AU2004205351A1

AU2004205351A1 - Pyrimido(5,4-e)(1,2,4)triazine-5,7-diones, methods for producing the same and their use

Info

Publication number: AU2004205351A1
Application number: AU2004205351A
Authority: AU
Inventors: Karl-Heinz Baringhaus; Guenter Mueller; Stefan Petry; Norbert Tennagels
Original assignee: Sanofi Aventis Deutschland GmbH
Current assignee: Sanofi Aventis Deutschland GmbH
Priority date: 2003-01-20
Filing date: 2004-01-07
Publication date: 2004-08-05
Also published as: WO2004065387A1; EP1587806B1; DE502004008447D1; JP2006515611A; DE10301788B4; DE10301788A1; CA2513285A1; EP1587806A1; BRPI0406828A; MXPA05007201A; ATE414086T1

Abstract

Pyrimidotriazine-dione derivatives (I) are new. Pyrimidotriazine-dione derivatives of formula (I) and their salts are new. R1-R4 = H, fluoro, chloro, bromo, hydroxy, trifluoromethyl, nitro, cyano, trifluoromethoxy, 1-6C alkyl, 2-6C alkenyl, 2-6C alkynyl, 1-10C alkoxy, 2-10C alkenyloxy, 2-10C alkynyloxy, 1-6C alkylthio, 2-6C alkenylthio, 2-6C alkynylthio, 3-7C cycloalkyl or 3-7C cycloalkyl(1-4C) alkyl (all optionally substituted on alkyl, alkenyl, alkynyl and/or cycloalkyl by one or more S1), 1-6C alkylsulfinyloxy, 1-6C alkylsulfonyloxy, 6-10C arylsulfonyloxy, 6-10C aryloxy (optionally aryl-substituted by 1 or 2 fluoro, chloro, cyano, OR13, R13, trifluoromethyl or trifluoromethoxy), 1-6C alkylsulfinyl, 1-6C alkylsulfonyl, 6-10C arylsulfonyl (optionally ring-substituted by 1 or 2 fluoro, chloro, bromo, cyano, OR13, R13, trifluoromethyl, trifluoromethoxy, C(O)OR13 or C(O)NR14R15), SO2NR14R15, C(O)OR13, C(O)heteroalkyl, NR14R15 or heteroalkyl; S1 = fluoro, chloro, bromo, phenylsulfinyl, phenylsulfonyl or phenyl (optionally phenyl-substituted by fluoro, chloro, bromo or R13), OR13, C(O)OR13, C(O)NR14R15, NR14R15 or C(O)heteroalkyl; and R13-R15 = H, 1-6C alkyl or phenyl.

Description

IN THE MATTER OF an Australian Application corresponding to PCT Application PCT/EP2004/000040 RWS Group Ltd, of Europa House, Marsham Way, Gerrards Cross, Buckinghamshire, England, hereby solemnly and sincerely declares that, to the best of its knowledge and belief, the following document, prepared by one of its translators competent in the art and conversant with the English and German languages, is a true and correct translation of the PCT Application filed under No. PCT/EP2004/000040 Date: 25 May 2005 C. E. SITCH Deputy Managing Director - UK Translation Division For and on behalf of RWS Group Ltd WO 2004/065387 PCT/EP2004/000040 Description Pyrimido[5,4-e][1,2,4]triazine-5,7-diones, methods for producing the same and their use 5 The invention relates to pyrimido[5,4-e][1,2,4]triazine-5,7-diones and to their physiologically tolerated salts and physiologically functional derivatives. 10 JP 96-67814 describes compounds of a similar structure as being antineoplastic agents. The invention was based on the object of making available compounds which can be used to prevent and treat diabetes type 1 and type 2. In 15 addition, the compounds should bring about a perceptible reduction in blood sugar level. The invention therefore relates to compounds of the formula I, R4 20 in which RI, R3 and R4 are, independently of each other, H, F, Cl, Br, OH, CE 3 , 25

NO

2 , CN, OCF 3 , (C 1

-C

6 )-alkyl, (C 2

-C

6 )-alkenyl, (C 2

-C

6 )-alkynyl, 0-(C 1 -C10)-alkyl, 0-(C 1 -C10)-alkenyl,

C-(C

2

-C

1 o)-alkynyl, S-(C 1 C 6 )-alkyl, S-(C 2

-C

6 )-alkenyl,

S-(C

2

-C

6 )-alIkynyl, (C 3

-C

7

)

cycloalkyl, (C3-C7)-cycloalkyl-(C 1

-C

4 )-alkyl, where alkyl, alkenyl, alkynyl and cycloalkyl can be substituted more than once by F, 30 Cl, Br, SO-phenyl, SO2-phenyl or phenyl, where the phenyl ring can be substituted by F, C, Br or R13, or by OR13, COOR13, CON(R14)(R1 5), N(R1 4)(R1 5) or CO-heteroalkyl, 0-SO-(C 1

