EP1347959A1

EP1347959A1 - Indole derivatives as ligands of thyroid receptors

Info

Publication number: EP1347959A1
Application number: EP01272011A
Authority: EP
Inventors: Helmut Haning; Michael Woltering; Gunter Schmidt; Hilmar Bischoff; Axel Kretschmer; Verena Vöhringer; Christiane Faeste
Original assignee: Bayer AG; Bayer Healthcare AG
Current assignee: Bayer AG
Priority date: 2000-12-27
Filing date: 2001-12-14
Publication date: 2003-10-01
Also published as: JP2004517851A; UY27098A1; WO2002051805A1; CA2433100A1; US20030078288A1; US6794406B2; US20050032874A1

Abstract

The invention relates to novel indole derivatives, to a method for the production of said derivatives and to the use thereof in medicaments.

Description

Indole derivatives

The invention relates to new indole derivatives, processes for their preparation and their use in medicaments.

EP-A-580 550 describes oxamic acid derivatives which have cholesterol-lowering properties in mammals. The reduction in plasma cholesterol, in particular LDL cholesterol, is emphasized as a pharmacological property. Cholesterol-lowering effects are also described in EP-A-188 351 for certain diphenyl ethers with thyroid hormone-like effects which clearly differ in chemical structure from the compounds according to the invention.

WO 00/51971 discloses oxamic acid derivatives with an --ndol partial structure as thyroid receptor ligands for the treatment of various explanations.

Other indoles which are connected in the 5-position via a bridge member to a substituted phenyhing are known (WO 94/14770; EP-A-674 619 AI or WO 94/26737). No thyroid hormone-like properties have been described for these 5-substituted indoles.

WO 99/50268 discloses substituted indolalkane carboxylic acids which are suitable for the treatment of chronic complications caused by diabetes mellitus.

WO 95/20588 discloses indole derivatives which act as 5-HT _r agonists.

WO 98/11895 discloses the use of 5-HTι agonists for the treatment of migraines; Indole derivatives are also indicated as suitable active ingredients. WO 98/06402 describes the use of the same structures for the treatment of colds or rhinitis. EP-A-639 573 discloses benzo-fused 5-ring heterocycles and their use in medicines and diagnostics. The compounds disclosed are inhibitors of the cellular sodium proton antiporter (Na ⁺ / H ⁺ exchanger).

US-A-5 468 899 relates to bicyclic aryl compounds with selective properties as LTB4 antagonists.

EP-A-377 450 discloses substituted indole, benzofuran and benzothiophene derivatives which act as 5-lipoxygenase inhibitors.

JP-A-07145 147 discloses testosterone-5-alpha-reductase inhibitors derived from benzoic acid, which can be used for the treatment of prostate cancer and certain hair loss conditions.

GB-A-2 253 848 describes di-ortho-substituted phenyl-indole in the phenyl part

Described ethers with herbicidal activity, which can be used as crop protection agents. Thyromimetic effects have so far not been known for these ortho-substituted indoles.

The object of the invention is to provide new compounds with improved, in particular pharmaceutical, effects.

It has now been found that compounds of the general formula (I)

in which Z stands for O, S, SO, SO ₂ , CH ₂ , CHF, CF ₂ or for NR ⁹ , in which R ⁹ denotes hydrogen or (dC) -alkyl,

R ¹ and R ^{2 are} identical or different and represent hydrogen, halogen, cyano, (C _j - C ₆ ) alkyl, CF ₃ , CHF ₂ , CH ₂ F, vinyl or (C ₃ -C ₇ ) cycloalkyl, where at least one of the two substituents is not hydrogen and is in the ortho position to the bridge bond,

R for a group of the formula

-A _m -D _n -E ₀ -G _p -LR 10

stands in what

A stands for O, S, NR ¹¹ or for the group - (CR ¹² = CR ¹³ ) -, in which R ¹¹

Hydrogen or and R ¹² and R ^{13 are the} same or different and are hydrogen, cyano, (dC ₄ ) alkyl or (dC ₄ ) alkoxy,

D stands for a straight-chain (dC ₃ ) alkylene group which, one or more times, identically or differently, by (C 1 -C ₄ ) alkyl, hydroxy, (dC ₄ ) alkoxy, halogen, amino, mono- (Cι- C ₄ ) -alkylamino, mono- (dC) -acylamino or (-C-C ₄ ) -alkoxycarbonylamino may be substituted,

E and L independently of one another represent a C (O) or SO ₂ group,

G is NR ¹⁴ , in which R ^{14 is} hydrogen or (dC) -alkyl, or represents a straight-chain (C ₁ -C ₃ ) -alkylene group which is mono- or polysilicon, the same or different, by (dC) -alkyl , Hydroxy, (CC) - Alkoxy, halogen, amino, mono- or di- (dC ₄ ) -alkylamino or mono- (dC ₄ ) -acylamino can be substituted,

m, n, o and p each independently represent the number 0 or 1, with the proviso that

in the event that L stands for a C = O group, the sum (m + n + o + p) is not equal to the number 0,

and

in the event that m and o each represent the number 1, A the remainder NR ¹¹ and E and L each represent a C = O group, the sum (n + p) is not equal to the number 0,

and

R ¹⁰ for OR ¹⁵ , NR ¹⁶ R ¹⁷ , (dC ₁₀ ) alkyl, (C ₃ -C ₈ ) cycloalkyl, (C ₂ -C ₆ ) alkenyl, (C ₆ -Cιo) aryl, (C ₆ -C ₁₀ ) arylmethyl or for a saturated, partially unsaturated or aromatic 5- to 10-membered

Heterocycle with up to four identical or different hetero atoms from the series N, O and / or S, the abovementioned radicals optionally being selected from the group halogen, hydroxyl, oxo, cyano, by one, two or three identical or different substituents, Nitro, amino, NR ¹⁸ R ¹⁹ , trifluoromethyl, (dC ₆ ) alkyl, optionally substituted by R ²⁰ (dC ₆ ) alkoxy, (C ₃ -C ₈ ) cycloalkyl, (C ₆ -C ₁₀ ) aryl, which in turn is optionally substituted by halogen, (C _r C ₄ ) alkyl, (dC ₄ alkoxy, trifluoromethyl, nitro or cyano, -OC (O) -R ²¹ , -C (O) -OR ²² , -C (O ) -NR ²³ R ²⁴ , -SO ₂ -NR ²⁵ R ²⁶ , -NH-C (O) -R ²⁷ and -NH-C (O) -OR ^{28 are} substituted, wherein R ¹⁵ , R ¹⁶ , R ¹⁷ , R ¹⁸ , R ¹⁹ , R ²⁰ , R ²¹ , R ²² , R ²³ , R ²⁴ , R ²⁵ , R ²⁶ , R ²⁷ and R ^{28 are the} same or different and each represents hydrogen,

Phenyl, benzyl, (dC ₆ ) -alkyl or (C ₃ -C ₈ ) -cycloalkyl, which in turn are optionally one or more, identical or different, by halogen, hydroxy, amino, carboxyl, (d- C ₄ ) - Alkoxy, (dC ₄ ) -alkoxy carbonyl, (C - C) -alkoxy-carbonylamino, (dC ₅ ) -alkanoyloxy, a heterocycle or phenyl which is optionally substituted by halogen or hydroxy,

or the group

-LR ^{10 represents} a group of the formula wherein

R ²⁹ denotes hydrogen or (dC ₄ ) -alkyl,

or

R for a group of the formula

stands in what

Q represents a 5- to 6-membered saturated, partially unsaturated or aromatic heterocycle with up to four identical or different heteroatoms from the series N, O and or S, which is in turn optionally substituted one to three times, identically or differently, by oxo (= O), thioxo (= S), hydroxy, (dC ₆ ) -alkyl or phenyl,

r represents the number 0, 1 or 2,

and

the ring Het is a 5- to 6-membered saturated or partially unsaturated heterocycle with up to three identical or different heteroatoms from the series N, O and / or S, which may be one to three times, identical or different, by oxo (= O), thioxo (= S), hydroxy, (-CC ₆ ) -alkyl or phenyl is substituted,

R and R ^{5 are the} same or different and each represents hydrogen, hydroxy, halogen, cyano, nitro, (C ₁ -C ₄ ) alkyl or the rest of the formula NR ³⁰ R ³¹ , where R ³⁰ and R ^{31 are} those for R ¹⁵ have the meaning given and, independently of one another, may be the same or different with this substituent,

R ^{6 represents} hydrogen, halogen or a group of the formula

-M _a -R 32

stands in what

M represents a carbonyl group, a sulfonyl group or a methylene group,

a represents the number 0 or 1,

and R ^{32 has} the meaning of R ¹⁰ given above and can be identical or different with this substituent,

R ^{7 represents} hydrogen or an acyl group which can be split off under physiological conditions to form an NH function, preferably represents hydrogen or acetyl,

and

R ^{8 has} the meaning of R ⁶ given above and can be identical or different with this substituent,

as well as their pharmaceutically acceptable salts, solvates, hydrates and hydrates of the salts,

preferably the compounds which are tri-, in particular tetra-substituted in the phenyl part, and are preferably substituted in the 1-, 2-, 4- and 6-positions and have a substituent in the 3-position in the indole ring,

show a pharmacological effect and can be used as pharmaceuticals or for the production of pharmaceutical formulations.

The following may preferably be mentioned as heterocycles in the definition of R ⁶ , R ⁸ or R ¹⁰ :

A 5- to 10-membered saturated, partially unsaturated or aromatic, optionally benzocondensed heterocycle with up to 4 heteroatoms from the series S, N and / or O, i.e. a heterocycle which can contain one or more double bonds and which is linked via a ring carbon atom or a ring nitrogen atom. Examples include: Tefr-d ydrofuryl, pyrrolidinyl, pyrrolinyl, piperidinyl, 1,2-dihydropyridinyl, 1,4-dihydropyridinyl, piperazinyl,

Moφholinyl, azepinyl, 1,4-diazepinyl, furanyl, pyrrolyl, thienyl, thiazolyl, oxa- zolyl, imidazolyl, triazolyl, tetrazolyl, pyridyl, pyrimidinyl, pyrazinyl, pyridazinyl, pyrimidinonyl, pyridazinonyl.

From this list, the following are preferred: pyridyl, pyrimidinyl, pyridazinyl, pyrimidinonyl, pyridazinonyl and thienyl.

In the context of the invention, alkyl represents a straight-chain or branched alkyl radical having preferably 1 to 15, 1 to 12, 1 to 10, 1 to 8, 1 to 6, 1 to 4 or 1 to 3 carbon atoms. A straight-chain or branched alkyl radical having 1 to 3 carbon atoms is preferred. Examples and preferably are:

Methyl, ethyl, n-propyl, isopropyl, n-, i-, s- or t-butyl, n-pentyl and n-hexyl.

In the context of the invention, aryl stands for an aromatic radical having preferably 6 to 10 carbon atoms. Preferred aryl radicals are phenyl and naphthyl.

Cycloalkyl in the context of the invention represents a cycloalkyl group with preferably 3 to 8, 3 to 7 or 3 to 6 carbon atoms. Examples and preferably mentioned are: cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl and cycloheptyl.

In the context of the invention, alkoxy preferably represents a straight-chain or branched alkoxy radical having 1 to 6, 1 to 4 or 1 to 3 carbon atoms. A straight-chain or branched alkoxy radical having 1 to 3 carbon atoms is preferred. The following may be mentioned as examples and preferably: methoxy, ethoxy, n-propoxy, isopropoxy, t-butoxy, n-pentoxy and n-hexoxy.

Alkoxycarbonyl in the context of the invention preferably represents a straight-chain or branched alkoxy radical having 1 to 6 or 1 to 4 carbon atoms, which is linked via a carbonyl group. A straight-chain or branched alkoxycarbonyl radical having 1 to 4 carbon atoms is preferred. The following may be mentioned as examples and preferably: methoxycarbonyl, ethoxycarbonyl, n-propoxycarbonyl, isopropoxycarbonyl and t-butoxycarbonyl. Alkanoyloxy in the context of the invention preferably represents a straight-chain or branched alkyl radical having 1 to 6, 1 to 5 or 1 to 3 carbon atoms, which bears a double-bonded oxygen atom in the 1 position and which is linked via a further oxygen atom in the 1 position is. A straight-chain or branched alkanoyloxy radical having 1 to 3 carbon atoms is preferred. Examples and preferably mentioned are: acetoxy, propionoxy, n-butyroxy, i-butyroxy, pivaloyloxy and n-hexanoyloxy.

In the context of the invention, monoalkylamino represents an amino group with a straight-chain or branched alkyl substituent which preferably has 1 to 6, 1 to 4 or 1 to 2 carbon atoms. A straight-chain or branched monoalkylamino radical having 1 to 4 carbon atoms is preferred. Examples and preferably mentioned are: methylamino, ethyl∑uriino, n-propylamino, isopropylamino, t-butylamino, n-pentylamino and n-hexylamino.

In the context of the invention, dialkylamino stands for an amino group with two identical or different straight-chain or branched alkyl substituents which preferably each have 1 to 6, 1 to 4 or 1 to 2 carbon atoms. Straight-chain or branched dialkylamino radicals each with 1 to 4 are preferred

Carbon atoms. Examples and preferably mentioned are: NN-dimethylamino, NN-diethylamino, N-ethyl-N-methylamino, N-methyl-Nn-propylamino, N-isopropyl-Nn-propylamino, Nt-butyl-N-memyl-ιmino, N-ethyl-Nn-pentylamino and Nn-hexyl-N-memyl-i-tnino.

In the context of the invention, monoacylamino represents an amino group having a straight-chain or branched alkanoyl substituent which preferably has 1 to 6, 1 to 4 or 1 to 2 carbon atoms and is linked via the carbonyl group. A monoacylamino radical having 1 to 2 carbon atoms is preferred. The following may be mentioned as examples and preferably: formamido, acetamido, propionamido, n-butyramido and pivaloylamido. In the context of the invention, alkoxycarbonylamino represents an amino group with a straight-chain or branched alkoxycarbonyl substituent which preferably has 1 to 6 or 1 to 4 carbon atoms in the alkoxy radical and is linked via the carbonyl group. An alkoxycarbonylamino radical having 1 to

4 carbon atoms. The following may be mentioned by way of example and preferably: methoxycarbonylamino, ethoxycarbonylamino, n-propoxycarbonylamino and t-butoxyc_trbonyl-mino.

Halogen in the context of the invention includes fluorine, chlorine, bromine and iodine. Fluorine, chlorine or bromine are preferred.

Depending on the substitution pattern, the compounds according to the invention can exist in stereoisomeric forms which either behave like image and mirror image (enantiomers) or do not behave like image and mirror image (diastereomers). The invention relates both to the enantiomers or diastereomers and to their respective mixtures. Like the diastereomers, the racemic forms can be separated into the stereoisomerically uniform constituents in a known manner.

Furthermore, certain compounds can exist in tautomeric forms. This is known to those skilled in the art and such compounds are also within the scope of the invention.

The compounds according to the invention can also be present as salts. Physiologically acceptable salts are preferred in the context of the invention.

Physiologically acceptable salts can be salts of the compounds according to the invention with inorganic or organic acids. Salts with inorganic acids such as hydrochloric acid, hydrobromic acid, phosphoric acid or sulfuric acid are preferred, or salts with organic carbon or sulfonic acids such as acetic acid, propionic acid, maleic acid, fumaric acid acid, malic acid, citric acid, tartaric acid, lactic acid, benzoic acid, or methanesulfonic acid, ethanesulfonic acid, benzenesulfonic acid, toluenesulfonic acid or naphthalene disulfonic acid.

Physiologically acceptable salts can also be salts of the invention

Be compounds with bases, such as metal or ammonium salts. Preferred examples are alkali metal salts (for example sodium or potassium salts), alkaline earth metal salts (for example magnesium or calcium salts), and also ammonium salts which are derived from ammonia or organic amines, such as, for example, ethylamine, di- or triethylamine, ethyldiisopropylamine, monoethanolamine, di- or triethanolamine, dicyclohexylamine, dimethylaminoethanol, dibenzylamine, N-methylmopholine, dihydroabietylamine, 1-ephenamine, methylpiperidine, arginine, lysine, ethylenediamine or 2-phenylethylamine.

The compounds according to the invention can also be present in the form of their solvates, in particular in the form of their hydrates.

The invention also includes prodrugs of the compounds according to the invention. According to the invention, “prodrugs” refer to those derivatives of the compounds of the general formula (I) which themselves may be less biologically active or also inactive but which, after application under physiological conditions, are converted into the corresponding biologically active form (for example metabolically, solvolytically or on other way).

Compounds of the general formula (I) are preferred

in which

Z represents O, S or CH ₂ , R ¹ and R ^{2 are the} same or different and represent hydrogen, fluorine, chlorine, bromine,

(C _r C ₄ ) -alkyl, CF ₃ , CHF ₂ , CH ₂ F, vinyl or (C ₃ -C ₅ ) -cycloalkyl, where at least one of the two substituents is not hydrogen and is in the ortho-position to the bridge bond, in particular both substituents are not equal to hydrogen and both are in the ortho position,

R ³ for a group of the formula

"A-jj-Uj-li) G _p -L- R 10

stands in what

A represents O, S, NR ^π or the group - (CR ¹² = CR ¹³ ) -, in which R ¹¹ denotes hydrogen or methyl, and R ¹² and R ^{13 are} identical or different and denote hydrogen or methoxy,

D stands for a straight-chain (C ₁ -C ₃ ) alkylene group which is mono- or divalent, identical or different, by (dC) - alkyl, hydroxy, methoxy, ethoxy, fluorine, chlorine, amino, mono- (C ₁ - C ₄ ) -alkylamino or mono- (-C-C ₄ ) -acylamino may be substituted,

E represents a C (O) group,

L represents a C (O) or SO ₂ group,

G represents an NH group or a straight-chain (dC ₃ ) alkylene group which can be substituted once or twice, identically or differently, by methyl, ethyl, hydroxy, methoxy, fluorine, chlorine, amino, methylamino or acetylamino,

m, n, o and p each independently represent the number 0 or 1 with which

Provided that in the event that L stands for a C = O group, the sum (m + n + o + p) is not equal to the number 0,

and

in the event that m and o each represent the number 1, A represents the radical NR ¹¹ and L represents a C- = O group, the sum (n + p) is not equal to the number 0,

and

R ¹⁰ for OR ¹⁵ , NR ¹⁶ R ¹⁷ , (dC ₆ ) alkyl, (C ₃ -C ₇ ) cycloalkyl, naphthyl, phenyl, benzyl or for a saturated, partially unsaturated or aromatic 5- to 6-membered heterocycle with up to four identical or different heteroatoms from the series N, O and / or S, the abovementioned radicals optionally being selected from the group halogen, hydroxyl, oxo, cyano, nitro, amino, by one, two or three identical or different substituents, NR ¹⁸ R ¹⁹ , trifluoromethyl, (dC ₄ ) alkyl, optionally substituted by R ²⁰ (dC ₄ ) alkoxy, (C ₃ -C ₆ ) cycloalkyl, -OC (O) -R ²¹ , -C (O) -OR ²² ,

-C (O) -NR ²³ R ²⁴ , -SO ₂ -NR ²⁵ R ²⁶ , -NH-C (O) -R ²⁷ and -NH-C (O) -OR ^{28 are} substituted, wherein

R ¹⁵ , R ¹⁶ , R ¹⁷ , R ¹⁸ , R ¹⁹ , R ²⁰ , R ²¹ , R ²² , R ²³ , R ²⁴ , R ²⁵ , R ²⁶ , R ²⁷ and R ^{28 are the} same or different and each represents hydrogen,

Phenyl, benzyl, (dC ₆ ) -alkyl or (C ₃ -C ₆ ) -cycloalkyl, which in turn are optionally one or more, identical or different, by halogen, hydroxy, amino, carboxyl, (d-C ₄ ) - Alkoxy, (dC ₄ ) alkoxycarbonyl, (dC ₄ ) alkoxy-carbonylamino, (d-C5) alkanoyloxy ,. a heterocycle or optionally substituted by halogen or hydroxy substituted phenyl,

or

R> 3 for a group of the formula

stands,

R ⁴ and R ^{5 are the} same or different and each represents hydrogen, halogen or (C _r C ₄ ) alkyl,

R ^{6 represents} hydrogen, halogen or a group of the formula

-M _a -R ³² , wherein

M represents a carbonyl group, a sulfonyl group or a methylene group,

a represents the number 0 or 1,

and R ^{32 represents} (dC ₁₀ ) alkyl, (C ₃ -C ₇ ) cycloalkyl, (C ₂ -C ₄ ) alkenyl, naphthyl, phenyl, benzyl, pyridyl, pyridazinyl or pyridazinonyl, where the abovementioned radicals may be replaced by a , two or three identical or different substituents selected from the group

Halogen, hydroxy, cyano, nitro, amino, NR ¹⁸ R ¹⁹ , trifluoromethyl, (dC ₄ ) alkyl, (dC ₄ ) alkoxy, (C ₃ -C ₇ ) cycloalkyl, phenyl, which in turn may be replaced by halogen, ( dC ₄ ) -alkyl, (dC ₄ ) - alkoxy, trifluoromethyl, nitro or cyano is substituted, -OC (O) - R ²¹ , -C (O) -OR ²² , -C (O) -NR ²³ R ²⁴ , -SO ₂ -NR ²⁵ R ²⁶ , -NH-C (O) -R ²⁷ and

-NH-C (O) -OR ^{28 are} substituted, wherein

R ¹⁸ , R ¹⁹ , R ²¹ , R ²² , R ²³ , R ²⁴ , R ²⁵ , R ²⁶ , R ²⁷ and R ^{28 are the} same or different and each represents hydrogen, phenyl, benzyl, (dC ₆ ) - alkyl or ( C ₃ -C ₆ ) cycloalkyl, which in turn are optionally one or more, identical or different, by halogen, hydroxy, amino, carboxyl, (C) -C) alkoxy, (dC ₄ ) alkoxycarbonyl, (Cι- C) -alkoxycarbonylamino, (d- C ₅ ) -alkanoyloxy, a heterocycle or phenyl which is optionally substituted by halogen or hydroxy,

R ^{7 represents} hydrogen,

and

as well as their pharmaceutically acceptable salts, solvates, hydrates and hydrates of

Salts. Compounds of the general formula (I) are particularly preferred

in which

Z represents O or CH ₂ ,

R ¹ and R ^{2 are the} same or different and represent hydrogen, fluorine, chlorine, bromine,

R for a group of the formula

-A _m -D _n -E ₀ -G _p -LR 10

stands in what

A represents O, S or NH,

D represents a straight-chain (C ₁ -C ₃ ) alkylene group which can be substituted once or twice, identically or differently, by methyl, ethyl, hydroxy, methoxy, fluorine, amino or acetylamino,

E represents a C (O) group,

L represents a C (O) or SO ₂ group,

G represents an NH group or a methylene group, and p independently of one another each represent the number 0 or 1, with the proviso that

and

in the event that m and o each represent the number 1, A represents the remainder NH and L represents a C = O group, the sum (n + p) is not equal to the number 0,

and

R ¹⁰ for OR ¹⁵ , NR ¹⁶ R ¹⁷ , (dC ₆ ) alkyl, phenyl, benzyl or for an aromatic 5- to 6-membered heterocycle with up to four identical or different heteroatoms from the series N, O and / or S stands, where the aforementioned radicals optionally by one, two or three identical or different substituents selected from the group fluorine, chlorine, hydroxy, oxo, cyano, nitro, amino, NR ¹⁸ R ¹⁹ , trifluoromethyl, (dC ₄ ) alkyl, optionally substituted by R ²⁰

(dC ₄ ) alkoxy, (C ₃ -C ₆ ) cycloalkyl, -OC (O) -R ²¹ , -C (O) -OR ²² , -C (O) -NR ²³ R ²⁴ , -SO ₂ - NR ²⁵ R ²⁶ , -NH-C (O) -R ²⁷ and -NH-C (O) -OR ^{28 are} substituted, wherein

R ¹⁵ , R ¹⁶ , R ¹⁷ , R ¹⁸ , R ¹⁹ , R ²⁰ , R ²¹ , R ²² , R ²³ , R ²⁴ , R ²⁵ , R ²⁶ , R ²⁷ and R ^{28 are the} same or different and each represents hydrogen, Phenyl, benzyl, (-C-C ₆ ) alkyl or (C ₃ -C ₆ ) cycloalkyl, which in turn are optionally one to two times, identical or different, by fluorine, chlorine, hydroxy, amino, carboxyl, (dC _4th ) -Alkoxy, (dC ₄ ) -alkoxycarbonyl, (dC ₄ ) -alkoxy-carbonylamino, (-C-C ₅ ) -alkanoyloxy, a heterocycle or phenyl optionally substituted by fluorine, chlorine or hydroxy,

R ⁴ and R ^{5 are the} same or different and each represents hydrogen, fluorine, chlorine or methyl,

R represents hydrogen, halogen or a group of the formula

-M _a -R ³² , wherein

M represents a sulfonyl group or a methylene group,

a represents the number 0 or 1,

and

R ^{32 stands} for (dd ^ -alkyl, (C ₃ -C ₇ ) cycloalkyl, phenyl, benzyl, pyridyl, pyridazinyl or pyridazinonyl, the aforementioned radicals optionally being selected from the group fluorine, chlorine by one or two identical or different substituents , Bromine, hydroxy, cyano, nitro, amino, NR ¹⁸ R ¹⁹ , trifluoromethyl, (dC) alkyl, (d- C ₄ ) alkoxy, (C ₃ -C ₇ ) cycloalkyl, -OC (O) -R ²¹ , -C (O) -OR ²² , -C (O) -NR ²³ R ²⁴ , -SO ₂ -NR ²⁵ R ²⁶ , -NH-C (O) -R ²⁷ and -NH-C (O) - OR ^{28 are} substituted, wherein

R ¹⁸ , R ¹⁹ , R ²¹ , R ²² , R ²³ , R ²⁴ , R ²⁵ , R ²⁶ , R ²⁷ and R ^{28 are the} same or different and each represents hydrogen, phenyl, benzyl,

(-C-C ₆ ) alkyl or (C ₃ -C ₆ ) cycloalkyl, which in turn are optionally one or two, identical or different, by fluorine, chlorine, hydroxy, amino, carboxyl, (dC ₄ ) - Alkoxy, (dC ₄ ) -alkoxycarbonyl, (dC ₄ ) -alkoxycarbonyl-a ino, (-C-C ₅ ) -alkanoyloxy, a heterocycle or optionally substituted by fluorine, chlorine or hydroxy-substituted phenyl,

R ^{7 represents} hydrogen,

R ^{8 represents} hydrogen, carboxyl, (dC ₄ ) alkoxycarbonyl, (CC ₆ ) alkyl, (C ₃ -C ₇ ) cycloalkyl, phenyl, benzyl, pyridyl, phenylsulfonyl or benzylsulfonyl, the above-mentioned radicals optionally being substituted by one or two identical or different substituents selected from the group fluorine, chlorine, bromine, hydroxy, cyano, nitro, amino, NR ¹⁸ R ¹⁹ , trifluoromethyl, (d- C ₄ ) -alkyl, (dC ₄ ) -alkoxy, (C ₃ - C ₆ ) -cycloalkyl, -OC (O) -R ²¹ , -C (O) -OR ²² , -C (O) -NR ²³ R ²⁴ , -SO ₂ -NR ²⁵ R ²⁶ , -NH-C (O ) -R ²⁷ and -NH-C (O) -OR ²⁸ are substituted, whereby

R ¹⁸ , R ¹⁹ , R ²¹ , R ²² , R ²³ , R ²⁴ , R ²⁵ , R ²⁶ , R ²⁷ and R ^{28 are the} same or different and each is hydrogen, phenyl, benzyl, (-C-C ₆ ) alkyl or (C ₃ -

C ₆ ) -cycloalkyl, which in turn are optionally one or more, identical or different, by fluorine, chlorine, hydroxy, amino,

Carboxyl, (dC) - alkoxy, (C ₁ -C ₄ ) alkoxycarbonyl, (dC) alkoxycarbonylamino, (C] -C ₅ ) alkanoyloxy, a heterocycle or optionally substituted by fluorine, chlorine or hydroxy-substituted phenyl .

and their pharmaceutically acceptable salts, solvates, hydrates and hydrates of the salts.

Compounds of the general formula (I) are very particularly preferred,

in which Z stands for O,

R ¹ and R ^{2 are the} same or different and represent hydrogen, fluorine, chlorine, bromine, (C _r C ₄ ) alkyl, CF ₃ , CHF ₂ , CH ₂ F, vinyl or (C ₃ -C ₅ ) cycloalkyl , wherein at least one of the two substituents is not hydrogen and is in the ortho position to the bridge bond, in particular both substituents are not hydrogen and both are in the ortho position,

R for a group of the formula

-A _m -D _n -E ₀ -G _p -LR ¹⁰ , wherein

A represents O, S or NH,

D represents a methylene or ethylene group which can be substituted one to two times, identically or differently, by methyl, ethyl, fluorine, amino or acetylamino,

E represents a C (O) group,

L represents a C (O) or SO ₂ group,

G represents an NH group or a methylene group,

in the event that L stands for a C = O group, the sum (m + n + o + p) is not equal to the number 0, and

and

R ¹⁰ is OR ^15, NR ¹⁶ R ¹⁷ or _(C, -C ₄₎ -alkyl, where R ^15, R ¹⁶ and R ¹⁷ are the same or different and each is hydrogen, phenyl,

Benzyl, (-C-C ₆ ) - alkyl or (C ₃ -C ₆ ) -cycloalkyl, which in turn are optionally one to two times, the same or different, by fluorine, chlorine, hydroxy, amino, carboxyl, (-C-C ₄ ) - alkoxy, (dC) - alkoxycarbonyl, (dC ₄ ) -alkoxycarbonylamino, (C ₁ -C ₅ ) -alkanoyloxy, a heterocycle or phenyl,

R ^{6 represents} hydrogen, halogen, (dC ₁₀ ) alkyl, (C ₃ -C ₇ ) cycloalkyl, (C ₃ -C ₇ ) cycloalkylmethyl, phenyl, benzyl, pyridazinonylmethyl, phenylsulfonyl or pyridylsulfonyl, the aforementioned aromatic radicals are optionally substituted by one or two identical or different substituents selected from the group consisting of fluorine, chlorine, cyano, nitro, trifluoromethyl, methyl, methoxy, carboxyl or methoxycarbonyl,

R ^{7 represents} hydrogen,

R ^{8 represents} hydrogen, (dC ₆ ) alkyl, (C ₃ -C ₇ ) cycloalkyl, phenyl, benzyl, phenylsulfonyl or benzylsulfonyl, the aforementioned aromatic

Residues optionally by one or two identical or different substituents selected from the group fluorine, chlorine, cyano, trifluoromethyl, methyl or methoxy are substituted,

Of particular importance are compounds of the general formula (I) in which

Z represents CH or in particular oxygen,

R ¹ and R ^{2 are the} same or different and represent methyl, ethyl, propyl, isopropyl, chlorine, bromine, CF, vinyl or cyclopropyl, where both substituents are in the ortho-position to the bridge bond,

R ⁴ and R ⁵ independently of one another represent methyl, fluorine or chlorine or in particular hydrogen,

and

R ^{7 represents} hydrogen.

