AU673329B2 - 1-(N-(halo-3-pyridylmethyl))-N-methylamino-1-alkylamino-2- nitroethylene derivatives for use against fleas on pets - Google Patents

Abstract

Described are compounds of the formula (I), in which Hal is a halogen such as fluorine, chlorine, bromine or iodine; R1 is hydrogen, C1-C6 alkyl or C3-C7 cycloalkyl; R2 is hydrogen, C1-C6 alkyl or C3-C7 cycloalkyl and R3 is hydrogen or C1-C6 alkyl, for use in a method of controlling fleas on pets, in particular dogs and cats. Systemic application is preferred. Application is carried out by administering an amount effective against fleas of a substance of the formula (I) via the digestive tract or the blood of the host animal, hence administering the substance systemically to the pet, particularly a dog or cat.

Description

DPI DATE 30/12/93 APPLN. ID 18746/92 A03P DATE 10/03/94 PCT NUMBER PCT/EP92/01161 1HI1111111111111111 11111111 ii111111111 AU921 8746 INTERNATIONALE ANMELDUNG VEROFFENTLICHT NACH DEM VERTRAG OBER DIE INTERNATIONALE ZUSAMMENARBEIT AUF DEM GEBIET DES PATENTWESENS (PCT) (51) Internationale Patentklassifikation 5 AOIN 4~3/40 (11) Internationale Verliffentlichungsnumnmer: IAl (43) lnternationaleos IVerdffentlichungsdatumn: 9. Dez WO 93/24002 ember 1993 (09.12.93) (21) lnternationales Aktenzeichen PCT/EP92/01 161 (22) Internationales Anmeldedatum: 23. Mai 1992 (23.05.92) (71)Annielder (ffir alle Besinimungsstaaten ausser US): CIBA- GEIGY AG [CH/CH]; Klybeckstrasse 141, CH-4002 Basel (CR).

(72) Erfinder; und Erf'inder/Anmelder (nurfiir US) FRIEDEL, Thomas [AU/ AU]; 49 The High Road, East lilaxiand, NSW 2774 MOYSES, Eric, William rCH/CR]; Laufenburgerstrasse 26, CH-4058 Base! (CH-U. TINEMBART, Olivier [CHICH]; Rue des Miriers 16, CH-2800 Delkmont MAIENFISCH, Peter WCHICH]; Aegertenstrasse 21, CH-41 18 Rodersdorf GSELL, Laurenz [C1-/ CHI; Maiengasse 56, CH-4056 Basel (CH).

(74) Gemeinsamer Vertreter: CIBA-GEIGY AG; Patentabteilung, Klybeckstrasse 141, CH-4002 Basel (CH), (81) Bestimniungsstaatcn: AU, BB, BG, BR, CA, CS, Fl, RU, JP, KP, KR, LK, MG, MN, MW, NO, PL. RO, RU, SD, UA, US, europflisches Patent (AT, BE, CR, DE, DK, ES, FR, GB, GR, IT, LU, MC, NL, SE), OAPI Patent (BF, BJ, CF, CG, CI, CM, GA, GN, ML, MR, SN, TD,

TG).

Vertiffentlicht it internationalem Rt'c/irchenbericht.

6 7 A* 44S Title: I -[N-(HALO.3.PYRI DYLMETRYL)]-N-METHYLAM INO- I -ALKYLAM INO-2-N ITRO ETHYLENE DERIVA- TIVES FOR USE AGAINST FLEAS ON PETS (54) Bezeichnung: I -[N-(HALO.3-PYRI DYLMETHYL)]-N-M ETH-YLAM INO-I -ALKYLAM INO-2-N ITROETH YLEN-DE- RIVATE ZUR BEKAMPFUNG VON FLOHEN BEI RAUSTIEREN <1NR 2

R

3 (57) Abstract Described are compounds of the formula in which Hal is a halogen such as fluorine, chlorine, bromine or iodine;, R, is hydrogen, CI-C 6 alkyl or C 3 -C7 cycloalkyl; R 2 is hydrogen, C 1

-C

6 alkyl or C 3

-C

7 cycloalkyl and R 3 is hydrogen or C 1

-C

6 alkyl, for use in a method of' controlling fleas on pets, in particular dogs and cats. Systemic application is preferred. Application is carried out by administering an amount effective against fklas of a substance of the formula via the digestive tract or the blood of the host animal, hence administering the substance systemically to the pet, particularly a dog or cat.

(57) Zusammenfassung Es werden die Verbindlungen der Formel wormn Hal f~r Halogen, wvie Flijor, Chior, Brom oder Jod steht;- R 1 Wasserstoff, C 1

-C

6 -Alkyl oder C 3

-C

7 -Cycloalkyl bedeutet; R 2 for Wasserstoff, C 1

-C

6 -Alkyl oder C 3

-C

7 -Cycloalkyl steht und R, for Wasserstoff oder C 1

-C

6 -Alkyl steht zur Verwendung in einem Verfabren zur Beklimpfung von Flfihen bei Raustieren, inshesondere bei Hunden und Katzen, wobei die systemnische Applikation bevorzugt ist, beschrieben. Die Applikation erfolgt dadurch, dass man eine gegen FI6he wirksamne Menge der Substanzen der Formel Oiber den Verdauungstrakt oder Oiber das Blut des Wirtstieres und somit systemisch an das Haustier, vorzugsweise den Hund oder die Katze, verabreicht.

PCT/EP 92/01161 -1- H-19097/P1

PCT

1-fN-(Halo-3-pyridvlmethyl)]-N-methylamino- -alkylamino-2-nitroethylene derivatives for controlling fleas in domestic animals The present invention relates to 1-[N-(halo-3-pyridylmethyl)]-N-methylamino- -alkylamino-2-nitroethylene derivatives of the following formula I for use in a method of controllirg fleas in domestic animals, especially in dogs and cats, wherein systemic administration is preferred. The invention relates also to a method of inhibiting the infestation of dogs and cats by fleas which comprises the systemic administration of the said compound, in an amount effective against fleas, to the said domestic animal, for example the dog or the cat, by way of the digestive tract or the blood of the host animal.

The 1-[N-(halo-3-pyridylmethyl)]-N-methylamino- -alkylamino-2-nitroethylene derivatives mentioned in the introduction have the following chemical structure of formula I:

R

HalN

NR

2 Hal (I)

NNO

NO

2 wherein Hal is halogen, such as fluorine, chlorine, bromine or iodine;

R

1 is hydrogen, Ci-C 6 alkyl or C 3

-C

7 cycloalkyl;

R

2 is hydrogen, C 1

-C

6 alkyl or C 3

-C

7 cycloalkyl, and

R

3 is hydrogen or CI-C 6 alkyl.

Owing to their pronounced activity against fleas, preference is given within the scope of -2formula I to the following subgroups: Group a: Compounds of formula I wherein Hal is in the 6-position. Special preference is given to such compounds wherein Hal is fluorine, chlorine or bromine, especially chlorine.

