USRE34299E

USRE34299E - 1-(4'-fluorophenyl)-3,5-substituted indoles useful in the treatment of psychic disorders and pharmaceutical compositions thereof

Info

Publication number: USRE34299E
Application number: US07/759,517
Authority: US
Inventors: Jens K. Perregaard
Original assignee: H Lundbeck AS
Current assignee: H Lundbeck AS
Priority date: 1985-04-10
Filing date: 1991-09-13
Publication date: 1993-06-29
Anticipated expiration: 2006-04-01
Also published as: FI90976B; FI861505A0; CA1256437A; IE58370B1; CA1338327B; NL970016I1; JPS61236764A; DK169674B1; FI90976C; LU90218I2; AU583607B2; JPH064587B2; IE860618L; DK157686D0; FI861505A7; US4710500A; HK116793A; NL970016I2; EP0200322B1; AU5590186A

Abstract

The present invention relates to novel indole derivatives which have interesting pharmacodynamic effects indicating pronounced activity in the treatment of psychic disorders, especially psychoses and, at the same time, a low degree of undesired side effects.

Moreover, the invention relates to methods for the preparation of said indole derivatives, pharmaceutical compositions containing same, and methods for the treatment of psychic disorders, especially psychoses, by administering a therapeutically active amount of one of said derivatives to a living animal body, including human beings.

The novel indole derivatives of the present invention are represented by the following formula; ##STR1## wherein R is phenyl, optionally substituted with halogen.[., lower alkyl or trifluoromethyl,.]. or a hetero aromatic group, such as 2-thienyl, 3-thienyl, .[.2-furoyl, 3-furoyl, 2-thiazol, 2-oxazol, 2-imidazole, 2-pyridyl, 3-pyridyl.]. .Iadd.2-oxazolyl, 2-imidazolyl, 2-pyridyl 3-pyridyl.Iaddend.or 4-pyridyl; R¹ is hydrogen, halogen, lower alkyl, lower alkoxy, hydroxy, cyano, nitro, lower alkylthio, trifluoromethyl, lower alkylsulfonyl, amino, lower alkylamino or lower di-alkylamino; "A" is nitrogen or carbon, and the dotted line indicates--when A is carbon--an optional bond; R² is hydrogen, cycloalkyl, lower alkyl or lower alkenyl, optionally substituted with one or two hydroxy groups, any hydroxy group present being optionally esterified with an aliphatic carboxylic acid radical having from two to twenty-four carbon atoms inclusive, or R² is the group ##STR2## wherein "n" is an integer of 2-6; X is oxygen or sulfur, or <C=X may constitute the group .[.>.]. =CH= when Y is =N-- or =CH--; Y is oxygen, sulfur, CH₂ or N R³, where R³ is hydrogen.Iadd., .[.or.]. lower alkyl, lower alkenyl or a cycloalkylmethyl group, said "cycloalkyl" having from three to six carbon atoms inclusive; Z is --(CH₂)_m --, "m" being 2 or 3, or Z is --CH=CH-- or 1,2-phenylene optionally substituted with halogen or trifluoromethyl, or Z is --CO(or S)CH₂ --; U is nitrogen or carbon provided that when R¹ is .Iadd.hydrogen, .Iaddend.chloro, .Iadd.lower alkyl, methoxy or hydroxy, .Iaddend.A is nitrogen and R² is .[.methyl or cyclohexyl.]. .Iadd.lower alky or .Iadd.cycloalkyl of C₃ --C₆, .Iaddend.R may not be phenyl; as well as their pharmaceutically acceptable acid addition salts.

Description

BACKGROUND OF THE INVENTION

In the past, several indole derivatives being substituted at the nitrogen atom with a carboxylic acid radical have been found to possess .[.analgetic.]. .Iadd.analgesic .Iaddend.and antiinflammatory properties. Recently it was suggested in German OLS No. 2811031 that also indoles having a phenylsubstituent at the nitrogen atom might have the desired .[.analgetic.]. .Iadd.analgesic .Iaddend.or antiinflammatory effects, but no data were given for the .[.1-phenyl-5-chloro-3-methylpiperanzineindole .Iadd.1-phenyl-5-chloro-3-(4-methyl-1-piperazinyl)-1-phenylindole or 1-phenyl-5-chloro-3-cyclohexyl-piperazineimdole actually disclosed in the specification. We have prepared the first-mentioned of these compound Lu23-015) and found that it was without interesting effects .Iadd.as compared to the closest related compound of the invention, i.e., 5-chloro-1-(4-fluorophenyl)-3-(4-methyl-1-piperazinyl)indole (Lu 23-011), .Iaddend.in the pharmacological testing carried out in our laboratories.

In European Patent application No. 80401005.6 some derivatives of tetrahydro-pyridinyl-indoles having at the 1-position either hydrogen or alkyl (1-3 C-atoms), were described as being neuroleptics. The pharmacological data given in the specification, however, indicate only weak to moderate neuroleptic activity.

We have prepared one of these compounds, .[.5-chloro-3-(1-(2-hydroxyethyl)-1,2,3,6-tetrahydropyrid-4-yl)indol.]. .Iadd.5-chloro-3-(1-(2-hydroxyethyl)-1,2,3,6-tetrahydropyrid-4-yl)indole .Iaddend.(Lu 23-143) and found that it was almost active compared with the compounds of Formula I.

It has now surprisingly been found that the novel indole derivatives of Formula I are potent dopaminergic antagonists in pharmacological tests.[., both in vivo and.]. in vitro.[.,.]. .Iadd.and many of them also in vivo, .Iaddend.as compared with well-known neuroleptics commonly used in the treatment of psychoses; and especially very long-lasting effects -- up to several days -- were observed with many of the compounds of Formula I. Additionally, most of the .[.the.]. indoles of Formula I are strong 5-HT antogonists both .[.periferically.]. .Iadd.peripherally .Iaddend.and centrally, which is considered to be important for the treatment of psychic disorders or cardiovascular diseases.

The terms lower alkyl, lower alkoxy, lower alkylthio and lower alkysulfonyl designate such groups having from one to four carbon atoms inclusive. Exemplary of such groups are methyl, ethyl, n-propyl, iso-propyl, n-butyl, sec.butyl, methoxy, ethoxy, propoxy, butoxy, methylthio, ethylthio, propylthio, methylsulfonyl, ethylsulfonyl, or the like.

The term lower alkenyl designates alkenyl groups having from two to four carbon atoms, for example ethenyl, 1-propenyl, 2-butenyl, or the like.

This invention also includes pharmaceutically acceptable salts of the compounds of Formula I formed with non-toxic acids. Such salts are easily prepared by methods known to the art.

The base is reacted with either the calculated amount of organic or inorganic acid in an aqueous miscible solvent, such as acetone or ethanol, with isolation of the salt by concentration and cooling or an excess of the acid in aqueous immiscible solvent, such as ethyl ether or chloroform, with the desired salt separating directly.

Exemplary of such organic salts are those with maleic, fumaric, benzoic, ascorbic, embonic, succinic, oxalic, bis-methylenesalicylic, methanesulfonic, ethanedisulfonic, acetic, propionic, tartaric, salicylic, citric, gluconic, lactic, malic, mandelic, cinnamic, citraconic, aspartic, stearic, palmitic, itaconic, glycolic, p-aminobenzoic, glutamic, benzene sulfonic and theophylline acetic acids, as well as the 8-halotheophyllines, for example 8-bromo-theophylline. Exemplary of such inorganic salts are those with hydrochloric, hydrobromic, sulfuric, sulfamic, phosphoric and nitric acids. Of course, these salts may also be prepared by the classical method of double decomposition of appropriate salts, which is well-known to the art.

