WO1996034865A1

WO1996034865A1 - Novel heterocyclic chemistry

Info

Publication number: WO1996034865A1
Application number: PCT/DK1996/000198
Authority: WO
Inventors: Jane Marie Lundbeck; Birgitte SØKILDE; Per Olaf SØRENSEN
Original assignee: Novo Nordisk A/S
Priority date: 1995-05-05
Filing date: 1996-05-01
Publication date: 1996-11-07
Also published as: AU5644296A; EP0823909A1; EP0823909B1; US5834482A; ATE223915T1; ES2182975T3; PT823909E; DE69623610D1; JPH11505217A; DE69623610T2; DK0823909T3

Abstract

A compound of formula (I). The present invention relates to therapeutically active β-carboline derivatives, a method of preparing the same and to pharmaceutical compositions comprising the compounds. The novel compounds are useful in treating a central nervous system ailment related to the inhibition of GABA uptake via the GAT-4 subtype carrier.

Description

Novel Heterocyclic Chemistry

Field of the invention

The present invention relates to novel substituted β-carboline derivatives, to methods for their preparation, to pharmaceutical compositions containing them and to their use in the clinical treatment of abnormal functioning of the γ-aminobutyric acid neurotransmission system.

Background of the invention

γ -Aminobutyric acid (GABA) is the major inhibitory neuro transmitter in the central nervous system (CNS) (for review see Enna, 1983, Biochem. Pharmacol., 30, 907-15; Enna and Mohler, 1987, Raven Press, New York, 265-79; Lloyd and Morselli, 1987, Medical Biology, 65, (2-3), 159-65; Krogsgaard-Larsen, 1988, Medical Res. Reviews, 8, 1, 27-56; Schwartz, 1988, Biochem. Pharmacol. 27, 3369-76). GABA has been estimated to be present in 60-70 % of all synapses within the CNS (Fahn, 1976, Raven Press, New York, 169-83). A reduction in GABA neurotransmission has been implicated in the etiology of a variety of neurological disorders including epilepsy (Krogsgaard- Larsen et al., 1988, Medical Res. Reviews, 8, 1, 27-56; Lόscher, 1985, Epilepsy and GABA Receptor Agonists: Basic and Therapeutic Research. L.E.R.S. Monograph. Vol. 3, G. Bartholoni, L. Bossi, K.G. Lloyd, P.L. Morselli (Eds.), Raven Press, New York, 109-18); Enna, 1981, Biochem. Pharmacol., 30, 907-14 and Neuropharmacology of Central Nervous System GABA and Behavioral Disorders, G. Palmer (Ed.). Academic Press, New York 1981, 507-25; Rebak et al. , 1979, Science, 205, 211-13; Ross and Craig, 1981, J.Neurochem. 36, 1006).

The GABA uptake system has traditionally been classified as either neuronal or glial GABA uptake carriers, on the basis of pharmacological selectivity for specific GABA uptake inhibitors (for review see: Krogsgaard-Larsen, 1988, Medical Res. Reviews, 8, 1, 27-56; Schousboe et al. , 1991, GABA Mechanisms in Epilepsy, G. Tunnicliff, B.U. Raess (Eds.) Wiley-Liss, New York, 165-87). Several investigators (Gaustella et al., 1990, Science, 249, 1303-1306; Clark et al., 1992, Neuron 9, 337-348; Borden et al., 1992, J.Biol. Chem. 267, 21098-21104; Liu et al. , 1993, J.Biol.Chem. 268, 2106-2112) have recently cloned, and sequenced, four

5 subtypes of the rat and mouse GABA uptake carrier, whose pharmacology cannot be totally explained by the traditional neuronal and glial GABA uptake carriers. Gaustella et al., (1990, Science, 249, 1303-1306) and Nelson et al. (1990, FEBS Lett. 269, 181-184) reported on the cloning of GAT-1, which appears to be a neuronal GABA uptake carrier due to its high sensitivity to nipecotic acid (Gaustella et al. , 1990, Science, 249, 1303-

10 1306), and lipophilic nipecotic acid based compounds and distribution within the central nervous system (CNS) (Radian et al., 1990, J.Neurosci. 10, 1319-1330; Mabjeesh et al. , 1992, J.Biol.Chem. 267, 2563-68). GAT-1 is not present outside the CNS (Nelson et al., 1990, FEBS Lett. 269, 181-184; Liu e al., 1992, FEBS. Lett. 305, 110-114). GAT-2 was initially cloned by Lopez-Corruera (1992, J.Biol.Chem. 267, 17491-17493) and is

15 present in the CNS, kidney and liver, and has a pharmacology resembling the glial GABA uptake carrier characterized in primary cell culture. GAT-3 which was initially cloned by Liu et al., (1993, J.Biol.Chem. 267, 2106-2112), appears to be under develop¬ mental control, as GAT-3 mRNA is highly expressed in neonatal brain, but weakly expressed in adult brain. GAT-3 is also present in kidney and liver. GAT-4 (Liu et al.,

20 1993, J.Biol.Chem. 268, 2106-2112; also termed GAT-B by Clark et al., (1992, Neuron 9, 337-348) and GAT-3 by Borden et al., (1992, J.Biol.Chem. 267, 21098-21104)), cDNA hybridized only in the CNS, and the mRNA for GAT-4 is highly enriched in the brain stem, but not present in the cerebellum or cerebral cortex. While GAT-4 has been shown to transport β-alanine, it appears to have neuronal localization (Clarke et al. ,

25 1992, Neuron 9, 337-348).

