EP1165556A1 - Derivatives of pyrimido[6,1-a]isoquinolin-4-one - Google Patents

Abstract

Compounds of general formula (I) wherein each of R?1 and R2¿ independently represents a C¿1-6? alkyl or C2-7 acyl group; X represents OCH2 or a group CR?3R4¿, wherein each of R3 or R4 independently represents a hydrogen atom or a C¿1-3? alkyl group; R?5¿ represents a hydrogen atom or a C¿1-3? alkyl, C2-3 alkenyl or C2-3 alkynyl group; R?6¿ represents a hydrogen atom or a C¿1-6? alkyl, C2-6 alkenyl, C2-6 alkynyl, amino, C1-6 alkylamino, di(C1-6) alkylamino or C2-7 acylamino group; each of R?7 and R8¿ independently represents a hydrogen or halogen atom or a hydroxy, trifluoromethyl, C¿1-6? alkyl, C2-6 alkenyl, C2-6 alkynyl, C2-7 acyl, C1-6 alkylthio, C1-6 alkoxy, C3-6 cycloalkyl; R?9¿ represents a hydrogen or halogen atom or a hydroxy, trifluoromethyl, C¿1-6? alkyl, C2-6 alkenyl, C2-6 alkynyl, C2-7 acyl, C1-6 alkylthio, C1-6 alkoxy or C3-6 cycloalkyl group, or salts thereof are useful for treatment of respiratory disorders such as asthma. Compounds of the invention have a longer duration of action than the known compound trequinsin (9,10-dimethoxy-3-methyl-2-mesitylimino-2,3,6,7-tetrahydro-4H-pyrimido[6,1-a]isoquinolin-4-one) and do not have trequinsin's very bitter taste.

Description

Derivatives of pyrimido[6J-a]isoquinolin-4-one

The present invention relates to derivatives of pyrimido[6J-a]isoquinolin-4-one and their application as inhibitors of phosphodiesterase (PDE) isoenzymes. More particularly the invention relates to 2-phenoxy derivatives of pyrimido[6J- a]isoquinolin-4-one and their use in medicine for example as bronchodilators with anti-inflammatory properties.

In all cells where cyclic AMP (cAMP) is present as a secondary messenger, intracellular concentrations of cAMP are regulated by the two processes involved in its formation and degradation. Stimulation of membrane bound receptors on the external surface of the cells (e.g. by β-adrenoceptor agonists) results in activation of adenylyl cyclase to generate cAMP from ATP. Phosphodiesterases present in the cell serve to reduce the concentration of cAMP by hydrolysing it to adenosine monophosphate (AMP).

In a disease such as asthma, the principal cells involved in the associated bronchoconstriction and inflammatory processes are subject to inhibitory control by cAMP. Inhibitors of type III phosphodiesterase raise intracellular levels of cAMP, leading to relaxation of bronchial smooth muscle, whereas inhibitors of type IV phosphodiesterase inhibit the release of damaging mediators from pro-inflammatory cells. Thus, in principle, a combined PDE III/IV inhibitor should have the desirable effects of a β-adrenoceptor agonist plus an inhaled anti-inflammatory steroid which are currently the mainstay of treatment in severe asthma. Moreover, a combined PDE III/IV inhibitor given by inhalation should achieve beneficial effects similar to a β- agonist plus inhaled steroid and should be an unusually effective treatment of asthma and other respiratory disorders without the undesirable glucocorticoid effects of the steroid such as osteoporosis and the stunting of growth. The potential adverse effects of a PDE III/IV inhibitor (e.g. nausea and vomiting, gastric acid secretion, cardiovascular effects such as increased cardiac contractility, vasodilation and potential arrhythmogenic activity) should be avoidable with a compound that is delivered directly to the lungs by inhalation. It is desirable that the substance is long acting, non irritant and has a taste which is not so unpleasant as to have any adverse effect on patient compliance.

An example of a pyrimido[6J-a]isoquinolin-4-one derivative with PDE III/IV inhibitory activity and known to possess antihypertensive vasodilator activity is trequinsin (9J0-dimethoxy-3-methyl-2-mesitylimino-2,3,6,7-tetrahydro-4H- pyrimido[6J-a]isoquinolin-4-one), which is described by De Souza et al, J. Med. Chem. 27 1470-1480 (1984) and in GB-A-1597717.

As described by De Souza et al. and in GB-A-1597717, trequinsin has valuable pharmacological properties, and can be administered to human subjects suffering from, for example, respiratory disorders. However, it is unsuitable for administration by inhalation because of its bitter taste and in vitro data indicate its persistence of action is less than desirable.

It has now been found that it is possible to design certain pyrimido[6J-a]isoquinolin-

4-one derivatives which are PDE inhibitors, which have a longer duration of action relative to trequinsin and other useful properties, such as improved taste.

According to a first aspect of the present invention there is provided a compound of general formula I:

wherein

each of R¹ and R² independently represents a Cι.₆ alkyl or C _-7 acyl group;

X represents OCH or a group CR³R⁴, wherein each of R^J and R⁴ independently represents a hydrogen atom or a Cι- alkyl group;

R³ represents a hydrogen atom or a Cι_-3 alkyl, C_2-3 alkenyl or C_2- alkynyl group; R⁶ represents a hydrogen atom or a Cι-₆ alkyl, C_2-6 alkenyl, C_2-6 alkynyl, amino, Cι- alkylamino, di(Cι_-6) alkylamino or C_2-7 acylamino group;

7 ϊ. • each of R and R independently represents a hydrogen or halogen atom or a hydroxy, trifluoromethyl, Cι-₆ alkyl, C_2-6 alkenyl, C _-6 alkynyl, C₂. acyl, Cι-₆ alkylthio, C_1-6 alkoxy or C_3-6 cycloalkyl group;

R⁹ represents a hydrogen or halogen atom or a hydroxy, trifluoromethyl, Cι_-6 alkyl, C_{2- 6} alkenyl, C _-6 alkynyl, C_2-7 acyl, Cι_-6 alkylthio, Cι-₆ alkoxy or C₃.₆ cycloalkyl group; or a salt thereof; excluding the compound 6,7-dihydro-2-phenoxy-9J0-dimethoxy-4H- pyrimido[6J a]isoquinolin-4-one.

The compound 6,7-dihydro-2-phenoxy-9J0-dimethoxy-4H- pyrimido[6Ja]isoquinolin-4-one, which is excluded from the scope of the first aspect of the present invention, is compound "8f ' in De Souza et al, cited above. 6,7-dihydro- 2-phenoxy-9J0-dimethoxy-4H-pyrimido[6Ja]isoquinolin-4-one is described in De Souza et al only as being a poor hypotensive agent and is not described as having bronchodilatory activity.

As used herein the term "halogen" or its abbreviation "halo" means fluoro, chloro, bromo or iodo.

As used herein the term "Cι-₆ alkyl" refers to straight chain or branched chain alkyl groups having from one to six carbon atoms. Illustrative of such alkyl groups are methyl, ethyl, propyl, isopropyl, butyl, isobutyl, -fee-butyl, tert-butyl, pentyl, neopentyl and hexyl. C alkyl groups are preferred.

As used herein the term "C_2-3 alkenyl" refers to straight chain or branched chain hydrocarbon groups having from two to three carbon atoms and having in addition one double bond, of either E or Z stereochemistry where applicable. This term would include for example, vinyl and 1-propenyl.

As used herein the term "C₂.₃ alkynyl" refers to straight chain hydrocarbon groups having from two to three carbon atoms and having in addition one triple bond. This term would include for example, ethynyl and 1-propynyl.

As used herein the term "C _-6 alkenyl" refers to straight chain or branched chain hydrocarbon groups having from two to six carbon atoms and having in addition one double bond, of either E or Z stereochemistry where applicable. This term would include for example, vinyl, 1-propenyl, 1- and 2-butenyl and 2-methyl-2-propenyl.

C .₃ alkenyl groups are preferred.

As used herein the term "C₂-₆ alkynyl" refers to straight chain or branched chain hydrocarbon groups having from two to six carbon atoms and having in addition one triple bond. This term would include for example, ethynyl, 1-propynyl, 1- and 2- butynyl, 2-methyl-2-propynyl, 2-pentanyl, 3-pentanyl, 4-pentanyl, 2-hexanyl, 3- hexanyl, 4-hexanyl and 5-hexanyl. C_2-3 alkynyl groups are preferred.

As used herein the term "Cι-₆ alkoxy" refers to straight chain or branched chain alkoxy groups having from one to six carbon atoms. Illustrative of such alkoxy groups are methoxy, ethoxy, propoxy, isopropoxy, butoxy, isobutoxy, see-butoxy, tert-butoxy, pentoxy, neopentoxy and hexoxy. Cι_-4 alkoxy groups are preferred.

As used herein the term "C₂-₇ acyl" refers to straight chain or branched chain acyl groups having from two to seven carbon atoms. Illustrative of such acyl groups are acetyl, propionyl (or propiono or propanoyl), isopropionyl (or isopropiono or isopropanoyl), butyryl (or butanoyl), isobutyryl (or isobutanoyl), pentanoyl (or valeryl), hexanoyl (or capronyl) and heptanoyl.

As used herein the term "C_2-7 acyloxy" refers to straight chain or branched chain acyloxy groups having from two to seven carbon atoms. Illustrative of such acyloxy groups are acetyloxy, propionyl (or propiono or propanoyl)oxy, isopropionyl (or isopropiono or isopropanoyl)oxy, butyryl (or butanoyl)oxy, isobutyryl (or isobutanoyl)oxy, pentanoyl (or valeryl)oxy, hexanoyl (or capronyl)oxy and heptanoyloxy. C_2- acyloxy groups are preferred.

As used herein the term "C_3-6 cycloalkyl" refers to an alicyclic group having from three to six carbon atoms. Illustrative of such cycloalkyl groups are cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl. Cyclopentyl and cyclohexyl groups are preferred.

As used herein the term "Cι-₆ alkylthio" refers to straight chain or branched chain alkylthio groups having from one to six carbon atoms. Illustrative of such alkylthio groups are methylthio, ethylthio, propylthio, isopropylthio, butylthio, isobutylthio, sec- butylthio, tert-butylthio, pentylthio, neopentylthio and hexylthio. Cι- alkylthio groups are preferred.

As used herein the term "Cι-₆ alkylamino" refers to straight chain or branched chain alkylamino groups having from one to six carbon atoms. Illustrative of such alkylamino groups are methylamino, ethylamino, propylamino, isopropylamino, butylamino, isobutylamino, -fec-butylamino, tert-butylamino, pentylamino, neopentylamino and hexylamino. alkylamino groups are preferred.

As used herein, the term "di(Cι-₆) alkylamino" refers to straight chain or branched chain di-alkylamino groups having from one to six carbon atoms in each of the alkyl groups. Illustrative of such dialkylamino groups are di-methylamino, di-ethylamino, di-propylamino, di-isopropylamino, di-butylamino, di-isobutylamino, άi-sec- butylamino, di-tert-butylamino, di-pentylamino, di-neopentylamino and di- hexylamino. Di(Cι- )alkylamino groups are preferred.