-C

6

)-

2 alkyl, O-SO 2

-(C

1

-C

6 )-alkyl, O-SO 2

-(C

6 -C1o)-aryl, O-(C6-C1o)-aryl, where aryl can be substituted up to two times by F, Cl, CN, OR13, R13, CF 3 or OCF 3 , SO-(C1-C)-alkyl, S0 2 -(C1-C 6 )-alkyl, S02-(C 6 -Clo)-aryl, where the phenyl ring can be substituted up 5 to two times by F, Cl, Br, CN, OR13, R13, CF 3 , OCF 3 , COOR13 or CON(R14)(R15), S0 2 -N(R14)(R15), COOR13, CO heteroalkyl, N(R14)(R15) or heteroalkyl; R13, R14 and R15, are, independently of each other, H, (C 1

-C

6 )-alkyl or 10 phenyl; and the physiologically tolerated salts thereof. Particular preference is given to compounds of the formula I in which one 15 or more radicals(s) has/have the following meaning: R1 is H or (C1-C)-alkyl; R3 and R4 are, independently of each other, H, F, Cl, Br, OH, CF 3 , NO 2 , 20 CN, OCF 3 , (C1-C)-alkyl, (C2-C6)-alkenyl, (C2-C6)-alkynyl, 0-(C1 C1o)-alkyl, 0-(C1-C1o)-alkenyl, 0-(C2-C1o)-alkynyl,

S-(C

1 -C6) alkyl, S-(C2-Ce)-alkenyl, S-(C2-C 6 )-alkynyl, (C3-C7)-cycloalkyl, (C3-C7)-cycloalkyl-(C1-C 4 )-alkyl, where alkyl, alkenyl, alkynyl and cycloalkyl can be substituted more than once by F, Cl, Br, SO 25 phenyl, S02-phenyl or phenyl, where the phenyl ring can be substituted by F, Cl, Br or R13, or by OR13, COOR13, CON(R14)(R15), N(R14)(R15) or CO-heteroalkyl, O-SO-(C1-C6) alkyl, O-SO2-(C1-C 6 )-alkyl, O-SO2-(C6-C1o)-aryl, 0-(C6-C1o)-aryl, where aryl can be substituted up to two times by F, C, CN, 30 OR13, R13, CF 3 or OCF 3 , SO-(C1-C 6 )-alkyl, S02-(C1-C 6 )-alkyl, SO2-(C6-Clo)-aryl, where the phenyl ring can be substituted up to two times by F, Cl, Br, CN, OR13, R13, CF 3 , OCF 3 , COOR13 or CON(R14)(R15), S0 2 -N(R14)(R15), COOR13, CO-hetero alkyl, N(R14)(R15) or heteroalkyl; 35 R13, R14 and R15 are, independently of each other, H, (C1-C 6 )-alkyl or phenyl; and the physiologically tolerated salts thereof.

3 Very particular preference is given to compounds of the formula I in which one or more radical(s) has/have the following meaning: R1 is (CI-C)-alkyl; 5 R3 is (CI-Cs)-alkyl-phenyl or (C2-CO)-alkenyl-phenyl, where the phenyl ring can be substituted by F, Cl, Br, OR13 or R13; R4 is (C-C)-alkyl or (Ci-C6)-alkylene-D; 10 R13 is (CrC 6 )-alkyl or phenyl; and the physiologically tolerated salts thereof. 15 The alkyl radicals in the substituents R1, R3 and R4 can be either straight chain or branched. If radicals or substituents, such as COOR13, can occur more than once in the compounds of the formula I, they can then all, independently of each 20 other, have the given meanings and be identical or different. Because they are more soluble in water than the starting compounds or basis compounds, pharmaceutically tolerated salts are particularly suitable for medical applications. These salts must possess a pharmaceutically 25 tolerated anion or cation. Suitable pharmaceutically tolerated acid addition salts of the compounds according to the invention are salts of inorganic acids, such as hydrochloric acid, hydrobromic acid, phosphoric acid, metaphosphoric acid, nitric acid and sulfuric acid, and also of organic acids, such as acetic acid, benzenesulfonic acid, benzoic acid, citric acid, 30 ethanesulfonic acid, fumaric acid, gluconic acid, glycolic acid, isethionic acid, lactic acid, lactobionic acid, maleic acid, malic acid, methanesulfonic acid, succinic acid, p-toluenesulfonic acid and tartaric acid. Suitable pharmaceutically tolerated basic salts are ammonium salts, alkali metal salts (such as sodium salts and potassium salts), alkaline earth metal salts 35 (such as magnesium salts and calcium salts), trometamol (2-amino-2 hydroxymethyl-1,3-propanediol), diethanolamine, lysine or ethylene diamine.