Group b: Compounds of formula I wherein R 1 is hydrogen, C 1

-C

3 alkyl or C 3

-C

6 cycloalkyl, preferably hydrogen, methyl or ethyl or cyclopropyl, especially ethyl.

Group c: Compounds of formula I wherein R 2 is C 1

-C

3 alkyl or cyclopropyl, especially methyl.

Group d: Compounds of formula I wherein Hal is halogen, such as fluorine, chlorine, bromine or iodine; R 1 is hydrogen, methyl, C 3

-C

6 alkyl or C 3

-C

7 cycloalkyl and R 2 is hydrogen or CI-C 6 alkyl.

Within groups to preference is given above all to those compounds wherein R 3 is hydrogen.

Owing to its pronounced systemic activity against fleas, special preference is given to the following compound: 1-[N-(6-chloro-3-pyridylmethyl)]-N-ethylamino- 1-methylamino-2-nitroethylene, and also to its immediate homologues.

Within the scope of the present invention, depending on the number of carbon atoms indicated, the term "alkyl" is to be understood as meaning, for example, the following straight-chained and branched groups: methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, tert-butyl, isobutyl, etc.. Here and hereinafter, Hal is to be understood as being fluorine, chlorine, bromine or iodine, preferably fluorine, chlorine or bromine, but especially chlorine. Depending on the number of carbon atoms indicated, cycloalkyl by itself or as part of a substituent is cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, etc., cyclopropyl being especially preferred.

Compounds of the structural type falling within the scope of formula I, including processes for their preparation, are described in EP-0 302 389. The compounds of formula I can be prepared in accordance with the methods disclosed in EP-0 302 389 or analogously to the compounds described therein. That publication discloses a broad class of compounds of which the above representatives constitute only a selected subgroup, although they do not appear therein as a group. The class of compounds disclosed in EP-0 302 389 is described as insecticidal and acaricidal. Plant-destructive insects and mites are given as the preferred area of application. There is no reference to activity against fleas.

EP-0 302 833 likewise discloses a group of compounds which are structurally similar to those of the above formula I or which to some extent overlap structurally therewith. The essential structural difference between the compounds specifically disclosed and those of formula I is that the former have an unsubstituted pyridyl group, whereas the compounds of formula I are mono-halogenated at the pyridyl radical. The compounds disclosed in EP-0 302 833 are said to be valuable active ingredients in pest control, while being well tolerated by warm-blooded animals and plants, and to be suitable for controlling pests in and on animals and plants. Among the animal-injurious insects, specific reference is made to the order Siphonaptera (fleas).

It has now been found, surprisingly, that in the case of the compounds of the above formula I, the introduction of a halogen atom into the pyridyl radical brings about quite unexpected and significantly increased activity against fleas. That is very clear from a comparison of the principal compound according to the invention and the structurally most similar compound from the prior art. The relevant comparison data are given below in the I) Biological Examples.

The outstanding activity against fleas exhibited by the compounds of formula I is of such significance because the infestation by fleas of domestic animals and pets, especially of dogs and cats, is a problem for vets and animal owners alike to which there is still no adequate solution.

Owing to the complicated life cycle of the flea, none of the known methods of controlling these extremely troublesome parasites, which not only transmit diseases but are also the cause of unpleasant allergies, is totally satisfactory, especially since most of the known methods of control are based on the application of the nh'ive compound to the habitat of the various flea stages. As a result of the complex life cycle of the flea, however, that procedure is very laborious and cannot, in practice, cover all of the habitats, and is accordingly unreliable.

-4- For example, control aimed at treating the adult fleas in the fur, which is generally effected by applying an anti-flea composition to the fur of the host animal, takes no account at all of the various juvenile stages of the fleas, which live not only in the fur of the animal, but also mainly on the floor, on carpets, on the animal's sleeping place, on chairs, in the garden and in all the other places with which the infested animal comes into contact. Adult cat and dog fleas (Ctenocephalides felis and C. canis) normally live in the fur of the host cat or host dog. They live on the blood of the host animal and lay their eggs in its fur. Since those eggs are not self-adhering, however, they generally soon fall off and can be found on the floor, on carpets, in the dog's or cat's basket, on the chairs used by the animal, in the garden, in the yard, etc..

That means that the whole of the pets' living area i" .ontaminated with flea eggs, from which the larvae develop within two days. The larvae have three distinct stages of development, each of which lasts three days. In the final stage the larva spins its cocoon and becomes a pupa. Under favourable conditions, i.e. at 33 0 C and a relative humidity of the metamorphosis from egg to pupa takes place in about 8 to 10 days. After about another 8 days the young, fully-formed fleas develop in the cocoons that are still lying on the floor, the carpets, the sleeping places, the chairs, etc.. The young adult fleas remain there until they sense the presence of an acceptable host animal, then they hatch from their cocoons and attempt to jump onto the host animal. Thus it takes at least three weeks for an egg to develop into a young adult flea that is capable of reinfesting the host animal.

The young flea may, however, remain in its cocoon for months, possibly for up to a year.

On the other hand, under less favourable conditions the development from egg to young adult flea may take from 4 to 5 months. To reach sexual maturity, fleas require blood as food in order to be able to reproauce, and that blood must be from the appropriate host animal. It is normally obtained from the excreta of the adult fleas living on the host animal. Those excreta contain large amounts of undigested blood.

That long life cycle, which proceeds separately from the host animal, has a significant influence on the successful control of fleas on the host animal.

Only when the fleas in the fur of the host animal can be successfully controlled very quickly, i.e. when all the adult fleas are killed within a very short time with a suitable active ingredient, is the cat or the dog protected against the risk of reinfestation by newly hatched young fleas from its living space.

Flea infestation of dogs and cats has unpleasant consequences not only for the animal to be treated but also for the animal's owner. Such drawbacks lead, for example, to local irritation or troublesome itching and often result in intense scratching. A large number of the animals become allergic to the excreta of the fleas, which leads to very itchy and crusty skin changes around the sites of the bites on the animal's body. Those skin changes normally have a diameter of approximately 3 mm or more and oftena make the animal prone to biting and cause it to scratch, leading to loss of fur in places.

Furthermore, flea-infested animals are constantly exposed to the risk of infestation by dipylidium, a species of tape worm, which is transmitted by fleas.

Flea infestation is not only extremely troublesome for the affected animal, but also has unpleasant consequences for the animal's owner, since it will eventually become evident to him from the unusual behaviour of his pet that it is ill and suffering and that he must help it. What is more, it can become unpleasant for the animal's owner if he gives up keeping his infested animal, or if it dies or is removed temporarily from its usual environment, since in the event of the prolonged absence of a suitable host animal, the newly hatched fleas on the floor will be forced to infest the human, although they are unable to live on human blood as their only source of food. Even when the dog or the cat is present, the animal's owner can still be bitten by the fleas.