As used herein, the term "C₂-₇ acylamino" refers to straight chain or branched chain acylamino groups having from two to seven carbon atoms. Illustrative of such acylamino groups are acetylamino, propionyl (or propiono or propanoyl)amino, isopropionyl (or isopropiono or isopropanoyl)amino, butyryl (or butanoyl)amino, isobutyryl (or isobutanoyl)amino, pentanoyl (or valeryl)amino, hexanoyl (or capronyl)amino and heptanoylamino. C₂. acylamino groups are preferred.

Where there is a substituent which renders a compound basic, for example when R⁶ is an amino, alkylamino or dialkylamino group, addition of an acid results in a salt. The acid may be any suitable acid, and can be organic or inorganic. Preferred compounds of general formula I include those in which, independently or in any compatible combination:

1 ? each of R and R represents a Cι-₆ alkyl, preferably a C alkyl, group; R^l and R² are the same as each other; each of R^"5 and R⁴ represents a hydrogen atom; R^D represents a hydrogen atom; R⁶ represents a hydrogen atom;

7 R each of R and R represents a Cι.₆ alkyl, preferably methyl, ethyl or isopropyl, group; R⁷ and R⁸ are the same as each other;

R⁹ represents a halogen atom or a methyl or acetyl group.

Exemplary compounds include:

1. 6,7-Dihydro-2-(2,6-dimethylphenoxy)-9J0-dimethoxy-4H-pyrimido-[6J-α]iso- quinolin-4-one;

2. 2-(2,6-diethylphenoxy)-6,7-dihydro-9J0-dimethoxy-4H-pyrimido-[6J---]iso- quinolin-4-one;

3. 6,7-Dihydro-2-(2,6-diisopropylphenoxy)-9, 10-dimethoxy-4H-pyrimido-[6, 1 - Ω]isoquinolin-4-one;

4. 6,7-Dihydro-9, 10-dimethoxy-2-(2,4,6-trimethylphenoxy)-4H-pyrimido-[6, 1 - α]isoquinolin-4-one;

5. 2-(4-Chloro-2,6-dimethylphenoxy)-6,7-dihydro-9J0-dimethoxy-4H-pyrimido- [6, 1 -α]isoquinolin-4-one; 6. 2-(4-Bromo-2,6-dimethylphenoxy)-6,7-dihydro-9J 0-dimethoxy-4H-pyrimido-

[6, 1 -α]isoquinolin-4-one; 7. 6,7-Dihydro-9, 10-dimethoxy-2-(4-ethanoyl-2,6-dimethylphenoxy)-4H-pyrimido- [6,1 -α]isoquinolin-4-one; S. 2-(2,6-Dichlorophenoxy)-6,7-dihydro-9, 10-dimethoxy-4H-pyrimido-[6, 1 - α]isoquinolin-4-one; 9. 9J0-Dimethoxy-2-(2-methylphenoxy)-6,7-dihydro-4H-pyrimido[6J-a] isoquinolin-4-one; 10. 9J0-Dimethoxy-2-(2-isobutylphenoxy)-6,7-dihydro-4H-pyrimido[6J-a] isoquinolin-4-one;

11. 2-(2-tert-butylphenoxy)-9J0-dimethoxy-6,7-dihydro-4H-pyrimido[6J-a] isoquinolin-4-one;

12. 9J 0-Dimethoxy-2-(2-ethylphenoxy)-6,7-dihydro-4H-pyrimido[6, 1 -a]isoquinolin- 4-one;

13. 2-(2-Cyclopentylphenoxy)-9, 10-dimethoxy-6,7-dihydro-4H-pyrimido[6, 1 -a] isoquinolin-4-one.

The compounds 2-(2,6-diethylphenoxy)-6,7-dihydro-9, 10-dimethoxy-4H pyrimido- [6J-α]isoquinolin-4-one and 6,7-Dihydro-2-(2,6-diisopropylphenoxy)-9J0- dimethoxy-4H-pyrimido-[6J- α]isoquinolin-4-one are particularly preferred.

Compounds of general formula I may be prepared by any suitable method known in the an and/or by the following process, which itself forms part of the invention.

According to a second aspect of the invention, there is provided a process for preparing a compound of general formula I as defined above, excluding the compound 6,7-dihydro-2-phenoxy-9J0-dimethoxy-4H-pyrimido[6Ja]isoquinolin-4-one, the process comprising:

(a) reacting a compound of general formula II:

II

wherein R¹, R², R^D, R⁶ and X are as defined for general formula I and LG represents a leaving group, with a compound of general formula III

III

wherein R', R⁸ and R⁹ are as defined for general formula I; or

(b) when X in general formula I represents a group CR³R⁴, wherein R³ represents a hydrogen atom, R⁴ represents a hydrogen atom or a C ₁.₃ alkyl group, and R⁵ represents a hydrogen atom or a C ₁.₃ alkyl group, hydrogenating a compound of general formula IX:

wherein R¹, R², R⁶, R⁷, R⁸ and R⁹ are as defined for general formula I; and

(c) optionally converting a compound of general formula I so formed into another compound of general formula I.

In compounds of general formula II, the leaving group LG may be chlorine, a thioalkyl group, preferably thiomethyl, or an alkylsulphonyl group, preferably methylsulphonyl. Preferably it is chlorine.

The reaction conditions of step (a) are generally such as to favour the reaction, which is a nucleophilic displacement which is preferably carried out in a suitable solvent such as dimethylformamide or isopropanol in the presence of a base such as potassium carbonate. Suitable reaction conditions may be found in GB-A-1597717 and EP-A- 0124893, which disclose the preparation of related compounds.

The reaction of step (a) is generally applicable for producing compounds of general formula I where R⁶ represents a hydrogen atom or a Cι_-6 alkyl, C_2-6 alkenyl, C_2-6 alkynyl, amino, Cι-₆ alkylamino or C₂-₇ acylamino group and R¹ to R³ and R⁷ to R⁹ and

X have the meanings given above. Compounds of general formula II where LG represents a chlorine atom may be prepared by reacting a compound of general formula IV or a compound of general formula V with phosphorous oxychloride, or by heating a compound of general formula IV with phosphorous pentachloride :

IV

V

wherein R¹, R², R⁵, R⁶ and X are as defined for general formula I. Compounds of general formula II where LG represents a thioalkyl group may be prepared from compounds of general formula IV by heating with phosphorous pentasulphide in a solvent such as dioxan or pyridine to give initially the intermediate thio derivative of compound of formula IV which, on treatment with an alkylating agent such as an alkyl iodide eg. methyl iodide, in a suitable solvent such as tetrahydrofuran or ethyl acetate, gives the thioalkyl compound. Oxidation of the thioalkyl compound with, for example, 3-chloroperbenzoic acid in a solvent such as methylene chloride, gives the alkylsulphone derivative.

Compounds of general formula III are substituted phenols which are either known in the art and available from commercial sources or may readily be prepared by methods known per se, for example from the correspondingly substituted aniline compound via hydrolysis of the diazonium salt.

Compounds of general formula IV may be prepared by reacting a compound of general formula V, wherein R¹, R², R^D and R⁶ are as defined for general formula I, with a cyclodehydrating agent such as phosphorous oxychloride, under less vigorous condition, ie lower temperatures, than those required to give compounds of the general formula II where LG represents a chlorine atom. An alternative method has been described in NL-A-6,401,827 (Hoffmann-La Roche) which involves reacting the carbamoylmethylene-tetrahydroisoquinoline, formula VIII, with diethyl carbonate in ethanolic sodium ethoxide:

VIII

Compounds of general formula V may be prepared by reacting a compound of general formula VI

VI

wherein R¹, R², R⁵ and X are as defined for general formula I with R⁶CH(CO₂Et)₂, wherein R⁶ is as defined for general formula I, and a strong base such as sodium ethoxide in hot ethanolic solution. Alternatively, the corresponding dimethyl ester can be employed in the presence of hot methanolic sodium methoxide.

Compounds of general formula VI may be prepared by reacting a compound of general formula VII

VII

wherein R¹, R², R⁵ and X are as defined for general formula I, with urea by heating at 160°C. Alternatively, compounds of formula VII may be reacted with potassium cyanate in the presence of acetic acid in a suitable solvent such as ethanol.

Compounds of general formula VII are either known in the art or may readily be prepared by methods known per se. For example, the preparation of l-(3,4- dimethoxyphenethyl)barbituric acid has been described by B. Lai et al. J.Med.Chem. 27 1470-1480 (1984). Turning now to step (b), the reaction conditions of step (b) are generally to favour the hydrogenation reaction, and the reaction is generally carried out in a suitable solvent such as an alcohol, eg ethanol, with a noble metal catalyst such as palladium, platinum, rhodium or nickel, at room temperature. The catalyst may be supported, for example on charcoal or alumina.

Compounds of general formula IX may be prepared from a compound of general formula X:

wherein R¹, R² and R⁶ are as defined for general formula I, and R and R³ independently represent a hydrogen atom or a Cι-₃ alkyl group. The reactions are conducted as described above for converting a compound of general formula IV to a compound of general formula I via compounds of general formula II and the preferred reaction conditions correspond accordingly.

Compounds of general formula X may be prepared from compounds of general formula IV (wherein X represents a group CR³R⁴, wherein R³ represents a hydrogen atom, R⁴ represents a hydrogen atom or a C _-3 alkyl group; and R³ represents a hydrogen atom or a Cι-₃ alkyl group) by heating with a noble metal catalyst such as palladium, platinum, rhodium or nickel at a temperature of 300 to 350°C. The catalyst may be supported on charcoal or alumina and the reaction carried out in an inert solvent such as an aromatic hydrocarbon,

In optional step (c), a compound of general formula I may be converted into another compound of general formula I. For example, compounds of general formula I where

R⁶ represents NH₂ may be converted into compounds of general formula I where R⁶ represents a Cι_-6 alkylamino group by standard chemistry, such as by alkylation of a protected derivative such as an acyl or a /?-toluenesulphonyl derivative followed by removal of the protecting group, such as by acid hydrolysis. Compounds of general formula I where R⁶ represents a di(Cι_-6) alkylamino group may be prepared by direct alkylation of the alkylamino derivative. Compounds of general formula I wherein R⁵,

R⁶, R⁷, R⁸ and/or R⁹ represent a C2-3 alkenyl, C₂-₆ alkenyl, C_2-3 alkynyl or C_2-6 alkynyl group may be hydrogenated to give the coreesponding compound with saturated bonds. The reaction conditions for the hydrogenation are as outlined above for step (b).

According to a third aspect, the present invention provides a composition comprising a compound of general formula I, including the excluded compound (6,7-dihydro-2- phenoxy-9J0-dimethoxy-4H-pyrimido[6Ja]isoquinolin-4-one), and a veterinarily or pharmaceutically acceptable carrier or diluent. Preferably the composition is a pharmaceutical composition for human medicine.