The general or preferred radical definitions given above apply both to the end products of the formula (I) and correspondingly to the starting materials or intermediates required in each case for the preparation.

The radical definitions specified in detail in the respective combinations or preferred combinations of radicals are also replaced by radical definitions of other combinations, irrespective of the respectively specified combinations of the radicals. Compounds of the formula (I) in which Z represents oxygen are particularly preferred.

Compounds of the formula (I) in which R ^{3 is} a group of the formula are particularly preferred

which is in the para position to the bridge bond and in which R is hydroxy or the radical -C (O) -R ^{10 has} the meanings given for R for a group which, in the sense of a prodrug to the carboxylic acid -C (O) -OH or their salts can be broken down.

Compounds of the formula (I) in which R ⁴ , R ⁵ and R ^{7 are} hydrogen are particularly preferred.

Compounds of the formula (I) in which R ¹ and R ^{2 are} both arranged in the ortho position to Z and are bromine, trifluoromethyl, ethyl, cyclopropyl and in particular methyl or chlorine are particularly preferred.

Compounds of the formula (Ia) are very particularly preferred in which

R ^{3 represents} a group of the formula -CH ₂ -C (O) -OH, -CHF-C (O) -OH or -CF ₂ -C (O) -OH,

and

R for straight-chain or branched (dC ₈ ) alkyl

stands.

Likewise, very particular preference is given to compounds of the formula (Ib)

in which

R ¹ and R ^{2 are} identical or different and represent bromine, trifluoromethyl, ethyl, cyclopropyl and in particular methyl or chlorine,

R ^{J stands} for a group of the formula -NH-C (O) -CH ₂ -C (O) -R 1 ^ι 0 ^υ , in which

R ^{10 represents} hydroxy or the radical -C (O) -R ^{10 has} the meanings given above of R ¹⁰ for a group which can be degraded as a prodrug to the carboxylic acid -C (O) -OH or its salts, and

R for straight-chain or branched (-CC ₈ ) - alkyl

stands.

The following individual compounds are mentioned by way of example and preferably:

Compounds of formula 1 in which R has the meanings given in Table 1

(* means the link in the table):

Table 1

Individual compounds of the formula 2 in which R ³ each has the meanings given in Table 1 and R ² instead of methyl from the formula 1 for each of the individual compounds 1 to 35 has the meanings given in Table 2 for R ² :

Table 2

Individual compounds of the formula 3 in which R ² and R ³ each have the meanings given in Tables 1 and 2 and R ¹ instead of methyl from the formula 2 for each of the individual compounds 1 to 490 each have the meanings given in Table 3 for R ¹ has:

Table 3

Individual compounds of the formula 4 in which R ¹ , R ² and R ³ each have the meanings given in Tables 1, 2 and 3 and R ⁶ instead of methyl from the formula 3 for each of the individual compounds 1 to 6860 each in the table 4 given meanings for R ⁶ has:

Table 4

The compounds of the general formula (I) according to the invention can be prepared by reacting reactive indole derivatives of the general formula (II) with reactive phenyl derivatives of the general formula (III)

(II) (III) (IN)

wherein the substituents R ¹ , R ² , R ⁴ , R ⁵ , R ⁶ , R ⁷ and R ⁸ are those given above

Have meanings, and

R ³ 'has the meaning given for R ³ or for ΝO ₂ , NH ₂ , NH-PG, OH, O-PG, SH, S-PG, or for an aldehyde, cyano, carboxyl or (dC- - Alkoxycarbonyl group,

where PG stands for a protective group,

X and Y each represent groups of opposite reactivity, where, for example, X can be an electrophilic radical which reacts with a nucleophilic Y substituent and vice versa, Z 'has the meaning given for Z or for ^ CH-OH or ^ .C = 0

stands,

if appropriate in the presence of inert solvents and catalysts and if appropriate with isolation of the intermediates of the general formula (IV) or directly to give compounds of the formula (I).

Coupling catalysts such as Pd, Rh and / or Cu compounds may be mentioned as examples of catalysts.

The following may be mentioned as examples of the reactive groups X and Y: halogen, hydroxy, CH ₂ Br, mercapto, amino, CHO, Li, magnesium, tin or boron derivatives.

The indoles of the general formula (II) which can be used according to the invention are known or can be prepared by known methods [compare e.g. Ozaki et al., Heterocycles 51, 727-731 (1999); Harvey et al., J. Chem. Soc, 473 (1959); Quadbeck et al., Hoppe-Seyler's Z. Physiolog. Chem. 297, 229 (1954); Chen et al., J. Org. Chem. 59, 3738 (1994); Synthesis, 480 (1988); J. Prakt. Chem. 340, 608 (1998)].

The phenyl derivatives of the general formula (III) are also known or can be prepared by known methods [compare e.g. van de Bunt, Recl. Trav. Chim. Pays-Bas 48, 131 (1929); Valkanas, J. Chem. Soc, 5554 (1963)].

The reaction of the starting compounds (II) with (III) generally proceeds

Normal pressure. However, it can also be carried out under increased or reduced pressure.

The reaction can be carried out in a temperature range from -100 ° C to 200 ° C, preferably between -78 ° C and 150 ° C in the presence of inert solvents become. The following may be mentioned as inert solvents: dimethyl sulfoxide (DMSO), dimethylformamide (DMF), N-methyl-2-pyrrolidinone (ΝMP), tetrahydrofuran (THF), diethyl ether, dichloromethane etc.

Depending on the specific substituent pattern, intermediates of the formula (IV) can also be formed in the reaction of (II) and (III), in which, for example, the substituent R ³ 'for a Νitro, aldehyde, cyano, carboxyl or alkoxycarbonyl group represents or Z 'represents a CHOH or C (O) group, which are then reacted with or without isolation of these intermediates by conventional methods to give compounds of formula (I).

The method according to the invention can be illustrated by the following formula schemes:

Process variant (A)

(II) m (IV)

X = F, Cl, Br, I, B (OH) ₂ ; Y = OH, SH, H ₂ or X = OH, SH, NH-; Y = F, Cl, Br, I, B (OH) ₂

Process variant (B)

(H) (in) (IVa)

X = CHO; Y = Li, MgCl, MgBr or X = Li, MgCl, MgBr; Y = CHO

(IVb)

Process variant (C)

(IVb) Depending on the meaning of the substituents R ¹ , R ² , R ⁴ , R ⁵ , R ⁶ , R ⁷ and R ⁸ , it may be expedient or necessary to vary these in the scope of meaning given in individual process stages.

Protective groups (PG) in the present application are understood to mean groups in starting, intermediate and / or end products which contain functional groups such as e.g. Protect carboxyl, amino, mercapto or hydroxy groups and which are common in preparative organic chemistry. The groups protected in this way can then be converted into free functional groups in a simple manner under known conditions.

The compounds of the formula (I) according to the invention have a surprising and valuable spectrum of pharmacological activity and can therefore be used as versatile medicaments for the treatment of humans and mammals, such as dogs and cats in particular. In particular, they can be used for all indications that can be treated with natural thyroid hormones, such as, for example and preferably, depression, goiter or thyroid cancer. Arteriosclerosis, hypercholesterolemia and dyslipidemia can preferably be treated with the compounds of formula (I) according to the invention. In addition, obesity and heart failure can be treated and a postprandial reduction in triglycerides can be achieved.

The compounds are also suitable for the treatment of certain respiratory diseases, in particular pulmonary emphysema and for the medicinal promotion of pulmonary maturation.

The compounds are also suitable for the treatment of pain and migraines, for neuronal repair (remyelination) and for the treatment of Alzheimer's disease. The compounds are also suitable for the treatment of osteoporosis, cardiac arrhythmias, hypothyroidisms and skin diseases.

The compounds can also be used to promote and regenerate hair growth and to treat diabetes.

The active compounds according to the invention open up a further treatment alternative and are an enrichment for the pharmaceutical industry. Compared to the known and previously used thyroid hormone preparations, the compounds according to the invention show an improved spectrum of action. They are preferably characterized by great specificity, good tolerance and fewer side effects, especially in the cardiovascular area.

The activity of the compounds according to the invention can e.g. Test in vitro using the T3 promoter assay cell test described below:

The test is carried out with a stably transfected human HepG2 hepatocarcinoma cell which expresses a luciferase gene under the control of a thyroid hormone-regulated promoter. The vector used for transfection carries a minimal thymidine kinase promoter with one in front of the luciferase gene

Thyroid hormone - responsive element (TRE), which consists of two inverted palindromes of 12 bp each and an 8 bp spacer.

For the test, the cell cultures are sown in 96-well plates in Eagle's Minimal Essential Medium with the following additives: glutamine, tricine [N- (tris (hydroxymethyl) methyl) glycine], sodium pyruvate, non-essential amino acids (L- Ala, L-Asn, L-Asp, L-Pro, L-Ser, L-Glu, Gly), insulin, selenium and transfenin. The cultures are grown for 48 hours at 37 ° C. and 10% CO atmosphere. Then serial dilutions of test substance or reference compound (T3, T4) and costimulator retinoic acid are added to the test cultures and these for a further 48 or

Incubated 72 hours as before. Each substance concentration is in four replicates tested. To determine the luciferase induced by T3 or other substances, the cells are then lysed by adding a buffer containing triton and luciferin (from Promega) and immediately measured luminometrically. The EC _5Q values of each connection are calculated. Representative results for the compounds according to the invention are shown in Table 5:

Table 5

The compounds according to the invention also show surprisingly advantageous properties in the tests described below:

Test descriptions for the detection of pharmacologically active substances:

The substances that are to be examined for their serum cholesterol-lowering effect in vivo are administered orally to male mice with a body weight between 25 and 35 g. The animals are divided into groups with the same number of animals, usually n = 7-10, one day before the start of the experiment. During the entire experiment, drinking water and feed are available to the animals ad libitum. The substances are administered orally once a day for 7 days. For this purpose, the test substances are, for example, in a solution of Solutol HS 15 + ethanol + saline (0.9%) in a ratio of 1 + 1 + 8 or in a solution of Solutol HS 15 + saline (0.9%) in a ratio of 2 + 8 solved. The application The dissolved substances are carried out in a volume of 10 ml / kg body weight with a pharyngeal tube. Animals that are treated in the same way but only receive the solvent (10 ml / kg body weight) without test substance serve as a control group.

Before the first substance application, blood is taken from each mouse to determine the serum cholesterol by puncturing the retroorbital venous plexus (previous value). The animals are then given the test substance for the first time using a pharyngeal tube. 24 hours after the last substance application, (on the 8th day after the start of treatment), blood is again taken from each animal for the determination of the serum cholesterol by puncturing the retroorbital venous plexus. The blood samples are centrifuged and after the serum has been obtained, the cholesterol is determined photometrically using an EPOS Analyzer 5050 (Eppendorf-Gerätebau, Netheler & Hinz GmbH, Hamburg). The determination is carried out using a commercially available enzyme test (Boehringer M-innheim, Mannheim).

The effect of the test substances on the serum cholesterol concentration is determined by subtracting the cholesterol value of the 1st blood sample (previous value) from the cholesterol value of the 2nd blood sample (after treatment). The differences of all cholesterol values in a group are averaged and compared with the mean value of the differences in the control group.

Statistical evaluation is carried out using Student's t-test after the variances have been checked for homogeneity.

Substances that compared the serum cholesterol of the treated animals with that of the

Control groups, statistically significant (p <0.05) lower by at least 10%, are considered to be pharmacologically active.

At the end of the experiment, the animals are weighed and killed after the blood is drawn. To check for potential cardiovascular side effects under the influence of the substance, the hearts are removed and weighed. An effect on the heart Circulatory system can be determined by a significant increase in heart weight. A change in body weight can be used as a further parameter for the substance effect.

Analogously, e.g. NMRI mice, whether ob mice, Wistar rats or fa, fa sugar rats are used as experimental animals for this test.

Another in vivo test in which the compounds according to the invention show surprisingly advantageous properties is the animal model of the cholesterol-fed rat [A. Taylor et al., Molecular Pha macology 52, 542-547 (1997);

Z. Stephan et al., Atherosclerosis 126, 53-63 (1996)].

Furthermore, the cholesterol-lowering action of the compounds according to the invention can also be exerted on normocholesterolemic dogs by oral administration of the test substances for 5-7 days.

For further investigation of potential cardiovascular side effects under the influence of substances, the determination of the expression of the mRNA of the "HCN2" ion channel ("hypeφolarization-activated cyclic nucleotide-gated channel") in mouse or rat hearts can be used [cf. also: Trost et al.,

Endocrinology 141 (9), 3057-3064 (2000); Gloss et al., Endocrinology 142 (2), 544-550 (2001); Pachuki et al., Circulation Research 85, 498-503 (1999)]:

HCN2 assay:

The mRNA of the "hypeφolarization-activated cyclic nucleotide-gated" cation channel (HCN2) in rat hearts was carried out by real-time PCR (TaqMan-PCR; Heid et al, Genome Res. 6 (10), 986-994). For this purpose, after preparation of the heart, the total RNA is isolated using RNaesy columns (Qiagen), digested with DNase and then rewritten into cDNA

(SUPERSCRTPT-II RT cDNA synthesis kit, Gibco). The HCN2 mRNA Determination is carried out on an ABI Prism 7700 device (from Applied Biosystems). The sequence of the "forward" and "reverse" primer was: 5'-GGGAATCGACTCCGAGGTC-3 'and 5'-GATCTTGGTGAAACGCACGA-3', that of the fluorescent sample 5'-6FAM-ACAAGACGGCCCGTGCACTACGC-TAMRA-3 (FAM = fluorescent 6-carboxyfluorescein; TAMRA =

Quencher 6-carboxytetramethylrhodamine). During the polymerase chain reaction, the 5'-exonuclease activity of the Taq polymerase cleaves the fluorescent dye FAM and thereby the previously quenched fluorescence signal is obtained. The number of cycles at which the fluorescence intensity was 10 standard deviations above the background fluorescence is recorded as the so-called “threshold cyle” (Ct value). The relative expression of the HCN2 mRNA calculated in this way is then normalized to the expression of the ribosomal protein L32.

This assay can also be carried out in an analogous manner with mouse hearts. The sequence of the "forward" and "reverse" primers in this case was 5'-

CGAGGTGCTGGAGGAATACC-3 'or 5'-CTAGCCGGTCAATAGCCACAG-3', that of the fluorescent sample 5'-6FAM-CATGATGCGGCGTGCCTTTGAG-TAMRA-3.

For the application of the compounds of the general formula (I), all customary application forms come into consideration, i.e. i.e. oral, parenteral, inhalative, nasal, sublingual, buccal, rectal or external, e.g. transdermally, particularly preferably orally or parenterally. In parenteral administration, intravenous, intramuscular, subcutaneous administration should be mentioned in particular, e.g. as a subcutaneous depot. Oral application is very particularly preferred.

Compounds of the general formulas (Ia) and (Ib) in particular have surprisingly advantageous pharmacokinetic properties after oral administration, for example with regard to the bioavailability, the active substance concentration in the blood, the half-life and / or the excretion rate. The active ingredients can be administered alone or in the form of preparations. Preparations suitable for oral administration include tablets, capsules, pellets, dragees, pills, granules, solid and liquid aerosols, syrups, emulsions, suspensions and solutions. The active ingredient must be present in such an amount that a therapeutic effect is achieved. In general, the active ingredient can be present in a concentration of 0.1 to 100% by weight, in particular 0.5 to 90% by weight, preferably 5 to 80% by weight. In particular, the concentration of the active ingredient should be 0.5-90% by weight, ie the active ingredient should be present in amounts which are sufficient to achieve the dosage range indicated.

For this purpose, the active ingredients can be converted into the customary preparations in a manner known per se. This is done using inert, non-toxic, pharmaceutically suitable carriers, auxiliaries, solvents, vehicles, emulsifiers and / or dispersants.

Examples of auxiliary substances are: water, non-toxic organic solvents such as e.g. Paraffins, vegetable oils (e.g. sesame oil), alcohols (e.g. ethanol, glycerin), glycols (e.g. polyethylene glycol), solid carriers such as natural or synthetic rock powder (e.g. talc or silicates), sugar (e.g.

Milk sugar), emulsifiers, dispersants (e.g. polyvinylpyrrolidone) and lubricants (e.g. magnesium sulfate).

In the case of oral administration, tablets can of course also contain additives such as sodium citrate together with additives such as starch, gelatin and the like. Aqueous preparations for oral administration can also be mixed with flavor enhancers or colorants.

In the case of oral administration, preferably dosages of 0.001 to 5 mg / kg, preferably 0.001 to 3 mg / kg body weight, are applied per 24 hours. The new active substances can be used alone and, if necessary, also in combination with other active substances, preferably from the group CETP inhibitors, antidiabetics, antioxidants, cytostatics, calcium antagonists, antihypertensive agents, thyroid hormones, inhibitors of HMG-CoA reductase, inhibitors of HMG-CoA reductase Gene expression, squalene synthesis J inhibitors, ACAT-J inhibitors, blood flow-promoting agents, platelet aggregation inhibitors, anticoagulants, angiotensin II receptor antagonists, cholesterol absorption inhibitors, MTP inhibitors, inhibitors, aldose reductibrase Anorectics, lipase inhibitors and PPAR agonists are administered.

The following exemplary embodiments are intended to explain the invention by way of example without restricting the scope of protection.

Used abbreviations:

DC thin layer chromatography DCI direct chemical ionization (in MS)

DMF N, N-dimethylformamide

DMSO dimethyl sulfoxide

EI electron impact ionization (for MS)

HPLC high pressure, high performance liquid chromatography conc. concentrated

MS mass spectroscopy

NMP Ν-methylpyrrolidinone

NMR nuclear magnetic resonance spectroscopy

Rf retention index (at DC)

Rt retention time (with HPLC)

THF tetrahydrofuran aq. aqueous

Dec. decomposition

Output connections:

Example I

5- (2,6-dichloro-4-nitrophenoxy) -3-isopropyl-lH-indole

5 g of 5-hydroxy-3-isopropylindole are dissolved in 10 ml of THF and 3.2 g of potassium tert-butoxide are added. The reaction mixture is stirred for 20 minutes at room temperature and the solvent is removed in vacuo. The phenolate is in 10 ml

DMF dissolved and added dropwise to 6.46 g of l, 2,6-trichloro-4-nitrobenzene in 10 ml of DMF at 0 ° C. The mixture is stirred at 0 ° C. for 30 minutes and the reaction mixture is allowed to warm up slowly to room temperature. The reaction mixture is poured onto water, extracted with ethyl acetate, dried over sodium sulfate and the solvent is removed in vacuo. Chromatographic purification (cyclohexane / ethyl acetate) gives 663 mg 5-

(2,6-dichloro-4-nitrophenoxy) -3-isopropyl-lH-indole.

1H-NMR (300 MHz, CDC1 ₃ ): δ = 1.30, d, 6H; 3.09, sept, 1H; 6.79, dd, 1H; 6.99, m, 2H; 7.31, s, 1H; 7.89, s, broad, 1H; 8.32, s, 2H.

Example II

5- (2-chloro-6-methyl-4-nitrophenoxy) -3-isopropyl-lH-indole

4.4 g of 5-hydroxy-3-isopropylindole are dissolved in 10 ml of THF and mixed with 2.82 g of potassium tert-butoxide at room temperature. The mixture is stirred at room temperature for 30 minutes and rotated in. The phenolate is dissolved in DMF, 5.17 g of 1,2-dichloro-4-nitro-5-methylbenzene are added at 0 ° C. and the mixture is stirred at 0 ° C. for 30 minutes. The mixture is stirred at room temperature for 15 minutes and then at 50 ° C. for 1 hour. You leave them

Cool reaction mixture, pour on water, extract 2 times with ether and wash the combined organic phases 2 times with water. The aqueous phases are extracted with dichloromethane, the combined organic phases are spun in and the residue is purified by chromatography (cyclohexane / ethyl acetate). 6.65 g of 5- (2-chloro-6-methyl-4-nitrophenoxy) -3-isopropyl-1H-indole are obtained.

1H-NMR (300 MHz, CDC1 ₃ ): δ = 1.28, d, 6H; 2.31, s, 3H; 3.07, sept, 1H; 6.75, dd, 1H; 6.92, m, 1H; 6.99, m, 1H; 7.29, s, 1H; 7.87, s, broad, 1H.

Example III

3-chloro-4 - [(3-isopropyl-lH-indol-5-yl) oxy] -5-methylaniline

500 mg of 5- (2-chloro-6-methyl-4-nitrophenoxy) -3-isopropyl-1H-indole (Example II) are suspended in 10 ml of ethanol and with 50 mg of palladium on activated carbon (10%) and at atmospheric pressure 2 Hours hydrogenated. It is filtered through diatomaceous earth, the solvent is removed in vacuo and the product is purified by chromatography (cyclohexane / ethyl acetate). 271 mg of 3-chloro-4 - [(3-isopropyl-1H-indol-5-yl) oxy] -5-methylaniline are obtained.

1H-NMR (300 MHz, CDC1 ₃ ): δ = 1.29, d, 6H; 2.11, s, 3H; 3.07, sept, 1H; 3.61, s, broad, 2H; 6.50, dd, 1H; 6.66, dd, 1H; 6.78, dd, 1H; 6.94, d, 2H; 7.20, s, 1H; 7.25, m, 1H; 7.78, s, broad, 1H.

Example IV

3,5-dichloro-4 - [(3-isopropyl-lH-indol-5-yl) oxy] aniline

500 mg of 5- (2,6-dichloro-4-nitrophenoxy) -3-isopropyl-1H-indole (Example I) are mixed with 6.18 g of tin (II) chloride dihydrate in 5 ml of NMP at 50 ° C. for 17 hours touched. The solvent is removed in vacuo and the residue is taken up in ethyl acetate. It is washed with saturated ammonium chloride solution and saturated sodium chloride solution, the organic phase is dried and the solvent is removed in vacuo. The product is precipitated with diethyl ether. Chromatographic purification (cyclohexane / ethyl acetate) of the solid gives 174 mg of 3,5-dichloro-4 - [(3-isopropyl-1H-indol-5-yl) oxy] aniline.

1H NMR (300 MHz, DMSO-d ₆ ): δ = 1.21, d, 6H; 2.95, sept, 1H; 5.56, s, 2H; 6.63, dd, 1H; 6.71, s, 2H; 6.75, m, 1H; 7.06, d, 1H; 7.24, d, 1H. Example V

4- (3-isopropyl-lH-indol-5-yloxy) -3,5-bis-trifluoromethyl-benzaldehyde

12.8 g (70.27 mmol) of 5-hydroxy-3-isopropyl-indole are dissolved in 275.8 ml of DMSO, 10.68 g (77.3 mmol) of potassium carbonate are added solidly, the mixture is subsequently stirred at room temperature for 10 minutes and then 19 , 43 g (70.27 mmol) of 3,5-bistrifluoromethyl-4-chlorobenzaldehyde were added in portions. After 3 hours of stirring at 50 ° C., the mixture is poured onto a mixture of 400 ml of ethyl acetate and 250 ml of saturated ammonium chloride solution. After phase separation, the aqueous phase is extracted again with ethyl acetate, the combined organic phases are washed twice with brine and dried over sodium sulfate. After the desiccant has been separated off and the solvent has been distilled off, the crude product is chromatographed on silica gel 60 (Merck 0.040-0.063 mm) using toluene. Yield: 18.55 g (56.6%) MS (DCI): 450 ([M + NH ₃ + NH ₄ ] ⁺ , 100%) R _f : 0.75 (toluene-ethyl acetate = 8: 2)

1H-NMR (300 MHz, CDC1 ₃ ): δ = 1.25, d, 6H; 3.04, quin, 1H; 6.73, dd, 1H; 6.87, d, 1H; 6.96, d, 1H; 7.22, d, 1H; 7.85, broad s, 1H; 8.45, s, 2H; 10.11, s, 1H. Example VI

4- (3-isopropyl-lH-indol-5-yloxy) -3,5-bis-trifluoromethyl-benzyl alcohol

To a solution of 1.0 g (2.41 mmol) of aldehyde derivative from Example V in 20 ml of methanol is added 0.27 g (7.22 mmol) of sodium borohydride in 4 portions at room temperature and stirred for 1 hour. The reaction solution is then concentrated in half, 60 ml of water are added and the mixture is concentrated until methanol has evaporated completely. The aqueous phase is extracted three times with ethyl acetate, the combined organic phases are washed with sodium chloride solution, dried, concentrated and dried under high vacuum. Yield: 0.996 g (96.8%) MS (ESI): 418 ([M + H] ⁺ , 35%) HPLC: R _t = 4.97 (97.7%)

0.5% HCIO ₄ / acetonitrile

Kromasil column C18 (60 x 2 mm)

Flow: 0.75 ml / minute; 210 nm

1H-NMR (300 MHz, CDC1 ₃ ): δ = 1.28, d, 6H; 1.96, t, 1H; 3.04, quin, 1H; 4.87, d,

2H; 6.72, dd, 1H; 6.85, d, 1H; 6.93, d, 1H; 7.2, d, 1H; 7.78, broad s, 1H; 7.94, s, 2H. Example VII

4- (3-isopropyl-lH-indol-5-yloxy) -3,5-bis-trifluoromethyl-benzyl bromide

1.273 g (3.02 mmol) of triphenylphosphine dibromide are added in portions to a solution of 0.97 g (2.32 mmol) of benzyl alcohol derivative from Example VI in 15 ml of acetonitrile and 0.3 ml (3.72 mmol) of pyridine at 0 ° C. After 15 minutes, the cooling bath is removed and the mixture is stirred at room temperature for 2 hours. The reaction solution is concentrated in vacuo, the residue is dissolved in a little toluene and purified by chromatography on silica gel 60 using toluene.

Yield: 61 l mg (54.7%) MS (EI): 481 ([M] ⁺ , 60%) HPLC: R _t = 5.30 (80.7%)

0.5% HClO ₄ / acetonitrile

Kromasil column C18 (60 x 2 mm)

Flow: 0.75 ml / minute; 210 nm

1H-NMR (300 MHz, CDC1 ₃ ): δ ^■ = 1.28, d, 6H; 3.06, quin, 1H; 4.56, s, 2H; 6.70, dd, 1H; 6.88, d, 1H; 6.95, d, 1H; 7.23, d, 1H; 7.8, broad s, 1H; 8.0, s, 2H.

Example VIII

4- (3-isopropyl-lH-indol-5-yloxy) -3,5-bis-trifluoromethyl-phenylacetonitrile

72.9 mg (1.49 mmol) of sodium cyanide are added to a solution of 0.57 g (1.19 mmol) of benzyl bromide from Example VII in 3.5 ml of dimethylformamide and 0.38 ml of water and the mixture is stirred 60 minutes at 50 ° C. Then dimethylformamide is distilled off, the concentrate is diluted with ethyl acetate and water, the aqueous phase is separated off and extracted again with ethyl acetate. The combined organic phases are washed with brine, dried over sodium sulfate, filtered and concentrated. The crude product is purified on silica gel 60 using toluene / ethyl acetate (toluene, toluene / ethyl acetate = 18: 1 or 18: 1.5). Yield: 374 mg (73.9%)

MS (EI): 426 ([M] ⁺ , 60%)

R _f : 0.51 (toluene / ethyl acetate = 9: 1)

1H-NMR (300 MHz, CDC1 ₃ ): δ = 1.28, d, 6H; 3.06, quin, 1H; 3.93, s, 2H; 6.72, dd, 1H; 6.84, d, 1H; 6.96, d, 1H; 7.23, d, 1H; 7.82, broad s, 1H; 7.9, s, 2H. Example IX tert-butyl (4-hydroxy-3,5-dimethylphenoxy) acetate

10 g of dimethyl hydroquinone are dissolved in 750 ml of a mixture of 40% DMF and 60% THF, and 117 g of cesium carbonate are added. 14.1 g of tert-butyl bromoacetate are added dropwise at -25 ° C. and the reaction mixture is stirred at room temperature for 17 hours. After addition of 10 g of potassium carbonate, the reaction mixture is stirred for 24 hours at room temperature, poured onto water and extracted twice with ethyl acetate. The combined organic phases are washed with NaCl solution, dried over sodium sulfate and the solvent removed in vacuo. Chromatographic purification (cyclohexane / ethyl acetate) gives 1.27 g of tert-butyl (4-hydroxy-3,5-dimethylphenoxy) acetate.

1H-NMR (300 MHz, CDC1 ₃ ): δ = 1.42, s, 9H; 2.11, s, 6H; 4.47, s, 2H; 6.48, s, 2H; 7.74, s, 1H. Example X

5-bromo-3-isopropyl-1 H-indole

10 g of bromophenylhydrazine hydrochloride are suspended in 50 ml of acetic acid and 3.85 g of 3-methylbutyraldehyde are added dropwise at 80 ° C. The reaction mixture is stirred under reflux for 3 hours, allowed to cool and the solvent is removed in vacuo. It is taken up in ethyl acetate, extracted with water, the aqueous phase is extracted with ethyl acetate, the combined organic phases are washed with water and sodium carbonate solution, dried over sodium sulfate and the solvent is removed in vacuo. Chromatographic purification (cyclohexane / ethyl acetate) gives 8.6 g of 5-bromo-3-isopropyl-1H-indole.

1H NMR (300 MHz, CDC1 ₃ ): δ = 1.35, d, 6H; 3.15, sept, 1H; 6.96, d, 1H; 7.24, m,

2H; 7.77, d, 1H; 7.89, s, broad, 1H.

Example XI

5-bromo-l- [tert-butyl (dimethyl) silyl] -3-isopropyl-lH-indole

0.50 g (12.6 mmol) of 60% sodium hydride on paraffin oil in 20 ml of THF are introduced under argon at room temperature. A solution of 2.0 g (8.40 mmol) of 5-bromo-3-isopropyl-1H-indole (Example X) in 20 ml of THF is added dropwise and the mixture is stirred until gas evolution can no longer be seen. Then 2.03 g (13.44 mmol) of tert-butyl (chloro) dimethylsilane are added dropwise. After a short reaction time, a precipitate is formed. The mixture is stirred for 3 hours at room temperature. 200 ml of water are added. The aqueous phase is extracted twice with ethyl acetate, the combined org. Phases dried and evaporated. The residue is chromatographed on silica gel (mobile phase: cyclohexane). 2.63 g (89%) of 5-bromo-l- [tert-butyl (dimethyl) silyl] -3-isopropyl-1H-indole are obtained.

