50 degrees Celsius), the decolorization process being accelerated by the application of heat. At the end of the exposure time of the decolorizing agent, the hair is rinsed with water, if necessary washed with a shampoo.

Although component (B) is particularly well suited for decolorizing keratin fibers dyed with the colorant (A), in particular human hair, component (B) can in principle also be used for decolorizing other natural or synthetic fibers dyed with the colorant (A) such as cotton, viscose, nylon, cellulose acetate can be used.

The present application further relates to compounds of the formula (I) or (Ia) in which R2 'or R2 is a methylene or methyl group when R10 is hydrogen or a methoxy group, and at least one of the radicals R5 to R12 are different from hydrogen if the radicals R1, R3 and R4 simultaneously represent a methyl group; as well as the compounds of formula (V).

The following examples are intended to explain the subject in more detail without restricting it to these examples. Examples

Examples 1.1 to 1.22: Synthesis of the indoline derivatives of the formula (I) / (Ia)

A) General instructions for the preparation of the 3H-indole derivatives of the formula (VII) variant 1:

1 mol of 5-halogeno-2,3,3, -trimethyl-3H-indole of the formula (II) 1.3 mol of arylboronic acid of the formula (III) are dissolved in 1, 2-dimethoxyethane. Argon is bubbled through this solution for 15 minutes. The Pd catalyst (0.1 to 0.12 mol) and 2 to 2.6 mol of potassium carbonate, dissolved in water, are then added. The reaction mixture is heated under reflux and under an argon atmosphere for 2 to 6 hours. After the reaction has ended, the reaction mixture is filtered through silica gel, taken up in dichloromethane and the resulting organic phase is washed twice with one molar sodium hydroxide solution and three times with water, dried over MgSO ₄ and then concentrated at 40 ° C. under reduced pressure. The residue is distilled in a high vacuum or purified by chromatography. Variant 2:

1 mol of 5-dioxaborinane-2,3,3-trimethyl-3H-indole of the formula (V) and 1.0 to 1.3 mol of aryl halogen compound of the formula (VI) are dissolved in 1, 2-dimethoxyethane. Argon is bubbled through this solution for 15 minutes. The Pd catalyst (0.1 to 0.2 mol) and 2 to 2.6 mol of potassium carbonate, dissolved in water, are then added. The reaction mixture is heated under reflux and under an argon atmosphere for 2 to 6 hours. After the reaction has ended, the reaction mixture is filtered through silica gel, taken up in dichloromethane and the resulting organic phase twice with single-molar sodium hydroxide solution, twice with Water and washed once with a saturated saline solution, dried over MgSO ₄ and then concentrated at 40 ° C. under reduced pressure. The residue is distilled under high vacuum or purified by chromatography. Variant 3:

To 1. 5 mol of 5-dioxaborinane-2,3,3-trimethyl-3H-indole of the formula (V) dissolved in 1, 2 dimethoxyethane, 1.95 mol of aryl halogen compound, 0.15 mol of Pd catalyst and 3.9 mol an aqueous K ₂ CO ₃ solution. The reaction mixture is then mixed with argon, heated to 80 ° C and rotated at 360 elliptical rounds per minute. The course of the reaction is monitored by means of thin layer chromatography (silica gel; hexane / ethanol or hexane / acetone). After the reaction has ended (after about 4 to 10 hours), the aqueous phase is separated off and the product dissolved in the organic phase is adsorbed on silica gel and then purified by chromatography (silica gel; hexane / ethanol).

B) General instructions for the preparation of the 5-dioxaborinane-2,3,3-trimethyl-3H-indole derivatives of the formula (V) 1 mol of aryl halogen compound of the formula (II) and 1.5 mol of diborone compound of the formula (IV) as well as the Pd catalyst (0.03 to 0.05 mol) and 3 to 3.2 mol of potassium acetate are added to anhydrous dioxane. The reaction mixture is then heated to 80 to 85 ° C. for 4 to 6 hours under a nitrogen atmosphere and with vigorous stirring. Then the reaction solution is mixed with water and extracted three times with ethyl acetate. The combined organic phases are washed once with saturated sodium chloride solution and twice with distilled water, then dried over MgSO ₄ and completely concentrated at 40 ° C. under reduced pressure. The residue is purified chromatographically (silica gel, hexane / acetone) or using Kugelrohr distillation.

C) General instructions for the N-alkylation of the 3H-indole derivatives of the formula (VII) variant 1:

1 mol of the intermediate product obtained in stage A) is dissolved in 1,2-dichloroethane, mixed with 1.2 mol of trimethyloxonium tetrafluoroborate and heated under reflux for 6 hours. The product precipitates if the reaction mixture is cooled to 4 ° C. or ethyl acetate or tert-butyl methyl ether is added. The solid obtained is filtered off, washed with a little ethyl acetate or tert-butyl methyl ether and recrystallized from methanol, ethanol, acetonitrile or ethyl acetate. Variant 2:

1 mol of the intermediate product obtained in stage A) is dissolved in chloroform, and 1.1 to 2.1 mol of methyl iodide are added. The solution obtained is then stirred under the exclusion of light and under an argon atmosphere at 25 ° C. for 24 hours. Then tert-butyl methyl ether is added to this solution, the yellow precipitate is filtered off with suction and recrystallized from ethanol. Variant 3:

1 mol of the intermediate product obtained in stage A) is dissolved in 1,2-dichloroethane. 1 to 2.5 mol of triethyloxonium tetrafluoroborate dissolved in 1, 2-dichloroethane are added. The reaction mixture is then heated to 80 ° C. and rotated at 360 elliptical rounds per minute. The course of the reaction is determined by means of thin layer chromatography (silica gel; ethyl acetate or butanol / acetic acid / H ₂ O 50:15:35) monitored. After the reaction has ended (after about 6 hours), the reaction mixture is concentrated under reduced pressure to a viscous oil which forms a precipitate by mixing with ethanol or ethyl acetate. The precipitated product is filtered off, washed and dried at 40 ° C.

Example 1.1: 5- (2,4-Dimethoxyphenyl) -1, 2,3,3-tetramethyl-3H-indole-1-ium tetrafluroborate

The preparation is carried out according to variant 1 of general synthesis instructions A), 0.92 g of 5-bromo-2,3,3-trimethyl-3H-indole and 1.01 g of 2,4-dimethoxyphenylboronic acid in 20 ml of 1,2-dimethoxyethane and 0.51 g of tetrakis (triphenylphosphine) palladium (0) and 1.38 g of potassium carbonate in 5 g of water. The resulting residue is purified by chromatography (silica gel; hexane / ethyl acetate 4/6).

0.86 g (76% of theory) of 5- (2,4-dimethoxyphenyl) -2,3,3-trimethyl-3H-indole are obtained.

0.82 g of the 5- (2,4-dimethoxyphenyl) -2,3,3-trimethyl-3H-indole thus obtained are, according to variant 1 of the general procedure C), with 0.49 g of trimethyloxonium tetrafluoroborate in 5 ml of 1, 2- Alkylated dichloroethane. The crude product is recrystallized from methanol.

Yield: 0.61 g (55% of theory) 5- (2,4-dimethoxyphenyl) -1, 2,3,3-tetramethyl-3H-indole-1-tetrafluroborate melting point: 184-187 ° C

¹ H-NMR (Dg-DMSO): δ = 1.53 ppm (s, 6H); 2.75 ppm (s, 3H); 3.77 ppm (s, 3H); 3.81 ppm (s, 3H); 3.97 ppm (s, 3H); 6.65 ppm (d, ³ J = 8 Hz, 1 H); 6.70 ppm (s, 1H); 7.29 ppm (d, ³ J = 8 Hz, 1 H); 7.66 ppm (d, ³ J = 9

Hz); 7.84 ppm (s, 1H); 7.85 ppm (d, ³ J = 9 Hz, 1 H).

FAB mass spectrum: M ⁺ = 310.2 (100% relative intensity)

Elemental analysis:

(C ₂₀ H ₂₄ NO ₂ BF ₄ )% C% H% N% F% O calc .: 60.48 6.09 3.53 19.13 8.06 found: 60.20 6.30 3.40 18.80 8.20

Example 1.2: 5- (1, 3-Benzodioxol-5-yl) -1, 2,3,3-tetramethyl-3H-indol-1-ium tetrafluoroborate

The preparation is carried out according to variant 1 of the general synthesis instructions A), 0.92 g of 5-bromo-2,3,3-trimethyl-3H-indole and 0.83 g of 3,4-methylenedioxyphenylboronic acid in 20 ml of 1,2-dimethoxyethane and 0.51 g of tetrakis (triphenylphosphine) palladium (0) and 1.38 g of potassium carbonate in 5 g of water. The resulting residue is purified by chromatography (silica gel; hexane / ethyl acetate 4/6).

0.89 g (83% of theory) of 5- (1,3-benzodioxol-5-yl) -2,3,3-trimethyl-3H-indole are obtained.

0.70 g of the 5- (1,3-benzodioxol-5-yl) -2,3,3-trimethyl-3H-indole thus obtained are, according to variant 1 of the general synthesis instruction C), with 0.44 g of trimethyloxonium tetrafluoroborate in 4 ml 1, 2-dichloroethane alkylated. The crude product is recrystallized from ethyl acetate / acetonitrile (1: 1).

Yield: 0.65 g (68% of theory) of 5- (1,3-benzodioxol-5-yl) -1, 2,3,3-tetramethyl-3H-indol-1-ium tetrafluoroborate

¹ H-NMR (D.-DMSO): δ = 1.55 ppm (s, 6H); 2.75 ppm (s, 3H), 3.97 ppm (s, 3H); 6.10 ppm (s, 2H); 7.05 ppm (d, ³ J = 8 Hz, 1 H); 7.28 ppm (d, ³ J = 8 Hz, 1 H); 7.40 ppm (s, 1H); 7.86 ppm (d, ³ J = 9 Hz; 1 H); 7.91 ppm

(d, ³ J = 9 Hz, 1 H); 8.11 (s, 1H).

FAB mass spectrum: M ⁺ = 294.30

Elemental analysis:

(C ₁₉ H ₂₀ NO ₂ BF ₄ )% C% H% N% F% O calc .: 59.87 5.29 3.67 19.94 8.39 found: 59.60 5.40 3.70 19.90 8.20

Example 1.3: 1, 2,3,3-tetramethyl-5 - (- 2-trifluoromethyl) phenyl) -3H-indole-1-ium tetrafluroborate

The preparation is carried out in accordance with variant 1 of the general synthesis instructions A), 0.92 g of 5-bromo-2,3,3-trimethyl-3H-indole and 0.95 g of 2-trifluoromethylphenylboronic acid in 20 ml of 1,2-dimethoxyethane and 0 , 51 g of tetrakis (triphenylphosphine) palladium (0) and 1.38 g of potassium carbonate in 5 g of water. The resulting residue is purified by chromatography (silica gel; hexane / ethyl acetate 4: 6).

0.77 g (66% of theory) of 5- (2- (trifluoromethyl) phenyl) -2,3,3-trimethyl-3H-indole are obtained.

0.76 g of the 5- (2- (trifluoromethyl) phenyl) -2,3,3-trimethyl-3H-indole thus obtained is, according to variant 1 of the general synthesis instructions C), with 0.44 g of trimethyloxonium tetrafluoroborate in 4 ml 1, 2 -Dichloroethane alkylated. The crude product is recrystallized from ethanol.

Yield: 0.46 g (46% of theory) 1, 2,3,3-tetramethyl-5 - (- 2-trifluoromethyl) phenyl) -3H-indole-1-ium tetrafluroborate.

Η NMR (Dg-DMSO): δ = 1.54 ppm (s, 6H); 2.77 ppm (s, 3H); 3.99 ppm (s, 3H); 7.40-8.05 ppm (m, 7H) FAB mass spectrum: M ⁺ = 318.0 (100% relative intensity) Example 1.4: 1, 2, 3, 3-tetra methyl-5- (thiophene-3-yl) -3 H-indole in m-iodide The preparation is carried out according to variant 1 of general synthesis instruction A), 1 g of 5- Bromo-2,3,3-trimethyl-3H-indole and 0.70 g of 3-thiophene boronic acid in 18 ml of 1,2-dimethoxyethane and 0.56 g of tetrakis (triphenylphosphine) palladium (0) and 1.51 g of potassium carbonate in 5 , 3 g of water can be used.

The resulting residue is purified by chromatography (silica gel; hexane / ethyl acetate 4: 6).

0.81 g (80% of theory) of 5- (thiophene-3-yl) -2,3,3-trimethyl-3H-indole are obtained.

1.03 g of the 5- (thiophene-3-yl) -2,3,3-trimethyl-3H-indole thus obtained are alkylated with 0.7 g of methyl iodide in 4 ml of chloroform in accordance with variant 2 of the general synthesis instructions C).

Yield: 0.37 g (23% of theory) 1, 2,3,3-tetramethyl-5- (thiophene-3-yl) -3H-indolium iodide

¹ H NMR (CD ₅ OD): δ = 1.65 ppm, (s, 6H); 4.06 ppm (s, 3H), 4.85 ppm (s, 3H); 7.53-7.59 ppm (m, 2H); 7.81-7.86 ppm (m, 2H); 7.93 ppm (dd, ³ J = 8.5 Hz, ⁴ J = 2 Hz, 1 H); 8.07 ppm (d, J = 2Hz, 1H) FAB mass spectrum: M ⁺ = 256.0 (100% relative intensity) Elemental analysis:

(C _1β H _1β NSI)% C% H% N calc .: 50.14 4.73 3.65 found: 50.14 4.80 3.35 Example 1.5: 5-phenyl-1, 2,2,3-tetramethyl-1 (3H) -indolium tetrafluoroborate

The preparation is carried out according to variant 1 of the general synthesis instructions A), 1 g of 5-bromo-2,3,3-trimethyl-3H-indole and 0.69 g of benzene boronic acid in 18 ml of 1, 2-dimethoxyethane and 0.56 g of tetrakis (triphenylphosphine) palladium (0) and 1.5 g of potassium carbonate in 5.3 g of water.