Compounds of the present invention are PDE inhibitors and thus possess valuable pharmacological properties, such as bronchodilator activity as demonstrated by the inhibition of field-stimulated contraction of guinea-pig isolated trachea, and anti- inflammatory activity as illustrated in studies on human mononuclear cells stimulated by PΗA (phytohaemagglutinin). In vitro and in vivo data indicate the compounds have a long duration of action, as demonstrated by their persistent protective effects against histamine induced bronchospasm in the guinea-pig when inhaled directly into the lungs as a dry powder. The invention therefore also relates to acute, chronic or prophylactic treatment of patients suffering from respiratory disorders including, in particular, asthma, allergic asthma, hay fever, allergic rhinitis, bronchitis, chronic obstructive pulmonary disease (COPD), adult respiratory distress syndrome (ARDS), and cystic fibrosis. They may also be used topically in skin disorders such as atopic dermatitis and psoriasis, or in ocular inflammation or any other disease including cerebral ischaemia or auto-immune diseases in which increasing intracellular concentrations of cAMP is considered beneficial.

One or more compounds as set out in the first aspect of the invention may be present in association with one or more non-toxic pharmaceutically and/or veterinarily acceptable carriers and/or diluents and/or adjuvants and/or propellants and, if desired, other active ingredients. Suitable carriers or diluents are known in the art (eg Handbook of Pharmaceutical Excipients (1994) 2^nd Edition, Eds. A. Wade/PJ Weller, The Pharmaceutical Press, American Pharmaceutical Association).

Preferably, the compounds and the compositions of the present invention are administered by inhalation, for example by aerosols or sprays which can disperse the pharmacological active ingredient in the form of a powder or in the form of a solution or suspension. Pharmaceutical compositions with powder-dispersing properties usually contain, in addition to the active ingredient, a liquid propellant with a boiling point below room temperature and, if desired, adjuncts, such as liquid or solid non- ionic or anionic surfactants and/or wetting agent to form a stable dispersion. Pharmaceutical compositions in which the pharmacological active ingredient is in solution contain, in addition to this, a suitable propellant, and furthermore, if necessary, an additional solvent and/or a stabiliser. Instead of the propellant, compressed air can also be use, it being possible for this to be produced as required by means of a suitable compression and expansion device. Pharmaceutical compositions may also be delivered by breath activated inhalation devices. Dry powder compositions are prefened for administration by inhalation.

According to a fourth aspect, the present invention provides a compound of general formula I or a composition containing a compound of general formula I, including the excluded compound (6,7-dihydro-2-phenoxy-9J0-dimethoxy-4H- pyrimido[6Ja]isoquinolin-4-one), for use in medicine.

Compounds of the present invention are useful as inhibitors of phosphodiesterase isoenzymes. The compounds or compositions of the present invention may be used to prevent or treat any disease in which the compounds or compositions are useful, but particularly a disease in which raising the intracellular concentration of cAMP is desirable. Examples of diseases against which compounds are useful include respiratory disorders including, in particular, asthma, bronchitis, chronic obstructive pulmonary disease (COPD), adult respiratory distress syndrome (ARDS), allergic asthma, hay fever, allergic rhinitis, and cystic fibrosis. They may also be used topically in skin disorders such as atopic dermatitis or psoriasis, ocular inflammation, or any other disease including cerebral ischaemia or auto-immune diseases in which increasing intracellular concentrations of cAMP is considered beneficial.

This aspect of the invention is particularly relevant to the treatment of humans, but is also applicable to general veterinary industry, in particular domestic animals such as dogs and cats and farm animals such as horses, pigs, cattle, sheep, etc.

Dosage levels of the order of about 0.02 mg to about 200mg, to be taken up to three times daily, are useful in the treatment of the above-mentioned conditions. More particularly, a dosage range of about 0.2 mg to about 20 mg, taken up to three times daily, is effective. The particular dosage regime will however ultimately be determined by the attending physician and will take into consideration such factors as the medication being used, age, weight, severity of symptoms and/or severity of treatment being or to be applied, method of administration of the medication, adverse reactions and/or other contraindications.

The medication according to this aspect of the invention may be given to a patient together with other active agents, which may for example be a different compound of the present invention, or other compounds. Examples include β₂-adrenoceptor agonists, glucocorticoid steroids, xanthine derivatives, antihistamine compounds, leukotriene antagonists, inhibitors of leukotriene synthesis and/or combinations thereof.

According to a fifth aspect, the present invention provides the use of a compound of general formula I, including the excluded compound (6,7-dihydro-2-phenoxy-9J0- dimethoxy-4H-pyrimido[6Ja]isoquinolin-4-one), in the manufacture of an inhibitor of a type III/IV phosphodiesterase isoenzyme. The invention encompasses the use of a compound of general formula I, including the excluded compound (6,7-dihydro-2- phenoxy-9J0-dimethoxy-4H-pyrimido[6Ja]isoquinolin-4-one), in the manufacture of a bronchodilator and/or an anti-asthmatic medication and/or a medicament for the prevention or treatment of chronic obstructive pulmonary disease (COPD).

The invention also relates to a method for the treatment or prevention of a disease in a mammal where a phosphodiesterase isoenzyme inhibitor and/or a bronchodilator would be expected to be of benefit, which method comprises administering to said mammal an amount of an effective, non-toxic amount of a compound of general formula I, including the excluded compound (6,7-dihydro-2-phenoxy-9J0-dimethoxy-

4H-pyrimido[6Ja]isoquinolin-4-one). The invention encompasses a method of treating or preventing asthma and/or chronic obstructive pulmonary disease (COPD) in a mammal. Prefened features of each aspect of the invention apply to each other aspect of the invention, mutatis mutandis.

The following examples, without being limiting, illustrate the invention, with reference to the following figures:

Figure 1 , refened to in Example A(i) below, is a graph showing the effect of DMSO (0.05%) on cholinergic contractile response in superfused guinea pig trachea number of experiments (n) is 10); Figure 2, refened to in Example A(i) below, is a graph showing the effect of 10 μM of the compound of Example 3 on the contraction of guinea pig trachea to electrical field stimulation over time (number of experiments (n) is 3), wherein the anow denotes commencement of washout period; Figure 3, refened to in Example A(i) below, is a graph showing the effect of 10 μM of the compound of Example 11 on cholinergic contractile response in superfused guinea-pig trachea (number of experiments (n) is 3), wherein the anow denotes commencement of washout period;

Figure 4, refened to in Example A(i) below, is a graph showing the effect of 10 μM of the compound of Example 12 on cholinergic contractile response in superfused guinea-pig trachea (number of experiments (n) is 3), wherein the anow denotes commencement of washout period;

Figure 5, refened to in Example A(i) below, is a graph showing the effect of 10 μM of the compound of Example 13 on cholinergic contractile response in superfused guinea-pig trachea (number of experiments (n) is 3), wherein the anow denotes commencement of washout period;

Figure 6, refened to in Example A(ii) below, is a graph showing the effect of lOμM of the compound of Example 1 on the contraction of guinea pig trachea to electrical field stimulation over time (n=l), wherein the anow denotes commencement of washout period; Figure 7, refened to in Example A(ii) below, is a graph showing the effect of lOμM of the compound of Example 8 on the contraction of guinea pig trachea to electrical field stimulation over time (n=l), wherein the anow denotes commencement of washout period;

Figure 8, refened to in Example A(ii) below, is a graph showing the effect of lOμM of the compound of Example 2 on contraction of guinea pig trachea to electrical field stimulation over time (n=l), wherein the anow denotes commencement of washout period;

Figure 9 refened to in Example A(i) below, is a graph showing the effect of lOμM of the compound of Example 10 on contraction of guinea pig trachea to electrical field stimulation;

Figure 10, refened to in Example B below, is a graph showing the effect of various compounds of the present invention against proliferation of human mononuclear cells stimulated by PHA, wherein each point represents the mean of six experiments, and vertical lines represent standard enor of the mean.

Preparation 1 : Synthesis of 2-Chloro-6.7-dihydro-9J0-Dimethoxy-4H-pyrimido-[6J- a]isoquinolin-4-one

A mixture of l-(3,4-dimethoxyphenyl) barbituric acid (70g, 0.24mol), prepared according to the method described in B. Lai et al. J.Med.Chem. 27 1470-1480 (1984), and phosphorus oxychloride (300ml, 3.22mol) was refluxed for 2.5h. The excess phosphorous oxychloride was removed by distillation (20mmHg) on warming. After cooling the residue was slurried in dioxan (100ml) and cautiously added to a vigorously stined ice/water solution (11). Chloroform (11) was added and the resulting mixture was basified with 30% sodium hydroxide solution. The organic layer was separated and the aqueous phase further extracted with chloroform (2x750ml). The combined organic extracts were washed with water (1.51), dried over magnesium sulphate and concentrated in vacuo to leave a gummy material (90g). This was stirred in methanol for a few minutes, filtered and washed with methanol (200ml), diethyl ether (2x200ml) and dried in vacuo at 40°C to yield the title compound as a yellow/orange solid. 47g, 62%

(300MHz, CDC1₃) δ 2.96(2H, t, C(₇₎ H₂); 3.96(6H, s, 2xOCH₃; 4.20(2H, t, C(₆) H₂); 6.61(1H, s, C_{( 1 )} H); 6.76(1H, s, Ar-H); 7J0(1H, s, Ar-H).

Preparation 2: 2.6-Diethylphenol

To a solution of 2,6-diethylaniline (14.9g, OJOmol) in glacial acetic acid (200ml) was added dropwise concentrated sulphuric acid (90ml) with stirring and cooling to maintain temperature between 10 - 20°C. The solution was then stined at 0°C while sodium nitrite (9.0g, 0J3mol) in water (50ml) was added dropwise at such a rate as to keep the temperature below 5°C. The mixture was stined for a further 20 minutes at 0°C then an ice cold solution of urea (3.0g) in water (300ml) was added slowly to produce an amber solution. A mixture of concentrated sulphuric acid (150ml) and water (600ml) was stined and heated to gentle reflux while the ice cold solution of the diazonium salt was added dropwise maintaining a gentle reflux. It is important that the diazonium salt solution drops directly into the sulphuric acid solution without touching the sides of the flask. After the addition the mixture was stined for a further 10 minutes at reflux then for 18h at room temperature. The dark red brown product was removed by filtration, washed with water and dissolved in dichloromethane. The solution was dried over magnesium sulphate and evaporated to obtain a solid which was purified by column chromatography (Silica gel; 2:1 petroleum ether 40 - 60°C : dichloromethane) to give the title compound as colourless crystals. 9.6g, 64% mpt.: 38-39°C

(60MHz, CDC1₃) δ 1.23(6H, t, CH₃); 2.63(4H, q, CH₂); 4.67 (IH, s, OH); 6.90- 7.20(3H, m, Ar-H).