1H-NMR (200 MHz, CDC1 ₃ ): δ = 0.58, s, 6H; 0.89, s, 9H; 1.33, d, 6H; 3.12, sept., 1H; 6.88, s, 1H; 7.20, dd, 1H; 7.32, d, 1H; 7.71, d, 1H.

Example XII 1- [tert-Butyl (dimethyl) silyl] -3-isopropyl-1H-indol-5-yl-boronic acid

Under argon, 1.30 g (3.69 mmol) of 5-bromo-l- [tert-butyl (dimethyl) silyl] -3-isopropyl-lH-indole (Example XI) are dissolved in 10 ml of THF at -78 ° C submitted. 2.50 ml (4.24 mmol) of a 1.6 N tert-butyllithium solution in n-hexane are added dropwise. The mixture is stirred at -78 ° C for 30 min. Then 1.70 ml (7.38 mmol) of triisopropyl borate are added dropwise. The mixture is stirred at -78 ° C for 2 h. 4 ml of water are then added. The aqueous phase is extracted three times with diethyl ether, the united org. Phases dried and evaporated. The residue is purified by chromatography (mobile phase: cyclohexane, cyclohexane / ethyl acetate 5: 1, 3: 1). 0.68 g (58%) of l- [tert-butyl (dimethyl) silyl] -3-isopropyl-1H-indol-5-yl-boronic acid are obtained.

1H-NMR (200 MHz, CDC1 ₃ ): δ = 0.65, s, 6H; 0.93, s, 9H; 1.48, d, 6H; 3.37, sept.,

1H; 6.93, s, 1H; 7.62, d, 1H; 8.08, d, 1H; 8.64, s, 1H.

MS (ESI): 318 (M + H).

Example XIII tert-Butyl [4 - ({1- [tert -butyl (dimethyl) silyl] -3-isopropyl-1H-indol-5-yl} oxy) -3,5-dimethylphenoxyjacetate

0.50 g (1.58 mmol) of l- [tert-butyl (dimethyl) silyl] -3-isopropyl-lH-indol-5-yl-boronic acid (Example XII), 0.437 g (1.73 mmol) are suspended. tert-Butyl- (4-hydroxy-3,5-dimethylphenoxy) acetate (Example IX), 0.286 g (1.58 mmol) copper (II) acetate and 0.50 g molecular sieve (4Ä, powdered) in 10 ml dried dichloromethane , 0.64 ml (7.88 mmol) of pyridine and 1.10 ml (7.88 mmol) are added dropwise at room temperature.

Triethylamine. The mixture is stirred at room temperature overnight. The mixture is then filtered through silica gel and washed with dichloromethane. The filtrate is concentrated and the residue is filtered through silica gel (dichloromethane). 0.525 g (62%) of tert-butyl- [4 - ({l- [tert-butyl- (dimethyl) silyl] -3-isopropyl-1H-indol-5-yl} oxy) -3.5- dimethylphenoxy] acetate. 1H-NMR (300 MHz, CDC1 ₃ ): δ = 0.54, s, 6H; 0.89, s, 9H; 1.27, d, 6H; 1.50, s, 9H; 2.12, s, 6H; 3.01, sept, 1H; 4.50, s, 2H; 6.63, s, 3H; 6.83, dd, 2H; 7.29, d, 1H.

Example XIV

3-isopropyl-5- (4-nitro-2,6-dimethyl-phenoxy) -lH-indole

11.44 g (58.76 mmol) 5-hydroxy-3-isopropyl-indole are dissolved in 350 ml DMSO,

8.93 g (64.63 mmol) of potassium carbonate are firmly added and then 9.94 g (58.76 mmol) of 3,5-dimethyl-4-fluoronitrobenzene are added. The reaction solution is stirred for 2 hours at 100 ° C. under argon. The mixture is then cooled to room temperature, 100 ml of ethyl acetate and 600 ml of H ₂ O are added; after phase separation, ethyl acetate is separated off and the aqueous phase is extracted twice with ethyl acetate. The combined organic phases are washed twice with brine, dried over sodium sulfate, filtered and evaporated to dryness. The residue is purified by chromatography on silica gel using cyclohexane / ethyl acetate (10: 1). Yield: 11.96 g (62.8%)

MS (DCI): 342 ([M + NH ₄ ] ⁺ , 100%)

R _f : 0.26 (cyclohexamethyl acetate = 8: 2)

1H-NMR (300 MHz, CDC1 ₃ ): δ = 1.28 (d, 6H); 2.24 (s, 6H); 3.05 (quin, 1H); 6.72 (dd, 1H); 6.84 (d, 1H); 6.99 (i.e. 1H); 7.27 (d, 1H); 7.87 (s, 1H); 8.03 (s, 2H). Example XV 4- (3-isopropyl-1H-indol-5-yloxy) -3,5-dimethyl-phenylamine

11.95 g (36.85 mmol) of nitro compound from Example XIV are hydrogenated in 500 ml of methanol / ethanol mixture with 550 mg of palladium / activated carbon (10%) at 3 bar. It is filtered through diatomaceous earth, the solvent is removed in vacuo and the product is purified by chromatography (toluene / ethyl acetate).

Yield: 10.75 g (97.9%) MS (DCI): 295 ([M + H] ⁺ , 100%)

R _f : 0.36 (toluene: ethyl acetate = 9: 1) HPLC: R _t = 4.15 (98.9%)

0.5% HClO ₄ / acetonitrile

Kromasil column C18 (60x2 mm)

Flow: 0.75 ml / min .; 210 nm

Example XVI

4- (3-isopropyl-lH-indol-5-yloxy) -3,5-dichloro-benzaldehyde

Analogously to the procedure of Example V, 10.0 g (57.07 mmol) of 5-hydroxy-3-isopropylol are dissolved in 300 ml of DMSO, and 8.68 g (62.77 mmol) of potassium carbonate are added, for 10 minutes at room temperature stirred and 11.95 g (57.07 mmol) of 4,5,6-trichlorobenzaldehyde added in portions and stirred for 2 hours at room temperature and 2 hours at 50 ° C. After quenching with ethyl acetate / ammonium chloride solution and silica gel chromatography using toluene, 12.01 g (85.4%) of the desired product are obtained. MS (CI-POS): 348 ([M + H] ⁺ , 100%) R _f : 0.60 (toluene: ethyl acetate = 9: 1)

1H-NMR (300 MHz, CDC1 ₃ ): δ = 1.29 (d, 6H); 3.08 (quin, IH); 6.78 (dd, IH); 6.99 (dd, 2H); 7.27 (d, IH); 7.85 (broad s, IH); 7.92 (s, 2H); 9.95 (s, IH).

Example XVII

4- (3-isopropyl-1 H -indol-5-yloxy) -3,5 -dichlorobenzyl alcohol

The preparation is carried out in analogy to the procedure of Example VI from 5.0 g (12.2 mmol) of aldehyde derivative from Example XVI using 1.39 g (36.61 mmol) of sodium borohydride.

Yield: 4.62 g (100%)

MS (CI-POS): 350 ([M + H] ⁺ , 100%)

R: 0.16 (toluene: ethyl acetate = 9: 1) 1H-NMR (300 MHz, CDC1 ₃ ): δ = 1.29 (d, 6H); 1.83 (weak t, IH); 3.08 (quin,

IH); 4.71 (d, 2H); 6.8 (dd, IH); 6.95 (d, IH); 6.99 (d, IH); 7.23 (d, IH); 7.42 (s, 2H);

7.82 (broad s, IH). Example XVIII

4- (3-isopropyl-lH-indol-5-yloxy) -3,5-dichlorobenzyl bromide

Analogously to the instructions of Example VII, 4.8 g (12.66 mmol) of benzyl alcohol derivative from Example XVII are mixed with 6.95 g (16.46 mmol) of dibromotriphenylphosphorane and 1.6 g (20.26 mmol) of pyridine in 80 ml Acetonitrile implemented. Yield: 2.03 g (35.5%)

MS (CI-POS): 413 ([M + H] ⁺ , 57%) HPLC: R _t = 5.62 (91.4%)

0.5% HClOJ acetonitrile Kromasil column C18 (60 x 2 mm) flow: 0.75 ml / min .; 210 nm

1H NMR (300 MHz, CDC1 ₃ ): δ = 1.3 (d, 6H); 3.1 (quin, IH); 4.43 (s, 2H); 6.77 (dd, IH); 6.97 (s, IH); 7.02 (d, IH); 7.24 (d, IH); 7.43 (s, 2H); 7.82 (broad s, IH).

Example XIX

4- (3-isopropyl-lH-indol-5-yloxy) -3,5-dichlθφhenylacetonitril

Analogously to the procedure of Example VIII, 1.0 g (2.42 mmol) of benzyl bromide from Example XVIII is mixed with 0.15 g (3.03 mmol) of sodium cyanide in DMF / H ₂ O (10: 1) at 50 ° C. in 60 Min. Implemented. After isolation of the crude product (distilling DMF and quenching with ethyl acetate / water), chromatography on silica gel 60 is carried out using toluene.

Yield: 0.763 g (65.4%)

MS (DCI): 359 ([M + H] ⁺ , 67%)

Rf. 0.47 (toluene: ethyl acetate = 9: 1)

1H NMR (300 MHz, CDC1 ₃ ): δ = 1.3 (d, 6H); 3.09 (quin, IH); 3.78 (s, 2H); 6.78 (dd, IH); 6.97 (d. 2H); 7.25 (d, IH); 7.4 (s, 2H); 7.85 (broad s, IH).

Example XX

4- (3-cyclohexylmethyl-lH-indol-5-yloxy) -3,5-bis-trifluoromethyl-benzaldehyde

Analogously to the procedure of Example V, 2.0 g (8.72 mmol) of 5-hydroxy-3-cyclohexylmethyl-indole are dissolved in 50 ml of DMSO, 1.33 g (9.59 mmol) of potassium carbonate are added, 10 minutes. stirred at room temperature and then 2.41 g (8.72 mmol) of 3,5-bis-trifluoromethyl-4-chlorobenzaldehyde added in portions. After stirring overnight at 50 ° C., the mixture is worked up analogously to Example V and the crude product is chromatographed on silica gel 60 using toluene. Yield: 2.23 g (49.8%) MS (DCI): 504 ([M + NH ₃ + NH ₄ , 100%) R _f : 0.57 (toluene: ethyl acetate = 9: 1)

1H-NMR (300 MHz, CDC1 ₃ ): δ = 0.91 (m, 2H); 1.15 (m, 4H); 1.5 (m, IH); 1.66 (m, 4H); 2.5 (d, 2H); 6.71 (dd, IH); 6.82 (d, IH); 6.97 (d, IH); 7.22 (d, IH); 7.89 (broad s, IH); 8.46 (s, 2H); 10.11 (s, IH).

Example XXI

4- (3-Cyclohexyhnethyl-lH-indol-5-yloxy) -3,5-bis-trifluoromethyl-benzyl alcohol

The preparation is carried out in analogy to the procedure of Example VI from 2.20 g

(4.29 mmol) aldehyde derivative from Example XX with 0.49 g (12.86 mmol) sodium borohydride.

Yield: 2.05 g (100%) MS (ESI): 4.72 ([M + H] ⁺ , 100%) HPLC: R _t = 5.34 (98.4%)

1H-NMR (200 MHz, CDC1 ₃ ): δ = 0.9 (m, 2H); 1.13 (m, 4H); 1.5 (m, IH); 1.63 (m, 4H); 1.95 (t, IH); 2.5 (d, 2H); 4.88 (d. 2H); 6.7 (dd, IH); 6.81 (d, IH); 6.93 (d, IH); 7.2 (d, IH); 7.83 (broad s, IH); 7.94 (s, 2H).

Example XXII

4- (3-cyclohexylmethyl-lH-indol-5-yloxy) -3,5-bis-trifluoromethyl-benzyl bromide

The preparation is carried out in analogy to the procedure of Example VII from 2.0 g (4.18 mmol) of benzyl alcohol derivative from Example XXI and 2.82 g (6.69 mmol) of dibromotriphenylphosphorane in 40 ml of acetonitrile. After 3 hours of stirring at room temperature, another 0.3 equivalents of dibromotriphenylphosphorane are added. The mixture is stirred for 5 hours at 70 ° C and then overnight at room temperature. The product is purified on silica gel using toluene as the eluent. Yield: 0.96 g (40.2%)

MS (ESI): 534 ([M + H] ⁺ , 100%)

R _f : 0.76 (toluene-ethyl acetate = 9: 1)

1H-NMR (200 MHz, CDC1 ₃ ): δ = 0.92 (m, 2H); 1.16 (m, 4H); 1.5 (m, IH); 1.66 (m, 4H); 2.5 (d, 2H); 4.58 (s, 2H); 6.69 (dd, IH); 6.83 (d, IH); 6.95 (d, IH); 7.21 (d, IH);

7.35 (broad s, IH); 7.95 (s, 2H). Example XXIII

4- (3-cyclohexylmethyl-lH-indol-5-yloxy) -3,5-bis-trifluoromethyl-phenylacetonitrile

The preparation is carried out in analogy to the procedure of Example VIII from 0.85 g (1.59 mmol) of benzyl bromide from Example XXII with 0.1 g (1.99 mmol) of sodium cyanide in 5 ml of dimethylformamide and 0.5 ml of water at 50 ° C in 1.5 hours. The crude product is chromatographed on silica gel 60 using toluene.

Yield: 0.32 g (37.7%) MS (ESI): 481 ([M + H] ⁺ , 100%) HPLC: R _t = 5.67 (90.0%)

0.5% HClO ₄ / acetonitrile Kromasil column C 18 (60 x 2 mm)

Flow: 0.75 ml / min .; 210 µm

1H-NMR (300 MHz, CDC1 ₃ ): δ = 0.92 (m, 2H); 1.16 (m, 4H); 1.5 (m, IH); 1.67 (m, 4H); 2.5 (d, 2H); 3.92 (s, 2H); 6.69 (dd, IH); 6.8 (d, IH); 6.95 (d, IH); 7.22 (d, IH); 7.84 (broad s, IH); 7.91 (s, 2H). Preparation Examples:

example 1

Methyl 3 - ({4 - [(3-isopropyl-1H-indol-5-yl) oxy] -3,5-dimethylphenyl} amino) -3-oxo-propanoate

0.2 g (0.68 mmol) of 4 - [(3-isopropyl-lH-indol-5-yl) oxy] -3,5-dimethylaniline (Example XV) are dissolved in 2 ml of acetone with 76 mg (0 , 75 mmol) of triethylamine and 102 mg (0.75 mmol) of methyl malonate were added at 0 ° C. The mixture is stirred for 1 h, diluted with dichloromethane and extracted with sodium chloride solution and with NaHCO ₃ solution. The organic phase is dried and the solvent is removed in vacuo. 211 mg (74%) of methyl 3 - ({4 - [(3-isopropyl-1H-indol-5-yl) oxy] -3,5-dimethylphenyl} amino) -3-oxo-propanoate are obtained

1H-NMR (300 MHz, CDC1 ₃ ): δ = 1.29, d, 6H; 2.16, s, 6H; 3.05, hept, IH; 3.50, s, 2H; 3.81, s, 3H; 6.72, dd, IH; 6.88, d, IH; 6.95, d, IH; 7.25, m, IH; 7.30, s, 2H; 7.77, s, broad, IH.

Example 2 3 - ({4 - [(3-Isopropyl-1H-indol-5-yl) oxy] -3,5-dimethylphenyl} amino) -3-oxopropanoic acid

50 mg of methyl 3 - ({4 - [(3-sopropyl-lH-indol-5-yl) oxy] -3,5-dimethyl-phenyl} amino) - 3-oxo-propanoate (Example 1) are added in 2 ml Ethanol stirred with 30 mg sodium hydroxide for 30 minutes. The solvent is removed in vacuo. It is taken up in ether / water, the organic phase is dried and the solvent is removed in vacuo. 23 mg (46%) of 3 - ({4 - [(3-isopropyl-1H-indol-5-yl) oxy] -3,5-dimethylphenyl} amino) -3-oxopropanoic acid are obtained.

1H NMR (300 MHz, DMSO-d ₆ ): δ = 1.18, d, 6H; 2.02, s, 6H; 2.92, hept, IH; 6.52, dd, IH; 6.64, d, IH; 7.02, s, 2H; 7.18, d, IH; 7.32, s, 2H.

Example 3

Ethyl-N- {4 - [(3-isopropyl-lH-indol-5-yl) oxy] -3,5-dimethylphenyl} glycinate

210 mg of 4 - [(3-isopropyl-1H-indol-5-yl) oxy] -3,5-dimethylaniline (Example XV) are mixed with 119 mg of ethyl bromoacetate and 117 mg of sodium acetate in 10 ml Ethanol refluxed for 24 h. After adding water, the mixture is extracted with ether, the organic phase is dried and evaporated. Chromatographic purification (cyclohexane / ethyl acetate) gives 143 mg (53%) of ethyl N- {4 - [(3-isopropyl-1H-indol-5-yl) oxy] -3,5-dimethylphenyl} glycinate.

1H-NMR (300 MHz, CDC1 ₃ ): δ = 1.27, d, 6H; 1.31, t, 3H; 2.09, s, 6H; 3.06, hept, IH; 3.92, s, 2H; 4.12, s, broad, IH; 4.26, fourth, 2H; 6.38, s, 2H; 6.72, dd, IH; 6.91, dd, 2H; 7.20, d, IH; 7.77, s, broad, IH.

Example 4a

Methyl 3 - ({3-chloro-4 - [(3-isopropyl-1H-indol-5-yl) oxy] -5-methylphenyl} amino) -3-oxo-propanoate

131 mg of 3-chloro-4 - [(3-isopropyl-lH-indol-5-yl) oxy] -5-methylaniline (Example III) are dissolved in 46 ml of triethylamine in 3 ml of acetone and with 62 mg of methyl malonate at 0 ° C added dropwise. The mixture is stirred at room temperature for 3 hours, poured onto 20 ml of dichloromethane, the organic phase is washed with sodium chloride solution, dried over sodium sulfate and rotated in. Chromatographic purification (cyclohexane / ethyl acetate) gives 134 mg of methyl 3 - ({3-chloro-4 - [(3-isopropyl-lH-indol-5-yl) oxy] -5-methylphenyl-yl} amino) - 3-oxo-propanoate.

1H-NMR (300 MHz, CDC1 ₃ ): δ = 1.28, d, 6H; 2.20, s, 3H; 3.07, sept, IH; 3.50, s,

2H; 3.83, s, 3H; 6.77, dd, IH; 6.92, d, IH; 6.95, d, IH; 7.24, m, IH; 7.36, d, IH; 7.65, d, IH; 7.81, s, broad, IH; 9.24, s, broad, IH. Example 4b

Ethyl 3- ({3-chloro-4 - [(3-isopropyl-1H-indol-5-yl) oxy] -5-methylphenyl} amino) -3-oxo-propanoate

Analogously to Example 4a, starting from 2.50 g (7.94 mmol) of 3-chloro-4- [(3-isopropyl-1H-indol-5-yl) oxy] -5-methylaniline (Example III) and 1.26 g (7.94 mmol) ethyl malonate 3.65 g (99% of theory) ethyl 3 - ({3-chloro-4- [(3-isopropyl-1H-indol-5-yl) oxy ] -5-methylphenyl} amino) -3-oxo-propanoate.

1H-NMR (200 MHz, CDC1 ₃ ): δ = 1.28, d, 6H; 1.34, t, 3H; 2.19, s, 3H; 3.08, sept, IH; 3.49, s, 2H; 4.27, fourth, 2H; 6.76, dd, IH; 6.93, m, 2H; 7.22, m, IH; 7.36, d, IH; 7.66, d, IH; 7.80, broad s, IH; 9.32, broad s, IH.

Example 4c

Isopropyl 3 - ({3-chloro-4 - [(3-isopropyl-1H-indol-5-yl) oxy] -5-methylphenyl} amino) - 3-oxo-propanoate

This compound can be prepared starting from 3-chloro-4 - [(3-isopropyl-1H-indol-5-yl) oxy] - 5-methylaniline (Example HI) in analogy to Example 4a. Example 4d

2-Hydroxyethyl-3 - ({3-chloro-4 - [(3-isopropyl-1H-indol-5-yl) oxy] -5-methylphenyl} - amino) -3-oxopropanoate

Starting from 3-chloro-4 - [(3-isopropyl-1H-indol-5-yl) oxy] - 5-methylaniline (Example III) or methyl-3 - ({3-chloro-4 - [( 3-isopropyl-1H-indol-5-yl) oxy] -5-methylphenyl} amino) -3-oxo-propanoate (Example 4a) can be prepared by methods known from the literature.

Example 5

N- {4 - [(3-isopropyl-lH-indol-5-yl) oxy] -3,5-dimethylphenyl} glycine

56 mg of ethyl N- {4 - [(3-isopropyl-lH-indol-5-yl) oxy] -3,5-dimethylphenyl} glycinate (Example 3) are dissolved in 7 ml of dioxane with 1.5 ml of 1N sodium hydroxide solution 2 Stirred for hours at room temperature. It is poured into water, acidified with 1N hydrochloric acid, extracted with ethyl acetate, dried and the solvent is removed in vacuo. 51 mg of N- {4 - [(3-isopropyl-1H-indol-5-yl) oxy] -3,5-dimethylphenyl} glycine are obtained. 1H-NMR (300 MHz, CDC1 ₃ ): δ = 1.29, d, 6H; 2.10, s, 6H; 3.07, sept, IH; 3.70, s, 2H; 6.41, s, 2H; 6.73, m, IH; 6.91, m, 2H; 7.21, d, IH; 7.77, s, broad, IH.

Example 6 3 - ({3-Chloro-4 - [(3-isopropyl-1H-indol-5-yl) oxy] -5-methylphenyl} amino) -3-oxo-propionic acid

101 mg methyl 3 - ({3-chloro-4 - [(3-isopropyl-1H-indol-5-yl) oxy] -5-methylphenyl} - amino) -3-oxo-propanoate (Example 4a) are dissolved in 2 ml of ethanol and 1 ml of 1N sodium hydroxide solution, stirred for 1 hour at room temperature and the solvent removed in vacuo. It is acidified, extracted with ethyl acetate, dried over sodium sulfate and the solvent is removed in vacuo. 87 mg of 3 - ({3-chloro-4 - [(3-isopropyl-1H-indol-5-yl) oxy] -5-methylphenyl} amino) -3-oxopropionic acid are obtained.

1H-NMR (300 MHz, MeOH-d ₄ ): δ = 1.25, d, 6H; 2.16, s, 3H; 2.99, sept, IH; 3.45, s, 2H; 6.69, dd, IH; 6.76, d, IH; 6.96, s, IH; 7.23, d, IH; 7.38, d, IH; 7.73, d, IH.

Example 6a

Potassium 3- ({3-chloro-4 - [(3-isopropyl-1H-indol-5-yl) oxy] -5-methylphenyl} amino) -3-oxopropanoate

1.16 g (2.89 mmol) 3 - ({3-chloro-4 - [(3-isopropyl-1H-indol-5-yl) oxy] -5-methylphenyl} amino) -3-oxopropionic acid ( Example 6) are dissolved in 15 ml of THF and 5.67 ml of a 0.51 molar potassium hydroxide solution are added dropwise at 0 ° C. The reaction mixture is stirred for one hour and then the solvent in

Vacuum removed. Co-evaporation with toluene gives 1.25 g (99% of theory) of potassium 3 - ({3-chloro-4 - [(3-isopropyl-lH-indol-5-yl) oxy] -5- methylphenyl} amino) -3-oxopropanoate.

1H NMR (200 MHz, DMSO-d ₆ ): δ = 1.20, d, 6H; 2.10, s, 3H; 2.83, s, 2H; 2.96, sept,

IH; 6.62, dd, IH; 6.73, d, IH; 7.04, d, IH; 7.26, m, 3H; 7.84, d, IH; 10.70, s, broad, IH; 13.03, s, broad, IH.

Example 6b Sodium 3 - ({3-chloro-4 - [(3-isopropyl-1H-indol-5-yl) oxy] -5-methylphenyl} amino) -3-oxopropanoate

This compound is obtained in a manner analogous to Example 6a, starting from 3 - ({3-chloro-4 - [(3-isopropyl-1 H-indole-5-yl) oxy] -5-methylphenyl} amino) -3-oxopropion - Acid (Example 6) and sodium hydroxide.

Example 6c

Magnesium bis [3 - ({3-chloro-4 - [(3-isopropyl-1H-indol-5-yl) oxy] -5-methylphenyl} - amino) -3-oxopropanoate]

This compound is obtained analogously to Example 6a starting from 3 - ({3-chloro-4 - [(3-isopropyl-1H-indol-5-yl) oxy] -5-methylphenyl} amino) -3-oxopropion- acid (Example 6) and magnesium methanolate

Example 6d

Calcium bis [3 - ({3-chloro-4 - [(3-isopropyl-1H-indol-5-yl) oxy] -5-methylphenyl} - amino) -3-oxopropanoate]

This compound is obtained analogously to Example 6a starting from 3 - ({3-chloro-4 - [(3-isopropyl-1H-indol-5-yl) oxy] -5-methylphenyl} amino) -3-oxopropion- acid (Example 6) and calcium hydroxide. Example 7

Methyl 3 - ({3,5-dichloro-4 - [(3-isopropyl-1H-indol-5-yl) oxy] phenyl} amino) -3-oxopropanoate

139 mg of 3,5-dichloro-4 - [(3-isopropyl-lH-indol-5-yl) oxy] aniline (Example IV) are dissolved in 46 ml of triethylamine in 3 ml of acetone and with 62 mg of methyl malonate at 0 ° C added dropwise. The mixture is stirred at room temperature for 1 hour, poured onto 20 ml of dichloromethane, the organic phase is washed with sodium chloride solution, dried over sodium sulfate and rotated in. Chromatographic purification (cyclohexane / ethyl acetate) gives 162 mg of methyl 3 - ({3,5-dichloro-4 - [(3-isopropyl-1H-indol-5-yl) oxy] phenyl} amino) -3-oxopropanoate ,

1H-NMR (300 MHz, CDC1 ₃ ): δ = 1.29, d, 6H; 3.09, sept, IH; 3.47, s, 2H; 3.82, s,

3H; 6.80, dd, IH; 6.96, m, IH; 7.19, s, IH; 7.24, m, IH; 7.70, s, 2H; 7.82, s, broad, IH; 9.43, s, broad, IH.

Example 8

3 - ({3,5-dichloro-4 - [(3-isopropyl-1H-indol-5-yl) oxy] phenyl} amino) -3-oxopropionic acid

193 mg of methyl 3 - ({3,5-dichloro-4 - [(3-isoropropyl-lH-indol-5-yl) oxy] phenyl} amino) -3-oxopropanoate (Example 7) are dissolved in 3 ml of ethanol with 1 ml IN NaOH stirred for one hour at room temperature. The solvent is removed in vacuo and the residue is taken up in dichloromethane. It is shaken with water, the organic phase is dried and the solvent is removed in vacuo. By stirring with diethyl ether, 143 mg of 3 - ({3,5-dichloro-4 - [(3-isopropyl-1H-indol-5-yl) oxy] - phenyl} amino) -3-oxopropionic acid are obtained.

1H-ΝMR (300 MHz, MeOH-d ₄ ): δ = 1.27, d, 6H; 3.00, sept, IH; 3.35, s, 2H; 6.70, dd, IH; 6.79, m, IH; 6.97, s, IH; 7.23, d, IH; 7.79, s, 2H.

Example 9

Ethyl N- {3-chloro-4 - [(3-isopropyl-lH-indol-5-yl) oxy] -5-methylphenyl} glycinate

120 mg of 3-chloro-4 - [(3-isopropyl-1H-indol-5-yl) oxy] -5-methylaniline (Example III) are refluxed with 62 mg of sodium acetate and 63 mg of ethyl bromoacetate in 5 ml of ethanol for 17 hours , A further 21 mg of ethyl bromoacetate are added and the mixture is refluxed for 3 hours. The solvent is removed in vacuo, the mixture is taken up in water and dichloromethane, the organic phase is washed with saturated sodium chloride solution, the organic phase is dried and the solvent is removed in vacuo. Chromatographic purification (cyclohexane / ethyl acetate) gives 56 mg of ethyl N- {3-chloro-4 - [(3-isopropyl-lH-indol-5-yl) oxyi-5-methylphenyl} glycinate

1H-NMR (300 MHz, CDC1 ₃ ): δ = 1.29, d, 6H; 1.32, t, 3H; 2.13, s, 3H; 3.08, sept. 1H; 3.91, s, 2H; 4.28, fourth, 2H; 6.43, d, IH; 6.56, d, IH; 6.77, dd, IH; 6.94, d, IH; 7.22, d, IH; 7.78, s, broad, IH.

Example 10 Ethyl N- {3,5-dichloro-4 - [(3-isopropyl-1H-indol-5-yl) oxy] phenyl} glycinate

100 mg of 3,5-dichloro-4 - [(3-isopropyl-1H-indol-5-yl) oxy] aniline (Example IV) are refluxed with 49 mg of sodium acetate and 50 mg of ethyl bromoacetate in 5 ml of ethanol for 17 hours. A further 21 mg of ethyl bromoacetate are added and the mixture is refluxed for 2 hours. The solvent is removed in vacuo, the mixture is taken up in water and dichloromethane, the organic phase is washed with saturated sodium chloride solution, the organic phase is dried and the solvent is removed in vacuo. Chromatographic purification (cyclohexane / ethyl acetate) gives 22 mg of ethyl N- {3,5-dichloro-4 - [(3-isopropyl-lH-indol-5-yl) oxy] phenyl} glycinate.

1H-NMR (300 MHz, DMSO-d ₆ ): δ = 1.21, t, 3H; 1.22, d, 6H; 2.96, m IH; 4.00, m, 2H; 4.15, fourth, 2H; 6.63, m, IH; 6.76, d, IH; 6.77, s, 2H; 7.06, d, IH; 7.24, d, IH.