The compounds of Formula I as well as the pharmaceutically acceptable acid addition salts thereof may be administered both orally and parenterally, for example in the form of tablets, capsules, powders, syrups or solutions for injection.

Of the indoles of Formula I, those wherein R¹ is chlorine, fluorine, trifluoromethyl, methyl, nitro or amino in the 5-position, R is phenyl substituted with fluroine in the 4'-or the 2'-position, R² is methyl, hydroxyethyl or 3-hydroxypropyl, and A is as defined above, have shown especially favourable effects in the pharmacological testing, and also have few undesired side effects.

The invention moreover relates to a method for the preparation of the novel indoles of Formula I, which comprises

(a) reacting an indole derivative of the following formula: ##STR3## wherein R¹ and R are as defined above, with a 4-piperidone of the formula: ##STR4## wherein R² is as defined above, or

(b) reducing a compound of the following formula: ##STR5## wherein R¹, R and R² are as defined above, or

(c) reacting a compound of the following formula: ##STR6## wherein R¹, R² and A are defined above, with a compound of formula:

wherein R is as defined above and "hal" is halogen, in the presence of a metal catalyst, or

(d) reacting a compound of the following formula: ##STR7## wherein R¹, R and A are as defined above, with a lower alkyl halide or an epoxide of formula ##STR8## wherein .[.R.]. .Iadd.R' .Iaddend.is hydrogen, methyl or ethyl, or

(e) reducing a compound of the following formula: ##STR9## wherein R¹, R and A are as defined above and R⁴ is hydrogen, lower alkyl (1-3 C-atoms) or lower alkoxy (1-3 C-atoms), or

(f) heating a compound of the following formula: ##STR10## wherein R¹ and R .Iadd.are .Iaddend.as defined above, with a piperazine of formula: ##STR11## wherein R² is as defined above, or

(g) reducing a compound of the following formula: ##STR12## wherein R¹, R and R² are as defined above, with a suitable reducing agent, whereupon the indole of Formula I is isolated in the form of the free base or a pharmaceutically acceptable acid addition salt thereof, and if the group R² contains one or two hydroxyl groups, if desired, acylating such a hydroxy group with a reactive derivative of an aliphatic carboxylic acid having from two to twenty-four carbon atoms, and isolating the ester formed as the free base or a pharmaceutically acceptable acid addition salt thereof.

In method (a) the reaction is performed under strong acidic conditions by heating. Trifluoroacetic acid or HCl in ethanol are preferred as acid catalysts. The starting compounds of Formula II are conveniently prepared according to procedures described in the literature, e.g. by reduction of R substituted isatins or oxindoles by a method described by H. Sirowej et al, in Synthesis 1972, 84, according to the following reaction scheme: ##STR13## Isatins and oxindoles are prepared by a .[.Fiedel-Craft.]. .Iadd.Friedel-Craft .Iaddend.ring closure under standard conditions from N-oxalylchloro-or N-(2-chloroacetyl) diphenylamines respectively. The compounds of Formula II may alternatively be prepared by arylation of N-unsubstituted indoles according to the method described by M.A. Khan and E.K. Rocha, Chem.Pharm.Bull. 25 (11), 3110-3114 (1977).

An alternative way of obtaining the intermediates of Formula II is that from an indoxyl-2-carboxylic ester as outlined below: ##STR14## in method (b) the reduction is preferably carried out at low hydrogen pressures (3 ato.) in the presence of platinum or palladium on carbon black.

In method (c) the arylation is preferably carried out at about 160°-210° C. in aprotic polar solvents as e.g. N-methyl-2-pyrrolidone or hexamethylphosphoric triamide with K₂ CO₃ as base and copper as a catalyst. In method (e) the reduction is preferably carried out with LiAlH₄ in THF or diethylether or with diborane in THF.

Method (f) is a two step procedure in which compound VII first is decarboxyalkylated in the presence of an inorganic salt as e.g. LiCl or MgCl₂ in a polar solvent as e.g. diglyme, hexamethylphosphoric triameide or N-methyl-2-pyrrolidone at elevated temperatures (120°-150° C.). Finally, the appropriate piperazine is added and the temperature raised to about 200° C. and kept there until the corresponding indoxyle has disappeared according to TLC analysis. The compounds of Formula VII are conveniently prepared according to the procedures reported by P. C. Unangst and M. E. Carethers, J.Heterocyclic Chem. 21, 709 (1984).

In method (g) diborane in THF is conveniently used as a reducing agent. The compounds of Formula VIII are prepared from the corresponding R-substituted isatins according to the following reaction scheme: ##STR15## The methods of the invention shall be illustrated in the following by some examples, which may not be construed as limiting:

EXAMPLE 1 (Method a)

1-(4'-Fluorophenyl)-5-methyl-3-(1-methyl-1,2,3,6-tetrahydropyridin-4-yl)-1H-indole, hydrochloride (Lu 20-089).

1-(4'-fluorophenyl)-5-methyl-1H-indole (4.5 g) and

1-methyl-4-piperidone (5 g) were dissolved in 25 ml of acetic acid and added dropwise to 50 ml of trifluoroacetic acid kept almost at the boiling point. The mixture was gently refluxed for another 1/2 h. Excess trifluoroacetic acid was evaporated and the reaction mixture was added to 50 ml of 6 M HCl and 50 ml of ether. The precipitated title compound was filtered off and dried. Yield: 3.1 g (43%). M.p. 262°-266° C.

In a corresponding manner the following tretrahydropyridin-4-ylindoes were prepared:

5-Fluoro-1-(4'-fluorophenyl)-3-(1-methyl-1,2,3,6-tetrahydropyridin-4-yl)-1H-indole, hydrochloride. (Lu 21-018). M.p. 256° C.

1-(4'-Fluorophenyl)-3-(1-methyl-1,2,3,6-tetrahydropyridin-4-yl)-5-trifluoromethyl-1H-indole, oxalate. (Lu 21-120). M.p. 228°-229° C.

1-(4'-Fluorophenyl)-5-nitro-3-(1-methyl-1,2,3,6-tetrahydropyridin-4yl)-1H-indole. (Lu 22-135). M.p. 168°-170° C.

1-(3'-Fluorophenyl)-5-nitro-3-(1-methyl-1,2,3,6-tetrahydropyridin-4-yl)-1H-indole, maleate. (Lu 24-004). M.p. 216°-217° C.

1-(2'-Fluorophenyl)-5-nitro-3-(1-methyl-1,2,3,6-tetrahydropyridin-4-yl)-1H-indole, maleate. (Lu 24-003). M.p. 208° C.

3-(1-(2-Hydroxyethyl)-1,2,3,6-tetrahydropyridin-4-yl)-1-(4'-trifluoromethylphenyl)-1H-indole, fumarate. (Lu 24-012). M.p. 174°-175° C.

1-(4'-Fluorophenyl)-3-(1-methyl-1,2,3,6-tetrahydropyridin-4-yl)-1H-indole, hydrochloride. (Lu 23-083). M.p. 268°-270° C.

1-(4'-Fluorophenyl)-5-nitro-3-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indole, maleate. (Lu 23-133). M.p. 204°-205° C.

5-Chloro-1-(4'-fluorophenyl)-3-(1-(2-hydroxyethyl)-1,2,3,6tetrahydropyridin -4yl)-1H indole, hydrochloride. (Lu 23-146). M.p. 280°-282° C.

5-Chloro-1-(4'-fluorophenyl)-3-(1,2,3,6-tetrahydropyri-din-4-yl)-1H-indole. (Lu 23-147). M.p. 105° C.

