GB2248836A

GB2248836A - Piperazine derivatives

Info

Publication number: GB2248836A
Application number: GB9118744A
Authority: GB
Inventors: Ian Anthony Cliffe
Original assignee: John Wyeth and Brother Ltd
Current assignee: John Wyeth and Brother Ltd
Priority date: 1990-10-19
Filing date: 1991-09-02
Publication date: 1992-04-22
Anticipated expiration: 2011-09-02
Also published as: AU8592091A; DE69122205D1; JPH04282371A; GR3021221T3; HU212943B; CA2053709A1; HU211587A9; IE913669A1; IE65379B1; CA2053709C; HUT60264A; KR100193928B1; PT99251A; ES2091879T3; HU913292D0; DE69122205T2; NZ240271A; EP0481744B1; DK0481744T3; ATE143012T1

Abstract

2,3,4,5,6,7-Hexahydro-1- &lsqbstr& 4-[1-[4-(2-methoxyphenyl)-piperazinyl]]-2-phenylbutyryl &rsqbstr& -1H-azepin e and the pharmaceutically acceptable acid addition salts thereof are 5-HT1A binding agents useful, for example, as anxiolytics.

Description

0 1 0 22433-50 PIPERAZINE DERIVATIVES This invention relates to piperazine

derivatives, to processes for their preparation, to their use and to pharmaceutical compositions containing them. The novel compounds act on the central nervous system by binding to 5-HT receptors (as more fully explained below) and hence can be used as medicaments for treating humans and other mammals.

The novel compounds of the invention are the compound of the formula OCH N C- 1 \--/ N-(CH 2) 2 -CH.CONC) (A) 1 1 and the pharmaceutically acceptable salts thereof.

Compound A is 2,3,4,5,6,7-hexahydro-l{4-[1-[4-(2me-Ihoxyphenyl)piperazinyll]-2-phenylbutyryl}-IHazepine.

Our copending U.K. application No. 9008925.1 describes compounds having a general formula which embraces the novel compounds of the present invention. The compounds of our copending application are those of the general formula R RI-N /- N-(CHA CR 2 R 3 -X (I) 2 n and the pharmaceutically acceptable acid addition salts thereof.

In formula (I) n is one of the integers 1 or 2, R is hydrogen or lower alkyl, R 1 is an aryl or nitrogen containing heteroaryl radical, R 2 is hydrogen or lower alkyl, R 3 is an aryl radical, an alkyl radical containing 4 to 8 carbon atoms or an aryl(lower)alkyl radical, X is -OCOR 10, - CO 2 R 6, -CONR 5 R 9, OCO 2 R 6, NR 4 COR 6 ' 11 - 6 4 6 _ 6 _ 6 OCONHR NHCO 2 R NR CONHR CONHNHR, CONHOR 0 4 R - ' N Y 0 R 13 Y R 14 or-N CO R and R 5 are each hydrogen or lower alkyl 6 7 8 R is -CHR R ' cycloalkyl of 3 to 12 qarbon atoms or aryl(lower)alkyl (where R 7 and R 8 are each hydrogen or lower alkyl), R 9 is hydrogen, an alkyl group of 1 to 8 carbon atoms other than a tertiary alkyl group, cycloalkyl of 3 to 12 carbon atoms, cycloalkyl(lower)alkyl, aryl, aryl(lower)alkyl or 8azaspiro[4.5]deca-7,9-dione-8-yl(lower)alkyl [with the proviso that when R 3 is aryl or aralkyl, R 9 is not a phenyl group substituted in the ortho position by halogen, nitro, trifluoroalkyl, cyano, sulphonic acid, sulphonamido, carboxy, carbalkoxy, carboxylanilino or a 4carboxylaminobenzosulphonamido group and that when R 9 is hydrogen,alkyl, aryl or aryl(lower)alkyl R 5 is hydrogen or -CHR 7 R 8 11 or R 5 and R 9 together with the nitrogen atom to which they are attached represent an azetidino, pyrrolidino, piperidino, hexahydroazepino, morpholino or piperazino ring which may be optionally substituted by lower alkyl, aryl or aryl(lower)alkyl R 10 is cycloalkyl of 3 to 12 carbon atoms, or 2,3-dihydro[1, 4]benzodioxinyl optionally substituted by lower alkyl, lower alkoxy or halogen or, when R3 is an alkyl radical containing 4 to 8 carbon atoms, R 10 can also be aryl; R 11 is cycloalkyl of 3 to 12 carbon atoms, aryl or aryl(lower)alkyl, R 12 and R 13 are each lower alkyl or together with the carbon atom to which they are both attached represent c 4-6 cycloalkyl, R 14 represents hydrogen, halogen, lower alkyl or lower alkyl and Y is CO or SO 2 4 The compounds of our copending application can be prepared by a number of methods from known starting materials or starting materials that may be prepared by conventional methods. Some of the disclosed methods are given below:

