Phenylpiperazine derivatives with a combination of partial dopamine-D2 receptor agonism and serotonin reuptake inhibition

Abstract

The invention relates to a group of novel phenylpiperazine derivatives with a dual mode of action: serotonin reuptake inhibition and partial agonism on dopamine-D2 receptors. The invention also relates to the use of a compound disclosed herein for the manufacture of a medicament giving a beneficial effect. The compounds have the general formula (1): wherein the symbols have the meanings given in the specification. and tautomers, stereoisomers and N-oxides thereof, as well as pharmacologically acceptable salts, hydrates and solvates of said compounds of formula (1) and its tautomers, stereoisomers and N-oxides.

Description

The present invention relates to a group of novel phenylpiperazine derivatives with a dual mode of action: serotonin reuptake inhibition and partial agonism on dopamine-D₂ receptors. The invention also relates to the use of a compound disclosed herein for the manufacture of a medicament giving a beneficial effect. A beneficial effect is disclosed herein or apparent to a person skilled in the art from the specification and general knowledge in the art. The invention also relates to the use of a compound of the invention for the manufacture of a medicament for treating or preventing a disease or condition. More particularly, the invention relates to a new use for the treatment of a disease or condition disclosed herein or apparent to a person skilled in the art from the specification and general knowledge in the art. In embodiments of the invention specific compounds disclosed herein are used for the manufacture of a medicament useful in the treatment of disorders in which dopamine-D₂ receptors and serotonin, reuptake sites are involved, or that can be treated via manipulation of those targets.

Compounds with a dual action as dopamine-D₂ antagonists and serotonin reuptake inhibitors are known from WO 00/023441, WO 00/069424 and WO 01/014330. This combination of activities is useful for the treatment of schizophrenia and other psychotic disorders: it enables a more complete treatment of all disease symptoms (e.g. positive symptoms and negative symptoms).

The goal of the present invention was to provide further compounds with a dual action as partial dopamine-D₂ antagonists and serotonin reuptake inhibitors.

The invention relates to a group of novel compounds of the formula (1):
wherein:

X═S or O,

R₁ is H, (C₁-C₆)alkyl, CF₃, CH₂CF₃, OH or O—(C₁-C₆)alkyl

R₂ is H, (C₁-C₆)alkyl, halogen or cyano

R₃ is H or (C₁-C₆)alkyl

R₄ is H, (C₁-C₆)alkyl, optionally substituted with a halogen atom

• T is a saturated or unsaturated carbon chain of 2-7 atoms, wherein one carbon atom may be replaced with a nitrogen atom, optionally substituted with an (C₁-C₃)alkyl, CF₃ or CH₂CF₃ group, an oxygen atom or a sulphur atom, which chain is optionally substituted with one or more substituents selected from the group consisting of (C₁-C₃)alkyl, (C₁-C₃)alkoxy, halogen, cyano, trifluoromethyl, OCF₃, SCF₃, OCHF₂ and nitro,
• Ar is selected from the groups:
• which Ar group is optionally further substituted with one or more substituents selected from the group consisting of (C₁-C₃)alkyl, (C₁-C₃)alkoxy, halogen, cyano, trifluoromethyl, OCF₃, SCF₃, OCHF₂ and nitro,
• and in which Ar groups that contain a five-membered ring, the double bond in the five-membered ring may be saturated,
• and tautomers, stereoisomers and N-oxides thereof, as well as pharmacologically acceptable salts, hydrates and solvates of said compounds of formula (1) and its tautomers, stereoisomers and N-oxides.

In the groups ‘Ar’, the dot represents the attachement point of group ‘T’.

In the description of the substituents the abbreviation ‘alkyl(C_1-3)’ means ‘methyl, ethyl, n-propyl or isopropyl’.

Prodrugs of the compounds mentioned above are in the scope of the present invention. Prodrugs are therapeutic agents which are inactive per se, but are transformed into one or more active metabolites. Prodrugs are bioreversible derivatives of drug molecules used to overcome some barriers to the utility of the parent drug molecule. These barriers include, but are not limited to, solubility, permeability, stability, presystemic metabolism and targeting limitations (Medicinal Chemistry: Principles and Practice, 1994, Ed.: F. D. King, p. 215; J. Stella, “Prodrugs as therapeutics”, Expert Opin. Ther. Patents, 14(3), 277-280, 2004; P. Ettmayer et al., “Lessons learned from marketed and investigational prodrugs”, J. Med. Chem., 47, 2393-2404, 2004). Pro-drugs, i.e. compounds which when administered to humans by any known route, are metabolised to compounds having formula (1), belong to the invention. In particular this relates to compounds with primary or secondary amino or hydroxy groups. Such compounds can be reacted with organic acids to yield compounds having formula (1) wherein an additional group is present which is easily removed after administration, for instance, but not limited to amidine, enamine, a Mannich base, a hydroxyl-methylene derivative, an O-(acyloxy-methylene carbamate) derivative, carbamate, ester, amide or enaminone.

N-oxides of the compounds mentioned above are in the scope of the present invention. Tertiary amines may or may not give rise to N-oxide metabolites. The extend to what N-oxidation takes place varies from trace amounts to a near quantitative conversion. N-oxides may be more active than their corresponding tertiary amines or less active. Whilst N-oxides are easily reduced to their corresponding tertiary amines by chemical means, in the human body this happens to varying degrees. Some N-oxides undergo nearly quantitative reductive conversion to the corresponding tertiary amines, in other cases the conversion is a mere trace reaction or even completely absent. (M. H. Bickel: “The pharmacology and Biochemistry of N-oxides”, Pharmaco-logical Reviews, 21(4), 325-355, 1969).

It has been found that the compounds according to the invention show high affinity for both the dopamine D₂ receptor and the serotonin reuptake site. The compounds show activity at dopamine D₂ receptors with varying degree of agonism. All of the compounds show activity as inhibitors of serotonin reuptake, as they potentiate 5-HTP induced behaviour in mice (B. L. Jacobs., ‘An animal behaviour model for studying central serotonergic synapses’; Life Sci., 1976, 19(6) 777-785).

In contrast to the use of full dopamine-D₂ receptor agonists or antagonists, the use of partial dopamine-D₂ receptor agonists offers a dynamic medication that self-adjusts on a moment-to-moment basis to the endogenous state of the patient. Thus, it provides the desired flexible modulation of the dopamine system and avoidance of the many adverse effects caused either by treatment using full dopamine-D₂ receptor agonists like bromocriptine (hallucinations, nausea, vomiting, dyskinesia, orthostatic hypotension, somnolescence) or full dopamine-D₂ receptor antagonists like haloperidol (emotional blunting, dysphoria, tardive dyskinesia). Because of these many adverse effects, full agonists and antagonists have found only very limited use in the therapy of depressive and anxiety disorders. Partial dopamine-D₂ receptor agonists not only show a flexible modulation and a favourable side-effect profile, they also have a pronounced anxiolytic profile in relevant animal models (Drugs of the Future 2001, 26(2): 128-132).

Partial dopamine-D₂ receptor agonists, according to the present invention, are compounds that—when tested in a concentration response range—achieve activation in the functional cAMP cell based assay (as described below). Partial dopamine-D₂ receptor agonists will act as an agonist in cases when the endogenous synaptic tone of dopamine is low, or in the the presence of a full dopamine-D₂ receptor antagonist, and will act as an antagonist in cases when the endogenous synaptic tone of dopamine is high, or in the presence of a full dopamine D₂ receptor agonist. Like full agonists, partial dopamine-D₂ receptor agonists in general are active in sensitized systems. They induce contralateral turning in rats with unilateral 6-hydroxy-dopamine (6-OHDA) lesions in the substantia nigra pars compacta. In MPTP-treated common marmosets they produce potent and long-lasting reversal of motor symptoms (Drugs of the Future 2001, 26(2): 128-132). In contrast to full agonists, however, partial dopamine-D₂ agonists are substantially less active in non-sensitized systems: they hardly reverse reserpine induced hypolocomotion in rats.

For the treatment of CNS disorders involving an overactive dopaminergic system a pharmaceutical preparation combining partial dopamine-D₂ receptor agonistic activity having low intrinsic functional activity with serotonin reuptake inhibitory activity is recommended. In case of a disorder involving dopamine insufficiency a pharmaceutical preparation combining partial dopamine-D₂ receptor agonistic activity with high intrinsic functional activity and serotonin reuptake activity according to the invention has considerable advantages.

Disorders characterized by dynamic fluctuations in dopamine neurotransmission like bipolar depression and addiction will profit in particular from the flexible adjustment of the dopamine system by the partial dopamine-D₂ receptor agonists in the pharmaceutical preparation. Combining this “dopaminergic neurotransmission stabilizing” activity with serotonin reuptake inhibitory activity will enhance antidepressive and anxiolytic efficacy. The compounds can be used for the treatment of affections or diseases of the central nervous system caused by disturbances in the dopaminergic and serotonergic systems, for example: aggression, anxiety, disorders, autism, vertigo, depression, disturbances of cognition or memory, Parkinson's disease, and in particular schizophrenia and other psychotic disorders.

Pharmaceutically acceptable salts may be obtained using standard procedures well known in the art, for example by mixing a compound of the present invention with a suitable acid, for instance an inorganic acid such as hydrochloric acid, or with an organic acid.

Pharmaceutical Preparations

The compounds of the invention can be brought into forms suitable for administration by means of usual processes using auxiliary substances such as liquid or solid carrier material. The pharmaceutical compositions of the invention may be administered enterally, orally, parenterally (intramuscularly or intravenously), rectally or locally (topically). They can be administered in the form of solutions, powders, tablets, capsules (including microcapsules), ointments (creams or gel) or suppositories. Suitable excipients for such formulations are the pharmaceutically customary liquid or solid fillers and extenders, solvents, emulsifiers, lubricants, flavorings, colorings and/or buffer substances. Frequently used auxiliary substances which may be mentioned are magnesium carbonate, titanium dioxide, lactose, mannitol and other sugars, talc, lactoprotein, gelatin, starch, cellulose and its derivatives, animal and vegetable oils such as fish liver oil, sunflower, groundnut or sesame oil, polyethylene glycol and solvents such as, for example, sterile water and mono- or polyhydric alcohols such as glycerol.

Compounds of the present invention are generally administered as pharmaceutical compositions which are important and novel embodiments of the invention because of the presence of the compounds, more particularly specific compounds disclosed herein. Types of pharmaceutical compositions that may be used include but are not limited to tablets, chewable tablets; capsules, solutions, parenteral solutions, suppositories, suspensions, and other types disclosed herein or apparent to a person skilled in the art from the specification and general knowledge in the art. In embodiments of the invention, a pharmaceutical pack or kit is provided comprising one or more containers filled with one or more of the ingredients of a pharmaceutical composition of the invention. Associated with such container(s) can be various written materials such as instructions for use, or a notice in the form prescribed by a governmental agency regulating the manufacture, use or sale of pharmaceuticals products, which notice reflects approval by the agency of manufacture, use, or sale for human or veterinary administration.

Pharmacological Methods

In Vitro Affinity for Dopamine-D₂ Receptors

Affinity of the compounds for dopamine-D₂ receptors was determined using the receptor binding assay described by 1. Creese, R. Schneider and S. H. Snyder: “[³H]-Spiroperidol labels dopamine receptors in rat pituitary and brain”, Eur. J. Pharmacol., 46, 377-381, 1977.

In Vitro Affinity for Serotonin Reuptake Sites

Affinity of the compounds for serotonin reuptake sites was determined using the receptor binding assay described by E. Habert et al.,: “Characterisation of [³H]-paroxetine binding to rat cortical membranes”, Eur. J. Pharmacol., 118, 107-114, 1985.