1-(4'-fluorophenyl)-3-(1-(2-hydroxyethyl)-1,2,3,6-tetrahydropyridin-4-yl)-5-nitro-1H-indole. (Lu 23-150). M.p. 151°-152° C.

1-(4'-Fluorophenyl)-3-(1,2,3,6-tetrahydropyridin-4-yl)-5-trifluoromethyl-1H-indole. (Lu 23-155). M.p. 128°-130° C.

1-(4'-Fluorophenyl)-3-1-(2-hydroxyethyl-1,2,3,6-tetrahydropyridin-4-yl)-5-trifluoromethyl-1H-indole. (Lu 23-156). M.p. 140°-141° C.

5-fluoro-1-(4'-fluorophenyl)-3-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indole. (Lu 23-159). M.p. 75°-77° C.

5-fluoro-1-(4'-fluorophenyl)-3-(1-(2-hydroxyethyl)-1,2,3,6-tetrahydropyridin-4-yl)-1H-indole, oxalate. (Lu 23-160). M.p. 180°-184° C.

5-fluoro-1-(4'-fluorophenyl)-3-(1-(2-propyl-1,2,3,6-tetrahydropyridin-4-yl)-1H-indole, fumarate. (Lu 23-167). M.p. 190°-195° C.

1-(4'-Fluorophenyl)-3-(1-(3-hydroxypropyl)-1,2,3,6-tetrahydropyridin-4-yl)-5trifluoromethyl-1H-indole. (Lu 23-171). M.p. 159°-161° C.

5-Fluoro-1-(4'-fluorophenyl)-3-(1-(3-hydroxypropyl-1,2,3,6-tetrahydropyridin-4-yl)-1H-indole, oxalate. (Lu 23-175). M.p. 173°-175° C.

EXAMPLE 2 (method b)

1-(4'-Fluorophenyl)-3-(1-methyl-4-piperidyl)-5-trifluoromethyl-1H-indole, oxalate. (Lu 21-131).

Compound Lu 21-120, oxalate (2.5 g) is dissloved in ethanol (200 ml), and PtO₂ (0.2 g) is added. Hydrogenation is continued for 3h at 3 atm. The catalyst was then filtered off, ethanol evaporated and the title compound crystallized from acetone/ether. Yield: 1.2 g (48%). M.p. 251°-252° C.

In a corresponding manner were also prepared:

.[.1-(4'-Fluorophenyl)-3-(1-(2-imidazolidinon-1-yl)ethyl)-4-piperidyl)-1H-indole..]. .Iadd.

1-(4'-Fluorophenyl)-3-(1-(2-(2-imidazolidinon-1-yl)ethyl)-4-piperidyl)-1H-indole. .Iaddend.(Lu 23-086). M.p. 174°-175° C.

.[.1-(4'-Fluorophenyl)-3-(1-(1-pyrrolidinon-2-onylethyl-4-piperidyl)-5-trifluoromethyl-1H-indole, fumarate..]. .Iadd.

1-(4'-Fluorophenyl)-3-(1-(2-(1-pyrrolidinon-2-onyl)ethyl)-4-piperidyl)-5-trifluoromethyl-1H-indole, fumarate. (Lu 23-158). M.p. 240°-241° C.

.[.5-Chloro-1-(4'-fluorophenyl)-3-(1-(2-imidazolidinon-1-ylethyl)-4-piperidyl)-1H-indole, maleate..]. .Iadd.

5-Chloro-1-(4'-fluorophenyl)-3-(1-(2-(2imidazolidinon-1-yl)ethyl)-4-piperidyl)-1H-indole, maleate..Iaddend.(Lu 23-174). M.p. 155°-160° C.

EXAMPLE 3 (Method c)

3-(1-Methyl-1,2,3,6-tetrahydropyridin-4-yl)-5-nitro-1-pyridin-3-yl-1H-indole. (Lu 24-016).

3-(1-Methyl-1,2,3,6-tetrahydropyridin-4-yl)-5-nitro-1H-indole (4.5 g), 3-bromopyridin (6.0 g), CuBr (4.5 g) and K₂ CO₃ (8.0 g) .Iadd.in N-methyl-2-pyrrolidone (25 ml) .Iaddend.were heated under stirring at 160° C. for 2.5 h. After cooling the reaction mixture was poured into diluted NH₄ OH (500 ml) and extracted with ethyl acetate (3×300 ml). The combined organic phases were dried (MgSO₄) and the solvent evaporated. The title compound was obtained by recrystallization from acetone. Yield: 3.4 g (58%). M.p. 175°-177° C.

In a corresponding manner were also prepared:

3-(1-Methyl-1,2,3,6-tetrahydropyridin-4-yl)-5-nitro-1-pyridin-2-yl-1H-indole. (Lu24-015). M.p. 134° C.

.[.3-(1-Methyl-1,2,3,6-tetrahydropyridin-4-yl)-5-nitro-1-(2-thiazolo-1H-indole. .Iadd.

3-(Methyl-1,2,3,6-tetrahydropyridin-4-yl)-5-nitro-1-(2-thiazolyl)-1H-indole. (Lu 24-022). M.p. 204°-206° C.

5-Chloro-3-(1-methyl-1,2,3,6-tetrahydropyridin-4-yl)-1-(3-thienyl)-1H-indole, maleate. (Lu 24-001). M.p. 168°-170° C.

3-(1-Methyl-1,2,3,6-tetrahydropyridin-4-yl)-5-nitro-1-(2-thienyl)-1H-indole, maleate. Lu 24-014). M.p. 206°-208° C.

EXAMPLE 4 (methods c and e)

5-Chloro-1-(4'-fluorophenyl)-1-methyl-1,2,3,6-tetrahydropyridin-4-yl)-1H-indole, hydrobromide. (Lu 22-117).

5-Chloro-3-(1-carbethoxy-1,2,3,6-tetrahydropyridin-4-yl)-1H-indole (10 g), 1,4-fluoroiodobenzene (15 g), CuBr (10 g) and K₂ CO₃ (15 g) in HMPA (50 ml) were heated (180°-200° C.) while stirring for 3h. After cooling the reaction mixture was poured into H₂ O (1 ltr.) and ethylenediamine (100 ml). The crude product was obtained by extraction twice with ether/ethyl acetate (2:1). The combined organic phases were dried .[.(MgSo₄).]. .Iadd.(MgSO₄) .Iaddend.and the solvents were evaporated. The pure 5-chloro-1-(4'-fluorophenyl)-3-(1-carbethoxy-1,2,3,6-tetrahydropyridin-4-yl)-1H-indole was obtained by column chromatography on silica gel (eluent 30% ether in dichloromethane). Yield: 8.9 g (68%). M.p. 120°-122° C. The carbethoxy compound .[.then.]. .Iadd.thus .Iaddend.obtained (3 g) was dissolved in dry THF (50 ml) and LiAlH₄ pellets (2 g) were added. The mixture was refluxed for 1h, cooled and H₂ O/THF added to destroy excess LiAlH₄. The precipitate was filtered off and THF evaporated. The remaining oil was dissolved in acetone and the title compound precipitated as a hydrobromide salt. Yield: 2.4 g (75%). M.p. 258° C.

In a corresponding manner were also prepared:

5Chloro-1-(4'-fluorophenyl)-3-(1-isobutyl-1,2,3,6-tetrahydropyridin-4yl)-1H-indole, hydrobromide. (Lu 22-134). M.p. 285°-286° C.

.[.5-Fluro-3-(1-methyl-1,2,3,6-tetrahydropyridin-4-yl)-1-(2-thiazolo)-1H-indole,.]. .Iadd.

5-Fluoro-3-(1-methyl-1,2,3,6-tetrahydropyridin-4-yl)-1-(2-thiazoloyl)-1H-indole, .Iaddend.fumarate. (Lu 24-013). M.p. 190°-194° C.