Example 1 : Synthesis of 6.7-Dihydro-2-(2.6-dimethylphenoxy)-9J0-dimethoxy-4H- pyrimido-[6.1 -a]isoquinolin-4-one

2-Chloro-6,7-dihydro-9J 0-dimethoxy-4H-pyrimido-[6, 1 --ϊjisoquinolin-4-one (20g, 68.4mmol), prepared according to Preparation 1, and 2,6-dimethylphenol (obtained from Aldrich) (25 Jg, 167mmol) were dissolved in anhydrous N,N-dimethyl formamide (160ml). Potassium carbonate (28.3g, 205mmol) was added and the mixture heated to 90°C under nitrogen for 3h. The mixture was then cooled, added to water (600ml) and extracted with ethyl acetate (3x300ml). The combined organic extracts were washed with sodium bicarbonate (300ml), water (2x 500ml) and brine (300ml), dried over magnesium sulphate and concentrated in vacuo to give a gummy residue. This was triturated with ether (250ml), isolated by filtration and re- crystallised from methanol (300ml) to give the title compound as a pale yellow solid.

20g, 67% mpt. : 216-218°C.

(300MHz, d₆DMSO) δ 2.05(6H, s, 2x CH₃); 2.95(2H, t, C(₇) H₂); 3.85 (3H, s, OCH₃); 3.90(3H, s, OCH3); 4.05(2H, t, C(₆) H₂); 6.95-7.15(5H, m, Ar-H); 7.55(1H, s, Ax-H). Example 2: Synthesis of 6.7-Dihydro-2-⁽2.6-diisopropylphenoxy)- 9J0-dimethoxy- 4H-pyrimido-[6.1 -a]isoquinolin-4-one

2-Chloro-6,7-dihydro-9, 10-dimethoxy-4H-pyrimido-[6, 1 -α]isoquinolin-4-one, prepared according to Preparation 1 (23 Jg, 79mmol) and 2,6-diisopropylphenol (42.2g, 237mmol) were dissolved in anhydrous N,N-dimethyl formamide (160ml). Potassium carbonate (32.3g, 234mmol) was added and the mixture heated to 90°C under nitrogen for 4.5h. The mixture was then cooled, added to water (800ml) and extracted with ethyl acetate (3x300ml). The combined organic extracts were washed with sodium bicarbonate (300ml), water (2x500ml) and brine (300ml), dried over magnesium sulphate and concentrated in vacuo. The residue was purified by column chromatography (Silica gel; dichloromethane then 2% methanol in dichloromethane. The isolated product was re-crystallised from ethyl acetate (250ml) as a pale yellow solid. Residual ethyl acetate was removed by dissolving the compound in dichloromethane and concentrating in vacuo to give the title compound as a pale yellow solid. 20.5g, 52% mpt. : 123-126°C. (300MHz, CDC1₃) δ 1J5(12H, d, 4x CH-Me); 3.0(4H, m); 4.00(6H, s, 2x OCH3); 4.25(2H, t, C(6) H₂); 6.40(1H, s, C(i) H);6.65(1H, s, Ar-H); 7.20(4H, m).

Example 3: Synthesis of 2-⁽2.6-diethylphenoxy)-6.7-dihydro-9J0-dimethoxy-4H- pyrimido-[6J-a]isoquinolin-4-one

2-Chloro-6,7-dihydro-9J0-dimethoxy-4H-pyrimido-[6J-fl]isoquinolin-4-one, prepared according to Preparation 1 (l.Og, 3.41rnmol), and 2,6-diethylphenol (1.53g,

10.2mmol) were dissolved in propan-2-ol (125ml). Potassium carbonate (1.41g, 10.2mmol) was added and the mixture heated to reflux under nitrogen for 24h. The mixture was then cooled and the solid removed by filtration. The filtrate was evaporated in vacuo and the residue purified by column chromatography (Silica gel; 2: 1 ethyl acetate : dichloromethane) to give the title compound as a pale yellow solid.

1.21g, 88%

mpt. : 180 - 181°C.

ΗPLC : Area (%) 100.00 Column ODS (150 x 4.6mm)

MP pΗ=4 KH PO4 / MeOH (50/50)

FR 0.8 ml/min R_T 11.634 Detection 250nm

(300MHz, CDC1₃) δ 1.21(6H, t, CH3); 2.54(4H, q, CH₂); 2.99(2H, t, J= 6.5 Hz, C₍₇₎ H₂); 3.98(3H, s, OCH3); 4.00 (3H, s, OCH3); 4.22(2H, t, J= 6.5 Hz, C₍₆₎ H₂);

6.42(1H, s, C(i) H); 6.79(1H, s, Ar-H); 7J0-7J9(3H, m, Ar-H); 7.22(1H, s, Ar-H).

Example 4: Synthesis of 6.7-Dihydro-9J0-dimethoxy-2-(2.4.6-trimethylphenoxy)- 4H-pyrimido-[6.1 -a]isoquinolin-4-one

2-Chloro-6,7-dihydro-9, 10-dimethoxy-4H-pyrimido-[6J -a]isoquinolin-4-one, as prepared in Preparation 1 (1.2g, 4J0mmol), and 2,4,6-trimethylphenol (obtained from

Aldrich) (1.68g, 12.34mmol) were dissolved in propan-2-ol (145ml). Potassium carbonate (1.70g, 12.30mmol) was added and the mixture heated under nitrogen for 16h. After cooling to room temperature, the mixture was filtered and the precipitate washed with acetone. The combined filtrates were evaporated in vacuo. The residue was dissolved in dichloromethane (200ml) and washed with 10% sodium hydroxide

(aq) (40ml) and then water (40ml). The organic layer was dried over magnesium sulphate, filtered and evaporated in vacuo to yield a brown oil. Column chromatography (Silica gel: 4:1 ethyl acetate : petroleum ether 40-60° followed by 4:1 ethyl acetate : dichloromethane) gave a yellow solid. This material was washed with diethyl ether, collected by filtration and dried in vacuo to yield the title compound as a pale yellow solid. 0.56g, 35%. mpt.: 230-231°C m/z: C 3H₂₄N₂θ4 requires M=392 found (M+l) = 393

HPLC : Area (%) 99.65

Column ODS (150 x 4.6mm)

MP 0.2M NH₄Ac / MeOH (30/70) FR (ml/min) 0.7

R_τ (min) 13.006

Detection 250nm

(300MHz, CDC1₃) δ 2J5(6H, s, 2x CH₃); 2.28(3H, s, CH3); 3.0 (2H, t, C(₇) H₂); 3.98(6H, s, 2xOCH₃); 4.23(2H, t, C(₆) H₂); 6.42(1H, s, C(i) H); 6.78(1H, s, Ar-H);

6.86(2H, s, 2x Ar-H); 7.20(1H, s, Ar-H).

Example 5: Synthesis of 2-(4-Chloro-2.6-dimethylphenoxyV 6,7-dihydro-9J0- dimethoxy-4H-pyrimido-[6J -a]isoquinolin-4-one

2-Chloro-6,7-dihydro-9J0-dimethoxy-4H-pyrimido-[6J-α]isoquinolin-4-one, prepared in Preparation 1, (1.5g, 5J3mmol) and 4-chloro-2,6-dimethylphenol (obtained from Lancaster Chemicals) (2.41g, 15.39mrnol) were dissolved in propan-2- ol (180ml). Potassium carbonate (2J3g, 15.41mmol) was added and the mixture heated under nitrogen for 16h. After cooling to room temperature, the mixture was filtered and the precipitate washed with acetone. The combined filtrates were evaporated in vacuo. The residue was dissolved in dichloromethane (200ml) and washed with 10% sodium hydroxide (_aq\ (45ml) and then water (45ml). The organic layer was dried over magnesium sulphate, filtered and evaporated in vacuo to yield an orange oil. Column chromatography (Silica gel: 4:1 ethyl acetate : dichloromethane) gave a yellow solid. This material was washed with diethyl ether, collected by filtration and dried in vacuo to yield the title compound as a pale yellow powder. 1.78g, 84%. mpt. 201 - 203°C. m/z: C₂₂Η₂₁ ³⁵ClN₂O₄ requires M=412 found (M+l) = 413

C₂₂H ₁ ³⁷ClN₂O4 requires M=414 found (M+l) = 415

HPLC Area 97.91 Column ODS (250 x 4.6mm)

MP 0JM NH₄Ac / MeCN (40/60)

FR (ml/min) 0.7

R (min) 12.466

Detection 250nm

(300MHz, CDC1₃) δ 2J3(6H, s, 2xCH₃); 2.99 (2H, t, C₍₇₎ H₂); 3.98(3H, s, OCH3); 4.02(3H, s, OCH3); 4.23(2H, t, C(₆) H₂); 6.43(1H, s, C_{( 1)} H); 6.78(1H, s, Ar-H); 7.04(2H, s, 2x Ar-H); 7.21(1H, s, Ar-H).

Example 6: Synthesis of 2-(4-Bromo-2.6-dimethylphenoxyV 6.7-dihydro-9J0- dimethoxy-4H-pyrimido-[6.1 -a]isoquinolin-4-one

2-Chloro-6,7-dihydro-9J0-dimethoxy-4H-pyrimido-[6J-α]isoquinolin-4-one, prepared in Preparation 1, (1.5g, 5J3mmol) and 4-bromo-2,6-dimethylphenol (obtained from Lancaster Chemicals) (3Jg, 15J3mmol) were dissolved in propan-2- ol (180ml). Potassium carbonate (2J3g, 15.41mmol) was added and the mixture heated under nitrogen for 16h. After cooling to room temperature, the mixture was filtered and the precipitate washed with acetone. The combined filtrates were evaporated in vacuo. The residue was dissolved in dichloromethane (200ml) and washed with 10% sodium hydroxide (_aq) (45ml) and then water (45ml). The organic layer was dried over magnesium sulphate, filtered and evaporated in vacuo to yield an orange oil. Column chromatography (Silica gel: 4:1 ethyl acetate : dichloromethane) gave a yellow solid. This material was washed with diethyl ether, collected by filtration and dried in vacuo to yield the title compound as a pale yellow powder

1.90g, 81%. mpt. : 232 - 234°C. m/z: C ₂H ι⁷⁹BrN O₄ requires M=456 found (M+l) = 457

C₂ H ₁ ⁸¹BrN₂0 requires M=458 found (M+l) = 459 HPLC : Area (%) 99.77

Column ODS (150 x 4.6mm)

MP 0JM NH₄Ac / MeCN (57/43)

FR (ml/min) 1.0 R_T (min) 1 1.565 Detection 250nm

(300MHz, CDC1₃) δ 2J4(6H, s, 2xCH₃); 2.98(2H, t, C(₇) H₂); 3.97(3H, s, OCH3); 3.99 (3H, s, OCH3); 4.22(2H, t, C(₆) H₂); 6.43(1H, s, C₍₁) H); 6.78(1H, s, Ar-H); 7J9(2H, s, 2x Ar-H); 7.21(1H, s, Ar-H).