Inhibition of Forskolin-Induced [³H]-cAMP Accumulation

The in vitro functional activity at dopamine-D₂ receptors, including the intrinsic activity (E) of the compounds of the invention was measured by their ability to inhibit forskolin-induced [³H]-cAMP accumulation.

Human dopamine D_2,L receptors were cloned in fibroblast cell line CHO-K1′ cells and obtained from Dr. Grandy, Vollum Institute, Portland, Oreg., USA. CHO cells were grown in a Dulbecco's modified Eagle's medium (DMEM) culture medium, supplemented with 10% heat-inactivated fetal calf serum, 2 mM glutamine, 1 mM pyruvate, 5000 units/ml penicillin, 5000 μg/ml streptomycin and 200 μg/ml G-418 at 37° C. in 93% air/7% CO₂. For incubation with test compounds, confluent cultures grown in 24 wells plates were used. Each condition or substance was routinely tested in quadruplicate. Cells were loaded with 1 μCi [³H]-adenine in 0.5 ml medium/well. After 2 hours, cultures were washed with 0.5 ml PBS containing 1 mM of the phosphodiesterase inhibitor isobutylmethylxanthine (IBMX) and incubated for 20 min with 0.5 ml PBS containing 1 mM IBMX and forskolin with or without test compound. After aspiration the reaction was stopped with 1 ml trichloroacetic acid 5% (w/v). The [³H]-ATP and [³H]-cAMP formed in the cellular extract were assayed as described by Solomon Y, Landos C, Rodbell M, 1974, A highly selective adenylyl cyclase assay, Anal Biochem 58:541-548 and Weiss S, Sebben M, Bockaert J J, 1985, Corticotropin-peptide regulation of intracellular cyclic AMP production in cortical neurons in primary culture, J Neurochem 45:869-874. 0.8 ml Extract was passed over Dowex (50WX-4 200-400 mesh) and aluminumoxide columns, eluted with water and 0.1M imidazole (pH=7.5). Eluates were mixed with 7 ml Insta-gel and radioactivity was counted with a liquid scintillation counter. The conversion of [³H]-ATP into [³H]-cAMP was expressed as the ratio in percentage radioactivity in the cAMP fraction as compared to combined radioactivity in both cAMP and ATP fractions, and basal activity was subtracted to correct for spontaneous activity.

Test compounds were obtained as 10 mM stock solutions in 100% DMSO, and diluted in PBS/IBMX to final concentrations. Typically, compounds were used in concentrations that ranged from 10⁻¹⁰M to 10⁻⁵M. From quadruplicate data counts, the mean was taken as an estimate for drug-induced, receptor-mediated effects at specified second messenger accumulation, expressed as percentage of control values (forskolin-stimulated cAMP accumulation, subtracted by basal activity). By using the non-linear curve-fitting program INPLOT or the Excel-add-in XL-Fit, mean values were plotted against drug concentration (in molar) and a sigmoid curve (four-parameter logistic curve) was constructed. The maximal forskolin-induced stimulated conversion is taken as maximum value and the maximal inhibition (usually at drug concentrations 10⁻⁴ M or 10⁻⁵ M) as minimum and these values were fixed during the fitting process. Thus, concentrations of the compound, causing 50% of the maximally obtained inhibition of forskolin-induced cAMP accumulation (EC₅₀), are averaged over several experiments and presented as mean pEC₅₀±SEM. Antagonist potency is assessed by co-incubating cells with a fixed agonist concentration and specified antagonist concentrations. Curve fitting procedures are identical to those used for estimating EC₅₀ values. Thus IC₅₀ values, i.e. the concentration that is able to achieve 50% of maximal antagonism that can be achieved by this compound. IC₅₀ values are corrected using a Cheng-Prussoff equation, correcting it for agonist concentration and EC₅₀ values that is obtained in the same experiment. Thus, K_b=IC₅₀/(1+[agonist]/EC₅₀, agonist). The corresponding pA₂ value is −log (K_b). Concentration-response curve fitting allows estimation of pEC₅₀ values and of maximal achievable effect (intrinsic activity or efficacy (ε). A full receptor agonist has ε=1, a full receptor antagonist has ε=0, and a partial receptor agonist has an intermediate intrinsic activity.

Dosages

The affinity of the compounds of the invention for dopamine-D₂ receptors and serotonine reuptake sites was determined as described above. From the binding affinity measured for a given compound of formula (1), one can estimate a theoretical lowest effective dose. At a concentration of the compound equal to twice the measured K_i-value, 100% of the receptors likely will be occupied by the compound. Converting that concentration to mg of compound per kg of patient yields a theoretical lowest effective dose, assuming ideal bioavailability. Pharmacokinetic, pharmacodynamic, and other considerations may alter the dose actually administered to a higher or lower value. The dosage expediently administered is 0.001-1000 mg/kg, preferably 0.1-100 mg/kg of patient's bodyweight.

Treatment

The term ‘treatment’ as used herein refers to any treatment of a mammalian, preferably human condition or disease, and includes: (1) preventing the disease or condition from occurring in a subject which may be predisposed to the disease but has not yet been diagnosed as having it, (2) inhibiting the disease or condition, i.e., arresting its development, (3) relieving the disease or condition, i.e., causing regression of the condition, or (4) relieving the conditions caused by the disease, i.e., stopping the symptoms of the disease.

Materials and Methods

¹H and ¹³C NMR spectra were recorded on a Bruker Avance DRX600 instrument (600 MHz), Varian UN400 instrument (400 MHz) or on a Varian VXR200 instrument (200 MHz) using DMSO-D₆ or CDCl₃ as solvents with tetramethylsilane as an internal standard. Chemical shifts are given in ppm (δ scale) downfield from tetramethylsilane. Peakshapes in the NMR spectra are indicated with the symbols ‘q’ (quartet), ‘dq’ (double quartet), ‘t’ (triplet), ‘dt’ (double triplet), ‘d’ (doublet), ‘dd’ (double doublet), ‘s’ (singlet), ‘bs’ (broad singlet) and ‘m’ (multiplet). Flash chromatography was performed using silica gel 60 (0.040-0.063 mm, Merck). Column chromatography was performed using silica gel 60 (0.063-0.200 mm, Merck). Mass spectra were recorded on a Micromass QTOF-2 instrument with MassLynx application software for acquisition and reconstruction of the data. Exact mass measurement was done of the quasimolecular ion [M+H]⁺. Melting points were recorded on a Buchi B-545 melting point apparatus.

Yields refer to isolated pure products. The preparation of the compounds having formula (I) will now be described in more detail in the following Examples.

EXAMPLES

The H-atom of the N-H moiety of amines I-H to X-H can be replaced by Q in two different chemical ways, A and B, eventually leading to the compounds of the invention which are listed in table 1 (see below.

Method A:

The compounds were prepared via the synthesis depicted in scheme A1: an amine (from FIG. 1) was reacted with Q-X (X=leaving group like e.g. Cl, Br, I) in e.g. acetonitrile or butyronitrile with Et(i-Pr)₂N acting as a base, in some cases KI (or NaI) was added. Et₃N ran be used instead of Et(i-Pr)₂N.

Example 1

Scheme A2, Step i: To a suspension of 0.6 g (2.35 mmol) of the piperazine hydrochloride I-H.HCl in 100 ml of acetonitril were added 0.77 g (2.35 mmol) of the iodide, 0.71 g (4.7 mmol) of NaI and 1.39 ml (8 mmol) of DIPEA. The mixture was refluxed for 20 hours and concentrated in vacuo. The residue was taken up in CH₂Cl₂ and the resulting mixture washed with water. The organic layer was dried on Na₂SO₄. The drying agent was removed by filtration and the solvent by concentration in vacuo.

The residue was purified by flash column chromatography (SiO₂, eluent CH₂Cl₂/MeOH/NH₄OH 960/37.5/2.5). The product containg fractions were concentrated in vacuo leaving a residue which was stirred in diisopropylether. The solid material was collected by filtration, yielding 0.79 g (81%) of compound 9. M.p.: 228-230° C.

Method B:

The compounds were prepared via the synthesis depicted in scheme B1: an amine (from FIG. 1) was alkylated by means of a reductive alkylation. Q-OH was oxidized to the corresponding aldehyde Q′-CHO after which reductive alkylation was performed. THF and DCE are suitable solvents for this type of reaction.

Example 2

The Swern oxidation was carried out according to literature: Anthony J. Mancuso, Daniel Swern; Synthesis, (1981) 165-184.
Scheme B2, Step i:

A solution of oxalyl chloride (0.45 ml, 5.2 mmol) in 15 ml DCM is placed in a three-necked round bottom flask equipped with a thermometer and two pressure-equalizing dropping funnels respectively containing dimethyl sulfoxide (0.74 ml, 10.4 mmol) in 3 ml DCM, and the 3-(6-chloro-indazo-1-yl)-propanol Q56-OH (1.0 g, 4.7 mmol) in 5 ml DCM under an N₂ atmosphere. The dimethyl sulfoxide is added to the stirred oxalyl chloride solution at −50° C. to −60° C. The reaction mixture is stirred for 2 minutes and the alcohol is added within 5 minutes; stirring is continued for an additional 15 minutes. Triethylamine (3.3 ml, 23.73 mmol) is added and the reaction mixture is stirred for 15 minutes and then allowed to warm to room temperature. Water is added and the aqueous layer is re-extracted with additional DCM. The organic layer is washed with 0.3 N HCl, water, 5% NaHCO₃, saturated NaCl solution and dried with Na₂SO₄. The filtered solution is evaporated yielding the corresponding aldehyde.

Scheme B2, Step ii:

The crude product containing the aldehyde (from step i) is added to a stirred solution of 3-7-piperazin-1-yl-3H-benzooxazole-2-one.2HCl (V.2HCl) (0.57 g, 2.44 mmol) and tri-ethyl amine (0.76 ml, 5.38 mmol) in 100 ml DCE. The reaction mixture is stirred for 1 hour and NaBH(OAc)₃ (0.83 g, 3.91 mmol) is added. The mixture is stirred for an additional 8 hours. Water was added and the resulting fraction extracted with DCM (3 times). The combined organic layers were evaporated. The crude product was purified by flash chromatography on silica (eluent: 1.5% MeOH in DCM→2% MeOH in DCM) to afford 128 as a crystalline solid in a 58% yield. Melting point: 118-120° C.