EXAMPLE 5 (method d)

.[.5-Fluoro-2-(4'-fluorophenyl)-3-(1-(2-imidazolidinon-1-ylethyl)-1,2,3,6-tetrahydropyridin-4-yl)-1H-indole,.]. .Iadd.

5-Fluoro-1-(4'-fluorophenyl)-3-(1-(2-(2-imidazolidinon-1yl)ethyl)-1,2,3,6-tetrahydropyridin-4-yl)-1H-indole, .Iaddend.oxalate. (Lu 21-046)

5-Fluoro-1-(4'-fluorophenyl)-3-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indole (2g) prepared as described in Example 1; .[.1chloroethyl-2-imidazolidinon.]. .Iadd.1-(2-chloroethyl)-2-imidazolidinone .Iaddend.(2 g), K₂ CO₃ (3 g) and a small crystal of KI were refluxed in methyl .[.isobytyl.]. .Iadd.isobutyl .Iaddend.ketone (50 ml) for 16 h. The reaction mixture was poured into H₂ O and CH₂ Cl₂ (200 ml) was added. The organic phase was separated, dried (MgSO₄) and the solvents evaporated. The crude product was dissolved in acetone and precipitated as an oxalate salt. Yield: 1.2 g (36%) . M.p. 186°-189° C.

In a corresponding manner the following indoles were prepared:

.[.1-(4'-Fluorophenyl)-3-(4-(2-imidazolidinon-1-ylethyl)-1-piperazino-5-trifluoromethyl-1H-indole,.]. .Iadd.

1-(4'-Fluorophenyl)-3-(2-(2-imidazolidinon-1-yl)ethyl-1-piperazinyl)-5-trifluoromethyl-1H-indole, .Iaddend.dihydrobromide. (Lu 23-001). M.p. 262°-263° C.

.[.1-(4'-Fluorophenyl)-3-(4-(1-pyrrolidin-2-onylethyl)-1-piperazino-5-trifluoromethyl-1H-indole..]. .Iadd.

1-(4'-Fluorophenyl)-3-(4-(2-(1-pyrrolidin-2-onyl)ethyl)-1-piperazinyl)-5-trifluoromethyl-1H-indole. .Iaddend.(Lu 22-133). M.p. 224°-227° C.

.[.1-(4'-Fluorophenyl)-5-nitro-3-(1-pyrrolidin-2-onlyethyl)-1,2,3,6-tetrahydropyridin-4yl)-1H indole,.]. .Iadd.

1-(4'-Fluorophenyl-5-nitro-3-(4-(2-(1-pyrrolidin-2-onyl)ethyl)-1,2,3,6-tetrahydropyridin-4-yl)-1H-indole, hydrochloride. (Lu 23-024). M.p. 263°-265° C.

.[.1(4'-Fluorophenyl)-3-(1-(2-imidazolidinon-1-ylethyl)-1,2,3,6-tetrahydropyridin-4-yl)-1H-indole,.]. .Iadd.

1-(4'-Fluorophenyl)-3-(1-(2-imidazolidinon-1-yl)ethyl)-1,2,3,6-tetrahydropyridin-4-yl)-1H-indole, .Iaddend.hydrochloride. (Lu 23-075). M.p. 259°-262° C.

.[.1-(4'-Fluorophenyl)-5-nitro-3-(1-(2-oxazolidinon-3-ylethyl)-1,2,36-tetrahydropyridin-4yl)-1H-indole,.]. .Iadd.

1-(4'-Fluorophenyl)-5-nitro-3-(2(2-(oxazolidinon-3-yl)ethyl)-1,2,3,6-tetrahydropyridin-4-yl)-1H-indole, .Iaddend.maleate. (Lu 23-134). M.p. 128°-130° C.

.[.1-(4'-Fluorophenyl)-3-(1-(2-imidazolidinon-1-ylethyl)-1,2,3,6-tetrahydropyridin-4-yl)-5-nitro-1H-indole..]. .Iadd.

1-(4'-Fluorophenyl)-3-(1-(2-(2-imidazolidinon-1-yl)ethyl)-1,2,3,6-tetrahydropyridin-4-yl)-5-nitro-1H-indole,.Iaddend.(Lu 23-142). M.p. 177°-179° C.

.[.5-Chloro-1-(4'-fluorophenyl)-3-(1-(2-imidazolidinon-1-ylethyl)-1,2,3,6-tetrahydropyridin-4-yl)-1H-indole..]..Iadd.

5-Chloro-1-(4'-fluorophenyl)-3-(1-(2-(2-imidazolidinon-1-yl)ethyl)-1,2,3,6-tetrahydropyridin-4-yl)-1H-indole..Iaddend. (Lu 23-148). M.p. 138°-140° C.

.[.1-(4'-Fluorophenyl)-3-(1-(2-imidazolidinon-1-ylethyl)-1,2,3,6-tetrahydropyridin-4-yl)-5-trifluoromethyl-1H-indole..]. .Iadd.

1-(4'-Fluorophenyl)-(1-(2-(2-imidazolidinon-1-yl)ethyl)-1,2,3,6-tetrahydropyridin-4-yl)-5-trifluoromethyl-1H-indole. .Iaddend.(Lu 23-157). M.p. 164°-165° C.

.[.1-(2'-Fluorophenyl)-3)-(1-(2-imidazolidinon-1-ylethyl)-1,2,3,6-tetrahydropyridin-4-yl)-5-nitro-1H-indole,.]. .Iadd.

1-(2'-Fluorophenyl)-3-(1-(2-(2-imidazolidinon-1-yl)ethyl)-1,2,3,6-tetrahydropyridin-4-yl)-5-nitro-1H-indole, .Iaddend.maleate. (Lu 24-024). M.p. 200°C.

.[.1-(4'-Fluorophenyl)-3-(1-pyrrolo-2-ethyl)-1,2,3,6-tetrahydropyridin-4-yl)-5-trifluoromethyl-1H-indole, .Iadd.

1-(4'-Fluorophenyl)-3-(1-(2-(1-pyrrolyl)ethyl)-1,2,3,6-tetrahydropyridin-4-yl)-5-trifluoromethyl-1H-indole, .Iaddend.maleate. (Lu 23-172).

.[.1-(4'-Fluorophenyl)-3-(1-pyrrolo-2-aceto-(1-1,2,3,6-tetrahydropyridin-4-yl)-5-trifluoromethyl-1H-indole .Iadd.

1-(4'-Fluorophenyl)-3(1-pyrrolyl)carbonylmethyl-1,2,3,6-tetrahydropyridin-4-yl-5-trifluoromethyl-1H-indole .Iaddend.(2.5 g) was refluxed with LiAlH₄ (1 g) in dry THF (50 ml) for 1.5h. After cooling H₂ O/THF was added to destroy excess of LiAlH₄. The precipitate was filtered off and THF evaporated. The remaining oil was dissolved in 2-propanol and the title compound precipitated as a maleate. Yield: 1.3 g (42%). M.p. 194°-195° C.

In a corresponding manner were also prepared:

.[.1-(4'-Fluorophenyl)-3-(1-(2-methyl-1-imidazoloe-2-ethyl)-1,2,3,6-tetrahydropyridin-4-yl)-5-trifluoromethyl-1H-indole,.]. .Iadd.

1-(4'-Fluorophenyl)-3(1-(2-(2-methylimidazol-1-yl)ethyl)-1,2,3,6-tetrahydropyridin-4-yl)-5-trifluoromethyl-1H-indole, .Iaddend.difumarate. (Lu 23-173). M.p. 189°-191° C.