0.81 g (82% of theory) of 5-phenyl-2,3,3-trimethyl-3H-indole are obtained.

1.5 g of the 5-phenyl-2,3,3-trimethyl-3H-indole thus obtained are alkylated in accordance with variant 1 of the general synthesis instructions C) with 1.11 g of trimethyloxonium tetrafluoroborate in 5 ml of 1,2-dichloroethane. The crude product is recrystallized from acetonitrile. Yield: 1.33 g (63% of theory) 5-phenyl-1, 2,2,3-tetramethyl-1 (3H) indolium tetrafluoroborate

Η NMR (Dg-DMSO): δ = 1.57 ppm (s, 6H); 2.76 ppm (s, 3H); 3.99 ppm (s, 3H); 7.35-7.60 ppm (m, 3H); 7.70-7.83 ppm (m; 2H); 7.88-8.02 ppm (m, 2H); 8.17 ppm (s, 1 H)

FAB mass spectrum: M ⁺ = 250.3 (100% relative intensity) Elemental analysis:

C ₁₈ H ₂₀ NBF ₄ % C% H% N% F calc .: 64.12 5.98 4.15 22.54 found: 63.60 6.10 4.20 22.50 Example 1.6: 1, 2,3,3-tetramethyl-5-p-tolyl-3H-indolium tetrafluoroborate The preparation is carried out in accordance with variant 2 of the general synthesis instructions A), 2.20 g of 5- (5,5-dimethyl- [1, 3.2] dioxaborinan-2-yl) -2,3,3-trimethyl-3H-indole and 1.8 g of 4-bromotoluene in 50 ml of 1,2-dimethoxyethane with 0.94 g of tetrakis (triphenylphosphine ) palladium (0) and 2.90 g of potassium carbonate in 10.5 g of H ₂ O are used. The resulting residue is distilled using Kugelrohr distillation in vacuo (0.004 mbar) at 107 ° C.

1.80 g (90% of theory) of 2,3,3-trimethyl-5-p-tolyl-3H-indole are obtained.

1.7 g of the 2,3,3-trimethyl-5-p-tolyl-3H-indole thus obtained are alkylated according to variant 1 of the general synthesis instructions C) with 1.27 g of trimethyloxonium tetrafluoroborate in 6 ml of 1,2-dichloroethane. The crude product is recrystallized from methanol.

Yield: 1.43 g (57% of theory) 1, 2,3,3-tetramethyl-5-p-tolyl-3H-indolium tetrafluoroborate

¹ H NMR (Dg-DMSO): δ = 1.57 ppm (s, 6H); 2.36 ppm (s, 3H); 2.76 ppm (s, 3H); 3.98 ppm (s, 3H); 7.32 ppm (~ d, ³ J ~ 8Hz, 2H); 7.68 ppm (~ d, ³ J ~ 8Hz, 2H); 7.88 ppm (~ d, ³ J ~ 9 Hz, 1H); 7.94 ppm (~ d, 3J ~ 9 Hz, 1H); 8.14 ppm (s, 1 H)

FAB mass spectrum: M ⁺ = 264.1 (100% relative intensity) Elemental analysis:

(C ₁₉ H ₂₂ NBF ₄ )% C% H% N% F calc .: 64.98 6.31 3.99 21.64 found: 64.90 6.20 3.90 21, 50 Example 1.7: 1, 2,3,3-tetramethyl-5-naphthalene-1-yl-3H-indolium tetrafluoroborate

The production takes place according to variant 1 of the general

Synthesis instructions A), 1.06 g of 5-bromo-2,3,3-trimethyl-3H-indole and

1.0 g of naphthalene-1-boronic acid in 20 ml of 1,2-dimethoxyethane and 0.57 g

Tetrakis (triphenylphosphine) palladium (0) and 1.6 g potassium carbonate in 5.8 g

Water can be used.

The resulting residue is distilled using Kugelrohr distillation in vacuo

(0.008 mbar) distilled at 200 ° C.

0.78 g (61% of theory) 2,3,3-trimethyl-5-naphthalen-1-yl-

Get 3H-indole.

0.65 g of the 2,3,3-trimethyl-5-naphthalen-1-yl-3H-indole obtained in this way are used in accordance with variant 1 of the general synthesis instructions C)

Alkylated 0.4 g of trimethyloxonium tetrafluoroborate in 5 ml of 1, 2-dichloroethane.

The reaction mixture is concentrated under reduced pressure. The oily residue is taken up in a little CH ₂ CI ₂ and by adding part. The product is precipitated in butyl methyl ether.

Yield: 0.32 g (36% of theory) 1, 2,3,3-tetramethyl-5-naphthalene

1-yl-3H-indolium tetrafluoroborate

Η NMR (CDgOD): δ = 1.61 ppm (s, 6H); 2.82 ppm (s, 3H); 4.06 ppm (s,

3H); 7.40 - 7.70 (m, 4H); 7.70-7.85 ppm (m, 2H); 7.95-8.15 ppm (m, 4H)

FAB mass spectrum: M ⁺ = 300.0 (100% relative intensity)

Example 1.8: 2,3,3-Trimethyi-5- (4,4,5,5-tetramethyl- [1,3,2] dioxaborolan-2-yl) -3H-indole

The preparation is carried out according to the general synthesis instructions B), 0.16 g of 5-bromo-2,3,3-trimethyl-3H-indole, 0.25 g of bis (pinacolato) diborone, 0.02 g [1, 1'-bis (diphenylphosphino) ferrocene] dichloro-palladium (II) and 0.20 g of potassium acetate in 10 ml of dioxane can be used.

The resulting residue is chromatographed (silica gel, hexane /

Acetone = 9/1) cleaned.

Yield: 0.13 g (68% of theory) 2,3,3-trimethyl-5- (4,4,5,5-tetramethyl- [1,3,2] dioxaborolan-2-yl) -3H-indole

¹ H-NMR (CDCIg): δ = 1.31 ppm (s, 6H); 1.36 ppm (s, 12H); 2.30 ppm (s,

3H); 7.53 ppm (d, ³ J = 8 Hz, 1 H); 7.73 ppm (s, 1H); 7.79 ppm (d, ³ J = 8

Hz, 1H);

El mass spectrum: 285 (100, M ⁺ ); 270 (53); 228 (7); 212 (10); 199 (62);

186 (62); 170 (18); 158 (8); 144 (16); 116 (15); 103 (6); 78 (14); 60 (14)

Example 1.9: 5- (5,5-Dimethyl- [1,3,2] dioxaborinan-2-yl) -2,3,3-trimethyl-3H-indole

The preparation is carried out according to general synthesis instructions B), 11.91 g of 5-bromo-2,3,3-trimethyl-3H-indole,

16.94 g of bis (neopentyl glycolato) diborone, 1, 10 g of [1, 1'-bis (diphenylphosphino) ferrocene] dichloro-palladium (II) and 15.21 g of potassium acetate in 150 ml of dioxane can be used.

The resulting oily residue is purified by means of Kugelrohr distillation (0.020 mbar, 160-170 ° C).

Yield: 9.50 g (70% of theory) 5- (5,5-dimethyl- [1,3,2] dioxaborinane

2-yl) -2,3,3-trimethyl-3H-indole

¹ H-NMR (CDCI ₃ ): δ = 1.03 ppm (s, 6H); 1.31 ppm (s, 6H); 2.30 ppm (s,

3H); 3.78 ppm (s, 4H); 7.52 ppm (d, ³ J = 8 Hz, 1 H); 7.73 ppm (s, 1H); 7.78 ppm (d, ³ J = 8 Hz, 1 H).

El mass spectrum: 271 (100, M ⁺ ); 256 (68); 230 (5); 184 (18); 170 (42);

144 (46); 129 (19); 115 (36); 91 (13); 77 (26); 57 (19). Example 1.10: 1-ethyl-2,3,3-trimethyl-5- (4-methylsulfanyl-phenyl) -3H-indolium tetrafluoroborate

The preparation is carried out according to variant 3 of the general synthesis instructions A), 407 mg of 5- (5,5-dimethyl- [1,3,2] dioxaborinan-2-yl) - 2,3,3-trimethyl-3H-indole and 396 mg of 4-bromothioanisole in 7.5 ml of 1,2-dimethoxyethane and 173 mg of tetrakis (triphenylphosphine) palladium (0) and 2.0 ml of potassium carbonate solution (2.76 g of potassium carbonate in 10 ml of H ₂ O) are used.

The resulting residue is purified by chromatography (silica gel; hexane / ethanol 9: 1).

219 mg (52% of theory) 2,3,3-trimethyl-5- (4-methylsulfanyl-phenyl) -3H-indole are obtained.

219 mg of the 2,3,3-thmethyl-5- (4-methylsulfanyl-phenyl) -3H-indole thus obtained is, according to variant 3 of the general synthesis instructions C), with 1.1 ml of 1, 2-dichloroethane and 0.93 ml a triethyloxonium tetrafluoroborate solution (= 1, 90 g triethyloxonium tetrafluoroborate in 10 ml 1, 2-dichloroethane) alkylated.

The product thus obtained is washed once with hot ethanol and once with methanol.

Yield: 171 mg (55% of theory) 1-ethyl-2,3,3-trimethyl-5- (4-methylsulfanylphenyl) -3H-indolium tetrafluoroborate ¹ H-NMR (Dg-DMSO): δ = 1 , 45 ppm (t, ³ J = 7 Hz, 3H); 1.57 ppm (s, 6H); 2.52 ppm (s, 3H); 2.82 ppm (s, 3H); 4.50 ppm (q, ³ J = 7 Hz, 2H); 7.39 ppm (d, ³ J = 8 Hz, 2H); 7.73 ppm (d, ³ J = 8 Hz, 2H); 7.90 ppm (d, ³ J ~ 8 Hz, 1H); 8.00 ppm (d, ³ J = 8 Hz, 1 H), 8.17 ppm (s, 1 H). ESI mass spectrum: M ⁺ = 310.1 (100% relative intensity)

[M + Na] = 332.1 (20% relative intensity) Example 1.11: 1'-acetyl-1-ethyl-2,3,3-trimethyl-2 ', 3'-dihydro-3H, 1Η-

[5,5 '] biindolyl-1-ium-tetrafluoroborate

The production takes place according to variant 3 of the general

Synthesis instructions A), where 407 mg of 5- (5,5-dimethyl- [1,3,2] dioxaborinane

2-yl) -2,3,3-trimethyl-3H-indole and 468 mg 1-acetyl-5-bromoindoline in 7.5 ml 1, 2-dimethoxyethane and 173 mg tetrakis (triphenylphosphine) palladium (O) and 2 , 0 ml of a potassium carbonate solution (= 2.76 g

Potassium carbonate in 10 ml H ₂ O) can be used.

The resulting residue is purified by chromatography (silica gel;

Hexane / ethanol 8: 2).

242 mg (51% of theory) of 1- (2 \ 3 \ 3'-trimethyl-2,3-dihydro-3Η-

Obtained [5,5 '] biindolyl-1-yl) ethanone.

242 mg of the thus obtained 1- ^(2, ^3, 3'-trimethyl-2,3-dihydro-3'H-

[5,5 '] biindolyl-1-yl) ethanol is used according to variant 3 of the general

Synthesis instructions C) with 1, 2 ml of 1, 2-dichloroethane and 0.91 ml of one

Triethyloxonium tetrafluoroborate solution (= 1.90 g triethyloxonium tetrafluoroborate in 10 ml 1, 2-dichloroethane) alkylated.

The product thus obtained is washed with hot ethanol.

Yield: 190 mg (58% of theory) of 1'-acetyl-1-ethyl-2,3,3-trimethyl-

2 ^, 3'-dihydro-3H, 1 ^, H- [5,5 '] biindolyl-1 -ium tetrafluoroborate

¹ H NMR (Dg-DMSO): δ = 1.45 ppm (t, ³ J = 7 Hz, 3H); 1.57 ppm (s, 6H);

2.18 ppm (s, 3H); 2.82 ppm (s, 3H); 3.22 ppm (t, ³ J ~ 8 Hz, 2H); 4.15 ppm (t, ³ J ~ 8Hz, 2H); 4.50 ppm (q, ³ J = 7 Hz, 2H); 7.58 ppm (d, ³ J ~ 9

Hz, 1H); 7.68 ppm (s, 1H); 7.87 ppm (d, ³ J ~ 8 Hz, 1 H); 7.98 ppm (d, ³ J ~

8 Hz, 1H); 8.12 ppm (d, ³ J ~ 9 Hz, 1H), 8.16 ppm (s, 1H).

ESI mass spectrum: M ⁺ = 347.2 (100% relative intensity)

[M + Na] = 369.1 (93% relative intensity) Example 1.12: 1-ethyl-2,3,3-trimethyl-5-naphthalene-2-yl-3H-indolium tetrafluoroborate

The preparation is carried out according to variant 3 of the general synthesis instructions A), 407 mg of 5- (5,5-dimethyl- [1,3,2] dioxaborinan-2-yl) - 2,3,3-trimethyl-3H-indole and 404 mg of 2-bromonaphthalene in 7.5 ml of 1,2-dimethoxyethane and 173 mg of tetrakis (triphenylphosphine) palladium (O) and 2.0 ml of a potassium carbonate solution (= 2.76 g of potassium carbonate in 10 ml of H ₂ O) be used. The resulting residue is purified by chromatography (silica gel; hexane / ethanol 9: 1).

256 mg (60% of theory) of 2,3,3-trimethyl-5-naphthalene-2-yl-3H-indole are obtained.