TABLE 1
examples of compounds of the invention.
Comp.				L-		melting
nr.	amine	Q	meth.	group	salt	r. ° C.
1	I	1	A	I	free base	194-196.5
2	I	2	A	I	free base	168-170
3	I	3	A	I	free base	206.5-207.5
4	I	4	A	I	free base	173.5-175
5	I	5	A	I	free base	173-176
6	I	6	A	I	free base	180-182
7	I	7	A	I	free base	211-213
8	I	8	A	I	free base	193-195
9	I	9	A	I	free base	228-230
10	I	10	A	I	free base	186-188
11	I	11	A	I	free base	176-178
12	I	12	A	I	free base	212-214
13	I	13	A	I	free base	183-184
14	I	14	A	I	HCl	225-227
15	I	15	A	I	HCl	255-260
16	I	16	A	I	free base	143-145
17	I	17	A	I	free base	152-157
18	I	18	A	I	free base	157-159
19	I	19	A	I	HCl	179-181
20	I	20	A	I	free base	174.5-177
21	I	21	A	Cl	free base	180-183
22	I	22	A	I	free base	206-208
23	I	23	A	I	free base	202-204
24	I	25	A	I	free base	154-156
25	I	29	A	I	free base	amorph
26	I	30	A	I	free base	177-179
27	I	31	A	I	free base	153-156
28	I	32	A	I	free base	174-177
29	I	33	A	Br	free base	187-190
30	I	34	A	Br	free base	190-192
31	I	35	A	Br	free base	174-177
32	I	36	A	Br	free base	198-200
33	I	37	A	Br	free base	194-195
34	I	38	A	Br	free base	137-138
35	I	39	A	Br	free base	136-138
36	I	40	A	Cl	free base	121-123
37	I	41	A	Br	free base	133-135
38	I	42	A	Br	free base	135-137
39	I	43	A	Cl	free base	111-112
40	I	44	B		free base	200-202
41	I	45	A	Br	free base	197-199
42	I	46	A	Cl	free base	162-164
43	I	47	A	Br	free base	204-206
44	I	48	A	Cl	free base	162-164
45	I	49	A	Br	free base	188-189
46	I	50	A	Cl	free base	146-149
47	I	51	A	Cl	free base	109-113
48	I	52	A	Br	free base	75-105
						amorph
49	I	53	A	Br	free base	209-210
50	I	54	B		free base	201-203
51	I	55	B		free base	161-162
52	I	56	B		free base	203-204
53	I	57	B		free base	83-86
54	I	58	B		free base	172-174
55	I	59	B		free base	134-137
56	I	60	A	Br	free base	214-6
57	I	61	A	I	HCl	214-6
58	I	62	A	I	HCl	275-7 (d)
59	I	63	A	I	free base	NMR**
60	I	64	A	Cl	free base	234-6
61	II	3	A	I	free base	187-189
62	II	5	A	I	free base	157-159
63	II	6	A	I	free base	154-156
64	II	8	A	I	free base	190-192
65	II	9	A	I	free base	234-236
66	II	11	A	I	free base	176-178
67	II	13	A	I	free base	236-239
68	II	15	A	I	free base	156-158
69	II	16	A	I	HCl	256-260
70	II	17	A	I	HCl	244-246
71	II	26	A	I	HCl	232-5 (d)
72	II	29	A	I	free base	157-158
73	II	31	A	I	free base	190-1
74	II	32	A	I	free base	168-170
75	II	35	A	Br	free base	170-173
76	II	36	A	Br	free base	193-196
77	II	45	A	Br	free base	166-169
78	II	47	A	Br	free base	108-113
79	II	49	A	Br	free base	168-170
80	II	50	A	Cl	free base	194-7
81	II	59	B		free base	153-5
82	II	61	A	I	free base	157-9
83	III	16	A	I	free base	153-154
84	IV	16	A	I	free base	163-5
85	V	1	A	I	free base	125-127
86	V	3	A	I	free base	153-155
87	V	4	A	I	HCl	182-183
88	V	5	A	I	free base	113-116
89	V	6	A	I	free base	162-164
90	V	8	A	I	free base	119-121
91	V	9	A	I	free base	150-152
92	V	10	A	I	free base	141-142
93	V	11	A	I	free base	124-126
94	V	12	A	I	free base	184-186
95	V	13	A	I	HCl	107
96	V	14	A	I	HCl	197-199
97	V	15	A	I	HCl	216-218
98	V	16	A	I	HCl	199-201
99	V	17	A	I	HCl	214-218
100	V	18	A	I	free base	228-229
101	V	19	A	I	free base	132-134
102	V	20	A	I	free base	138-140
103	V	22	A	I	free base	143-145
104	V	23	A	I	free base	150-152
105	V	24	A	I	free base	179-181
106	V	25	A	I	HCl	197-199
107	V	26	A	I	free base	105-107
108	V	28	A	I	free base	146-147
109	V	31	A	I	free base	119-21
110	V	33	A	Br	HCl	>240 d
111	V	34	A	Br	free base	108-111
112	V	35	A	Br	free base	129-132
113	V	36	A	Br	HCl	>240 d
114	V	37	A	Br	free base	146-149
115	V	41	A	Br	free base	117-118
116	V	42	A	Br	free base	110-112
117	V	43	A	Cl	free base	167-170
118	V	45	A	Br	free base	111-113
119	V	46	A	Cl	free base	88-91
120	V	47	A	Br	free base	131-133
121	V	49	A	Br	free base	124-126
122	V	50	A	Cl	free base	103-105
123	V	51	A	Cl	free base	112-115
124	V	52	A	Br	free base	203-205
125	V	53	A	Br	HCl	262-264
126	V	54	B		free base	116-118
127	V	55	B		free base	104-107
128	V	56	B		free base	118-120
129	V	57	A	I	free base	108-112
130	V	58	B		free base	102-104
131	V	59	B		free base	125-128
132	V	60	A	Br	free base	202-3
133	V	61	A	I	HCl	194-7
134	V	62	A	I	HCl	274-6 (d)
135	V	63	A	I	free base	NMR**
136	V	64	A	Cl	free base	154-5
137	VI	16	A	I	free base	134-6
138	VI	31	A	I	free base	125-6
139	VI	50	A	Cl	free base	116-8
140	VI	59	B		free base	130-2
141	VII	16	A	I	HCl	274-276
142	VIII	16	A	I	free base	135-137
143	IX	3	A	I	free base	106-108
144	IX	6	A	I	free base	117-119
145	IX	49	A	Br	HCl	204-206
146	IX	50	A	Cl	free base	107-109
NMR**, compound 59: (d, ppm) 3.36 (t, broad, Ph—N(CH2CH2)2N—)
NMR**, compound 135: (d, ppm) 3.29 (t, broad, Ph—N(CH2CH2)2N—)
**CDCl3/d6-DMSO = ¼

Structures of the phehylpiperazine part of the compounds of formula (1), herein termed ‘amines’, and groups ‘Q’ are given below. In the column ‘method’, the general method (A or B) is given, and in case of method A, the next column gives the leaving group.

The phenylpiperazine parts of the compounds of formula (1) used in these methods are indicated as I-H to IX-H, wherein the dot on the N-atom is the attachment point for the group Q:

The syntheses of the piperazines I-H, III-H and V-H are described in WO97/36893.
Synthesis of Amine II-H:

The synthesis of the starting material has been described (patent DE487014).

Scheme II, Step i:

30 g ((0.14 mol) of the starting material was suspended in 600 ml of MeOH. Then a small amount of Raney nickel was added after which hydrogenation was started (atmospheric, room temperature). After 24 hours 7.2 liters (theoretical amount 9.4 liters) of hydrogen was absorbed. To the reaction mixture 150 ml of THF was added and another small amount of Raney nickel. After one hour the reaction mixture was filtered over hyflo, the residue washed with THF. The filtrate was concentrated in vacuo, yielding 25.2 g (98%) of the correspondig aniline.

Scheme II, Step ii:

24.2 g (131.2 mmol) of the aniline of the previous step and 25.8 g (144.3 mmol) of bis (2-chloroethyl)amine were suspended in 675 ml of chlorobenzene. While stirring, 25 ml of solvent were distilled off with the aid of a Dean-Stark apparatus. After removal of the Dean-Stark apparatus, the reaction was allowed to reflux for 48 hours. When the reaction mixture had come to room temperature, the mixture was decanted and the residue washed twice with Et₂O. Then 400 ml of MeOH were added after which the mixture was warmed until almost all of the residue was dissolved. Then 200 ml of silica were added after which the whole was concentrated in vacuo. Then the residue was put on top of a flash chromatography column using DMA 0.75 as the eluent. After removal of the solvent a residue was isolated which was suspended in about 100 ml of acetonitrile and stirred for 4 hours. Filtration and drying yielded 17 g of the desired piperazine II-H as a free base.
Synthesis of Amine IV-H:

The toluene used in this experiment was degassed for three hours prior to usage. 1.48 g (1.61 mmol) of Pd₂(dba)₃ and 3.02 g (4.85 mmol) of BINAP were put into 400 ml of toluene after which the mixture was stirred and heated to 105° C. for 0.5 hours after which the mixture was allowed to room temperature. Subsequently were added to the reaction mixture: 27.

Scheme IV, Step i:

20.5 g (81.3 mmol) of dibromophenol and 20 g of potassium carbonate were suspended in 400 ml of aceton, after which 15.7 ml of benzylbromide were added. The reaction mixture was refluxed for 24 hours. After the mixture had reached room temperature, it was concentrated in vacuo. Subsequently water was added and CH₂Cl₂. The organic layer was filtered with a water repellant filter, the dry filtrate concentrated in vacuo after which it was dissolved again in 200 ml of acetonitrile. Subsequently, 15 ml of piperidine were added after which the temperature was raised to 60° C. for one hour. The reaction mixture was concentrated in vacuo and CH₂Cl₂ was added. The latter was washed with: 1N HCl (3×), water, 2N NaOH, and again water. The organic layer was filtered with a water repellant filter, the dry filtrate concentrated in vacuo yielding 27.6 g (99%) of the corresponding benzylated phenol.

Scheme IV, Step ii:

6 g (80.7 mmol) of the benzylated compound (step i) dissolved in 50 ml of toluene, 9.2 g (80.7 mmol) of the (α,α′)-dimethylpiperazine and 10.08 g (104.9 mmol) of sodium tertbutoxide. The resulting mixture was heated at 105° C. for 20 hours, after which it was allowed to reach room temperature. The mixture was diluted with CH₂Cl₂ after which it was filtered over hyflo and concentrated in vacuo. The residue was put on top of a flash chromatography column (SiO₂) using DMA 0.125. The combined product containing fractions yielded after concentration in vacuo 7.7 g (26%) of the almost pure phenylpiperazine.

Scheme IV, Step iii:

This step was done analogously to the procedure described in the previous step ii (scheme IV). In this case benzylamine was used in the Buchwald reaction. Yield: 88%.

Scheme IV, Step iv:

7 ml (98 mmol) of acetyl chloride was added dropwise to 70 ml of cooled absolute ethanol, stirring was continued for 15 minutes. The latter solution was added to a solution of 11.5 g (28.7 mmol) of the dibenzyl product of step iii in 250 ml of methanol. Subsequently 1.5 g of Pd/C (10%) was added, after which the reaction mixture was hydrogenated for 24 hours. The mixture was filtered over hyflo, the filtrate concentrated in vacuo. The residue containing the amino phenol HCl salt was directly used in step v.

Scheme IV Step v:

The residue (28.7 mmol) obtained in step iv, 52 ml of DIPEA (298 mmol), and 20.9 g (129 mmol) of CDI were added to 750 ml of THF after which the mixture was refluxed for 20 hours under a nitrogen atmosphere. After cooling to room temperature, the mixture was concentrated in vacuo, to the residue CH₂Cl₂ and 5% NaHCO₃ were added, the whole being stirred for one hour. Extraction with CH₂Cl₂ (3×), the water fraction was concentrated and extracted again (CH₂Cl₂, 3×). The combined organic fractions were concentrated in vacuo, the residue contained a considerable amount of imidazol. The whole was solved in 120 ml of acetonitrile after which the solution was allowed to reach room temperature. The precipitate which formed was filtered yielding almost pure piperazine IV.
Synthesis of Amine V-H:
Scheme V, Steps i, ii and iii:

Synthesis of V-H has been described in WO97/36893. The steps i, ii and iii were done analogously to steps i, ii and iii in scheme VI.
Synthesis of Amine VI-H:
Scheme VI, Step i:

While stirring, 3.8 g (15 mmol) of piperazine II-H were suspended in 5.48 ml (31.5 mmol) of DIPEA and the mixture was brought to −40° C. A solution of 3.14 g (14.4 mmol, 0.96 eq) of Boc-anhydride in 30 ml of CH₂Cl₂ was added dropwise in 100 minutes. Stirring was continued at −40° C. (1 hour), then at −30° C. (2 hours), and the reaction mixture was allowed to come to room temperature (16 hours). Then water and some MeOH were added after which it was extracted with CH₂Cl₂. The combined organic fractions were filtered with a water repellant filter, the dry filtrate mixed with 50 ml of silica after which the whole was concentrated in vacuo. Then the residue was put on top of a dry chromatography column (SiO₂) using CH₂Cl₂/MeOH (98/2) as the eluent. The part of the column containing the product was cut out, and the product washed out of the column material with CH₂Cl₂/MeOH (98/2) yielding 3.55 g (67%) of the desired N-Boc II.