Example 11

4- (3-isopropyl-lH-indol-5-yloxy) -3,5-bis-trifluoromethyl-phenylacetic acid

A mixture of 5 ml of concentrated sulfuric acid and 5 ml of water is added dropwise to a solution of 0.35 g (0.82 mmol) of nitrile derivative from Example VIII in 5 ml of acetic acid (100%). The reaction solution is stirred for 4 hours at 105 ° C., then cooled to room temperature and mixed with ice-cold water and ethyl acetate. The organic phase is separated off, the aqueous solution extracted again with ethyl acetate, the combined organic phases dried over sodium sulfate, filtered and concentrated to an oil. The crude product (120.3 mg) is chromatographed on silica gel 60 using methylene chloride / methanol (95: 5 and 95:11). Yield: 55 mg (15.3%) MS (DCI): 446 ([M + H] ⁺ , 100%)

R _f : 0.38 (methylene chloride: methanol = 9: 1)

1H-NMR (300 MHz, CDC1 ₃ ): δ = 1.28, d, 6H; 3.05, quin, IH; 3.81, s, 2H; 6.69, dd,

IH; 6.89, d, IH; 6.94, d, IH; 7.21, d, IH; 7.8, broad s, IH; 7.88, s, 2H.

Example 12

4- (3-isopropyl-lH-indol-5-yloxy) -3,5-bis-trifluoromethyl-benzyltetrazol

251 mg (4.69 mmol) of ammonium chloride and 305 mg (4.69 mmol) of sodium azide are added to a solution of 200 mg (0.469 mmol) of nitrile derivative from Example VIII in 8 ml of dimethylformamide and the mixture is boiled under reflux for 4 hours. The solution is then strongly concentrated, treated with 6N hydrochloric acid and extracted three times with ethyl acetate. The combined organic phases are dried, filtered and concentrated in vacuo to an oil. The crude product is dissolved in dichloromethane and chromatographed on silica gel 60 with dichloromethane with the addition of methanol in the gradient mode (90: 5 to 90:40). Yield: 126 mg (57.3%) MS (ESI): 470 ([M + H] ⁺ , 100%)

R _f : 0.30 (dichloromethamethanol = 9: 1)

1H-NMR (200 MHz, CDC1 ₃ ): δ = 1.27, d, 6H; 3.06, quin, IH; 4.49, s, 2H; 6.67, dd, IH; 6.88, d, IH; 6.94, d, IH; 7.2, d, IH; 7.84, broad s, IH; 7.92, s, 2H; 8.01, s, IH.

Example 13

4- (3-isopropyl-lH-indol-5-yloxy) -3,5-bis-trifluoromethyl-cinnamate

1.0 g (2.41 mmol) of aldehyde derivative from Example V is dissolved in 10 ml of toluene and 0.92 g (2.65 mmol) of ethoxycarbonylmethylene triphenylphosphorane is added in portions. After 2 days of stirring at room temperature, the reaction mixture is concentrated to half the volume and chromatographed on silica gel 60 using toluene.

Yield: 1.076 g (88.4%)

MS (ESI): 486 ([M + H] ⁺ , 100%)

R _f : 0.68 (toluene-ethyl acetate = 8: 2)

HPLC: R _t = 5.44 (94.5%) 0.5% HClO ₄ / acetonitrile

Kromasil column C18 (60 x 2 mm) flow: 0.75 ml / minute; 210 nm

1H-NMR (200 MHz, CDC1 ₃ ): δ = 1.27, d, 6H; 1.37, t, 3H; 3.05, quin, IH; 4.3, fourth, 2H; 6.55, broad d, IH; 6.72, dd, IH; 6.87, d, IH; 6.95, d, IH; 7.21, d, IH; 7.73, broad d, IH; 7.84, broad s, IH; 8.04, s, 2H. Example 14

4- (3-isopropyl-lH-indol-5-yloxy) -3,5-bis-trifluoromethyl-cinnamic acid

0.23 g (0.46 mmol) of ethyl cinnamate from Example 13 are dissolved in 10 ml of dioxane, 4 ml of 1 molar sodium hydroxide solution are added and the mixture is stirred at room temperature for 5 hours. The reaction solution is acidified to pH 4 with 1N hydrochloric acid, ethyl acetate is added and the aqueous phase is extracted twice more with ethyl acetate. The combined organic phases are washed with sodium chloride solution, dried over sodium sulfate, filtered, concentrated and dried under high vacuum overnight.

Yield: 0.175 g (79.0%) MS (DCI): 475 ([M + NH ₄ ] ⁺ , 100%) HPLC: R _t = 4.99 (96.3%)

0.5% HClO ₄ / acetonitrile

Kromasil column C18 (60 x 2 mm)

Flow: 0.75 ml / minute; 210 nm

1H-NMR (200 MHz, CDC1 ₃ ): δ = 1.28, d, 6H; 3.06, quin, IH; 6.59, broad d, IH;

6.73, dd, IH; 6.88, d, IH; 6.97, d, IH; 7.23, d, IH; 7.83, broad s and broad d, 2H; 8.09, s, 2H. Example 15

4- (3-isopropyl-lH-indol-5-yloxy) -3,5-bis-trifluoromethyl-phenylρropionsäure

150 mg (0.328 mmol) of cinnamic acid derivative from Example 14 are dissolved in 10 ml of methanol, 75 mg of palladium on activated carbon (10%) are added and the mixture is hydrogenated at hydrostatic hydrogen pressure for 18 hours. The palladium catalyst is over

Aspirated kieselguhr, washed with methanol and the filtrate to a solid

Product restricted.

Yield: 86.2 mg (57.2%)

MS (LC): 460 ([M + H] ⁺ , 100%)

R _f : 0.76 (methylene chloride: methanol = 10: 1)

1H-NMR (200 MHz, DMSO-d ₆ ): δ = 1.19, d, 6H; 2.7, t, 2H; 2.95, quin, IH; 3.03, t,

2H; 6.58, dd, IH; 6.1, d, IH; 7.08, d, IH; 7.24, d, IH; 8.05, s, 2H; 10.72, d, IH; 12.25, broad s, IH.

Example 16

{4 - [(3-isopropyl-lH-indol-5-yl) oxy] -3,5-dimethylphenoxy} acetic acid

0.24 g (0.46 mmol) of tert-butyl- [4 - ({l- [tert-butyl- (dimethyl) silyl] -3-isopropyl-1H-indol-5-yl} oxy) -3,5-dimethylphenoxy] acetate (Example XIII) dissolved in 5 ml of ethanol and adds 2.5 ml (2.50 mmol) of 1 N sodium hydroxide solution. The mixture is stirred at room temperature for 2.5 h. The solvent is spun off, the mixture is diluted with 50 ml of water and acidified with 1 N hydrochloric acid solution. The aqueous phase is extracted twice with ethyl acetate, the combined organic phases are dried and the solvent is removed in vacuo. 0.186 g (87.3%) of {4 - [(3-isopropyl-1H-indol-5-yl) oxy] -3,5-dimethylphenoxy} acetic acid is obtained.

1H-NMR (200 MHz, CDC1 ₃ ): δ = 1.28, d, 6H; 2.10, s, 6H; 2.96, m, IH; 3.08, sept,

IH; 4.58, s, 2H; 6.68, s, 3H; 6.90, dd, 2H; 7.81, s, IH.

Example 17

4- (3-isopropyl-lH-indol-5-yloxy) -3,5-dichlθφhenylessigsäure

5 ml of conc. Are first added dropwise to a solution of 0.43 g (0.90 mmol) of nitrile derivative from Example XIX in 10 ml of dioxane. Add sulfuric acid and then 5 ml of water. The reaction mixture is stirred for 4 hours at 100 ° C., then poured onto ice and extracted twice with ethyl acetate. The combined organic phases are washed with brine, dried over sodium sulfate, filtered and concentrated in vacuo. The crude product is chromatographed on silica gel 60 using toluene / ethyl acetate (1: 1) in the isocratic mode. Yield: 0.266 g (68.7%) MS (DCI): 395 ([M + NH »] ^{" 1 "} , 100%) HPLC: R _t = 4.79 (87.8%)

0.5% HClO ₄ / acetonitrile

Kromasil column C18 (60 x 2 mm)

Flow: 0.75 ml / min .; 210 µm

1H-NMR (200 MHz, CDC1 ₃ ): δ = 1.4 (d, 6H); 3.1 (quin, IH); 3.65 (s, 2H); 6.76 (dd,

IH); 6.95 (d, IH); 7.03 (d, IH); 7.24 (d, IH); 7.34 (s, 2H); 7.81 (broad s, IH).

Example 18

5- {4 - [(3-isopropyl-1H-indol-5-yl) oxy] -3,5-bis-trifluoromethyl-phenyl} -imidazolidine-2,4-dione

3.0 g (7.22 mmol) of aldehyde are added to a solution of 0.581 g (14.4 mmol) of sodium cyanide and 3.63 g (36.1 mmol) of ammonium carbonate in 30 ml of water

Example V dissolved in 30 ml of ethanol and stirred at 60 ° C. for 24 hours. On- finally the reaction solution is distilled off from ethanol, diluted with water, acidified to pH 2 with 1 N hydrochloric acid while cooling with ice and extracted twice with ethyl acetate. After drying and distilling off the solvent, the crude product (4.03 g) is chromatographed on silica gel 60 with methylene chloride with the addition of a little methanol in a ratio of 20: 1 to 20: 2.5. Yield: 2.73 g (78.1%) MS (ESI): 486 ([M + H] ⁺ , 100%) HPLC: R _t = 4.58 (85.1%)

0.5% HClOJ acetonitrile

Kromasil column C18 (60 x 2 mm)

Flow: 0.75 ml / min .; 210 nm

1H-NMR (200 MHz, CDC1 ₃ ): δ = 1.26 (d, 6H); 3.06 (quin, IH); 5.29 (s, IH); 6.23 (s, IH); 6.65 (dd, IH); 6.9 (d, IH); 6.95 (d, IH); 7.2 (d, IH); 7.8 (broad s, IH); 7.97 (s, 2H); 8.27 (broad s, IH).

Example 19

DL-amino- {4 - [(3-isopropyl-lH-indol-5-yl) oxy] -3,5-bis-trifluoromethyl-phenyl} -acetic acid

1.0 g (2.06 mmol) of hydantoin from Example 18 are heated to 100 ° C. overnight with 0.493 g (20.6 mmol) of lithium hydroxide in 15 ml of water. The reaction solution is cooled to 0 ° C. and directly reacted further with di-tert-butyl dicarbonate (Example 20). R _f : 0.39 (methylene chloride: methanol = 8: 2) Example 20

DL-tert-butoxycarbonylamino- {4 - [(3-isopropyl-1H-indol-5-yl) oxy] -3,5-bis-trifluoromethylphenyl} acetic acid

The reaction solution from Example 19 (approx. 2.06 mmol - 100%) is mixed with 50 ml of dioxane and at 0 ° C. with 0.899 g (4.12 mmol) of di-tert-butyl dicarbonate dissolved in 5 ml of dioxane dropwise implemented. The reaction solution is then left on

Come to room temperature and stir for 2 hours at room temperature. After dioxane had been distilled off, the reaction solution was acidified at 0 ° C. with 1 N hydrochloric acid to pH 2 and extracted twice with ethyl acetate. The combined ethyl acetate phases are washed with sodium chloride solution, dried, filtered and concentrated. The crude product (1.234 g) is on silica gel 60 with methylene chloride

Chromatographed methanol (9: 1) in isocratic mode. Yield: 0.271 g (23.5%)

A second fraction of 0.531 g (HPLC content: 64.0%) is obtained. MS (LC-MS): 561 ([M + H] ⁺ , 100%) HPLC: R _t = 0.503 (91.4%)

0.5% HClO- _t / acetonitrile Kromasil C18 column (60 x 2 mm) flow: 0.75 ml / min .; 210 nm 1H-NMR (200 MHz, d ₆ -DMSO): δ = 1.18 (d, 6H); 1.38 (s, 9H); 2.93 (m, IH); 3.33 (broad s, IH); 4.99 (d, IH); 6.59 (d, IH); 6.1 (s, IH); 7.08 (d, IH); 7.25 (d, IH); 8.1 (s, 2H); 10.75 (s, IH).

Example 21

DL-amino- {4 - [(3-isopropyl-lH-indol-5-yl) oxy] -3,5-bis-trifluoromethyl-phenyl} -acetic acid acetate salt

0.526 g (0.945 mmol) of tert-butoxycarbonyl-protected amino acid from Example 20 are dissolved in 7 ml of dichloromethane, cooled to 0 ° C. and 7 ml of trifluoroacetic acid are added dropwise under argon. The solution is then stirred for 45 minutes at room temperature, then concentrated to an oil, the oily residue is stirred with ether and ether is distilled off. Yield: 0.526 g (as trifluoroacetate salt)

The residue is dissolved in 20% acetic acid (20 ml) with the addition of 10 ml of methanol and passed through a column filled with 80 ml of Amberlite IR-67 (acetate form; Fluka). It is then washed with a water / methanol mixture (1: 1), the eluate is freed from methanol in vacuo and lyophilized. Yield: 120 mg (27.8%) MS (EI): 460 ([M] ⁺ , 14%)

HPLC: R _t = 4.29 (79.8%) 0.5% HClO ₄ / acetonitrile

Kromasil column C18 (60 x 2 mm) flow: 0.75 ml min .; 210 nm Example 22

5 - {4- [(3-isopropy 1- 1 H-indol-5-yl) oxy] -3, 5-bis-trifluoromethyl 1-benzylidene} - thiazolidine-2,4-dione

A mixture of 0.52 g (1.25 mmol). Aldehyde derivative from Example V, 0.21 g

(1.63 mmol) 2,4-thiazolidine-2,4-dione, 0.2 g (1.63 mmol) benzoic acid and 0.14 g (1.63 mmol) piperidine in 47.5 ml toluene are left overnight in the presence of

Molecular sieve 4A powder cooked under reflux. The reaction solution is then cooled to room temperature, diluted with 47.5 ml of toluene, suction filtered from the molecular sieve and washed with ethyl acetate. The organic filtrate is washed twice with ammonium chloride solution, dried, filtered and concentrated in vacuo. Chromatography on silica gel 60 using toluene / ethyl acetate (10: 1) in the isocratic mode gives the thiazolidinedione derivative. Yield: 50 mg (4.9%) MS (ESI): 515 ([M + H] ⁺ , 100%) HPLC: R _t = 3.72 (63.2%) 0.3 g 30% HC1 pro 1 1 H ₂ O

Symmetry column C18 (150 x 2.1 mm) flow: 0.9 ml / min .; 210 µm Example 23

6- {4- [(3-isopropyl-1 H -indol-5-yl) oxy] -3, 5-bis-trifluoromethyl-pheny 1} - [1, 3] - thiazinan-2,4-dione

The thiazine derivative is formed as a further product in the preparation of the benzylidene-2,4-thiazolidinedione derivative (Example 22). Yield: 0, 123 g (14.7%) MS (LC): 517 ([M + H] ⁺ , 100%) HPLC: R _t = 3.26 (77.3%)

0.3 g of 30% HC1 per 1 1 H ₂ O

Symmetry column C18 (150 x 2.1 mm)

Flow: 0.9 ml / min .; 210 µm

Example 24

3- {4 - [(3-isopropyl-lH-indol-5-yl) oxy] -3,5-bis-trifluoromethyl-benzylidene} dihydro-furan-2-one

0.36 g (0.87 mmol) of aldehyde derivative from Example V are dissolved in 10 ml of toluene and 0.36 g (1.04 mmol) of butyrolactonylidene triphenylphosphorane are added in portions. After 3 days of stirring at room temperature, the reaction mixture is filtered, the filtrate is concentrated to half the volume and chromatographed on silica gel 60 using toluene / ethyl acetate (9: 1). Yield: 0.334 g (72.5%) MS (DCI): 501 ([M + NH ₄ ] ⁺ , 100%) R _f : 0.87 (toluene: ethyl acetate = 9: 1)

1H-NMR (200 MHz, CDC1 ₃ ): δ = 1.27 (d, 6H); 3.05 (quin, IH); 3.31 (sext, 2H); 4.55 (t. 2H); 6.71 (dd, IH); 6.88 (d, IH); 6.96 (d, IH); 7.2 (d, IH); 7.62 (t, IH); 7.84 (broad s, IH); 8.03 (s, 2H).

Example 25

3 - {4 - [(3-isopropyl-1 H-indol-5-yl) oxy] -3, 5-bis-trifluoromethyl-benzyl} -dihydrofuran-2-one

0.2 g (0.38 mmol) of benzylidene compound from Example 24 are dissolved in 100 ml of methanol and hydrogenated with hydrogen in the presence of palladium on activated carbon for 18 hours. The catalyst is suctioned off through kieselguhr and the filtrate is concentrated in vacuo. The raw product is cleaned by chromato- graph on silica gel 60 in isocratic gradient mode with toluene / ethyl acetate

(10: 1).

Yield: 94 mg (48.7%)

MS (ESI): 486 ([M + H] ⁺ , 100%)

R _f : 0.35 (toluene: ethyl acetate = 9: 1)

1H-NMR (300 MHz, CDC1 ₃ ): δ = 1.28 (d, 6H); 2.04 (m, IH); 2.37 (m, IH); 2.91 (m. 2H); 3.05 (quin, IH); 3.4 (quart, IH); 4.23 (m, IH); 4.39 (sext, IH); 6.69 (dd, IH); 6.85 (d, IH); 6.94 (d, IH); 7.2 (d, IH); 7.77 (s, 2H); 7.8 (s, IH).

Example 26

5- {4 - [(3-Isopropyl-1H-indol-5-yl) oxy] -3,5-bis-trifluoromethyl-phenyl} -3-oxo-pent-4-ene carboxylic acid ethyl ester

Analogously to the procedure of Example 24, 0.35 g (0.84 mmol) of aldehyde derivative from Example V with 0.36 g (0.93 mmol) of ethyl 4- (triphenylphosphoranylidene) in 10 ml of toluene were added for 2 days Room temperature and then 18 hours at 75 ° C and 6 hours at 120 ° C implemented. The crude product is purified by column chromatography on silica gel 60 using toluene. Yield: 0.24 g (47.3%) MS (ESI): 528 ([M + H] ⁺ , 100%)

HPLC: R _t = 6.00 (27.3%) and R _t = 5.35 (51.2%); E / Z-mixture

0.5% HClO acetonitrile

Kromasil column Cl 8 (60 x 2 mm)

Flow: 0.75 ml / min .; 210 nm

Example 27

5- {4 - [(3-Isopropyl-1H-indol-5-yl) oxy] -3,5-bis-trifluoromethyl-phenyl} -3-oxopentanecarboxylic acid, ethyl ester

Analogously to the procedure of Example 25, 0.2 g (0.38 mmol) of 3-oxopentene-4-carboxylic acid derivative from Example 26 are hydrogenated overnight in methanol with palladium on activated carbon under a hydrogen atmosphere. The crude product is chromatographed on silica gel with toluene / ethyl acetate (10: 1) in the isocratic mode.

Yield: 89 mg (38.6%)

MS (ESI): 530 ([M + H] ⁺ , 100%)

R _f : 0.37 (toluene: ethyl acetate = 9: 1) 1H-NMR (200 MHz, CDC1 ₃ ): δ = 1.28 (d and t, 9H); 3.03 (m, 5H); 3.49 (s, 2H); 4.2

(quart, 2H); 6.1 (dd, IH); 6.87 (d, IH); 6.95 (d, IH); 7.21 (d, IH); 7.73 (s, 2H); 7.8

(s, IH). Example 28

Ethyl 5- {4 - [(3-isopropyl-1H-indol-5-yl) oxy] -3,5-bis-trifluoromethyl-phenyl} pentanecarboxylic acid

The pentanecarboxylic acid derivative is formed as a by-product in the catalytic hydrogenation of the 3-oxopentecarboxylic acid derivative in Example 27. Yield: 15 mg (6.2%)

MS (ESI): 516 ([M + H] ⁺ , 100%)

R _f : 0.4 (toluene: ethyl acetate = 9: 1)

1H-NMR (200 MHz, CDC1 ₃ ): δ = 1.28 (d and t, 9H); 1.73 (quin, 3H); 2.39 (m, 2H); 2.78 (m. 2H); 3.04 (sext, 2H); 4.15 (fourth, 2H); 6.7 (dd, IH); 6.86 (d, IH); 6.93 (d,

IH); 7.21 (d, IH); 7.71 (s, 2H); 7.8 (broad s, IH). Example 29

4- (3-cyclohexylmethyl-lH-indol-5-yloxy) -3,5-bis-trifluoromethyl-phenylacetic acid

The preparation is carried out in analogy to the procedure of Example 17 from 0.3 g (0.62 mmol) of phenylacetonitrile derivative from Example XXIII by dissolving the nitrile in 10 ml of dioxane and adding 4 ml of conc. Treated sulfuric acid and 4 ml of water at 100 ° C for 4 hours. The crude product is chromatographed on silica gel 60 using toluene / ethyl acetate (1: 1) in the isocratic mode.

Yield: 65 mg (17.5%) MS (ESI): 500 ([M + H] ⁺ , 100%) HPLC: R _t = 5.23 (82.6%)

0.5% HClO ₄ / acetonitrile Kromasil column C18 (60 x 2 mm)

Flow: 0.75 ml / min .; 210 n R _f : 0.29 (toluene: ethyl acetate = 1: 1)

1H-NMR (200 MHz, CDC1 ₃ ): δ = 0.92 (m, 2H); 1.17 (m, 4H); 1.5 (, IH); 1.65 (m, 4H); 2.49 (d, 2H); 3.82 (s, 2H); 6.68 (dd, IH); 6.84 (d, IH); 6.93 (d, IH); 7.2 (d, IH);

7.85 (d and s, 3H). The following can be produced in an analogous manner:

Example 30

{4 - [(3-isopropyl-lH-indol-5-yl) oxy] -3,5-dimethylphenoxy} acetic acid

Example 31

{4 - [(3-cyclopropyl-lH-indol-5-yl) oxy] -3,5-dimethylphenoxy} acetic acid

Example 32 {4 - [(3-Cyclobutyl-1H-indol-5-yl) oxy] -3,5-dimethylphenoxy} acetic acid

Example 33

{4 - [(3-cyclopentyl-lH-indol-5-yl) oxy] -3,5-dimethylphenoxy} acetic acid

Example 34

{4 - [(3-cyclohexyl-lH-indol-5-yl) oxy] -3,5-dimethylphenoxy} acetic acid

Example 35

{3,5-dimethyl-4 - [(3-propyl-lH-indol-5-yl) oxy] phenoxy} acetic acid

Example 36

{4 - [(3-butyl-1H-indol-5-yl) oxy] -3, 5-dimethylphenoxy} acetic acid

Example 37 {3,5-Dimethyl-4 - [(3-pentyl-1H-indol-5-yl) oxy] phenoxy} acetic acid

Example 38

{4 - [(3-hexyl-lH-indol-5-yl) oxy] -3,5-dimethylphenoxy} acetic acid

Example 39

{4 - [(3-isobutyl-lH-indol-5-yl) oxy] -3,5-dimethylphenoxy} acetic acid Example 40

{4 - [(3-sec-butyl-lH-indol-5-yl) oxy] -3,5-dimethylphenoxy} acetic acid

Example 41

(4- {[3- (Cyclohexylmethyl) -1 H-indol-5-yl] oxy} -3,5-dimethylphenoxy) acetic acid

Example 42

(4 - {[3- (cyclopentylmethyl) -lH-indol-5-yl] oxy} -3,5-dimethylphenoxy) acetic acid

Example 43 (4 - {[3- (Cyclobutylmethyl) -IH-indol-5-yl] oxy} -3,5-dimethylphenoxy) acetic acid

Example 44 (4- {[3 - (Cyclopropylmethyl) -1 H-indol-5-yl] oxy} -3,5-dimethylphenoxy) acetic acid

Example 45

{3,5-dichloro-4 - [(3-isopropyl-lH-indol-5-yl) oxy] phenoxy} acetic acid

Example 46

{3,5-dichloro-4 - [(3-cyclopropyl-lH-indol-5-yl) oxy] phenoxy} acetic acid

Example 47

(3,5-dichloro-4 - [(3-cyclobutyl-lH-indol-5-yl) oxy] phenoxy} acetic acid

Example 48 {3,5-dichloro-4 - [(3-cyclopentyl-1H-indol-5-yl) oxy] phenoxy} acetic acid

Example 49 {3,5-dichloro-4 - [(3-cyclohexyl-lH-indol-5-yl) oxy] phenoxy} acetic acid Example 50

{3,5-dichloro-4 - [(3-propyl-lH-indol-5-yl) oxy] phenoxy} acetic acid

Example 51 {4 - [(3-Butyl-1H-indol-5-yl) oxy] -3,5-dichloropheneoxy} acetic acid

Example 52

{3,5-dichloro-4 - [(3-pentyl-lH-indol-5-yl) oxy] phenoxy} acetic acid

Example 53

{3,5-dichloro-4 - [(3-hexyl-lH-indol-5-yl) oxy] phenoxy} acetic acid

Example 54

{3,5-dichloro-4 - [(3 -isobutyl-1H-indol-5 -yl) oxy] phenoxy} acetic acid

Example 55 {4 - [(3-sec-Butyl-1H-indol-5-yl) oxy] -3,5-dichloφhenoxy} acetic acid

Example 56 (3,5-dichloro-4- {[3- (cyclohexylmethyl) - 1H-indol-5-yl] oxy} phenoxy) acetic acid

Example 57

(3,5-dichloro-4 - {[3- (cyclopentylmethyl) -lH-indol-5-yl] oxy} phenoxy) acetic acid

Example 58

(3,5-dichloro-4 - {[3- (cyclobutylmethyl) -lH-indol-5-yl] oxy} phenoxy) acetic acid

Example 59

(3,5-dichloro-4 - {[3- (cyclopropylmethyl) -lH-indol-5-yl] oxy} phenoxy) acetic acid Example 60

{3,5-dibromo-4 - [(3-isopropyl-lH-indol-5-yl) oxy] phenoxy} acetic acid

Example 61 {3,5-Dibromo-4 - [(3-cyclopropyl-lH-indol-5-yl) oxy] phenoxy} acetic acid

Example 62

{3,5-dibromo-4 - [(3-cyclobutyl-lH-indol-5-yl) oxy] phenoxy} acetic acid

Example 63

{3,5-dibromo-4- [(3-cy clopenty 1- 1 H-indol-5-yl) oxy] phenoxy} acetic acid

Example 64

{3,5-dibromo-4 - [(3-cyclohexyl-lH-indol-5-yl) oxy] phenoxy} acetic acid

Example 65 {3,5-dibromo-4 - [(3-propyl-1H-indol-5-yl) oxy] phenoxy} acetic acid

Example 66 {3,5-dibromo-4 - [(3-butyl-lH-indol-5-yl) oxy] phenoxy} acetic acid

Example 67

{3,5-dibromo-4 - [(3-pentyl-lH-indol-5-yl) oxy] phenoxy} acetic acid

Example 68

{3,5-dibromo-4 - [(3-hexyl-lH-indol-5-yl) oxy] phenoxy} acetic acid

Example 69

{3,5-dibromo-4 - [(3-isobutyl-1H-indol-5-yl) oxy] phenoxy} acetic acid Example 70

{3,5-dibromo-4 - [(3-sec-butyl-lH-indol-5-yl) oxy] phenoxy} acetic acid

Example 71 (3,5-dibromo-4 - {[3- (cyclohexylmethyl) -IH-indol-5-yl] oxy} phenoxy) acetic acid

Example 72

(3,5-dibromo-4 - {[3- (cyclopentylmethyl) -lH-indol-5-yl] oxy} phenoxy) acetic acid

Example 73

(3,5-dibromo-4 - {[3- (cyclobutylmethyl) -lH-indol-5-yl] oxy} phenoxy) acetic acid

Example 74

(3,5-dibromo-4 - {[3- (cyclopropylmethyl) -lH-indol-5-yl] oxy} phenoxy) acetic acid

Example 75

[4 - [(3-isopropyl-lH-indol-5-yl) oxy] -3,5-bis (trifluoromethyl) phenoxy] acetic acid

Example 76 [4 - [(3-Cyclopropyl-1H-indol-5-yl) oxy] -3,5-bis (trifluoromethyl) phenoxy] acetic acid

Example 77

[4 - [(3-cyclobutyl-lH-indol-5-yl) oxy] -3,5-bis (trifluoromethyl) phenoxy] acetic acid

Example 78

[4 - [(3-cyclopentyl-lH-indol-5-yl) oxy] -3,5-bis (trifluoromethyl) phenoxy] acetic acid

Example 79

[4 - [(3-cyclohexyl-lH-indol-5-yl) oxy] -3,5-bis (trifluoromethyl) phenoxy] acetic acid Example 80

[4 - [(3-propyl-lH-indol-5-yl) oxy] -3,5-bis (trifluoromethyl) phenoxy] acetic acid

Example 81 [4- [(3-butyl-1H-indol-5-yl) oxy] -3,5-bis (trifluoromethyl) phenoxy] acetic acid

Example 82

[4 - [(3-pentyl-lH-indol-5-yl) oxy] -3,5-bis (trifluoromethyl) phenoxy] acetic acid

Example 83

[4 - [(3-hexyl-lH-indol-5-yl) oxy] -3,5-bis (trifluoromethyl) phenoxy] acetic acid

Example 84

[4- [(3-isobutyl-1 H -indol-5-yl) oxy] -3, 5-bis (trifluoromethyl) phenoxy] acetic acid

Example 85 [4 - [(3-sec-butyl-1H-indol-5-yl) oxy] -3,5-bis (trifluoromethyl) phenoxy] acetic acid

Example 86 [4- {[3- (Cyclohexylmethyl) -IH-indol-5-yl] oxy} -3,5-bis (trifluoromethyl) phenoxy] acetic acid

Example 87

[4 - {[3- (Cyclopentylmethyl) -IH-indol-5-yl] oxy} -3,5-bis (trifluoromethyl) phenoxy] acetic acid

Example 88

[4 - {[3- (Cyclobutylmethyl) -IH-indol-5-yl] oxy} -3,5-bis (trifluoromethyl) phenoxy] acetic acid Example 89

[4- {[3 - (Cyclopropylmethyl) -1 H-indol-5-yl] oxy} -3,5-bis (trifluoromethyl) phenoxy] acetic acid

Example 90

[4 - [(3-isopropyl-lH-indol-5-yl) oxy] -3-methyl-5- (trifluoromethyl) phenoxy] acetic acid

Example 91

[4 - [(3-Cyclopropyl-1H-indol-5-yl) oxy] -3-methyl-5- (trifluoromethyl) phenoxy] acetic acid

Example 92

[4- [(3-Cyclobutyl-1 H -indol-5-yl) oxy] -3-methyl-5 - (trifluoromethyl) phenoxy] acetic acid