The distribution of GAT-1, closely resembles the previously reported distribution of ³H- Tiagabine receptor autoradiography (Suzdak et al., 1994, Brain Research, 647(2), 231- 41), as would be expected due to the high affinity of lipophilic nipecotic acid based 30 GABA uptake inhibitors for the GAT-1 transporter (Clarke et al., 1992, Neuron 9, 337- 348). While in situ hybridization has revealed the presence of GAT-4 mRNA in the CNS, there has been no direct demonstration of a discretely localized neuronal GABA uptake carrier, which is not sensitive to lipophilic nipecotic acid based GABA uptake inhibitors.

The inhibition of GABA uptake results in enhanced availability of this inhibitory neurotransmitter in the synaptic cleft and thus to increased GABA'ergic activity. Increased GABA'ergic activity can be useful in the treatment, for example of anxiety, pain and epilepsy, as well as muscular and movement disorders (see, for example, P. Krogsgaard-Larsen et al., Progress in Medicinal Chemistry, 1985, 22, 68-112).

A well-known and potent inhibitor of GABA uptake from the synaptic cleft into presynaptic nerve terminals and glial cells is, for example, 3-piperidinecarboxylic acid (nipecotic acid). However, being a relatively polar compound and therefore unable to cross the blood-brain barrier, 3-piperidinecarboxylic acid itself has found no practical utility as a drug.

In US Patent No. 4,383,999 and No. 4,514,414 and in EP 236342 as well as in EP 231996 some derivatives of N-(4,4-disubstituted-3-butenyl)azaheterocyclic carboxylic acids are claimed as inhibitors of GABA uptake. In EP 342635 and EP 374801, N- substituted azaheterocyclic carboxylic acids in which an oxime ether group and vinyl ether group forms part of the N-substituent respectively are claimed as inhibitors of GABA uptake. Further, in WO 9107389 and WO 9220658, N-substituted azacyclic carboxylic acids are claimed as inhibitors of GABA uptake. EP 221572 claims that l-aryloxyalkylpyridine-3 -carboxylic acids are inhibitors of GABA uptake.

According to Yunger, L.M. et al., J.Pharm.Exp.Ther. 1984, 228, 109, N-(4,4-diphenyl- 3-buten-l-yl)nipecotic acid (designated SK&F 89976A), N-(4,4-diρhenyl-3-buten-l- yl)guvacine (designated SK&F 100330A), N-(4,4-diphenyl-3-buten-l-yl)-homo-β-proline (designated SK&F 100561) and N-(4-phenyl-4-(2-thienyl)-3-buten-l-yl)nipecotic acid (designated SK&F 100604 J) are orally active inhibitors of GABA uptake. These data are summarized in Krogsgaard-Larsen, P. et al., Epilepsy Res. 1987, 1, 77-93.

The above cited references all disclose compounds inhibiting the uptake of GABA via the GAT-1 subtype carrier. US Patent No. 4,539,407 discloses β-carboline-3-carboxylate ester derivatives having anticonvulsant activity.

The present invention is directed to identifying novel compounds with affmity for the neuronal subtype of the GABA uptake carrier whose pharmacology resembles that of GAT-4.

Description of the invention

The present invention relates to novel substituted β-carboline derivatives of formula I

wherein

R¹ and R² independently are hydrogen, halogen, hydroxy, nitro, -(CH₂)_n-(C=O)-(CH₂)_mCH₃, -NR⁹R¹⁰, -SONRⁿR¹², -COOR¹³, -CONR¹⁴R¹⁵, C,.₆-alkyl,

C^-alkoxy, trifluoromethyl or trifluoromethoxy wherein R⁹, R¹⁰, R", R¹², R¹³, R¹⁴ and

R¹⁵ independently are hydrogen, ._e-alkyl, C₂.₆-alkenyl or C₂.₆-alkynyl, and wherein n and m independently are 0, 1, 2, 3 or 4; and

R³ is C_ι.₅-alkylene optionally substituted with one or two C_1-6-alkyl or C₃.₇-cycloalkyl, C₂.₅-alkenylene or C₂.₅-alkynylene or R³ is -(CH₂)_m-A-(CH₂)_n-, -(CH₂)_m-C-(CH₂)_n- or -(CH₂)_m-CH-CH-(CH₂)_n-

wherein A is C₃.₇-cycloalkylene and B is C^-alkylene and C is .s-alkylene and m and n independently are 0, 1 or 2; and R⁴ is hydrogen or C_1-6-alkyl; and

R⁵ and R⁶ independently are hydrogen, halogen, hydroxy, nitro, -NR¹⁶R¹⁷, -COOR¹⁸, C,. ₆-alkyl, C,,.₆-alkoxy, trifluoromethyl or trifluoromethoxy wherein R¹⁶, R¹⁷ and R¹⁸ independently are hydrogen, C,.₆-alkyl, C₂._<*-alkenyl or C₂.₆-alkynyl; and

wherein X is -NH-, oxygen or sulphur; and

R⁷ is hydrogen, C,.₆-alkyl, C₂.₆-alkenyl, C₂.₆-alkynyl, phenyl, C₃.₇-cycloalkyl, -OR⁸ or -

SR⁸ wherein R⁸ is hydrogen or C_1-6-alkyl; or a pharmaceutically acceptable salt thereof.

The compounds of formula I may exist as geometric and optical isomers and all isomers and mixtures thereof are included herein. Isomers may be separated by means of standard methods such as chromatographic techniques or fractional crystallization of suitable salts.

The compounds according to the invention may optionally exist as pharmaceutically acceptable acid addition salts.