Scheme VI, Step ii:

4.5 g (12.7 mmol) N-Boc II together with 5.8 g (3.3 eq) of potassium carbonate were suspended in 100 ml of aceton. While stirring, the reaction mixture was cooled to −10° C. after which 0.87 ml (14 mmol, 1.1 eq) of methyl iodide was added dropwise. After 15 minutes, the reaction mixture was allowed to reach room temperature and stirring was continued for 14 hours. Subsequently, the reaction mixture was concentrated in vacuo, the residue mixed with water and CH₂Cl₂. The water layer was separated and extracted twice with CH₂Cl₂. The combined organic layers were filtered with a water repellant filter, the dry filtrate concentrated in vacuo yielding 4.5 g (98%) of the corresponding N′-methylated N-Boc II.

Scheme VI, Step iii:

While stirring at −10° C., 5 ml of acetyl chloride (70.4 mmol, 5.8 eq) was added dropwise to 65 ml of ethanol. The latter solution was added to 4.5 g (12.2 mmol) of the N′-methylated N-Boc II isolated in step ii. The resulting mixture was stirred for 3 hours at 55° C., then the reaction mixture was allowed to reach room temperature and stirring was continued for 14 hours. Subsequently, the mixture was concentrated in vacuo after which the residue was suspended in di-isopropyl ether and stirred for 2 hours. The precipitate was isolated by filtration yielding 3.6 g (97%) of piperazine VI-H.HCl.
Synthesis of Amine VII-H:
Scheme VII, Step i:

This step was done analogously to step i in scheme IV. After chromatograhic purification an oil containing the benzylated product, was isolated in 88% yield. The oil solidified upon standing.

Scheme VII, Step ii:

This step was done analogously to step ii in scheme IV. Boc-piperazine was used in this Buchwald reaction. Yield after chromatographic purification: 44% of a brown oil.

Scheme VII, Step iii:

This step was done analogously to the procedure described in the previous step ii (scheme VII). In this case benzylamine was used in the Buchwald reaction. Yield after chromatographic purification: 73% of a brown oil.

Scheme VII, Step iv:

11.91 g (24.3 mmol) of the dibenzylated product isolated in previous step iii (scheme, VII) was suspended in a mixture of 110 ml of ethanol, 72 ml of water and 11 ml of acetic acid. While stirring, 0.5 g of Pd(OH)₂/C was added and hydrogenation was started for 6 days. After one day and after 3 days an additional small amount of Pd(OH)₂/C was added. The reaction mixture was filtered over hyflo, the filtrate concentrated in vacuo. The residue was treated with toluene and concentrated in vacuo, this procedure was repeated, leaving a dark sirup 7.9 g (88%), containing the amino phenol.

Scheme VII, Step v:

This step (ring closure with CDI) was done analogously to step v in scheme IV. The crude product after work up was chromatographed (flash column, SiO₂, eluent DCM/MeOH 97/3) yielding 7.6 g of an impure brown foam. A second chromatography (flash column, SiO₂, eluent EtOAc/petroleum ether 1/2) yielded 3.3 g (42%) of pure brown foam, containing the N-Boc protected benzoxazolinone piperazine.

Scheme VII, Step vi:

This methylation step was done analogously to the procedure described in step ii (scheme VI). Yield: 98% of a brown foam of 97% purity.

Scheme VII, Step vii:

This deprotection step was done analogously to the procedure described in step iii (scheme VI). Yield: 94% of a light pink solid of 98% purity, containing the product VII-H.HCl.
Synthesis of Amine VIII-H:
Scheme VIII, Step i:

The starting material synthesis has been described in EP0189612.

4.91 g (32.7 mmol) of the anilin was suspended in 75 ml of 48% of HBr/water, while it was cooled to −5° C. Subsequently 2.27 g (33 mmol) of sodium nitrite dissolved in 4 ml of water, were added dropwise during 15 minutes. Stirring was continued at 0° C. for 15 minutes.

Subsequently, the reaction mixture was added, in one time, to a 0° C. solution of 2.42 g (16.9 mmol) CuBr in 20 ml of 48% HBr/water. After 30 minutes the reaction mixture was heated to 85° C. for one hour, after which it was allowed to reach room temperature, stirring was continued for 14 hours. To the mixture diethyl ether and water were added, after shaking the organic layer was isolated which was washed with water. The organic layer, together with some silica, was concentrated in vacuo, and the residue was put on top of a flash chromatography column (SiO₂) using Et₂O/petroleum ether (1/1), and later on pure Et₂O as the eluent. The combined product containing fractions yielded after concentration in vacuo 3.3 g (47%) of the desired corresponding bromo product.

Scheme VIII, Step ii:

This step was carried out identical to step ii in scheme VI. Yield: 92% of the corresponding methylated bromo compound.

Scheme VIII, Step iii:

In the following order 6.82 g (29.9 mmol) of the methylated bromo compound, 4.03 g (35.9 mmol) of the dimethyl piperazine, 13.6 g (41.9 mmol) of Cs₂CO₃, 1.42 g (2.99 mmol) of X-Phos (see Huang et al., J. Am. Chem. Soc., 125(2003)6653). and 0.55 g (0.6 mmol) of Pd₂(dba)₃ were added to 225 ml of toluene which was degassed for 4 hours prior to usage. While stirring and under a nitrogen atmosphere the temperature was raised to 100° C. for 20 hours, after which it was allowed to reach room temperature. The mixture was diluted with CH₂Cl₂ after which it was filtered and concentrated in vacuo. The residue was put on top of a flash chromatography column (SiO₂) using DMA 0.25. The combined product containing fractions yielded after concentration in vacuo 0.73 g (9%) of the desired pure piperazine VIII-H.
Synthesis of Amine IX-H:
Scheme IX, Steps i, ii and iii:

Synthesis of I-H has been described in WO97/36893. The steps i, ii and iii were done analogously to steps i, ii and iii in scheme VI.

Below, the different structures of Q1 to Q64 are given:

In these formulae ‘Q’, the dot represents the attachment to the phenylpiperazine part of the compounds of formula (1).
Synthesis of Q1-6:

All starting materials (phenols and alkynes) were prepared according to procedures described in the literature:

Alkynes: Davison, Edwin C.; Fox, Martin E.; J. Chem. Soc. Perkin Trans. 1; 12(2002). 1494-1514. Yu, Ming; Alonso-Alicia, M.; Bioorg. Med. Chem.; 11 (2003)2802-2822. Phenols: Buchan; McCombie; J. Chem. Soc.; 137 (1931) 144. Finger et al; J. Amer. Chem. Soc.; 81 (1959) 94, 95, 97. Berg; Newbery; J. Chem. Soc.; (1949) 642-645.

Scheme 1-6, Step i:

R═CN, n=2

A stirred solution of the silylated alcohol (3.35 g, 10 mmol) in 20 ml of dry THF was cooled to −70° C. 2.5M n-BuLi (4.8 ml, 12 mmol) was slowly added dropwise at such a rate that the temperature was kept below −65° C. The solution was allowed to warm to −20° C. and stirring was continued for 1 hour during which the color of the solution changed from light to dark yellow. The solution is again cooled to −70° C. and a solution of tert-butyldimethylsilylchloride (1.66 g, 11 mmol) in 15 ml of dry THF is slowly added dropwise in 10 minutes. The reaction mixture was allowed to warm to room temperature and stirring was continued for 20 h. The reaction mixture was quenched by the addition of saturated NH₄Cl and extracted 2× with Et₂O. The combined Et₂O layers were washed with 5% NaHCO₃ (1×) and H₂O (1×) and dried (Na₂SO₄). The Et₂O fraction was concentrated under reduced pressure and the residue was chromatographed (SiO₂) using DMA/petroleum ether 1/5 as eluent to give 3.35 g (75%) of the silylated alkyne as a colorless oil.

Scheme 1-6, Step ii:

A mixture of 4-cyano-2-iodophenol (1.23 g, 5 mmol), silylated alkyne (from step i) (2.18 g, 5 mmol), LiCl (0.21 g, 5 mmol) and Na₂CO₃ (2.38 g, 22.5 mmol) in 20 ml DMF was degassed by bubbling nitrogen through the solution for 2 h. Pd(OAc)₂ (50 mg, 0.20 mmol) was added and the reaction mixture was stirred for 7 hours at 100° C. H₂O and hexane were added and the mixture was filtered over hyflo. After separation of the hexane layer, the aqueous layer was extracted with hexane (1×). The combined hexane layers were washed with H₂O (1×) and brine 1×). The hexane fraction was partially evaporated under reduced pressure and 8 g of silicagel was added and stirring was continued for 15 minutes. The silica is filtered off and the filtrate is concentrated under reduced pressure. The residue was chromatographed (SiO₂) using Et₂O/petroleum ether 1/9 as the eluent to give 0.93 g (35%) of the benzfurane derivative as a light yellow oil.

Scheme 1-6, Step iii:

A mixture of the cyclized compound (29.58 g, 52.17 mmol), KF.2H₂O (14.73 g, 156.51 mmol), benzyltriethylammoniumchloride (14.26 g, 62.60 mmol) in 450 ml of CH₃CN was refluxed for 4 h. After cooling to room temperature, CH₃CN was washed 2× with hexane. The CH₃CN fraction was evaporated under reduced pressure. H₂O was added the residue and this was extracted twice with EtOAc. The combined organic layers were washed with respectively H₂O (1×) and brine (1×). The organic layer was dried (Na₂SO₄) and concentrated in vacuo. The residue was subjected to column chromatography (SiO2, eluent: EtOAc/petroleum ether 1:3→EtOAc/petroleum ether 1:1) to yield 9.20 g (82%) of the alcohol Q3-OH as a yellow oil.

Scheme 1-6, Step iv:

PPh₃ (14.38 g, 54.84 mmol) and imidazole (3.73 g, 54.84 mmol) were dissolved in 160 ml of CH₂Cl₂. Iodine (13.92 g, 54.84 mmol) was added and the resulting suspension was stirred for 20 minutes at room temperature. A solution of the alcohol obtained at step iii (9.07 g, 42.19 mmol) in 70 ml of CH₂Cl₂ was added dropwise and the reaction mixture was stirred for 20 h at room temperature. Water was added and after separation the H₂O layer was extracted with CH₂Cl₂. The combined organic layers were washed with respectively 5% NaHSO₃ solution (1×) and H₂O (1×) and dried on Na₂SO₄. The drying agent was removed by filtration and the solvent by concentration in vacuo. The residue was chromatographed (SiO₂) using CH₂Cl₂ as the eluent to give 12.9 g (94%) of the iodide Q3-I as a thick oil which crystallized on standing.
Synthesis of Q7-9:

The 5-bromobenzthiophene was prepared according to: Leclerc, V.; Beaurain, N.; Pharm. Pharmacol. Commun., 6(2000)61-66.

Scheme 7-9, Step i:

Sodium metal (4.5 g, 195.9 mmol) was added in pieces to 260 ml of absolute EtOH. The malonic ester (116 ml, 779 mmol) was added and the reaction mixture was stirred under a nitrogen atmosphere for 30 minutes. The 5-bromobenzthiophene (29.5 g, 97.2 mmol) was added as a suspension in 125 ml of absolute EtOH and stirring was continued at reflux for 18 h. The solvent was evaporated under reduced pressure after which 250 ml H₂O and 15 g NH₄Cl were added to the residue. The aqueous layer was extracted with CH₂Cl₂ (2×) and the combined organic layers were dried (Water Repelling Filter) and the filtrate concentrated in vacuo (by means of an oil pump, 8 mbar). The residue was chromatographed (SiO₂) with CH₂Cl₂/petroleumether 3/2 to give 23.9 g (64%) of the di-ester.