.[.1-(4'-Fluorophenyl)-3-(1-(1-imidazole-2-ethyl-1,2,3,6-tetrahydropyridin-4-yl)-5-trifluoromethyl-1H-indole,.]. .Iadd.

1-(4'-Fluorophenyl)-3-(2-2-(imidazol-1-yl)ethyl)-1,2,3,6-tetrahydropyridin-4-yl)-5-trifluoromethyl-1H-indole, .Iaddend.dimaleate. (Lu 24-002). M.p. 165°-167° C.

EXAMPLE 7 (method f)

.[.1-(4'-Fluorophenyl)-3-(4-methyl-piperazino-1-)-5-trifluoromethyl-1H-indole,.]. .Iadd.

1-(4'-Fluorophenyl)-3-(4-methyl-1-piperazinyl)-5-trifluoromethyl-1H-indole, .Iaddend.dihydrochloride. (Lu 21-123).

.[.2-Carboxymethyl-1-(4'-fluorophenyl)-5-trifluoromethylindolin-3-on.]..Iadd.

2-Carboxymethyl-1-(4'-fluorophenyl)-5-trifluoromethylindolin-3-one .Iaddend.(15 g) and MgCl₂ ·6H₂ O (30 g) in HMPA (100 ml) were heated under N₂ at 120°-140° C. for 1 h and finally at 150° C. for another 1/2 h. .[.1-Methyl-piperazin.]. .Iadd.1-Methyl-piperazine .Iaddend.(25 ml) was added and the mixture was refluxed under N₂ at an oil bath temperature of 200° C. for 16 h. The mixture was cooled and poured into 1 ltr. of H₂ O and extracted with ether 3×200 ml). The combined ether extracts were washed with 0.5 M HCl (3×300 ml). The acidic H₂ O phase was made alkaline and reextracted with ether (2×200 ml). The combined organic phase was dried (MgSO₄) and the ether evaporated. The remaining oil was dissolved in acetone and the title compound precipitated as a dihydrochloride. Yield: 6.7 g (35%). M.p. 245°-247° C.

In a corresponding manner the following 3-piperazinoindoles were prepared:

.[.1-(4'-Fluorophenyl)-3-(4-(2-hydroxyethyl)-1-piperazino-5-trifluoromethyl-1H-indole..]. .Iadd.

1-(4'-Fluorophenyl)-3-(4-(2-hydroxyethyl)-1-piperazinyl)-5-trifluoromethyl-1H-indole. .Iaddend.(Lu 21-152). M.p. 164° C.

.[.1-(4'-Fluorophenyl)-3-piperazino-5-trifluoromethyl-1H-indole..]. .Iadd.

1-(4'-Fluorophenyl)-3-(1-piperazinyl-5-trifluoromethyl-1H-indole. .Iaddend.(Lu 21-153). M.p. 168°-170° C.

.[.1-(4'-Fluorophenyl)-3-(4-isopropyl-piperazino-5-trifluoromethyl-1H-indole,.[. .Iadd.

1-(4'-Fluorophenyl)-3-(4-isopropyl-1-piperazinyl-5-trifluoromethyl-1H-indole, .Iaddend.dihydrochloride. (Lu 23-016). M.p. 278°-280° C.

.[.5-Chloro-3-(4-methylpiperazino-1-phenyl-1H-indole..]. .Iadd.

5-Chloro-3-(4-methyl-1-piperazinyl)-1-phenyl-1H-indole. .Iaddend.(Lu 23-015). M.p. 174°-175° C. .Iadd.Lu 23-011 (see Table 1). .Iaddend.

EXAMPLE 8 (method g)

1-(4'-Fluorophenyl)-5-methyl-3-(1-methyl-4-piperidyl)-1H-indole, hydrobromide. (Lu 21-037).

To 14 g of Mg turnings was added 4-chloro-1-methylpiperidine (35 g) in dry THF (500 ml). The mixture was refluxed for 1 hour and filtered under N₂ into an ice cooled solution of 1-(4'-fluorophenyl)-5-methylisatin (60 g) in dry THF (500 ml). The mixture was heated to reflux and poured into H₂ O (1 ltr.) saturated with NH₄ Cl and extracted with ether (2×300 ml). The combined organic phases were dried (MgSO₄), the ether evaporated yielding 48.5 g (58%) of 1-(4'-fluorophenyl-3-hydroxy-5-methyl-3-(1-methyl-4-piperidyl)indolin-2-on. M.p. 177°-179° C.//To a suspension of LiAlH₄ (1 g) in dry THF (100 ml) was added 2.5 g of the above prepared indolin-2-on. The mixture was refluxed for 1 hour, excess of .[.LiAlH₄ destroyed.]. .Iadd.LiAlH₄ destroyed .Iaddend. by addition of H₂ O / THF, and filtered; and 2 M HCl (500 ml) was added to the filtrate and gently heated. The H₂ O phase was made alkaline and the product extracted with ether (2×300 ml). The combined ether phases were dried (MgSO₄) and the ether evaporated. The remaining oil was dissolved in acetone and 1-(4'-fluorophenyl)-5-methyl-3-(1-methyl-4-piperidyl) .[.indolin-2-on.]. .Iadd.indolin-2-one .Iaddend.was precipitated an oxlate. Yield: 2.0 g (66%). M.p. 222° C. To a solution of .[.B₂ H₆ in.]. .Iadd.B₂ H₆ in .Iaddend.THF (100 ml) kept under N₂ at 0°C. was added 11.0 g of the oxalate salt prepared as above. The mixture was heated slowly to 50° C. and kept there for 2 hours. It was finally poured onto ice (1 ltr.) and extracted with ether (2×200 ml). The combined ether phases were dried (MgSO₄) and the ether evaporated. The remaining oil was dissolved in 2-propanol and the title compound precipitated as a hydrobromide salt. Yield: 3.7 g (36%). M.p. 254°-256° C.

EXAMPLE 9

5-Amino-1-(4'-fluorophenyl)-3-(1-methyl-1,2,3,6-tetrahydropyridin-4-yl)-1H-indole, fumarate. (Lu 23-149)

.[.1-(4'-Fluorophenyl)-3-(methyl-1,2,3,6-tetrahydropyridin-4yl)-5-nitro-1H-indole.]. .Iadd.

1-(4'-Fluorophenyl)-3-(1-methyl-1,2,3,6-tetrahydropyridin-4-yl)-5-nitro-1H-indole .Iaddend.(Lu 22-135) (10 g) in 90% ethanol (150 ml) was heated to reflux and dil. HCl (2 ml) and Fe-powder (5 g) were added within 0.5 hour. Reflux was continued for another hour. The reaction mixture was filtered, cooled down and subsequently poured into 1 liter of .[.NH₄ Oh.]. .Iadd.NH₄ OH .Iaddend.and extracted with ethyl acetate (2×400 ml). The combined organic phases were dried (MgSO₄) and the solvent evaporated. The remaining oil .[.and.]. .Iadd.was .Iaddend.purified by column chromatography on silica gel (eluted with ethyl acetate/methanol 1:1 containing 2% of triethylamine). The title compound was finally precipitated as a fumarate from ethanol/acetone (1:1). Yield 4.2 g (34%). M.p. 128°-134° C.

EXAMPLE 10

.[.1-(4'-Fluorophenyl)-3-(4-(2-(pyrrolidin-2-thion-1-yl)-ethyl-1-piperazino-5-trifluoromethyl-1H-indole.]. .Iadd. 1-(4'-Fluorophenyl )-3-(4-(2-(pyrrolidin-2-thion-1-yl)-ethyl)-1-piperaziny)-5-trifluor methyl-1H-indole .Iaddend. (Lu 23-018).