Example 7: Synthesis of 6.7-Dihydro-9J0-dimethoxy-2-(4-ethanoyl-2_T6- dimethylphenoxy)- 4H-pyrimido-[6J -a]isoquinolin-4-one

6,7-Dihydro-2-chloro-9, 10-dimethoxy-4H-pyrimido-[6, 1 -α]isoquinolin-4-one, prepared in Preparation 1, (1.5g, 5J3mmol) and 2,6-dimethyl-4-hydroxyacetophenone (obtained from Maybridge Chemicals) (2.53g, 15.41mmol) were dissolved in propan- 2-ol (180ml). Potassium carbonate (2J3g, 15.41mmol) was added and the mixture heated under nitrogen for 23h. After cooling to room temperature, the mixture was filtered and the precipitate washed with acetone. The combined filtrates were evaporated in vacuo. The residue was dissolved in dichloromethane (200ml) and washed with water (2x 45ml). The organic layer was dried over magnesium sulphate, filtered and evaporated in vacuo to yield an orange oil. Column chromatography (Silica gel: 4:1 ethyl acetate : dichloromethane) gave a yellow solid. This material was washed with diethyl ether, collected by filtration and dried in vacuo to yield the title compound as a pale yellow powder 1.81g, 84%. mpt. : 228- 230°C. m/z: C₂₄Η₂₄N₂θ5 requires M-420 found (M+l) = 421 HPLC : Area (%) 99.32

Column ODS MP 0JM NH₄Ac / MeCN (65/35)

FR (ml/min) 1.0

Rχ (min) 13.840

Detection 250nm

(300MHz, CDC1₃) δ 2.25(6H, s, 2xCH₃); 2.60(3H, s, CH3CO); 3.02(2H, t, C₍₇₎ H₂); 3.99(3H, s, OCH3); 4.01 (3H, s, OCH3); 4.23(2H, t, C₍₆₎ H₂); 6.47(1H, s, C(i) H); 6.78(1H, s, Ar-H); 7.21(1H, s, Ar-H); 7.68(2H, s, 2xAr-H).

Example 8: Synthesis of 2J2.6-DichlorophenoxyV 6.7-dihydro-9J0-dimethoxy-4H- pyrimido-[6.1 -a]isoquinolin-4-one

2-Chloro-6,7-dihydro-9, 10-dimethoxy-4H-pyrimido-[6, 1 -α]isoquinolin-4-one, prepared in Preparation 1 (25g, 85mmol) and 2,6-dichlorophenol (25Jg, 153mmol) were dissolved in anhydrous N,N-dimethyl formamide (150ml). Potassium carbonate (30g, 217mmol) was added and the mixture heated to 90°C under nitrogen for 2h. The mixture was then cooled, partitioned between water (11) and ethyl acetate (500ml). The resulting precipitate was filtered, washed with ethyl acetate (100ml) and water (100ml), re-dissolved in dichloromethane (500ml) and washed with brine (200ml), dried over magnesium sulphate and concentrated in vacuo. The residue was re-crystallised from acetonitrile (600ml) to give the title compound as a pale yellow solid. 22g, 53%

mpt. 240-242°C.

(300MHz, d₆DMSO) δ 2.05(2H, t, C₍₇₎ H₂₎; 3.85(3H, s, OCH₃); 3.90 (3H, s, OCH3); 4.05(2H, t, C(₆) H₂); 7.00(1H, s, C₍₁₎ H); 7J5(1H, s, Ar-H); 7.35(1H, t, Ar- H); 7.65(1H, s, Ar-H).

Example 9: Synthesis of 9J0-Dimethoxy-2J2-methyιphenoxy)-6.7-dihydro-4H- pyrimido[6.1 -a]isoquinolin-4-one

2-Chloro-9J0-dimethoxy-6,7-dihydro-4H-pyrimido[6J-a]isoquinolin-4-one (1) (1.5g, 5J3 mmol) and o-cresol (1.66g, 15.4 mmol) were dissolved in iso-propanol (180 ml).

Potassium carbonate (2J3g, 15.4 mmol) was added and the mixture was heated at reflux, under nitrogen, for 18h. After cooling to room temperature, the mixture was filtered and the precipitate washed with acetone. The combined filtrates were evaporated in vacuo and the residue was dissolved in dichloromethane (220 ml), washed with 10% NaOH (40 ml), then with water (40 ml) and dried (MgSO₄). Evaporation in vacuo gave a brown oil which was purified by column chromatography on silica gel (EtOAc / petroleum ether 80:20). The title compound was obtained as a pale yellow solid, 0.56g, 35%.

M.p.: 201-203°C m/z: C21H20N2O₄ requires M=364 found (M+l) = 365 HPLC: Area (%) 99.01

Column ODS (150 x 4.6 mm) MP 0.2M NH₄OAc / MeOH (40/60)

FR (ml/min) 0.8 RT (min) 14.976 Detection 235 nm

JJ NMR (300 MHz, CDC1₃): δ 2.22 (3H, s, ArCH₃), 2.97 (2H, t, CH₂), 3.98 (6H, s, 2xOCH₃), 4.21 (2H, t, CH₂), 6.40 (IH, s, C=CH), 6.78 (IH, s, ArH), 7.04-7.25 (5H, m, 5 ArH).

Example 10: Synthesis of 9J0-Dimethoxy-2-(2-isobutylphenoxy)-6.7-dihydro-4H- pyrirnido[6J-a] isoquinolin-4-one

2-Isobutylphenol

Potassium tert-butoxide (44.8g, 400mmol) was suspended in degassed heptane (1300ml) and butyllithium (258ml, 400mmol) added. The reaction mixture was allowed to stir at room temperature for 20 min and then O-cresol (10.8g, lOOmmol) added followed by heating at reflux for 3 hours. The mixture was then cooled to room temperature and the precipitate allowed to settle. The excess solvent was decanted off and the residue washed with pentane. This process was repeated once more and the resultant precipitate suspended in THF (1500ml). This suspension was transfened, via cannula, to a solution of isopropylbromide (10.33ml, HOmmol) in THF (500ml) and the reaction mixture stirred at room temperature overnight. The mixture was quenched by addition of water (50ml) and acidified with HC1 (5M). The aqueous phase was separated and extracted with chloroform (3 x 100ml). The organic phases were combined, dried (MgSO ), filtered and concentrated to give a red brown liquid. The crude material was purified by flash column chromatography (90:10 petrohEtOAc) to give the title compound as a yellow oil (7.63g, 51%).

9J0-Dimethoxy-2-(2-isobutylphenoxy)-6.7-dihydro-4H-pyrimido[6J-a]isoquinolin- 4-one

2-Isobutylphenol (1.24g, 8J6mmol) was dissolved in TΗF (40ml) and cooled to - 78°C. Butyllithum (5J2ml, 8J6mmol) was then added and the reaction mixture stined at -78°C for 1 hour and then slowly warmed to room temperature overnight. The reaction was quenched by addition of NΗ C1 (40ml) and the mixture extracted with EtOAc (3 x 50ml). The combined organic phases were washed with NH C1

(50ml). This aqueous phase was combined with that from the previous washing and extracted with EtOAc (50ml). All the organic phases were now combined and washed with brine, dried (MgSO ), filtered and concentrated to give a yellow oily solid. Ether was added to the residue and the resultant solid filtered off and washed with ice cold ether. The residue was purified by flash column chromatography eluting with ethyl acetate to give the title compound as a white solid (0.5g, 18%).

Example 1 1 : Synthesis of 2-(2-tert-butylphenoxyV9J0-dimethoxy-6.7-dihydro-4H- pyrimido[6.1 -a]isoquinolin-4-one

2-Chloro-9J0-dimethoxy-6,7-dihydro-4H-pyrimido[6J-a]isoquinolin-4-one (1.47g, 5.0 mmol) and 2-tert-butylphenol (2.25g, 15.0 mmol) were dissolved in 2-propanol

(180 ml). Potassium carbonate (2.07g, 15.0 mmol) was added and the mixture was stined and heated to reflux, under nitrogen, for 6h. After cooling to room temperature the mixture was filtered and the filtrate was evaporated in vacuo. The residue was purified by column chromatography on silica gel [ethyl acetate/dichloromethane (3:2)] to provide the above compound (1.35g, 66%) as an off-white solid.

M.p.: 226-228°C

M/z: C₂₄H₂₆N₂0₄ requires M=406, found m/z [ES+] = 407

HPLC: Area (%) 99.68

Column S5 C8 (250 x 4.6 mm)

MP pH 4 0.02M KH₂PO₄ / CHjCN (35/65) RT (min) 9J75

FR (mlΛnin) 0.7 Detection 254 nm

Η NMR (300 MHz, CDC1₃): δ 1.39 (9H, s, CH(CH)₃), 2.97 (2Η, t, CH₂), 3.97 (3H, s, OCH₃), 3.98 (3H, s, OCH₃), 4.23 (2H, t, CH₂), 6.38 (IH, s, C=CH), 6.78 (IH, s,

ArH), 7.05-7.27 (4H, m, 4xArH), 7.40 (IH, m, ArH).

Example 12: Synthesis of 9J0-Dimethoxy-2-f2-ethylphenoxyV6.7-dihydro-4H- pyrimido[6.1 -a]isoquinolin-4-one

2-Chloro-9J0-dimethoxy-6,7-dihydro-4H-pyrimido[6J-a]isoquinolin-4-one (lJ7g, 5.0 mmol) and 2-ethylphenol (1.22g, 10.0 mmol) were dissolved in 2-propanol (180 ml). Potassium carbonate (1.38g, 10.0 mmol) was added and the mixture was stined and heated to reflux, under nitrogen, for 6h. After cooling to room temperature the mixture was filtered and the filtrate was evaporated in vacuo. The residue was purified by column chromatography on silica gel [ethyl acetate/dichloromethane (3:2)] to provide the above compound (1.27g, 67%) as a pale yellow solid.

M.p.: 167-169°C

M/z: C₂₂H₂₂N₂O₄ requires M=378, found m/z [ES+] = 379

HPLC: Area (%) 99.46 Column S5 C8 (250 x 4.6 mm)

MP pH 4 0.02M KH₂PO₄ / CH₃CN (35/65)

RT (min) 7.725

FR (ml/min) 0.7

Detection 254 nm

^!H NMR (300 MHz, CDCI₃): δ 1.21 (3H, t, CH₂CH₃), 2.59 (2Η, q, CH₂CH₃), 2.97 (2H, t, CH₂), 3.97 (6H, s, 2xOCH₃), 4.21 (2H, t, CH₂), 6.41 (IH, s, C=CH), 6.78 (IH, s, ArH), 7.05-7.28 (5H, m, 5xArH).

Example 13: Synthesis of 2-(2-CyclopentylphenoxyV9J0-dimethoxy-6.7-dihydro-4H- pyrimido[6J-a]- isoquinolin-4-one

2-Chloro-9J0-dimethoxy-6,7-dihydro-4H-pyrimido[6,l-a]isoquinolin-4-one (1.20g, 4J 1 mmol) and 2-cyclopentylphenol (l.Og, 6J7 mmol) were dissolved in 2-propanol (150 ml). Potassium carbonate (lJ4g, 8.23 mmol) was added and the mixture was stined and heated to reflux, under nitrogen, for 18h. After cooling to room temperature the mixture was filtered and the filtrate was evaporated in vacuo. The residue was purified by column chromatography on silica gel [ethyl acetate/dichloromethane (3:2)] to provide the above compound (0.51g, 30%) as a pale yellow solid.