4 Salts containing an anion which is not pharmaceutically tolerated, such as trifluoroacetate, also belong within the scope of the invention as useful intermediates for preparing or purifying pharmaceutically tolerated salts and/or for use in nontherapeutic applications, for example in-vitro 5 applications. The term "physiologically functional derivative", which is used here, denotes any physiologically tolerated derivative of a compound of the formula I according to the invention, e.g. an ester which is able, on being 10 administered to a mammal, such as a human, to form (directly or indirectly) a compound of the formula I or an active metabolite thereof. The physiologically functional derivatives also include prodrugs of the compounds according to the invention, as described, for example, in H. 15 Okada et al., Chem. Pharm. Bull. 1994, 42, 57-61. Such prodrugs can be metabolized in vivo to give a compound according to the invention. These prodrugs may or may not themselves be active. The compounds according to the invention can also be present in different 20 polymorphic forms, for example as amorphous and crystalline polymorphic forms. All the polymorphic forms of the compounds according to the invention belong within the scope of the invention and are another aspect of the invention. 25 In that which follows, all references to "compound(s) according to formula I" relate to (a) compound(s) of the formula I as described above and to its (their) salts, solvates and physiologically functional derivatives as described herein. 30 The compound(s) of the formula (1) can also be administered in combination with (an) other active compound(s). The quantity of a compound according to formula I which is required in order to achieve the desired biological effect depends on a number of 35 factors, e.g. the specific compound which is selected, the intended use, the type of administration and the clinical state of the patient. In general, the daily dose lies in a range from 0.3 mg to 100 mg (typically from 3 mg to 50 mg) per day per kilogram of body weight, e.g. 3-10 mg/kg/day. An intravenous dose can, for example, lie in the range from 0.3 mg to 5 1.0 mg/kg, with it being possible for this dose to be expediently administered as an infusion of from 10 ng to 100 ng per kilogram per minute. Infusion solutions which are suitable for these purposes can contain, for example, from 0.1 ng to 10 mg, typically from 1 ng to 10 mg per 5 millilitre. Single doses can contain, for example, from 1 mg to 10 g of the active compound. Consequently, ampoules for injections can contain, for example, from 1 mg to 100 mg, while single dose formulations which can be administered orally, such as tablets or capsules, can, for example, contain from 1.0 to 1000 mg, typically from 10 to 600 mg. While the 10 compounds according to formula I can themselves be used as the compound for treating the abovementioned conditions, they are preferably present, together with a tolerated excipient, in the form of a pharmaceutical composition. The excipient naturally has to be tolerated, in the sense that it is compatible with the other constituents of the composition and is not 15 harmful to the health of the patient. The excipient can be a solid or a liquid or both and is preferably formulated with the compound as a single dose, for example as a tablet which can contain from 0.05% to 95% by weight of the active compound. Other pharmaceutically active substances can also be present, including other compounds according to formula 1. The pharma 20 ceutical compositions according to the invention can be prepared using one of the known pharmaceutical methods, which essentially consist in mixing the constituents with pharmacologically tolerated carrier substances and/or auxiliary substances. 25 Pharmaceutical compositions according to the invention are those which are suitable for oral, rectal, topical, peroral (e.g. sublingual) or parenteral (e.g. subcutaneous, intramuscular, intradermal or intravenous) administration even if the most suitable mode of administration depends, in each individual case, on the nature and severity of the condition to be 30 treated and on the nature of the compound according to formula I which is in each case employed. Sugar-coated formulations and sugar-coated delayed-release formulations also belong within the scope of the invention. Formulations which are acid-resistant and gastric juice-resistant are preferred. Suitable gastric juice-resistant coatings include cellulose acetate 35 phthalate, polyvinyl acetate phthalate, hydroxypropylmethyl cellulose phthalate and anionic polymers of methacrylic acid and methyl methacrylate.