Examples of such salts include inorganic and organic acid addition salts such as hydrochloride, hydrobromide, sulphate, phosphate, acetate, phthalate, fumarate, maleate, citrate, lactate, tartrate, oxalate, or similar pharmaceutically acceptable inorganic or organic acid addition salts, and include the pharmaceutically acceptable salts listed in Journal of Pharmaceutical Science, 66, 2 (1977) which are hereby incorporated by refe- rence.

Alkyl, alkenyl and alkynyl are intended to mean straight or branched alkyl, alkenyl or alkynyl chains.

The compounds of formula I have a greater lipophilicity - and thus a greater availability to the brain - as well as a far higher affinity to the GABA uptake sites than the parent compounds without the β-carboline moiety.

It has been demonstrated that the novel compounds of formula I which inhibit the uptake of GABA from the synaptic cleft possess useful pharmacological properties in the central nervous system, in that they cause a selective enhancement of GABA'ergic activity.

Compounds of formula I may be used to treat for example, pain, anxiety, extrapyrimi- dinal dyskinesia, epilepsy and certain muscular and movement disorders. They are also useful as sedatives, hypnotics and antidepressants.

The invention also relates to a method of preparing the above mentioned compounds of formula I. These methods comprise:

Method A:

II III

A compound of formula II wherein R¹, R², R³ and Z are as defined above and X is a suitable leaving group such as halogen, p-toluene sulphonate or mesylate may be reacted with an azaheterocyclic compound of formula III wherein R⁴, R⁵ and R⁶ are as defined above. This alkylation reaction may be carried out in a suitable solvent such as acetone, dibutylether, 2-butanone, tetrahydrofuran, methylisobutyl ketone, methylisopropyl ketone, toluene, benzene or DMF in the presence of a base e.g. potassium carbonate, sodiumhydride or potassium tert.-butoxide at a temperature up to reflux for the solvent used for e.g. 1 to 200 h.

Method B:

IV A compound of formula IV wherein R¹, R² and Z are as defined above may be reacted with an azaheterocyclic compound of formula V wherein R³, R⁴, R⁵, R⁶ and X are as defined above. This alkylation may be carried out in a suitable solvent as defined above in the presence of a base as defined above and a catalyst e.g. an alkali metal iodide at a temperature up to reflux for the solvent used for e.g. 1 to 200 h.

Method C:

VI VII

An azaheterocyclic ketone of formula VI wherein R¹, R², R³, R⁴ and Z are defined as above may be reacted with a Grignard reagent of formula VII wherein R⁵ and R⁶ are as defined above and Y is chloro, bromo or iodo. This reaction may be carried out in a suitable solvent such as diethylether, THF, toluene or benzene at a suitable temperature up to reflux temperature for the solvent used for e.g. 1 to 5 h.

Compounds of formula II may readily be prepared according to the procedure described in EP 0 130 141 or EP 0 161 574.

Pharmacological Methods

³H-GABA uptake was measured by a modification of the method of Fjalland et al. , (1978). A crude membrane preparation was prepared from selected brain areas by homogenization in 20 ml of ice-cold 0.32 M sucrose with a hand driven teflon/glass Potter-El vehj em homogenizer. The homogenate was centrifuged at 4°C for 10 min. at 1.000 x g, and the pellet was discarded. The supernatant was recentrifuged at 4°C for 20 min. at 20.000 x g. The pellet was then homogenized in 50 volumes 0.32 M sucrose. To 300 μl uptake-buffer (200 nM NaCl, 15.3 mM KC1, 6.67 mM MgSO₄, 3.83 mM CaCl₂, 16.67 mM glucose, 66.67 mM Tris, pH 7.5 at 30°C) was added l-(2-(((diphenylme- thylene)amino)oxy)ethyl)-l,2,5,6-tetrahydro-3-pyridinecarboxylic acid (NNC 05-0711) (1 mM final concentration), 100 μl test substance and 50 μl tissue suspension. The samples were mixed and incubated at 30°C for 8 min. Then ³H-GABA (0.9 nM final concentration) and unlabelled GABA (25 nM final concentration) was added, and the incubation was continued for an additional 8 min. The reaction was terminated by rapid filtration through Whatman GF/F glass fiber filters under vacuum. The filters were then washed twice in 10 ml of ice-cold isotonic saline, and the tritium trapped on the filters was quantified by conventional scintillation spectroscopy. Non-GABA uptake carrier mediated uptake of ³H-GABA was determined in the presence of 500 μl nipecotic acid.

Values for non-GABA uptake carrier mediated uptake of ³H-GABA for some representative compounds are recorded in Table I.

Table I

Non-GABA uptake carrier mediated uptake of ³H-GABA.

Compound No. IC₅₀ (nM) in vitro

4 932

7 1089

10 1439

15 6375

20 5385

24 4692

26 1641

28 1241 For the above indications the dosage will vary depending on the compound of formula I employed, on the mode of administration and on the therapy desired. However, in general, satisfactory results are obtained with a dosage of from about 0.5 mg to about 5 1000 mg, preferably from about 1 mg to about 500 mg of compounds of formula I, conveniently given from 1 to 5 times daily, optionally in sustained release form. Usually, dosage forms suitable for oral administration comprise from about 0.5 mg to about 1000 mg, preferably from about 1 mg to about 500 mg of the compounds of formula I admixed with a pharmaceutical carrier or diluent. 0

The compounds of formula I may be administered in pharmaceutically acceptable acid addition salt form or where possible as a metal or a lower alkylammonium salt.

This invention also relates to pharmaceutical compositions comprising a compound of 5 formula I or a pharmaceutically acceptable salt thereof and, usually, such compositions also contains a pharmaceutical carrier or diluent. The compositions containing the compounds of this invention may be prepared by conventional techniques and appear in conventional forms, for example capsules, tablets, solutions or suspensions.