In one method for preparing an amide of formula (I), where X represents CONR 5 R 9 an amine of formula NHR 5 R 9 (II) where R 5 and R 9 are as defined above is acylated with an acid of formula 1 R - N 1 0 R N-(CH 2)n CR 2 R 3 COOH (III) 1 2 3 (where R, R, R and R are as defined above) or with an acylating derivative thereof. Examples of acylating derivatives include the acid halides (eg acid chlorides), azides, anhydrides, imidazolides (eg obtained from carbonyldiimidazole), activated esters or O-acyl ureas obtained from a carbodiimide such as a dialkylcarbodiimide particularly dicyclohexylcarbodiimide. Preferably the amine is acylated with the acid in presence of a coupling agent such as 1,1'carbonyldiimidazole, iso-butylchloroformate or diphenylphosphinyl chloride.

An alternative method of preparing the compounds of formula (I) comprises alkylation of a piperazine of formula a R R 1 - N /, NH (where R and R 1 are as defined above) with an alkylating agent providing the group -(CH 2) n CR 2 R 3 X (where n, R 2, R 3 and X are as defined above).

(IV) (V) The alkylating agent may be, for example, a compound of formula Z-CH 2 CR 2 R 3 X (VI) where R 2 ' R 3 and X are as defined above and Z is a leaving group such as halogen or an alkyl- or aryl-sulphonyloxy group. Alternatively the alkylating agent may be an unsaturated compound of formula CH 2 =CR 3 X 1 b (VII) (where R 3 and X are as defined above) and the compound of formula (VII) is reacted with the piperazine of formula (IV) by means of a Michael reaction. The reaction may be carried out at elevated temperature in the presence of an alcohol. A small.quantity of an acid catalyst may be employed in the reaction when X 9 represents -CONR R The compound of the invention of formula A may be prepared in an analogous manner using appropriate starting materials. A preferred method of preparing compound A comprises reacting a compound of formula OCH 3 N- (CH 2) 2 -X where X is a leaving group, such as halogen, with an anion of the amide of formula O-CH 2 CON The anion may be prepared by reacting the amide with a strong base, eg lithium diisopropylamide.

The processes described above may be carried out to give a compound of the invention in the form of a free base or as an acid addition salt. If the compound of the invention-is obtained as an cid addition salt, the free base can be obtained by basifying a solution of the acid addition salt. Conversely, if the product of the process is a free base an acid addition salt, particularly a pharmaceutically acceptable acid addition salt, may be obtained by dissolving the free base in a suitable organic solvent and treating the solution with an acid, in accordance with conventional procedures for preparing acid addition salts from base compounds.

Examples of acid addition salts are those formed from inorganic and organic acids, such as sulphuric, hydrochloric, hydrobromic, phosphoric, tartaric, fumaric, maleic, citric, acetic, formic, b methanesulphonic, p-toluenesulphonic, oxalic and succinic acids.

The compounds of the invention contain an asymmetric carbon atom, so that the compounds can exist in different steroisomeric forms. The compounds can be, for example, racemates or optically active forms. The optically active forms can be obtained by resolution of the racemates or by asymmetric synthesis. For example resolution may be carried out by forming diastereoisomeric salts of the racemic base with an optically active acid (eg dibenzoyl-L-tartaric acid), separating the diastereoisomeric salts and converting them to the optically active base or other salts.