6 Suitable pharmaceutical compounds for oral administration can be present -in separate units, such as capsules, cachets, sucking tablets or tablets which in each case contain a specific quantity of the compound according to formula I; as powders or granulates; as a solution or suspension in an 5 aqueous or non-aqueous liquid; or as an oil-in-water or a water-in-oil emulsion. As has already been mentioned, these compositions can be prepared using any suitable pharmaceutical method which includes a step in which the active compound and the excipient (which can consist of one or more additional constituents) are brought into contact. In general, the 10 compositions are prepared by uniformly and homogeneously mixing the active compound with a liquid and/or finely divided solid excipient, after which the product is molded, if necessary. Thus, a tablet can be prepared, for example, by means of a powder or granulate of the compound being pressed or molded, where appropriate together with one or more additional 15 constituents. Pressed tablets can be prepared by tableting the compound in freely flowing form, such as a powder or granulate, which is mixed, where appropriate, with a binder, lubricant, inert diluent and/or a (several) surface active/dispersing agent(s) in a suitable machine. Molded tablets can be prepared by molding the pulverulent compound, which is moistened with an 20 inert, liquid diluent, in a suitable machine. Pharmaceutical compositions which are suitable for peroral (sublingual) administration include sucking tablets which contain a compound according to formula I together with a flavoring agent, usually sucrose and gum arabic 25 or tragacanth, and lozenges, which include the compound in an inert base such as gelatin and glycerol or sucrose and gum arabic. Suitable pharmaceutical compositions for parenteral administration preferably include sterile, aqueous preparations of a compound according 30 to formula I which are preferably isotonic with the blood of the intended recipient. These preparations are preferably administered intravenously even if the administration can also take place subcutaneously, intra muscularly or intradermally as an injection. These preparations can preferably be prepared by mixing the compound with water and making the 35 resulting solution sterile and isotonic with the blood. In general, injectable compositions according to the invention contain from 0.1 to 5% by weight of the active compound.

7 Suitable pharmaceutical compositions for rectal administration are preferably present as single-dose suppositories. These can be prepared by mixing a compound according to formula I with one or more conventional solid excipients, for example cocoa butter, and molding the resulting 5 mixture. Suitable pharmaceutical compositions for topical application on the skin are preferably present as an ointment, cream, lotion, paste, spray, aerosol or oil., Vaseline, lanolin, polyethylene glycols, alcohols, and combinations of 10 two or more of these substances can be used as the excipient. In general, the active compound is present at a concentration of from 0.1 to 15% by weight of the composition, for example of from 0.5 to 2%. Transdermal administration is also possible. Suitable pharmaceutical 15 compositions for transdermal applications can be present as individual plasters which are suitable for long-term, close contact with the epidermis of the patient. Such plasters expediently contain the active compound in an optionally buffered, aqueous solution, dissolved and/or dispersed in an adhesive or dispersed in a polymer. A suitable active compound 20 concentration is from approx. 1% to 35%, preferably from approx. 3% to 15%. As a special option, the active compound can, as described, for example, in Pharmaceutical Research, 2(6): 318 (1986), be released by means of electrotransport or iontophoresis. 25 The following are suitable to use as additional active compounds for the combination preparations: all the antidiabetics which are named in chapter 12 in the Roten Liste [Red List] 2001. They can be combined with compounds of the formula I according to the invention, particularly for the purpose of synergistically improving the effect. The active compound 30 combination can be administered either by separately administering the active compounds to the patient or administering them in the form of combination preparations in which several active compounds are present in one pharmaceutical preparation. Most of the active compounds which are cited below are disclosed in USP Dictionary of USAN and International 35 Drug Names, US Pharmacopoeia, Rockville 2001. Antidiabetics include insulin and insulin derivatives, such as Lantus@ (see www.lantus.com) or HMR 1964, rapidly acting insulins (see US 6,221,633), GLP-1 derivatives, such as those which Novo Nordisk A/S has disclosed in WO 98/08871, and also orally active hypoglycaemic active compounds.

8 The orally active hypoglycaemic active compounds preferably include sulfonylureas, biguanidines, meglitinides, oxadiazolidinediones, thiazolidinediones, glucosidase inhibitors, glucagon antagonists, GLP-1 agonists, potassium channel openers, such as those which Novo Nordisk 5 A/S has disclosed in WO 97/26265 and WO 99/03861, insulin sensitizers, inhibitors of liver enzymes which are involved in stimulating gluconeo genesis and/or glycogenolysis, modulators of glucose uptake, compounds which alter fat metabolism, such as antihyperlipidaemic active compounds and antilipidaemic active compounds, compounds which decrease food 10 intake, PPAR agonists and PXR agonists, and active compounds which act on the ATP-dependent potassium channel in the beta cells. In one embodiment of the invention, the compounds of formula I are administered in combination with an HMGCoA reductase inhibitor, such as 15 simvastatin, fluvastatin, pravastatin, lovastatin, atorvastatin, cerivastatin or rosuvastatin. In one embodiment of the invention, the compounds of formula I are administered in combination with a cholesterol absorption inhibitor, such as 20 Ezetimibe, Tiqueside or Pamaqueside. In one embodiment of the invention, the compounds of the formula I are administered in combination with a PPAR gamma agonist, such as rosiglitazone, pioglitazone, JTT-501 or GI 262570. 25 In one embodiment of the invention, the compounds of formula I are administered in combination with a PPAR alpha agonist, such as GW 9578 or GW 7647. 30 In one embodiment of the invention, the compounds of the formula I are administered in combination with a mixed PPAR alpha/gamma agonist, such as GW 1536, AVE 8042, AVE 8134 or AVE 0847, or as described in PCT/USOO/1 1833, PCT/USOO/1 1490 or DE10142734.4. 35 In one embodiment of the invention, the compounds of formula I are administered in combination with a fibrate, such as Fenofibrate, Clofibrate or Bezafibrate.