0 The pharmaceutical carrier employed may be a conventional solid or liquid carrier. Examples of solid carriers are lactose, terra alba, sucrose, talc, gelatin, agar, pectin, acacia, magnesium stearate and stearic acid. Examples of liquid carriers are syrup, peanut oil, olive oil and water.

5 Similarly, the carrier or diluent may include any time delay material known to the art, such as glyceryl monostearate or glyceryl distearate, alone or mixed with a wax.

If a solid carrier for oral administration is used, the preparation can be tabletted, placed in a hard gelatin capsule in powder or pellet form or it can be in the form of a troche or 0 lozenge. The amount of solid carrier will vary widely, but will usually be from about 25 mg to about 1 g. If a liquid carrier is used, the preparation may be in the form of a syrup, emulsion, soft gelatin capsule or sterile injectable liquid such as an aqueous or non-aqueous liquid suspension or solution.

Generally, the compounds of this invention are dispended in unit dosage form comprising 50-200 mg of active ingredient in or together with a pharmaceutically acceptable carrier per unit dosage.

The dosage of the compounds according to this invention is 1-500 mg/day, e.g. about 100 mg per dose, when administered to patients, e.g. humans, as a drug.

A typical tablet, which may be prepared by conventional tabletting techniques contains:

Core:

Active compound (as free compound 100 mg or salt thereof) Colloidal silicon dioxide (Aerosil.TM) 1.5 mg

Cellulose, microcryst. (Avicel,TM) 70 mg

Modified cellulose gum (Ac-Di-Sol,TM) 7.5 mg

Magnesium stearate

Coating:

HPMC approx. 9 mg

^*Mywacett,TM 9-40 T approx. 0.9 mg

"Acylated monoglyceride used as plasticizer for film coating.

The route of administration may be any route, which effectively transports the active compound to the appropriate or desired site of action, such as oral or parenteral e.g. rectal, transdermal, subcutaneous, intravenous, intraurethral, intramuscular, topical, intranasal, ophthalmic solution or an ointment, the oral route being preferred. Examples

The process for preparing compounds of formula I is further illustrated in the following examples which however are not to be construed as limiting.

Hereinafter, DMF is N,N-dimethylformamide, TEA is triethylamine, TLC is thin layer chromatography and THF is tetrahydrofuran, CDC1₃ is deuterio chloroform and DMSO-d₆ is hexadeuterio dimethylsulfoxide. The structures of the compounds are confirmed by either elemental analysis or NMR, where peaks assigned to characteristic protons in the title compounds are presented where appropriate. NMR shifts (δ) are given in parts per million (ppm). M.p. is melting point and is given in °C. Column chromatography was carried out using the technique described by W.C. Still et al, J. Org. Chem. 1978, 43, 2923-2925 on Merck silica gel 60 (Art. 9385). Compounds used as starting materials are either known compounds or compounds which can readily be prepared by methods known per se.

EXAMPLE 1

(9H-β-Carbolin-3-yl)-imidazol-l-ylmethanone (Compound 1)

To a suspension of 9H-β-carboline-3-carbocylic acid (1.98 g, 9.3 mmol) in a mixture of anhydrous DMF (100 mL) and anhydrous THF (100 mL), l,l '-carbonyldiimidazole (1.60 g, 10 mmol) was slowly added. The reaction mixture was stirred under a nitrogen atmosphere for 7 days. The solvents were removed in vacuo. the solid residue washed with water, and dried in vacuo to give the title compound (1.12 g, 45%). White solid, M.p. > 280°C. EXAMPLE 2

3-(3-Ethyl-l,2,4-oxadiazol-5-yl)-9H-β-carboline (Compound 2)

To a solution of Compound 1 (1.05 g, 4 mmol) in a mixture of toluene (50 mL) and DMF (50 mL), N-hydroxypropanimidamide (0.53 g, 6 mmol) was added. The resulting mixture was heated at 140-150°C for 7 h, and stirring continued for 3 days at room tem- perature. The solvents were removed in vacuo. and the oily residue precipitated from water. The white solid (1.0 g) was dried and submitted to column chromatography on silica gel with CH₂Cl₂/methanol(9: 1) as eluent. This afforded the titie compound (0.6 g, 56%). M.p. 146-149°C.

EXAMPLE 3

9-(3-Chloro- 1 -propyl)-3-(3-ethyl- 1 ,2 ,4-oxadiazol-5-yl)-9H-β-carboline (Compound 3)

To a solution of Compound 2 (0.73 g, 2.8 mmol) in anhydrous DMF (100 mL), sodium hydride (60% in mineral oil, 0.13 g, 3.3 mmol) was carefully added. The resulting mixture was stined at room temperature for 30 min, until hydrogen evolution had ceased. The reaction mixture was slowly added to a solution of l-bromo-3-chloropropane (0.52 g, 3.3 mmol) in anhydrous DMF (150 mL). The resulting mixture was stirred at room temperature for 12h. The solvents were removed in vacuo to give a yellow solid (1.59 g). The residue was dissolved in acetone, filtered and the filtrate concentrated in vacuo. giving the title compound (1.07 g, 100%). 'H- and ¹³C-NMR revealed that the crude product was a mixture of the bromo and chloro isomers in the ratio 70:8. The crude product was used without further purification. EXAMPLE 4

l-(3-(3-(3-Ethyl-l,2,4-oxadiazol-5-yl)-9H-β-carbolin-9-yl)-l-propyl)-4-phenylpiperidin- 4-ol (Compound 4)

To a solution of Compound 3 (1.0 g, 3 mmol) in anhydrous DMF (50 mL), 4- phenylpiperidin-4-ol (0.63 g, 3.5 mmol) and TEA (1 mL) were added. The resulting mixture was heated at 85°C for 76 h under a nitrogen atmosphere. The solvent was removed in vacuo. and the solid residue was submitted to column chromatography on silica gel with CH₂Cl₂/methanol (9: 1) as eluent. The purified compound was precipitated as the hydrochloride, giving the title compound (0.6 g, 36%) as an yellow solid. M.p. 169-170°C.