M.p.: 122-125°C

M/z: C₂₅Η₂₆N₂O₄ requires M=418, found m/z [ES+] = 419

HPLC: Area (%) 99.43

Column S5 C8 (250 x 4.6 mm)

MP pH 4 0.02M KH₂PO₄ / CH₃CN (35/65) RT (min) 10.191

FR (ml/min) 0.7

Detection 254 nm

Η NMR (300 MHz, CDC1₃): δ 1.57-2.05 (8H, m, cyclopentyl 4xCH₂), 2.97 (2H, t, CH₂), 3J3 (IH, m, ArCH), 3.97 (6Η, s, 2xOCH₃), 4.21 (2H, t, CH₂), 6.38 (IH, s,

C=CH), 6.78 (IH, s, ArH), 7.07 (IH, m, AxH), 7.18 (3H, m, 3xArH), 7.32 (IH, m, ArH).

The pharmacological utility of the compounds of the present invention has been demonstrated in studies using compounds previously synthesised as described in the above Examples. The results below serve to illustrate the generic application of the compounds of the present invention. Example A: Efficacy of compounds of the invention against electrical-induced contraction of guinea-pig isolated trachea

The efficacy of compounds of the invention was tested against electrical-induced contraction of guinea-pig isolated trachea. The results demonstrate that the compounds of Examples 2, 3, 10, 11, 12 and 13 inhibit the contractile responses with a long duration of action .

Example A (ϊ) - Superfusion experiments Method

Superfusion of guinea-pig tracheal rings was performed according to a previously described method (Coleman et al. Pulmonary Pharmacology 9 107-1 17 (1996)). Briefly, guinea-pig tracheal preparations were cut into rings and then opened by sectioning the ring opposite the smooth muscle and suspended between two platinum electrodes under lg tension. The tissues were superfused at a rate of from 1 to 3.25 ml/min with Krebs-Henseleit solution at 37°C containing the cyclooxygenase inhibitor, indomethacin (5μM) and bubbled with 95% O₂ and 5% CO₂. Tracheal preparations were allowed to equilibrate for 40 minutes before commencement of electrical stimulation, delivered as a 10 s train of square wave pulses at 3Hz, OJms duration and 20V (approx 400 mAmps) generated every 100 sec by means of physiological square wave-stimulator. The compounds of the present invention were superfused at a rate of 0.2 to 0.3 ml/min and contractile responses to electrical field stimulation were recorded on a Macintosh computer using MacLab software. The drug was prepared in DMSO and diluted in Krebs-Henseleit solution which yielded a final superfusion concentration of 0.05 to 0J % DMSO.

Results

The duration of action was determined and expressed as onset time (OT₅₀) and recovery time (RT₅₀). The time taken to reach 50% of the maximum inhibition of the contractile response (onset time: OT) was determined and similarly, the time taken for a 50%) reversal of the maximum inhibition of the contractile response (recovery time: RT₅o) following the termination of exposing the tissue to compound. These values are shown in Table 1.

As shown in Table 1 , all the tested compounds caused a time dependent inhibition of the contractile response to electrical field stimulation in guinea-pig isolated trachea. The recovery of the contractile response to electrical field stimulation was slow, with the inhibitory responses not reversing 4 hours after cessation of administration of the drug. The vehicle, DMSO, failed significantly to inhibit the contractile response to electrical field stimulation (Figure 1).

Table 1. OTsn and RT^values

(Each value is the mean and s.e. mean of three observations except where otherwise indicated, as "n")

Example A fii - Organ bath experiments Method

Guinea-pig tracheal rings were suspended in organ baths under 1 g tension between two electrodes and subjected to electrical field stimulation (3Ηz, OJms duration and 20V (approx 400mAmps) generated every 100 sec by means of physiological square wave-stimulator. The compounds of Examples 1, 2 and 8 were dissolved in DMSO containing Tween 80 (10%) and distilled water (0.01M), which were then added to the organ bath to give a final concentration of lOμM.

Results The results are shown in Figures 6 (for compound of Example 1), 7 (for compound of

Example 8) and 8 (for compound of Example 2). All compounds caused complete inhibition of the contractile response to electrical field stimulation and the effect was maintained for more than 2-4 hours.

Example B: Efficacy of compounds of the invention against proliferation of human mononuclear cells stimulated by PHA The effect of compounds of the invention against proliferation of human mononuclear cells stimulated by PHA was also investigated. Proliferation was significantly inhibited by these compounds, indicating that they possess anti-inflammatory activity. The results below serve to illustrate the generic application of the novel compounds of the present invention.

Method

Normal healthy volunteers underwent phlebotomy and 25ml of blood was collected. Mononuclear cells were separated and purified according to the method of Banner et al. (Banner et al. Br. J. Pharmacol. 116 3169-3174 (1995)). Human peripheral mononuclear cells (100,000 per well) were stimulated for 24h with phytohaemagglutinin (PHA, 2μg/ml) in the absence or presence of the compounds of Examples 1, 2 and 8 (0.001-100μM) at 37°C in a 95% air, 5% CO₂ atmosphere. Twenty four hours later, [³H] -thymidine (OJμCi) was added to each well and the cells were incubated for a further 24h period. Cells were then harvested onto glass fibre filters using a cell harvester (ICN Flow, Buckinghamshire) and counted in a scintillation counter.

Results

All the compounds under test caused a concentration dependent inhibition of the proliferation of human mononuclear cells stimulated with PHA (n=6; Figure 9). The IC₅₀ values and 95%) confidence limits for these compounds are indicated in Table 2. The results are also shown in the graph of Figure 10.

Table 2: TCsn values for various compounds against proliferation of human mononuclear cells stimulated with PHA (n=6)

Example C

6,7-Dihydro-2-(2,6-diisopropylphenoxy)- 9J0-dimethoxy-4H-pyrimido-[6J- a]isoquinolin-4-one (compound of Example 2) has been shown to be a potent inhibitor of phosphodiesterase (PDE) type 3 and 4 isozymes. The IC₅₀ value is shown below.

PDE3 (nM) PDE4 (nM)

(human platelet) (human neutrophil)

Example 2 107 1195

Rolipram ND 6412

Cilostamide 89 ND

Rolipram is a known PDE 4 inhibitor and cilostamide is a known PDE3 inhibitor ND - Not determined

Example D 6,7-Dihydro-2-(2,6-diisopropylphenoxy)- 9, 10-dimethoxy-4H-pyrimido-[6, 1 - a]isoquinolin-4-one (compound of Example 2) was tested for effects on LPS induced TNF-α release from human monocytes. Results are below.

IC50 (nM)

Compound 250 n=6

CDP 840 (PDE4 inhibitor) 92 n=6

Siguazodan (PDE3 inhibitor) >100μM

Example E: in vivo tests on 6.7-Dihvdro-2-f2.6-diisopropylphenoxy)- 9J0-dimethoxy-

4H-pyrimido-[6J-a]isoquinolin-4-one (compound of Example 2)

1. The above compound was tested in a model of histamine induced bronchospasm. Conscious guinea-pigs were exposed to dry powder (micronised) of the compound. The drug was blended with lactose so that the final concentration was 0.25, 2.5 and

25%o. At various times after exposure to drug the animals were anaesthetised and challenged with varying doses of histamine. Total airway resistance and mean arterial blood pressure were recorded. Exposure to dry powder (25%) provided significant protection against histamine induced bronchospasm without changing mean arterial blood pressure.

2. Intravenous administration of the compound of Example 2 (0J to 300μg/kg) to urethane anaesthetised guinea-pigs produced a dose dependant reduction in mean arterial blood pressure. The compound was dissolved in DMSO then diluted with saline (there was evidence that the compound had come out of solution).

3. In a model of antigen induced eosinophilia in the ovalbumin sensitised guinea-pig, the compound of Example 2 (lOmg/kg) administered orally 1 hour prior to antigen challenge, significantly inhibited the recruitment of eosinophils to the lungs following antigen challenge (aerosol) in sensitised guinea-pigs.

Example F: Taste of compounds

For pharmaceutical compounds which are administered orally, how the compounds taste is a very important factor in ensuring patient compliance. Unexpectedly, the compounds of the present invention are substantially tasteless. They are therefore particularly suitable for oral administration, for example as dry powder to be inhaled.

Method

Small amounts of all the compounds of the above Examples 1 to 13, trequinsin (9J0- dimethoxy-3-methyl-2-mesitylimino-2,3,6,7-tetrahydro-4H-pyrimido[6J- a]isoquinolin-4-one) and desmethyl trequinsin (9J0-dimethoxy-2-mesitylimino- 2,3,6,7-tetrahydro-4H-pyrimido[6J-a]isoquinolin-4-one) were placed on the tip of the tongue of an informed, healthy male volunteer and the taste of each compound was assessed.

Results All the compounds of Examples 1 to 13 were not bitter, and therefore have significantly improved taste compared wth trequinsin or desmethyl trequinsin, which are both very bitter.

Claims

1. A compound of general formula I:

wherein

each of R¹ and R² independently represents a Q-₆ alkyl or C _-7 acyl group;

X represents OCH or a group CR³R⁴, wherein each of R³ and R⁴ independently represents a hydrogen atom or a Cι_-3 alkyl group;

R represents a hydrogen atom or a C_1- alkyl, C_2-3 alkenyl or C_2-3 alkynyl group;

R⁶ represents a hydrogen atom or a Cι_-6 alkyl, C_2-6 alkenyl, C .₆ alkynyl, amino, Cι_-6 alkylamino, di(Cι-₆) alkylamino or C_2- acylamino group; each of R⁷ and R⁸ independently represents a hydrogen or halogen atom or a hydroxy, trifluoromethyl, Cι-₆ alkyl, C₂.₆ alkenyl, C₂.₆ alkynyl, C -₇ acyl, Cι-₆ alkylthio, Cι-₆ alkoxy or C_3-6 cycloalkyl group;

R⁹ represents a hydrogen or halogen atom or a hydroxy, trifluoromethyl, Cι_-6 alkyl, C_2- alkenyl, C₂-₆ alkynyl, C_2-7 acyl, Cι-₆ alkylthio, Cι-₆ alkoxy or C_3-6 cycloalkyl group; or a salt thereof; excluding the compound 6,7-dihydro-2-phenoxy-9J0-dimethoxy-4H- pyrimido[6Ja]isoquinolin-4-one.

2. A compound as claimed in claim 1 wherein, independently or in any compatible combination,

1 7 each of R and R represents a Cι-₆ alkyl, preferably a C_M alkyl, group;

R¹ and R² are the same as each other; each of R³ and R⁴ represents a hydrogen atom; R³ represents a hydrogen atom; R⁶ represents a hydrogen atom;

7 P* each of R and R represents a Cι-₆ alkyl, preferably methyl, ethyl or isopropyl, group;

R⁷ and R⁸ are the same as each other; R⁹ represents a halogen atom or a methyl or acetyl group.

3. 6,7-Dihydro-2-(2,6-dimethylphenoxy)-9J0-dimethoxy-4H-pyrimido-[6J-α]iso- quinolin-4-one.

4. 2-(2,6-Diethylphenoxy)-6,7-dihydro-9J0-dimethoxy-4H-pyrimido-[6J-α]iso- quinolin-4-one.