The compounds of the present invention possess pharmacological activity. In particular, they act on the central nervous system by binding to 5-HT receptors. In pharmacological testing it has been shown that the compounds particularly bind to receptors of the 5-HT 1A type. The compounds selectively bind to receptors of the 5-HT 1A type to a much greater extent than they bind to other receptors such as a I receptors. They exhibit activity as 5-HT 1A antagonists in pharmacological testing. The pharmacological testing of the compounds indicates that they can be used for the treatment of CNS disorders, such as anxiety in mammals, particularly humans. They may also be useful as antidepressants, hypotensives and,as agents for regulating the sleep/wake cycle, feeding behaviour and/or sexual function.

1 1 5 8- The compounds of the invention were tested for 5-HT IA receptor binding activity in rat hippocampal membrane homogenate by the method of B S Alexander and M D Wood, J Pharm Pharmacol, 1988, 40, 888-891.

The results indicate that the compounds of the invention are more potent than other compounds of formula I including the related compound 2,3,4,5, 6,7-hexahydro-lf3-{1-E4-(2methoxyphenyl)piperazinylll-2-phenylpropionyl}IHazepine (compound B) described in Example 34 of our copending application. Compound B was one of the most potent compounds disclosed in the copending application. The results are given below, in which compound C is the isomer described in Example 2(a) below:

Compound A Compound B Compound C IC50 (nM) 3 9 1 The compounds were also tested for 5HT IA receptor antagonism activity in a test involving the antagonism of 8-hydrox,-2-(di-n-propylamino)- tetralin (8-OH DPAT) svndrome in the rat. The results are given below Compound A Compound B MED (mglkg; s.c.) 0.03 - 0.3 Lhe compounds were also tested for potential anxiolytic activity by a test procedure measuring mouse exploratory activity in a two-compartment light/dark box based upon the procedure of B Costall et al, 1 1 Neuropharmacology, 1987, 26, 195-200 and J.N. Crawley et al, Pharmac. Biochem. Behav. 1980, 13, 167-170. The results are given below Compound A Compound B MED (mg/kg; s.c.) 0.03 1 The invention also provides a pharmaceutical composition comprising a compound of formula A or a pharmaceutically acceptable acid addition salt thereof in association with a pharmaceutically acceptable carrier. Any suitable carrier known in the art can be used to prepare the pharmaceutical composition. In such a composition, the carrier is generally a solid or liquid or a mixture of a solid or liquid.

Solid form compositions include powders, granules, tablets, capsules (eg hard and soft gelatine capsules), suppositories and pessaries. A solid carrier can be, for example, one or more substances which may also act as flavouring agents, lubricants, solubilisers, suspending agents, fillers, glidants, compression aides, binders or tablet-disintegrating agents; it can also be an encapsulating material. In powders the carrier is a finely divided solid which is in admixture with the finely divided active ingredient. In tablets the active ingredient is mixed with a carrier having the necessary compression properties in suitable proportions and compacted in the shape and size desired. The powders and tablets preferably contain up to 99%, eg from 0.03 to 99% preferably 1 to 80% of the active ingredient. Suitable solid carriers include, for example, calcium phosphate, magnesium stearate, 1 A 1 0 talc, sugars, lactose, dextrin, starch, gelatin, cellulose, methyl cellulose, sodium carboxymethyl cellulose, polyvinylpyrrolidine, low melting waxes and ion exchange resins.

The term 'composition" is intended to include the formulation of an active ingredient with encapsulating material as carrier to give a capsule in which the active ingredient (with or without other carriers) is surrounded by the carrier, which is thus in association with it. Similarly cachets are included.

Liquid form compositions include, for example, solutions, suspensions, emulsions, syrups, elixirs and pressurised compositions. The active ingredient, for example, can be dissolved or suspended in a pharmaceutically acceptable liquid carrier such as water, an organic solvent, a mixture of both or pharmaceutically acceptable oils or fats. The liquid carrier can coptain other suitable pharmaceutical additives such as solubilisers, emulsifiers, buffers, preservatives, sweeteners, flavouring agents, suspending agents, thickening agents, colours, viscosity regulators, stabilisers or osmo-regulators. Suitable examples of liquid carriers for oral and parenteral administration include water (particularly containing additives as above, eg cellulose derivatives, preferably sodium carboxymethyl cellulose solution), alcohols, eg glycerol and glycols) and their derivatives, and oils (eg fractionated coconut oil and arachis oil). For parenteral administration the carrier can also be an oily-ester such as ethyl oleate and isopropyl myristate. Sterile liquid carriers are used in sterile liquid form compositions for parenteral administration.