In addition, dog and cat fleas, or their excreta, can lead to allergy-like skin disorders in some people, which in many cases means that the pet must be given up. The desire for effective control of fleas in dogs and cats has therefore existed for centuries.

A number of conventional methods of control are known, but they have various disadvantages. If, for example, flea combs surface-coded with an insecticide are used, the animal's owner has no alternative but to comb the animal intensively and often which, depending on the size of the animal, may take from a few minutes to an hour and will not be accepted patiently by every animal. However, not every animal owner is prepared to devote the time to this. The use of corresponding anti-flea shampoos is often unsuccessful, since most cats, and also many dogs, can be bathed, if at all, only by force, with the result that water and active ingredient are spilt and have to be cleared up. In addition, the effect of such a bath treatment lasts about a week at most, and the laborious procedure has to be repeated. The same or very similar problems can be expected with the use of dips or rinses. The use of dusting powders is generally also not accepted by the animal without resistance, since it takes several minutes to treat the whole surface of the fur uniformly, and some of the dust will inevitably get into the mouth, nose and eyes of the animal. Even with careful application, it cannot be ensured that the animal and the human will not inhale any powder. It is virtually inevitable that the human will also come into contact with the composition to a greater or lesser extent.

When using sprays, many people may be unpleasantly surprised to find that most animals, especially cats, run away or react aggressively at the mere sound of the spray. In addition, sprays also have all the disadvantages listed for dusting powders, added to which they become even more finely dispersed in the atmosphere and are therefore inhaled by human and animal. Fleas are frequently controlled by means of so-called flea collars, which ensure good effectiveness temporarily. This treatment has a certain weakness, owing especially to its locally very limited area of application. Although the killing action in the region of the neck and chest is generally 100 more remote parts of the body are scarcely affected. In addition, those collars are active for a limited time. Furthermore, many of the collars are unattractive and may annoy the animal. It is also possible nowadays to buy medallions, which can be hung from conventional collars and are supposed to be effective. Although they are attractive in appearance, tbh action of those medallions is unsatisfactory, since they have inadequate contact with the fur. Some antiflea organophosphorus compounds are also available as spot-on formulations and are thus applied to a locally limited area of the fur. They generally have good short-term activity against adult fleas, but the compositions used often have toxic properties that present problems. Some organophosphorus compounds have also been administered orally, but they are subject to strict safety restrictions and must on no account be administered simultaneously with other organophosphorus compounds.

Overall it may be said that the conventional methods, which seek to kill the adult flea, produce such unsatisfactory results chiefly because they depend on the patience and the skill of the user when handling the infested host animal. The success of the current compositions stands and falls with the frequency and thoroughness with which the user, normally the animal's owner, applies the active ingredient to the host animal and the thoroughness with which he disinfects the environment in which the host animal lives.

The conventional methods are relatively expensive, time-consuming and not especially successful in thdie long term. In the short term, relief can certainly be obtained with the -7conventional compositions.

What has hitherto not been adequately taken into account in the case of the conventional methods and compositions is the fact that, owing to the particular life cycle of the flea, dogs and cats are repeatedly reinfested by new fleas, partly because contact with the flea eggs, flea larvae and young adult fleas on the floor and/or in the immediate vicinity of the animal is unavoidable, and partly because many pet animals constantly come into contact with infested members of their own species.

Constantly recurring reinfestation is inadequately prevented by conventional compositions or can be prevented only by the application of large amounts of disinfectant, etc..

It has now been found, surprisingly, that using certain systemic methods of administration and using compounds of formula I as active ingredients, it is possible to eliminate the adult fleas very rapidly and completely and thus to intervene in the complex development cycle of the flea by blocking that cycle. Since those compounds exhibit all of their outstanding anti-flea activity also when they are administered to the host animal systemically, i.e. orally, parenterally, subcutaneously, intramuscularly or intravenously, it is possible, by means of their specific periodic administration, in a simple manner to break the vicious circle of constantly recurring reinfestation described above until all the juvenile stages in the living area of the host animal have died. The fleas are killed and prevented from reproducing, the juvenile stages are prevented from maturing and are no longer able to infest the host animal, so that the living area of dogs and cats can be kept free of fleas for a prolonged period. The only unavoidable source of reinfestation is contact with infested members of the same species and that aspect can of course be excluded one hundred percent only by means of long-term treatment. That residual risk is, however, of minor importance.

It has now been found that by oral administration, parenteral administration or administration by means of an implant, of compounds of formula I in an amount effective against fleas, it is possible for infestation by fleas of domestic animals, such as cats and dogs, to be drstically reduced or completely prevented.

What is astonishing in connection with the present invention, however, is that full activity can be achieved even when an active ingredient is administered to the host animal in relatively low concentrations and reaches its target of the adult flea only by the circuitous -8route via the gastro-intestinal tract and thus via the blood sucked up by the flea. Since systemic administration of the active ingredient brings about the total mortality of the adult fleas, it is now possible to eradicate the fleas. A combination of this systemic administration of the active ingredient with accompanying measures, for example disinfection of the living area of the host animal, makes it possible to eliminate the flea problem even more rapidly, but even without those accompanying measures the flea population is reduced completely or to an acceptable minimum within a few weeks or at the most months.

The compounds of formula I exhibit activity against juvenile flea stages insofar as flea larvae that hatch from the flea eggs are substantially dependent on the excreta of the adult fleas, since they live on that excrement, However, flea excreta comprise large amounts of undigested blood from the host animal and serve as a source of protein for the developing fleas. Since, however, the compounds of formula I kill the adult fleas very rapidly, the necessary excreta are not available and the juvenile stages are deprived of their nutrient base and therefore die before they reach the adult stage. This is also a decisive contributing factor in the interruption of the complex life cycle of the flea and prevents the host animals from being constantly reinfected in their preferred living area by the eggs, and the larvae hatching therefrom, that are scattered all over it.

The present invention thus has two objects, on the one hand the afore-described method of preventing the reinfestation of domestic animals by fleas, and simultaneously of course the inhibition of the reproduction of fleas.

It is essential to the invention that the compounds of formula I are administered in such a manner that they can be taken up in sufficient amounts by the adult, sucking flea with the blood of the host animal and kill the adult flea rapidly before it can provide sufficient uncontaminated food for the flea larvae by way of its excreta. This is achieved with tilhe compounds of the invention using various forms of administration, for example by administering the formulated active ingredient orally. "Formulated" in this case means, for example, in the form of a powder, a tablet, granules, a capsule, an emulsion or a foam, in microencapsulated form, etc.; the animal need not necessarily be given the composition directly, rather it is advantageously mixed with its food, since that form of administration presents the fewest problems both to the host animal and to the person administering the composition. In addition to customary formulation ingredients, any composition that is to be administered orally may of course comprise further adjuvan's that encourage the host -9animal to take the composition voluntarily, for example suitable odorants and flavourings.