The pyrrolidonyl indole derivative (Lu 22-133) (2.8 g) prepared in Example 4 and p-methoxyphenylthionophosphine sulfide dimer (2.0 g) (Lawesson reagent) were heated in HMPA (25 ml) at 110° C. for 1 hour. The reaction mixture was poured into H₂ O (500 ml) and K₂ CO₃ (10 g) added. The product was extracted with ether containing 10% of ethyl acetate (2×200 ml). The combined organic phases were dried (MgSO₄), the solvents evaporated and the resulting crystalline product was recrystallized from ethanol yielding 2.1 g (73%) of the title compound. M.p. 199°-201° C.

EXAMPLE 11

.[.3-(4-(1-Acetyloxyethyl)-1-piperazino-1-(4'-fluorophenyl)-5-trifluoromethyl-1H-indole..]. .Iadd.

3-(4-(2-(1-Acetyloxy)ethyl)-1-piperazinyl)-1-(4'-fluorophenyl)-5-trifluoromethyl-1H-indole. .Iaddend.(Lu 23-161).

.[.1-(4'Fluorophenyl-3-(4-(2-hydroxyethyl)-1-piperazinol)-5-trifluoromethyl-1H-indole.]. .Iadd.

1-(4'-Fluorophenyl)-3-(4-(2-hydroxyethyl)-1-piperazinyl)-5-trifluoromethyl-1H-indole .Iaddend.(Lu 21-152) (5 g) was heated to reflux in acetone (50 ml). Acetylchloride (2 ml) was added slowly. Refluxing was continued for 1.5 h. The solvent was evaporated and the remaining oil was extracted with CH₂ Cl₂ (2×200 ml) from NH₄ OH at .[.Ph.]. .Iadd.pH 10. The combined organic phases were dried (MgSO₄) and the solvent evaporated. The title compound precipitated from ether. Yield: 3.7 g (72%). M.p. 129°-131° C.

In a corresponding manner the following esterified indole derivatives were prepared:

3-(4-(1-decanoyloxyethyl)-1-piperazino)-1-(4'-fluorophenyl)-5-trifluoromethyl-1H-indole. (Lu 23-162). M.p. 71°-73° C.

1-(4'-Fluorophenyl)-3-(4-(1-oleyloxyethyl)-1-piperazino)-5-trifluoromethyl-1H-indole, dihydrochloride. (Lu 23-163). M.p. 158°-162° C.

The compounds of Formula I were tested according to reliable and well recognized pharmacological tests as follows:

1. Methylphenidate antagonism

The inhibiting effect of test substances on the methylphenidate-induced gnawing in mice is determined as described by Pedersen and Christensen (1972).

The test substance is given i.p. in different doses, while methylphenidate is given s.c. in the dose 60 mg/kg, 1/2, 2 or 24 hours after injection of test substance. Per dose of the test substance is used 3×2 mice σ, 18-25 g). The results are given in fractions: 0/3, 1/3, 2/3 and 3/3, where 0,1,2 and 3 are the number of pairs, which .[.has.]. .Iadd.have .Iaddend. not been gnawing on receipt of the test substance.

Ref:

Pedersen, V. and Christensen, A.V.; Acta pharmacol. et toxicol. 31, 488-496, 1972.

2. Catalepsy

Evaluation of catalepsy is made according to Arnt (1983). The rat is placed on a vertical wire mesh (mesh diameter 12 mm) and considered as cataleptic if it remains immobile for more than 15 seconds. The number of cataleptic rats in each dose group is determined every hour, 1-6 hours and 24 hours following peroral administration of test compound. The maximal numbers of cataleptic rats in each of at least 3 dose groups, each consisting of at least 4 rats, is recorded. These numbers are used for calculation of .[.ED₅₀ values.]. .Iadd.ED₅₀ values by log-probit analysis.

Ref.:

Arnt, J.: European J. Pharmacol. 90, 47-55, 1983.

3. Quipazine inhibition

Quipazine and a number of other compounds, which increase .[.5-HT₂ receptor.]. .Iadd.5-HT₂ receptor .Iaddend.activity in the CNS, induce a characteristic rapid shake (twitch) of the head. This response is inhibited by 5-HT₂ receptor antagonists (Vetulani et al. 1980, Arnt et al. 1984).

The test compound or saline is injected subcutaneously 2 hours before subcutaneous injection of quipazine hemimaleate (15 μmol/kg). At least 3 dose groups, each consisting of at least 4 rats, are used. The rats are individually placed in observation cages (12×25 cm) and the number of head twitches are counted 30-40 min after quipazine administration. Inhibition of head twitches is expressed in per cent of the number of head twitches in the control group. .[.ED 50.]. .Iadd.ED₅₀ .Iaddend.values are calculated by log-probit analysis.

Ref.:

Vetulani, J., B.B. Beduarczyk, K. Reichenberg and A. Rokost: Neuropharmacology 19, 155-158, .[.1983.]..

Arnt, J., J. Hyttel and J.-J. Larsen: Acta pharmacol. et toxicol. 55, 363-372, 1984.

4. ³ H-spiroperidol bindings

The affinity of compounds to dopamine (DA) D-2 receptors and serotomin₂ (5-HT₂) receptors was determined by in vitro receptor binding technique. Binding of ³ H-spiroperidol to DA D-2receptors in rat striatal membranes and to 5HT₂ receptors in rat cortical membranes was determined as described in detail by Arnt et al. (1984).

Ref.:

Arnt, J.,J. Hyttel and J.-J. Larsen: Acta pharmacol. et toxicol. 55, 363-372 1984.