Example 93

[4- [(3-Cyclopentyl-1 H -indol-5-yl) oxy] -3-methyl-5- (trifluoromethyl) phenoxy] acetic acid

Example 94

[4 - [(3-Cyclohexyl-1H-indol-5-yl) oxy] -3-methyl-5- (trifluoromethyl) phenoxy] acetic acid

Example 95 [3-methyl-4 - [(3-propyl-1H-indole-5-yl) oxy] -5 - (trifluoromethyl) phenoxy] acetic acid

Example 96

[4- [(3-butyl-1 H -indol-5-yl) oxy] -3-methyl-5 - (trifluoromethyl) phenoxy] acetic acid

Example 97

[3-Methyl-4 - [(3-pentyl-lH-indol-5-yl) oxy] -5- (trifluoromethyl) phenoxy] acetic acid Example 98

[4 - [(3-hexyl-lH-indol-5-yl) oxy] -3-methyl-5- (trifluoromethyl) phenoxy] acetic acid

Example 99

[4 - [(3-isobutyl-lH-indol-5-yl) oxy] -3-methyl-5- (trifluoromethyl) phenoxy] acetic acid

Example 100

[4 - [(3-sec-butyl-lH-indol-5-yl) oxy] -3-methyl-5- (trifluoromethyl) phenoxy] acetic acid

Example 101

[4 - {[3- (Cyclohexylmethyl) -lH-indol-5-yl] oxy} -3-methyl-5- (trifluoromethyl) phenoxy] acetic acid

Example 102

[4- {[3 - (Cyclopentylmethyl) -1 H-indol-5-yl] oxy} -3-methyl-5 - (trifluoromethyl) phenoxy] acetic acid

Example 103 [4- {[3- (Cyclobutylmethyl) - 1H-indol-5-yl] oxy} -3-methyl-5- (trifluoromethyl) phenoxy] acetic acid

Example 104

[4 - {[3- (Cyclopropylmethyl) -IH-indol-5-yl] oxy} -3-methyl-5- (trifluoromethyl) phenoxy] acetic acid

Example 105

{3-bromo-4 - [(3-isopropyl-lH-indol-5-yl) oxy] -5-methylphenoxy} acetic acid

Example 106

{3-bromo-4 - [(3-cyclopropyl-lH-indol-5-yl) oxy] -5-methylphenoxy} acetic acid Example 107

{3-bromo-4 - [(3-cyclobutyl-lH-indol-5-yl) oxy] -5-methylphenoxy} acetic acid

Example 108

{3-bromo-4 - [(3-cyclopentyl-lH-indol-5-yl) oxy] -5-methylphenoxy} acetic acid

Example 109

{3-bromo-4 - [(3-cyclohexyl-lH-indol-5-yl) oxy] -5-methylphenoxy} acetic acid

Example 110

{3-bromo-5-methyl-4 - [(3-propyl-1H-indol-5-yl) oxy] phenoxy} acetic acid

Example 111 {3 -Brom-4 - [(3-butyl-1 H -indol-5-yl) oxy] -5-methylphenoxy} acetic acid

Example 112

{3-bromo-5-methyl-4 - [(3-pentyl-lH-indol-5-yl) oxy] phenoxy} acetic acid

Example 113

{3-bromo-4 - [(3-hexyl-lH-indol-5-yl) oxy] -5-methylphenoxy} acetic acid

Example 114

{3-bromo-4 - [(3-isobutyl-lH-indol-5-yl) oxy] -5-methylphenoxy} acetic acid

Example 115 {3-Bromo-4 - [(3-sec-butyl-1H-indol-5-yl) oxy] -5-methylphenoxy} acetic acid

Example 116 (3-bromo-4 - {[3- (cyclohexylethyl) -lH-indol-5-yl] oxy} -5-methylphenoxy) acetic acid Example 117

(3 -Brom-4- {[3 - (cyclopentylmethyl) - 1 H -indol-5 -yl] oxy} -5 -methylphenoxy) acetic acid

Example 118

(3-bromo-4 - {[3- (cyclobutylmethyl) -lH-indol-5-yl] oxy} -5-methylphenoxy) acetic acid

Example 119

(3 -Brom-4- {[3 - (cyclopropylmethyl) -1 H -indol-5-yl] oxy} -5-methylphenoxy) acetic acid

Example 120

{3-Chloro-4 - [(3-isopropyl-lH-indol-5-yl) oxy] -5-methylphenoxy} acetic acid

Example 121

{3-Chloro-4 - [(3-cyclopropyl-lH-indol-5-yl) oxy] -5-methylphenoxy} acetic acid

Example 122

{3-Chloro-4 - [(3-cyclobutyl-lH-indol-5-yl) oxy] -5-methylphenoxy} acetic acid

Example 123 {3-Chloro-4 - [(3-cyclopentyl-1H-indol-5-yl) oxy] -5-methylphenoxy} acetic acid

Example 124 {3-Chloro-4 - [(3-cyclohexyl-lH-indol-5-yl) oxy] -5-methylphenoxy} acetic acid

Example 125

{3-Chloro-5-methyl-4 - [(3-propyl-lH-indol-5-yl) oxy] phenoxy} acetic acid

Example 126

{4 - [(3-butyl-lH-indol-5-yl) oxy] -3-chloro-5-methylphenoxy} acetic acid Example 127

{3-Chloro-5-methyl-4 - [(3-pentyl-lH-indol-5-yl) oxy] phenoxy} acetic acid

Example 128

{3 -Chlor-4- [(3 -hexyl- 1 H -indol-5-yl) oxy] -5-methylphenoxy} acetic acid

Example 129

{3-Chloro-4 - [(3-isobutyl-lH-indol-5-yl) oxy] -5-methylphenoxy} acetic acid

Example 130

{4- [(3-sec-butyl-1 H -indol-5-yl) oxy] -3-chloro-5-methylphenoxy} acetic acid

Example 131 (3-Chloro-4 - {[3- (cyclohexylmethyl) -lH-indol-5-yl] oxy} -5-methylphenoxy) acetic acid

Example 132

(3-Chloro-4 - {[3- (cyclopentylmethyl) -lH-indol-5-yl] oxy} -5-methylphenoxy) acetic acid

Example 133 (3-Chloro-4 - {[3- (cyclobutylmethyl) -lH-indol-5-yl] oxy} -5-methylphenoxy) acetic acid

Example 134 (3-chloro-4 - {[3- (cyclopropylmethyl) -lH-indol-5-yl] oxy} -5-methylphenoxy) acetic acid

Example 135

{3-bromo-5-chloro-4 - [(3-isopropyl-lH-indol-5-yl) oxy] phenoxy} acetic acid Example 136

{3-bromo-5-chloro-4 - [(3-cyclopropyl-lH-indol-5-yl) oxy] phenoxy} acetic acid

Example 137 {3-Bromo-5-chloro-4 - [(3-cyclobutyl-1H-indol-5-yl) oxy] phenoxy} acetic acid

Example 138

{3-bromo-5-chloro-4 - [(3-cyclopentyl-lH-indol-5-yl) oxy] phenoxy} acetic acid

Example 139

{3 -Bromo-5-chloro-4- [(3 -cyclohexyl-1H-indole-5-yl) oxy] phenoxy} acetic acid

Example 140

{3-bromo-5-chloro-4 - [(3-propyl-lH-indol-5-yl) oxy] phenoxy} acetic acid

Example 141 {3-Bromo-4 - [(3-butyl-1H-indol-5-yl) oxy] -5-chloro-phenoxy} acetic acid

Example 142 {3-Bromo-5-chloro-4 - [(3-pentyl-1H-indol-5-yl) oxy] phenoxy} acetic acid

Example 143

{3-bromo-5-chloro-4 - [(3-hexyl-lH-indol-5-yl) oxy] phenoxy} acetic acid

Example 144

{3-bromo-5-chloro-4 - [(3-isobutyl-lH-indol-5-yl) oxy] phenoxy} acetic acid

Example 145

{3-bromo-4 - [(3-sec-butyl-lH-indol-5-yl) oxy] -5-chloφhenoxy} acetic acid Example 146

(3-Bromo-5-chloro-4 - {[3- (cyclohexylmethyl) -lH-indol-5-yl] oxy} phenoxy) acetic acid

Example 147 (3-bromo-5-chloro-4 - {[3- (cyclopentylmethyl) -IH-indol-5-yl] oxy} phenoxy) acetic acid

Example 148

(3-Bromo-5-chloro-4- {[3 - (cyclobutylmethyl) -1 H -indol-5-yl] oxy} phenoxy) acetic acid

Example 149

(3-Bromo-5-chloro-4 - {[3- (cyclopropylmethyl) -lH-indol-5-yl] oxy} phenoxy) acetic acid

Example 150

[3-chloro-4 - [(3-isopropyl-lH-mdol-5-yl) oxy] -5- (trifluoromethyl) phenoxy] acetic acid

Example 151 3-Chloro-4 - [(3-cyclopropyl-1H-indol-5-yl) oxy] -5- (trifluoromethyl) phenoxy] acetic acid

Example 152 [3-Chloro-4- [(3 -cyclobutyl-1H-indol-5-yl) oxy] -5- (trifluoromethyl) phenoxy] acetic acid

Example 153

[3-chloro-4 - [(3-cyclopentyl-lH-indol-5-yl) oxy] -5- (trifluoromethyl) phenoxy] acetic acid

Example 154

[3-chloro-4 - [(3-cyclohexyl-lH-indol-5-yl) oxy] -5- (trifluoromethyl) phenoxy] acetic acid

Example 155

[3-chloro-4 - [(3-propyl-lH-indol-5-yl) oxy] -5- (trifluoromethyl) phenoxy] acetic acid Example 156

[4 - [(3-butyl-lH-indol-5-yl) oxy] -3-chloro-5- (trifluoromethyl) phenoxy] acetic acid

Example 157 [3-Chloro-4- [(3-pentyl-1 H -indol-5-yl) oxy] -5 - (trifluoromethyl) phenoxy] acetic acid

Example 158

[3-chloro-4 - [(3-hexyl-lH-indol-5-yl) oxy] -5- (trifluoromethyl) phenoxy] acetic acid

Example 159

[3-Chloro-4- [(3 -isobutyl-1H-indol-5-yl) oxy] -5 - (trifluoromethyl) phenoxy] acetic acid

Example 160

[4- [(3-sec-butyl-1 H -indol-5-yl) oxy] -3-chloro-5 - (trifluoromethyl) phenoxy] acetic acid

Example 161

[3-Chloro-4 - {[3- (cyclohexylmethyl) -lH-indol-5-yl] oxy} -5- (trifluoromethyl) -phen-oxy] acetic acid

Example 162

[3-Chloro-4- {[3 - (cyclopentylmethyl) - 1 H -indol-5-yl] oxy} -5 - (trifluoromethyl) phenoxy] acetic acid

Example 163 [3-Chloro-4 - {[3- (cyclobutylmethyl) -lH-indol-5-yl] oxy} -5- (trifluoromethyl) ρhenoxy] acetic acid

Example 164

[3-Chloro-4 - {[3- (cyclopropylmethyl) -IH-indol-5-yl] oxy} -5- (trifluoromethyl) phenoxy] acetic acid Example 165

[3-bromo-4 - [(3-isopropyl-lH-indol-5-yl) oxy] -5- (trifluoromethyl) phenoxy] acetic acid

Example 166 [3-bromo-4 - [(3-cyclopropyl-lH-indol-5-yl) oxy] -5- (trifluoromethyl) phenoxy] acetic acid

Example 167

[3-bromo-4 - [(3-cyclobutyl-lH-indol-5-yl) oxy] -5- (trifluoromethyl) phenoxy] acetic acid

Example 168

[3 -Brom-4- [(3 -cyclopentyl-1 H -indol-5 -yl) oxy] -5 - (trifluoromethyl) phenoxy] acetic acid

Example 169

[3-bromo-4 - [(3-cyclohexyl-lH-indol-5-yl) oxy] -5- (trifluoromethyl) phenoxy] acetic acid

Example 170

[3 -Brom-4- [(3-propyl-1H-indol-5-yl) oxy] -5 - (trifluoromethyl) phenoxy] acetic acid

Example 171 [3-bromo-4 - [(3-butyl-1H-indol-5-yl) oxy] -5- (trifluoromethyl) phenoxy] acetic acid

Example 172

[3 -Brom-4- [(3-pentyl-1 H -indol-5-yl) oxy] -5 - (trifluoromethyl) phenoxy] acetic acid

Example 173

[3-bromo-4 - [(3-hexyl-lH-indol-5-yl) oxy] -5- (trifluoromethyl) phenoxy] acetic acid

Example 174

[3-bromo-4 - [(3-isobutyl-lH-indol-5-yl) oxy] -5- (trifluoromethyl) phenoxy] acetic acid Example 175

[3 -Brom-4- [(3 -sec-butyl-1 H -indol-5-yl) oxy] -5- (trifluoromethyl) phenoxy] acetic acid

Example 176 [3-bromo-4 - {[3- (cyclohexylmethyl) -IH-indol-5-yl] oxy} -5- (trifluoromethyl) phenoxy] acetic acid

Example 177

[3-bromo-4 - {[3- (cyclopentylmethyl) -IH-indol-5-yl] oxy} -5- (trifluoromethyl) phenoxy] acetic acid

Example 178

[3-bromo-4 - {[3- (cyclobutylmethyl) -IH-indol-5-yl] oxy} -5- (trifluoromethyl) phenoxy] acetic acid

Example 179

[3-bromo-4 - {[3- (cyclopropylmethyl) -IH-indol-5-yl] oxy} -5- (trifluoromethyl) phenoxy] acetic acid

Example 180

({4 - [(3-isopropyl-1H-indol-5-yl) oxy] -3,5 -dimethylphenyl} sulfanyl) acetic acid

Example 181

({3,5-dichloro-4 - [(3-isopropyl-lH-indol-5-yl) oxy] phenyl} sulfanyl) acetic acid

Example 182 ({3,5-dibromo-4 - [(3-isopropyl-1H-indol-5-yl) oxy] phenyl} sulfanyl) acetic acid

Example 183 {[4- [(3-isopropyl-1H-indol-5-yl) oxy] -3,5-bis (trifluoromethyl) phenyl] sulfanyl} acetic acid Example 184

{[4 - [(3-isopropyl-lH-indol-5-yl) oxy] -3-methyl-5- (trifluoromethyl) phenyl] sulfanyl} acetic acid

Example 185 ({3-chloro-4 - [(3-isopropyl-1H-indol-5-yl) oxy] -5-methylphenyl} sulfanyl) acetic acid

Example 186 ({3-bromo-4 - [(3-isopropyl-1H-indol-5-yl) oxy] -5-methylphenyl} sulfanyl) acetic acid

Example 187

({3-bromo-5-chloro-4 - [(3-isopropyl-lH-indol-5-yl) oxy] phenyl} sulfanyl) acetic acid

Example 188

{[3-bromo-4 - [(3-isopropyl-lH-indol-5-yl) oxy] -5- (trifluoromethyl) phenyl] sulfanyl} - acetic acid

Example 189 {[3-Chloro-4 - [(3-isopropyl-lH-indol-5-yl) oxy] -5- (trifluoromethyl) phenyl] sulfanyl} acetic acid

Example 190

N- [3-chloro-4 - [(3-isopropyl-lH-indol-5-yl) oxy] -5- (trifluoromethyl) phenyl] glycine

Example 191 N- [3-bromo-4 - [(3-isopropyl-1H-indol-5-yl) oxy] -5- (trifluoromethyl) phenyl] glycine

Example 192 N- {3-bromo-5-chloro-4 - [(3-isopropyl-1H-indol-5-yl) oxy] phenyl} glycine Example 193

N- {3-bromo-4 - [(3-isopropyl-lH-indol-5-yl) oxy] -5-methylphenyl} glycine

Example 194 N- {3-Chloro-4 - [(3-isopropyl-1H-indol-5-yl) oxy] -5-methylphenyl} glycine

Example 195

N- [4 - [(3-isopropyl-lH-indol-5-yl) oxy] -3-methyl-5- (trifluoromethyl) phenyl] glycine

Example 196

N- [4 - [(3-isopropyl-lH-indol-5-yl) oxy] -3,5-bis (trifluoromethyl) phenyl] glycine

Example 197

N- {3,5-dibromo-4 - [(3-isopropyl-lH-indol-5-yl) oxy] phenyl} glycine

Example 198

N- {3,5-dichloro-4 - [(3-isopropyl-lH-indol-5-yl) oxy] phenyl} glycine

Example 199 N- {4 - [(3-isopropyl-1H-indol-5-yl) oxy] -3,5-dimethylphenyl} glycine

Example 200

3 - {[3-chloro-4 - [(3-isopropyl-lH-indol-5-yl) oxy] -5- (trifluoromethyl) phenyl] amino} -3-oxopropionic acid

Example 201

3 - {[3-bromo-4 - [(3-isopropyl-lH-indol-5-yl) oxy] -5- (trifluoromethyl) phenyl] amino} -3-oxopropionic acid Example 202

3 - ({3-Bromo-5-chloro-4 - [(3-isopropyl-1H-indol-5-yl) oxy] phenyl} amino) -3-oxopropionic acid

Example 203

3 - ({3-Bromo-4 - [(3-isopropyl-1H-indol-5-yl) oxy] -5-methylphenyl} amino) -3-oxopropionic acid

Example 204 3 - ({3-Chloro-4 - [(3-isopropyl-1H-indol-5-yl) oxy] -5-methylphenyl} amino) -3-oxo-propionic acid

Example 205

3 - {[4- [(3-isopropyl-1H-indol-5-yl) oxy] -3-methyl-5- (trifluoromethyl) phenyl] amino} - 3-oxopropionic acid

Example 206

3 - {[4 - [(3-isopropyl-1H-indol-5-yl) oxy] -3,5-bis (trifluoromethyl) phenyl] amino} -3-oxopropionic acid

Example 207

3 - ({3,5-Dibromo-4 - [(3-isopropyl-1H-indol-5-yl) oxy] phenyl} amino) -3-oxopropionic acid

Example 208

Example 209 3 - ({4 - [(3-Isopropyl-1H-indol-5-yl) oxy] -3,5-dimethylphenyl} amino) -3-oxopropionic acid Example 210

3 - {[3-chloro-4 - [(3-isopropyl-lH-indol-5-yl) oxy] -5- (trifluoromethyl) phenyl] amino} -2-oxopropionic acid

Example 211

3 - {[3-bromo-4- [(3-isopropyl-1H-indol-5-yl) oxy] -5- (trifluoromethyl) phenyl] amino} - 2-oxopropionic acid

Example 212

3 - ({3-Bromo-5-chloro-4 - [(3-isopropyl-1H-indol-5-yl) oxy] phenyl} amino) -2-oxopropionic acid

Example 213 3 - ({3 -Brom-4- [(3-isopropyl-1H-indole-5-yl) oxy] -5-methylpheny 1} amino) -2-oxo-propionic acid

Example 214

3 - ({3-Chloro-4 - [(3-isopropyl-1H-indol-5-yl) oxy] -5-methylphenyl} amino) -2-oxopropionic acid

Example 215

3 - {[4- [(3-isopropyl-1H-indol-5-yl) oxy] -3-methyl-5 - (trifluoromethyl) phenyl] amino} - 2-oxopropionic acid

Example 216

3 - {[4 - [(3-isopropyl-1H-indol-5-yl) oxy] -3,5-bis (trifluoromethyl) phenyl] a-nino} -2-oxopropionic acid Example 217

3 - ({3,5-Dibromo-4 - [(3-isopropyl-1H-indol-5-yl) oxy] phenyl} amino) -2-oxopropionic acid

Example 218

3 - ({3,5-dichloro-4 - [(3-isopropyl-1H-indol-5-yl) oxy] phenyl} amino) -2-oxopropionic acid

Example 219 3- ({4 - [(3-Isopropyl-1H-indol-5-yl) oxy] -3,5-dimethylphenyl} amino) -2-oxopropionic acid

Example 220

3- [3-Chloro-4 - [(3-isopropyl-1H-indol-5-yl) oxy] -5- (trifluoromethyl) phenyl] propionic acid

Example 221

3- [3-bromo-4 - [(3-isopropyl-1H-indol-5-yl) oxy] -5- (trifluoromethyl) phenyl] propionic acid

Example 222

3 - {3-Bromo-5-chloro-4- [(3-isopropyl-1H-indole-5-yl) oxy] phenyl} propionic acid

Example 223 3 - {3-Bromo-4- [(3-isopropyl-1H-indole-5-yl) oxy] -5-ethylpheny 1} propionic acid

Example 224 3- {3-Chloro-4 - [(3-isopropyl-1H-indol-5-yl) oxy] -5-methylphenyl} propionic acid Example 225

3- [4 - [(3-isopropyl-1H-indol-5-yl) oxy] -3-methyl-5- (trifluoromethyl) phenyl] propionic acid

Example 226

3- [4 - [(3-isopropyl-lH-indol-5-yl) oxy] -3,5-bis (trifluoromethyl) phenyl] propionic acid

Example 227

3- {3,5-dibromo-4 - [(3-isopropyl-lH-indol-5-yl) oxy] phenyl} propionic acid

Example 228 3- {3,5-dichloro-4 - [(3-isopropyl-1H-indol-5-yl) oxy] phenyl} propionic acid

Example 229 3- {4 - [(3-Isopropyl-1H-indol-5-yl) oxy] -3,5-dimethylphenyl} propionic acid

Example 230

[3-Chloro-4- [(3-isopropyl-1H-indol-5-yl) oxy] -5- (trifluoromethyl) phenyl] acetic acid

Example 231

[3-chloro-4 - [(3-cyclopropyl-lH-mdol-5-yl) oxy] -5- (trifluoromethyl) phenyl] acetic acid

Example 232

[3-chloro-4 - [(3-cyclobutyl-lH-indol-5-yl) oxy] -5- (trifluoromethyl) phenyl] acetic acid

Example 233 [3-Chloro-4 - [(3-cyclopentyl-1H-indol-5-yl) oxy] -5- (trifluoromethyl) phenyl] acetic acid

Example 234 [3-Chloro-4 - [(3-cyclohexyl-1H-indol-5-yl) oxy] -5- (trifluoromethyl) phenyl] acetic acid Example 235

[3-chloro-4 - [(3-propyl-lH-indol-5-yl) oxy] -5- (trifluoromethyl) phenyl] acetic acid

Example 236 [4 - [(3-Butyl-1H-indol-5-yl) oxy] -3-chloro-5- (trifluoromethyl) phenyl] acetic acid

Example 237

[3-chloro-4 - [(3-pentyl-lH-indol-5-yl) oxy] -5- (trifluoromethyl) phenyl] acetic acid

Example 238

[3-chloro-4 - [(3-hexyl-lH-indol-5-yl) oxy] -5- (trifluoromethyl) phenyl] acetic acid

Example 239

[3-chloro-4 - [(3-isobutyl-lH-indol-5-yl) oxy] -5- (trifluoromethyl) phenyl] acetic acid

Example 240

[4- [(3-sec-butyl-1 H -indol-5-yl) oxy] -3-chloro-5- (trifluoromethyl) pheny 1] acetic acid

Example 241 [3-Chloro-4- {[3 - (cyclohexylmethyl) -1 H -indol-5-yl] oxy} -5 - (trifluoromethyl) phenyl] acetic acid

Example 242

[3-chloro-4- {[3- (cyclopentylmethyl) - 1H-indol-5-yl] oxy} -5- (trifluoromethyl) phenyl] acetic acid

Example 243

[3-chloro-4- {[3- (cyclobutylmethyl) - 1H-indol-5-yl] oxy} -5- (trifluoromethyl) phenyl] acetic acid Example 244

[3-Chloro-4 - {[3- (cyclopropylmethyl) -IH-indol-5-yl] oxy} -5- (trifluoromethyl) phenyl] acetic acid

Example 245

[4 - [(3 -B enzyl-1 H -indol-5-yl) oxy] -3-chloro-5 - (trifluoromethyl) phenyl] acetic acid

Example 246

[3-Chloro-4 - {[3- (4-chlorobenzyl) -IH-indol-5-yl] oxy} -5- (trifluoromethyl) phenyl] acetic acid

Example 247

[3 -Chlor-4- {[3 - (4-fluorobenzyl 1) -1 H -indol-5-y 1] oxy} -5 - (trifluoromethyl) phenyl] acetic acid

Example 248

[3-Chloro-4 - ({3 - [(4-fluorophenyl) sulfonyl] -lH-indol-5-yl} oxy) -5- (tri-luormethyl) phenyl] acetic acid

Example 249

[3-Chloro-4 - ({3 - [(4-chloro-phenyl) sulfonyl] -lH-indol-5-yl} oxy) -5- (trifluoromethyl) phenyl] acetic acid

Example 250 [3-Chloro-4 - {[3- (phenylsulfonyl) -1H-indol-5-yl] oxy} -5- (trifluoromethyl) phenyl] acetic acid

Example 251

[3-bromo-4 - [(3-isopropyl-lH-indol-5-yl) oxy] -5- (trifluoromethyl) phenyl] acetic acid Example 252

[3 -Brom-4 - [(3 -cyclopropyl-1H-indol-5-yl) oxy] -5 - (trifluoromethyl) phenyl] acetic acid

Example 253 [3-Bromo-4 - [(3-cyclobutyl-1H-indol-5-yl) oxy] -5- (trifluoromethyl) phenyl] acetic acid

Example 254

[3-bromo-4 - [(3-cyclopentyl-lH-indol-5-yl) oxy] -5- (trifluoromethyl) phenyl] acetic acid

Example 255

[3-bromo-4 - [(3-cyclohexyl-lH-indol-5-yl) oxy] -5- (trifluoromethyl) phenyl] acetic acid

Example 256

[3-bromo-4 - [(3-propyl-lH-indol-5-yl) oxy] -5- (trifluoromethyl) phenyl] acetic acid

Example 257 [3-Bromo-4 - [(3-butyl-1H-indol-5-yl) oxy] -5- (trifluoromethyl) phenyl] acetic acid

Example 258 [3-bromo-4 - [(3-pentyl-1H-indol-5-yl) oxy] -5- (trifluoromethyl) phenyl] acetic acid

Example 259

[3-bromo-4 - [(3-hexyl-lH-indol-5-yl) oxy] -5- (trifluoromethyl) phenyl] acetic acid

Example 260

[3-bromo-4 - [(3-isobutyl-lH-indol-5-yl) oxy] -5- (trifluoromethyl) phenyl] acetic acid

Example 261

[3 -Brom-4 - [(3 -sec-butyl-1H-indol-5-yl) oxy] -5 - (trifluoromethyl) phenyl] acetic acid Example 262

[3 -Brom-4- {[3 - (cyclohexylmethyl) - 1 H -indol-5 -yl] oxy} -5 - (trifluoromethyl) phenyl] acetic acid

Example 263

[3-bromo-4 - {[3- (cyclopentylmethyl) -IH-indol-5-yl] oxy} -5- (trifluoromethyl) phenyl] acetic acid

Example 264 [3-Bromo-4 - {[3- (cyclobutylmethyl) -IH-indol-5-yl] oxy} -5- (trifluoromethyl) phenyl] acetic acid

Example 265

[3-bromo-4 - {[3- (cyclopropylmethyl) -IH-indol-5-yl] oxy} -5- (trifluoromethyl) phenyl] acetic acid

Example 266

[4 - [(3-benzyl-lH-indol-5-yl) oxy] -3-bromo-5- (trifluoromethyl) phenyl] acetic acid

Example 267

[3-bromo-4 - {[3- (4-chlorobenzyl) -IH-indol-5-yl] oxy} -5- (trifluoromethyl) phenyl] acetic acid

Example 268 [3-Bromo-4 - {[3- (4-fluorobenzyl) -1H-indol-5-yl] oxy} -5- (trifluoromethyl) phenyl] acetic acid

Example 269

[3-Bromo-4 - ({3 - [(4-fluoφhenyl) sulfonyl] -lH-indol-5-yl} oxy) -5- (trifluoromethyl) phenyl acetic acid Example 270

[3-bromo-4 - ({3 - [(4-chloro-phenyl) sulfonyl] -lH-indol-5-yl} oxy) -5- (trifluoromethyl) phenyl] acetic acid

Example 271

[3 -Brom-4- {[3 - (phenylsulfonyl) -1 H -indol-5 -yl] oxy} -5 - (trifluoromethyl) phenyl] acetic acid

Example 272 {3-Bromo-5-chloro-4 - [(3-isopropyl-1H-indol-5-yl) oxy] phenyl} acetic acid

Example 273

{3-bromo-5-chloro-4 - [(3-cyclopropyl-lH-indol-5-yl) oxy] phenyl} acetic acid

Example 274

{3-bromo-5-chloro-4- [(3 -cyclobutyl-1 H -indol-5 -yl) oxy] phenyl} acetic acid

Example 275

{3-bromo-5-chloro-4 - [(3-cyclopentyl-lH-indol-5-yl) oxy] phenyl} acetic acid

Example 276 {3-Bromo-5-chloro-4 - [(3-cyclohexyl-1H-indol-5-yl) oxy] phenyl} acetic acid

Example 277 {3-Bromo-5-chloro-4 - [(3-propyl-1H-indol-5-yl) oxy] phenyl} acetic acid

Example 278

{3-bromo-4 - [(3-butyl-lH-indol-5-yl) oxy] -5-chloφhenyl} acetic acid

Example 279

{3-Bromo-5-chloro-4- [(3-pentyl-1 H -indol-5-yl) oxy] ρhenyl} acetic acid Example 280

{3-bromo-5-chloro-4 - [(3-hexyl-lH-indol-5-yl) oxy] phenyl} acetic acid

Example 281

{3-bromo-5-chloro-4 - [(3-isobutyl-lH-indol-5-yl) oxy] phenyl} acetic acid

Example 282

{3 -Brom-4- [(3 -sec-butyl-1 H -indol-5 -yl) oxy] -5 -chloφhenyl} acetic acid

Example 283 (3-bromo-5-chloro-4 - {[3- (cyclohexylmethyl) -IH-indol-5-yl] oxy} phenyl) acetic acid

Example 284 (3-bromo-5-chloro-4 - {[3- (cyclopentylmethyl) -IH-indol-5-yl] oxy} phenyl) acetic acid

Example 285

(3-Bromo-5-chloro-4 - {[3- (cyclobutylmethyl) -lH-indol-5-yl] oxy} phenyl) acetic acid

Example 286

(3-Bromo-5-chloro-4- {[3 - (cyclopropylmethyl) -1 H -indol-5-yl] oxy} phenyl) acetic acid