Scheme 7-9, Step ii:

This step was carried out analogous to step ii from Scheme 51.

Scheme 7-9, Step ii:

This step was carried out analogous to step iii from Scheme 51.

Scheme 7-9, Step iv:

This step was carried out analogous to step iii from scheme 10-12.

Scheme 7-9, Step v

This step was carried out analogous to step v from scheme 10-12.

Scheme 7-9, Step vi:

This step was carried out analogous to step iv from scheme 1-6.

Derivatives of Q7 and Q8 were prepared analogously to the above described procedures.
Synthesis of Q10-12:

All reagents were commercially available. The 5-bromobenzthiophene was prepared according to Badger et al., J. Chem. Soc., (1957) 2624, 2628.

Scheme 10-12, Step i:

To a stirred mixture of 5-bromobenzthiophene (22.5 g, 105.6 mmol) and the acid chloride (17.4 ml, 141.3 mmol) in 135 ml benzene at 0° C., SnCl₄ (43.1 ml, 368 mmol) was added in 2 h. Stirring was continued for 4 hours at the same temperature. The reaction mixture was poured into a mixture of 95 ml concentrated HCl (36-38%) in ice. The reaction mixture was extracted with EtOAc and the organic layer was washed with H₂O (3×), 1N NaOH (1×), 5% NaHCO₃ and H₂O (2×). The EtOAc fraction was dried (MgSO₄). The drying agent was removed by filtration and the solvent by evaporation under reduced pressure. The residue was recrystallized from 950 ml MeOH and chromatographed with Et₂O/petroleum ether 1/1 as eluent to give 23.3 g (68%) of the acylated benzthiophene.

Scheme 10-12, Step ii:

To a stirred mixture of the acylated benzthiophene (23.3 g, 71.3 mmol) and powdered NaOH (23 g, 575 mmol) in 285 ml diethyleneglycol, hydrazine hydrate (23 ml, 474 mmol) was added. Stirring was continued for 2 hours at 145° C. after which additional stirring for 2 hours at 180° C. was needed to complete the conversion. The reaction mixture was poured onto ice and acidified with concentrated HCl (36-38%). The aqueous layer was extracted with Et₂O and the organic layer was washed with H₂O (3×) and brine (1×) and dried (MgSO₄). The drying agent was removed by filtration and the solvent by evaporation under reduced pressure yielded 19.7 g (93%) of the acid.

Scheme 10-12, Step iii:

At −5° C., 29 ml of thionyl chloride were added dropwise in 30 minutes to 250 ml of MeOH. The mixture was stirred for 15 minutes during which the temperature was kept between −10° C. and −5° C. The acid (19.7 g, 65.9 mmol) was added in one time to the cooled solution. The reaction mixture was stirred for 1 hour after which is was allowed to warm to room temperature and stirred for an additional 20 h. The reaction mixture was concentrated in vacuo and the residue was chromatographed (SiO₂) with CH₂Cl₂ as the eluent to give 20.6 g (100%) of the methyl ester.

Scheme 10-12, Step iv:

A mixture of the methyl ester (20.6 g, 65.8 mmol) and zinc cyanide (4.64 g, 39.5 mmol) in 85 ml of dry DMF was degassed by bubbling nitrogen through the solution for 1 h. Palladium tetrakis, Pd(PPh₃)₄, (3.8 g, 3.29 mmol) was added under a nitrogen atmosphere and the reaction mixture was stirred for 16 hours at 90° C. The reaction mixture was diluted with 200 ml toluene and filtered through a pad of Hyflo. The organic layer was washed with 5% NaHCO₃ (2×) and brine (1×). The organic layer was dried (MgSO₄). The drying agent was removed by filtration and the solvent by evaporation under reduced pressure. The residue was chromatographed (SiO₂) using CH₂Cl₂/petroleum ether 3/2→CH₂Cl₂ as eluent to give 15.6 g (92%) of the 5-cyanobenzthiophene.

Scheme 10-12, Step v:

To a stirring solution of the 5-cyanobenzthiophene (15.6 g, 60.2 mmol) in 250 ml 96% EtOH at 15° C. was added sodium borohydride (22.8 g, 602 mmol) in one time. The reaction mixture was stirred at room temperature for 48 h. H₂O was added and the aqueous layer was extracted with Et₂O (3×). The combined organic layers were washed with brine (1×). The Et₂O fraction was dried (MgSO₄). The drying agent was removed by filtration and the solvent by evaporation under reduced pressure. The residue was chromatographed (SiO₂) with Et₂O/CH₂Cl₂ 1/9 as eluent to give 9.2 g (66%) of the alcohol Q12-OH.

Scheme 10-12, Step vi:

Was prepared according to the procedure described in Scheme 1-6, Step iii.

Q10-OH and Q11-OH were prepared similarly using steps i, ii, iii and v respectively.
Synthesis of Q13-20:

All starting materials were commercially available.

Scheme 13-20 Step i:

To a stirring solution of 3-nitro-p-tolunitrile (16.58 g, 102.3 mmol) in 55 ml DMF was added DMF-dimethylacetale (15.24 g, 128.1 mmol). The reaction mixture turned dark red and was stirred at 110° C. for 3 h. The solvent was removed under reduced pressure and taken up in a mixture of 300 ml EtOH and 300 ml acetic acid. The reaction mixture was heated to 60° C. and iron powder (33 g, 594 mmol) was added in portions. The reaction mixture was refluxed for 2 hours and filtered over a pad of Hyflo. Et₂O was added to the filtrate and the acidic layer was extracted with Et₂O (1×). The Et₂O fraction was concentrated in vacuo. The residue was chromatographed (SiO₂) with CH₂Cl₂ as the eluent to give 7.02 g (48%) of a solid, containing the 6-cyano-indole.

Scheme 13-20 Step ii:

To a stirring suspension of NaH (60%) (1.13 g, 25.96 mmol) in 60 ml DMF under a nitrogen atmosphere was added 6-cyanoindole of step i (3.51 g, 24.72 mmol) in portions. After stirring at room temperature for 1 hour the 1-(dimethyl-tert.butylsilyl)-3-bromo propane (6.30 ml, 27.29 mmol) was added dropwise at −5° C. The reaction mixture is stirred at room temperature for 20 h. 400 ml H₂O and 400 ml Et₂O were added. The Et₂O layer was separated and the aqueous layer was extracted 1× with Et₂O. The combined Et₂O layers were concentrated in vacuo. The residue was chromatographed (SiO₂) with CH₂Cl₂/petroleum ether 3/1 as the eluent to give 5.50 g (71%) as a light yellow oil.

Scheme 13-20 Step iii:

Was performed analogously to step iii in scheme 1-6, and yielded Q19-OH.

Scheme 13-20 Step iv:

The conversion of the resulting alcohols to the corresponding iodo derivatives was performed analogously to the procedure described in scheme 1-6 step iv.

The 6-cyano-indole derivative Q20-OH was prepared according to the procedure described above.

The indole, 6-Fluoroindole and 6-Chloroindole were commercially available and were further converted to the indole derivatives Q13-18-OH according to the procedures given above.
Synthesis of Q21:
Scheme 21 Step i:

To a stirred suspension of NaH (55%) (0.48 g, 20 mmol) in 20 ml NMP at room temperature was added dropwise a solution of benzimidazole (1.18 g, 10 mmol) in 20 ml NMP. The reaction mixture turned light red and hydrogen forming was observed. After stirring at room temperature for 30 minutes 3-chlorobromopropane (1.08 ml, 11 mmol) in 10 ml NMP was added dropwise. The reaction mixture was stirred at room temperature for 2 hours after which the reaction mixture was heated at 100° C. for 2 h. After additional stirring at room temperature for 72 h, H₂O and EtOAc were added. The layers were separated and the aqueous layer was extracted with EtOAc (2×). The combined organic layers were washed with brine (1×) and dried (MgSO₄). The drying agent was removed by filtration and the solvent by evaporation under reduced pressure to give 2.9 g of Q21-Cl (150%, still NMP present) as an oil. This was used in coupling reactions with amines.
Synthesis of Q22-23:

All reagents were commercially available.

Scheme 22-23 Step i:

To a stirring solution of 2,4-difluoronitrobenzene (8 g, 50.3 mmol) in 100 ml CH₃CN was added 4-aminobutanol (5.61 ml, 60.4 mmol) and DIPEA (20.9 ml, 120.7 mmol). The reaction mixture was stirred at room temperature for 72 h. The solvent was evaporated under reduced pressure and CH₂Cl₂ was added to the residue. The CH₂Cl₂ fraction was washed with H₂O (2×), dried (by a Water Repelling Filter) and the filtrate evaporated under reduced pressure. The residue was chromatographed (SiO₂) with Et₂O as the eluent to give 9.68 g (84%) of the amino-alkylated product.

Scheme 22-23 Step ii:

To a solution of the amino-alkylated product (from step i) (9.68 g, 42.5 mmol) in 250 ml EtOH (96%) was added 1 g 10% Pd/C after which the mixture was hydrogenated at room temperature (1 atm) for 3 h. The reaction mixture was filtered through a pad of Hyflo and the black filtrate was concentrated in vacuo under reduced pressure to give 8.42 g (100%) of the corresponding aniline.

Scheme 22-23 Step iii:

A mixture of the aniline (from step ii) (8.42 g, 42.5 mmol) in 25 ml formic acid (96%) was refluxed for 2.5 hours after which it was allowed to cool to room temperature. H₂O was added and after cooling, to the reaction mixture 50 ml of 50% NaOH was added. After stirring for 2 hours the aqueous layer was extracted with CH₂Cl₂. The CH₂Cl₂ fraction was dried (by a Water Repelling Filter) and concentrated in vacuo under reduced pressure. The residue was chromatographed (SiO₂) with CH₂Cl₂/MeOH 9:1 as the eluent to give 8.1 g (92%) of the benzimidazole.

Scheme 22-23 Step iv:

The conversion of the resulting alcohols to the corresponding iodo derivatives was performed according to the procedure described in scheme 1-6 step iv. In this case triphenylphosphine on solid support was used.

Q22-OH was prepared via the same procedure as described above.
Synthesis of Q24:

All reagents were commercially available.

Scheme 24 Step i:

A suspension of sodium borate tetrahydrate (32.5 g, 211.2 mmol) in 195 ml of acetic acid was heated until the temperature of the reaction mixture was above 50° C. The reaction temperature was kept this way while 2-chloro-4-cyanoaniline (5.93 g, 38.9 mmol) was added in portions over 1 h. Stirring and heating were continued for 2 hours on an oil bath of 62° C. After cooling to room temperature the reaction mixture was poured into 1 L icewater. The aqueous layer was extracted with Et₂O (3×). The combined organic layers were washed with H₂O (2×) and dried (MgSO₄). The drying agent was removed by filtration and the solvent by evaporation under reduced pressure. The residue was chromatographed (SiO₂) with Et₂O/petroleum ether 1/3 as eluent to give 5.27 g (74%) of the oxidized product.

Scheme 24 Step ii:

To a stirring solution of 2-chloro-4-cyanonitrobenzene from step i (2.48 g, 13.6 mmol) in 12 ml DMF was cooled in ice. 4-aminobutanol (5.50 ml, 59.3 mmol) was added and the reaction mixture was slowly allowed to warm to room temperature after which stirring was continued at room temperature for 72 h. H₂O was added and the aqueous layer was extracted with CH₂Cl₂ (2×) The combined organic layers were washed with H₂O (3×), dried (by a Water Repelling Filter) and evaporated under reduced pressure. The residue was chromatographed with Et₂O/petroleum ether 4:1 as eluent to give 2.6 g (49%) of the amino-alkylated product.

Scheme 24 Step iii:

Prepared according to step ii, in scheme 22-23.

Scheme 24 Step iv:

Prepared according step iii, in scheme 22-23.