                                  TABLE 1                                 
__________________________________________________________________________
Pharmacology of Indoles                                                   
         MePh  Catalep.      Qvipaz. .sup.3 H-Spiroperidol bindings       
         Antg. ED50(po)      inh.    DA-2  5-HT.sub.2                     
Compound ED50(ip)                                                         
               (μmol/kg)  ED50(sc)                                     
                                     receptors                            
No.      (μmol/kg)                                                     
               1-6 h   24 h  (μmol/kg)                                 
                                     IC.sub.50 /10.sup.-9                 
__________________________________________________________________________
                                     M                                    
Lu 20-089                                                                 
         0.18  0.43    6.5   0.12    0.34  1.8                            
Lu 21-018                                                                 
         0.58  2.00    >6.9  0.15    0.74  3.0                            
Lu 21-037                                                                 
         2.10                                                             
Lu 21-046                                                                 
         48.1                0.23                                         
Lu 21-120                                                                 
         0.08  0.32    0.35  0.03    0.61  3.1                            
Lu 21-123                                                                 
         0.09  0.08    0.62  0.035   1.7   6.7                            
Lu 21-131                                                                 
         0.60  0.59    2.2                                                
Lu 21-152                                                                 
         0.11  0.17    0.28  0.023   2.8   7.4                            
Lu 21-153                                                                 
         2.0   7.1     16.0  0.37    3.7   6.7                            
Lu 22-117                                                                 
         0.06  0.09*   >0.37*                                             
                             0.052   1.2   0.66                           
Lu 22-133                                                                 
         0.82  0.66*   1.7*  0.15          1.9                            
Lu 22-134                                                                 
         1.7   2.7*    >2.7* 2.5     5.3                                  
Lu 22-135                                                                 
         0.10  0.078   >0.89*                                             
                             0.009   1.1   1.9                            
Lu 23-001                                                                 
         0.22  1.2     2.6   0.047   6.6   18                             
Lu 23-011                                                                 
         0.12* 0.55    >1.8  0.041         0.38                           
Lu 23-015                                                                 
         8.8   12.0    >15   0.062   12.0  3.9                            
Lu 23-018                                                                 
         53.0  1.2     2.9                                                
Lu 23-024                                                                 
         0.65  6.8*    >10*                5.3                            
Lu 23-075                                                                 
         19*                 0.18                                         
Lu 23-083                                                                 
         1.3*  9.4     >14   0.15    1.8                                  
Lu 23-086                                                                 
         >98*                0.036   42    2.9                            
Lu 23-133                                                                 
         18*   11.0    >11           5.9                                  
Lu 23-134                                                                 
         9.0*  1.1     >8.8          2.8   15                             
Lu 23-142                                                                 
         2.6*                              6.7                            
Lu 23-143                                                                 
         72.0* >18*    >18*  [4.5] >4.5                                   
Lu 23-146                                                                 
         0.73* 1.0*                                                       
Lu 23-147                                                                 
         >99*                                                             
Lu 23-148                                                                 
         >91*                                                             
Lu 23-149                                                                 
         0.45*                                                            
Lu 23-150                                                                 
         0.07* 0.21                  4.7   10                             
Lu 23-155                                                                 
         3.8*                                                             
Lu 23-156                                                                 
         0.07* <0.19*  1.1*  0.03    19    15                             
Lu 23-157                                                                 
         0.37* 0.49*   2.6*  0.12                                         
Lu 23-158                                                                 
         2.9*                0.11                                         
Lu 23-159                                                                 
         47*                                                              
Lu 23-160                                                                 
         3.4*  5.2*    [5.2*]        11    34                             
Lu 23-161                                                                 
         0.05* 0.09*   0.18*                                              
Lu 23-162                                                                 
         1.7*                                                             
Lu 23-163                                                                 
         1.1*                                                             
Lu 23-167                                                                 
         2.7*  2.7*    >11.0*                                             
Lu 23-171                                                                 
         0.11*                                                            
Lu 23-172                                                                 
         >70*                >0.55   31                                   
Lu 23-173                                                                 
         0.77* 1.8*          >7.1    42    60                             
Lu 23-174                                                                 
         >72*                0.49    20    6.6                            
Lu 23-175                                                                 
         0.32* 0.68*                 11    6.7                            
Lu 24-001                                                                 
         2.6*                0.19          8.8                            
Lu 24-002                                                                 
         0.45*               >0.45                                        
Lu 24-003                                                                 
         0.09*                       6.0   14                             
Lu 24-004                                                                 
         1.1*                                                             
Lu 24-012                                                                 
         >20*                                                             
Lu 24-013                                                                 
         >20*                                                             
Lu 24-014                                                                 
         >22*                                                             
Lu 24-015                                                                 
         3.8*                                                             
Lu 24-016                                                                 
         >30*                                                             
Lu 24-022                                                                 
Lu 24-024                                                                 
Clorpromazine                                                             
         23    70            0.38    24    30                             
Cis(Z)Flupentizol                                                         
         0.14  2.4     19    0.042   3.2   13                             
Haloperidol                                                               
         0.11  1.0           0.99    8.2   58                             
Tefludazine                                                               
         0.06  0.61    0.9   0.06    19    8.6                            
__________________________________________________________________________
 *ED50 from sc administration                                             
  The compound Lu 23011 is                                                
 5chloro-1-(4-fluorophenyl)-3-(4-methyl-1-piperazinyl)indole. (See Column 
 9).   LD.sub.50 i.v. in mice was determined for Lu 21-152 and Lu 22-135 t
 be 147 μmol/kg and 276 μmol/kg respectively which indicates a
 comparatively low acute toxicity as compared with known neuroleptics such
 as chlorpromazine, cis(Z)-flupentixol and tefludazin having values between
 120-180 μmol/kg.

The compounds of Formula I and the non-toxic acid addition salts thereof may be administered to animals such as dogs, cats, horses, sheeps or the like, including human beings, both orally and parenterally, and may be used for example in the form of tables, capsules, powders, syrups or in the form of the usual sterile solutions for injection. .[.-Results upon administration to human beings have been very gratifying..].

Most conveniently the compounds of Formula I are administered orally in unit dosage form such as tablets or capsules, each dosage unit containing the free amine or a non-toxic acid addition salt of one of the said compounds in an amount of from about 0.10 to about 100 mg, most preferably, however, from about 5 to 50 mg, calculated as the free amine, the total daily dosage usually ranging from about 1.0 to about 500 mg. The exact individual dosages as well as daily dosages in a particular case will, of course, be determined according to established medical principles under the direction of a physician.

When preparing tablets, the active ingredient is for the most part mixed with ordinary tablet adjuvants such as corn starch, potato starch, talcum, magnesium stearate, gelatine, lactose, gums, or the like.

When the compound of Formula I is an ester, preferably a decanoic acid ester, palmitic acid ester or a behenic acid ester, the composition may advantageously be an oily solution for injection, and such solutions often have a very prolonged effect when compared with the corresponding unesterified compound.

Typical examples of formulas for composition containing .[.1-(4'fluorophenyl)-3-(4-(2-hydroxyethyl-1-piperazinyl)-5-trifluoromethylindole.]. .Badd.1-(4'-fluorophenyl)-3-(4-(2-hydroxyethyl)-188-piperazinyl)-5-trifluoromethylindole .Baddend.(called Lu 21-132 for short) as the active ingredient, are as follows:

______________________________________                                    
(1) Tablets containing 5 milligrams of Lu 21-152                          
calculated as the free base:                                              
Lu 21-152              5      mg                                          
Lactose                18     mg                                          
Potato starch          27     mg                                          
Saccharose             58     mg                                          
Sorbitol               3      mg                                          
Talcum                 5      mg                                          
[Gelatine] Gelatin     2      mg                                          
Povidone               1      mg                                          
Magnesium stearate     0.5    mg                                          
(2) Tablets containing 50 milligrams of Lu 21-152                         
calculated as the free base:                                              
Lu 21-152              50     mg                                          
Lactose                16     mg                                          
Potato starch          45     mg                                          
Saccharose             106    mg                                          
Sorbitl                6      mg                                          
Talcum                 9      mg                                          
[Gelatine] Gelatin     2      mg                                          
Povidone               3      mg                                          
Magnesium stearate     0.6    mg                                          
(3) Syrup containing per milliliter:                                      
Lu 21-152              10     mg                                          
Sorbitol               500    mg                                          
Tragacanth             7      mg                                          
Glycerol               50     mg                                          
Methyl-paraben         1      mg                                          
Proyl-paraben          0.1    mg                                          
Ethanol                0.005  ml                                          
Water                  ad 1   ml                                          
(4) Solution for injection containing per milliliter:                     
Lu 21-152              50     mg                                          
Acetic acid            17.9   mg                                          
Sterile water          ad 1   ml                                          
(5) Solution for injection containing per milliliter:                     
Lu 21-152              10     mg                                          
Sorbitol               42.9   mg                                          
Acetic acid            0.63   mg                                          
Sodium hydroxide       22     mg                                          
Sterile water          ad 1   ml                                          
______________________________________

Any other pharmaceutical tableting adjuvants may be used provided that they are compatible with the active ingredient, and additional compositions and dosage forms may be similar to those presently used for neuroleptics, such as .[.chlorpenthixol.]. .Iadd.clopenthixol, .Iaddend.flupentixol or fluphenazine.

Also combinations of the compounds of Formula I as well as their non-toxic acid salts with other active ingredients, especially other neuroleptics, thymoleptics, tranquilizers, .[.analgetics.]. .Iadd.analgesics .Iaddend.or the like, fall within the scope of the present invention.