9 In one embodiment of the invention, the compounds of the formula I are administered in combination with an MTP inhibitor, such as -Implitapide, BMS-201038 or R-1 03757. 5 In one embodiment of the invention, the compounds of formula I are administered in combination with a bile acid absorption inhibitor (see, e.g., US 6,245,744 or US 6,221,897), such as HMR 1741. In one embodiment of the invention, the compounds of the formula I are 10 administered in combination with a CETP inhibitor, such as JTT-705. In one embodiment of the invention, the compounds of formula I are administered in combination with a polymeric bile acid adsorber, such as Cholestyramine or Colesevelam. 15 In one embodiment of the invention, the compounds of formula I are administered in combination with an LDL receptor inducer (see US 6,342,512), such as HMR1171 or HMR 1586. 20 In one embodiment of the invention, the compounds of the formula I are administered in combination with an ACAT inhibitor, such as Avasimibe. In one embodiment of the invention, the compounds of the formula I are administered in combination with an antioxidant, such as OPC-14117. 25 In one embodiment of the invention, the compounds of the formula I are administered in combination with a lipoprotein lipase inhibitor, such as NO 1886. 30 In one embodiment of the invention, the compounds of the formula I are administered in combination with an ATP citrate lyase inhibitor, such as SB-204990. In one embodiment of the invention, the compounds of the formula I are 35 administered in combination with a squalene synthetase inhibitor, such as BMS-1 88494.

10 In one embodiment of the invention, the compounds of the formula I are administered in combination with a lipoprotein(a) antagonist, such as Cl-1 027 or nicotinic acid. 5 In one embodiment of the invention, the compounds of the formula I are administered in combination with a lipase inhibitor, such as Orlistat. In one embodiment of the invention, the compounds of the formula I are administered in combination with insulin. 10 In one embodiment, the compounds of the formula I are administered in combination with a sulfonylurea, such as Tolbutamide, Glibenclamide, Glipizide or Glimepiride. In one embodiment, the compounds of the formula I are administered in combination with a biguanide, such as Metformin. 15 In yet another embodiment, the compounds of formula I are administered in combination with a Meglitinide, such as Repaglinide. In one embodiment, the compounds of formula I are administered in combination with a thiazolidinedione, such as Troglitazone, Ciglitazone, 20 Pioglitazone, Rosiglitazone or the compounds disclosed by Dr. Reddy's Research Foundation in WO 97/41097, in particular 5-[[4-[(3,4-dihydro-3 methyl- 4 -oxo-2-quinazolinylmethoxy]phenyl]methyl]-2,4-thiazolidinedione. In one embodiment, the compounds of the formula I are administered in combination with an a-glucosidase inhibitor, such as Miglitol or Acarbose. 25 In one embodiment, the compounds of the formula I are administered in combination with an active compound which acts on the ATP-dependent potassium channel in beta cells, such as Tolbutamide, Glibenclamide, Glipizide, Glimepiride or Repaglinide. In one embodiment, the compounds of formula I are administered in 30 combination with more than one of the abovementioned compounds, e.g. in combination with a sulfonylurea and Metformin, a sulfonylurea and Acarbose, Repaglinide and Metformin, insulin and a sulfonylurea, insulin and Metformin, insulin and Troglitazone, insulin and Lovastatin, etc. 35 In another embodiment, the compounds of the formula I are administered in combination with CART modulators (see "cocaine-amphetamine-regulated transcript influences energy metabolism, anxiety and gastric emptying in mice" Asakawa, A, et al., M.: Hormone and Metabolic Research (2001), 33(9), 554-558), NPY antagonists, e.g. naphthalene-1 -sulfonic acid-{4-[(4- 11 aminoquinazolin-2-ylamino)methyl]cyclohexylmethyl}amide hydrochloride (CGP 71683A)), MC4 agonists (e.g. 1-amino-1,2,3,4-tetrahydro naphthalene-2-carboxylic acid [2-(3a-benzyl-2-methyl-3-oxo-2,3,3a,4,6,7 hexahydropyrazolo[4,3-c]pyridin-5-yl)-1 -(4-chlorophenyl)-2-oxoethyl]amide; 5 (WO 01/91752)), Orexin antagonists (e.g. 1-(2-methylbenzoxazol-6-y)-3 [1,5]naphthyridin-4-yl urea hydrochloride (SB-334867-A)), H3 agonists (3 cyclohexyl-1 -(4,4-dimethyl-1,4,6,7-tetrahydroimidazo[4,5-c]pyridin-5-yl) propan-1-one oxalic acid salt (WO 00/63208)); TNF agonists, CRF antagonists (e.g. [2-methyl-9-(2,4,6-trimethylphenyl)-9H-1 , 3,9-triazafluoren 10 4-yl]dipropylamine (WO 00/66585)), CRF BP antagonists (e.g. Urocortin), Urocortin agonists, p3-agonists (e.g. 1-(4-chloro-3-methanesulfonyl methylphenyl)-2-[2-(2,3-dimethyl-1 H-indol-6-yloxy)ethylamino]ethanoI hydrochloride (WO 01/83451)), MSH (melanocyte-stimulating hormone) agonists, CCK-A agonists (e.g. {2-[4-(4-chloro-2,5-dimethoxyphenyl)-5-(2 15 cyclohexylethyl)thiazol-2-ylcarbamoyl]-5,7-dimethylindol-1 -yl}acetic acid trifluoroacetic acid salt (WO 99/15525)), serotonin reuptake inhibitors (e.g. Dexfenfluramine), mixed serotoninergic and noradrenergic compounds (e.g. WO 00/71549), 5HT agonists, e.g. 1-(3-ethylbenzofuran-7 yl)piperazine oxalic acid salt (WO 01/09111), Bombesin agonists, Galanin 20 antagonists, growth hormone (e.g. human growth hormone), growth hormone-releasing compounds (tert-butyl 6-benzyloxy-1-(2 diisopropylaminoethylcarbamoyl)-3,4-dihydro-1 H-isoquinoline-2 carboxylate (WO 01/85695)), TRH agonists (see, e.g. EP 0 462 884) uncoupling protein 2 or protein 3 modulators, leptin agonists (see, e.g. Lee, 25 Daniel W.; Leinung, Matthew C.; Rozhavskaya-Arena, Marina; Grasso, Patricia. Leptin agonists as a potential approach to the treatment of obesity. Drugs of the Future (2001), 26(9), 873-881), DA agonists (Bromocriptin, Doprexin), lipase/amylase inhibitors (e.g. WO 00/40569), PPAR modulators (e.g. WO 00/78312), RXR modulators or TR-p-agonists. 30 In one embodiment of the invention, the other active compound is leptin; see, e.g., "Perspectives in the therapeutic use of leptin", Salvador, Javier; Gomez-Ambrosi, Javier; Fruhbeck, Gema, Expert Opinion on Pharmacotherapy (2001), 2(10), 1615-1622. 35 In one embodiment, the other active compound is Dexamphetamine or amphetamine. In one embodiment, the other active compound is Fenfluramine or Dexfenfluramine.