Oral administration, being easy to carry out, is preferred according to the invention. A further form of administration is parenteral administration, for example by subcutaneous injection or intravenous injection, or with a long-term composition (depot form) in the form of an implant.

Oral administration includes, for example, the administration of dog and cat food ready mixed with the active ingredient, for example in the form of biscuits or treats, chewable tablets, water-soluble capsules or tablets, in a water-soluble form that can be added to the food in the form of drops or in other forms that can be mixed with the animal food. The implants also include any means that can be introduced into the body of the animal in order to release active ingredient.

Percutaneous forms of administration include, for example, subcutaneous, dermal, intramuscular and even intravenous administration of injectable forms. In addition to the customary syringes with needles, needle-less high-pressure syringe devices, as well as pour-on and spot-on formulations, may be expedient By selection of a suitable formulation, it is possible to promote the ability of the active ingredient to penetrate through the living tissue of the animal, and/or to maintain its availability. That is important when, for example, a very sparingly soluble active ingredient is used, the low solubility of which requires means for enhancing solubility, since the animal's body fluid is capable of dissolving only small amounts of active ingredient at a time.

The active ingredient may also be present in a matrix formulation which physically prevents the active ingredient from decomposing and maintains the constant availability of active ingredient. The matrix formulation is injected into the body and remains there as a form of depot from which active ingredient is released continuously. Such matrix formulations are known to a person skilled in the art. They are generally wax-like, semisolid substances, for example vegetable waxes and polyethylene glycols having a high molecular weight.

A high degree of availability of the active ingredient is also obtained by tile introduction of an implant of the active ingredient into the animal. Such implants are widely used in veterinary medicine and often consist of silicone-containing rubber. The active ingredient is dispersed in the solid rubber or is located inside a hollow rubber body. Care must be taken that the active ingredient selected is soluble in the rubber implant, since it is first dissolved in the rubber and then seeps continuously out of the rubber material and into the body fluid of the animal to be treated.

The rate of release of the active ingredient from the implant, and thus the length of time during which the implant exhibits activity, is generally determined by the accuracy of the calibration of the implant (amount of active ingredient in the implant), the environment of the implant and the polymer formulation from which the implant has been produced.

Administration of the active ingredient by means of an implant is a further preferred component of the present invention. Such administration is extremely economical and effective, because a correctly dimensioned implant ensures that the concentration of active ingredient in the tissue of the host animal is constant. It is possible nowadays for implants to be so made and implanted in a simple manner that they are capable of supplying the active ingredient over a period of several months. Once the implant has been made, the animal is not disturbed further, and there is no further need to be concerned about the dose.

The administration of veterinary medicinal additives to animal food is well known in the field of animal health. It is usual first to prepare a so-called premix in which the active ingredient is dispersed in a liquid or is in finely divided form in solid carriers. That premix can normally comprise about 1 to 800 g of compound per kg of premix, depending on the desired final concentration in the food.

It is also known that active ingredients may be hydrolysed or weakened by the constituents of the food. Such active ingredients are routinely formulated in a protective matrix, for example in gelatin, before being added to the premix.

The present invention therefore relates to the object of eliminating tile adult fleas on the domestic animal, as well as to preventing the further development of the flea larvae by depriving them of food, which is equivalent to systemic prevention of the reinfection of domestic animals, especially of domestic animals by fleas. This is achieved by administering* to the said host animal orally, parcnterally or by means of an implant at least one compound t formula I in an amount effective against fleas.

*Translator's note: "zusetzt" presumably in error for "verabrcicht" 1.1 The present invention thus also relates to the object preventing the reproduction of fleas, which comprises making available to fleas as food, by means of the systemic administration of the active ingredient to the host animal, contaminated blood that comprises at least one compound of formula I in an amount effective against fleas. This is most easily achieved by administering to the host animal, in the form of a food additive, a compound of formula I in an amount effective against fleas, and in that way allowing it to reach the fleas living on the host animal.

The compounds of formula I are advantageously administered in a dose of from 0.01 to 800, preferably from 0.1 to 200, especially from 0.5 to 30, mg/kg of body weight of the host animal, oral administration being preferred.

A good dose that can be administered to the host animal regularly is from 0.5 to 100 mg/kg of body weight. Administration is advantageously effected daily or weekly.

The total dose may vary for the same active ingredient from one species of animal to another as well as within a species of animal, since it depends inter alia on the weight and thdie constitution of the animal.

When used according to the invention, the active ingredient is not normally administered in pure formn, but preferably in the form of a composition which comprises in addition to tx,: active ingredient constituents that assist administration, suitable constituents being those that are tolerated by the host animal. It is of course possible, as well as controlling the adult ficas in accordance with the invention, additionally to use conventional methods that control the juvenile flea stages, although the latter is not absolutely essential.

Such compositions to be administered in accordance wilh the invention generally comprise from 0.1 to 99 by weight, especially from 0. I to 95 by weight, of a compound of formula I and from 99.9 to 1 by weight, especially from 99.9 to 5 by weight, of a solid or liquid, non-toxic adjuvant, including from 0 to 25 by weight, especially from 0.1 to 25 by weight, of a non-toxic surfactant.

Whereas commercial products will preferably be formulated as concentrates, the end user will normally employ dilute formulations.

The compositions may also contin further auxiliaries such as stabilisers, antifoams, -12viscosity regulators, binders, tackifiers as well as other active ingredients for obtaining special effects.

The materials known from veterinary medicinal practice for oral and parenteral administration and for implants can be used as formulation excipients. Some examples are given below.

Suitable excipients are especially fillers, such as sugars, for example lactose, saccharose, mannitol or sorbitol, cellulose preparations and/or calcium phosphates, for example tricalcium phosphate or calcium hydrogen phosphate, and binders, such as starch pastes using, for example, corn, wheat, rice or potato starch, gelatin, tragacanth, methylcellulose and/or, if desired, disintegrators, such as the above-mentioned starches, also carboxymethyl starch, cross-linked polyvinylpyrrolidone, agar, alginic acid or a salt thereof, such as sodium alginate. Adjuvants are especially flow conditioners and lubricants, for example silicic acid, talc, stearic acid or salts thereof, such as magnesium or calcium stearate, and/or polyethylene glycol. Dragde cores can be provided with suitable, optionally enteric, coatings, there being used inter alia concentrated sugar solutions which may comprise gum arabic, talc, polyvinylpyrrolidone, polyethylene glycol and/or titanium dioxide, or coating solutions in suitable organic solvents or solvent mixtures, or, for the preparation of enteric coatings, solutions of suitable cellulose preparations, such as acetylcellulose phthalate or hydroxypropylmethylcellulose phthalate. Dyes, flavourings or pigments may be added to the tablets or dragde coatings, for example for identification purposes or to indicate different doses of active ingredient.

Other orally administrable compositions are dry-filled capsules comprising gelatin, and also soft sealed capsules comprising gelatin and a plasticiser, such as glycerol or sorbitol.