256 mg of the 2,3,3-trimethyl-5-naphthalen-2-yl-3H-indole thus obtained is, according to variant 3 of the general synthesis instructions C), with 1.3 ml of 1,2-dichloroethane and 1.08 ml of a triethyloxonium -tetrafluoroborat- solution (= 1, 90 g triethyloxonium tetrafluoroborate in 10 ml 1, 2-dichloroethane) alkylated. The product thus obtained is washed with ethanol. Yield: 244 mg (68% of theory) of 1-ethyl-2,3,3-trimethyl-5-naphthalene-2-yl-3H-indolium tetrafluoroborate

Η NMR (Dg-DMSO): δ = 1.48 ppm (t, ³ J = 7 Hz, 3H); 1.61 ppm (s, 6H); 2.85 ppm (s, 3H); 4.53 ppm (q, ³ J = 7 Hz, 2H); 7.53-7.68 ppm (m, 2H); 7.92-8.17 ppm (m, 6H); 8.35 ppm (s, 2H). ESI mass spectrum: M ⁺ = 314.1 (100% relative intensity)

[M + Na] = 336.1 (27% relative intensity) Example 1.13: 1-Ethyl-5- (6-hydroxy-naphthalen-2-yl) -2,3,3-trimethyl-3H-indolium tetrafluoroborate

The preparation is carried out according to variant 3 of the general synthesis instructions A), 407 mg of 5- (5,5-dimethyl- [1,3,2] dioxaborinan-2-yl) - 2,3,3-trimethyl-3H-indole and 435 mg of 6-bromo-2-naphthol in 7.5 ml of 1, 2-dimethoxyethane and 173 mg of tetrakis (triphenylphosphine) palladium (O) and 2.0 ml of a potassium carbonate solution (= 2.76 g of potassium carbonate in 10 ml H ₂ O) can be used. The resulting residue is purified by chromatography (silica gel; hexane / ethanol 8: 2).

427 mg (94% of theory) of 6- (2,3,3-trimethyl-3H-indol-5-yl) -naphthalen-2-ol are obtained.

427 mg of the 6- (2,3,3-trimethyl-3H-indol-5-yl) -naphthalene-2-ol thus obtained is treated according to variant 3 of the general synthesis instructions C) with 4.1 ml of 1,2-dichloroethane and 1.70 ml of a triethyloxonium tetrafluoroborate solution (= 1.90 g of triethyloxonium tetrafluoroborate in 10 ml of 1,2-dichloroethane) is alkylated. The product thus obtained is washed with ethyl acetate. Yield: 194 mg (33% of theory) of 1-ethyl-5- (6-hydroxy-naphthalene-2-yl) -2,3,3-trimethyl-3H-indolium tetrafluoroborate

¹ H NMR (Dg-DMSO): δ = 1.48 ppm (m, 9H); 2.54 ppm (s, 3H); 4.52 ppm (m, 2H); 7.11-7.14 ppm (m, 2H); 7.63 ppm (d, ³ J = 8 Hz, 1 H); 7.78-7.76 ppm (m, 4H); 8.07 ppm (s, 1H); 8.13 ppm (s, 1H). ESI mass spectrum: M ⁺ = 330.1 (100% relative intensity) Example 1.14: 5-Anthracen-9-yl-1-ethyl-2,3,3-trimethyl-3H-indolium tetrafluoroborate

The preparation is carried out according to variant 3 of the general synthesis instructions A), 407 mg of 5- (5,5-dimethyl- [1,3,2] dioxaborinan-2-yl) - 2,3,3-trimethyl-3H-indole and 501 mg 9-bromo-anthracene in 7.5 ml 1, 2-dimethoxyethane and 173 mg tetrakis (triphenylphosphine) palladium (O) and 2.0 ml potassium carbonate solution (= 2.76 g potassium carbonate in 10 ml H ₂ O ) are used. The resulting residue is purified by chromatography (silica gel; hexane / ethanol 9: 1). 251 mg (50% of theory) of 5-anthracen-9-y! -2,3,3-trimethyl-3H-indole are obtained.

251 mg of the 5-anthracen-9-yl-2,3,3-trimethyl-3H-indole thus obtained is, according to variant 3 of the general synthesis instructions C), with 1.3 ml of 1,2-dichloroethane and 0.90 ml of a triethyloxonium -tetrafluoroborat- solution (= 1, 90 g triethyloxonium tetrafluoroborate in 10 ml 1, 2-dichloroethane) alkylated. The product thus obtained is washed with ethanol. Yield: 179 mg (53% of theory) of 5-anthracen-9-yl-1-ethyl-2,3,3-trimethyl-3H-indolium tetrafluoroborate

¹ H NMR (Dg-DMSO): δ = 1.54-1.61 ppm (m, 9H); 2.90 ppm (s, 3H); 4.61 ppm (q, ³ J = 7 Hz, 2H); 7.47-7.58 ppm (m, 6H); 7.69 ppm (d, ³ J = 8 Hz, 1H); 7.97 ppm (s, 1H); 8.18-8.23 ppm (m, 3H); 8.75 ppm (s, 1H) ESI mass spectrum: M ⁺ = 364.2 (100% relative intensity)

[M + Na] = 386.1 (33% relative intensity) Example 1.15: 5- (3,5-Dimethyl-phenyl) -1-ethyl-2,3,3-trimethyl-3H-indolium tetrafluoroborate

The preparation is carried out according to variant 3 of the general synthesis instructions A), 407 mg of 5- (5,5-dimethyl- [1,3,2] dioxaborinan-2-yl) - 2,3,3-trimethyl-3H-indole and 361 mg of 1-bromo-3,5-dimethylbenzene in 7.5 ml of 1, 2-dimethoxyethane and 173 mg of tetrakis (triphenylphosphine) palladium (O) and 2.0 ml of a potassium carbonate solution (= 2.76 g of potassium carbonate in 10 ml H ₂ O) can be used. The resulting residue is purified by chromatography (silica gel; hexane / ethanol 9: 1). 193 mg (49% of theory) of 5- (3,5-dimethyl-phenyl) -2,3,3-trimethyl-3H-indole are obtained.

193 mg of the 5- (3,5-dimethyl-phenyl) -2,3,3-trimethyl-3H-indole thus obtained is, according to variant 3 of the general synthesis instructions C), with 1.0 ml of 1,2-dichloroethane and 0, Alkylated 88 ml of a triethyioxonium tetrafluoroborate solution (= 1.90 g triethyioxonium tetrafluoroborate in 10 ml 1, 2-dichloroethane). The product thus obtained is washed with acetic acid.

Yield: 167 mg (60% of theory) 5- (3,5-dimethyl-phenyl) -1-ethyl-2,3,3-trimethyl-3H-indolium tetrafluoroborate H-NMR (Dg-DMSO): δ = 1.45 ppm (t, ³ J = 7 Hz, 3H); 1.57 ppm (s, 6H); 2.35 ppm (s, 6H); 2.82 ppm (s, 3H); 4.50 ppm (q, ³ J = 7Hz, 2H); 7.06 ppm (s, 1H); 7.37 ppm (s, 2H); 7.87 ppm (d, ³ J = 8 Hz, 1 H); 8.00 ppm (d, ³ J = 8 Hz, 1 H); 8.15 ppm (s, 1H) ESI mass spectrum: M ⁺ = 292.3 (100% relative intensity) Example 1.16: 5-Acenaphthen-5-yl-1-ethyl-2,3,3-trimethyl-3H-indolium tetrafluoroborate

The preparation is carried out according to variant 3 of the general synthesis instructions A), 407 mg of 5- (5,5-dimethyl- [1,3,2] dioxaborinan-2-yl) - 2,3,3-trimethyl-3H-indole and 455 mg 5-bromoacenaphten in 7.5 ml 1, 2-dimethoxyethane and 173 mg tetrakis (triphenylphosphine) palladium (O) and 2.0 ml potassium carbonate solution (= 2.76 g potassium carbonate in 10 ml H ₂ O) be used. The resulting residue is purified by chromatography (silica gel; hexanes / ethanol 9: 1). 237 mg (51% of theory) of 5-acenaphthen-5-yl-2,3,3-trimethyl-3H-indole are obtained.

237 mg of the 5-acenaphthen-5-yl-2,3,3-trimethyl-3H-indole thus obtained is, according to variant 3 of the general synthesis instructions C), with 1.2 ml of 1, 2-dichloroethane and 0.91 ml of a triethyloxonium -tetrafluoroborat- solution (= 1, 90 g triethyloxonium tetrafluoroborate in 10 ml 1, 2-dichloroethane) alkylated. The product thus obtained is washed with ethanol. Yield: 108 mg (33% of theory) of 5-acenaphthen-5-yl-1-ethyl-2,3,3-trimethyl-3H-indolium tetrafluoroborate

¹ H-NMR (Dg-DMSO): δ = 1.50 ppm (t, ³ J = 7 Hz, 3H); 1.60 ppm (s, 6H); 2.85 ppm (s, 3H); 3.42 ppm (s, 4H); 4.55 ppm (q, ³ J = 7 Hz, 2H); 7.38-7.58 ppm (m, 5H); 7.77 ppm (d, ³ J = 8 Hz, 1H); 8.04 ppm (s, 1H); 8.08 ppm (d, ³ J = 8 Hz, 1 H). ESI mass spectrum: M ⁺ = 340.1 (100% relative intensity)

[M + Na] = 362.3 (25% relative intensity) Example 1.17: 1-ethyl-5- (4-methoxy-2-methylphenyl) -2,3,3-trimethyl-3H-indolium tetrafluoroborate

The preparation is carried out according to variant 3 of the general synthesis instructions A), 407 mg of 5- (5,5-dimethyl- [1,3,2] dioxaborinan-2-yl) - 2,3,3-trimethyl-3H-indole and 392 mg of 4-bromo-3-methylanisole in 7.5 ml of 1, 2-dimethoxyethane and 173 mg of tetrakis (triphenylphosphine) palladium (O) and 2.0 ml of a potassium carbonate solution (= 2.76 g of potassium carbonate in 10 ml H ₂ O) can be used. The resulting residue is purified by chromatography (silica gel; hexane / ethanol 9: 1). 173 mg (43% of theory) of 5- (4-methoxy-2-methylphenyl) -2,3,3-trimethyl-3H-indole are obtained.

173 mg of the 5- (4-methoxy-2-methylphenyl) -2,3,3-trimethyl-3H-indole thus obtained is, according to variant 3 of the general synthesis instructions C), with 0.9 ml of 1,2-dichloroethane and 0.78 ml of a triethyloxonium tetrafluoroborate solution (0 1, 90 g triethyloxonium tetrafluoroborate in 10 ml 1, 2-dichloroethane) alkylated. The resultant is washed with ethanol. Yield: 134 mg (52% of theory) 1-ethyl-5- (4-methoxy-2-methylphenyl) -2,3,3-trimethyl-3H-indolium tetrafluoroborate ¹ H-NMR (Dg-DMSO) : δ = 1.46 ppm (t, ³ J = 7 Hz, 3H); 1.55 ppm (s, 6H); 2.24 ppm (s, 3H); 2.82 ppm (s, 3H); 3.78 ppm (s, 3H); 4.50 ppm (q, ³ J = 7 Hz, 2H); 6.87 ppm (d, ³ J = 8 Hz, 1 H); 6.92 ppm (s, 1H); 7.18 ppm (d, ³ J = 8 Hz, 1 H); 7.54 ppm (d, ³ J = 8 Hz, 1H); 7.82 ppm (s, 1H); 7.97 ppm (d, ³ J = 8 Hz, 1 H). ESI mass spectrum: M ⁺ = 308.1 (100% relative intensity)

[M + Na] = 330.1 (20% relative intensity) Example 1.18: 5-Biphenyl-4-yl-1-ethyl-2,3,3-trimethyl-3H-indolium tetrafluoroborate

The preparation is carried out according to variant 3 of the general synthesis instructions A), 407 mg of 5- (5,5-dimethyl- [1,3,2] dioxaborinan-2-yl) - 2,3,3-trimethyl-3H-indole and 455 mg of 4-bromobiphenyl in 7.5 ml of 1,2-dimethoxyethane and 173 mg of tetrakis (triphenylphosphine) palladium (O) and 2.0 ml of a potassium carbonate solution (= 2.76 g of potassium carbonate in 10 ml of H ₂ O) be used. The resulting residue is purified by chromatography (silica gel; hexane / ethanol 9: 1). 264 mg (57% of theory) of 5-biphenyl-4-yl-2,3,3-trimethyl-3H-indole are obtained. 264 mg of the 5-biphenyl-4-yl-2,3,3-trimethyl-3H-indole thus obtained is, according to variant 3 of the general synthesis instructions C), with 1.3 ml of 1,2-dichloroethane and 1.02 ml of a triethyloxonium -tetrafluoroborate solution (= 1, 90 g triethyloxonium tetrafluoroborate in 10 ml 1, 2-dichloroethane) alkylated. The product thus obtained is washed with ethanol.

Yield: 220 mg (61% of theory) of 5-biphenyl-4-yl-1-ethyl-2,3,3-trimethyl-3H-indolium tetrafluoroborate

¹ H-NMR (Dg-DMSO): δ = 1.47 ppm (t, ³ J = 7 Hz, 3H); 1.60 ppm (s, 6H); 2.84 ppm (s, 3H); 4.52 ppm (q, ³ J = 7 Hz, 2H); 7.40-7.52 ppm (m, 3H); 7.73-7.91 ppm (m, 6H); 8.00-8.06 ppm (m, 2H); 8.25 ppm (s, 1H). ESI mass spectrum: M ⁺ = 340.3 (100% relative intensity)

[M + Na] = 362.1 (30% relative intensity) Example 1.19: 5-Benzofb1thiophen-3-yl-1-ethyl-2,3,3-trimethyl-3H-indolium tetrafluoroborate

The preparation is carried out according to variant 3 of the general synthesis instructions A), 407 mg of 5- (5,5-dimethyl- [1,3,2] dioxaborinan-2-yl) - 2,3,3-trimethyl-3H-indole and 416 mg of 3-bromothianaphtene in 7.5 ml of 1,2-dimethoxyethane and 173 mg of tetrakis (triphenylphosphine) palladium (O) and 2.0 ml of a potassium carbonate solution (= 2.76 g of potassium carbonate in 10 ml of H ₂ O) be used. The resulting residue is purified by chromatography (silica gel; hexane / ethanol 9: 1). 254 mg (58% of theory) of 5-benzo [b] thiophene-3-yl-2,3,3-trimethyl-3H-indole are obtained.