Example 287

{4- [(3 -B enzyl- 1 H -indol-5 -yl) oxy] -3 -bromo-5 -chloφhenyl} acetic acid

Example 288 (3-bromo-5-chloro-4 - {[3- (4-fluorobenzyl) -IH-indol-5-yl] oxy} phenyl) acetic acid

Example 289 (3-bromo-5-chloro-4 - {[3- (4-chlorobenzyl) -IH-indol-5-yl] oxy} phenyl) acetic acid Example 290

[3-bromo-5-chloro-4 - ({3 - [(4-chloro-phenyl) sulfonyl] -lH-indol-5-yl} oxy) phenyl] acetic acid

Example 291

[3-bromo-5-chloro-4- ({3 - [(4-fluoφhenyl) sulfonyl] - 1H-indol-5-yl} oxy) phenyl] acetic acid

Example 292 (3-bromo-5-chloro-4 - {[3- (phenylsulfonyl) -IH-indol-5-yl] oxy} phenyl) acetic acid

Example 293

{3-bromo-4 - [(3-isopropyl-lH-indol-5-yl) oxy] -5-methylphenyl} acetic acid

Example 294

{3-bromo-4 - [(3-cyclopropyl-lH-indol-5-yl) oxy] -5-methylphenyl} acetic acid

Example 295

{3-bromo-4 - [(3-cyclobutyl-lH-indol-5-yl) oxy] -5-methylphenyl} acetic acid

Example 296 {3-Bromo-4 - [(3-cyclopentyl-1H-indol-5-yl) oxy] -5-methylphenyl} acetic acid

Example 297 {3-Bromo-4 - [(3-cyclohexyl-1H-indol-5-yl) oxy] -5-methylphenyl} acetic acid

Example 298

{3-bromo-5-methyl-4 - [(3-propyl-lH-indol-5-yl) oxy] phenyl} acetic acid

Example 299

{3-bromo-4 - [(3-butyl-lH-indol-5-yl) oxy] -5-methylphenyl} acetic acid Example 300

{3-bromo-5-methyl-4 - [(3-pentyl-lH-indol-5-yl) oxy] phenyl} acetic acid

Example 301

{3-bromo-4 - [(3-hexyl-lH-indol-5-yl) oxy] -5-methylphenyl} acetic acid

Example 302

{3-bromo-4 - [(3-isobutyl-lH-indol-5-yl) oxy] -5-methylphenyl} acetic acid

Example 303 {3-Bromo-4 - [(3-sec-butyl-1H-indol-5-yl) oxy] -5-methylphenyl} acetic acid

Example 304 (3-bromo-4 - {[3- (cyclohexylmethyl) -lH-indol-5-yl] oxy} -5-methylphenyl) acetic acid

Example 305

(3-bromo-4- {[3- (cyclopentylmethyl) - 1H-indol-5-yl] oxy} -5-methylphenyl) acetic acid

Example 306

(3 -Brom-4- {[3 - (cyclobutylmethyl) -1 H -indol-5-yl] oxy} -5-methylphenyl) acetic acid

Example 307

(3-bromo-4 - {[3- (cyclopropylmethyl) -lH-indol-5-yl] oxy} -5-methylphenyl) acetic acid

Example 308 {4 - [(3-benzyl-1H-indol-5-yl) oxy] -3-bromo-5-methylphenyl} acetic acid

Example 309 (3-bromo-4 - {[3- (4-fluorobenzyl) -1H-indol-5-yl] oxy} -5-methylphenyl) acetic acid Example 310

(3-bromo-4 - {[3- (4-chlorobenzyl) -lH-indol-5-yl] oxy} -5-methylphenyl) acetic acid

Example 311 [3-bromo-4 - ({3 - [(4-chlθφhenyl) sulfonyl] -lH-indol-5-yl} oxy) -5-methylphenyl] acetic acid

Example 312

[3 -Brom-4- ({3 - [(4-fluoφhenyl) sulfonyl] - 1 H -indol-5 -yl} oxy) -5-methylphenyl] acetic acid

Example 313

(3-Bromo-5-methyl-4- {[3 - (phenylsulfonyl) -1 H -indol-5-yl] oxy} phenyl) acetic acid

Example 314

{3-Chloro-4 - [(3-isopropyl-lH-indol-5-yl) oxy] -5-methylphenyl} acetic acid

Example 315

{3-Chloro-4 - [(3-cyclopropyl-lH-indol-5-yl) oxy] -5-methylphenyl} acetic acid

Example 316 {3-chloro-4 - [(3-cyclobutyl-1H-indol-5-yl) oxy] -5-methylphenyl} acetic acid

Example 317 {3-Chloro-4 - [(3-cyclopentyl-1H-indol-5-yl) oxy] -5-methylphenyl} acetic acid

Example 318

{3-Chloro-4 - [(3-cyclohexyl-lH-indol-5-yl) oxy] -5-methylphenyl} acetic acid

Example 319

{3-Chloro-5-methyl-4 - [(3-propyl-lH-indol-5-yl) oxy] phenyl} acetic acid Example 320

{4 - [(3-butyl-lH-indol-5-yl) oxy] -3-chloro-5-methylphenyl} acetic acid

Example 321

{3-Chloro-5-methyl-4 - [(3-pentyl-lH-indol-5-yl) oxy] phenyl} acetic acid

Example 322

{3-Chloro-4 - [(3-hexyl-lH-indol-5-yl) oxy] -5-methylphenyl} acetic acid

Example 323 {3-Chloro-4 - [(3-isobutyl-1H-indol-5-yl) oxy] -5-methylphenyl} acetic acid

Example 324 {4 - [(3-sec-Butyl-1H-indol-5-yl) oxy] -3-chloro-5-methylphenyl} acetic acid

Example 325

(3-chloro-4- {[3- (cyclohexylmethyl) - 1H-indol-5-yl] oxy} -5-methylphenyl) acetic acid

Example 326

(3-chloro-4 - {[3- (cyclopentylmethyl) -lH-indol-5-yl] oxy} -5-methylphenyl) acetic acid

Example 327

(3-chloro-4 - {[3- (cyclobutylmethyl) -lH-indol-5-yl] oxy} -5-methylphenyl) acetic acid

Example 328 (3-chloro-4 - {[3- (cyclopropylmethyl) -IH-indol-5-yl] oxy} -5-methylphenyl) acetic acid

Example 329 {4 - [(3-Benzyl-1H-indol-5-yl) oxy] -3-chloro-5-methylphenyl} acetic acid Example 330

(3-chloro-4 - {[3- (4-fluorobenzyl) -lH-indol-5-yl] oxy} -5-methylphenyl) acetic acid

Example 331 (3-Chloro-4- {[3 - (4-chlorobenzyl) -1 H -indol-5-yl] oxy} -5-methylphenyl) acetic acid

Example 332

[3-Chloro-4 - ({3 - [(4-chloro-phenyl) sulfonyl] -lH-indol-5-yl} oxy) -5-methylphenyl] acetic acid

Example 333

[3-Chloro-4 - ({3 - [(4-fluoφhenyl) sulfonyl] -lH-indol-5-yl} oxy) -5-methylphenyl] acetic acid

Example 334

(3-chloro-5-methyl-4 - {[3- (phenylsulfonyl) -lH-indol-5-yl] oxy} phenyl) acetic acid

Example 335

[4- [(3-isopropyl-1 H -indol-5-yl) oxy] -3-methyl-5 - (trifluoromethyl) phenyl] acetic acid

Example 336 [4 - [(3-Cyclopropyl-1H-indol-5-yl) oxy] -3-methyl-5- (trifluoromethyl) phenyl] acetic acid

Example 337 [4 - [(3-Cyclobutyl-1H-indol-5-yl) oxy] -3-methyl-5- (trifluoromethyl) phenyl] acetic acid

Example 338

[4 - [(3-cyclopentyl-lH-indol-5-yl) oxy] -3-methyl-5- (trifluoromethyl) phenyl] acetic acid

Example 339

[4 - [(3-cyclohexyl-lH-indol-5-yl) oxy] -3-methyl-5- (trifluoromethyl) phenyl] acetic acid Example 340

[3-Methyl-4 - [(3-propyl-lH-indol-5-yl) oxy] -5- (trifluoromethyl) phenyl] acetic acid

Example 341

[4 - [(3-butyl-lH-indol-5-yl) oxy] -3-methyl-5- (trifluoromethyl) phenyl] acetic acid

Example 342

[3-Methyl-4 - [(3-pentyl-lH-indol-5-yl) oxy] -5- (trifluoromethyl) phenyl] acetic acid

Example 343 [4 - [(3-Hexyl-1H-indol-5-yl) oxy] -3-methyl-5- (trifluoromethyl) phenyl] acetic acid

Example 344 [4 - [(3-isobutyl-1H-indol-5-yl) oxy] -3-methyl-5- (trifluoromethyl) phenyl] acetic acid

Example 345

[4 - [(3-sec-butyl-lH-indol-5-yl) oxy] -3-methyl-5- (trifluoromethyl) phenyl] acetic acid

Example 346

[4 - {[3- (Cyclohexylmethyl) -lH-indol-5-yl] oxy} -3-methyl-5- (trifluoromethyl) phenyl] acetic acid

Example 347 [4 - {[3- (Cycloρentylmethyl) -lH-indol-5-yl] oxy} -3-methyl-5- (trifluoromethyl) phenyl] acetic acid

Example 348

[4 - {[3- (Cyclobutylmethyl) -IH-indol-5-yl] oxy} -3-methyl-5- (trifluoromethyl) phenyl] acetic acid Example 349

[4 - {[3- (Cyclopropylmethyl) -IH-indol-5-yl] oxy} -3-methyl-5- (trifluoromethyl) phenyl] acetic acid

Example 350

[4 - [(3-benzyl-lH-indol-5-yl) oxy] -3-methyl-5- (trifluoromethyl) phenyl] acetic acid

Example 351

[4- {[3- (4-fluorobenzyl) -1 H -indol-5-yl] oxy} -3-methyl-5- (trifluoromethyl) phenyl] acetic acid

Example 352

[4 - {[3- (4-Chlorobenzyl) -IH-indol-5-yl] oxy} -3-methyl-5- (trifluoromethyl) phenyl] acetic acid

Example 353

[4 - ({3 - [(4-chloro-phenyl) sulfonyl] -lH-indol-5-yl} oxy) -3-methyl-5- (trifluoromethyl) phenyl] acetic acid

Example 354

[4 - ({3 - [(4-Fluoφhenyl) sulfonyl] -1H-indol-5-yl} oxy) -3-methyl-5- (trifluoromethyl) phenyl] acetic acid

Example 355 [3-Methyl-4- {[3- (phenylsulfonyl) -IH-indol-5-yl] oxy} -5- (trifluoromethyl) phenyl] acetic acid

Example 356

[4 - [(3-isopropyl-lH-indol-5-yl) oxy] -3,5-bis (trifluoromethyl) phenyl] acetic acid Example 357

[4 - [(3-cyclopropyl-lH-indol-5-yl) oxy] -3,5-bis (trifluoromethyl) phenyl] acetic acid

Example 358 [4- [(3-Cyclobutyl-1H-indol-5-yl) oxy] -3, 5-bis (trifluoromethyl) phenyl] acetic acid

Example 359

[4 - [(3-cyclopentyl-lH-indol-5-yl) oxy] -3,5-bis (trifluoromethyl) phenyl] acetic acid

Example 360

[4 - [(3-cyclohexyl-lH-indol-5-yl) oxy] -3,5-bis (trifluoromethyl) phenyl] acetic acid

Example 361

[4 - [(3-propyl-lH-indol-5-yl) oxy] -3,5-bis (trifluoromethyl) phenyl] acetic acid

Example 362 [4 - [(3-Butyl-1H-indol-5-yl) oxy] -3,5-bis (trifluoromethyl) phenyl] acetic acid

Example 363 [4 - [(3 -pentyl-1H-indol-5-yl) oxy] -3,5-bis (trifluoromethyl) phenyl] acetic acid

Example 364

[4 - [(3-hexyl-lH-indol-5-yl) oxy] -3,5-bis (trifluoromethyl) phenyl] acetic acid

Example 365

[4 - [(3-isobutyl-lH-indol-5-yl) oxy] -3,5-bis (trifluoromethyl) phenyl] acetic acid

Example 366

[4 - [(3-sec-butyl-lH-indol-5-yl) oxy] -3,5-bis (trifluoromethyl) phenyl] acetic acid Example 367

[4 - {[3- (Cyclohexylmethyl) -IH-indol-5-yl] oxy} -3,5-bis (trifluoromethyl) phenyl] acetic acid

Example 368

[4 - {[3- (Cyclopentylmethyl) -IH-indol-5-yl] oxy} -3,5-bis (trifluoromethyl) phenyl] acetic acid

Example 369 [4 - {[3- (Cyclobutylmethyl) -IH-indol-5-yl] oxy} -3,5-bis (trifluoromethyl) phenyl] acetic acid

Example 370

[4- {[3 - (Cyclopropylmethyl) -1 H-indol-5-yl] oxy} -3,5-bis (trifluoromethyl) phenyl] acetic acid

Example 371

[4- [(3 -B-enzyl-1 H -indol-5-yl) oxy] -3, 5-bis (trifluoromethyl) phenyl] acetic acid

Example 372

[4 - {[3- (4-fluorobenzyl) -lH-indol-5-yl] oxy} -3,5-bis (trifluoromethyl) phenyl] acetic acid

Example 373

[4 - {[3- (4-chlorobenzyl) -lH-indol-5-yl] oxy} -3,5-bis (trifluoromethyl) phenyl] acetic acid

Example 374

[4 - ({3 - [(4-Chlθφhenyl) sulfonyl] -lH-indol-5-yl} oxy) -3,5-bis (trifluoromethyl) phenyl] acetic acid Example 375

[4 - ({3 - [(4-Fluoφhenyl) sulfonyl] -lH -indol-5-yl} oxy) -3,5-bis (trifluoromethyl) phenyl] acetic acid

Example 376

[4- {[3 - (phenylsulfonyl) -1 H -indol-5 -y 1] oxy} -3.5 -bis (trifluoromethyl) pheny 1] acetic acid

Example 377

{3,5-dibromo-4 - [(3-isopropyl-lH-indol-5-yl) oxy] phenyl} acetic acid

Example 378 {3,5-dibromo-4 - [(3-cyclopropyl-1H-indol-5-yl) oxy] phenyl} acetic acid

Example 379 {3,5-dibromo-4 - [(3-cyclobutyl-1H-indol-5-yl) oxy] phenyl} acetic acid

Example 380

{3,5-dibromo-4 - [(3-cyclopentyl-lH-indol-5-yl) oxy] phenyl} acetic acid

Example 381

{3,5-dibromo-4 - [(3-cyclohexyl-lH-indol-5-yl) oxy] phenyl} acetic acid

Example 382

{3,5-dibromo-4 - [(3-propyl-lH-indol-5-yl) oxy] phenyl} acetic acid

Example 383 {3,5-dibromo-4 - [(3-butyl-1H-indol-5-yl) oxy] phenyl} acetic acid

Example 384 {3,5-dibromo-4 - [(3-pentyl-1H-indol-5-yl) oxy] phenyl} acetic acid Example 385

{3,5-dibromo-4- [(3-hexyl-1H-indol-5-yl) oxy] phenyl} acetic acid

Example 386 {3,5-dibromo-4 - [(3-isobutyl-1H-indol-5-yl) oxy] phenyl} acetic acid

Example 387

{3,5-dibromo-4 - [(3-sec-butyl-lH-indol-5-yl) oxy] phenyl} acetic acid

Example 388

(3,5-dibromo-4 - {[3- (cyclohexylmethyl) -lH-indol-5-yl] oxy} phenyl) acetic acid

Example 389

(3,5-dibromo-4 - {[3- (cyclopentylmethyl) -lH-indol-5-yl] oxy} phenyl) acetic acid

Example 390 (3,5-dibromo-4 - {[3- (cyclobutylmethyl) -1H-indol-5-yl] oxy} phenyl) acetic acid

Example 391 (3,5-Dibromo-4- {[3 - (cyclopropylmethyl) -1 H -indol-5-yl] oxy} phenyl) acetic acid

Example 392

{4 - [(3-benzyl-lH-indol-5-yl) oxy] -3,5-dibromophenyl} -acetic acid

Example 393

(3,5-dibromo-4 - {[3- (4-fluorobenzyl) -lH-indol-5-yl] oxy} phenyl) acetic acid

Example 394

(3,5-dibromo-4 - {[3- (4-chlorobenzyl) -lH-indol-5-yl] oxy} phenyl) acetic acid Example 395

[3,5-dibromo-4 - ({3 - [(4-chloφhenyl) sulfonyl] -lH-indol-5-yl} oxy) phenyl] acetic acid

Example 396 [3,5-Dibromo-4 - ({3 - [(4-fluoφhenyl) sulfonyl] -lH-indol-5-yl} oxy) phenyl] acetic acid

Example 397

(3, 5 -Dibromo-4- {[3 - (phenylsulfonyl) -1 H -indol-5-yl] oxy} phenyl) acetic acid

Example 398

{3,5-dichloro-4 - [(3-isopropyl-lH-indol-5-yl) oxy] phenyl} acetic acid

Example 399

{3,5-dichloro-4 - [(3-cyclopropyl-lH-indol-5-yl) oxy] phenyl} acetic acid

Example 400

{3,5-dichloro-4- [(3 -cyclobutyl-1 H -indol-5 -yl) oxy] phenyl} acetic acid

Example 401 {3,5-dichloro-4 - [(3-cyclopentyl-1H-indol-5-yl) oxy] phenyl} acetic acid

Example 402

{3,5-dichloro-4 - [(3-cyclohexyl-lH-indol-5-yl) oxy] phenyl} acetic acid

Example 403

{3,5-dichloro-4 - [(3-propyl-lH-indol-5-yl) oxy] phenyl} acetic acid

Example 404 {4 - [(3-Butyl-1H-indol-5-yl) oxy] -3,5-dichloφhenyl} acetic acid Example 405

{3,5-dichloro-4 - [(3-pentyl-lH-indol-5-yl) oxy] phenyl} acetic acid

Example 406 {3,5-dichloro-4 - [(3-hexyl-1H-indol-5-yl) oxy] phenyl} acetic acid

Example 407

{3,5-dichloro-4 - [(3 -isobutyl-1H-indole-5-yl) oxy] phenyl} acetic acid

Example 408

{4 - [(3-sec-butyl-lH-indol-5-yl) oxy] -3,5-dichloφhenyl} acetic acid

Example 409

(3,5-dichloro-4 - {[3- (cyclohexylmethyl) -lH-indol-5-yl] oxy} phenyl) acetic acid

Example 410

(3, 5 -Dichlor-4- {[3 - (cyclopentylmethyl) -1 H -indol-5-yl] oxy} phenyl) acetic acid

Example 411 (3,5-dichloro-4 - {[3- (cyclobutylmethyl) -IH-indol-5-yl] oxy} phenyl) acetic acid

Example 412

(3,5-dichloro-4 - {[3- (cyclopropyhnethyl) -lH-indol-5-yl] oxy} phenyl) acetic acid

Example 413

{4 - [(3-benzyl-lH-indol-5-yl) oxy] -3,5-dichloφhenyl} acetic acid

Example 414

(3,5-dichloro-4 - {[3- (4-fluorobenzyl) -lH-indol-5-yl] oxy} phenyl) acetic acid Example 415

(3,5-dichloro-4- {[3 - (4-chlorobenzyl) -1 H -indol-5-y 1] oxy} phenyl) acetic acid

Example 416 [3,5-dichloro-4 - ({3 - [(4-chloro-phenyl) sulfonyl] -lH-indol-5-yl} oxy) phenyl] acetic acid

Example 417

[3,5-dichloro-4 - ({3 - [(4-fluoφhenyl) sulfonyl] -lH-indol-5-yl} oxy) phenyl] acetic acid

Example 418

(3,5-dichloro-4 - {[3- (phenylsulfonyl) -lH-indol-5-yl] oxy} phenyl) acetic acid

Example 419

{4 - [(3-isopropyl-lH-indol-5-yl) oxy] -3,5-dimethylphenyl} acetic acid

Example 420

{4 - [(3-cyclopropyl-lH-indol-5-yl) oxy] -3,5-dimethylphenyl} acetic acid

Example 421 {4 - [(3-Cyclobutyl-1H-indol-5-yl) oxy] -3,5-dimethylphenyl} acetic acid

Example 422

{4 - [(3-cyclopentyl-lH-indol-5-yl) oxy] -3,5-dimethylphenyl} acetic acid

Example 423

{4- [(3-Cyclohexyl-1 H -indol-5-yl) oxy] -3,5 -dimethylphenyl} acetic acid

Example 424

{3,5-dimethyl-4- [(3-propyl-1H-indol-5-yl) oxy] phenyl} acetic acid Example 425

{4 - [(3-butyl-lH-indol-5-yl) oxy] -3,5-dimethylphenyl} acetic acid

Example 426 {3,5-Dimethyl-4- [(3-pentyl-1 H-indole-5-yl) oxy] phenyl} acetic acid

Example 427

{4- [(3-Hexyl-1 H -indol-5-yl) oxy] -3,5-dimethylphenyl} acetic acid

Example 428

{4 - [(3-isobutyl-lH-indol-5-yl) oxy] -3,5-dimethylphenyl} acetic acid

Example 429

{4 - [(3-sec-butyl-lH-indol-5-yl) oxy] -3,5-dimethylphenyl} acetic acid

Example 430 (4 - {[3- (Cyclohexylmethyl) -IH-indol-5-yl] oxy} -3,5-dimethylphenyl) acetic acid

Example 431 (4 - {[3- (Cyclopentylmethyl) -IH-indol-5-yl] oxy} -3,5-dimethylphenyl) acetic acid

Example 432

(4 - {[3- (cyclobutylmethyl) -lH-indol-5-yl] oxy} -3,5-dimethylphenyl) acetic acid

Example 433

(4 - {[3- (cyclopropylmethyl) -lH-indol-5-yl] oxy} -3,5-dimethylphenyl) acetic acid

Example 434

{4 - [(3-benzyl-lH-indol-5-yl) oxy] -3,5-dimethylphenyl} acetic acid Example 435

(4 - {[3- (4-fluorobenzyl) -lH-indol-5-yl] oxy} -3,5-dimethylphenyl) acetic acid

Example 436 (4 - {[3- (4-chlorobenzyl) -IH-indol-5-yl] oxy} -3,5-dimethylphenyl) acetic acid

Example 437

[4- ({3 - [(4-chloro-phenyl) sulfonyl] -1 H -indol-5-y 1} oxy) -3,5-dimethylphenyl] acetic acid

Example 438

[4 - ({3 - [(4-Fluoφhenyl) sulfonyl] -lH-indol-5-yl} oxy) -3,5-dimethylphenyl] acetic acid

Example 439

(3,5-dimethyl-4 - {[3- (phenylsulfonyl) -lH-indol-5-yl] oxy} phenyl) acetic acid

Example 440

(3,5-dimethyl-4- {[3 - (phenylsulfonyl) -1 H -indol-5-yl] oxy} phenoxy) acetic acid

Example 441 (3,5-dichloro-4 - {[3- (phenylsulfonyl) -1H-indol-5-yl] oxy} phenoxy) acetic acid

Example 442

(3,5-Dibromo-4- {[3 - (phenylsulfonyl) -1 H -indol-5-yl] oxy} phenoxy) acetic acid

Example 443

[4 - {[3- (Phenylsulfonyl) -1H-indol-5-yl] oxy} -3,5-is (trifluoromethyl) phenoxy] acetic acid

Example 444 (3,5-Dimethyl-4- {[3- (phenylsulfonyl) -1H-indol-5-yl] oxy} phenyl) acetic acid Example 445

3, 5-dichloro-4- {[3 - (phenylsulfonyl) -1 H -indol-5-y 1] oxy} phenyl) acetic acid

Example 446 (3,5-dibromo-4 - {[3- (phenylsulfonyl) -1H-indol-5-yl] oxy} phenyl) acetic acid

Example 447 [4 - {[3- (Phenylsulfonyl) -IH-indol-5-yl] oxy} -3,5-bis (trifluoromethyl) phenyl] acetic acid

Example 448

3, 5-Dimethyl-O- [3- (phenylsulfonyl) -1 H -indol-5-yl] -D-tyrosine

Example 449

3,5-dichloro-O- [3- (phenylsulfonyl) -lH-indol-5-yl] -D-tyrosine

Example 450

3,5-dibromo-O- [3- (phenylsulfonyl) -lH-indol-5-yl] -D-tyrosine

Example 451 O- [3- (phenylsulfonyl) -IH-indol-5-yl] -3,5-bis (trifluoromethyl) -D-tyrosine

Example 452

3, 5-Dimethyl-O- [3 - (phenylsulfonyl) -1 H -indol-5-yl] -L-tyrosine

Example 453

3,5-dichloro-O- [3- (phenylsulfonyl) -lH-indol-5-yl] -L-tyrosine

Example 454

3,5-dibromo-O- [3- (phenylsulfonyl) -lH-indol-5-yl] -L-tyrosine

Example 455

O- [3-φhenylsulfonyl) -lH-indol-5-yl] -3,5-bis (trifluoromethyl) -L-tyrosine Example 456

(3,5-dimethyl-4- {[3 - (phenylsulfonyl) -1 H -indol-5-yl] oxy} phenyl) methanesulfonic acid

Example 457 (3,5-dichloro-4 - {[3- (phenylsulfonyl) -1H-indol-5-yl] oxy} phenyl) methanesulfonic acid

Example 458

(3,5-dibromo-4- {[3 - (phenylsulfonyl) -1 H -indol-5-yl] oxy} phenyl) methanesulfonic acid

Example 459

[4 - {[3- (phenylsulfonyl) -1H-indol-5-yl] oxy} -3,5-bis (trifluoromethyl) phenyl] methanesulfonic acid

Example 460 [(3,5-Dimethyl-4 - {[3- (phenylsulfonyl) -1H-indol-5-yl] oxy} phenyl) sulfanyl] acetic acid

Example 461

[(3,5-dichloro-4 - {[3- (phenylsulfonyl) -lH-indol-5-yl] oxy} phenyl) sulfanyl] acetic acid

Example 462 [(3,5-dibromo-4 - {[3- (phenylsulfonyl) -IH-indol-5-yl] oxy} phenyl) sulfanyl] acetic acid

Example 463 {[4 - {[3- (phenylsulfonyl) -1H-indol-5-yl] oxy} -3,5-bis (trifluoromethyl) ρhenyl] sulfanyl} acetic acid

Example 464

(2R) -Amino (3,5-dimethyl-4 - {[3- (ρhenylsulfonyl) -lH-indol-5-yl] oxy} phenyl) ethanoic acid Example 465

(2R) -Amino (3,5-dichloro-4 - {[3- (phenylsulfonyl) -lH-indol-5-yl] oxy} phenyl) ethanoic acid

Example 466

(2R) -Amino (3,5-dibromo-4 - {[3- (phenylsulfonyl) -lH-indol-5-yl] oxy} phenyl) ethanoic acid

Example 467 (2R) -amino [4- {[3- (phenylsulfonyl) - lH-indol-5-yl] oxy} -3,5-bis (trifluoromethyl) phenyl] ethanoic acid

Example 468

(2S) -Amino (3,5-dimethyl-4 - {[3- (phenylsulfonyl) -IH-indol-5-yl] oxy} phenyl) ethanoic acid

Example 469

(2S) -Amino (3,5-dichloro-4 - {[3- (phenylsulfonyl) -lH-indol-5-yl] oxy} phenyl) ethanoic acid

Example 470

(2S) -Amino (3,5-dibromo-4 - {[3- (phenylsulfonyl) -lH-indol-5-yl] oxy} phenyl) ethanoic acid

Example 471

(2S) -Amino [4 - {[3- (phenylsulfonyl) -IH-indol-5-yl] oxy} -3,5-bis (trifluoromethyl) phenyl] ethanoic acid

Example 472 [4 - ({3 - [(4-Fluoφhenyl) sulfonyl] -1H-indol-5-yl} oxy) -3,5-dimethylphenoxy] acetic acid Example 473

[3,5-dichloro-4 - ({3 - [(4-fluoφhenyl) sulfonyl] -lH-indol-5-yl} oxy) phenoxy] acetic acid

Example 474

[3, 5-Dibromo-4- ({3 - [(4-fluoφhenyl) sulfonyl] - 1 H -indol-5-yl} oxy) phenoxy] acetic acid

Example 475

[4 - ({3 - [(4-Fluoφhenyl) sulfonyl] -1H-indol-5-yl} oxy) -3,5-bis (trifluoromethyl) phenoxy] acetic acid

Example 476

Example 477

Example 478

[3,5-dibromo-4 - ({3 - [(4-fluoφhenyl) sulfonyl] -lH-indol-5-yl} oxy) phenyl] acetic acid

Example 479

Example 480

O- {3 - [(4-fluoφhenyl) sulfonyl] -lH-indol-5-yl} -3,5-dimethyl-D-tyrosine

Example 481

3,5-dichloro-O- {3 - [(4-fluorophenyl) sulfonyl] - 1H-indol-5-yl} -D-tyrosine Example 482

3,5-dibromo-O- {3 - [(4-fluoφhenyl) sulfonyl] -lH-indol-5-yl} -D-tyrosine

Example 483 O- {3 - [(4-fluorophenyl) sulfonyl] -1 H -indol-5-yl} -3,5-bis (trifluoromethyl) -D-tyrosine

Example 484

O- {3 - [(4-fluoφhenyl) sulfonyl] -lH-indol-5-yl} -3,5-dimethyl-L-tyrosine

Example 485

3,5-dichloro-O- {3 - [(4-fluoφhenyl) sulfonyl] -lH-indol-5-yl} -L-tyrosine

Example 486

3,5-dibromo-O- {3 - [(4-fluoφhenyl) sulfonyl] -lH-indol-5-yl} -L-tyrosine

Example 487 O- {3 - [(4-fluorophenyl) sulfonyl] -IH-indol-5-yl} -3,5-bis (trifluoromethyl) -L-tyrosine

Example 488 [4 - ({3 - [(4-fluorophenyl) sulfonyl] -1H-indol-5-yl} oxy) -3,5-dimethylphenyl] methanesulfonic acid

Example 489

[3,5-dichloro-4- ({3 - [(4-fluorophenyl) sulfonyl] - 1H-indol-5-yl} oxy) phenyl] methanesulfonic acid

Example 490

[3,5-dibromo-4 - ({3 - [(4-fluoφhenyl) sulfonyl] -lH-indol-5-yl} oxy) phenyl] methanesulfonic acid Example 491