The dry-filled capsules may comprise the active ingredient in the form of granules, for example in admixture with fillers, such as lactose, binders, such as starches, and/or glidants, such as talc or magnesium stearate, and, if desired, stabilisers. In soft capsules, the active ingredient is preferably dissolved or suspended in suitable liquids, such as fatty oils, paraffin oil or liquid polyethylene glycols, to which stabilisers may also have been added. Preference is given inter alia to capsules that are easily bitten through or swallowed without being chewed.

Suitable for parenteral administration are especially aqueous solutions of an active ingredient in water-soluble form, for example in the form of a water-soluble salt, and also 13suspensions of the active ingredient, such as corresponding oily injection suspensions, there being used suitable lipophilic solvents or vehicles, such as fatty oils, for example sesame oil, or synthetic fatty acid esters, for example ethyl oleate, or triglycerides, or aqueous injection suspensions that comprise viscosity-increasing substances, for example sodium carboxymethylcellulose, sorbitol and/or dextran, and, optionally, stabilisers.

The compositions of the present invention can be prepared in a manner known per se, for example by means of conventional mixing, granulating, confectioning, dissolving or lyophilising processes. For example, pharmaceutical compositions for oral administration can be obtained by combining the active ingredient with solid carriers, optionally granulating a resulting mixture, and processing the mixture or granules, if desired or necessary after the addition of suitable excipients, to form tablets or drag6e cores.

The following Examples illustrate the invention described above, but do not limit its scope in any way. Temperatures are given in degrees Celsius.

14- Table: Examples of compounds of formula I that can be used in accordance with the invention

R

N

NR

2

R

3 H-al(I 22 Comp. Hal R, R R 3 melting point No. in 0

C

1.1 6-Cl CH 3

CH

3 H 87-90 1.2 6-Cl C 2

H

5

CH

3 H yellow oil 1.3 6-Cl CH 3 CA11 H- 112-114 1.4 6-Cl CH 3

C

3

H

7 -i H- 133-135 6-Cl Cl- 3

C

4

-H

9 -n H 1.6 6-Cl CH 3

C

4

-H

9 -t H- 1.7 6-Cl CH 3

C

4 -Hg-s H- 1.8 6-Cl CH 3

C

5 -l-1-n H- 1.9 6-Cl CH 3

C

6

-H

13 -n H 1.10 6-F CH 3

CH-

3 I-I 100-100.5 1.11 5-Br CL- 3

CH

3 H- 1 t6-117 1.12 2-Cl CH 3 Cl- 3 H 106-113 1.13 6-Cl C 3 1- 7 -iso Cl- 3 1-I 1.14 6-Cl C 4

-H

9 -n Cl-1 3

H-

1.15 6-Cl C 4

-H

9 -tert CH- 3

H

1.16 6-Cl C 4

-H

9 -sec CH 3

H-

1.17 6-Cl C 6

-H

13 -n CH 3

H

1.18 6-Cl cyclopropyl CL- 3 HI 104-105 1.19 6-Cl cyclobutyl Cl- 3

HI

1.20 6-Cl cyclopentyl CI- 3

H

1.21 6-Cl cyclohexyl Cl-1 3 1-I 1.22 6-Cl cycloheptyl Cl- 3 I-1 1.23 6-Cl 1-I Cl-1 3 1-1 158-161 Comp. H-al R, 2R melting point No. in 0

C

1.24 6-Cl C 2

H

5 H H 159-161 1.25 6-Cl CH 3 H H 202 decomp.

1.26 5-Cl CH 3

CH

3

H

1.27 4-Cl CR 3

CR

3

H

1.28 6-Cl cyclopropyl C 2

H

5 H 144-146 1.29 6-F CAH CH 3 H oil 1.30 6-Br CAH CH 3 H 79-80 1.31 6-Cl H CH 3

CH

3 97-98 1.32 6-Br CH 3

CH

3 H 130-131 1.33 6-C1 CH 3

CH

3

CR

3 110-112 1.34 6-Cl. H CAH CR 3 87-88 1.35 6-Cl C 3

H

7 -iSO H H resin 1.36 6-Cl H H H 188-190 1.37 6-Cl C 3

H

7 -n H H- 185-186 1.38 6-Cl C 3

H

7 -n H Cl- 3 102-103 1.39 6-Cl C 3

H

7 -iSO H CR 3 119-120 1.40 6-Cl cyclopropyl H cyclo- 113-115 propyl In the Formulauon Examples that follow, the term active ingredient stands for Il-[N- (6-cliloro-3-pyridylmethiyl)]-N-ethiylamino- 1-methiylamino-2-nitroethiylene.

Example t: Tablets comprising 25 mg of active ingredient can be prepared as follows: Constituents (for 1000 tablets) active ingredient lactose wheat starch polyethylene glycol 6000 talcum magnesium stearate 25.0 g 100.7 g 7.5 g 5.O g 1.8 g 16demineralised water q.s.

Preparation: All the solid ingredients are first forced through a sieve having a mesh size of 0.6 mm. Then the active ingredient, the lactose, the talcum and half the starch are mixed together. The other half of the starch is suspended in 40 ml of water and the suspension is added to a boiling solution of the polyethylene glycol in 100 ml of water. The resulting starch paste is added to the main batch and the mixture is granulated, if necessary with the addition of water. The granules are dried overnight at 350, forced through a sieve having a mesh size of 1.2 mm, mixed with the magnesium stearate and compressed to form tablets having a diameter of about 6 mm which are concave on both sides.

Example 2: Tablets comprising 0.02 g of active ingredient are prepared as follows: Composition (for 10 000 tablets) active ingredient 200.00 g lactose 290.80 g potato starch 274.70 g stearic acid 10.00 g talcum 200.00 g magnesium stearate 2.50 g colloidal silica 32.00 g ethanol q.s.

A mixture of the active ingredient, the lactose and 194.70 g of potato starch is moistened with an ethanolic solution of the stearic acid and granulated through a sieve. After drying, the remaining potato starch, the talcum, the magnesium stearate and the colloidal silica are mixed in and the mixture is compressed to form tablets each weighing 0.1 g, which may, if desired, be provided with dividing notches for finer adaptation of the dose.

Example 3: Capsules comprising 0.025 g of active ingredient can be prepared as follows: Composition (for 1000 capsules) active ingredient 25.00 g lactose 249.80 g gelatin 2.00 g corn starch 10.00 g 17talcum 15.00 g water q.s.

The active ingredient is mixed with the lactose, the mixture is moistened uniformly with an aqueous solution of the gelatin and granulated through a sieve having a mesh size of 1.2-1.5 mm. The granules are mixed with the dried corn starch and the talcum and introduced in 300 mg portions into hard gelatin capsules (size 1).