EXAMPLE 5

3-(3-Cyclopropyl-l,2,4-oxadiazol-5-yl)-9H-β-carboline (Compound 5)

To a solution of sodium ethoxide, prepared from sodium metal (0.6 g, 26 mmol) and anhydrous ethanol (50 mL), cyclopropylmethanimidamide (1.67 g, 16 mmol) and 9H-β- carboline-3-carboxylic acid ethyl ester (2.0 g, 8.0 mmol) were added. Toluene (50 mL) was added and the resulting mixture was heated to 120-130°C. The ethanol and water formed during the reaction were removed by azeotropic distillation. The reaction was complete after 30 min. The solid was filtered from the reaction mixture, washed with water and dried. This afforded the title compound (1.15 g, 52%) as an yellow solid. M.p. 256-257°C. EXAMPLE 6

9-(3-Chloro- 1 -propyl)-3-(3-cyclopropyl- 1,2, 4-oxadiazol÷5-yl)-9H-β-carboline (Compound 6)

The compound was synthesized by mixing (Compound 5) (1.0 g, 3.6 mmol), NaH (0.22 g, 4.3 mmol) and l-bromo-3-chloropropane (0.68 g, 4.3 mmol)in DMF, in the same manner as illustrated in example 3, to give the tide compound (0.76 g, 63%) as a white solid. M.p. 165-169°C.

EXAMPLE 7

l-(3-(3-(3-Cyclopropyl-l,2,4-oxadiazol-5-yl)-9H-β-carbolin-9-yl)-l-propyl)-4- phenylpiperidin-4-ol hydrochloride (Compound 7)

The compound was synthesized by mixing (Compound 6) (0.76 g, 2.2 mmol), 4- phenylpiperidin-4-ol (0.48 g, 2.7 mmol), TEA (0.55 g, 5.4 mmol) in DMF, in the same manner as illusterated in example 3. The compound was isolated as the hydrochloride (0.15 g, 12%) as an yellow solid. M.p. 184-185°C.

EXAMPLE 8

3-(3-Phenyl-l,2,4-oxadiazol-5-yl)-9H-β-carboline (Compound 8)

The compound was synthesized by mixing 9H-β-carboline-3-carbocylic acid ethylester (2.0 g, 8.0 mmol), N-hydroxyphenylimidamide (1.30 g, 9.6 mmol), Na (0.91 g, 40 mmol) in ethanol (50 mL) and toluene (100 mL), in the same manner as illustrated in example 5 to give the title compound (0.66 g, 25%). M.p. 279-283°C. EXAMPLE 9

9-(3-Chloro-l-propyl)-3-(3-phenyl-l,2,4-oxadiazol-5-yl)-9H-β-carboline (Compound 9)

The compound was synthesized by mixing (Compound 8) (0.6 g, 1.9 mmol), 1-bromo- 3-chloropropane (0.45 g, 2.9 mmol), NaH (0.09 g, 2.3 mmol) in DMF, in the same manner as illustrated in example 3 to give the title compound (0.72 g, 97%). M.p. 192- 195°C (and 235.5-236°C).

EXAMPLE 10

l-(3-(3-(3-Phenyl-l,2,4-oxadiazol-5-yl)-9H-β-carbolin-9-yl)-l-propyl)-4-phenylpiperidin- 4-ol hydrochloride (Compound 10)

The compound was synthesized by mixing (Compound 9) (0.7 g, 1.8 mmol), 4- phenylpiperidin-4-ol (0.38 g, 2.2 mmol) and TEA (0.55 g, 5.4 mmol) in DMF, in the same manner as illustrated in example 4 to give the title compound (0.47 g, 43%). M.p. 184-185°C.

EXAMPLE 11

6-Dimethylsulfamoyl-9H-β-carbolin-3-carboxylic acid ethyl ester (Compound 11)

To chlorosulfonic acid (20 mL), sodium chloride (2.9 g, 49.6 mmol) was carefully added at room temperature. When the evolution of hydrochloride had ceased the resulting mixture was cooled on an ice-bath. 9H-β-Carbolin-3-carboxylic acid ethyl ester (6.0 g, 25 mmol) was slowly added, and the mixture stirred at room temperature for 2 days. The reaction mixture was poured into iced water (100 g). The precipitate was collected and washed with water. This compound was added under stirring to icecold dimethylamine 17 (60% in toluene, 100 mL). The mixture was stirred at 0°C for an additional 30 min, and at room temperature for 1.5 h. Acetic acid (70 mL) was carefully added (exothermic!). To the resulting mixture was added water (100 mL) and the precipitate filtered, washed with water and dried. This afforded the titie compound (3.0 g, 34%). M.p. 310-311°C.

EXAMPLE 12

6-Dimethylsulfamoyl-3-(3-ethyl-l,2,4-oxadiazol-5-yl) 9H-β-carboline (Compound 12)

The ester, Compound 11 ( 10 g, 28.8 mmol) was heated at 100°C, in a mixture of ethanol (200 mL) and KOH (5.5 g, 98.2 mmol), suspended in water (15 mL) for 4 h. Acetic acid was added. The precipitate was washed with water and dried. This afforded the acid (6.8 g, 21.3 mmol). The free acid (2.5 g, 7.8 mmol) was treated as described in example 1 and example 2 to give the title compound (1.3 g, 44%) as a white solid. M.p. 266-268°C.