5. 6,7-Dihydro-2-(2,6-diisopropylphenoxy)-9J0-dimethoxy-4H-pyrimido-[6J- α]isoquinolin-4-one.

6. 6,7-Dihydro-9J0-dimethoxy-2-(2J,6-trimethylphenoxy)-4H-pyrimido-[6,l- α]isoquinolin-4-one.

7. 2-(4-Chloro-2,6-dimethylphenoxy)-6,7-dihydro-9, 10-dimethoxy-4H-pyrimido- [6, 1 -α]isoquinolin-4-one.

8. 2-(4-Bromo-2,6-dimethylphenoxy)-6,7-dihydro-9, 10-dimethoxy-4H-pyrimido- [6, 1 -α]isoquinolin-4-one.

9. 6,7-Dihydro-9J 0-dimethoxy-2-(4-ethanoyl-2,6-dimethylphenoxy)-4H-pyrimido- [6J-α]isoquinolin-4-one.

10. 2-(2,6-Dichlorophenoxy)-6,7-dihydro-9, 10-dimethoxy-4H-pyrimido-[6, 1 - α]isoquinolin-4-one.

11. 9,10-Dimethoxy-2-(2-methylphenoxy)-6,7-dihydro-4H-pyrimido[6J- a]isoquinolin-4-one

12. 9J0-Dimethoxy-2-(2-isobutylphenoxy)-6,7-dihydro-4H-pyrimido[6J-a] isoquinolin-4-one.

13. 2-(2-tert-butylphenoxy)-9, 10-dimethoxy-6,7-dihydro-4H-pyrimido[6, 1 -a] isoquinolin-4-one.

14. 9,10-Dimethoxy-2-(2-ethylphenoxy)-6,7-dihydro-4H-pyrimido[6J-a]isoquinolin- 4-one.

15. 2-(2-Cyclopentylphenoxy)-9, 10-dimethoxy-6,7-dihydro-4H-pyrimido[6J -a] isoquinolin-4-one.

16. A process for preparing a compound of general formula I as defined in claim 1, excluding the compound 6,7-dihydro-2-phenoxy-9J0-dimethoxy-4H- pyrimido[6Ja]isoquinolin-4-one, the process comprising:

(a) reacting a compound of general formula IT.

II

wherein R¹, R², R^, R⁶ and X are as defined for general formula I and LG represents a leaving group, with a compound of general formula III

III

wherein R , R and R are as defined for general formula I; or

(b) when X in general formula I represents a group CR³R⁴, wherein R³ represents a hydrogen atom, R⁴ represents a hydrogen atom or a C₁-₃ alkyl group, and R⁵ represents a hydrogen atom or a C₁-₃ alkyl group, hydrogenating a compound of general formula IX:

wherein R¹, R², R⁶, R⁷, R⁸ and R⁹ are as defined for general formula I; and

(c) optionally converting a compound of general formula I so formed into another compound of general formula I.

17. A process as claimed in claim 16, wherein LG in general formula II represents a chlorine atom.

18. A process as claimed in claim 16 or claim 17, wherein step (a) is carried out in a suitable solvent such as dimethylformamide or isopropanol in the presence of a base such as potassium carbonate.

19. A process as claimed in claims 16, 17 or 18 wherein the compound of general formula I is as defined in any of claim 1 to 15.

20. A composition comprising a compound of general formula I:

wherein

each of R and R² independently represents a Cι_-6 alkyl or C₂.₇ acyl group;

. A "ϊ J X represents OCH₂ or a group CR R , wherein each of R and R independently represents a hydrogen atom or a Cι_-3 alkyl group;

R⁵ represents a hydrogen atom or a C1-3 alkyl, C _3 alkenyl or C_2-3 alkynyl group;

R⁶ represents a hydrogen atom or a Cι-₆ alkyl, C_2-6 alkenyl, C _-6 alkynyl, amino, Cι_-6 alkylamino, di(Cι-₆) alkylamino or C₂-₇ acylamino group; each of R⁷ and R⁸ independently represents a hydrogen or halogen atom or a hydroxy, trifluoromethyl, Cι-₆ alkyl, C_2-6 alkenyl, C__-6 alkynyl, C_2- acyl, Cι-₆ alkylthio, Cι.₆ alkoxy or C₃.₆ cycloalkyl group;

R⁹ represents a hydrogen or halogen atom or a hydroxy, trifluoromethyl, d-₆ alkyl, C?.

₆ alkenyl, C₂.₆ alkynyl, C₂.₇ acyl, Cι-₆ alkylthio, Cι-₆ alkoxy or C₃-₆ cycloalkyl group; or a salt thereof; and a veterinarily or pharmaceutically acceptable carrier or diluent.

21. A composition as claimed in claim 20, further comprising an active agent such as a β₂-adrenoceptor agonist or a glucocorticoid steroid.

22. A composition as claimed in claim 20 or claim 21, wherein the composition is a pharmaceutical composition for human medicine.

23. A composition as claimed in claim 20, 21 or 22, adapted for administration by aerosol.

24. A composition as claimed in any of claims 20 to 23, wherein the compound is as defined in any of claims 1 to 15.

25. A compound of general formula I

wherein

1 7 each of R and R independently represents a Cι-₆ alkyl or C₂.₇ acyl group;

X represents OCH₂ or a group CR³R⁴, wherein each of R³ and R⁴ independently represents a hydrogen atom or a Cι-₃ alkyl group;

R⁵ represents a hydrogen atom or a Cι-₃ alkyl, C₂-₃ alkenyl or C_2-3 alkynyl group;

R⁶ represents a hydrogen atom or a Cι_-6 alkyl, C_2-6 alkenyl, C_2-6 alkynyl, amino, Cι_-6 alkylamino, di(Cj_-6) alkylamino or C_2-7 acylamino group; each of R⁷ and R⁸ independently represents a hydrogen or halogen atom or a hydroxy, trifluoromethyl, Cι-₆ alkyl, C₂.₆ alkenyl, C₂.₆ alkynyl, C_2-7 acyl, Cι_-6 alkylthio, Cι-₆ alkoxy or C₃-₆ cycloalkyl group; R represents a hydrogen or halogen atom or a hydroxy, trifluoromethyl, Cι-₆ alkyl, C₂. ₆ alkenyl, C_2-6 alkynyl, C_2-7 acyl, Cι_-6 alkylthio, Cι_-6 alkoxy or C₃.₆ cycloalkyl group; or a salt thereof; for use in medicine.

26. A compound of general formula I:

wherein

each of R¹ and R² independently represents a Cι.₆ alkyl or C₂-7 acyl group;

X represents OCH₂ or a group CR³R⁴, wherein each of R³ and R⁴ independently represents a hydrogen atom or a C ₁-₃ alkyl group;

R⁵ represents a hydrogen atom or a C₁-₃ alkyl, C₂-₃ alkenyl or C₂-₃ alkynyl group; R⁶ represents a hydrogen atom or a Cι-₆ alkyl, C₂-₆ alkenyl, C₂.₆ alkynyl, amino, Ci-6 alkylamino, di(Cι_-6) alkylamino or C₂.₇ acylamino group; each of R⁷ and R⁸ independently represents a hydrogen or halogen atom or a hydroxy, trifluoromethyl, Cι_-6 alkyl, C_2-6 alkenyl, C₂-₆ alkynyl, C_2-7 acyl, Cι_-6 alkylthio, Cι_-6 alkoxy or C_3-6 cycloalkyl group; R⁹ represents a hydrogen or halogen atom or a hydroxy, trifluoromethyl, Cι-₆ alkyl, C₂.

₆ alkenyl, C_2-6 alkynyl, C2-7 acyl, Cι_-6 alkylthio, Ci-6 alkoxy or C _-6 cycloalkyl group; or a salt thereof; for use as an inhibitor of a phosphodiesterase isoenzyme.

27. A compound of general formula I:

wherein

each of R and R independently represents a Cι_-6 alkyl or C_2-7 acyl group;

X represents OCH₂ or a group CR R⁴, wherein each of R³ and R⁴ independently represents a hydrogen atom or a C ₁-3 alkyl group;

R⁵ represents a hydrogen atom or a C_1-3 alkyl, C_2-3 alkenyl or C_2-3 alkynyl group;

R represents a hydrogen atom or a Cι_-6 alkyl, C_2-6 alkenyl, C_2-6 alkynyl, amino, Cι_-6 alkylamino, di(Cι-₆) alkylamino or C₂_₇ acylamino group; each of R⁷ and R⁸ independently represents a hydrogen or halogen atom or a hydroxy, trifluoromethyl, Cι_-6 alkyl, C₂-₆ alkenyl, C_2-6 alkynyl, C_2-7 acyl, Cι-₆ alkylthio, Cι-₆ alkoxy or C₃-₆ cycloalkyl group;

R⁹ represents a hydrogen or halogen atom or a hydroxy, trifluoromethyl, Cι-₆ alkyl, C₂-

6 alkenyl, C₂-₆ alkynyl, C₂-₇ acyl, Cι-₆ alkylthio, Cι-₆ alkoxy or C₃-₆ cycloalkyl group; or a salt thereof; for use in the prevention or treatment of a disease in which raising the intracellular concentration of cAMP is desirable.

8. A compound of general formula I:

wherein

1 7 each of R and R independently represents a Cι_-6 alkyl or C_2-7 acyl group;

X represents OCH₂ or a group CR³R⁴, wherein each of R³ and R⁴ independently represents a hydrogen atom or a C₁-₃ alkyl group;

R⁵ represents a hydrogen atom or a C ₁.₃ alkyl, C₂-₃ alkenyl or C₂-₃ alkynyl group; R⁶ represents a hydrogen atom or a Cι_-6 alkyl, C2-₆ alkenyl, C2_-6 alkynyl, amino, Cι_-6 alkylamino, di(Cι_-6) alkylamino or C2-_? acylamino group; each of R⁷ and R⁸ independently represents a hydrogen or halogen atom or a hydroxy, trifluoromethyl, C_1-6 alkyl, C2-₆ alkenyl, C₂-₆ alkynyl, C2-7 acyl, Cj-6 alkylthio, Cι_-6 alkoxy or C_3-6 cycloalkyl group; R⁹ represents a hydrogen or halogen atom or a hydroxy, trifluoromethyl, Cι-₆ alkyl, C2-

6 alkenyl, C₂-₆ alkynyl, C2-7 acyl, Cι_-6 alkylthio, Cι_-6 alkoxy or C_3-6 cycloalkyl group; or a salt thereof; for use in the prevention or treatment of asthma.