Example 4: Premix (food additive) 0.25 part by weight of active ingredient and 4.75 parts by weight of secondary calcium phosphate, alumina, Aerosil, carbonate or chalk are mixed until homogeneous with parts by weight of an animal food.

Example 5: Premix (food additive) 0.40 part by weight of active ingredient and 5.00 parts by weight of Aerosil/chalk are mixed until homogeneous with 94.6 parts by weight of a commercial dry food.

Example 6: Emulsifiable concentrate parts by weight of active ingredient are mixed with parts by weight of the emulsifier, e.g. a mixture of alkylarylpolyglycol ether with alkylarylpolysulfonates, and with parts by weight of a solvent, until the solution has been completely homogenised.

Emulsions of the desired concentration are obtained by dilution with water.

Example 7: Solutions for use as a drink additive) percent by weight active ingredient in 2,2-dimethyl-4-hydroxymethyl-1,3-dioxolane, percent by weight active ingredient in diethylene glycol monoethyl ether, percent by weight in polyethylene glycol 300, and percent by weight in glycerol.

Example 8: Soluble powder parts by weight of active ingredient 1 part by weight of sodium lauryl sulfate, 3 parts by weight of colloidal silica gel, and 18- 71 parts by weight of urea.

The ingredients are mixed together and ground with one another until homogeneous.

Other biologically active compounds or adjuvants that are neutral towards the active ingredients and that have no adverse effect on the host animal to be treated, as well as mineral salts or vitamins, can be added to the compositions described.

Biological Examples Example 9: Comparison test of action against Ctenocephalides felis (cat flea) In accordance with the following protocol, both the active ingredient according to the invention, 1-[N-(6-chloro-3-pyridylmethyl)]-N-ethylamino-l-methylamino-2-nitroethylene having the chemical structure: Compound of the invention NMHCH 3 and the structurally most similar compound mentioned in EP-0 302 833, of the formula: Compound (B) of the prior art NHCH 3

NO

are tested for comparison purposes against an untreated control group of fleas.

Test protocol: adult fleas of the species Ctenocephalides felis are introduced into a flat round cage closed off at both ends with gauze. A vessel sealed at the bottom with a parafilm membrane is then placed on the cage. The vessel contains blood comprising 1.0 ppm of 19active ingredient and is heated to a constant temperature of 37°C. The fleas take up the blood through the membrane. Evaluation is effected 24 and 48 hours after the start of the test. The percentage reduction in population activity) is determined from a comparison of the number of dead fleas given treated blood with those given untreated blood (control group). 24 hours after treatment the blood is replaced with fresh blood that has likewise been treated and the test is continued with the surviving fleas. The untreated blood for the control group is also replaced after 24 hours.

Results: All three groups of fleas [(Control group/untreated blood); (Group A/blood treated with compound A of the invention) and (Group B/blood treated with compound B from the prior art)] begin to take up blood as soon as they are placed in the test apparatus.

The behaviour of the control group and of Group B (prior art) remains virtually unchanged over the duration of the test. In contrast, only half an hour after dithe start of the test the first toxic signs appear in Group A (treatment according to the invention). After 24 hours the following individual results are observed using 2 x 20 fleas in each case (in mortality): Compound ppm a.i. Test 1 Test 2 Test 3 Test 4 B 1.0 0% 5% 0% 0% A 1.0 100% 95% 95% 100% Control 0.0 0% 0% 0% 0% Example 10: In vivo comparison test of the action against Ctcnocephalides felis (cat flea) In this comparative test, as in Example 9, compound A of the invention is again tested on cats and compared with the structurally most similar compound B of the prior art.

When other compounds from the Table are tested with the compounds of formula I given by way of example, entirely comparable results are obtained.

Test protocol: 6 female domestic cats 1-2 years old and having a body weight of from 3.0 to 4.0 kg are divided into three groups of two animals. One group is already infested with fleas, but remains untreated and serves as control group. One of the other groups receives test compound A and the other receives test compound B, in each case in a dose of 10 ing/kg 1 a* of body weight, by means of a gelatin capsule directly into the back of the throat. Each of the test compounds has been mixed beforehand with lactose 1:1. Immediately after administration of the test compounds the cats are infested with 20 fleas each (16 female and 4 male fleas) in the region of the ridge between the shoulderbones. Further infestation with a further 20 fleas is effected in the case of compound A on days +4 and In the case of the cats treated with compound B and in the case of the comparison group, further infestation with fleas is unnecessary, since all the fleas from the initial infestation have survived.

The flea eggs are collected daily and counted. The number of dead fleas found is also determined daily. The results for the 2 treated groups are compared both with each other and with those for the control group.

Results: The number of dead fleas found and the egg production are shown in the following Tables 1 and 2: Table 1: Number of fleas killed Compound Cat no. dead fleas on day. 0 +1 +2 +3 +4 +5 +6 +7 +8 +9 325 12 3. 0* 11 5* 0 2* 0 0 0

A

343 9* 1 0* 8 2* 0 2* 0 0 0 351 0* 1 0 0 0 0 00 0 0

B

266 0* 0 0 0 0 0 0 0 0 0 Control 339 599 0* 0 0 0 0 0 0 0 0 0 0* 0 0 0 0 0 0 0 0 0 Infestation with 20 fleas -21 In the case of compound A, only 6 hours after infestation with the first 20 fleas there is mortality. Even on the second day after fresh infestation with a further 20 fleas, a further 55 of the fleas are killed. Not until day 6 does the activity of compound A fall to approximately 10 In contrast, no significant difference is found between the control group and the group of cats treated with compound B. Compound B proves ineffective and unusable for oral administration against fleas at the low test concentrations.

Table 2: Egg production Compound Cat no. egg production on day...

+2 +3 +4 +5 +6 +7 +8 +9 325 0* 0 0* 0 37* 233 250 370

A

343 0* 0 0* 60 0* 186 240 283 351 240 306 403 423 350 333 343 290

B

266 106 266 386 313 286 290 326 303 339 60 133 186 300 310 313 290 233 Control 599 96 110 156 146 166 116 200 170 Infestation with 20 fleas In the group treated with compound A, no flea eggs are found after the first and second infestations with fleas. In the group of cats treated with compound B and in the control group, the female fleas produce the usual number of eggs; no significant differences are found.

The comparison test shows that compound A has good systemic activity against adult fleas for a period of about 3-4 days. Compound B, on the other hand, can be classed as completely ineffective at the test dose. It could be icither predicted nor expected that the mono-halogenation of the pyridyl group would bring about such a significant increase in activity as regards the systemic action against fleas.

I -22- The compounds for which physical data are given in the Table of compounds that may be used in accordance with the invention exhibit activity against fleas that is comparable with that of compound A of the invention. Especially striking is the outstanding activity of compounds 1.1 to 1.4, 1.10 to 1.12, 1.18, 1.28, 1.29 and 1.36 to 1.40.