EXAMPLE 13

9-(3-Chloro-l-propyl)-6-dimethylsulfamoyl-3-(3-ethyl-l,2,4-oxadiazol-5-yl)-9H-β- carboline (Compound 13)

The compound was synthesized by mixing (Compound 12) (3.0 g, 8.8 mM), NaH (0.46 g, 11.0 mmol) and l-bromo-3-chloropropane ( 1.5 g, 9.7 mmol) in DMF, in the same manner as illustrated in example 3 to give the title compound (0.25 g, 7%). M.p. 223- 224°C. EXAMPLE 14

l-(3-(3-(3-Ethyl-l,2,4-oxadiazol-5-yl)-6-dimethylsulfamoyl-9H-β-carbolin-9-yl)-l- propyl)-4-phenylpiperidin-4-ol hydrochloride (Compound 14)

The compound was synthesized by mixing (Compound 13) (0.25 g, 0.64 mmol), 4- phenylpiperidin-4-ol (0.136 g, 0.77 mmol) and TEA (0.19 g, 1.9 mmol) in DMF, in the same manner as illustrated in example 4 to give the title compound (0.09 g, 21 %). M.p. 186-189°C.

EXAMPLE 15

6-Nitro-9H-β-carboline-3-carboxylic acid ethyl ester (Compound 15)

9H-β-carboline-3-carboxylic acid ethyl ester (20 g, 833 mmol) was slowly added to concentrated nitric acid (400 mL). The reaction mixture was stirred at 70-75°C for 2 h. After cooling to room temperature the resulting mixture was poured onto ice (1 kg). The precipitated compound was collected, and recrystallized from pyridine (650 mL). This afforded the title compound C14.9 g, 63%). M.p. 339-341°C.

EXAMPLE 16

6-Amino-9H-β-carboline-3-carboxylic acid ethyl ester (Compound 16)

A suspension of Pd (10% on carbon, 1.0 g), and Compound 15 (8.0 g, 28 mmol) in anhydrous ethanol (300 mL) was hydrogenated (2280 mL) at 1 atm. The reaction mixture was filtered through a filter aid. The filtrate was concentrated in vacuo to give the title compound (5.62 g, 79%). M.p. 226-228°C. EXAMPLE 17

6-Dipropenylamino-9H-β-carboline-3-carboxylic acid ethyl ester (Compound 17)

To a solution of Compound 16 (15.8 g, 62 mmol) in anhydrous ethanol (300 mL), allylbromide (8.4 g, 69.4 mmol) and TEA (20 mL) were added. The reaction mixture was stirred under a nitrogen atmosphere at 80°C for 2 h. Additionally allylbromide (8.4 g, 69.4 mmol) and TEA (12 mL) were added, and stirring continued at 80°C for 48h. The reaction mixture was concentrated in vacuo. and the residual oil was poured into water (300 mL). The solid was filtered and dried, to give the title compound (16.5 g, 80%). M.p. 235-238°C.

EXAMPLE 18

6-Dipropenylamino-3-(3-ethyl- 1 ,2 ,4-oxadiazol-5-yl)-9H-β-carboline (Compound 18)

The compound was synthesized by mixing Na (2.6 g, 114 mmol) dissolved in ethanol (200 mL), (Compound 17) (13.2 g, 38 mmol), N-hydroxypropylimidamide (5.1 g, 57 mmol) in toluene, in the same manner as illustrated in example 5 to give the title compound (4.4 g, 32%). M.p. 151-156°C.

EXAMPLE 19

9-(3-Chloro-l-propyl)-6-dipropenylamino-3-(3-ethyl-l,2,4-oxadiazol-5-yl)-9H-β- carboline (Compound 19)

The compound was synthesized by mixing (Compound 18) (1 g, 2.8 mmol), NaH (50 % in oil) (0.075 g, 3.1 mmol) and l-bromo-3-chloropropane (0.44 g, 3.1 mmol) in DMF in the same manner as illustrated in example 3 to give the title compound (0.35 g, 28%). The 1H-NMR in (CDC1₃): 1.45 (t,3H), 2.35 (t,2H), 2,9 (q,2H), 3.5 and 3.35 (t,t,additio- nal 2H), 4.0 (d,4H), 4.5 (t,2H), 5.25 (2d,4H), 5.95 (m,2H), 7.15 (d,lH), 7.4 (s and d,2H), 8.7 (s, lH), 9.0 (s,lH).

EXAMPLE 20

l-(3-(3-(3-Ethyl-l,2,4-oxadiazol-5-yl)-6-dipropenylamino-9H-β-carbolin-9-yl)-l-propyl)- 4-phenylpiperidin-4-ol hydrochloride (Compound 20)

The compound was synthesized by mixing (Compound 19) (0.35 g, 0.8 mmol), 4- phenylpiperidin-4-ol (0.14 g, 0.8 mmol) and TEA (0.32 g, 3.2 mmol) in the same manner as illustrated in example 4 to give the title compound (0.33 g, 60%). M.p. 133- 139°C (dec).