1 5 Liquid pharmaceutical compositions which are sterile solutions or suspensions can be utilized by, for example, intramuscular, intraperitoneal or subcutaneous injection. Sterile solutions can also be administered intravenously. When the compound is orally active it can be administered orally either in liquid or solid composition form.

Preferably the pharmaceutical composition is in unit dosage form, eg as tablets or capsules. In such form, the composition is sub-divided in unit dose containing appropriate quantities of the active ingredient; the unit dosage forms can be packaged composition, for example packeted powders, vials, ampoules, prefilled syringes or sachets containing liquid. The unit dosage form can be, for example, a capsule or tablet itself, or it can be the appropriate number of any such compositions in package form. The quantity of the active ingredient in unit dose of composition may be varied or adjusted from 0.5 mg or less to 750 mg or more, according to the particular need and the activit of the active ingredient.

The following Examples illustrate the invention:

1 Example 1

2,3,4,5,6,7-Hexahydro-l-{4-El-E4-( methoxyphenyl)piperazinylll2phenylbutyryl}-1H-azepine Butyl lithium (1.5M in hexane: 5 ml, 7.5 mmol) was added dropwise over 5 min, maintaining the temperature below 80C, to a stirred solution of 2,3, 4,5,6,7-hexahydro-l-phenylacetyl-IH-azepine (1.48 g, 6.8 mmol) and diisopropylamine (2.0 ml, 1.4 g, 14 mmol) in dry toluene (16 ml) under argon. The mixture was stirred at OOC for 1 h, and a solution of freshly chromatographed 1-(2-chloroethyl)-4(2methoxyphenyl)piperazine (1.73 g, 6. 8 mmol) in dry toluene (4 ml) was added dropwise. The mixture was stirred at OOC to 200C for 18 h, and water (50 ml) was added. The layers were separated, and the aqueous phase was extracted with ethyl acetate (2 x 50 ml). The combined organic phases were concentrated in vacuo. The crude product (2.91 g) was chromatographed on silica with eluant ethyl acetate 'to give the title compound as the free base (0.15 g). The product was dissolved in ethyl acetate (30 ml), and the solution was acidified with ethereal hydrogen chloride. The product was collected to give the title compound as the dihydrochloride three quarters hydrate (0.36 g), m.p. 1750-1780C (Found: C, 62.05; H, 7.8; N, 7.75. C27 H 37 N 3 0 2 2HCl.0.75 H 2 0 requires C, 62.1; H, 7.8; N, 8.05%).

1 0 Example 2

Resolution of 2,3,4,5,6,7-hexahydro-l{4-[1-[4(2methoxyphenyl)piperazinvlll-2-phenylbutyryl}-IH-azepine 2,3,4,5,6,7-Hexahydro-l-4-[l-[4-(2methoxyphenyl)-piperazinylll-2phenylbutyryll-iHazepine (12.1 g) was dissolved in eth yl acetate (2.5 volumes, ie 30 ml) and a solution of dibenzoylL-tartaric acid monohydrate (1 mol eq) in ethyl acetate (2.5 volumes) added. The initially formed oil was -ity of redissolved by the addition of the minimum quant acetonitrile (3. 6 ml). After 3 d, filtration gave crystals (6.2 g) which had an optical purity of 28% as judged by chiral H.P.L.C.. Recrystallisation first from ethyl acetate - acetonitrile (3:10, 13 volumes), which gave a sample with an optical purity of 84%, and secondly from methanol (7.5 volumes) gave the first enantiomer (isomer I) of the product as a dibenzoyl- 22 L-tartrate (2.1 g) m.p. 147-1500C, [a] D = - 260(1% in MeOH) (Found: C, 66.7; H, 6.7; N, 5.1 C 27 H 37 N 3 0 2' C 18 H 14 0 8 H 2 0 requires C, 66.6; H, 6.6; N, 5.2%) with he sample was converted an optical purity of 97.4%. rIL 26 to the free base of isomer (1) (1-1 g, [a] +530 (1% in CHC1) and D Lhence to the hydrochloride salt in the usual manner to afford a colourless powder 10.65 g), m.p. 181-184"C, Ect] 23 = +350(1% in MeOH) (Found: D 63.1; H, 7.8; N, 7.9. C 27 H 37 N 3 0 2 2HC1.0.25H 2 0 requires C, 63.2; H, 7.7; N, 8.2%) with an optical purity of 97.6%.

