GB2075973A - Indoloquinolizines - Google Patents

Abstract

Indoloquinolizines of the formula (I> <IMAGE> and their pharmaceutically acceptable acid addition salts [wherein R<1> represents hydrogen, lower alkyl or lower aralkyl, R<2> and R<3> each represent hydrogen, halogen, lower alkoxy or lower alkyl, R<4> represents hydrogen, halogen or lower alkyl and R<5> represents lower alkyl or aryl] possesses antihypertensive activity.

Description

SPECIFICATION Indole derivatives The invention relates to novel indole derivatives, more particularly to novel indoloquinolizines, to processes for preparing the compounds, to their use and to pharmaceutical compositions containing them.

The present invention provides novel indoloquinolizines of the general formula (I)

and the pharmaceutically acceptable acid addition salts thereof, wherein R' represents hydrogen, lower alkyl or lower aralkyl, R2 and R3 each represent hydrogen, halogen, lower alkoxy or lower alkyl, R4 represents hydrogen, halogen or lower alkyl and R5 represents lower alkyl or aryl.

The terms "lower aklyl" and "lower alkoxy" as used herein indicate the the alkyl and alkoxy radicals each contain from 1 to 6 carbon atoms. Those radicals containing from 1 to 4 carbon atoms are preferred. The term "lower aralkyl" indicates that the radical contains from 7 to 10, preferably 7 to 9, carbon atoms. When a radical is referred to as "aryl" or part of a radical is "aryl" as in "aralkyl" the aryl group is preferably a phenyl or substituted phenyl group. The substituted phenyl group can be a phenyl group substituted by one or more substituents chosen from, for example, halogen (e.g. chlorine, fluorine or bromine), lower alkoxy (e.g. methoxy or ethoxy), lower alkyl (e.g. methyl, ethyl, propyl or butyl), alkylenedioxy (e.g. methylenedioxy or ethylenedioxy), amino, lower alkylamino, diloweralkylamino ortrifluoromethyl.

Examples of the group R1 are hydrogen, methyl, ethyl, propyl, butyl, benzyl and p-chlorobenzyl. Preferably R' is hydrogen or methyl. Examples of R2 and R3 are hydrogen, halogen such as fluorine, chlorine or bromine, lower alkoxy such as methoxy, ethoxy, propoxy or butoxy and lower alkyl such as methyl, ethyl, propyl or butyl. Preferably both R2 and R3 are hydrogen. Examples of R4 are hydrogen, halogen such as fluorine, chlorine or bromine and lower alkyl such as methyl, ethyl, propyl or butyl. Preferably R4 is hydrogen. R5 can be lower alkyl (e.g. methyl, ethyl, propyl or butyl) or aryl (e.g. phenyl or substituted phenyl as mentioned above). Preferably Rs is lower alkyl such as methyl.

The compounds of the invention can be prepared by a process in which an amine of general formula (II)

(where R', R2, R3 and R4 have the meanings given above) organ acid addition saltthereof, is reacted with a reactive derivative of a sulphonic acid compound of formula (III) R5SO2OH (Ill) As a reactive derivative of the sulphonic acid it is preferable to use an acid halide (for example the chloride or bromide) or an anhydride. The reaction may be carried out under basic conditions. The amine of formula (II) and the reactive derivatives of the acid of formula (III) are known compounds or they can be prepared by methods known in the art for preparing analagous compounds.For example, amines of formula (II) are disclosed in U.K. patent specification No. 1,453,573.

An alternative method of preparing the novel compounds of the invention comprises cyclising an N-oxide of general formula (IV)

where R', R2, R3, R4 and R5 are as defined hereinabove. The cyclisation of compounds of general formula (IV) may be brought about in a number of ways. For example a compound of formula (IV) may be cyclised by heating in the presence of ferrous ions and a suitable acidic medium. Examples of suitable acidic media are methanol/acetic acid or sulphuric acid/pyridine. Examples of compounds giving ferrous ions are ferrous sulphate and ferrous chloride. Alternatively cyclisation of compounds of general formula (IV) may be accomplished by reaction with trifluoroacetic anhydride /H+ mixtures, e.g.

a mixture of trifluoroacetic an hydride and trifluoroacetic acid. The starting material of general formula (IV) may be prepared by N-oxidising a compound of general formula (V)

where R',R2, R3, R4 and Rs are as defined above. The N-oxidisation may be effected with an N-oxidising agent e.g. hydrogen peroxide or a peroxy acid (e.g.

m-chloroperbenzoic acid).