Claims (21)

1. A method for the systemic control of fleas in a domestic animal, which comprises administering to the said domestic animal systematically, in an amount effective against fleas, a compound of formula I R 1 3 1 f Ha N NR 2 R 3 S2 H NO 2 wherein Hal is halogen; R 1 is hydrogen, CI-C 6 alkyl or C 3 -C 7 cycloalkyl; R 2 is hydrogen, C 1 -C 6 alkyl or C 3 -C 7 cycloalkyl, and R 3 is hydrogen or Ci-C 6 alkyl.

2. A method according to claim 1, wherein the active ingredient is a compound of formula I wherein Hal is in the 6-position and is fluorine, chlorine or bromine.

3. A method according to claim 1, wherein the active ingredient is a compound of formula I wherein RI is hydrogen, Ci-C 3 alkyl or C 3 -C 6 cycloalkyl.

4. A method according to claim 1, wherein the active ingredient is a compound of formula I wherein R 2 is C 1 -C 3 alkyl or cyclopropyl. A method according to any one of claims 2 to 4, wherein R 3 is hydrogen.

6. A method according to claim 1, wherein the active ingredient is 1-[N-ethyl-N- (6 -chloro-3'-pyridylmethyl)amino]-l-methylamino-2-nitroethylene or one of its S 20 immediate homologues.

7. A method according to any one of claims 1 to 6, wherein the domestic animal is a dog or a cat. 8 A method according to claim 7, which comprises, as an accompanying measure, controlling the juvenile flea stages using conventional larvicidal or ovicidal anti-flea compositions.

9. A method according to any one of claims 1 to 8, which comprises administering orally in regular individual doses a composition comprising the active ingredient. A method according to any one of claims 1 to 9, which comprises administering the active ingredient to the host animal in concentrations of from 0.01 mg/kg of body weight to 800 mg/kg of body weight.

11. A method according to claim 10, which comprises administering the active ingredient to the host animal in concentrations of from 0.1 mg/kg of body weight to 200 mg/kg of body weight. (N:\Alll(X)542:SAK 24

12. A method according to claim 11, which comprises administering the active ingredient to the host animal in concentrations of from 0.5 mg/kg of body weight to mg/kg of body weight.

13. A method according to either claim 10 or claim 11, which comprises administering the active ingredient to the domestic animal orally.

14. A method according to any one of claims 1 to 8, which comprises administering the active ingredient regularly to the domestic animal in a dose of from mg/kg of body weight to 100 mg/kg of body weight. A method of preventing the reproduction of fleas in a domestic animal, which comprises introducing into the blood of the said domestic animal, in an amount effective against fleas, a compound of formula I S R1 -lN NR 2 R 3 Hal- (I) 6 N 2' H NO 2 wherein Hal is halogen; 15 R is hydrogen, CI-C 6 alkyl or C 3 -C 7 cycloalkyl; S R 2 is hydrogen, Ci-C 6 alkyl or C 3 -C 7 cycloalkyl, and R 3 is hydrogen or C 1 -C 6 alkyl.

16. A method according to claim 15, wherein the active ingredient is one of the compounds of formula I defined in claims 2 to 6.

17. A method according to claim 15, which comprises administering an effective amount of the active ingredient to the host animal with its food and allowing the active ingredient to be taken up by the fleas on the host animal with the blood they suck up.

18. A method for the systemic control of fleas in a domestic animal, which comprises administering to the said domestic animal systematically, in an amount effective against fleas, any one of compounds 1.1 to 1.40 as hereinbefore described. Dated 13 September, 1996 Ciba-Geigy AG Patent Attorneys for the Applicant/Nominated Person SPRUSON FERGUSON T c~ [N:\libZ]00542:SAK 4 wherein Hal is halogen, such as fluorine, chlorine, bromine or iodine; RI is hydrogen, Ci-C 6 alkyl or C 3 -C 7 cycloalkyl; R 2 is hydrogen, Ci-C 6 alkyl or C 3 -C 7 cycloalkyl, and R 3 is hydrogen or C 1 -C 6 alkyl. A method according to claim 14, wherein the active ingredient is one of the compounds of formula I defined in claims 2 to 4. 16. A method according to claim 14, which comprises administering an effective amount of the active ingredient to the host animal with its food and allowing the active ingredient to be taken up by the fleas on the host animal with the blood they suck up. 17. A systemically active composition for preventing the infestation of domestic animals, especially of dogs and cats by fleas, which comprises in food, in an amount effective against fleas, a compound of formula I R 3I N tR 2 R 3 Hal I (I) SN 2 2 NO 2 wherein Hal is halogen, such rs fluorine, chlorine, biomine or iodine; RI is hydrogen, Ci-C 6 alkyl or C 3 -C 7 cycloalkyl; R 2 is hydrogen, C 1 -C 6 alkyl or C 3 -C 7 cycloalkyl, and R 3 is hydrogen or C 1 -C 6 alkyl. 18. A composition according to claim 17 comprising dog or cat food.

19. A composition according to claim 17, wherein the active ingredient is a compound of formula I according to any one of claims 2 to 4. 0, -26- A compound of formula I R N3 NR 2 R 3 Hal j (I) 6SNN 2 NO 2 Swherein Hal is halogen, such as fluorine, chlorine, bromine or iodine; R, is hydrogen, C 1 -C 6 alkyl or C 3 -C 7 cycloalkyl; R2 is hydrogen, CI-C 6 alkyl or C 3 -C 7 cycloalkyl, and R 3 is hydrogen or C 1 -C 6 alkyl, for use in a method for the systemic control of fleas, especially adult fleas in domestic animals.

21. A compound of formula I according to claim 20 method for the systemic control of fleas, especially adult fleas in domestic animals, wherein Hal is in the 6-position and is preferably fluorine, chlorine or bromine, but especially chlorine.

22. A compound of formula I according to claim 20 for use in a method for the systemic control of fleas, especially adult fleas in domestic animals, wherein R, is hydrogen, Ci-C 3 alkyl or C 3 -C 6 cycloalkyl, preferably hydrogen, methyl or cyclopropyl, especially methyl.

23. A compound of formula I according to claim 20 for use in a method for the systemic control of fleas, especially adult fleas in domestic animals, wherein R 2 is Ci-C 3 alkyl, especially methyl. A compound of formula I according to any one of claims 17 to 23 for use in a method for the systemic control of fleas, especially adult fleas in domestic animals, wherein R 3 is hydrogen. Food additive for the systemic control of fleas in domestic animals, which comprises as active ingredient, in an amount effective against fleas, a compound of formula I I 'I -27- R 3 NRR Hal Hal N NR 2 R (I) 6 N NO 2 wherein Hal is halogen, such as fluorine, chlorine, bromine or iodine; RI is hydrogen, C 1 -C 6 alkyl or C 3 -C 7 cycloalkyl; R 2 is hydrogen, CI-C 6 alkyl or C 3 -C 7 cycloalkyl, and R 3 is hydrogen or C 1 -C 6 alkyl.