[4 - ({3 - [(4-fFuoφhenyl) sulfonyl] -1H-indol-5-yl} oxy) -3,5-bis (trifluoromethyl) phenyl] methanesulfonic acid

Example 492

{[4 - ({3 - [(4-Fluoφhenyl) sulfonyl] -1H-indol-5-yl} oxy) -3,5-dimethylphenyl] sulfanyl} acetic acid

Example 493 {[3,5-dichloro-4 - ({3 - [(4-fluorophenyl) sulfyl] -lH-indol-5-yl} oxy) phenyl] sulfanyl} acetic acid

Example 494

{[3,5-Dibromo-4 - ({3 - [(4-fluoφhenyl) sulfonyl] -lH-indol-5-yl} oxy) phenyl] sulfanyl} - acetic acid

Example 495

{[4 - ({3 - [(4-Fluoφhenyl) sulfonyl] -lH-indol-5-yl} oxy) -3,5-bis (trifluoromethyl) - phenylj-sulfanyl} acetic acid

Example 496

(2R) -Amino [4 - ({3 - [(4-fluoφhenyl) sulfonyl] -lH-indol-5-yl} oxy) -3,5-dimethylphenylj-ethanoic acid

Example 497

(2R) -Amino [3,5-dichloro-4 - ({3 - [(4-fluoφhenyl) sulfonyl] -lH-indol-5-yl} oxy) ρhenyl] - ethanoic acid

Example 498 (2R) -Amino [3,5-dibromo-4 - ({3 - [(4-fluorophenyl) sulfonyl] -lH-indol-5-yl} oxy) ρhenyl] ethanoic acid Example 499

(2R) -Amino [4 - ({3 - [(4-fluoφhenyl) sulfonyl] -lH-indol-5-yl} oxy) -3,5-bis (trifluoromethyl) phenyl] ethanoic acid

Example 500

(2S) -Amino [4 - ({3 - [(4-fluoφhenyl) sulfonyl] -lH-indol-5-yl} oxy) -3,5-dimethylphenyl] ethanoic acid

Example 501

(2S) -Amino [3,5-dichloro-4 - ({3 - [(4-fluorophenyl) sulfonyl] -lH-indol-5-yl} oxy) phenyl] ethanoic acid

Example 502 (2S) -Amino [3,5-dibromo-4 - ({3 - [(4-fluorophenyl) sulfonyl] -lH-indol-5-yl} oxy) phenyl] ethanoic acid

Example 503

(2S) -Amino [4 - ({3 - [(4-fluoφhenyl) sulfonyl] -lH-indol-5-yl} oxy) -3,5-bis (trifluoromethyl) phenyl] ethanoic acid

Example 504

[4- ({3 - [(4-Chlθφhenyl) sulfony 1] - 1 H -indol-5 -yl} oxy) -3,5-dimethylphenoxy] acetic acid

Example 505 [3,5-dichloro-4 - ({3 - [(4-chloro-phenyl) sulfonyl] -lH-indol-5-yl} oxy) phenoxy] acetic acid

Example 506 [3,5-dibromo-4 - ({3 - [(4-chloro-phenyl) sulfonyl] -lH-indol-5-yl} oxy) phenoxy] acetic acid Example 507

[4 - ({3 - [(4-chloro-phenyl) sulfonyl] -lH-indol-5-yl} oxy) -3,5-bis (trifluoromethyl) phenoxy] acetic acid

Example 508

Example 509

[3,5-dichloro-4- ({3 - [(4-chloro-phenyl) sulfonyl] -1 H -indol-5-yl} oxy) phenyl] acetic acid

Example 510 [3,5-dibromo-4 - ({3 - [(4-chlθφhenyl) sulfonyl] -lH-indol-5-yl} oxy) phenyl] acetic acid

Example 511 [4 - ({3 - [(4-Chlθφhenyl) sulfonyl] -lH-indol-5-yl} oxy) -3,5-bis (trifluoromethyl) phenyl] acetic acid

Example 512

O- {3 - [(4-chloφhenyl) sulfonyl] -lH-indol-5-yl} -3,5-dimethyl-D-tyrosine

Example 513 3,5-dichloro-O- {3 - [(4-chlorophenyl) sulfonyl] -1H-indol-5-yl} -D-tyrosine

Example 514 3,5-dibromo-O- {3 - [(4-chlorophenyl) sulfonyl] - 1H-indol-5-yl} -D-tyrosine

Example 515

O- {3 - [(4-chloφhenyl) sulfonyl] -lH-indol-5-yl} -3,5-bis (trifluoromethyl) -D-tyrosine

Example 516

O- {3 - [(4-chlθφhenyl) sulfonyl] -lH-indol-5-yl} -3,5-dimethyl-L-tyrosine Example 517

3,5-dichloro-O- {3 - [(4-chloro-phenyl) sulfonyl] - 1H-indol-5-yl} -L-tyrosine

Example 518

3,5-dibromo-O- {3 - [(4-chloφhenyl) sulfonyl] -lH-indol-5-yl} -L-tyrosine

Example 519

O- {3 - [(4-chloφhenyl) sulfonyl] -lH-indol-5-yl} -3,5-bis (trifluoromethyl) -L-tyrosine

Example 520

[4 - ({3 - [(4-Cloφhenyl) sulfonyl] -lH-indol-5-yl} oxy) -3,5-dimethylphenyl] methanesulfonic acid

Example 521

[3,5-dichloro-4 - ({3 - [(4-chloro-phenyl) sulfonyl] -lH-indol-5-yl} oxy) phenyl] methanesulfonic acid

Example 522 [3,5-dibromo-4- ({3 - [(4-chloro-phenyl) sulfonyl] - 1H-indol-5-yl} oxy) phenyl] methanesulfonic acid

Example 523

[4 - ({3 - [(4-chloro-phenyl) sulfonyl] -lH-indol-5-yl} oxy) -3,5-bis (trifluoromethyl) phenyl] methanesulfonic acid

Example 524

{[4 - ({3 - [(4-Chlθφhenyl) sulfonyl] -lH-indol-5-yl} oxy) -3,5-dimethylphenyl] sulfanyl} acetic acid Example 525

{[3,5-dichloro-4 - ({3 - [(4-chlθφhenyl) sulfonyl] -lH-indol-5-yl} oxy) phenyl] sulfanyl} - acetic acid

Example 526

{[3,5-dibromo-4 - ({3 - [(4-chlθφhenyl) sulfonyl] -lH-indol-5-yl} oxy) phenyl] sulfanyl} - acetic acid

Example 527: {[4 - ({3 - [(4-chloro-phenyl) sulfonyl] -lH-indol-5-yl} oxy) -3,5-bis (trif [uonnethyl) phenyl] -sulfanyl} acetic acid

Example 528

(2R) -Amino [4 - ({3 - [(4-chloro-phenyl) sulfonyl] -lH-indol-5-yl} oxy) -3,5-dimethylphenyl] ethanoic acid

Example 529

(2R) -Amino [3,5-dichloro-4 - ({3 - [(4-chloro-phenyl) sulfonyl] -lH-indol-5-yl} oxy) -phenyljethanoic acid

Example 530

(2R) -Amino [3,5-dibromo-4 - ({3 - [(4-chlθφhenyl) sulfonyl] -lH-indol-5-yl} oxy) - phenyl] ethanoic acid

Example 531

(2R) -Amino [4 - ({3 - [(4-chloro-phenyl) sulfonyl] -lH-indol-5-yl} oxy) -3,5-bis (trifluoromethyl) phenyl] ethanoic acid

Example 532 (2S) -Amino [4 - ({3 - [(4-chloro-phenyl) sulfonyl] -lH-indol-5-yl} oxy) -3,5-dimethylphenyl] ethanoic acid Example 533

(2S) -Amino [3,5-dichloro-4 - ({3 - [(4-chlθφhenyl) sulfonyl] -lH-indol-5-yl} oxy) - pheny 1] ethanoic acid

Example 534

(2S) -Amino [3,5-dibromo-4 - ({3 - [(4-chlθφhenyl) sulfonyl] -lH-indol-5-yl} oxy) - phenyl] ethanoic acid

Example 535

(2S) -Amino [4 - ({3 - [(4-chlθφhenyl) sulfonyl] -lH-indol-5-yl} oxy) -3,5-bis (trifluoromethyl) phenyl] ethanoic acid

Example 536 [3,5-Dimethyl-4 - ({3 - [(4-methylphenyl) sulfonyl] -1H-indol-5-yl} oxy) phenoxy] acetic acid

Example 537

[3,5-dichloro-4 - ({3 - [(4-methylphenyl) sulfonyl] -lH-indol-5-yl} oxy) phenoxy] acetic acid

Example 538

[3,5-dibromo-4 - ({3 - [(4-methylphenyl) sulfonyl] -lH-indol-5-yl} oxy) phenoxy] acetic acid

Example 539

[4 - ({3 - [(4-Methylρhenyl) sulfonyl] -lH-indol-5-yl} oxy) -3,5-bis (trifluoromethyl) - ρhenoxy] acetic acid Example 540

[3,5-Dimethyl-4 - ({3 - [(4-methylphenyl) sulfonyl] -lH-indol-5-yl} oxy) phenyl] acetic acid

Example 541

[3,5-dichloro-4 - ({3 - [(4-methylphenyl) sulfonyl] -lH-indol-5-yl} oxy) phenyl] acetic acid

Example 542

[3,5-dibromo-4 - ({3 - [(4-methylphenyl) sulfonyl] -lH-indol-5-yl} oxy) phenyl] acetic acid

Example 543

[4 - ({3 - [(4-Methylphenyl) sulfonyl] -1H-indol-5-yl} oxy) -3,5-bis (trifluoromethyl) phenyl] acetic acid

Example 544

3,5-dimethyl-O- {3 - [(4-methylphenyl) sulfonyl] -lH-indol-5-yl} -D-tyrosine

Example 545

3,5-dichloro-O- {3 - [(4-methylphenyl) sulfonyl] -1H-indol-5-yl} -D-tyrosine

Example 546 3,5-Dibromo-O- {3 - [(4-methylphenyl) sulfonyl] -IH-indol-5-yl} -D-tyrosine

Example 547 O- {3 - [(4-methylphenyl) sulfonyl] -1H-indol-5-yl} -3,5-bis (trifluoromethyl) -D-tyrosine

Example 548

3,5-dimethyl-O- {3 - [(4-methylphenyl) sulfonyl] -lH-indol-5-yl} -L-tyrosine

Example 549

3,5-dichloro-O- {3 - [(4-methylphenyl) sulfonyl] -lH-indol-5-yl} -L-tyrosine Example 550

3,5-dibromo-O- {3 - [(4-methylphenyl) sulfonyl] -lH-indol-5-yl} -L-tyrosine

Example 551

O- {3 - [(4-methylphenyl) sulfonyl] -lH-indol-5-yl} -3,5-bis (trifluoromethyl) -L-tyrosine

Example 552

[3,5-Dimethyl-4- ({3 - [(4-methylphenyl) sulfonyl] - 1 H -indol-5-y 1} oxy) phenyl] methanesulfonic acid

Example 553

[3,5-dichloro-4- ({3 - [(4-methylphenyl) sulfonyl] - 1H-indol-5-yl} oxy) phenyl] methanesulfonic acid

Example 554

[3,5-dibromo-4 - ({3 - [(4-methylphenyl) sulfonyl] -1H-indol-5-yl} oxy) phenyl] methanesulfonic acid

Example 555

[4 - ({3 - [(4-Methylphenyl) sulfonyl] -1H-indol-5-yl} oxy) -3,5-bis (trifluoromethyl) phenyl] methanesulfonic acid

Example 556 {[3,5-Dimethyl-4 - ({3 - [(4-methylphenyl) sulfonyl] -1H-indol-5-yl} oxy) phenyl] sulfanyl} acetic acid

Example 557

{[3,5-dichloro-4 - ({3 - [(4-methylphenyl) sulfonyl] -1H-indol-5-yl} oxy) phenyl] sulfanyl} acetic acid Example 558

{[3,5-Dibromo-4 - ({3 - [(4-methylphenyl) sulfonyl] -1H-indol-5-yl} oxy) phenyl] sulfanyl} acetic acid

Example 559

{[4 - ({3 - [(4-Methylphenyl) sulfonyl] -lH-indol-5-yl} oxy) -3,5-bis (trifluoromethyl) - pheny 1] sulfanyl} acetic acid

Example 560 (2R) -amino [3,5-dimethyl-4 - ({3 - [(4-methylphenyl) sulfonyl] -lH-indol-5-yl} oxy) phenyl] ethanoic acid

Example 561

(2R) -Amino [3,5-dichloro-4 - ({3 - [(4-methylphenyl) sulfonyl] -lH-indol-5-yl} oxy) - phenyl] ethanoic acid

Example 562

(2R) -Amino [3,5-dibromo-4 - ({3 - [(4-methylphenyl) sulfonyl] -lH-indol-5-yl} oxy) - pheny 1] ethanoic acid

Example 563

(2R) -Amino [4 - ({3 - [(4-methylphenyl) sulfonyl] -1H-indol-5-yl} oxy) -3,5-bis (trifluoromethyl) phenyl] ethanoic acid

Example 564

(2S) -Amino [3,5-dimethyl-4 - ({3 - [(4-methylphenyl) sulfonyl] -lH-indol-5-yl} oxy) - phenyl] ethanoic acid Example 565

(2S) -Amino [3,5-dichloro-4 - ({3 - [(4-methylphenyl) sulfonyl] -lH-indol-5-yl} oxy) phenyl] -ethanoic acid

Example 566

(2S) -Amino [3,5-dibromo-4 - ({3 - [(4-methylphenyl) sulfonyl] -lH-indol-5-yl} oxy) - pheny 1] ethanoic acid

Example 567 (2S) -amino [4 - ({3 - [(4-methylphenyl) sulfonyl] -1H-indol-5-yl} oxy) -3,5-bis (trifluoromethyl) phenyl] ethanoic acid

Example 568

(3,5-dimethyl-4 - {[3- (4-pyridinylsulfonyl) -lH-indol-5-yl] oxy} phenoxy) acetic acid

Example 569 (3,5-dichloro-4 - {[3- (4-pyridinylsulfonyl) -IH-indol-5-yl] oxy} phenoxy) acetic acid

Example 570 (3,5-dibromo-4 - {[3- (4-pyridinylsulfonyl) -IH-indol-5-yl] oxy} phenoxy) acetic acid

Example 571

[4 - {[3- (4-Pyridinylsulfonyl) -1H-indol-5-yl] oxy} -3,5-bis (trifluoromethyl) phenoxy] acetic acid

Example 572 (3,5-Dimethyl-4 - {[3- (4-pyridinylsulfonyl) -1H-indol-5-yl] oxy} phenyl) acetic acid

Example 573 (3,5-dichloro-4 - {[3- (4-pyridinylsulfonyl) -1H-indol-5-yl] oxy} phenyl) acetic acid Example 574

(3,5-dibromo-4 - {[3- (4-pyridinylsulfonyl) -lH-indol-5-yl] oxy} phenyl) acetic acid

Example 575 [4 - {[3- (4-Pyridinylsulfonyl) -1H-indol-5-yl] oxy} -3,5-bis (trifluoromethyl) phenyl] acetic acid

Example 576

3,5-dimethyl-O- [3- (4-pyridinylsulfonyl) -lH-indol-5-yl] -D-tyrosine

Example 577

3, 5-dichloro-O- [3 - (4-pyridinylsulfonyl) -1 H-indole-5-y 1] -D-tyrosine

Example 578 3,5-Dibromo-O- [3- (4-pyridinylsulfonyl) -1H-indol-5-yl] -D-tyrosine

Example 579

O- [3- (4-pyridinylsulfonyl) -lH-indol-5-yl] -3,5-bis (trifluoromethyl) -D-tyrosine

Example 580

3,5-dimethyl-O- [3- (4-pyridinylsulfonyl) -lH-indol-5-yl] -L-tyrosine

Example 581

3,5-dichloro-O- [3- (4-pyridinylsulfonyl) -lH-indol-5-yl] -L-tyrosine

Example 582 3,5-Dibromo-O- [3- (4-pyridinylsulfonyl) -IH-indol-5-yl] -L-tyrosine

Example 583 O- [3- (4-pyridinylsulfonyl) -IH-indol-5-yl] -3,5-bis (trifluoromethyl) -L-tyrosine Example 584

(3,5-Dimethyl-4 - {[3- (4-pyridinylsulfonyl) -1H-indol-5-yl] oxy} phenyl) methanesulfonic acid

Example 585

(3,5-dichloro-4- {[3- (4-pyridinylsulfonyl) -1 H -indol-5-y 1] oxy} phenyl) methanesulfonic acid

Example 586 (3,5-dibromo-4- {[3- (4-pyridinylsulfonyl) -IH-indol-5-yl] oxy} phenyl) methanesulfonic acid

Example 587

[4 - {[3- (4-Pyridinylsulfonyl) -1H-indol-5-yl] oxy} -3,5-bis (trifluoromethyl) phenyl] methanesulfonic acid

Example 588

[(3,5-Dimethyl-4 - {[3- (4-pyridinylsulfonyl) -1H-indol-5-yl] oxy} phenyl) sulfanyl] acetic acid

Example 589

[(3,5-dichloro-4 - {[3- (4-pyridinylsulfonyl) -IH-indol-5-yl] oxy} phenyl) sulfanyl] acetic acid

Example 590

[(3,5-dibromo-4 - {[3- (4-pyridinylsulfonyl) -lH-indol-5-yl] oxy} phenyl) sulfanyl] acetic acid Example 591

{[4 - {[3- (4-pyridinylsulfonyl) -1H-indol-5-yl] oxy} -3,5-bis (trifluoromethyl) phenyl] sulfanyl} acetic acid

Example 592

(2R) -Amino (3,5-dimethyl-4 - {[3- (4-pyridinylsulfonyl) -IH-indol-5-yl] oxy} phenyl) ethanoic acid

Example 593 (2R) -Amino (3,5-dichloro-4 - {[3- (4-pyridinylsulfonyl) -lH-indol-5-yl] oxy} phenyl) ethanoic acid

Example 594

(2R) -Amino (3,5-dibromo-4 - {[3- (4-pyridinylsulfonyl) -lH-indol-5-yl] oxy} phenyl) ethanoic acid

Example 595

(2R) - Amino [4- {[3 - (4-pyridinylsulfony 1) - 1 H -indol-5-y 1] oxy} -3, 5-bis (trifluoromethyl) phenyl] ethanoic acid

Example 596

(2S) -Amino (3,5-dimethyl-4- {[3 - (4-pyridinylsulfonyl) -1 H -indol-5-yl] oxy} phenyl) ethanoic acid

Example 597

(2S) -Amino (3,5-dichloro-4 - {[3- (4-pyridinylsulfonyl) -IH-indol-5-yl] oxy} phenyl) ethanoic acid

Example 598 (2S) -Amino (3,5-dibromo-4 - {[3- (4-pyridinylsulfonyl) -IH-indol-5-yl] oxy} phenyl) ethanoic acid Example 599

(2S) -Amino [4 - {[3- (4-pyridinylsulfonyl) -IH-indol-5-yl] oxy} -3,5-bis (trifluoromethyl) pheny 1] ethanoic acid

Example 600

[4- ({3 - [(4-methoxyphenyl) sulfonyl] - 1H-indol-5-yl} oxy) -3,5-dimethylphenoxy] acetic acid

Example 601

[3,5-dichloro-4 - ({3 - [(4-methoxyphenyl) sulfonyl] -lH-indol-5-yl} oxy) phenoxy] acetic acid

Example 602 [3,5-dibromo-4 - ({3 - [(4-methoxyphenyl) sulfonyl] -1H-indol-5-yl} oxy) phenoxy] acetic acid

Example 603

[4- ({3 - [(4-methoxyphenyl) sulfonyl] -1 H -indol-5-yl} oxy) -3,5-bis (trifluoromethyl) phenoxy] acetic acid

Example 604

[4 - ({3 - [(4-methoxyphenyl) sulfonyl] -lH-indol-5-yl} oxy) -3,5-dimethylphenyl] acetic acid

Example 605

[3,5-dichloro-4 - ({3 - [(4-methoxyphenyl) sulfonyl] -lH-indol-5-yl} oxy) phenyl] acetic acid Example 606

[3, 5-Dibromo-4- ({3 - [(4-methoxyphenyl) sulfonyl] -1 H-indole-5-yl} oxy) pheny 1] acetic acid

Example 607

[4- ({3 - [(4-methoxyphenyl) sulfonyl] -1 H -indol-5-y 1} oxy) -3,5-bis (trifluoromethyl) phenyl] acetic acid

Example 608 O- {3 - [(4-methoxyphenyl) sulfonyl] -IH-indol-5-yl} -3,5-dimethyl-D-tyrosine

Example 609

3,5-dichloro-O- {3 - [(4-methoxyphenyl) sulfonyl] -lH-indol-5-yl} -D-tyrosine

Example 610

3,5-dibromo-O- {3 - [(4-methoxyphenyl) sulfonyl] -lH-indol-5-yl} -D-tyrosine

Example 611

O- {3 - [(4-methoxyphenyl) sulfonyl] - 1H-indol-5-yl} -3,5-bis (trifluoromethyl) -D-tyrosine

Example 612 O- {3 - [(4-methoxyphenyl) sulfonyl] -IH-indol-5-yl} -3,5-dimethyl-L-tyrosine

Example 613 3,5-dichloro-O- {3 - [(4-methoxyphenyl) sulfonyl] -IH-indol-5-yl} -L-tyrosine

Example 614

3,5-dibromo-O- {3 - [(4-methoxyphenyl) sulfonyl] -lH-indol-5-yl} -L-tyrosine

Example 615

O- {3 - [(4-methoxyphenyl) sulfonyl] -lH-indol-5-yl} -3,5-bis (trifluoromethyl) -L-tyrosine Example 616

[4 - ({3 - [(4-methoxyphenyl) sulfonyl] -1H-indol-5-yl} oxy) -3,5-dimethylphenyl] methane sulfonic acid

Example 617

[3,5-dichloro-4 - ({3 - [(4-methoxyphenyl) sulfonyl] -lH-indol-5-yl} oxy) phenyl] methanesulfonic acid

Example 618

[3,5-dibromo-4 - ({3 - [(4-methoxyphenyl) sulfonyl] -lH-indol-5-yl} oxy) phenyl] methanesulfonic acid

Example 619 [4 - ({3 - [(4-methoxyphenyl) sulfonyl] -1H-indol-5-yl} oxy) -3,5-bis (trifluoromethyl) phenyl] methanesulfonic acid

Example 620

{[4 - ({3 - [(4-methoxyphenyl) sulfonyl] -1H-indol-5-yl} oxy) -3,5-dimethylphenyl] sulfanyl} acetic acid

Example 621

{[3,5-dichloro-4 - ({3 - [(4-methoxyphenyl) sulfonyl] -1H-indol-5-yl} oxy) phenyl] sulfanyl} acetic acid

Example 622

{[3,5-Dibromo-4 - ({3 - [(4-methoxyphenyl) sulfonyl] -lH-indol-5-yl} oxy) phenyl] sulfanyl} acetic acid Example 623

{[4 - ({3 - [(4-methoxyphenyl) sulfonyl] -lH-indol-5-yl} oxy) -3,5-bis (trifluoromethyl) phenyl] sulfanyl} acetic acid

Example 624

(2R) -Amino [4 - ({3 - [(4-methoxyphenyl) sulfonyl] -lH-indol-5-yl} oxy) -3,5-dimethylphenyljethanoic acid

Example 625 (2R) -Amino [3,5-dichloro-4 - ({3 - [(4-methoxyphenyl) sulfonyl] -IH-indol-5-yl} oxy) phenyl] ethanoic acid

Example 626

(2R) -Amino [3,5-dibromo-4 - ({3 - [(4-methoxyphenyl) sulfonyl] -lH-indol-5-yl} oxy) -phenyl] ethanoic acid

Example 627

(2R) -Amino [4 - ({3 - [(4-methoxyphenyl) sulfonyl] -1H-indol-5-yl} oxy) -3,5-bis (trifluoromethyl) phenyl] ethanoic acid

Example 628

(2S) -Amino [4 - ({3 - [(4-methoxyphenyl) sulfonyl] -1H-indol-5-yl} oxy) -3,5-dimethylphenyl] ethanoic acid

Example 629

(2S) -Amino [3,5-dichloro-4- ({3 - [(4-methoxyphenyl) sulfonyl] - 1 H -indol-5-yl} oxy) phenyl] ethanoic acid

Example 630 (2S) -Amino [3,5-dibromo-4 - ({3 - [(4-methoxyphenyl) sulfonyl] -lH-indαl-5-yl} oxy) -phenyl] ethanoic acid Example 631

(2S) -Amino [4 - ({3 - [(4-methoxyphenyl) sulfonyl] -1H-indol-5-yl} oxy) -3,5-bis (trifluoromethyl) phenyl] ethanoic acid

Example 632

{3,5-Dimethyl-4 - [(3 - {[4- (trifluoromethyl) ρhenyl] sulfonyl} -lH-indol-5-yl) oxy] - phenoxy} acetic acid

Example 633

{3,5-dichloro-4 - [(3 - {[4- (trifluoromethyl) phenyl] sulfonyl} -lH-indol-5-yl) oxy] -phen-oxy} acetic acid

Example 634 {3,5-Dibromo-4 - [(3 - {[4- (trifluoromethyl) phenyl] sulfonyl} -lH-indol-5-yl) oxy] -phen-oxy} acetic acid

Example 635

{3,5-bis (trifluoromethyl) -4 - [(3 - {[4- (trifluoromethyl) phenyl] sulfonyl} -lH-indol-5-yl) - oxy] phenoxy} acetic acid

Example 636

{3,5-Dimethyl-4 - [(3 - {[4- (trifluoromethyl) phenyl] sulfbnyl} -lH-indol-5-yl) oxy] phenyl} acetic acid

Example 637

{3,5-dichloro-4 - [(3- {[4- (trifluoromethyl) phenyl] sulfonyl} - 1H-indol-5-yl) oxy] phenyl} acetic acid Example 638

{3,5-dibromo-4 - [(3- {[4- (trifluoromethyl) phenyl] sulfonyl} -lH-indol-5-yl) oxy] phenyl} acetic acid

Example 639

{3,5-bis (trifluoromethyl) -4 - [(3 - {[4- (trifluoromethyl) phenyl] sulfonyl} -lH-indol-5-yl) - oxy] phenyl} acetic acid

Example 640 3,5-Dimethyl-O- (3 - {[4- (trifluoromethyl) ρhenyl] sulfonyl} -lH-indol-5-yl) -D-tyrosine

Example 641

3,5-dichloro-O- (3 - {[4- (trifluoromethyl) ρhenyl] sulfonyl} -lH-indol-5-yl) -D-tyrosine

Example 642

3,5-dibromo-O- (3 - {[4- (trifluoromethyl) phenyl] sulfonyl} -lH-indol-5-yl) -D-tyrosine

Example 643

3,5-bis (trifluoromethyl) -O- (3- {[4- (trifluoromethyl) phenyl] sulfonyl} -1H-indol-5-yl) -D-tyrosine

Example 644

3,5-dimethyl-O- (3 - {[4- (trifluoromethyl) phenyl] sulfonyl} -lH-indol-5-yl) -L-tyrosine

Example 645

3,5-dichloro-O- (3 - {[4- (trifluoromethyl) p enyl] sulfonyl} -lH-indol-5-yl) -L-tyrosine

Example 646

3,5-dibromo-O- (3 - {[4- (trifluoromethyl) phenyl] sulfonyl} -lH-indol-5-yl) -L-tyrosine Example 647

3,5-bis (trifluoromethyl) -O- (3- {[4- (trifluoromethyl) phenyl] sulfonyl} - 1H-indol-5-yl) -L-tyrosine

Example 648

{3,5-Dimethyl-4 - [(3 - {[4- (trifluoromethyl) phenyl] sulfonyl} -lH-indol-5-yl) oxy] phenyl} methanesulfonic acid

Example 649 {3,5-dichloro-4 - [(3 - {[4- (trifluoromethyl) phenyl] sulfonyl} -lH-indol-5-yl) oxy] phenyl} methanesulfonic acid

Example 650

{3,5-dibromo-4 - [(3 - {[4- (trifluoromethyl) phenyl] sulfonyl} -lH-indol-5-yl) oxy] phenyl} methanesulfonic acid

Example 651

{3,5-bis (trifluoromethyl) -4 - [(3 - {[4- (trifluoromethyl) phenyl] sulfonyl} -lH-indol-5-yl) - oxy] phenyl} methanesulfonic acid

Example 652

({3,5-Dimethyl-4 - [(3 - {[4- (trifluoromethyl) phenyl] sulfonyl} -lH-indol-5-yl) oxy] -phenyl} sulfanyl) acetic acid

Example 653

({3,5-dichloro-4 - [(3 - {[4- (trifluoromethyl) phenyl] sulfonyl} -lH-indol-5-yl) oxy] -phenyl} sulfanyl) acetic acid

Example 654 ({3,5-dibromo-4 - [(3 - {[4- (trifluoromethyl) ρhenyl] sulfonyl} -lH-indol-5-yl) oxy] phenyl} sulfanyl) acetic acid Example 655

({3,5-bis (trifluoromethyl) -4 - [(3 - {[4- (trifluoromethyl) phenyl] sulfonyl} -lH-indol-5-yl) - oxy] phenyl} sulfanyl) acetic acid

Example 656

(2R) -Amino {3,5-dimethyl-4 - [(3 - {[4- (trifluoromethyl) ρhenyl] sulfonyl} -lH-indol-5-yl) oxy] phenyl} ethanoic acid

Example 657

(2R) -Amino {3,5-dichloro-4 - [(3 - {[4- (trifluoromethyl) phenyl] sulfonyl} -lH-indol-5-yl) -oxyphenyl} ethanoic acid

Example 658 (2R) -An-ύno {3,5-dibromo-4 - [(3 - {[4- (trifluoromethyl) phenyl] sulfonyl} -lH-indol-5-yl) - oxy] phenyl} ethanoic acid

Example 659

(2R) -Amino {3,5-bis (trifluoromethyl) -4 - [(3 - {[4- (trifluoromethyl) phenyl] sulfonyl} -lH-indol-5-yl) oxy] phenyl} ethanoic acid

Example 660

(2S) -Andno {3,5-dimethyl-4 - [(3 - {[4- (trifluoromethyl) phenyl] sulfonyl} -lH-indol-5-yl) oxy] phenyl} ethanoic acid

Example 661

(2S) -Amino {3,5-dichloro-4 - [(3- {[4- (trifluoromethyl) ρhenyl] sulfonyl} -lH-indol-5-yl) - oxy] phenyl} ethanoic acid Example 662