254 mg of the 5-benzo [b] thiophene-3-yl-2,3,3-trimethyl-3H-indole thus obtained is, according to variant 3 of the general synthesis instructions C), with 1.3 ml of 1,2-dichloroethane and 1, 05 ml of a triethyloxonium tetrafluoroborate solution (= 1.90 g triethyloxonium tetrafluoroborate in 10 ml 1, 2-dichloroethane) alkylated. The product thus obtained is washed with ethanol.

Yield: 180 mg (51% of theory) of 5-benzo [bjthiophen-3-yl-1-ethyl-2,3,3-trimethyl-3H-indolium tetrafluoroborate

¹ H-NMR (Dg-DMSO): δ = 1.48 ppm (t, ³ J = 7 Hz, 3H); 1.60 ppm (s, 6H); 2.85 ppm (s, 3H); 4.55 ppm (q, ³ J = 7 Hz, 2H); 7.43-7.55 ppm (m, 2H); 7.84-7.93 ppm (m, 2H); 7.98 ppm (s, 1H); 8.08-8.13 ppm (m, 3H). ESI mass spectrum: M ⁺ = 320.1 (100% relative intensity)

[M + Na] = 342.1 (12% relative intensity) Example 1.20: 1-ethyl-5- (1-ethyl-3-pyridiniumyl) -2,3,3-trimethyl-3H-indolium ditetrafluoroborate

The preparation is carried out in accordance with variant 2 of the general synthesis instructions A), 0.77 g of 5- (5,5-dimethyl- [1,3,2] dioxaborinan-2-yl) -2,3,3-trimethyl-3H- indole and 0.38 g of 3-bromopyridine in 10 ml of 1,2-dimethoxyethane with 0.23 g of tetrakis (triphenylphosphine) palladium (0) and 0.66 g of potassium carbonate in 2.4 g of H ₂ O are used. The resulting residue is adsorbed onto silica gel and purified by chromatography (silica gel, hexane / acetone 6: 4).

0.36 g (77% of theory) of 2,3,3-trimethyl-5- (3-pyridinyl) -3H-indole are obtained.

0.36 g of the 2,3,3-trimethyl-5- (3-pyridinyl) -3H-indole thus obtained is alkylated according to variant 3 of the general synthesis instructions C) with 0.64 g of triethyloxonium tetrafluoroborate in 5 mM, 2-dichloroethane. The product thus obtained is washed with ethyl acetate and recrystallized in methanol.

Yield: 0.26 g (37% of theory) of 1-ethyl-5- (1-ethyl-3-pyridiniumyl) -2,3,3-trimethyl-3H-indolium ditetrafluoroborate

¹ H-NMR (Dg-DMSO): δ = 1.50 ppm (t, ³ J = 7 Hz, 3H); 1.50-1.75 ppm

(m, 9H); 2.90 ppm (s, 3H); 4.57 ppm (q, ³ J = 7 Hz, 2H); 4.70 ppm (q, ³ J = 7 Hz, 2H); 8.18 ppm (d, ³ J ~ 8Hz, 1H); 8.25 ppm (d, ³ J ~ 8Hz, 1H); 8.32 ppm (~ dd, ³ J ~ 8 Hz, 1H); 8.41 ppm (s, 1H); 9.02 ppm (d; ³ J ~ 8Hz, 1H); 9.15 ppm (d, ³ J ~ 8 Hz, 1 H); 9.55 ppm (s, 1 H) ESI mass spectrum: [M-1] ⁺ = 293.2 (100% relative intensity) Example 1.21: 1-Ethyl-5-furan-3-yl-2,3,3-trimethyl-3H-indolium tetrafluoroborate

The preparation is carried out in accordance with variant 2 of the general synthesis instructions A), 0.77 g of 5- (5,5-dimethyl- [1,3,2] dioxaborinan-2-yl) -2,3,3-trimethyl-3H- indole and 0.50 g of 3-bromo-furan in 10 ml of 1,2-dimethoxyethane with 0.33 g of tetrakis (triphenylphosphine) palladium (0) and 0.94 g of potassium carbonate in 3.40 g of H ₂ O are used. The resulting residue is adsorbed on silica gel and purified by chromatography (silica gel, hexane / acetone 8: 2).

0.42 g (66% of theory) of 5-furan-3-yl-2,3,3-trimethyl-3H-indole are obtained.

0.35 g of the 5-furan-3-yl-2,3,3-trimethyl-3H-indole thus obtained are alkylated according to variant 3 of general synthesis instructions C) with 0.35 g of triethyloxonium tetrafluoroborate in 5 ml of 1,2-dichloroethane , The product thus obtained is washed with ethyl acetate. Yield: 0.18 g (34% of theory) of 1-ethyl-5-furan-3-yl-2,3,3-trimethyl-3H-indolium tetrafluoroborate

Η NMR (Dg-DMSO): δ = 1.45 ppm (t, ³ J = 7 Hz, 3H); 1.57 ppm (s

6H); 2.82 ppm (s, 3H); 4.50 ppm (q, ³ J = 7 Hz, 2H); 7.11 ppm (s, 1H); 7.83 ppm (s, 1H); 7.90 ppm (d, ³ J ~ 9 Hz, 1 H); 8.00 ppm (d, ³ J ~ 9 Hz, 1H); 8.15 ppm (s, 1H); 8.35 ppm (s, 1H).

Example 1.22: 1-Ethyl-2,3,3-trimethyl-5- (2-thienyl) -3H-indolium tetrafluoroborate

The preparation is carried out in accordance with variant 2 of the general synthesis instructions A), 0.77 g of 5- (5,5-dimethyl- [1,3,2] dioxaborinan-2-yl) -2,3,3-trimethyl-3H- indole and 0.56 g of 2-bromo-thiophene in 10 ml of 1, 2-dimethoxyethane with 0.33 g of tetrakis (triphenylphosphine) palladium (0) and 0.94 g Potassium carbonate in 3.40 g H ₂ O can be used. The resulting one

Residue is adsorbed on silica gel and purified by chromatography

(Silica gel, hexane / acetone 8: 2).

0.35 g (51% of theory) of 5- (thiophene-2-yl) -2,3,3-trimethyl-3H-indole are obtained.

0.32 g of the 5- (thiophene-2-yl) -2,3,3-trimethyl-3H-indole obtained in this way are used in accordance with variant 3 of the general synthesis instructions C)

0.30 g of triethyloxonium tetrafluoroborate in 5 ml of 1, 2-dichloroethane alkylated.

The product thus obtained is washed with ethyl acetate.

Yield: 0.31 g (65% of theory) of 1-ethyl-2,3,3-trimethyl-5- (2-thienyl) -3H-indolium tetrafluoroborate

¹ H NMR (Dg-DMSO): δ = 1.46 ppm (t, ³ J = 7 Hz, 3H); 1.59 ppm (s

6H); 2.83 ppm (s, 3H); 4.50 ppm (q, ³ J = 7 Hz, 2H); 7.22 ppm (m, 1H);

7.68 ppm (m, 2H); 7.90 ppm (d, ³ J ~ 8 Hz, 1 H); 8.00 ppm (d, ³ J ~ 8 Hz,

1H); 8.19 ppm (s, 1H).

Examples 2.1 to 10.3: Hair dye

Component A1

Compound of the formula (I) / (Ia) quantitative data according to Table 1-9

Cetylstearyl alcohol 12 g

Lauryl ether sulfate, 28% aqueous solution 10 g

Ethanol 23 g

Water, fully desalinated to 100 g

The cetylstearyl alcohol is melted at 80 ° C. The lauryl ether sulfate is heated to 80 ° C with 95% of the water and melted Cetylstearyl alcohol added and stirred until a cream results. At room temperature, the compound of formula (I) / (Ia), with the ethanol and the remaining water added. The pH of the cream is optionally adjusted to the value given in Tables 1 to 9 with 20% aqueous monoethanolamine solution.

Component A2

Carbonyl compound / imine compound Quantity according to

Table 1-9 Cetylstearyl alcohol 12 g

Lauryl ether sulfate, 28% aqueous solution 10 g

Ethanol 23 g

Water, fully desalinated to 100 g

The cetylstearyl alcohol is melted at 80 ° C. The lauryl ether sulfate is heated to 80 ° C. with 95% of the water and added to the melted cetylstearyl alcohol and stirred until a cream is obtained. At room temperature the carbonyl compound / imine compound is added together with the ethanol and the remaining water. The pH of the cream is optionally adjusted to the value given in Tables 1 to 9 with 20% aqueous monoethanolamine solution.

Component A1 and component A2 are mixed together in a ratio of 1: 1. The measured pH of the ready-to-use agent thus obtained is referred to in Tables 1 to 9 as pH _m . The ready-to-use hair dye thus obtained is applied to the hair and evenly distributed with a brush. After an exposure time of 30 minutes at 40 ° C, the hair is treated with a Washed shampoo, then rinsed with lukewarm water and then dried.

The hair can be completely decolorized at any time (for example after several days or weeks) within 20 minutes at 40 ° C. with an acidic (pH = 5) 5% sodium sulfite solution (component B).

The dyeing and bleaching results are summarized in Tables 1 to 9 below.

The L * a * b * color measurement values given in the present examples were determined using a color measuring device from Minolta, type Chromameter II. Here, the L-value stands for the brightness (i.e. the lower the L-value, the greater the color intensity), while the a-value is a measure of the red component (i.e. the larger the a-value, the greater the red component is larger). The b-value is a measure of the blue component of the color, the more negative the b-value, the greater the blue component.

Unless stated otherwise, all percentages in the present application represent percentages by weight.

Table 1: Color Results No. Component A1); pH = 9.3 hue color measurement values component A2); pH = 4.5 after L a b staining / decolorization

2.1 A1) 5- (2,4-dimethoxyphenyl) -1, 2,3,3- untreated hair: +83.30; -0.48; +10.40 tetramethyI-3H-indole-1 -ium green-blue After staining: +44.16; +20.20; -12.55 tetrafluroborate: 1.14 g

A2) 3,5-Dimethoxy-4-hydroxy after the white benzaldehyde: 0.52 g decolorization pH _m = 8.2

2.2 A1) 5- (2,4-dimethoxyphenyl) -1, 2,3,3- untreated hair: +83.30; -0.48; +10.40 tetramethyl-3H-indole-1-ium red After staining: +51, 64; +35.83; 0.00 tetrafluroborate: 1.14 g

A2) 4-Hydroxy-3-methoxy after the white benzaldehyde: 0.44g decolorization

_P H _m = 8.1

Table 1: (continued) No. Component A1); pH = 9.3 hue color measurement values component A2); pH = 4.5 after L a b staining / decolorization

2.3 A1) 5- (2,4-dimethoxyphenyl) -1, 2,3,3- untreated hair: +83.30; - 0.48; +10.40 tetramethyl-3H-indoI-1 -ium-orange After staining: +69.55, +21, 52; +36.57 tetrafluroborate: 1, 14 g

A2) 3-Hydroxy-4-methoxy according to the white benzaldehyde: 0.44 g decolorization pH _m = 8.5

2.4 A1) 5- (2,4-dimethoxyphenyl) -1, 2,3,3- untreated hair: +83.30; -0.48; +10.40 tetramethyl-3H-indol-1-ium green After staining: +43.42; +0.46; -7.12 tetrafluroborate: 1.14 g

A2) 3,4,5-trihydroxybenzaldehyde: after the

0.50 g decolorization: white pH _m = 7.9

2.5 A1) 5- (2,4-dimethoxyphenyl) -1, 2,3,3- untreated hair: +83.30; -0.48; +10.40 tetramethyl-3H-indole-1-ium pink After staining: +66.20; +25.17; -2.63 tetrafluroborate: 1.14 g

A2) 4- (Dimethy! Amino) benzaIdehyde: after the

0.43 g decolorization: pale pink

_P H _m = 8.6

Table 2: Color Results No. Component A1); pH = 9.3 hue color measurement values component A2); pH = 4.5 after L a b staining / decolorization

3.1 A1) 5- (1, 3-benzodioxol-5-yl) -1, 2,3,3- untreated hair: +83.30; -0.48; +10.40 tetramethyl-3H-indole-1 -ium green-blue After staining: +45.21; +19.49; -13.48 tetrafluoroborate: 1, 10 g

A2) 3,5-Dimethoxy-4- after the hydroxybenzaldehyde: 0.52 g decolorization white pH _m = 7.8

3.2 A1) 5- (1, 3-benzodioxol-5-yl) -1, 2,3,3- untreated hair: +83.30; -0.48; +10.40 tetramethyl-3H-indoI-1-ium red After staining: +50.63; +35.31; -1.86 tetrafluoroborate: 1.10 g

A2) 4-hydroxy-3-methoxy after the benzaldehyde: 0.44 g decolorization white pH _m = 7.8

Table 2: (continued) No. Component A1); pH = 9.3 hue color measurement values component A2); pH = 4.5 after L a b staining / decolorization

3.3 A1) 5- (1, 3-benzodioxol-5-yl) -1, 2,3,3- untreated hair: +83.30; -0.48; +10.40 tetramethyl-3H-indole-1 -ium orange After staining: +69.73; +21, 11; +34.32 tetrafluoroborate: 1, 10 g