Scheme 24 Step v:

Prepared according step iv, in scheme 22-23.
Synthesis of Q25-28:

All reagents were commercially available.

Scheme 25-28 Step i:

To a stirring solution of 3-nitro-p-tolunitrile (8.1 g, 50 mmol) in 30 ml DMF was added DMF-dimethylacetale (13.3 ml, 100 mmol) and the reaction mixture was stirred at 120° C. for 3 h. The solvent was evaporated under reduced pressure and the residue was taken up in CH₂Cl₂. The CH₂Cl₂ fraction was washed with H₂O (2×), dried (by a Water Repelling Filter). The drying agent was removed by filtration and the solvent by evaporation under reduced pressure to give 10.6 g (98%) of the adduct.

Scheme 25-28 Step ii:

To a stirring emulsion of the adduct (from step i) (6 g, 27.6 mmol) in 175 ml Et₂O was added 8.1 g NH₄Cl and 29 g zinc granules (40 mesh). After stirring at room temperature for 2 hours 100 ml THF was added to dissolve the starting material. After an additional stirring for 6 hours the reaction mixture was filtered over a pad of Hyflo. Half of the resulting filtrate was used in the next step.

Scheme 25-28 Step iii:

To the filtrate of the former step ii was added 2-bromoethanol (7.9 ml, 112 mmol), Aliquat (0.6 g, 10 mol %) and 90 ml 10% NaOH. The reaction mixture was stirred at room temperature for 20 h. After separation of the layers, the aqueous layer was extracted with Et₂O (1×). The combined organic layers were washed with H₂O (4×) and dried (MgSO₄). The drying agent was removed by filtration and the solvent by evaporation under reduced pressure (by means of an oil pump). The residue was chromatographed (SiO₂, eluent: CH₂Cl₂ 4 CH₂Cl₂/Et₂O 4:1) to give 1 g (36%) of the corresponding alcohol Q27-OH.

Scheme 25-28 Step iv:

The conversion of the resulting alcohols to the corresponding iodo derivatives was performed according to the procedure described in scheme 1-6 step iv.

Q25-OH, Q26-OH and Q28-OH were prepared analogously to the procedure described above.
Synthesis of Q29:

The naphtylpropylalcohol was prepared according to: Searles, J. Amer. Chem. Soc., 73 (1951) 124.

Scheme 29 Step i:

The conversion of the resulting alcohol to the corresponding iodo derivative was performed according to the procedure described in scheme 1-6 step iv.
Synthesis of Q30:

2-chloro-7-iodo-naphtalene was prepared according to the literature (Beattie; Whitmore; J. Chem. Soc. 1934, 50, 51, 52)

Scheme 30 Step i:

A 100 ml roundbottom flask under an nitrogen atmosphere was charged with 2-chloro-7-iodo-napthalene (11 mmol, 3.60 g), allyl-tributyltin (13 mmol, 4.30 g, 3.96 ml), tetrakis(triphenylphosphine)palladium(0) (0.55 mmol, 0.635 g) and 10 ml degassed benzene. The mixture was heated to relfux under a nitrogen atmosphere and after 20 hours another portion of tetrakis(triphenylphosphine)palladium(0) (0.55 mmol, 0.635 g) was added. The mixture was again heated at reflux for 20 hours after which it was allowed to cool to room temperature after which it was poured into 70 ml of a 10% KF-solution. After 30 min stirring at room temperature the suspension was filtered over Hyflo Supercel®. The filtrate was washed with water, brine and dried (Na₂SO₄). Column chromatography on silica gel (eluens 1/9 toluene/petroleum ether) afforded almost pure 2-allyl-7-chloro-napthalene (1.80 g, 80%).

Scheme 30 Step ii:

A 100 ml threeneck roundbottom flask under a nitrogen atmosphere was charged with 2-allyl-7-chloro-napthalene (1.80 g, 8.9 mmol) and 12 ml of dry THF. The mixture was cooled in an ice-bath and borane-THF (3.05 mmol, 3.05 ml 1.0 M borane in THF) was added dropwise in about 20 minutes After the addition the mixture was allowed to warm to room temperature and stirred for 20 hours. 3.0 N NaOH solution (2.65 mmol, 0.89 ml) was then added to the solution and the mixture was cooled in a waterbath while adding 30% hydrogen peroxide (10.62 mmol, 1.1 ml) dropwise at such a rate that the temperature did not exceed 30° C. After the addition the mixture was stirred for 6 hours at room temperature.

Water and diethyl ether were added and the organic layer was separated. The water layer was extracted again with ethyl ether and the combined organic extracts were washed with water, brine and dried (Na₂SO₄). The drying agent was removed by filtration and the solvent by evaporation in vacua. Flash column chromatography on silica gel (eluent: 1/99 methanol/dichloromethane) afforded 3-(7-chloro-napthalene-2-yl)-propan-1-ol (0.79 g, 40%) Q30-OH.

Scheme 30 Step iii:

The conversion of the resulting alcohol to the corresponding iodo derivative was performed according to the procedure described in scheme 79-84 step iii, yielding Q30-I.
Synthesis of Q31:

The fluorobromonaphtalene was prepared according to: Adcock, W. et al., Aust. J. Chem., 23 (1970)1921-1937.

Scheme 31 Step i:

To a stirred suspension of magnesium turnings (0.49 g, 20 mmol) and 0.1 ml 1,2-dibromoethane in 20 ml THF was added the fluoronaphtalene (0.45 g, 2 mmol) in one time. After the start of the grignard a solution of the fluoronaphtalene (4.06 g, 18 mmol) in 25 ml THF was slowly added dropwise. The temperature rose during the addition to 40° C. The reaction mixture was stirred at room temperature for 2 hours until all the magnesium had disappeared. A freshly prepared solution from LiCl and CuCN in THF was added dropwise at −10° C. which resulted in a dark green solution. At the same temperature was added dropwise a solution of allyl bromide (1.9 ml, 22 mmol) in 15 ml THF. After the complete addition the reaction mixture was stirred at −10-0° C. for 30 minutes. The green color disappeared and stirring was continued at room temperature for 20 h. The reaction mixture was poured into 200 ml of saturated NH₄Cl and extracted with CH₂Cl₂ (3×). The combined organic layers were washed with brine and dried (MgSO₄). The drying agent was removed by filtration and the solvent by evaporation under reduced pressure. The residue was chromatographed (SiO₂) using petroleum ether as eluent to give 1.65 g (44%) of the corresponding allylfluoro-naphtalene.

Scheme 31 Step ii:

To a cooled stirring solution of the allyl-fluoronaphtalene (1.65 g, 8.8 mmol) in 10 ml THF at −5° C. was slowly added dropwise 3.05 ml 1.0 M Borane.THF-complex. After stirring for 20 minutes at the same temperature and additional stirring at room temperature iodine (2.11 g, 8.6 mmol) was added in one time. 3.1 ml of a freshly prepared 2.7 M solution of sodium metal in MeOH) was slowly added dropwise (exothermic) after which the reaction mixture is stirred at room temperature for 20 h. 75 ml NaHSO₃ was added and the aqueous layer was extracted with CH₂Cl₂ (3×). The organic layer was washed with brine (1×) and dried (MgSO₄). The drying agent was removed by filtration and the solvent by evaporation under reduced pressure. The residue was chromatographed (SiO₂) using petroleum ether as eluent to give 1.25 g (46%) of the iodide Q31-I as a white solid.
Synthesis of Q32-39, Q41-42:
Scheme 32-39, 41-42 Step i:

A mixture of KOH pellets (140 g, 2.5 mol) and 10 ml H₂O in a nickel crucible was heated to 250° C. with a Bunsen burner while being stirred with a stainless steel stirrer. The flame is removed and 7-amino-2-naphtalenesulfonic acid sodium salt (0.245 mol, 60.0 g) was added to the clear liquid in 3 portions. The clear liquid changes into a thick black slurry which is again strongly heated with a Bunsen burner. At about 280° C. gas evolved and the temperature of the mixture quickly rises to 310-320° C. This temperature was maintained for 8 minutes after which the mixture was allowed to cool to about 200° C. The thick black paste was carefully transferred to a 3 litre beaker filled with ice. The product of 2 runs were combined and neutralized with concentrated HCl under cooling with an ice-salt bath. The suspension wa filtered and the black solid wa washed with 4 500 ml portions of 1.0 N HCl and discarded. The brown, clear filtrate that is obtained was cooled in an ice-salt bath and KOH-pellets are added until a light suspension was obtained. After addition of a saturated NH₄OAc-solution the green-grey solid fully precipitates and was collected through filtration to obtain 7-amino-naphtalene-2-ol (27.9 g, 36%) after drying in the air.

Scheme 32-39, 41-42 Step ii:

7-amino-naphtalene-2-ol (0.169 mol, 27.0 g) is suspended in 750 ml DCM and TEA (0.169 mol, 17.2 g, 23.6 ml) was added. The mixture wais stirred for 30 min at room temperature after which it was cooled to −5° C. in an ice-salt bath. A solution of p-Tosylchloride (0.17 mol, 32.4 g) in 250 ml DCM was added over a period of 2.5 hours at −5-0° C. The mixture was stirred for 10 minutes at −5-0° C. after which it was allowed to warm to room temperature and stirred for 18 hours. 1 L of H₂O was added to the mixture and the resulting suspension was filtered over Hyflo Super Cel® and the filtrate was transferred to a separatory funnel. After extracting the organic layer, the water-layer was again extracted with DCM (2×). The combined organic layers are washed with brine, dried (Na₂SO₄) and concentrated in vacuo to give 51.5 g of a black oil which was purified by column chromatography on silica gel (eluens 1/1 ethylacetate/petroleum ether) to afford toluene-4-sulfonic acid-7-amino-napthalene-2-yl-ester (12.1 g, 23%).

Scheme 32-39, 41-42 Step iii:

A 500 ml threeneck roundbottom flask made from PFA was charged with 100 g Pyridine/HF complex (30:70% w/w) and cooled to −10° C. with an ice/EtOH bath toluene-4-sulfonic acid-7-amino-napthalene-2-yl-ester (38.6 mmol, 12.1 g) was added in one portion and the mixture was stirred for 10 minutes after which a clear purple solution was obtained. This solution was cooled to <−30° C. in an dry-ice cooling bath and sodium nitrite (42.5 mmol, 2.93 g, dried by heating at 140° C. for 3 days) was added in one portion. The dry-ice bath was replaced by a normal ice-bath and the mixture was stirred at 0° C. for 20 minutes after which it was heated to 55-60° C. on an oilbath (evolution of nitrogen was observed). After 1.5 hours nitrogen evolution ceased and the mixture was allowed to cool to room temperature and poured into a large beaker filled with ice. The mixture was transferred to a separatory funnel and extracted 3 times with DCM. The organic layers where pooled together, washed with brine and dried (Na₂SO₄). Concentration in vacuo afforded 10.4 g of a red oil which was purified by flash column chromatography on silica gel (eluens 1/4 ethylacetate/petroleum ether) to give toluene-4-sulfonic acid-7-fluoro-napthalene-2-yl-ester (7.1 g, 58%)

Scheme 32-39, 41-42 Step iv:

A 500 ml roundbottom flask protected with a CaCl₂-tube was charged with toluene-4-sulfonic acid-7-fluoro-napthalene-2-yl-ester (22.4 mmol, 7.1 g) and 200 MeOH. The suspension was heated until a clear solution was obtained and then cooled down to room temperature in a waterbad to afford a fine suspension. Magnesium (179 mmol, 4.36 g) was added to the mixture which was then stirred for 4 hours at room temperature. The brown suspension was cooled in an ice-EtOH bath and acidified with 6N HCl and then concentrated in vacua. The mixture was transferred to a separatory funnel and extracted 3 times with ethylether. The organic extracts are pooled together, washed with brine and dried (Na₂SO₄). The drying agent was removed by filtration and the solvent by evaporation in vacua. Flash column chromatography on silica gel (eluens dichloromethaan) afforded unpure 7-fluoro-napthalene-2-ol (4.69 g) as an off white solid. This solid was dissolved in DCM and extracting 3 times with 2N NaOH-solution. The basic extracts were combined and acidified with 3N HCl while cooling with an ice bath. White crystals precipitated from the solution and were collected by filtration and dried in the air to afford pure 7-fluoro-napthalene-2-ol. (3.16 g, 87%)

Scheme 38-45: 47-48, Step v:

To a stirred suspension at −5° C. 0.97 g (6 mmol) of 2-hydroxy-7-fluoronaphtalene, 2.83 g (10.8 mmol) of triphenylphosphine and 1.11 ml (12.6 mmol) of 3-bromo-1-propanol in 30 ml of toluene, was added dropwise a solution of 2.13 ml (10.8 mmol) DIAD in 5 ml toluene. The reaction mixture was allowed to reach room temperature after which stirring was continued overnight. The reaction mixture was concentrated in vacuo and the residue taken up in 30 ml of diethylether. The mixture was filtered an the filtrate concentrated in vacuo and the residue subjected to flash column chromatography (SiO2, eluent: CH₂Cl₂/petroleum ether 1/5). Yield 1.28 g (75%) of Q37-Br.