12 In yet another embodiment, the other active compound is Sibutramine. In one embodiment, the other active compound is Orlistat. In one embodiment, the other active compound is Mazindol or Phentermine. 5 In one embodiment, the compounds of the formula I are administered in combination with ballast substances, preferably insoluble ballast substances (see, e.g., carob/Caromax@) (Zunft H J; et al., Carob pulp preparation for treatment of hypercholesterolemia, ADVANCES IN 10 THERAPY (2001 Sep-Oct), 18(5), 230-6). Caromax is a carob-containing product from Nutrinova, Nutrition Specialties & Food Ingredients GmbH, Industriepark Hoechst, 65926 Frankfurt/Main)). The combination with Caromax@ can be effected in one preparation or by means of separating administering compounds of the formula I and Caromax@. In this 15 connection, Caromax@ can also be administered in the form of foodstuffs, for example in bread, cakes and pastries or muesli bars. It will be understood that each suitable combination of the compounds according to the invention with one or more of the abovementioned 20 compounds and, if desired, one or more additional pharmacologically active substances, is regarded as coming within the protected scope of the present invention.

13

CH

3

CH

3 0 N -O .H3 OH HN 0 NH CH H 3 C H 3 S I

OH

3

OH

3 OPC-14117

CH

3 JTT-705 CI 40 Br NCl S SB-204990 HO OH No

CH

3 HO CHa NO-1886 0 OH

H

3 C OH 0 CH 3

H

3 C

CH

3 O C-1027 Ol:S, |

H

3 C CH 3 0

H

3 0 OH 3 BMS-188494 OCH 00 O H 3 O N O OH 0 GI 262570 0 OH 3 0N N O N -0 H JTT-501 The examples which are produced below serve to explain the invention without, however, restricting it.