A2) 3-hydroxy-4-methoxy after the benzaldehyde: 0.44 g decolorization white pH _m = 8.4

3.4 A1) 5- (1, 3-benzodioxol-5-yl) -1, 2,3,3- untreated hair: +83.30; -0.48; +10.40 tetramethyl-3H-indol-1-ium green After staining: +43.78; -1.37; -8.67 tetrafluoroborate: 1.10 g

A2) 3,4,5-trihydroxybenzaldehyde: after the

0.50 g decolorization: pale green pH _m = 7.2

3.5 A1) 5- (1, 3-benzodioxol-5-yl) -1, 2,3,3- untreated hair: +83.30; -0.48; +10.40 tetramethyl-3H-indole-1 -ium pink After staining: +61, 70; +28.88; -6.46 tetrafluoroborate: 1, 10 g A2) 4- (dimethylamino) benzaldehyde: after the 0.43 g decolorization: pale pink pH _m = 8.3

Table 3: Color Results No. Component A1); pH = 8.3 hue color measurement values component A2); pH = 4.5 after L a b staining / decolorization

4.1 A1) 1, 2,3,3-tetramethyl-5 - (- 2 untreated hair: +83.30; -0.48; +10.40 trifluoromethyl) phenyl) -3H-indole-1 -ium violet After dyeing: +50.78; +25.19; -8.79 tetrafluroborate: 1.17 g

A2) 3,5-Dimethoxy-4- after the hydroxybenzaldehyde: 0.52 g decolorization white pH _m = 7.3

4.2 A1) 1, 2,3,3-tetramethyl-5 - (- 2 untreated hair: +83.30; -0.48; +10.40 trifluoromethyl) phenyl) -3H-indole-1 -ium- red After dyeing: +58.54; +38.06; +7.11 tetrafluor roborate: 1.17 g

A2) 4-hydroxy-3-methoxy after the benzaldehyde: 0.44 g decolorization white pH _m = 7.2

Table 3: (continued) No. Component A1); pH = 8.3 hue color measurement values component A2); pH = 4.5 after L a staining / decolorization

4.3 A1) 1, 2,3,3-tetramethyl-5 - (- 2 untreated hair: +83.30; -0.48; +10.40 trifluoromethyl) phenyl) -3H-indole-1 -ium-orange After dyeing: +77.82; +12.45; +33.30 tetrafluroborate: 1.17 g

A2) 3-Hydroxy-4-methoxy according to the white benzaldehyde: 0.44 g decolorization pH _m = 7.3

4.4 A1) 1, 2,3,3-tetramethyl-5 - (- 2 untreated hair: +83.30; -0.48; +10.40 trifluoromethyl) phenyI) -3H-indole-1 -ium- green After dyeing: +49.50; +1, 16; -5.41 tetrafluroborate: 1.17 g

A2) 3,4,5-trihydroxybenzaldehyde: after the

0.50 g decolorization: pale yellow pH _m = 7.1

Table 3: (continued) No. Component A1); pH = 8.3 hue color measurement values component A2); pH = 4.5 after L a b staining / decolorization

4.5 A1) 1, 2,3,3-tetramethyl-5 - (- 2 untreated hair: +83.30; -0.48; +10.40 trifluoromethyl) phenyl) -3H-indole-1-ium pink After dyeing: +65.31; +37.51; -2.58 tetrafluroborate: 1.17 g after A2) 4- (dimethylamino) benzaldehyde: decolorization: pale pink 0.43 g pH _m = 7.2

Table 4: Color Results No. Component A1); pH = 7.7 hue color measurement values component A2); pH = 4.5 after L a b staining / decolorization

5.1 A1) 1, 2,3,3-tetramethyl-5- (thiophene-untreated hair: +83.30; -0.48; +10.40 3-yI) -3H-indolium iodide: 1.10 g violet after dyeing: +28.95; +31.75; -9.93 A2) 3,5-dimethoxy-4-hydroxybenzaldehyde: 0.52 g after pH _m = 7.5 decolorization: white

5.2 A1) 1, 2,3,3-tetramethyl-5- (thiophene-untreated hair: +83.30; -0.48; +10.40

3-yl) -3H-indolium iodide: 1, 10 g red After staining: +40.66; +46.78; +11, 39

A2) 4-Hydroxy-3-methoxybenzaldehyde: 0.44 g after pH _m = 7.7 Decolorization: white

Table 4: (continued) No. Component A1); pH = 7.7 hue color measurement values component A2); pH = 4.5 after L a b staining / decolorization

5.3 A1) 1, 2,3,3-tetramethyl-5- (thiophene-untreated hair: +83.30; -0.48; +10.40 3-yl) -3H-indolium iodide: 1.10 g orange after coloring: +64.49 +19.44 +56.13

A2) 3-Hydroxy-4-methoxybenzaldehyde: 0.44 g after pH _m = 7.6 Decolorization: white

5.4 A1) 1, 2,3,3-tetramethyl-5- (thiophene-untreated hair: +83.30; -0.48; +10.40 3-yl) -3H-indolium iodide: 1, 10 g green after dyeing: +32.98; +9.90; -11, 34

A2) 3,4,5-trihydroxybenzaldehyde:

0.50 g after pH _m = 7.5 decolorization: white

5.5 A1) 1, 2,3,3-tetramethyl-5- (thiophene-untreated hair: +83.30; -0.48; +10.40 3-yl) -3H-indolium iodide: 1.10 g pink after dyeing: +57.41; +36.87; -8.02 A2) 4- (dimethylamino) benzaldehyde: 0.43 g after pH _m = 7.5 decolorization: white

Table 5: Color Results No. Component A1); pH = 3.6 hue color measurement values component A2); pH = 9.5 after a b staining / decolorization

6.1 A1) 5-phenyl-1, 2,2,3-tetramethyl- untreated hair: +83.30; -0.48; +10.40 1 (3H) -indolium tetrafluoroborate: blue After staining: +28.29; +33.60; -20.98 3.88 g

A2) 3,5-Dimethoxy-4-hydroxy after the benzaldehyde: 2.10 g decolorization: white pH _m = 8.1

6.2 A1) 5-phenyl-1, 2,2,3-tetramethyl- untreated hair: +83.30; -0.48; +10.40 1 (3H) -indolium tetrafluoroborate: red After staining: +33.79; +51.63; -4.12 3.88 g

A2) 4-hydroxy-3-methoxy after the benzaldehyde: 1.75 g decolorization white pH _m = 8.2

Table 5: (continued) No. Component A1); pH = 3.6 hue color measurement values component A2); pH = 9.5 after L a b staining / decolorization

6.3 A1) 5-phenyl-1, 2,2,3-tetramethyl- untreated hair: +83.30; -0.48; +10.40 1 (3H) -indolium tetrafluoroborate: orange After staining: +64.24; +24.12; +47.90 3.88 g

A2) 3-hydroxy-4-methoxy after the benzaldehyde: 1.75 g decolorization: white pH _m = 8.9

6.4 A1) 5-phenyl-1, 2,2,3-tetramethyl untreated hair: +83.30; -0.48; +10.40 1 (3H) -indolium tetrafluoroborate: intense - after n staining:. +24.68; +22.92; -13.41 3.88 g burgundy

A2) 3,4-dihydroxybenzaldehyde:

1.59 g after pH _m = 8.3 Decolorization: white

Table 5: (continued) No. Component A1); pH = 3.6 hue color measurement values

Component A2); pH = 9.5 according to L a b

Coloring/

discoloration

6.5 A1) 5-phenyl-1, 2,2,3-tetramethyl- untreated hair: +83.30; -0.48; +10.40

1 (3H) -indolium tetrafluoroborate: intense - after staining: +42.56; +55.06; -16.87

3.88 g pink

A2) 4- (Dimethylamino) benzaldehyde:

1.72 g after pH _m = 8.9 decolorization: light pink

Table 6: Color Results No. Component A1); pH = 3.2 hue color measurement values component A2); pH = 9.5 after L a b staining / decolorization

7.1 A1) 1,2,3,3-tetramethyl-5-p-tolyl-3H untreated hair: +83.30; -0.48; +10.40 indolium tetrafluoroborate: 4.04 g green After staining: +35.40; +25.32; -17.35 A2) 3,5-dimethoxy-4-hydroxybenzaldehyde: 2.10 g after pH _m = 7.6 Decolorization: white

7.2 A1) 1, 2,3,3-tetramethy! -5-p-toIyl-3H- untreated hair: +83.30; -0.48; +10.40 indolium tetrafluoroborate: 4.04 g red After staining: +42.05; +43.01; -1.98 A2) 4-hydroxy-3-methoxybenzaldehyde: 1.75 g after pH _m = 7.1 Decolorization: white

Table 6: (continued) No. Component A1); pH = 3.2 hue color measurement values component A2); pH = 9.5 after L a b staining / decolorization

7.3 A1) 1, 2,3,3-tetramethyl-5-p-tolyl-3H untreated hair: +83.30; -0.48; +10.40 indolium tetrafluoroborate: 4.04 g orange After staining: +67.60; +20.74; -37.67 A2) 3-hydroxy-4-methoxybenzaldehyde: 1.75 g after pH _m = 8.4 decolorization: white

7.4 A1) 1, 2,3,3-tetramethyl-5-p-tolyl-3H untreated hair: +83.30; -0.48; +10.40 indolium tetrafluoroborate: 4.04 g wine red After dyeing: +33.64; +19.55; -9.90 A2) 3,4-dihydroxybenzaldehyde:

1.59 g after pH _m = 7.4 Decolorization: light pink

Table 6: (continued)

Component A1); pH = 3.2 hue color measurement values component A2); pH = 9.5 after L a b staining / decolorization

7.5 A1) 1, 2,3,3-tetramethyl-5-p-tolyl-3H- intensive- untreated hair: +83.30; -0.48; +10.40 indolium tetrafluoroborate: 4.04 g pink After staining: +41.30; +53.23; -19.57

A2) 4- (Dimethylamino) benzaldehyde:

1.72 g after pH _m = 8.0 Decolorization: light pink

Table 7: Color Results No. Component A1); pH = 3.2 hue color measurement values component A2); pH = 9.5 after L a b staining / decolorization

8.1 A1) 1, 2,3,3-tetramethyl-5 untreated hair: +83.30; -0.48; +10.40 naphthalene-1-yl-3H-indo! Ium; blue after dyeing: +36.90; +29.93; -21.87 tetrafluoroborate: 2.23 g

A2) 3,5-Dimethoxy-4- after the white hydroxybenzaldehyde: 2.10 g decolorization pH _m = 7.3

8.2 A1) 1, 2,3,3-tetramethyl-5 untreated hair: +83.30; -0.48; +10.40 naphthalene-1-yl-3H-indolium; red after dyeing: +46.06; +42.94; -6.26 tetrafluoroborate: 2.23 g

A2) 4-hydroxy-3-methoxy according to the white benzaldehyde: 1.75 g decolorization _P H _m = 7.1

Table 7: (continued) No. Component A1); pH = 3.2 hue color measurement values component A2); pH = 9.5 after L a b staining / decolorization

8.3 A1) 1, 2,3,3-tetramethyl-5 untreated hair: +83.30; -0.48; +10.40 naphthalene-1-yl-3H-indo! Ium; violet after dyeing: +39.36; +15.86; -12.47 tetrafluoroborate: 2.23 g

A2) 3,4, -Dihydroxybenzaldehyde: after the

1.59 g decolorization: white pH _m = 7.4

8.4 A1) 1, 2,3,3-tetramethyl-5 untreated hair: +83.30; -0.48; +10.40 naphthalene-1-yl-3H-indolium; pink after dyeing: +51, 44; +44.31; -16.38 tetrafluoroborate: 2.23 g

A2) 4- (DimethyIamino) benzaldehyde: after 1.72 g decolorization: white pH _m = 8.3

Table 8: Color Results No. Component A1); pH = 4.0 hue color measurement values component A2); pH = 9.5 after L a b staining / decolorization

9.1 A1) 1-ethyl-2,3,3-trimethyl-5- (4- untreated hair 63.30; -0.48; +10.40 methylsulfanyl-phenyl) -3H-indolium-green-blue after dyeing : 47.81; +15.05; -12.33 tetrafluoroborate: 2.28 g

A2) Syringaldehyde: 1.05 g after the yellow pH _m = 8.0 decolorization

Table 8: (continued) No. Component A1); pH = 3.2 hue color measurement values component A2); pH = 9.5 after L a b staining / decolorization

9.2 A1) 1'-acetyl-1-ethyl-2,3,3-trimethyl-untreated hair 63.30; -0.48; +10.40

2 ', 3'-dihydro-3H, 1Η- [5,5'] biindolyl-1-blue After staining: 32.60; +14.44; -17.04 ium tetrafluoroborate: 2.50 g A2) Syringaldehyde: 1.05 g after the yellow pH _m = 7.9 decolorization

Table 8: (continued) No. Component A1); pH = 4.0 hue color measurement values component A2); pH = 9.5 after L a b staining / decolorization

9.3 A1) 1-ethyl-2,3,3-trimethyl-5 untreated hair 63.30; -0.48; +10.40 naphthalene-2-yl-3H-indolium green After staining: 54.74; +8.51; -5.53 tetrafluoroborate: 2.31 g A2) Syringaldehyde: 1.05 g after the yellow pH _m = 7.7 decolorization

Table 8: (continued) No. Component A1); pH = 2.3 hue color measurement values component A2); pH = 9.5 after a b staining / decolorization

9.4 A1) 1-ethyl-5- (6-hydroxy-naphthalene-untreated hair: 63.30; -0.48; +10.40

2-yl) -2,3,3-trimethyl-3H-indolium green After staining: 58.78; +3.75; -0.52 tetra uoroborate: 2.40 g