As previously stated, when isolating the compounds of Formula I in the form of an acid addition salt the acid is preferably selected so as to contain an anion which is non-toxic and pharmacologically acceptable, at least in usual therapeutic doses. Representative salts which are included in this preferred group are the hydrochlorides, hydrobromides, sulphates, acetates, phosphates, nitrates, methanesulphonates, ethane-sulphonates, lactates, citrates, tartrates or bitartrates, pamoates and maleates of the amines of Formula I. Other acids are likewise suitable and may be employed if desired. For example: .[.fumaric.]. .Iadd.fumaric, .Iaddend.benzoic, ascorbic, succinic, salicylic, bismethylenesalicylic, propionic, malic, malonic, mandelic, cannamic, citraconic, stearic, palmitic, itaconic, glycolic, benzenesulphonic, and sulphamic acids may also be employed as acid addition saltforming acids.

When is it desired to isolate a compound of the invention in the form of the free base, this may be done according to conventional procedure as by dissolving the isolated or unisolated salt in water, treating with a suitable alkaline material, extracting the liberated free base with a suitable organic solvent drying the extract and evaporating to dryness or fractionally distilling to effect isolation of the free basic amine.

The invention also comprises a method for the alleviation, palliation, mitigation or inhibition of the manifestations of certain physiological-psychological abnormalities of animals, including psychoses, by administering to a living animal body, including human beings, an adequate quantity of a compound of Formula I or a non-toxic acid addition salt thereof. An adequate quantity would be from about 0.001 mg to about 10 mg per kg of body weight in each unit dosage, and from about 0.003 milligrams to about 7 milligrams/kg of body weight per day.

It is to be understood that the invention is not limited to the exact details of operation or exact compound or compositions shown and described, as obvious modifications and equivalents will be apparent to one skilled in the art. and equivalents will be apparent to one skilled in the art.

Claims

I claim:

1. A compound selected from the group consisting of (a) an indole derivative of the following formula: ##STR16## wherein R is selected from .Iadd.(a) .Iaddend.phenyl, optionally substituted with .[.one substituent selected from.]. halogen .[.and trifluoromethyl.]. and .Iadd.(b) .Iaddend.a hetero aromatic group selected from 2-thienyl, 3-thienyl, .[.2-furoyl, 3-furoyl, 2-thiazol, 2-oxazol, 2-imidazole, 2-pyridyl, 3-pyridy.]. .Iadd.2-oxazolyl, 2-imidazolyl, 2-pyridyl .Iaddend.and 4-pyridyl;

R¹ is selected from hydrogen, halogen, lower alkyl, lower alkoxy, hydroxy, cyano, nitro, lower alkylthio, trifluoromethyl, lower alkylsulfonyl, amino, lower alkylamino and lower di-alkylamino;

"A" is selected from nitrogen and carbon, and the dotted line indicates--when A is carbon--an optional bond;

R² is selected from hydrogen, .[.cycloakyl.]. .Iadd.cycloalkyl .Iaddend.of .[.C₃ -C₄ .]. .Iadd.C₃ -C₆ .Iaddend..].inclusive.]. .Iadd.inclusive, .Iaddend.lower alkyl and lower alkenyl, optionally substituted with one or two hydroxy groups, any hydroxy group present being optionally esterified with an aliphatic carboxylic acid having from two to twenty-four carbon atoms inclusive, and the group ##STR17## wherein "n" is an integer of 2-6; X is selected from oxygen and sulfur, .[.C=X.]. .Iadd.>C=X .Iaddend.may constitute the group .[.CH.]. .Iadd.--CH .Iaddend.= when Y is selected from ═N-- and ═CH--;

Y is selected from oxygen, sulfur, CH₂ and N-R³, where R³ is selected from .[.hydrogen and.]. .Iadd.hydrogen, .Iaddend.lower alkyl, lower alkenyl and a cycloalkylmethyl group, said "cycloalkyl" having from three to six carbon atoms inclusive;

Z is selected from --(CH₂)_m --, "m" being selected from 2 and 3, .[.and --CH═CH and.]. .Iadd.--CH═CH, .Iaddend.1,2-phenylene optionally substituted with a group selected from halogen and trifluoromethyl, and --CO (or S) CH₂ --;

U is selected from nitrogen and carbon, provided that when R¹ is .Iadd.hydrogen, .Iaddend.chloro, .Iadd.lower alkyl, methoxy or hydroxy, .Iaddend.A is nitrogen and R² is selected from .[.methyl.]. .Iadd.lower alkyl .Iaddend.and .[.cyclohexyl,.]. .Iadd.cycloalkyl of C₃ -C₆, .Iaddend.R may not be phenyl; .[.and.]. .Iadd.or .Iaddend.

(b) a pharmaceutically acceptable acid addition salt thereof.

2. An indole derivative of claim 1, wherein R¹ is selected from chlorine, fluorine, trifluoromethyl, methyl, nitro and amino in the 5-position, R is phenyl substituted with fluorine in the 4'- or 2'-position, .[.R² is.]. .Iadd.R² is .Iaddend.selected from methyl, 2-hydroxyethyl and 3-hydroxypropyl, and A is as defined in claim 1.

3. .Iadd.An indole derivative of claim .Iaddend..[.Claim.]. 1 .Iadd.wherein the .Iaddend.compound .Iadd.is .Iaddend.selected from .[.1-(4'-Fluorophenyl)-3-(4-(2-hydroxyethyl)-piperazino)-5-trifluoromethyl-1H-indole,.]. .Iadd.1-(4'-Fluorophenyl)-3-(4-(2-hydroxyethyl)-1-piperazinyl-5-trifluoromethyl-1H-indole,

1-(4'-Fluorophenyl)-5-nitro-3-(1-methyl-1,2,3,6-tetrahydropyridin-4-yl)-1H-indole,

5-Chloro-1-(4'-fluorophenyl)-3-(1-methyl-1,2,3,6-tetrahydropyridin-4-yl)-1H-indole,

1-(4'-Fluorophenyl)-3-(1-(2-hydroxyethyl)-1,2,3,6-tetrahydropyridin-4-yl)-5-nitro-1H-indole,

1(4'-Fluorophenyl)-3-(1-(2-hydroxyethyl)-1,2,3,6-tetrahydropyridin-4-yl)-5-trifluoromethyl-1H-indole,

5-Fluoro-1-(4'-fluorophenyl)-3-(1-(3-hydroxypropyl)-1,2,3,6-tetrahydropyridin-4-yl)-1H-indole, .[.and.]. .Iadd.or .Iaddend.pharmaceutically acceptable acid addition salts thereof.

4. A neuroleptic or thymoleptic pharmaceutical composition suitable for use in the treatment of disorders amenable to such medication in unit dosage form comprising, as an active ingredient, a compound as defined in claim 1 in an amount effective for such purpose, together with one or more pharmaceutical diluents or carriers.

5. A pharmaceutical composition in unit dosage form, according to claim 4, wherein the active ingredient is present in an amount from 0.10 to 100 milligrams per unit dosage.

6. A pharmaceutical composition in unit dosage form, according to claim 4 wherein the active ingredient is a compound of claim 3.

7. A method for the treatment of disorders amenable to .[.neuroleptic or.]. thymoleptic medication comprising administering a .[.neuroleptic or.]. thymoleptically-effective amount in unit dosage form of a compound of claim 1, as an active ingredient, optionally together with one or more pharmaceutical diluents or carriers, to a warmblooded animal including a human being.

8. A method according to claim 7, wherein the active ingredient is present in an amount from 0.1 to about 100 mg per unit dosage.

9. A method according to claim 8, wherein the active ingredient is 1-(4'-fluorophenyl)-3-(4(2-hydroxyethyl)-1-piperazinyl)-5-trifluoromethyl-indole, or a pharmaceutically acceptable salt thereof.