Q32 was synthesized as Q32-I, Q33-36, Q38-39 and Q41-42 derivatives were prepared similarly to the above described procedures (as bromides).
Synthesis of Q40, Q43:
Scheme 40, 43 Step i:

A mixture of 7-fluoro-2-naphtol (see Scheme 32-39, 41-42 step iv) (0.62 g, 3.82 mmol), the alkene (1.11 ml, 9.56 mmol) and K₂CO₃ (1.58 g, 11.5 mmol) in 35 ml CH₃CN was refluxed for 3 hours after which was was cooled to room temperature and evaporated under reduced pressure. The residue was taken up in H₂O and Et₂O and extracted with Et₂O (2×). The combined organic layers were washed with H₂O (1×) and brine (1×) after which it was dried (Na₂SO₄). The drying agent was removed by filtration and the solvent by evaporation under reduced pressure. The residue was chromatographed (SiO₂) with CH₂Cl₂/petroleum ether 1/5 as eluent to give 0.56 g (58%) of the fluoronaphthol derivative Q43-Cl as a colorless oil.
Synthesis of Q44:
Scheme 44 Step i:

For the fluornaphtol, see Scheme 32-39, 41-42 step iv. This Mitsunobu reaction was performed analogously to step v in scheme 32-39, 41-42.

Scheme 44 Step ii:

This step can be performed similar to step iii in scheme 1-6, and yielded Q44-OH.

Scheme 44 Step iii:

Q44-OH was oxidized following the procedure of step i in scheme B2. The product, Q′44-C═O was used in the reductive alkylation of amines.
Synthesis of Q45-50:

The starting acid and reagents were commercially available. The Cl-C4-MgBr was prepared according to: C. R. Hebd, Seances Acad. Ser. C, 268 (1969)1152-1154.

Scheme 45-50 Step i:

To a solution of the acid (25 g, 148.8 mmol) in 140 ml benzene was added 0.07 ml DMF after which oxalylchloride was added all at once. Immediate foaming of the reaction mixture was observed. The reaction mixture was stirred for at room temperature 18 hours and the solvent was removed by evaporation under reduced pressure. Acetonitrile was added to the residue for co-evaporation and again removed by evaporation under reduced pressure to give 27.75 g (100%).

Scheme 45-50 Step ii:

AlCl₃ (27.8 g, 208 mmol) was suspended in 200 ml 1,2-dichloroethane. The mixture was cooled under a nitrogen atmosphere to 0-5° C. and a solution of the acid chloride (27.75 g, 148.8 mmol) in 140 ml 1,2-dichloroethane was added dropwise in 1 h. The cooling bath was removed and after stirring for 30 min., stirring was continued for 2 hours at 70° C. After cooling to room temperature the reaction mixture was poured into a mixture of ice and 330 ml concentrated HCl (36-38%). The aqueous layer was extracted with CH₂Cl₂ and the resulting organic layer was washed with H₂O (2×), 5% NaHCO₃ and brine. The organic layer was dried (MgSO₄). The drying agent was removed by filtration and the solvent by evaporation under reduced pressure to give 19.02 g (85%).

Scheme 45-50 Step iii:

To a cooled solution of 0.5M cyclopropyl magnesiumbromide in THF (100 ml, 50 mmol) at 15° C. was added a solution of the ketone (5.3 g, 35.3 mmol) in 40 ml THF. The reaction mixture was stirred at reflux for 2 hours after which was was cooled in an ice bath. 50 ml saturated NH₄Cl was added dropwise and the aqueous layer was extracted with Et₂O. The Et₂O was washed with brine (1×), dried (MgSO₄) and evaporated under reduced pressure. The residue was dissolved in 85 ml acetic acid and 62 ml of a 20% HBr solution was added. The reaction mixture was stirred for 20 h. H₂O was added and the aqueous layer was extracted with CH₂Cl₂. The organic layer was further washed with H₂O (1×) and 5% NaHCO₃ (1×). The organic layer was dried (by a Water Repelling Filter) and evaporated under reduced pressure. The residue was chromatographed with CH₂Cl₂/petroleum ether 2.5/97.5 as eluent to give 4.44 g (49%) of the indene Q49-Br.

Scheme 45-50 Step iv:

Was prepared according to the procedure as described for step iii, yielding Q50-Cl Q45, Q46, Q47, and Q48 derivatives were made analogously to the above described procedure.
Synthesis of Q51:

The starting materials were commercially available.

Scheme 51 Step i:

A mixture of the Grignard reagent (90 ml, 90 mmol) and CuI (18 mg, 0.02 mmol) was stirred for 15 minutes after which it was cooled in an ice bath. A solution of the di-ester (18.9 ml, 96.7 mmol) in 25 ml THF was added in 90 min and the reaction mixture was, stirred at 0° C. for 2 h. 100 ml saturated NH₄Cl was added dropwise and the aqueous layer was extracted with Et₂O. The Et₂O fraction was washed with brine (1×) and dried (MgSO₄). The drying agent was removed by filtration and the solvent by evaporation under reduced pressure. The residue was chromatographed with CH₂Cl₂/petroleum ether 1/1 as eluent to give 26.17 g (98%) of the adduct.

Scheme 51 Step ii:

To a stirring solution of the adduct (26.17 g, 88.4 mmol) in 222 ml EtOH was added 265 ml 10% NaOH. The reaction mixture was refluxed for 3 hours and the solvent was evaporated under reduced pressure. The residue was cooled in ice and acidified with concentrated HCl (36-38%). The aqueous layer was extracted with EtOAc. The EtOAc fraction was washed with brine (1×) and dried (MgSO₄). The drying agent was removed by filtration and the solvent by evaporation under reduced pressure to give 20.9 g (99%) of the di-acid.

Scheme 51 Step iii:

A mixture of the di-acid (20.9 g, 87.1 mmol) and Cu₂O (0.62 g, 4.34 mmol) in 600 ml CH₃CN was refluxed for 16 h. The solvent was removed by evaporation under reduced pressure and 125 ml 3N HCl was added to the residue. The aqueous layer was extracted with EtOAc. The EtOAc fraction was washed with brine (1×) and dried (MgSO₄). The drying agent was removed by filtration and the solvent by evaporation under reduced pressure to give 16.9 g (99%) of the de-carboxylated product.

Scheme 51 Step iv:

Was prepared according to step i in scheme 45-50.

Scheme 51 Step v:

Was prepared according to step ii in scheme 45-50.

Scheme 51 Step vi:

Was prepared according to step iii in scheme 45-50, yielding Q51-Cl.
Synthesis of Q52-53:
Scheme 52-53 Step i:

A 3 litre beaker was charged with 2-amino-5-fluoro-benzoic acid (64 mmol, 10 g), 100 ml H₂O and 110 ml concentrated HCl and the suspension was cooled to 0° C. in an ice/aceton bath. A solution of natrium nitrite (64 mmol, 4.44 g) in 68 ml H₂O was added dropwise to the mixture while the temperature was maintained at below 3° C. After the addition was complete the brown solution was added in portions over 20 minutes, under a stream of sulfurdioxide, to a solution of 760 ml H₂O saturated with sulfurdioxide cooled at 0-5° C. with an ice-bath. After the addition was complete the ice-bath was removed and the solution was allowed to warm to room temperature while the stream of sulfurdioxide was maintained. After 1 hour the supply of sulfurdioxide was discontinued and the solution was allowed to stand at room temperature overnight. To the dark yellow solution which was obtained was added 620 ml concentrated HCl and after cooling the mixture a yellow precipitate separates which was collected on a cooled buchner funnel. The solid was suspended in a solution of 2 ml concentrated HCl and 200 ml H₂O and the mixture was heated to reflux. After a time the solid dissolves and a clear solution was obtained. After 1.5 hours of reflux a orange/brown solid has crystallized and the mixture was allowed to cool to room temperature and was concentrated to about 50 ml in vacuo. The solid was collected and dried in the air to afford 5-fluoro-1,2-dihydro-indazol-3-one (5.05 g, 52%)

Scheme 52-53 Step ii:

5-fluoro-1,2-dihydro-indazol-3-one (32 mmol 5.05 g) was suspended in 30 ml pyridine and under cooling with an ice-bath chloroethylformiate (64 mmol, 6.94 g, 6.09 ml) was, added dropwise. The mixture was heated to reflux for 3 hours and was then allowed to cool to room temperature ad concentrated in vacuo to afford a dark red oil which crystallizes after the addition of water. The solid was filtered and dried in the air to afford the corresponding urethane (5.52 g, 77%)

Scheme 52-53 Step iii:

To 20 ml toluene under a nitrogen atmosphere was added the urethane derivative (from step ii) (0.45 g, 2 mmol), 3-bromopropanol (0.18 ml, 2.1 mmol), Bu₃P (0.40 g, 2 mmol) and ADDP (0.5 g, 2 mmol). After the addition of ADDP the solution turned clear. The reaction mixture was heated at 85° C. for 20 hours and cooled to room temperature. 2N NaOH and EtOAc were added and the aqueous layer was extracted with EtOAc (2×). The combined organic layers were washed with 2N NaOH (1×), H₂O (1×) and brine (1×) after which the EtOAc was dried (Na₂SO₄) and evaporated under reduced pressure. The residue was chromatographed with CH₂Cl₂/MeOH 99:1 as eluent to give 0.22 g (32%) of the alkylated indazol-3-one.

Scheme 52-53 Step iv:

Was performed according to the procedure as described in scheme A2, Step i.

Scheme 52-53 Step v:

A mixture of the ethyl carbamate (0.38 g, 0.79 mmol) and K₂CO₃ (0.38 g, 2.74 mmol) in 21 ml of MeOH/DME/H₂O (5/1/1) was stirred at room temperature for 4 h. The reaction mixture was further purified using a SCX-column (ion exchange column) with 1N NH₃/MeOH as eluent to rinse the product off the column. The eluate was evaporated under reduced pressure and the residue refluxed in 20 ml CH₃CN. The suspension was filtered by suction to give 0.28 g (86%) of the de-protected product as a light orange solid containing compound 125 which was later transformed into its mono HCl salt (AcCl/MeOH), 125-HCl.

The Q53 analogue can be synthesized as well, as described above.

Compounds 48, 49 and 124 were prepared analogously to the procedures given above.
Synthesis of Q54-59:

The indazoles were preapared according to Christoph Rüchardt, Volkert Hassemann; Liebigs Ann. Chem.; (1980) 908-927.