A2) Syringaldehyde: 1.05 g after the yellow pH _m = 7.2 decolorization

Table 8: (continued) No. Component A1); pH = 3.8 hue color measurement values component A2); pH = 9.5 after L a b staining / decolorization

9.5 A1) 5-anthracen-9-yl-1-ethyl-2,3,3- untreated hair: 63.30; -0.48; +10.40 trimethyl-3H-indolium green After staining: 56.27; +13.39; -6.08 tetrafluoroborate: 2.60 g

A2) Syringaldehyde: 1.05 g after the slightly yellow pH _m = 7.6 decolorization

Table 8: (continued) No. Component A1); pH = 3.1 hue color measurement values component A2); pH = 9.5 after L a b staining / decolorization

9.6 A1) 5- (3,5-dimethyl-phenyl) -1-ethyl- untreated hair 63.30; -0.48; +10.40

2,3,3-trimethyl-3H-indolium blue After staining: 45.89; +18.46; -17.00 tetrafluoroborate: 2.18 g

A2) Syringaldehyde: 1.05 g after the white pH _m = 7.8 decolorization

9.7 A1) 1-ethyl-5- (4-methoxy-2-methyl- untreated hair: 63.30; -0.48; +10.40 phenyl) -2,3,3-trimethyl-3H-indolium-blue After dyeing: 40.85; +26.18; -17.64 tetrafluoroborate: 2.27 g

A2) Syringaldehyde: 1.05 g after the yellow pH _m = 8.2 decolorization

9.8 A1) 5-benzo [b] thiophene-3-yl-1-ethyl- untreated hair: 63.30; -0.48; +10.40

2,3,3-trimethyl-3H-indolium-blue-green After staining: 48.66; +16.20; -14.90 tetrafluoroborate: 2.34 g

A2) Syringaldehyde: 1.05 g after the yellow pH _m = 8.0 decolorization

Table 9: Color Results No. Component A1); pH = 4.1 hue color measurement values component A2); pH = 9.4 after L a b staining / decolorization

10.1 A1) 1-ethyl-5- (1-ethyl-3-pyridiniumyl) - untreated hair 82.17; +0.55; +11, 38

2,3,3-trimethyl-3H-indolium green-blue After staining: 33.68; +22.38; -6.94 ditetrafluoroborate: 2.43 g A2) Syringaldehyde: 1.05 g after the yellow pH _m = 8.0 decolorization

Table 9: (continued) No. Component A1); pH = 2.8 hue color measurement values component A2); pH = 9.4 after L a b staining / decolorization

10.2 A1) 1-ethyl-5-furan-3-yl-2,3,3- untreated hair 82,17; +0.55; +11.38 trimethyl-3H-indolium tetrafluoroborate: green-blue After staining: 39.69; +22.66; -17.58 2.34 g

A2) Syringaldehyde: 1.05 g after the white pH _m = 7.6 decolorization

Table 9: (continued) No. Component A1); pH = 3.6 hue color measurement values component A2); pH = 9.4 after L a b staining / decolorization

10.3 A1) 1-Ethyl-2,3,3-trimethyl-5- (2- untreated hair 82.17; +0.55; +11, 38 thienyl) -3H-indo! Ium tetrafluoroborate: blue After dyeing: 40.05; +19.91; -22.64 2.05 g

A2) Syringaldehyde: 1.05 g after the white pH _m = 7.5 decolorization

Claims

Patent claims

1. Agent for coloring keratin fibers (A), which is produced by mixing two components (A1) and (A2) and is characterized in that component (A1) has at least one compound of the formula (I) and / or (Ia) contains

(I) (la) where:

R1 is equal to a straight-chain or branched C1-C8 alkyl group, a C1 to C8 monohydroxyalkyl group, a C2-C8 polyhydroxyalkyl group, a C1-C8 alkoxy (C1-C8) alkyl group, a thio (C1- C8) alkyl group, a - (CH ₂ ) _m -X- (CH ₂ ) _n -Y- (CH ₂ ) _p R ^a group, a - (CH ₂ ) _n -XR ^a group, a - (CH ₂ ) _m -Y- (CH ₂ ) _n -X- (CH ₂ ) _p -R ^a group, one - (CH ₂ ) _m -CO- (CH ₂ ) _p -XR ^a group, one - (CH ₂ ) _p -R ^a group, a - (CH ₂ ) _m -X- (CH ₂ ) _p -CO-YR ^a group or one of the following 3 groups

where X and Y are independently an oxygen atom, a sulfur atom or an NR group, R ^a and R ^{b are} independently a hydrogen atom, one optionally are substituted aromatic carbocycle or heterocycle or a straight or branched C1-C8 alkyl group; m and n are independently an integer from 1 to 6 and p is an integer from 0 to 6; R2 is a straight chain C1-C6 alkyl group; R2 'is a CH-R' group with R 'is hydrogen or a C1-C5 alkyl group;

R3 and R4 independently of one another are equal to a straight-chain or branched C1-C4-alkyl group, a - (CH ₂ ) _n -R ^c group, a - (CH ₂ ) _m -CHR ^c -X- (CH ₂ ) _n -R ^c group, a - (CH ₂ ) _n -CO-R ^c group, a - (CH ₂ ) _n -CO-XR ^c group, a - (CH ₂ ) _n -CN group, a - (CH ₂ ) _n -CH = C (CH ₃ ) ₂ group, a - (CH ₂ ) _m -X-CHR ^c - (CH ₂ ) _n -R ^c group or a - (CH ₂ ) _n CH = CH - Group where X is an oxygen atom, a sulfur atom or an NR ^b group, m and n are independently an integer from 1 to 6 and R ° is a hydrogen atom, an optionally substituted aromatic carbocycle or heterocycle or a straight-chain or is C1-C6 branched alkyl group; with the proviso that the radicals R3 and R4, also connected via a (CH ₂ ) _n group (with n equal to an integer from 1 to 3), can form a spiro compound together with the 3H carbon;

R5, R6 and R7 are independently a hydrogen atom, a straight-chain or branched C1-C4-alkyl group, a C1-C4-hydroxyalkyl group, a hydroxy group, a methoxy group, a benzyl group, a halogen atom, a nitro group, a nitroso group, a cyano group, a trifluoromethyl group, a -CHO group, a -COR ^d group, a -COOH group, a -CO ₂ R ^d group, a -OCOR ^d group, a -OCH ₂ aryl group, one -S0 ₂ NH ₂ group, an -NH ₂ group, an -NH ₃ ⁺ group, an -NHR ^d group, an -NH ₂ R ^{d +} group, an -N (R ^d ) ₂ group , a -N (R ^d ) ₃ ⁺ group, an -NHCOR ^d group, an -NHCOOR ^d group, a -CH ₂ NH ₂ group, a -CH ₂ NHR ^d group, a -CH ₂ N (R ^d ) ₂ group, a -CO ₂ CF ₃ group, a -PO (OR ^d ) ₂ group, an -SO ₂ CHF ₂ group, an -SO ₂ CF ₃ group, an -SO ₂ R ^d group or an -SR ^d group, where R ^d is a hydrogen atom, an optionally substituted aromatic carbocycle or heterocycle or a C1-C6 alkyl group, with the proviso that the adjacent radicals R6 and R7 also together with the Carbon atoms of the aromatic nucleus can form a 5- or 6-membered alicyclic or aromatic ring which can optionally contain one or more sulfur atoms, nitrogen atoms and / or oxygen atoms; and

(IX) (X) (XI) (XU)

wherein R8, R9, R10, R11, R12, R13, R14, R15, R16, R17, R18 and R19 independently of one another are equal to a hydrogen atom, a straight-chain or branched C1-C4-alkyl group, a C1-C4-hydroxyalkyl group, one Hydroxyl group, a methoxy group, a benzyl group, a halogen atom, a nitro group, a nitroso group, a cyano group, a trifluoromethyl group, a -CHO group, a -COR ^e group, a -COOH group, a -CO ₂ R ^e group, a -OCOR ^e group, an -OCH ₂ aryl group, an -SO ₂ NH ₂ group, an -NH ₂ group, a - (NH ₃ ) ⁺ group, an -NHR ^e group, a - (NH ₂ R ^e ) ⁺ Group, an -N (R ^e ) ₂ group, a - (N (R ^e ) ₃ ) ⁺ group, an -NHCOR ^β group, an -NHCOOR ^e group, a -CH ₂ NH ₂ group , a -CH ₂ NHR ^e group, a -CH ₂ N (R ^e ) ₂ group, a -CO ₂ CF ₃ group, a -PO (OR ^e ) ₂ group, an -SO ₂ CHF ₂ - Group, an -SO ₂ CF ₃ group, an -SO ₂ R ^e group or an -SR ^Θ group, with R ^e being a hydrogen atom, an optionally substituted aromatic carbocycle or heterocycle or a C1-C6 alkyl group , with the proviso that two adjacent residues R8 to R19 also together with the carbon atoms of the aromatis chen core can form a 5- or 6-membered alicyclic or aromatic ring which may optionally contain one or more sulfur atoms, nitrogen atoms and / or oxygen atoms; and

Z is sulfur, nitrogen, oxygen or an N ⁽⁺⁾ -R ^f group; Q is sulfur, nitrogen, oxygen or an NR ^f group; R ^f is hydrogen, a CC ₆ -alkyl group, a C2-C4-hydroxyalkyl group, a phenyl group, an acetyl group or sulfonyl group. A ^" is equal to the anion of an organic or inorganic acid; and component (A2) contains at least one carbonyl compound and / or imine compound.

2. Composition according to claim 1, characterized in that the compound of formula (I) / (Ia) is selected from 5- (2,4-dimethoxy phenyl) -1,3,3-trimethyl-2-methylene-indoline, 5- (1,3-benzodioxol-5-yl) -1,3,3-trimethyl-2-methylene-indoline, 5- (2- (trifluoromethyl) phenyl) -1,3,3-triethyl-2-methylene-indoline, 5- (phenyl) -1, 3,3-trimethyl-2-methylene-indoline, 5- (p-tolyl) - 1,3,3-trimethyl-2-methylene-indoline, 5- (naphthalen-1-yl) -1,3,3-trimethyl-2-methylene-indoline, 5- (4-methylsulfanyl-phenyl) -1, 3,3-trimethyl-2-methylene-indoline, 5- (4-hydroxyphenyl) -1, 3,3-trimethyl-2-methylene-indoline, 5- (naphthalen-2-yl) -1, 3,3- trimethyl-2-methylene-indoline, 5- (2-hydroxy-naphthalene-6-yl) -1, 3,3-trimethyl-2-methylene-indoline, 5- (anthracen-9-yl) - 1, 3, 3-trimethyl-2-methylene-indoline, 5- (3,5-dimethyl-phenyl) -1, 3,3-trimethyl-2-methylene-indoline, 5- (acenaphthen-5-yl) -1, 3, 3-trimethyl-2-methylene indoline, 5- (4-methoxy-2-methylphenyl) -1, 3,3-trimethyl-2-methylene indoline, 5- (biphenyl-4-yl) -1, 3,3-trimethyl-2-methylene-indoline, 5- (benzo [b] thiophene-3-yl) -1-ethyl, 3,3-dimethyl-2-methylene-indoline, 1-ethyl-3- ( 1-ethyl-3,3-dimethyl-2-methylene-2,3-dihyd ro-1 H-indol-5-yl) pyridinium tetrafluoroborate, 5- (furan-3-yl) -1-ethyl-3,3-dimethyl-2-methylene-indoline, 5- (thiophene-3-yl) - 1, 3,3-trimethyl-2-methylene-indoline, 5- (thiophene-2-yl) -1 - ethyl-3,3-dimethyl-2-methylene-indoline, and 1 - (1 '.S' ^ '-Trimethyl ^' - methylene-2,3,2 ', 3'-tetrahydro-1 Η- [5,5'] biindolyl-1 -yl) -ethanone and their salts.