(2S) -Amino {3,5-dibromo-4 - [(3 - {[4- (trifluoromethyl) phenyl] sulfonyl} -lH-indol-5-yl) oxy] phenyl} ethanoic acid

Example 663

(2S) -Amino {3,5-bis (trifluoromethyl) -4 - [(3 - {[4- (trifluoromethyl) phenyl] sulfonyl} -lH-indol-5-yl) oxy] ρhenyl} ethanoic acid

Example 664 Difluoro (4 - {[3- (4-fluorobenzyl) -IH-indol-5-yl] oxy} -3,5-dimethylphenyl) acetic acid

Example 665

(4 - {[3- (4-chlorobenzyl) -lH-indol-5-yl] oxy} -3,5-dimethylphenyl) (difluoro) acetic acid

Example 666

[4 - ({3 - [(4-chloro-phenyl) sulfonyl] -lH-indol-5-yl} oxy) -3,5-dimethylphenyl] (difluoro) acetic acid

Example 667 Difluoro [4 - ({3 - [(4-fluorophenyl) sulfonyl] -1H-indol-5-yl} oxy) -3,5-dimethylρhenyl] acetic acid

Example 668

Fluorine [4 - ({3 - [(4-fluorophenyl) sulfonyl] -lH-indol-5-yl} oxy) -3,5-dimethylphenyl] acetic acid

Example 669

[4 - ({3 - [(4-Chlθφhenyl) sulfonyl] -lH-indol-5-yl} oxy) -3,5-dimethylphenyl] (fluoro) acetic acid Example 670

(4- {[3 - (4-Chlorbenzy 1) - 1 H-indol-5 -y 1] oxy} -3,5 -dimethylphenyl) (fluoro) acetic acid

Example 671 Fluorine (4 - {[3- (4-fluorobenzyl) -IH-indol-5-yl] oxy} -3,5-dimethylphenyl) acetic acid

Example 672

(3-chloro-4 - {[3- (4-fluorobenzyl) -lH-indol-5-yl] oxy} -5-methylphenyl) (fluoro) acetic acid

Example 673

(3-Chloro-4 - {[3- (4-chlorobenzyl) -lH-indol-5-yl] oxy} -5-methylphenyl) (fluoro) acetic acid

Example 674 [3-chloro-4 - ({3 - [(4-chloro-phenyl) sulfonyl] - 1 H -indol-5-yl} oxy) -5-methylphenyl] -

(Fluoro) acetic acid

Example 675

3-Chloro-4 - ({3 - [(4-fluoro-phenyl) sulfonyl] -lH-indol-5-yl} oxy) -5-methylphenyl] (fluoro) - acetic acid

Example 676

[3-Chloro-4 - ({3 - [(4-fluoφhenyl) sulfonyl] -lH-indol-5-yl} oxy) -5-methylphenyl] - (difluoro) acetic acid

Example 677

[3-chloro-4 - ({3 - [(4-chloφhenyl) sulfonyl] -lH-indol-5-yl} oxy) -5-methylphenyl] -

(Difluoro) acetic acid Example 678

(3-Chloro-4 - {[3- (4-chlorobenzyl) -lH-indol-5-yl] oxy} -5-methylphenyl) (difluoro) acetic acid

Example 679

(3-Chloro-4 - {[3- (4-fluorobenzyl) -lH-indol-5-yl] oxy} -5-methylphenyl) (difluoro) acetic acid

Example 680 (3,5-dichloro-4- {[3 - (4-fluorobenzyl 1) -1 H -indol-5-yl] oxy} phenyl) (difluoro) acetic acid

Example 681

(3,5-dichloro-4 - {[3- (4-chlorobenzyl) -lH-indol-5-yl] oxy} phenyl) (difluoro) acetic acid

Example 682

[3,5-dichloro-4 - ({3 - [(4-chlθφhenyl) sulfonyl] -lH-indol-5-yl} oxy) phenyl] (difluoro) acetic acid

Example 683 [3,5-dichloro-4 - ({3 - [(4-fluθφhenyl) sulfonyl] -lH-indol-5-yl} oxy) phenyl] (difluoro) acetic acid

Example 684

[3,5-dichloro-4 - ({3 - [(4-fluorophenyl) sulfonyl] -lH-indol-5-yl} oxy) phenyl] (fluoro) acetic acid

Example 685

[3,5-dichloro-4 - ({3 - [(4-chloro-phenyl) sulfonyl] -lH-indol-5-yl} oxy) phenyl] (fluoro) -acetic acid Example 686

(3,5-dichloro-4 - {[3- (4-chlorobenzyl) -lH-indol-5-yl] oxy} phenyl) (fluoro) acetic acid

Example 687 (3,5-dichloro-4 - {[3- (4-fluorobenzyl) -IH-indol-5-yl] oxy} phenyl) (fluoro) acetic acid

Example 688

(3,5-dibromo-4 - {[3- (4-fluorobenzyl) -lH-indol-5-yl] oxy} phenyl) (fluoro) acetic acid

Example 689

(3,5-dibromo-4 - {[3- (4-chlorobenzyl) -lH-indol-5-yl] oxy} phenyl) (fluoro) acetic acid

Example 690

[3,5-dibromo-4 - ({3 - [(4-chloro-phenyl) sulfonyl] -lH-indol-5-yl} oxy) phenyl] (fluoro) - acetic acid

Example 691

[3,5-dibromo-4 - ({3 - [(4-fluorophenyl) sulfonyl] -lH-indol-5-yl} oxy) phenyl] (fluoro) acetic acid

Example 692

[3,5-dibromo-4 - ({3 - [(4-fluoφhenyl) sulfonyl] -lH-indol-5-yl} oxy) phenyl] (difluoro) acetic acid

Example 693

[3,5-dibromo-4 - ({3 - [(4-chloro-phenyl) sulfonyl] -lH-indol-5-yl} oxy) phenyl] (difluoro) acetic acid

Example 694 (3,5-dibromo-4 - {[3- (4-chlorobenzyl) -IH-indol-5-yl] oxy} phenyl) (difluoro) acetic acid Example 695

(3,5-dibromo-4- {[3 - (4-fluorobenzyl) -1 H -indol-5-yl] oxy} phenyl) (difluoro) acetic acid

Example 696 Difluoro [4 - {[3- (4-fluorobenzyl) -IH-indol-5-yl] oxy} -3,5-bis (trifluoromethyl) phenyl] acetic acid

Example 697

[4 - {[3- (4-Chlorobenzyl) -IH-indol-5-yl] oxy} -3,5-bis (trifluoromethyl) phenyl] (difluoro) acetic acid

Example 698

[4 - ({3 - [(4-Chlθφhenyl) sulfonyl] -lH-indol-5-yl} oxy) -3,5-bis (trifluoromethyl) phenyl] - (difluoro) acetic acid

Example 699

Difluoro [4 - ({3 - [(4-fluorophenyl) sulfonyl] -1H-indol-5-yl} oxy) -3,5-bis (trifluoromethyl) phenyl] acetic acid

Example 700

Fluorine [4- ({3 - [(4-fluoφhenyl) sulfonyl] - 1H-indol-5-yl} oxy) -3,5-bis (trifluoromethyl) phenyl] acetic acid

Example 701 [4 - ({3 - [(4-chloro-phenyl) sulfonyl] -lH-indol-5-yl} oxy) -3,5-bis (trifluoromethyl) phenyl] -

(Fluoro) acetic acid

Example 702

[4 - {[3- (4-chlorobenzyl) -IH-indol-5-yl] oxy} -3,5-bis (trifluoromethyl) phenyl] - (fluoro) - acetic acid Example 703

Fluorine [4- {[3 - (4-fluorobenzyl) - 1 H -indol-5 -yl] oxy} -3, 5-bis (trifluoromethyl) pheny 1] - acetic acid

Claims

claims

1. Compounds of the general formula (I)

in which

Z stands for O, S, SO, SO ₂ , CH ₂ , CHF, CF ₂ or for NR ⁹ , where R ⁹

Represents hydrogen or (C - C ₄ ) -alkyl,

1

R and R are the same or different and represent hydrogen, halogen, cyano, (-CC ₆ ) alkyl, CF ₃ , CHF ₂ , CH ₂ F, vinyl or (C ₃ -C ₇ ) cycloalkyl, at least one the two substituents are not equal to hydrogen and are in the ortho position to the bridge bond,

R for a group of the formula

-A _m -D _n -E ₀ -G _p -LR 10

stands in what

A represents O, S, NR ¹¹ or the group - (CR ¹² = CR ¹³ ) -, in which R ¹¹ denotes hydrogen or (C1-C4) alkyl, and R ¹² and R ^{13 are} identical or different and are hydrogen, Mean cyano, (dC ^ -A-kyl or (CrC ₄ ) - alkoxy, D represents a straight-chain (C ₁ -C ₃ ) alkylene group which one or more times, identically or differently, by (CrC ₄ ) alkyl, hydroxy,

(-C-C ₄ ) alkoxy, halogen, amino, mono- (-C-C) alkylamino, mono-

(-CC) -acylamino or (-C ^ -alkoxycarbonylamino may be substituted,

E and L independently of one another represent a C (O) or SO ₂ group,

G represents NR ¹⁴ , in which R ^{14 represents} hydrogen or (-C ₄ ) -alkyl, or represents a straight-chain (C * -C ₃ ) -alkylene group which one or more times, identically or differently, by (Cj-C) -Alkyl, hydroxy, (-C-C ₄ ) - alkoxy, halogen, amino, mono- or di- (-C-C ₄ ) -Alkylamino or mono- (C ₁ -C ₄ ) -acylamino can be substituted,

and

R ¹⁰ for OR ¹⁵ , NR ¹⁶ R ¹⁷ , (CC ₁₀ ) alkyl, (C ₃ -C ₈ ) cycloalkyl, (C ₂ -C ₆ ) alkenyl, (C ₆ -Cι _. O) aryl, ( C ₆ -Cιo) arylmethyl or for a saturated, partially unsaturated or aromatic 5- to 10-membered Heterocycle with up to four identical or different heteroatoms from the series N, O and / or S, the abovementioned radicals optionally being selected from the group halogen, hydroxy, oxo, cyano, nitro, by one, two or three identical or different substituents, Amino, NR ^{I 8} R ¹⁹ , trifluoromethyl, (-

90

C ₆ ) alkyl, optionally substituted by R (QC _Ö ) - alkoxy, (C ₃ -C ₈ ) cycloalkyl, (C ₆ -Cιo) aryl, which in turn optionally by halogen, (-C-C ₄ ) alkyl , (-C ^ alkoxy, trifluoromethyl, nitro or cyano is substituted, -OC (O) -R ²¹ , -C (O) -OR ²² , -C (O) -NR ²³ R ²⁴ , -SO ₂ -NR ²⁵ R ²⁶ , -NH-C (O) -R ²⁷ and -NH-C (O) -OR ^{28 are} substituted, wherein

R ¹⁵ , R ¹⁶ , R ¹⁷ , R ¹⁸ , R ¹⁹ , R ²⁰ , R ²¹ , R ²² , R ²³ , R ²⁴ , R ²⁵ , R ²⁶ , R ²⁷ and R ^{28 are the} same or different and each represents hydrogen, Phenyl, benzyl, (CC ₆ ) -alkyl or (C ₃ -C ₈ ) -cycloalkyl, which in turn are optionally one or more, identical or different, by halogen, hydroxy, amino, carboxyl, (C- _. -C ₄ ) -Alkoxy, (-C- -alkoxycarbonyl, (C-ι-C ₄ ) -alkoxy-carb- onylamino, (-CC) alkanoyloxy, a heterocycle or optionally substituted by halogen or hydroxy

Phenyl are substituted,

or the group

-LR ιo represents a group of the formula in which

R ²⁹ denotes hydrogen or (Ci -C ₄ ) alkyl,

or R ³ for a group of the formula

stands in what

Q represents a 5- to 6-membered saturated, partially unsaturated or aromatic heterocycle with up to four identical or different heteroatoms from the series N, O and / or S, which in turn is optionally one to three times, identical or different, by oxo (= O), thioxo (= S), hydroxy, (-

C ₆ ) - alkyl or phenyl is substituted,

r represents the number 0, 1 or 2,

and

the ring Het is a 5- to 6-membered saturated or partially unsaturated heterocycle with up to three identical or different heteroatoms from the series N, O and / or S, which may be one to three times, identical or different, by oxo (= O),

Thioxo (= S), hydroxy, (C - C ₆ ) alkyl or phenyl is substituted,

R ⁴ and R ^{5 are the} same or different and each represents hydrogen, hydroxy,

Halogen, cyano, nitro, (C1-C4) -alkyl or the radical of the formula NR ³⁰ R ³¹ , where R ³⁰ and R ^{31 have} the meaning given for R ¹⁵ and, independently of one another, can be identical or different with this substituent,

R ^{6 represents} hydrogen, halogen or a group of the formula -M _a -R 32

stands in what

M represents a carbonyl group, a sulfonyl group or a methylene group,

a represents the number 0 or 1,

and

R ^{32 has} the meaning of R ¹⁰ given above and can be identical or different with this substituent,

and

2. Compounds according to claim 1,

in which Z represents O, S or CH ₂ ,

Rl and R ^ are the same or different and represent hydrogen, fluorine, chlorine,

Bromine, (-CC ₄ ) alkyl, CF ₃ , CHF ₂ , CH ₂ F, vinyl or (C3-C5) - cycloalkyl, where at least one of the two substituents is not equal to hydrogen and is in the ortho position to the bridge bond, in particular both substituents are not equal to hydrogen and both are in the ortho position,

R for a group of the formula

-A _m -D _n -E ₀ -G _p -LR 10

stands in what

A represents O, S, NR ¹¹ or the group - (CR ¹² = CR ¹³ ) -, in which R ¹¹ denotes hydrogen or methyl, and R ¹² and R ^{13 are} identical or different and denote hydrogen or methoxy,

D stands for a straight-chain (C ₁ -C ₃ ) alkylene group, which is mono- or divalent, identical or different, by (Q-) alkyl,

Hydroxy, methoxy, ethoxy, fluorine, chlorine, amino, mono- (Cp

C ₄ ) -alkylamino or mono- (C ₁ -C ₄ ) -acylamino may be substituted,

E represents a C (O) group,

L represents a C (O) or SO group, G represents an NH group or a straight-chain (dC ₃ ) alkyl group which is mono- or disubstituted, identically or differently, by methyl, ethyl, hydroxy, methoxy, fluorine, chlorine, amino, methylamino or acetylamino can

and

in the event that m and o each represent the number 1, A represents the radical NR ¹¹ and L represents a C = O group, the sum (n + p) is not equal to the number 0,

and

R ¹⁰ for OR ¹⁵ , NR ¹⁶ R ¹⁷ , (dC ₆ ) alkyl, (C ₃ -C ₇ ) cycloalkyl, naphthyl,

Phenyl, benzyl or for a saturated, partially unsaturated or aromatic 5- to 6-membered heterocycle with up to four identical or different heteroatoms from the series N, O and / or S, the aforementioned radicals optionally being substituted by one, two or three same or different substituents selected from the

Group halogen, hydroxy, oxo, cyano, nitro, amino, NR ¹⁸ R ¹⁹ , trifluoromethyl, (dC ₄ ) alkyl, optionally substituted by R ²⁰ (dC ₄ ) alkoxy, (C ₃ -C ₆ ) cycloalkyl, OC (O) -R ²¹ , -C (O) -OR ²² , -C (O) -NR ²³ R ²⁴ , -SO ₂ -NR ²⁵ R ²⁶ , -NH-C (O) -R ²⁷ and -NH -C (O) -OR ^{28 are} substituted, wherein R ¹⁵ , R ¹⁶ , R ¹⁷ , R ¹⁸ , R ¹⁹ , R ²⁰ , R ²¹ , R ²² , R ²³ , R ²⁴ , R ²⁵ , R ²⁶ , R ²⁷ and R ^{28 are the} same or different and each represents hydrogen,

Phenyl, benzyl, (-CC ₆ ) -alkyl or (C ₃ -C ₆ ) -cycloalkyl, which in turn are optionally one or more, identical or different, by halogen, hydroxy, amino, carboxyl, (d-

C ₄ ) - alkoxy, (dC) -alkoxycarbonyl, (Cι-C ₄ ) -alkoxy-carb-onylamino, (Cι-C ₅ ) -alkanoyloxy, a heterocycle or optionally substituted by halogen or hydroxy substituted phenyl,

or

R for a group of the formula

stands,

R4 and R-5 are the same or different and each represents hydrogen, halogen or (C i -C4) alkyl,

R ^{6 represents} hydrogen, halogen or a group of the formula

-M _a -R ³² stands in what

M represents a carbonyl group, a sulfonyl group or a methylene group,

a represents the number 0 or 1,

and

R ^{32 represents} (-C-Cιo) alkyl, (C ₃ -C ₇ ) fcycloalkyl, (C ₂ -C ₄ ) alkenyl, naphthyl, phenyl, benzyl, pyridyl, pyridazinyl or pyridazinonyl, the aforementioned radicals optionally being one, two or three identical or different substituents selected from the group halogen, hydroxy,

Cyano, nitro, amino, NR ¹⁸ R ¹⁹ , trifluoromethyl, (dC) - alkyl, (dC ₄ ) - alkoxy, (C ₃ -C ₇ ) cycloalkyl, phenyl, which in turn may be halogen, (dC ₄ ) alkyl , (dC ₄ ) - alkoxy, trifluoromethyl, nitro or cyano, -O- C (O) -R ²¹ , -C (O) -OR ²² , -C (O) -NR ²³ R ²⁴ , -SO ₂ -NR ²⁵ R ²⁶ , -NH-

C (O) -R ²⁷ and -NH-C (O) -OR ^{28 are} substituted, wherein

R ¹⁸ , R ¹⁹ , R ²¹ , R ²² , R ²³ , R ²⁴ , R ²⁵ , R ²⁶ , R ²⁷ and R ^{28 are the} same or different and each represents hydrogen, phenyl, benzyl, (dC ₆ ) -alkyl or ( C ₃ -C ₆ ) cycloalkyl, which in turn are optionally one or more, identical or different, by halogen, hydroxy, amino, carboxyl, (dC ₄ ) alkoxy, (dC ₄ ) alkoxycarbonyl, (C ₁ -C ₄ ) -A-koxycarbonylamino, (d- C ₅ ) -alkanoyloxy, a heterocycle or phenyl which is optionally substituted by halogen or hydroxy, R7 represents hydrogen,

and

3. Compounds according to claim 1,

in which

represents O or CH,

Rl and R2 are the same or different and represent hydrogen, fluorine, chlorine,

Bromine, (C ₁ -C 4) alkyl, CF ₃ , CHF ₂ , CH ₂ F, vinyl or (C ₃ -C ₅ ) cycloalkyl, where at least one of the two substituents is not hydrogen and is ortho to the bridge bond is, in particular both substituents are not equal to hydrogen and both are in the ortho position,

R for a group of the formula

stands in what

A represents O, S or NH, D represents a straight-chain (C ₁ -C ₃ ) alkylene group which can be substituted once or twice, identically or differently, by methyl, ethyl, hydroxy, methoxy, fluorine, amino or acetylamino,

E represents a C (O) group,

L represents a C (O) or SO ₂ group,

G represents an NH group or a methylene group,

and

R ^{10 represents} OR ¹⁵ , NR ¹⁶ R ¹⁷ , (dC ₆ ) - alkyl, phenyl, benzyl or an aromatic 5- to 6-membered heterocycle with up to four identical or different heteroatoms from the series N, O and or S. , wherein the aforementioned radicals optionally selected from the group by one, two or three identical or different substituents

Group fluorine, chlorine, hydroxy, oxo, cyano, nitro, amino, NR ¹⁸ R ¹⁹ , Trifluoromethyl, (-CC ₄ ) alkyl, optionally substituted by R ²⁰ (C ₁ -C ₄ ) alkoxy, (C ₃ -C ₆ ) cycloalkyl, -OC (O) -R ²¹ , -C (O) -OR ²² , -C (O) -NR ²³ R ²⁴ , -SO ₂ -NR ²⁵ R ²⁶ , -NH-C (O) -R ²⁷ and -NH-C (O) -OR ^{28 are} substituted, wherein

Phenyl, benzyl, (dC ₆ ) -alkyl or (C ₃ -C ₆ ) -cycloalkyl, which in turn are optionally one to two times, identical or different, by fluorine, chlorine, hydroxyl, amino, carboxyl,

(CC ₄ ) alkoxy, (-C-C ₄ ) alkoxycarbonyl, (C] -C ₄ ) alkoxycarbonylamino, (dC ₅ ) alkanoyloxy, a heterocycle or optionally substituted by fluorine, chlorine or hydroxy-substituted phenyl,

R4 and R5 are the same or different and each represents hydrogen, fluorine, chlorine or methyl,

R »6 for hydrogen, halogen or a group of the formula

-M _a - 32

stands in what

M represents a sulfonyl group or a methylene group,

a represents the number 0 or 1,

and R ^{32 represents} (dC ₁₀ ) alkyl, (C ₃ -C ₇ ) cycloalkyl, phenyl, benzyl, pyridyl, pyridazinyl or pyridazinonyl, the above-mentioned radicals optionally being selected from the group fluorine by one or two identical or different substituents, Chlorine, bromine, hydroxy, cyano, nitro, amino, NR ¹⁸ R ¹⁹ ,

Trifluoromethyl, (-CC ₄ ) - alkyl, (CC ₄ ) alkoxy, (C ₃ -C ₇ ) - cycloalkyl, -OC (O) -R ²¹ , -C (O) -OR ²² , -C (O ) -NR ²³ R ²⁴ , -SO ₂ -NR ²⁵ R ²⁶ , -NH-C (O) -R ²⁷ and -NH-C (O) -OR ^{28 are} substituted, wherein

R ¹⁸ , R ¹⁹ , R ²¹ , R ²² , R ²³ , R ²⁴ , R ²⁵ , R ²⁶ , R ²⁷ and R ^{28 are the} same or different and each represents hydrogen, phenyl,

Are benzyl, (dC ₆ ) -alkyl or (C ₃ -C ₆ ) -cycloalkyl, which in turn are optionally one or two, identical or different, by fluorine, chlorine, hydroxy, amino,

Carboxyl, (dC ₄ ) -alkoxy, (dC) -alkoxycarbonyl, (Ci-C ₄ ) -alkoxycarbonyl-amino, (d-C ₅ ) -alkanoyloxy, a heterocycle or optionally substituted by fluorine, chlorine or hydroxy-substituted phenyl,

R ^ represents hydrogen,

R ^{8 is} hydrogen, carboxyl, (dC ₄ ) alkoxycarbonyl, (dC ₆ ) alkyl, (C ₃ -C ₇ ) cycloalkyl, phenyl, benzyl, pyridyl, phenylsulfonyl or

Benzylsulfonyl, where the abovementioned radicals are optionally selected from the group fluorine, chlorine, bromine, hydroxy, cyano, nitro, amino, NR ¹⁸ R ¹⁹ , trifluoromethyl, (dC ₄ ) - alkyl, (dC.) By one or two identical or different substituents ₄ ) -alkoxy, (C ₃ - C ₆ ) -cycloalkyl, -OC (O) -R ²¹ , -C (O) -OR ²² , -C (O) -NR ²³ R ²⁴ , -SO ₂ -NR ²⁵ R ²⁶ , -NH-C (O) -R ²⁷ and -NH-C (O) -OR ^{28 are} substituted, wherein

(-C ₆ ) alkyl or (C ₆ -C ₆ ) cycloalkyl, which in turn, if necessary, one or more times, identically or differently, by fluorine, chlorine, hydroxyl, amino, carboxyl, (C 1 -C ₄ ) alkoxy , (-C-C) -alkoxycarbonyl, (dC ₄ ) -alkoxycarbonyl-amino, (dC ₅ ) -alkanoyloxy, a heterocycle or optionally substituted by fluorine, chlorine or hydroxy-substituted phenyl,

4. Compounds according to claim 1,

in which

stands for O,

Rl and R2 are the same or different and represent hydrogen, fluorine, chlorine,

Bromine, (C ₁ -C ₄ ) alkyl, CF ₃ , CHF ₂ , CH ₂ F, vinyl or (C3-C5) cycloalkyl, where at least one of the two substituents is not hydrogen and is in the ortho-position to the bridge bond , in particular both substituents are not equal to hydrogen and both are in the ortho position,

R ³ for a group of the formula -A _m -D _n -E ₀ -G _p -LR 10

stands in what

A represents O, S or NH,

represents a methylene or ethylene group which can be substituted one to two times, identically or differently, by methyl, ethyl, fluorine, amino or acetylamino,

E represents a C (O) group,

L represents a C (O) or SO group,

G represents an NH group or a methylene group,

in the case that L stands for a C = O group, the sum

(m + n + o + p) is not equal to the number 0,

and

in the event that m and o each represent the number 1, A represents the remainder NH and L represents a C = O group, the sum (n + p) is not equal to the number O,

and R ^{10 represents} OR ¹⁵ , NR ¹⁶ R ^Π or (dC ₄ ) alkyl, where R ¹⁵ , R ¹⁶ and

R ^{17 are the} same or different and each represents hydrogen, phenyl,

Benzyl, (-C-C ₆ ) -alkyl or (C ₃ -C ₆ ) -cycloalkyl are available, which in turn are optionally one to two times, identical or different, by fluorine, chlorine, hydroxy, amino, carboxyl, (dC ₄ ) - Alkoxy, (dC ₄ ) -

Alkoxycarbonyl, (-C-C4) -alkoxycarbonylamino, (Cι-C ₅ ) -alkanoyl-oxy, a heterocycle or phenyl are substituted,

R ^{6 represents} hydrogen, halogen, (C - C ₁₀ ) alkyl, (C ₃ -C ₇ ) cycloalkyl, (C ₃ - C ₇ ) cycloalkylmethyl, phenyl, benzyl, pyridazinonylmethyl, phenylsulfonyl or pyridylsulfonyl, where the aforementioned aromatic radicals are optionally substituted by one or two identical or different substituents selected from the group consisting of fluorine, chlorine, cyano, nitro, trifluoromethyl, methyl, methoxy, carboxyl or methoxycarbonyl,

R ^{7 represents} hydrogen,

R ^{8 is} hydrogen, (dC ₆ ) alkyl, (C ₃ -C ₇ ) cycloalkyl, phenyl, benzyl,

Phenylsulfonyl or benzylsulfonyl, the abovementioned aromatic radicals optionally being selected from the group fluorine, chlorine by one or two identical or different substituents,

Cyano, trifluoromethyl, methyl or methoxy are substituted,

5. Compounds according to claim 1, in which Z represents CH ₂ or in particular oxygen,

Rl and R2 are identical or different and represent methyl, ethyl, propyl, isopropyl, chlorine, bromine, CF ₃ , vinyl or cyclopropyl, where both substituents are in the ortho position to the bridge bond,

R4 and R-5 independently of one another represent methyl, fluorine or chlorine or in particular hydrogen,

and

R ^{7 represents} hydrogen.

6. A compound according to any one of claims 1 to 5, in which Z represents oxygen.

7. A compound according to any one of claims 1 to 6, in which R3 represents a group of the formula

is in the para position to the bridge bond and in which R ^{10 is} hydroxy or the radical -C ^ -R ¹ ° has the stated meanings of R ¹⁰ for a group which is a prodrug to the carboxylic acid -C (O ) - OH or its salts can be broken down.

Compounds according to any one of claims 1 to 7, in which R ⁴ , R ⁵ and R ^{7 represent} hydrogen.

Compounds according to one of claims 1 to 8, in which R and R-2 are both arranged in the ortho position to Z and represent bromine, trifluoromethyl, ethyl, cyclopropyl and in particular methyl or chlorine.

10. Compounds of formula (Ia)

in which

and

R for straight-chain or branched (dC ₈ ) alkyl

stands, and their pharmaceutically acceptable salts, solvates, hydrates and hydrates of the salts.

11. Medicament containing at least one compound of the general formula (I) or (Ia) as defined in claims 1 to 10.

12. Medicament containing at least one compound of the general formula (I) or (Ia) as defined in claims 1 to 10, and at least one auxiliary and / or excipient customary in pharmacology.

13 Process for the preparation of medicaments, characterized in that at least one compound of the general formula (I) or (Ia) as defined in claims 1 to 10 is converted into a suitable application form with auxiliaries and excipients.

14. Use of the compounds of general formula (I) as defined in claims 1 to 10 in the prevention and control of diseases.

15. Use of compounds of general formula (I) as defined in claims 1 to 10, in the treatment and / or prophylaxis of arteriosclerosis and hypercholesterolemia.

16. Use of compounds of general formula (I) according to at least one of claims 1 to 8 for the manufacture of medicaments for the prophylaxis and / or treatment of disease forms which can be treated with natural thyroid hormone.

17. Use of compounds of general formula (I) according to at least one of claims 14 to 16 in combination with other medicaments.

18. A method for the prevention and control of diseases, characterized in that treating patients with a compound as defined in claims 1 to 10.

19. A process for the preparation of compounds of the general formula (I) as defined in claim 1, characterized in that reactive indole derivatives of the general formula (II) with reactive phenyl derivatives of the general formula (III)

(II) (III) (IV)

wherein the substituents R ¹ , R ² , R ⁴ , R ⁵ , R ⁶ , R ⁷ and R ^{s have} the meanings given in claim 1, and

R ³ 'has the meaning given for R ³ or for NO, NH ₂ , NH-PG, OH, O-PG, SH, S-PG, or for an aldehyde, cyano, carboxyl or (Ci-C ₄ ) Alkoxy-carbonyl group,

where PG stands for a protective group,

X and Y each represent groups of opposite reactivity, e.g. X can be an electrophilic radical which reacts with a nucleophilic Y substituent and vice versa,

Z 'has the meaning given for Z or stands for _/ CH-OH or ^ C = O, if appropriate in the presence of inert solvents and catalysts and if appropriate with isolation of the intermediates of the general formula (IV) or directly to give compounds of the formula (I).

20. Compounds of the formula (Ib)

in which

R 1 and R are identical or different and represent bromine, trifluoromethyl, ethyl, cyclopropyl and in particular methyl or chlorine,

R ^{3 represents} a group of the formula -NH-C (O) -CH ₂ -C (O) -R ¹⁰ , wherein

R ^{10 represents} hydroxy or the radical -C (O) -R ^{10 has} the meanings given above of R ¹⁰ for a group which can be degraded as a prodrug to the carboxylic acid -C (O) -OH or its salts,

and

R ⁶ for straight-chain or branched (dC ₈ ) alkyl

stands.