29. A compound of general formula I:

wherein

1 7 each of R and R independently represents a Cι-₆ alkyl or C₂-₇ acyl group; X represents OCH₂ or a group CR³R⁴, wherein each of R³ and R⁴ independently represents a hydrogen atom or a C_1-3 alkyl group;

R⁵ represents a hydrogen atom or a Cι_-3 alkyl, C₂-₃ alkenyl or C₂.₃ alkynyl group;

R⁶ represents a hydrogen atom or a Cι_₆ alkyl, C₂-₆ alkenyl, C₂.₆ alkynyl, amino, Cι-₆ alkylamino, di(Cι-₆) alkylamino or C2-7 acylamino group; each of R⁷ and R⁸ independently represents a hydrogen or halogen atom or a hydroxy, trifluoromethyl, Cι-₆ alkyl, C_2-6 alkenyl, C2-₆ alkynyl, C₂_₇ acyl, Cι-₆ alkylthio, Cι_-6 alkoxy or C_3-6 cycloalkyl group;

R⁹ represents a hydrogen or halogen atom or a hydroxy, trifluoromethyl, Cι_-6 alkyl, C₂-

₆ alkenyl, C_2-6 alkynyl, C₂-₇ acyl, Cι-₆ alkylthio, C_..₆ alkoxy or C₃.₆ cycloalkyl group; or a salt thereof; for use in the prevention or treatment of chronic obstructive pulmonary disease

(COPD).

30. A compound as claimed in any of claims 25 to 29 wherein the compound is as defined in any of claims 1 to 15.

31. The use of a compound of general formula I:

wherein

each of R¹ and R² independently represents a Ci_-6 alkyl or C_2-7 acyl group;

X represents OCH₂ or a group CR³R⁴, wherein each of R^J and R⁴ independently represents a hydrogen atom or a Cι- alkyl group;

R⁵ represents a hydrogen atom or a Cι_-3 alkyl, C₂-₃ alkenyl or C_2-3 alkynyl group;

R⁶ represents a hydrogen atom or a Cι-₆ alkyl, C₂.₆ alkenyl, C_2-6 alkynyl, amino, Cι.₆ alkylamino, di(Cι-₆) alkylamino or C_2-7 acylamino group;

7 » each of R and R independently represents a hydrogen or halogen atom or a hydroxy, trifluoromethyl, Cι_-6 alkyl, C2_-6 alkenyl, C₂-6 alkynyl, C₂-₇ acyl, C_{1 -6} alkylthio, Cι-₆ alkoxy or C₃-₆ cycloalkyl group;

R⁹ represents a hydrogen or halogen atom or a hydroxy, trifluoromethyl, Cι-₆ alkyl, C₂. ₆ alkenyl, C₂-₆ alkynyl, C₂-7 acyl, Cι_-6 alkylthio, Cι-₆ alkoxy or C₃-₆ cycloalkyl group; or a salt thereof; in the manufacture of an inhibitor of a type III/IV phosphodiesterase isoenzyme.

32. The use of a compound of general formula I:

wherein

I 7 each of R and R^" independently represents a d-₆ alkyl or C₂-₇ acyl group; X represents OCH₂ or a group CR³R⁴, wherein each of R³ and R⁴ independently represents a hydrogen atom or a C₁-₃ alkyl group;

R^D represents a hydrogen atom or a Cι-₃ alkyl, C₂-₃ alkenyl or C₂-₃ alkynyl group; R represents a hydrogen atom or a Ci-₆ alkyl, C2-6 alkenyl, C_2-6 alkynyl, amino, Cι_-6 alkylamino, di(Cι-₆) alkylamino or C2-7 acylamino group;

7 Jϊ each of R and R independently represents a hydrogen or halogen atom or a hydroxy, trifluoromethyl, d-6 alkyl, C_2-6 alkenyl, -₆ alkynyl, -₇ acyl, Cι_-6 alkylthio, Ci-6 alkoxy or -₆ cycloalkyl group;

R⁹ represents a hydrogen or halogen atom or a hydroxy, trifluoromethyl, Ci-6 alkyl, C₂.

6 alkenyl, -₆ alkynyl, -7 acyl, Ci-6 alkylthio, Cι-₆ alkoxy or d-₆ cycloalkyl group; or a salt thereof; in the manufacture of a bronchodilator.

33. The use of a compound of general formula I:

wherein

each of R and R independently represents a Ci-₆ alkyl or C₂-₇ acyl group; X represents OCH2 or a group CR³R⁴, wherein each of R³ and R⁴ independently represents a hydrogen atom or a Cι-₃ alkyl group;

R⁵ represents a hydrogen atom or a C 1.₃ alkyl, C₂-₃ alkenyl or -₃ alkynyl group;

R represents a hydrogen atom or a alkyl, C₂-₆ alkenyl, C₂_₆ alkynyl, amino, Ci-₆ alkylamino, di(Cι.₆) alkylamino or C2-7 acylamino group; each of R⁷ and R⁸ independently represents a hydrogen or halogen atom or a hydroxy, trifluoromethyl, Ci-6 alkyl, C₂-6 alkenyl, C₂-₆ alkynyl, C₂-7 acyl, Cι_-6 alkylthio, Cι_₆ alkoxy or C₃-₆ cycloalkyl group;

R⁹ represents a hydrogen or halogen atom or a hydroxy, trifluoromethyl, Cι.₆ alkyl, d-

₆ alkenyl, d-₆ alkynyl, C2-₇ acyl, Cι-₆ alkylthio, Cι-₆ alkoxy or -₆ cycloalkyl group; or a salt thereof; in the manufacture of an anti-asthmatic.

34. The use of a compound of general formula I:

wherein

each of R¹ and R² independently represents a Ci-₆ alkyl or C₂-₇ acyl group; X represents OCH₂ or a group CR³R⁴, wherein each of R³ and R⁴ independently represents a hydrogen atom or a C 1.₃ alkyl group;

R⁵ represents a hydrogen atom or a C1-₃ alkyl, C₂-₃ alkenyl or d-₃ alkynyl group;

R⁶ represents a hydrogen atom or a Cι.₆ alkyl, C₂.₆ alkenyl, C₂-₆ alkynyl, amino, Ci-₆ alkylamino, di(Cι_6) alkylamino or C₂-7 acylamino group; each of R⁷ and R⁸ independently represents a hydrogen or halogen atom or a hydroxy, trifluoromethyl, Ci-₆ alkyl, C₂-6 alkenyl, -₆ alkynyl, d-₇ acyl, d_-6 alkylthio, Cι.₆ alkoxy or d-₆ cycloalkyl group;

R⁹ represents a hydrogen or halogen atom or a hydroxy, trifluoromethyl, Cι.₆ alkyl, d.

₆ alkenyl, -6 alkynyl, -7 acyl, Ci-6 alkylthio, Ci-₆ alkoxy or -₆ cycloalkyl group; or a salt thereof; in the manufacture of a medicament for the prevention or treatment of chronic obstructive pulmonary disease (COPD).

35. The use as claimed in any of claims 31 to 34, wherein the compound is as defined in any of claims 1 to 15.

36. A method for the treatment or prevention of a disease in a mammal where a phosphodiesterase isoenzyme inhibitor and/or a bronchodilator would be expected to be of benefit, which method comprises administering to said mammal an effective, non-toxic amount of a compound of general formula I:

wherein

each of R¹ and R² independently represents a Cι-₆ alkyl or -₇ acyl group;

X represents OCH₂ or a group CR³R⁴, wherein each of R³ and R⁴ independently represents a hydrogen atom or a Cι-₃ alkyl group;

R^D represents a hydrogen atom or a C ₁-₃ alkyl, -₃ alkenyl or C₂-₃ alkynyl group;

R⁶ represents a hydrogen atom or a Cι-₆ alkyl, -₆ alkenyl, C₂-₆ alkynyl, amino, Ci-6 alkylamino, di(Cι-₆) alkylamino or C₂-₇ acylamino group; each of R⁷ and R⁸ independently represents a hydrogen or halogen atom or a hydroxy, trifluoromethyl, Ci-₆ alkyl, -₆ alkenyl, -6 alkynyl, C2-7 acyl, d-6 alkylthio, Ci-6 alkoxy or d_-6 cycloalkyl group;

R⁹ represents a hydrogen or halogen atom or a hydroxy, trifluoromethyl, Ci-6 alkyl, C₂. 6 alkenyl, C₂-₆ alkynyl, d-7 acyl, Ci-₆ alkylthio, Ci-₆ alkoxy or C3.6 cycloalkyl group; or a salt thereof.

37. A method for the treatment or prevention of asthma in a mammal, which method comprises administering to said mammal an effective, non-toxic amount of a compound of general formula I:

wherein

each of R¹ and R² independently represents a Cι_-6 alkyl or C₂-₇ acyl group; X represents OCH₂ or a group CR³R⁴, wherein each of R³ and R⁴ independently represents a hydrogen atom or a Cι-₃ alkyl group;

R⁵ represents a hydrogen atom or a Cι-₃ alkyl, C₂-₃ alkenyl or C₂-₃ alkynyl group;

R⁶ represents a hydrogen atom or a Cι-₆ alkyl, -₆ alkenyl, C₂.₆ alkynyl, amino, Cι-₆ alkylamino, di(Cι_-6) alkylamino or C2-7 acylamino group; each of R⁷ and R⁸ independently represents a hydrogen or halogen atom or a hydroxy, trifluoromethyl, Ci-6 alkyl, -6 alkenyl, d-6 alkynyl, C₂-7 acyl, Ci-6 alkylthio, Cj.6 alkoxy or C_3-6 cycloalkyl group;

R⁹ represents a hydrogen or halogen atom or a hydroxy, trifluoromethyl, Ci-6 alkyl, d-

₆ alkenyl, C₂-₆ alkynyl, C₂-₇ acyl, Cι_₆ alkylthio, Ci-₆ alkoxy or C₃-₆ cycloalkyl group; or a salt thereof.

38. A method for the treatment or prevention of chronic obstructive pulmonary disease (COPD) in a mammal, which method comprises administering to said mammal an effective, non-toxic amount of a compound of general formula I:

wherein

each of R¹ and R² independently represents a Ci-₆ alkyl or d-₇ acyl group; X represents OCH₂ or a group CR³R⁴, wherein each of R³ and R⁴ independently represents a hydrogen atom or a C_1-3 alkyl group;

R⁵ represents a hydrogen atom or a C ι.₃ alkyl, -₃ alkenyl or C₂-₃ alkynyl group;

R represents a hydrogen atom or a Cι_₆ alkyl, -₆ alkenyl, -6 alkynyl, amino, Ci-6 alkylamino, di(Cι-₆) alkylamino or -7 acylamino group; each of R⁷ and R⁸ independently represents a hydrogen or halogen atom or a hydroxy, trifluoromethyl, Ci-₆ alkyl, -6 alkenyl, d-₆ alkynyl, d-₇ acyl, Ci-₆ alkylthio, Ci-₆ alkoxy or d_-6 cycloalkyl group;

R⁹ represents a hydrogen or halogen atom or a hydroxy, trifluoromethyl, Cι-₆ alkyl, d-

6 alkenyl, d-₆ alkynyl, C₂_7 acyl, Ci-6 alkylthio, Cι-₆ alkoxy or -6 cycloalkyl group; or a salt thereof.

39. A method as claimed in claim 36, 37 or 38, wherein the compound is as defined in any of claims 1 to 15.

40. A method as claimed in any of claims 36 to 39, wherein the compound is administered by aerosol.

41. A method as claimed in any of claims 36 to 40, wherein the animal is a human.

42. A compound substantially as hereinbefore described in any of the examples.

43. A process substantially as hereinbefore described in any of the examples.