1 1 (b) The second enantiomer (isomer II) was formed in a similar manner from the racemate of Example 1 and dibenzoyl-D-tartartic acid monohydrate. Isomer II dibenzoyl-D-tartrate m.p. 141-1420C, [a] 25 = +2500% in D MeOH) (Found: C, 67.3; H, 6.7; N, 5.2. C 27 H 37 N 3 0 2 C 18 H 14 0 8 0.25H 2 0 requires C, 67.3; H, 6.5; N, 5.2%).

Isomer II base: [a] 26 620(1% solution in CHCl D 26 3 Isomer II hydrochloride m.p. 181-1840C, [a] D 360(1% in MeOH) (Found: C, 60.2; H, 7.7; N, 7.75 C 27 H 37 N 3 0 2 2HCl-1.75H 2 0 requires C, 60.05; H, 7.9; N, 7.8%) with an optical purity of 98.2%.

1 p

Claims

CLAIMS i. 2,3,4,5,6,7-Hexahydro-l-4-[l-[4-(2methoxyphenyl)piperazinyll]-2-

phenylbutyryll-IH-azepine or a pharmaceutically acceptable acid addition salt thereof.
2. A compound as claimed in claim 1 which is the enantiomer of 2,3,4,5,6, 7-hexahydro-l-4-[l-[4-(2methoxyphenyl)piperazinylll-2-phenylbutyryll-lHazepine in which the free base has the [a] 26 of about +530 D (1% in CHC1 3), or a pharmaceutically acceptable salt thereof.
3. A compound as claimed in claim I which is the enantiomer of 2,3,4,5,6, 7-hexahydro-l-4-[l-[4-(2methox,phenyl)piperazinylll-2-phenylbutyryll-IHazepine in which the free base has the [a] 26 of about -620 D (1% in CHC1 3), or a pharmaceutically acceptable salt thereof.
4. A process for preparing a compound claimed in claim 1 which comprises (a) acylating an amine of formula with an acid of formula 1. 1 OCH 3 N \,\.. 1 - \_ N-(CH 2) 2 -CH.COOH 1 (1 -:z )I,, or with an acylating derivative thereof or (b) alkylating a piperazine of formula OCH 3 -1 N NH with an alkylating agent providing the group -CCH 2) 2 -CH.CON, or (c) reacting a compound of formula OCH 3 ji 1 N \--/ N-(CH 2) 2 -X (where X is a leaving group) with an anion of the amide of formula 1. 91 G-CH 2 CO N or (d) converting a base claimed in claim 1 into a pharmaceutically acceptable acid addition salt thereof or (e) converting a pharmaceutically acceptable acid addition salt claimed in claim I into a free base or (f) resolving a racemic compound claimed in claim 1
5. A process for preparing a compound claimed in claim 1 substantially as hereinbefore described with reference to Example 1.
6. A process for preparing a compound claimed in claim 1 substantially as hereinbefore described with reference to Example 2a or 2b.
7. A compound as claimed in claim 1 whenever prepared by the process claimed in any one of claims 4 to 6.
8. A pharmaceutical composition comprising a compound claimed in any one of claims 1,2,3 and 7 in association with a pharmaceutically acceptable carrier.
9. A compound claimed in claim 1,2 or 3 for use as a pharmaceutical.
10. A compound claimed in claim 1,2 or 3 for use as an anxiolytic, an antidepressant, a hypotensive or as an agent for regulating the sleep/wake cycle, feeding behaviour andlor sexual function.

1