EXAMPLE 21

6-Dimethylamino-β-carboline-3-carboxylic acid ethyl ester (Compound 21)

To a solution of compound 16 (1.00 g, 0.0039 mol) in CH₃CN (30 mL) were added 35% formaldehyde (aq) (3.4 mL, 0.0392 mol) and acetic acid (0.4 mL). The mixture was stirred at room temperature for 2 h, and methanol (20 mL) and NaBH₄ (0.74 g, 0.0117 mol) were added. After stirring for an additional 15 min. at room temperature the solvent as removed in vacuo from the reaction mixture, and the residue dissolved in IM KOH (20 mL), and the resulting solution extracted with CH₂C1₂ (100 mL). The organic phase was washed with IM KOH (2x20 mL) and dried (MgSO₄). The solvent was removed in vacuo to give the title compound 0.76 g (69%). M.p. 220-221°C.

EXAMPLE 22

6-Dimethylamino-3-(3-ethyl-l,2,4-oxadiazol-5-yl)-β-carboline (Compound 22) Sodium (0.11 g, 0.0048 mol) was carefully added to absolute ethanol (100 mL). To the sodium ethoxide solution were added compound 21 (0.53 g, 0.0019 mol), propionamide oxime (0.20 g, 0.0022 mol) and toluene (150 mL). The resulting mixture was heated at reflux temperature and the water removed from the mixture by azeotropic distillation. The solvent was removed from the reaction in vacuo. and the residue washed with water until neutral pH, and dried in vacuo to give the title compound 0.25 g (43%). M.p. 235-

240°C.

EXAMPLE 23

9-(3-Chloro- 1 -propyl)-6-dimethylamino-3-(3-ethyl- 1 ,2 ,4-oxadiazol-5-yl)-β-carboline (Compound 23)

To a solution of compound 22 (0.25 g, 0.0009 mol) in anhydrous DMF (30 mL) was added 50% sodium hydride in mineral oil (0.05 g, 0.0012 mol). The mixture was stirred for 30 min. at room temperature, and then added to a solution of l-bromo-3-chloro- propane (0.15 g, 0.001 mol) in anhydrous DMF (50 mL). The resulting mixture was stirred at ambient temperature over night, and the product then precipitated by d e addition of water. The crude product was purified on a silica gel column (Eluent: CH₂Cl₂/methanol (9:1)) to give the title compound 0.22 g (65%). M.p. 183-186°C.

EXAMPLE 24

l-(3-(3-Ethyl-l,2,4-oxadiazol-5-yl)-6-dimethylamino-β-carbolin-9-yl)-l-propyl)-4- phenylpiperidin-4-ol hydrochloride (Compound 24)

A solution of compound 23 (0.22 g, 0.0008 mol), TEA (0.32 g, 0.003 mol) and 4- phenylpiperidin-4-ol (0.17 g, 0.0009 mol) in anhydrous DMF was stined at room temperature for 96 h. The reaction mixture was filtered and the solvent was removed in vacuo. The residue was purified on a silica gel column (Eluent: CH₂Cl₂/methanol (9: 1)). The product was acidified with 2M HCl(g) in diethyl etiier, to give the title compound 0.08 g (16%). M.p. 199-201°C. EXAMPLE 25

9-(3-Chloro-l-propyl)-3-(3-methyl-l,2,4-oxadiazol-5-yl)-β-carboline 5 (Compound 25)

To a solution of 3-(3-methyl-l,2,4-oxadiazol-5-yl)-β-carboline (2.00 g, 0.008 mol) in anhydrous DMF (50 mL) was added 50% sodium hydride in mineral oil (0.42 g, 0.01

10 mol). The mixture was stirred for 1 h at room temperature, and then carefully added to a solution of l-bromo-3-chloropropane (1.39 g, 0.0088 mol) in anhydrous DMF (150 mL). The resulting mixture was stined at ambient temperature over night. The reaction mixture was concentrated in vacuo. and the crude product was purified on a silica gel column (Eluent: CH₂Cl₂/methanol (9: 1)) to give the title compound 2.11 g (81 %). M.p. 180-

15 185°C.

EXAMPLE 26

l-(3-(3-Methyl-l,2,4-oxadiazol-5-yl)-_β-carbolin-9-yl)-l-propyl)-4-phenylpiperidin-4-ol 20 hydrochloride (Compound 26)

A solution of compound 25 (1.00 g, 0.0031 mol), TEA (1.25 g, 0.0124 mol) and 4- phenylpiperidin-4-ol (0.60 g, 0.0034 mol) in anhydrous DMF (50 mL) was stirred at 25 room temperature overnight, and then heated at 80°C for 6 h. The reaction mixture was filtered and the solvent was removed in vacuo. The residue was purified on a silica gel column (Eluent: CH₂Cl₂/methanol (9: 1)). The product was acidified with 2M HCl(g) in diethyl ether, to give the title compound 0.69 g (44%). M.p. 179.5-180.5°C.

30 EXAMPLE 27

9-(3-Chloro-l-propyl)-3-(5-methyl-l,2,4-oxadiazol-3-yl)-β-carboline (Compound 27)

To a solution of 3-(5-methyl-l,2,4-oxadiazol-3-yl)-β-carboline (0.25 g, 0.001 mol) in anhydrous DMF (30 mL) was added 50% sodium hydride in mineral oil (0.03 g, 0.0011 mol). The mixture was stined for 1 h at room temperature, and then carefully added to a solution of l-bromo-3-chloropropane (0.17 g, 0.0011 mol) in anhydrous DMF (20 mL). The resulting mixture was stined at ambient temperature for 96 h. The reaction mixture was concentrated in vacuo. and the crude product was purified twice on a silica gel column 1) (Eluent: CH₂Cl₂/methanol (9: 1)); 2) (Eluent: ethyl acetate/toluene (1: 1)) to give the title compound 0.21 g (64%). M.p. 130-135°C.