26. The use of a compound of formula I R 1 N NR 2 R 3 Hal (I) N NO NO 2 wherein Hal is halogen, such as fluorine, chlorine, bromine or iodine; R 1 is hydrogen, Ci-C 6 alkyl or C 3 -C7cycloalkyl; R 2 is hydrogen, C 1 -C 6 alkyl or C 3 -C7cycloalkyl, and R 3 is hydrogen or Ci-C 6 alkyl, for the preparation of a veterinary medicinal composition for systemic administration to domestic animals for controlling fleas that are parasites of domestic animals.

27. The use according to claim 26, wherein the systemic administration is oral or parenteral administration or administration in the form of an implant to the said domestic animal.

28. A pack containing individual doses of a compound of formula I I I -28- R 3 I HN NR 2 R 3 Hal (I) NO 2 wherein Hal is halogen, such as fluorine, chlorine, bromine or iodine; RI is hydrogen, CI-C 6 alkyl or C 3 -C 7 cycloalkyl; R 2 is hydrogen, CI-C 6 alkyI or C 3 -C 7 cycloalkyl, and R 3 is hydrogen or C 1 -Cralkyl, in formulated form for oral administration against fleas in domestic animals, wherein the active ingredient is present in individual ready-for-use doses of from 0.01 mg/kg of body weight to approximately 800 mg/kg of body weight. I 4 H-19097/P1 PCT 1-rN-(Halo-3-pyridylmethyl)1-N-methylamino- -alkylamino-2-nitroethvlene derivatives for controiline fleas in domestic animals Abstract The compounds of formula I are described R 3a 3 N NR 2 R 3 Hal I 6 N 2 wherein Hal is halogen, such as fluorine, chlorine, bromine or iodine; R 1 is hydrogen, C 1 -C 6 alkyl or C 3 -C 7 cycloalkyl; R 2 is hydrogen, C 1 -C 6 alkyl or C 3 -C 7 cycloalkyl, and R 3 is hydrogen or Ci-C 6 alkyl, for use in a method of controlling fleas in domestic animals, especially in dogs and cats, wherein systemic administration is preferred. The compounds of formula I are adminis- tered in an amount effective against fleas via the digestive tract or via the blood of the host animal and thus systemically to the domestic animal, especially the dog or the cat. INTERNATIONAL SEARCH REPORT international application No. PCT/EP 92/01161 A. CLASSIFICATION OF SUBJECT MATTER Int.C1. 5 A01N43/40 According to International Patent Classification (IPC) or to both national classification and IPC B. FIELDS SEARCHED Minimum documentation searched (elassification system followed by classification symbols) Int.C1. 5 A01N Documentation searched other than minimum documentation to the extent that such documents are included in the fields searched Electronic data base consulted during the international search (name of data base and, where practicable. search terms used) C. DOCUMENTS CONSIDERED TO BE RELEVANT Category' Citation of document, with indication, where appropriate, of the relevant passages Relevant to claim No. X EP,A,0 302 389 (TAKEDA CHEMICAL 20-25 INDUSTRIES, LTD) 8 February 1989 cited in the application see page 2, line 36 page 3, line 4 see page 18, line 21 line see examples 10, 11, 41, 57, 58, 61, 64, 80-83 A EP,A,0 255 803 (CIBA-GEIGY AG) 1-27 February 1988 see page 2, page 4, line 8 see claims D Further documents are listed in the continuation of Box C. See patent family annex. Special categories of ciled documents: later document publishedafter the interational filing dateor priority "A i general stae e at is nt date ar41 not in conflict with ith application but cited to understand document defiing the general state of the ar l which is not considered the pnnciple or theory underlying the invention to be of particular relevance earlier document but published on or after the interntional filing date document of particular relevance: the claimed invention cannot be considered novel or cannot be considered to involve an inventive L" document which may throw doubts on pinoriy claim(s) or which is step when the document is taken alone cited to establish the publication date of another citation or other special reason (as specified) document of particular relevance: the claimed invention cannot be document referring to an oral disclosure, use, exhibition or other dered to nvolven inventive step when the document means combined with one or more othersuch documents, such combination being obvious to a person sklled in the art document published prior to the international filing date but later than en o ou ersonsenthea the priority date claimed document member of the same patent family D ,e of the actual completion of the international search Date of mailing of the international search report 27 January 1993 (27.01.93) 2 February 1993 (02.02.93) Name and mailing address of the ISA/ Authorized officer European Patent Office Facsimile No. Telephone No. Form PCT/ISA/210 (second sheet) (July 1992) -2- INTERNATIONAL SEARCH RE PORT International application No, PCT/EP 92/01161 C (Continuation). DOCUMIENTS CONSIDERED TO BE RELEVANT Category* Citation of document, with indication, where appropriate, of the relevant passages Relevant to claim No. A EPA, 375 907 (NIHON TOKUSHU NOYAKU SEIZO 1-27 K.K.) 4 July 1990 see page 2, line 10 line 29 see page 9, lines 1-5, 51 see page 10, line 2 line 7 see compounds No. 8, 11, 28-30 A EP,A,0 302 833 (CIBA-GEIGY AG) 1-27 8 February 1989 cited in the application see page 2, line 3 -line 31 see page 7, line 27 -line 51 compound No. 3.3 see claims 1-4,9,18,19,24-26 Form PCr/ISA/21O (continuation of second sheet) (July 1992) ANNEX TO THE INTERNATIONAL SEARCH REPORT ON INTERNATIONAL PATENT APPLICATION NO. EP 9201161 SA 59981 This annex lists the patent family members relating to the patent documents cited in the above-mentioned international search report. The members are as contained in the European Patent Office EDP file on The European Patent Office is in no way liable for these particulars wtich are merely given for the purpose of information. 27/01/93 Patent documaent Publication Patent family Publication cited in search report date uember(s) date EP-A-0302389 08-02-89 EP-A- 0509559 21-10-92 JP-A- 2000171 05-01-90 EP-A-0255803 10-02-88 AU-B- 606349 07-02-91 AU-A- 7658187 11-02-88 JP-A- 63072631 02-04-88 US-A- 4973589 27-11-90 ZA-A- 8705776 08-02-88 EP-A-0375907 04-07-90 AU-B- 623219 07-05-92 AU-A- 4939090 16-08-90 CA-A- 2009735 13-08-90 EP-A- 0383091 22-08-90 US-A- 5051434 24-09-91 US-A- 5084467 28-01-92 US-A- 5054194 08-10-91 JP-A- 2288859 28-11-90 JP-A- 2288860 28-11-90 EP-A-0302833 08-02-89 AU-A- 2051088 09-03-89 JP-A- 1070468 15-03-89 US-A- 4918086 17-04-90 US-A- 5049571 17-09-91 o mo d out thian Ol Jo of the Euopn at Ofi, No. 8 For more details about this annex se Official Journal of the European Patent Office, No. I2/81