I Z Z-Ir 0= K I I 00 L3L M0) CU) E cu

I-

0 CL cu~ 0 Eu -C E co) c Cu cu) A2 A) C m-r +~ £( o C.., * I 2:

E

16 The compounds of the formula 1, and/or their physiologically tolerated salts and/or their prodrugs can be used for producing pharmaceuticals. These pharmaceuticals are suitable, in particular for treating diabetes type I 5 and type 2, insulin resistance and pathological obesity. In addition to this, they are also suitable for treating excessively high blood fat values, high blood pressure, atherosclerosis, malfunctions of the immune system, autoimmune diseases, allergic diseases such as asthma, in connection with osteoporosis, proliferation disturbances such as cancer and psoriasis, 10 diseases involving a reduced or increased production of growth factors, hormones or cytokines which induce the release of growth hormones, infectious diseases or diseases of the nervous system, such as Alzheimer's and schizophrenia. 15 In addition, the compounds of the formula I, and/or their physiologically tolerated salts and/or their prodrugs can be used for producing a pharmaceutical, with this pharmaceutical inhibiting a PTPase. In this connection PTP1B, CD45, LAR, SHP-1, SHP-2, PTPa or HePTP can, in particular, occur as PTPases. 20 Finally, compounds of formula 1, and/or their physiologically tolerated salts and/or their prodrugs can be used for producing a pharmaceutical, with it being possible to employ this pharmaceutical for treating diseases, in particular diabetes type I and type 2, insulin resistance, pathological 25 obesity, excessively high blood fat values, high blood pressure, athero sclerosis, malfunctions of the immune system, autoimmune diseases, allergic diseases such as asthma, in connection with osteoporosis, proliferation disturbances such as cancer and psoriasis, diseases involving a reduced or increased production of growth factors, hormones or 30 cytokines which induce release of growth hormones, diseases of the nervous system such as Alzheimer's and schizophrenia and infectious diseases. In addition, compounds of the formula 1, and/or their physiologically 35 tolerated salts and/or their prodrugs can be employed for producing a pharmaceutical for treating late damage in diabetes (such as nephropathy, retinopathy and neuropathy), and also cardiac infarction, myocardial infarction, peripheral arterial occlusion diseases, thromboses, arterio sclerosis, syndrome X, obesity, insulin resistance, inflammations, immune 17 diseases, autoimmune diseases, such as AIDS, asthma, osteoporosis, cancer, psoriasis, Alzheimer's, schizophrenia and infectious diseases. The invention relates to the production of a pharmaceutical which comprises at least one compound of this invention, with the active 5 compound being mixed with a pharmaceutically suitable excipient and this mixture being brought into a form which is suitable for administration. The activity of the compounds was tested as follows: 10 Inhibiting phosphotyrosin phosphatase 1B (PTP1B) The setting up and implementation of an in-vitro assay for detecting a phosphatase-inhibiting effect of the compounds according to the invention are described below. The isolation of the enzyme preparation and the 15 implementation of the assay are described. Isolating the enzyme preparation: A) Cell culture: Sf9 (invitrogen) cells are cultured in spinner flasks at 28 0 C in Grace's 20 supplement medium (Gibco-BRL) containing 10% heat-inactivated foetal calf serum (Gibco-BRL) following the protocol of Summers and Smith (A Manual for Methods for Baculovirus Vectors and Insect Culture Procedures [Bulletin No. 15555]. Texas A & M University, Texas Agricultural Experiment Station, College Station, TX, 1987). 25 Constructing recombinant baculovirus transfer vectors: cDNA encoding the regulatory and catalytic domains of human PTP1B, but without the carboxy terminal hydrophobic region (corresponding to 1-299 aa), was obtained by means of the polymerase chain reaction, using primers containing favorable cloning sites and suitable cDNA templates, and then cloned into 30 baculovirus expression vectors (Amersham Pharmacia Biotech.). The recombinant baculoviruses were prepared using the Bac-to-Bac baculovirus expression system (Gibco-BRL). In brief, the gene was cloned into the pFASTBAC donor plasmid, which possesses a FLAG sequence at the 5' end of the cDNA. The resulting plasmid was transformed into 35 competent DH10BAC Escherichia coli cells. Following transposition and antibiotic selection, the recombinant plasmid DNA was isolated from selected E. coli colonies and then used for transfecting Sf9 insect cells. The virus particle in the supernatant medium was amplified three times up to a viral stock volume of 500 ml.