EXAMPLE 28

l-(3-(5-Methyl-l,2,4-oxadiazol-3-yl)-β-carbolin-9-yl)-l-propyl)-4-phenylpiperidin-4-ol hydrochloride (Compound 28)

A solution of compound 27 (0.21 g, 0.0007 mol), TEA (0.26 g, 0.0003 mol) and 4- phenylpiperidin-4-ol (0.11 g, 0.0007 mol) in anhydrous DMF (30 mL) was stined at 50° C for 5 d. The reaction mixture was filtered and the solvent was removed in vacuo. The residue was purified on a silica gel column (Eluent: CH₂Cl₂/methanol/25 % NH₄OH (aq) (90:9: 1)). The product was acidified with 2M HCl(g) in diethyl ether, to give the title compound 0.15 g (43%). M.p. decomposes at 157-159°C.

Claims

A compound of formula I

wherein

R¹ and R² independently are hydrogen, halogen, hydroxy, nitro, -(CH₂)_n-(C=O)-(CH₂)_mCH₃, -NR⁹R¹⁰, -SONRⁿR¹², -COOR¹³, -CONR¹⁴R¹⁵, C^-alkyl, Cι_₆-alkoxy, trifluoromethyl or trifluoromethoxy wherein R⁹, R¹⁰, R", R¹², R¹³, R¹⁴ and R¹⁵ independently are hydrogen, C-^-alkyl, C₂.₆-alkenyl or C₂.₆-alkynyl, and wherein n and m independently are 0, 1, 2, 3 or 4; and R³ is C-^-alkylene optionally substituted with one or two C^-alkyl or C₃.₇-cycloalkyl, C₂.₅-alkenylene or C₂.₅-alkynylene or

R³ is -(CH₂)_m-A-(CH₂)_n-,

or -(CH₂)_m-CH-CH-(CH₂)_n-

wherein A is C₃.₇-cycloalkylene and B is .s-alkylene and C is C-^-alkylene and m and n independently are 0, 1 or 2; and R⁴ is hydrogen or C-^-alkyl; and

R⁵ and R^δ independently are hydrogen, halogen, hydroxy, nitro, -NR¹⁶R¹⁷, -COOR¹⁸, C,. ₆-alkyl, Cι.₆-alkoxy, trifluoromethyl or trifluoromethoxy wherein R¹⁶, R¹⁷ and R¹⁸ independently are hydrogen, C,_-6-alkyl, C₂.₆-alkenyl or C_2-6-alkynyl; and

Z is

wherein X is -NH-, oxygen or sulphur; and R⁷ is hydrogen, Cι_-6-alkyl, C₂.₆-alkenyl, C₂.₆-alkynyl, phenyl, C₃.₇-cycloalkyl, -OR⁸ or - SR⁸ wherein R⁸ is hydrogen or C,.₆-alkyl; or a pharmaceutically acceptable salt thereof.

2_ A compound according to claim 1 which is l-(3-(3-(3-Ethyl-l ,2,4-oxadiazol-5-yl)-9H-β-carbolin-9-yl)-l-propyl)-4-phenylpiperidin- 4-ol, l-(3-(3-(3-Cyclopropyl-l,2,4-oxadiazol-5-yl)-9H-β-carbolin-9-yl)-l-propyl)-4- phenylpiperidin-4-ol , l-(3-(3-(3-Phenyl-l ,2,4-oxadiazol-5-yl)-9H-β-carbolin-9-yl)-l-propyl)-4-phenylpiperidin-

4-ol, 1 -(3-(3-(3-Ethyl- 1 ,2 ,4-oxadiazol-5-yl)-6-dimethylsulfamoyl-9H-β-carbolin-9-yl)- 1 - propyl)-4-phenylpiperidin-4-ol,

1 -(3-(3-(3-Ethyl- 1 ,2,4-oxadiazol-5-yl)-6-dipropenylamino-9H-β-carbolin-9-yl)- 1 -propyl)-

4-phenylpiperidin-4-ol , or a pharmaceutically acceptable salt thereof.

3_i A method of preparing a compound according to claim 1 ,

CHARACTERIZED IN a) reacting a compound of formula II

wherein R¹, R², R³ and Z are as defined above and X is a leaving group with a compound of formula III

wherein R , R and R are as defined above; or

b) reacting a compound of formula IV

T wherein R R² and Z are as defined above with a compound of formula V

wherein R³, R , R⁵, R⁶ and X are as defined above; or

c) reacting a compound of formula VI

wherein R , R , R , R and Z are as defined above with a compound of formula VII

wherein R , R and Y are as defined above. _ A pharmaceutical composition comprising as active component a compound according to claim 1 together with a pharmaceutically acceptable carrier or diluent.

5_i A pharmaceutical composition suitable for treating a central nervous system ailment related to the inhibition of GABA uptake via the GAT-4 subtype carrier com¬ prising an effective amount of a compound according to claim 1 together with a pharmaceutically acceptable carrier or diluent.

β__ The pharmaceutical composition according to claim 4 or 5 comprising between 0.5 mg and 1000 mg of the compound according to claim 1 per unit dose.

1_ A method of treating a central nervous system ailment related to the inhibition of GABA uptake via the GAT-4 subtype carrier in a subject in need of such treatment comprising administering to said subject an effective amount of a compound according to claim 1.

%__ A method of treating a central nervous system ailment related to the inhibition of GABA uptake via the GAT-4 subtype carrier in a subject in need of such treatment comprising administering to said subject a pharmaceutical composition according to claim 5.

__ The use of a compound according to claim 1 for the preparation of a medicament for treatment of a central nervous system ailment related to the inhibition of GABA uptake via the GAT-4 subtype carrier.

SUBSTITUTE SHEET