If necessary in the reactions herein before described, reactive substituent groups may be pro tected during a reaction and the protecting group removed at a later stage. Once the compound of general formula (I) has been prepared then if neces sary a substituent in the molecule may be converted into another substituent specified in connection with general formula (I).

If in the processes described above the compound of the invention is obtained as an acid 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, methanesulphonic and p-toluenesulphonic acids.

The compounds of the invention possess at least two asymmetric carbon atoms and hence they can exist in various stereochemical forms. In addition they can exist ascis or trans isomers. It will be realised that if, for example,the starting material of formula (II) is a mixture of isomers the product of formula (I) will also be a mixture of isomers which can be separated, if required, by standard procedures. The preferred compounds of the invention are the trans isomers in which the -NH SOURS group is in the equatorial position i.e. compounds ofthe general formula (VI)

and the pharmaceutically acceptable acid addition salts thereof (wherein R1, R2, R3, R4 and Rs are as defined above).These compounds can be prepared by the methods described above e.g. starting from the corresponding trans isomer of general formula (II).

The compounds of the invention have pharmacological activity. For example, the compounds exhibit anti-hypertensive activity upon administration to warm-blooded animals according to a standard pharmacological procedure. One such pharmacological test procedure is described below: Female rats are rendered hypertensive by implanting subcutaneously two wax pellets (30 mg) containing desoxycorticostemne acetate (15 mg) followed immediately by uninephrectomy. The drinking water is replaced by normal salineadlib for4weeks. Blood pressure stabilises at a hypertensive level after 6 weeks. Systolic pressure is measured indirectly before dosing with a test compound using an E and M pneumatic pulse transducer and a Devices MX2 recorder.Groups of 4 rats are dosed orally with suspensions of solution of the test compound in 0.5% hydroxypropylmethylcellulose 0.9% saline vehicle.

Blood pressures are recorded again at 2, 6 and 24 hours and the results, expressed as a percentage of the pre-dose values compared with those of a similar group of rats receiving vehicle alone.

In the aforementioned test Ni1, 2,3,4,6,7, 12, 12ba - octahydro - 2W - indolo i2, 3 - aJ quinolizin - yll methanesulphonamide, a representative compound of the present invention, was found to lower blood pressure by 51.7% 2 hours after dosing and by 46.2% 6 hours after dosing when administered at 50 mg/kg.

The invention further provides a pharmaceutical composition comprising a compound of general formula (I) or a pharmaceutically acceptable 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 and a liquid.

Solid form compositions include powders, granules, tablets, capsules (e.g. hard and soft gelatin 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 aids, binders ortablet-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%, e.g. from 0.03 to 99%, preferably 1 to 80% of the active ingredient.Suitable solid carriers include, for example, calcium phosphate, magnesium stearate, 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 encapsu lat- ing 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 phar maceutically acceptable liquid carrier such as water, an organic solvent, a mixture of both or pharmaceutically acceptable oils or fats. The liquid carrier can contain other suitable pharmaceutical additives such as solubilizers, emulsifiers, buffers, preservatives, sweeteners, flavouring agents, suspending agents, thickening agents, colours, viscosity regulators, stabilisers, or osmo-regulators.Suitabie examples of liquid carriers for oral and parenteral administration include water (particularly containing additives as above e.g. cellulose derivatives, preferably sodium carboxymethyl cellulose solution), alcohols (including monohydric alcohols and polyhydric alcohols e.g. glyceroland glycols) and their derivatives, and oils (e.g. fractionated coconut oil and arachis oil). For parental 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 parental administration. The liquid carrier for pressurised compositions can be a halogenated hydrocarbon or other pharmaceutically acceptable propellant.

Liquid pharmaceutical compositions which are sterile solutions or suspensions can be utilised 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, e.g. as tablets or capsules. In such form, the composition is sub-divided in unit doses containing appropriate quantities of the active ingredient; the unit dosage forms can be packaged compositions, for example packeted powders, vials, ampoules, prefilled syringes or sachets containing liquids. The unit dosage forms 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 a unit dose of composition may be varied or adjusted from 0.5mg.

or less to 750mg. or more, according to the particular need and the activity of the active ingredient. The invention also includes the compounds in the absence of the carrier where the compounds are in unit dosage form.

The following Examples illustrate the invention.