Scheme 54-59, Step i:

56; R=Cl, n=3:

NaH (55%) (2.14 g, 49.15 mmol) was suspended in 70 ml of dry DMF under a N₂ atmosphere. 6-chloro-indazole (7.5 g, 49.15 mmol) was added at room temperature. The mixture was stirred for 1 hour before cooling with an ice bath and (3-bromo-propoxy)-tert-butyl-dimethyl-silane (11.4 ml, 49.15 mmol) was added dropwise. After stirring for an additional 15 minutes the mixture was allowed to reach room temperature, stirring was continued for another 8 hours. Subsequently, the mixture was concentrated in vacuo and the residue was dissolved in DCM, the organic layer was then washed with water (3×). The organic layer was concentrated in vacuo. The crude product was purified by column chromatography on silica gel (SiO₂, eluent: petroleum ether/diethyl ether 5/1 ? 4/1) to afford the N1 substituted indazole in 61% yield.

Scheme 54-59, Step ii:

To a stirred solution of KF.2H₂O (4.3 g, 45.24 mmol) and benzyl tri-ethyl ammonium chloride (7.6 g, 33.18 mmol) in 300 ml acetonitrile, the N1 substituted indazole (from step i) (9.8 g, 30.16 mmol) was added. The mixture was warmed to reflux and stirred for 8 hours. The solvent was evaporated and DCM was added to the residue. The organic layer was washed with water (3×). De organic layer was concentrated in vacuo. The crude product was purified by flash chromatography on silica (eluent: diethylether→1% MeOH in diethylether) to afford the 3-(indazol-1-yl)-propanol in 95% yield.

The other indazolyl alcohols were prepared analogously. In step ii, tetrabutyl ammonium chloride in THF can be used instead of the combination KF.2H₂O/benzyl tri-ethyl ammonium chloride.

Synthesis of Q60:

Q60-Br was synthesized analogously to the synthesis depicted in Scheme 52-53, using bromoethanol in the Mitsunobu step iii.

Synthesis of Q61-62:

Q61-1 and Q62-1 were synthesized analogously to the synthesis depicted in scheme 13-20, Steps ii, iii and iv.

Synthesis of Q63:

Q63-1 was synthesized as depicted in scheme 63:
Scheme 63, Step i:

Through a suspension containing the fluorobromonapthalene (0.90 g, 4 mmol), tri-phenylphospine (0.21 g, 0.8 mmol), dichlorobis(tri-phenylphospine)palladium (0.28 g, 0.4 mmol) in 15 ml Et₃N, nitrogen was bubbled for 1 hour. 3-Butyn-1-ol (0.4 g, 0.45 ml, 6 mmol) was added and the mixture was heated to 40-50° C. on an oilbath. After 15 minutes of stirring at this temperature, CuI (0.15 g, 0.8 mmol) was added and the mixture was heated at 70° C. and stirred for 48 hours.

The resulting black suspension was allowed to reach room temperature and diethyl ether and water were added. The fractions were separated and the water layer was extracted twice with diethyl ether. The combined organic extracts were washed with water, brine and dried (Na₂SO₄). After removal of the drying agent by filtration and solvent by concentration in vacuo, the residue was subjected to flash chromatography (SiO₂, eluent: DCM) affording Q63-OH, 4-(2-fluoro-napthalene-7-yl)-3-butyne-1-ol (0.30 g, 1.46 mmol).

Scheme 63, Step ii:

The conversion of the alcohol of step i to the corresponding iodo-derivative was performed according to scheme 1-6 step iv, yielding Q63-1.
Synthesis of Q64:
Scheme 64, Step i:

A solution of Red-Al (4.47 ml of a 3.4 M solution in toluene) in 25 ml of dry diethyl ether was cooled in an ice-bath under nitrogen to which a solution of Q63-OH (1.90 g, 9.5 mmol) in 40 ml of diethylther (dry) was added dropwise. After the addition was complete, the resulting mixture is stirred for 10 min at 0° C. after which it was allowed to reach room temperature and stirred for an additional 2.5 hours. The reaction mixture was again cooled in a ice-bath and quenched by the careful addition of 50 ml of 3.6 M H₂SO₄. The reaction mixture was extracted three times with diethyl ether. The combined organic extracts are washed with water, brine, and dried Na₂SO₄). After removal of the drying agent by filtration and solvent by concentration in vacuo, the residue was subjected to flash chromatography (SiO₂, eluent: DCM) affording 1.17 g of Q64-OH, 4-(2-fluoro-naphtalene-7-yl)-3-butene-1-ol (5.8 mmol).

Scheme 64, Step ii:

5 ml of concentrated hydrochloric acid is added to a solution of Q64-OH (1.17 g, 5.8 mmol) in 5 ml of THF. The mixture is stirred for 4.5 hours at room temperature after which another 2 ml of concentrated hydrochloric acid and 2 ml of THF are added. After another 30 minutes diethyl ether and water are added and the resulting fractions were separated. The water layer is extracted twice with diethyl ether. The combined organic fractions are washed with water, brine, dried (Na₂SO₄). After removal of the drying agent by filtration and solvent by concentration in vacuo, the residue was subjected to flash chromatography (SiO₂, eluent: DCM) affording 1.03 g of Q64-Cl (4.67 mmol).

The specific compounds of which the synthesis is described above are intended to further illustrate the invention in more detail, and therefore are not deemed to restrict the scope of the invention in any way. Other embodiments of the invention will be apparent to those skilled in the art from consideration of the specification and practice of the invention disclosed herein. It is thus intended that the specification and examples be considered as exemplary only, with a true scope and spirit of the invention being indicated by the claims.

ABBREVIATIONS
AcCl	acetylchloride
ADDP	1,1′-(azodicarbonyl)dipiperidine
CDI	carbonyldiimidazol
Dba	see Huang et al., J. Am. Chem. Soc., 125(2003)6653
DCE	dichloroethane
DCM	dichloromethane
DIAD	diisopropyldiazodicarboxylate
DIPE	diisopropylether
DIPEA	diisopropylethylamine
	CH2Cl2(ml)	MeOH(ml)	NH4OH(ml)
DMA 0.125	980	18.75	1.25
DMA 0.187	970	28.13	1.87
DMA 0.25	960	37.5	2.5
DMA 0.50	920	75.0	5.0
DMA 0.75	880	112.5	7.5
DMA 1.00	840	150.0	10.0
DMAP	4-dimethylaminopyridin
DME	dimethoxyethane
DMF	N,N-dimethylformamide
EtOH	ethanol
MeOH	methanol
MTBE	methyl(tert.)-butylether
NMP	N-methylpyrrolidon
PA	petroleum ether
TBAB	tetrabutylammoniumbromide
TBAC	tetrabutylammoniumchloride
TBAF	tetrabutylammoniumfluoride
THF	tetrahydrofurane
XPHOS	see Huang et al., J. Am. Chem. Soc., 125(2003)6653

Example

Formulation of Compound 56 Used in Animal Studies

For oral (p.o.) administration: to the desired quantity (0.5-5 mg) of the solid compound 56 in a glass tube, some glass beads were added and the solid was milled by vortexing for 2 minutes. After addition of 1 ml of a solution of 1% methylcellulose in water and 2% (v/v) of Poloxamer 188 (Lutrol F68), the compound was suspended by vortexing for 10 minutes. The pH was adjusted to 7 with a few drops of aqueous NaOH (0.1N). Remaining particles in the suspension were further suspended by using an ultrasonic bath.

For intraperitoneal (i.p.) administration: to the desired quantity (0.5-15 mg) of the solid compound 56 in a glass tube, some glass beads were added and the solid was milled by vortexing for 2 minutes. After addition of 1 ml of a solution of 1% methylcellulose and 5% mannitol in water, the compound was suspended by vortexing for 10 minutes. Finally the pH was adjusted to 7.

Example

Pharmacological Test Results

TABLE 2
In vitro affinities and functional activity
of compounds of the invention
	Dopamine-D2	5-HT reuptake	Dopamine-D2
	binding	binding	cAMP accum
compound	pKi	pKi	ε (intrinsic activity)
6	7.7	9.8	0.85
7	8.2	8.5	0.39
8	8.3	8.9	0.10
16	8.5	9.1	0.73
53	8.8	8.8	0.62
56	8.9	8.1	0.38
79	7.1	8.5	0.10
94	7.8	8.5	0.70
98	6.9	9.0	0.75
102	7.4	9.0	0.81
108	7.7	8.1	0.95
117	8.1	>9.0	0.29
135	7.2	8.7	0.45
140	7.0	7.3	0.24

Dopamine-D₂ and serotonin reuptake receptor affinity data obtained according to the protocols given above are shown in the table below. In vitro functional activity at cloned human dopamine D_2,L receptors as measured by accumulation of radiolabeled cAMP (potency: pEC₅₀, intrinsic activity ε)

Claims

1. Compounds of the general formula (1): wherein

X═S or O,

R1 is H, (C1-C6)alkyl, CF3, CH2CF3, OH or O—(C1-C6)alkyl

R2 is H, (C1-C6)alkyl, halogen or cyano

R3 is H or (C1-C6)alkyl

R4 is H, (C1-C6)alkyl, optionally substituted with a halogen atom

T is a saturated or unsaturated carbon chain of 2-7 atoms, wherein one carbon atom may be replaced with a nitrogen atom optionally substituted with an (C1-C3)alkyl, CF3 or CH2CF3 group, an oxygen atom or a sulphur atom, which chain is optionally substituted with one or more substituents selected from the group consisting of (C1-C3)alkyl, (C1-C3)alkoxy, halogen, cyano, trifluoromethyl, OCF3, SCF3, OCHF2 and nitro,

Ar is selected from the groups:

which Ar group is optionally further substituted with one or more substituents selected from the group consisting of (C1-C3)alkyl, (C1-C3)alkoxy, halogen, cyano, trifluoromethyl, OCF3, SCF3 OCHF2 and nitro,

and in which Ar groups that contain a five-membered ring, the double bond in the five-membered ring may be saturated,

and tautomers, stereoisomers and N-oxides thereof, as well as pharmacologically acceptable salts, hydrates and solvates of said compounds of formula (1) and its tautomers, stereoisomers and N-oxides.

2. Compounds of the formula (1) as claimed in claim 1, wherein the phenylpiperazine part of the molecule is selected from the group consisting of: in which formulae the dot represents the attachment to ‘T’ of formula (1), and wherein the second part of the molecule, represented by the symbols -T-Ar in formula (1), is selected from the group consisting of: in which formulae the dot represents the attachment to the phenylpiperazine part of the compounds of formula (1). and tautomers, stereoisomers and N-oxides thereof, as well as pharmacologically acceptable salts, hydrates and solvates of said compounds of formula (1) and its tautomers, stereoisomers and N-oxides.

3. A pharmaceutical composition comprising, in addition to a pharmaceutically acceptable carrier and/or at least one pharmaceutically acceptable auxiliary substance, a pharmacologically active amount of at least one compound of claim 1, or a salt thereof, as an active ingredient.

4. A method of preparing a composition as claimed in claim 3, characterised in that at least one compound of claims 1 or a salt thereof, is brought into a form suitable for administration

5. A compound as claimed in claim 1, or a salt thereof, for use as a medicament.

6. Use of a compound as claimed in claim 1 for the preparation of a pharmaceutical composition for the treatment of CNS disorders.

7. Use as claimed in claim 6, characterized in that said disorders are aggression, anxiety disorders, autism, vertigo, depression, disturbances of cognition or memory, Parkinson's disease, schizophrenia and other psychotic disorders.

8. Use as claimed in claim 6, characterized in that said disorder is depression.

9. Use as claimed in claim 6, characterized in that said disorders are schizophrenia and other psychotic disorders.

10. Use as claimed in claim 6, characterized in that said disorder is Parkinson's disease.