3. Composition according to claim 1, characterized in that the carbonyl compound / imine compound is selected from 4-hydroxy-3-methoxy-benzaldehyde, 3-hydroxy-4-methoxy-benzaldehyde, 3,4-dihydroxy-benzaldehyde, 4-hydroxybenzaldehyde, 3,5-dimethoxy-4-hydroxy-benzaldehyde, 4-dimethylaminobenzaldehyde, 4-methyl-5-imidazole-carboxaldehyde, 4-dimethylamino-cinnamaldehyde, 4-hydroxy-2-methoxy-benzaldehyde, 3,5-dimethyl-4- hydroxybenzaldehyde, 4-dimethylamino-2- methoxybenzaldehyde, 2-hydroxybenzaldehyde, 4-hydroxy-1-naphthaldehyde, 4-methoxy-1-naphthaldehyde, 4-dimethylamino-1-naphthaldehyde, 4'-hydroxy-biphenyl-1-carbaldehyde, 2-hydroxy-3-methoxybenzaldehyde, 2 , 4-dihydroxybenzaldehyde, 3,4-dihydroxybenzaldehyde, 2,5-dihydroxybenzaldehyde, 2,3,4-trihydroxybenzaldehyde, 3,4,5-trihydroxybenzaldehyde, 2,4,6-trihydroxybenzaldehyde, 2,4-dimethoxybenzaldehyde , 2,3-dimethoxybenzaldehyde, 2,5-dimethoxybenzaldehyde, 3,5-dimethoxybenzaldehyde, 3,4-dimethoxybenzaldehyde, indole-3-carbaldehyde, benzene-1, 4-dicarbaldehyde, 4-ethoxybenzaldehyde, 2 -Methyl-1, 4-naphthoquinone, 4-carboxybenzaldehyde, 4-hydroxy-3-methoxycinnamaldehyde, 3,5-dimethoxy-4-hydroxycinnamaldehyde, 3-methoxy-4- (1-pyrrolidinyl) benzaldehyde, 4 -Diethylamino-3-methoxybenzaldehyde, 1,2-phthalaldehyde, pyrrole-2-aldehyde, thiophene-2-aldehyde, thiophene-3-aldehyde, chromone-3-carboxaldehyde, 6-methyl-4-oxo-1 (4H) - benzopyran-3-carbaldehyde, N-methylpyrrole-2-aldehyde, 5-methyl-furfural, 6-hydroxychromene-3-carbox aldehyde, 6-methylindole-3-carboxaldehyde, 4-dibutylamino-benzaldehyde, N-ethylcarbazole-3-aldehyde, 4-diethylamino-2-hydroxybenzaldehyde, 3,4-dimethoxy-5-hydroxybenzaldehyde, 5- (4th - (Diethylamino) phenyl) -2,4-pentadienal, 2,3-thiophene dicarboxaldehyde, 2,5-thiophene dicarboxaldehyde, 2-methoxy-1-naphthaldehyde, 3-ethoxy-4-hydroxybenzaldehyde, 2-nitrobenzaldehyde, 3-nitro - benzaldehyde and 4-nitrobenzaldehyde, 4 - (((2-hydroxyethyl) imino) methyl) -2-methoxyphenol, 5 - (((2-hydroxyethyl) imino) methyl) -2-methoxyphenol, 2,6-dimethoxy-4 - ((((2-Hydroxyethyl) imino) methyl) phenol, 4 - (((2-hydroxyethyl) imino) methyl) phenol, 1, 2-dihydroxy-4 - (((2-hydroxyethyl) imino) methyl) ) benzene, N, N-dimethyl-4 - (((2-hydroxyethyl) imino) methyl) aniline, 1, 2-dihydroxy-3 - (((2-hydroxyethyl) imino) methyl) benzene, 4 - (( (3-hydroxypropyl) imino) methyl) phenol, 2,6-dimethoxy-4 - (((3-hydroxypropyl) imino) - methyl) phenol, 4 - (((2,3-dihydroxypropyl) imino) methyl) phenol, 2,6-Dimethoxy-4 - (((2,3-dihydroxypropyl) imino) methyl) phenol, 2 - [(4-hydroxybenzylidene) amino] propane-1,3-diol, 2 - [(4th -Hydroxy-3,5-dimethoxy-benzylidene) -amino] -propane-1,3-diol, 4 - (((2-hydroxy-2-henyl-ethyl) imino) methyl) phenol, 2,6-dimethoxy-4 - (((1-phenyl-2-hydroxyethyl) imino) methyl) phenol, 4 - (((2-hydroxyphenyl) imino) methyl) phenol, 2,6-dimethoxy-4 - (((2-hydroxyphenyl) imino ) methyl) phenol, 5-guanidino-2- [(4-hydroxybenzylidene) amino] pentanoic acid, 2 - [(4-dimethylamino-naphthalene-1-ylmethylene) amino] ethanol, 5-guanidino-2 - [(4-hydroxy-3,5-dimethoxybenzylidene) amino] pentanoic acid, 2 - [(4-hydroxy-3,5-dimethoxybenzylidene) amino] -3- (3H-imidazole-4- yl) propanoic acid, 2 - [(4-hydroxybenzylidene) amino] -3- (3 / - / - imidazol-4-yl) propanoic acid, 2 - [(4-hydroxy-3,5-dimethoxy- benzylidene) amino] -3- (1 / - / - indol-3-yl) propanoic acid, 2 - [(4-hydroxybenzylidene) amino] -3- (1H-indol-3-yl) propanoic acid , 2 - (((2-Hydroxyethyl) imino) methyl) phenol, 1, 2-dihydroxy-3 - (((2-hydroxyethyl) imino) methyl) benzene, 1, 2,3-trihyd roxy-4 - (((2-hydroxyethyl) imino) methyl) benzene, 1, 2,3,4-tetrahydroxy-5 - (((2-hydroxyethyl) imino) methyl) benzene and 1, 2,4-trihydroxy-4 - (((2-hydroxyethyl) imino) methyl) benzene.

4. Composition according to one of claims 1 to 3, characterized in that the ready-to-use preparation (A) has a pH of 3 to 11.

5. Composition according to one of claims 1 to 4, characterized in that the compound of formula (l) / (la) in component (A1) in a total amount of 0.02 to 20 percent by weight and the carbonyl compound / lminverbindung in component (A2) is contained in a total amount of 0.02 to 20 percent by weight.

6. Composition according to one of claims 1 to 5, characterized in that it is the compound of formula (l) / (la) and the carbonyl compound / imine compound, based on the ready-to-use preparation, in each case in a total amount of 0.01 to 10 percent by weight contains.

7. Agent according to one of claims 1 to 6, characterized in that the ready-to-use agent (A) and the components (A1) and (A2) are each in the form of a solution, an emulsion, a foam, a cream or a gel.

8. Composition according to one of claims 1 to 7, characterized in that component (A1) and / or (A2) additionally contains at least one substantive dye from the group of acidic or basic dyes, nitro dyes, azo dyes, quinone dyes and triphenylmethane dyes.

9. Composition according to one of claims 1 to 8, characterized in that the component (A1) and / or (A2) consists of several individual components.

10. A process for the temporary coloring of keratin fibers, in which the keratin fiber is dyed with an agent according to one of claims 1 to 9 and the dyeing thus obtained is removed again at any later time by a sulfite-containing preparation (decolorizing agent).

11. The method according to claim 10, characterized in that the decolorizing agent is allowed to act on the keratin fiber for 5 to 60 minutes at a temperature of 20 to 50 ° C.

12. Process for the preparation of 5-aryl-1,3,3-trimethyl-2-methylene-indoline derivatives of the formula (I) or their salts of the formula (Ia),

(I) da) characterized in that in a first step by reacting a 5-halogeno-2,3,3-trimethyl-3H-indole derivative of the formula (II) with an arylboronic acid derivative of the formula (III) in the presence of a suitable catalyst and / or a suitable organic or inorganic base the 5-aryl-2,3,3-trimethyl-3H-indole derivative of the formula (VII) is prepared, and then in a second step in an apolar aprotic or polar Protic or polar aprotic solvent 1 mole of the 5-aryl-2,3,3-trimethyl-3H-indole derivative of the formula (VII) with 1 to 50 moles of a compound of the formula R1-A at a temperature of 20 to 180 ° C is reacted for 1 to 44 hours;

where: R1 is equal to a straight-chain or branched C1-C8 alkyl group, a C1 to C8 monohydroxyalkyl group, a C2-C8 polyhydroxyalkyl group, a C1-C8 alkoxy (C1-C8) alkyl group, a thio (C1- C8) alkyl group, a - (CH ₂ ) _m -X- (CH ₂ ) _n -Y- (CH ₂ ) _p R ^a group, a - (CH ₂ ) _n -XR ^a group, a - (CH ₂ ) _m -Y- (CH ₂ ) _n -X- (CH ₂ ) _p -R ^a group, one - (CH ₂ ) _m -CO- (CH ₂ ) _p -XR ^a group, one - (CH ₂ ) _p -R ^a group, a - (CH ₂ ) _m -X- (CH ₂ ) _p -CO-YR ^a group or one of the following 3 groups

R2 is a straight chain C1-C6 alkyl group;

R2 'is a CH-R' group with R 'being hydrogen or one

C1-C5 alkyl group;

R3 and R4 are, independently of one another, equal to a straight-chain or branched C1-C4-alkyl group, a - (CH ₂ ) _n -R ° group, one

- (CH ₂ ) _m -CHR ^c -X- (CH ₂ ) _n -R ^c group, one - (CH ₂ ) _n -CO-R ^c group, one

- (CH ₂ ) _n -CO-XR ^c group, one - (CH ₂ ) _n -CN group, one

- (CH ₂ ) _n -CH = C (CH ₃ ) ₂ group, a - (CH ₂ ) _m -X-CHR ^c - (CH ₂ ) _n -R ^c group or a - (CH ₂ ) _n CH = CH group, where X is an oxygen atom, a sulfur atom or an NR ^b group, m and n are independently an integer from 1 to 6 and R ^{c is the} same is a hydrogen atom, an optionally substituted aromatic carbocycle or heterocycle or a straight-chain or branched C1-C6 alkyl group; with the proviso that the radicals R3 and R4, also connected via a (CH ₂ ) _n group (with n equal to an integer from 1 to 3), can form a spiro compound together with the 3H carbon;

R5, R6 and R7 are independently a hydrogen atom, a straight-chain or branched C1-C4-alkyl group, a C1-C4-hydroxyalkyl group, a hydroxy group, a methoxy group, a benzyl group, a halogen atom, a nitro group, a nitroso group, a cyano group, a trifluoromethyl group, a -CHO group, a -COR ^d group, a -COOH group, a -CO ₂ R ^d group, a -OCOR ^d group, a -OCH ₂ aryl group, a -SO ₂ NH ₂ group, an -NH ₂ group, an -NH ₃ ⁺ group, an -NHR ^d group, an -NH ₂ R ^{d +} group, an -N (R ^d ) ₂ group, an - N (R ^d ) ₃ ⁺ group, an -NHCOR ^d group, an -NHCOOR ^d group, a -CH ₂ NH ₂ group, a -CH ₂ NHR ^d group, a -CH ₂ N (R ^d ) ₂ group, a -CO ₂ CF ₃ group, a -PO (OR ^d ) ₂ group, an -SO ₂ CHF ₂ group, an -SO ₂ CF ₃ group, an -SO ₂ R ^d - Group or an -SR ^d group, where R ^d is a hydrogen atom, an optionally substituted is aromatic carbocycle or heterocycle or a C1-C6-alkyl group, with the proviso that the adjacent radicals R6 and R7 together with the carbon atoms of the aromatic nucleus can also form a 5- or β-membered alicyclic or aromatic ring, which optionally has one or more May contain sulfur atoms, nitrogen atoms and / or oxygen atoms; and Aryl is equal to a substituted pyrimidyl group, a cyclic radical of the formula (IX) or a heterocyclic radical of the formula (X) or (XI) or (XII).

wherein R8, R9, R10, R11, R12, R13, R14, R15, R16, R17, R18 and R19 independently of one another are equal to a hydrogen atom, a straight-chain or branched C1-C4-alkyl group, a C1-C4-hydroxyalkyl group, one Hydroxy group, a methoxy group, a benzyl group, a halogen atom, a nitro group, a nitroso group, a cyano group, a trifluoromethyl group, a -CHO group, a -COR ^e group, a -COOH group, a -CO ₂ R ^e group , an -OCOR ^β group, an -OCH ₂ aryl group, an -SO ₂ NH ₂ group, an -NH ₂ group, an - (NH ₃ ) ⁺ group, an -NHR ^e group, an - (NH ₂ R ^Θ ) ⁺ group, an -N (R ^e ) ₂ group, a - (N (R ^e ) ₃ ) ⁺ group, an -NHCOR ^e group, an -NHCOOR ^e group, a -CH ₂ NH ₂ group, a -CH ₂ NHR ^e group, a -CH ₂ N (R ^e ) ₂ group, a -CO ₂ CF ₃ group, a -PO (OR ^e ) ₂ group , an -SO ₂ CHF ₂ group, an -SO ₂ CF ₃ group, an -SO ₂ R ^θ group or an -SR ^e group nen, with R ^e equal to a hydrogen atom, an optionally substituted aromatic carbocycle or heterocycle or a C1-C6 alkyl group, with the proviso that two adjacent radicals R8 to R19 also together with the carbon atoms of the aromatic nucleus form a 5- or δ-membered alicyclic or can form aromatic ring, optionally one or more

May contain sulfur atoms, nitrogen atoms and / or oxygen atoms; and

Z is sulfur, nitrogen, oxygen or an N ⁽⁺⁾ -R ^f group;

Q is sulfur, nitrogen, oxygen or an NR ^f group;

R ^f is hydrogen, a C _r C ₆ alkyl group, a C2-C4-hydroxyalkyl group, a phenyl group, an acetyl group or sulfonyl group;

Shark stands for an iodine atom, a bromine atom, a chlorine atom or one

CF ₃ -SO ₂ -O group;

R23 and R'23 are independently hydrogen or one

C ^ C _ß alkyl group, or R23 and R'23 form together with the

Group -O-B-O- a ring of the formula (VIII),

with R20 and R21 independently of one another being a hydrogen atom or a straight-chain or branched C1-C4-alkyl group and R22 being a straight-chain or branched C1-C4-alkyl group, where x is 0 or 1; and A ^" is the anion of an organic or inorganic acid.