Example 7 N - | 1,2, 3, 4, 6, 7, 12, 12ba - Octahydro - 2H - indolo [2,3- a] quinolizin - 2,8 - ylJ methansulphonamide A solution of 2ss - amino - 1,2,3,4,6, 7, 12, 12ba- octahydro - 2H- indolo L2, 3 - aj quniolizine (4.879; 20.18mM) and triethylamine (2.19; 20.3mM) in dichloromethane (50cm3) was stirred at 0 (ice) as a solution of methanesulphonic anhydride (3.51 g; 20.17mM) in dichloromethane (25cm3) was added slowly.The clear solution was then warmed to room temperature and allowed to stand over the weekend (70h). The mixture was washed with water (2 x 50cm3) and dried (MgSO4). Filtration and evaporation afforded a dark glass (5.289) which was purified by chromatography on silica and eluted with 10% ethanol in ethyl acetate, to give the title compound as a yellow solid (2.779). The base was converted to the hydrochloride giving the hydrochloride quarterhydrate (2.309) as cream-yellow needles, m.p.

247-253 (dec) (with signs of decomposition at temp- eratures above 220 ).

A sample (0.259) of the hydrochloride was converted to the base with aqueous bicarbonate and dichloromethane. Crystallisation from ethanol gave the free base quarterhydrate (0.139) as cream cubes, m.p. 250-255 (dec).

Found: C, 59.28%; H, 7.00%; N, 12.82% C16H31 N3O2S.

1/4 H2O requires C,59.32%; H, 6.69%; N,12.97%.

The NMR and IR spectra confirmed the 2,8 and 12buy stereochemistry.

Examples 2 to 4 By procedures analogous to that of Example 1 the following compounds are prepared: Example Product 2 N-1 1,2,3,4,6,7,12, 12b-octahydro-2H - indolo l 2,3 - al quinolizin - 2 - ylJ ethanesulphonamide 3 - j1,2,3,4,6,7,12,12b-octahydro-2H -indolo[2,3-a] quinolizin-2-ylj benzenesulphanamide 4 N-!12-ethyl-1,2,3,4,6,7,12,12b- octahydro - 2H indolo 12,3 - aJ quinolizin 2 - ylj methane - sulphonamide

Claims (15)

1. An indoquinolizine of the general formula

or a pharmaceutically acceptable acid addition salt wherein R' represents hydrogen, lower alkyl or lower aralkyl, R2 and R3 each represent hydrogen, halogen, lower alkoxy or lower alkyl, R4 represents hydrogen, halogen or lower alkyl and R5 represents lower alkyl or aryl.

2. A compound as claimed in Claim 1 wherein R1 is hydrogen, methyl, ethyl, propyl, butyl, benzyl or p-chlorobenzyl.

3. Acompound as claimed in Claim 1 or Claim 2 wherein RI, RI and RI are each hydrogen.

4. A compound as claimed in any one of Claims 1 to 3 wherein R5 is lower alkyl.

5. A compound as claimed in any one of Claims 1 to 4 in the form of the trans isomer in which the -NHSO2Rs is in the equatorial position.

6. N- j1,2,3,4,6,7,12,12bo-octahydro-2H- indolo 12,3 - ad - quinolizin - 2ss - ylj methanesulphonamide or a pharmaceutically acceptable acid addition salt thereof.

7. A process for preparing a compound claimed in Claim 1 which comprises reacting an amine of general formula (II)

(where R', R2, RI and R4 are as defined in Claim 1) or an acid addition salt thereof with a reactive derivative of a sulphonic acid compound of formula (Ill) RISO2OH (Ill) (where R5 is as defined in Claim 1) and, if desired, converting a base of general formula (I) into a pharmaceutically acceptable acid addition salt.

8. A process as claimed in Claim 7 wherein the reactive derivative is the acid halide or the anhydride.

9. A process for preparing a compound claimed in Claim 1 which comprises cyclising an N-oxide of general formula (IV)

10. A process for preparing an indoloquinolizine substantially as herein before described with reference to any one of the Examples.

11. An indoloquinolizine whenever prepared by the process claimed in any one of Claims 7 to 10.

12. A pharmaceutical composition comprising a compound as claimed in any one of Claims 1 to 6 and 11 in association with a pharmaceutically acceptable carrier.

13. Acomposition as claimed in Claim 12 in the form of a tablet or capsule.

14. A compound as claimed in any one of Claims 1 to 6 and 11 for use as a pharmaceutical.

15. Acompound as claimed in any one of Claims 1 to 6 and 11 for use as an antihypertensive.