13. A process for the preparation of 5-aryl-1,3,3-trimethyl-2-methylene-indoline derivatives of the formula (I) or their salts of the formula (Ia),

(I) (la) characterized in that in a first step by reacting a 5-halogeno-2,3,3-trimethyl-3H-indole derivative of the formula (II) with a diborone compound of the formula (IV) and a Arylhalogeno compounds of formula (VI) in the presence of a suitable catalyst and / or a suitable organic or inorganic base, the 5-aryl-2,3,3-trimethyl-3H-indole derivative of the formula (VII) is prepared, and then in one 2. Step in an apolar aprotic or polar protic or polar aprotic solvent 1 mol of the 5-aryl-2,3,3-trimethyl-3H-indole derivative of the formula (VII) with 1 to 50 mol of a compound of the formula R1- A is reacted at a temperature of 20 to 180 ° C for 1 to 44 hours;

(IV) where:

R2 is a straight chain C1-C6 alkyl group;

R2 'is a CH-R' group with R 'being hydrogen or one

C1-C5 alkyl group;

R3 and R4 are, independently of one another, equal to a straight-chain or branched C1-C4-alkyl group, a - (CH ₂ ) _n -R ^c group, one

- (CH ₂ ) _n -CO-XR ^c group, one - (CH ₂ ) _n -CN group, one

- (CH ₂ ) _n -CH = C (CH ₃ ) ₂ group, a - (CH ₂ ) _m -X-CHR ^c - (CH ₂ ) _n -R ^c group or a - (CH ₂ ) _n CH = CH group, where X is an oxygen atom, is a sulfur atom or an NR group, m and n independently of one another are an integer from 1 to 6 and R ^c is a hydrogen atom, an optionally substituted aromatic carbocycle or heterocycle or a straight-chain or branched C1-C6-alkyl group; with the proviso that the radicals R3 and R4, also connected via a (CH ₂ ) _n group (with n equal to an integer from 1 to 3), can form a spiro compound together with the 3H carbon;

R5, R6 and R7 are independently a hydrogen atom, a straight-chain or branched C1-C4-alkyl group, a C1-C4-hydroxyalkyl group, a hydroxyl group, a methoxy group, a benzyl group, a halogen atom, a nitro group, a nitroso group, one Cyano group, a trifluoromethyl group, a -CHO group, a -COR ^d group, a -COOH group, a -CO ₂ R ^d group, a -OCOR ^d group, a -OCH ₂ aryl group, a - SO ₂ NH ₂ group, an -NH ₂ group, an -NH ₃ ⁺ group, an -NHR ^d group, an -NH ₂ R ^{d +} group, an -N (R ^d ) ₂ group, an -N (R ^d ) ₃ ⁺ group, an -NHCOR ^d group, an -NHCOOR ^d group, a -CH ₂ NH ₂ group, a -CH ₂ NHR ^d group, a -CH ₂ N ( R ^d ) ₂ group, a -CO ₂ CF ₃ group, a -PO (OR ^d ) ₂ group, an -SO ₂ CHF ₂ group, an -SO ₂ CF ₃ group, an -S0 ₂ R ^d group or an -SR ^d group, where R ^d is a hydrogen atom, an optionally substi is aromatic carbocycle or heterocycle or a C1-C6-alkyl group, with the proviso that the adjacent radicals R6 and R7 together with the carbon atoms of the aromatic nucleus can also form a 5- or 6-membered alicyclic or aromatic ring, which optionally has one or more May contain sulfur atoms, nitrogen atoms and / or oxygen atoms; and

(IX) (X) (XI) (XU)

wherein R8, R9, R10, R11, R12, R13, R14, R15, R16, R17, R18 and R19 independently of one another are equal to a hydrogen atom, a straight-chain or branched C1-C4-alkyl group, a C1-C4-hydroxyalkyl group, one Hydroxy group, a methoxy group, a benzyl group, a halogen atom, a nitro group, a nitroso group, a cyano group, a trifluoromethyl group, a -CHO group, a -COR ^e group, a -COOH group, a -CO ₂ R ^e group , an -OCOR ^e group, an -OCH ₂ aryl group, an -SO ₂ NH ₂ group, an -NH ₂ group, an - (NH ₃ ) ⁺ group, an -NHR ^e group, one - (NH ₂ R ^e ) ⁺ group, an -N (R ^Θ ) ₂ group, a - (N (R ^e ) ₃ ) ⁺ group, an -NHCOR ^e group, an -NHCOOR ⁶ group, a -CH ₂ NH ₂ group, a -CH ₂ NHR ^e group, a -CH ₂ N (R ⁸ ) ₂ group, a -C0 ₂ CF ₃ group, a -PO (OR ^e ) ₂ group , an -SO ₂ CHF ₂ group, an -S0 ₂ CF ₃ group, an -SO ₂ R ^e group or an -SR ^e group n, where R ^e is a hydrogen atom, an optionally substituted aromatic carbocycle or heterocycle or one C1-C6-alkyl group, with the proviso that two adjacent

Residues R8 to R19 can also form together with the carbon atoms of the aromatic nucleus a 5- or 6-membered alicyclic or aromatic ring, which optionally has one or more

May contain sulfur atoms, nitrogen atoms and / or oxygen atoms; and

Z is sulfur, nitrogen, oxygen or an N ⁽⁺⁾ -R ^f group;

Q is sulfur, nitrogen, oxygen or an NR ^f group;

R ^f is hydrogen, a C, -C ₆ alkyl group, a C2-C4-hydroxyalkyl group, a phenyl group, an acetyl group or sulfonyl group;

Shark stands for an iodine atom, a bromine atom, a chlorine atom or one

CF ₃ -SO ₂ -O group;

R20 and R21 independently of one another are equal to a hydrogen atom or a straight-chain or branched C1-C4-alkyl group and

R22 is a straight or branched C1-C4 alkyl group, where x is 0 or 1; and

A ^' is the anion of an organic or inorganic acid.

14. The method according to claim 12 or 13, characterized in that the second step is carried out with the aid of ultrasound or in an autoclave or a bomb tube under excess pressure at 0.1 to 50 bar.

15. The method according to any one of claims 12 to 14, characterized in that the first step in an apolar aprotic solvent or a polar aprotic solvent, optionally with the addition of water, at 20 to 180 ° C.

16. The method according to any one of claims 12 to 15, characterized in that in the 1st step, the reaction medium is oxygen-free.

17. The method according to any one of claims 12 to 16, characterized in that the first step is carried out under a protective gas.

18. The method according to any one of claims 12 to 17, characterized in that the reaction time in the 1st step is 1 to 24 hours.

19. Compound of formula (I) or (la)

(I) (la) where:

R1 is equal to a straight-chain or branched C1-C8 alkyl group, a C1 to C8 monohydroxyalkyl group, a C2-C8 polyhydroxyalkyl group, a C1-C8 alkoxy (C1-C8) alkyl group, a thio (C1- C8) alkyl group, a - (CH ₂ ) _m -X- (CH ₂ ) _n -Y- (CH ₂ ) _p R ^a group, a - (CH ₂ ) _n -XR ^a group, a - (CH ₂ ) _m -Y- (CH ₂ ) _n -X- (CH ₂ ) _p -R ^a group, one - (CH ₂ ) _m -CO- (CH ₂ ) _p -XR ^a group, one - (CH ₂ ) _P -R ^a group, a - (CH ₂ ) _m -X- (CH ₂ ) _p -CO-YR ^a group or one of the following 3 groups wherein X and Y are independently an oxygen atom, a sulfur atom or an NR ^b group, R ^a and R ^{b are} independently a hydrogen atom, an optionally substituted aromatic carbocycle or heterocycle or a straight-chain or branched C1-C8-alkyl group; m and n are independently an integer from 1 to 6 and p is an integer from 0 to 6; R2 is a straight chain C1-C6 alkyl group; R2 'is a CH-R' group with R 'is hydrogen or a C1-C5 alkyl group;

R3 and R4 independently of one another are equal to a straight-chain or branched C1-C4-alkyl group, a - (CH ₂ ) _n -R ^c group, a - (CH ₂ ) _m -CHR ^c -X- (CH ₂ ) _n -R ^c group, a - (CH ₂ ) _n -CO-R ^c group, a - (CH ₂ ) _n -CO-XR ^c group, a - (CH ₂ ) _n -CN group, a - (CH ₂ ) _n -CH = C (CH ₃ ) ₂ group, a - (CH ₂ ) _m -X-CHR ^c - (CH ₂ ) _n -R ^c group or a - (CH ₂ ) _n CH = CH - Group where X is an oxygen atom, a sulfur atom or an NR ^b group, m and n are independently an integer from 1 to 6 and R ° is a hydrogen atom, an optionally substituted aromatic carbocycle or heterocycle or a straight-chain or is C1-C6 branched alkyl group; with the proviso that the radicals R3 and R4, also connected via a (CH ₂ ) _n group (with n equal to an integer from 1 to 3), can form a spiro compound together with the 3H carbon; R5, R6 and R7 are independently a hydrogen atom, a straight-chain or branched C1-C4-alkyl group, a C1-C4-hydroxyalkyl group, a hydroxyl group, a methoxy group, a benzyl group, a halogen atom, a nitro group, a nitroso group, one Cyano group, a trifluoromethyl group, a -CHO group, a -COR ^d group, a -COOH group, a -CO ₂ R ^d group, a -OCOR ^d group, a -OCH ₂ aryl group, a - S0 ₂ NH ₂ group, an -NH ₂ group, an -NH ₃ ⁺ group, an -NHR ^d group, an -NH ₂ R ^{d +} group, an -N (R ^d ) ₂ group, an -N (R ^d ) ₃ ⁺ group, an -NHCOR ^d group, an -NHCOOR ^d group, a -CH ₂ NH ₂ group, a -CH ₂ NHR ^d group, a -CH ₂ N ( R ^d ) ₂ group, a -CO ₂ CF ₃ group, a -PO (OR ^d ) ₂ group, an -SO ₂ CHF ₂ group, an -SO ₂ CF ₃ group, an -SO ₂ R ^d group or an -SR ^d group, where R ^d is a hydrogen atom, an optionally substi tuiert aromatic carbocycle or heterocycle or a C1-C6-alkyl group, with the proviso that the adjacent radicals R6 and R7 together with the carbon atoms of the aromatic nucleus can form a 5- or 6-membered alicyclic or aromatic ring, optionally one or more May contain sulfur atoms, nitrogen atoms and / or oxygen atoms; and

(IX) (X) (XI) (XII)

where R8, R9, R10, R11, R12, R13, R14, R15, R16, R1, R18 and R19 independently of one another are equal to a hydrogen atom, a straight-chain or branched C1-C4-alkyl group, a C1-C4-hydroxyalkyl group, one Hydroxy group, a methoxy group, a benzyl group, a halogen atom, a nitro group, a nitroso group, a cyano group, a trifluoromethyl group, a -CHO group, a -COR ^e group, a -COOH group, a -CO ₂ R ^e group , an -OCOR ⁶ group, an -OCH ₂ aryl group, an -SO ₂ NH ₂ group, an -NH ₂ group, an - (NH ₃ ) ⁺ group, an -NHR ^e group, one - (NH ₂ R ^e ) ⁺ group, an -N (R ^e ) ₂ group, a - (N (R ^e ) ₃ ) ⁺ group, an -NHCOR ^e group, an -NHCOOR ^e group, a -CH ₂ NH ₂ group, a -CH ₂ NHR ^e group, a -CH ₂ N (R ^e ) ₂ group, a -CO ₂ CF ₃ group, a -PO (OR ^e ) ₂ group , an -SO ₂ CHF ₂ group, an -SO ₂ CF ₃ group, an -SO ₂ R ^e group or an -SR ^e group , with R ^e equal to a hydrogen atom, an optionally substituted aromatic carbocycle or heterocycle or a C1-C6-alkyl group, with the proviso that two adjacent radicals R8 to R19 also together with the carbon atoms of the aromatic nucleus form a 5- or 6-membered alicyclic or aromatic Can form a ring, which may optionally contain one or more sulfur atoms, nitrogen atoms and / or oxygen atoms; and Z is sulfur, nitrogen, oxygen or an N ⁽⁺⁾ -R ^f group; Q is sulfur, nitrogen, oxygen or an NR ^f group; R ^f is hydrogen, a C ₁ -C ₆ -alkyl group, a C2-C4-hydroxyalkyl group, a phenyl group, an acetyl group or sulfonyl group. A ^" is equal to the anion of an organic or inorganic acid; on the condition that when R10 is hydrogen or a methoxy group, R2 'or R2 is a methylene or methyl group and when the radicals R1, R3 and R4 simultaneously represent a methyl group, at least one of the radicals R5 to R12 is different from hydrogen.

20. Compound of formula (V)

where:

R2 is a straight chain C1-C6 alkyl group;

- (CH ₂ ) _n -CO-XR ^G group, one - (CH ₂ ) _n -CN group, one

- (CH ₂ ) _n -CH = C (CH ₃ ) ₂ group, a - (CH ₂ ) _m -X-CHR ^c - (CH ₂ ) _n -R ^c group or a - (CH ₂ ) _n CH = CH group, where X is an oxygen atom, a sulfur atom or an NR ^b group, m and n independently are an integer from 1 to 6 and R ^c is a hydrogen atom, an optionally substituted aromatic carbocycle or heterocycle or a straight or branched C1-C6 alkyl group; with the proviso that the radicals R3 and R4, also connected via a (CH ₂ ) _n group (with n equal to an integer from 1 to 3), can form a spiro compound together with the 3H carbon;

R5, R6 and R7 are independently a hydrogen atom, a straight-chain or branched C1-C4-alkyl group, a C1-C4-hydroxyalkyl group, a hydroxy group, a methoxy group, a benzyl group, a halogen atom, a nitro group, a nitroso group, a cyano group, a trifluoromethyl group, a -CHO group, a -COR ^d group, a -COOH group, a -C0 ₂ R ^d group, a -OCOR ^d group, a -OCH ₂ aryl group, a -S0 ₂ NH ₂ group, an -NH ₂ group, an -NH ₃ ⁺ group, an -NHR ^d group, an -NH ₂ R ^{d +} group, an -N (R ^d ) ₂ group, an - N (R ^d ) ₃ ⁺ group, an -NHCOR ^d group, an -NHCOOR ^d group, a -CH ₂ NH ₂ group, a -CH ₂ NHR ^d group, a -CH ₂ N (R ^d ) ₂ group, a -CO ₂ CF ₃ group, a -PO (OR ^d ) ₂ group, an -SO ₂ CHF ₂ group, an -SO ₂ CF ₃ group, an -SO ₂ R ^d - Group or an -SR ^d group, where R ^d is a hydrogen atom, an optionally substituted ized aromatic carbocycle or heterocycle or a C1-C6 alkyl group, with the proviso that the adjacent radicals R6 and R7 together with the carbon atoms of the aromatic nucleus can also form a 5- or 6-membered alicyclic or aromatic ring, which optionally has one or more May contain sulfur atoms, nitrogen atoms and / or oxygen atoms; R20 and R21 are independently a hydrogen atom or a straight-chain or branched C1-C4-alkyl group and R22 is a straight-chain or branched C1-C4-alkyl group, where x is 0 or 1.