18 B) Producing recombinant protein: The infection of a 500 ml spinner culture of Sf9 cells with baculovirus was essentially carried out as described by Summers and Smith (see above). 5 Sf9 cells, at a density of 1-3 x 106 cells/ml, were pelleted by centrifuging at 300 g for 5 min, after which the supernatant was removed and the cells were resuspended, at a density of 1 x 10 7 cells/ml, in a suitable recombinant viral stock (MOI 10). After gently shaking at room temperature for 1.5 hrs, fresh medium was added in order to achieve a cell density of 10 1 x 106 cells/ml. The cells were then cultured in suspension at 28 0 C for suitable periods post infection. C) Cellular fractionation and total cell extracts from infected Sf9 cells: A suitable time after the post infection, aliquots were subjected to an 15 analysis of protein expression using SDS-PAGE and Western blot analysis. The cellular fractionation was carried out as described (Cromlish, W. and Kennedy, B. Biochem. Pharmacol. 52: 1777-1785, 1996). Total cell extracts were obtained from 1 ml aliquots of the infected Sf9 cells after specified times post infection. The pelleted cells (300 g, 5 min) were washed once in 20 phosphate-buffered saline (4 0 C), resuspended in 50 pal of water and disrupted by being repeatedly frozen and thawed. Protein concentrations were determined using the Bradford method (Pierce) and bovine serum albumin as standard. 25 Implementing the assay: A) Dephosphorylating a phosphopeptide: This assay is based on releasing phosphate from a consensus substrate peptide which is detected in the nanomolar concentration range using the malachite green/ammonium molybdate method (Lanzetta, P.A., Alvarez, 30 L.J., Reinach, P.S., Candia, O.A. Anal Biochem. 100: 95-97, 1979) as adapted for the microtiter plate format. The dodecatrisphosphopeptide, TRDIYETDYYRK (Biotrend, Cologne), corresponds to amino acids 1142 1153 of the catalytic domain of the insulin receptor and is (auto) phosphorylated at tyrosine residues 1146, 1150 and 1151. The 35 recombinant hPTP1B was diluted with assay buffer (40 mM tris/HCI, pH 7.4, 1 mM EDTA, 20 mM DTT), in accordance with an activity of 1000-1500 nmol/min/mg of protein, and (a 20 pal portion) was then preincubated (15 min, 30 0 C) in the absence or presence of the test substance (5 pd) at the desired concentration (final conc. DMSO 2% max.) 19 in a total volume of 90 pl (assay buffer). In order to start the dephosphorylation reaction, the peptide substrate (10 pI, prewarmed at 30 0 C) was added to the preincubated enzyme preparation with or without test substance (final conc. 0.2 - 200 piM) and the incubation was continued 5 for 1 hr. The reaction was terminated by adding 100 jil of malachite green hydrochloride (0.45%, 3 parts), ammonium molybdate tetrahydrate (4.2% in 4 N HCI, 1 part) and 0.5% Tween 20 as the stop solution. After incubating at 220C for 30 min, in order to develop the color, the absorption at 650 nm was determined using a microtiter plate reader (Molecular Devices). 10 Samples and blanks were measured in triplicate. The PTP1B activity was calculated as nanomoles of phosphate released per min and mg of protein using potassium phosphate as the standard. The inhibition of the recombinant hPTP1 B by test substances was calculated as percentages of the phosphatase control. Using a four-parameter non-linear logistic 15 regression curve, the IC50 values show significant agreement. B) Cleaving p-nitrophenyl phosphate: This assay is based on the change in the absorption of the non physiological substrate p-nitrophenylphosphate while it is being cleaved, 20 under standard conditions, to give nitrophenol (Tonks, N.K., Diltz, C.D.; Fischer, E.H. J. Biol. Chem. 263: 6731-6737, 1988; Burke T.R., Ye, B., Yan, X.J., Wang, S.M., Jia, Z.C., Chen, L., Zhang, Z.Y., Barford, D. Biochemistry 35: 15989-15996, 1996). The inhibitors are pipetted, at suitable dilutions, into the reaction mixtures, which contain 0.5-5 mM p 25 nitrophenyl phosphate. The following buffers are used (total volume, 100 ptl): (a) 100 mM sodium acetate (pH 5.5), 50 mM NaCl, 0.1% (w/v) bovine serum albumin, 5 mM glutathione, 5 mM DTT, 0.4 mM EGTA and 1 mM EDTA; (b) 50 mM Hepes/KOH (pH 7.4), 100 mM NaCl, 0.1% (w/v) bovine serum albumin, 5 mM glutathione, 5 mM DTT and 1 mM EDTA. The 30 reaction was started by adding enzyme and was carried out, at 250C for 1 hr, in microtiter plates. The reaction was terminated by adding 100 pl of 0.2 N NaOH. The enzyme activity was determined by measuring the absorption at 405 nm using suitable corrections for the absorption of the test substances of p-nitrophenyl phosphate. The results were expressed as 35 percentages of the control, with the quantity of p-nitrophenol formed in the test substance-treated samples (nmol/min/mg protein) being compared with the quantity in the untreated samples. The mean value and the standard deviation were calculated, with the IC50 values being determined by regression analysis of the linear portion of the inhibition curves.

20 C) Cleaving DIFMUP This assay is based on the change in the absorption of the non physiological substrate 6,8-difluoro-4-methylumbellifery phosphate 5 (DFMUP) while it is being cleaved to give 6,8-difluoro-4-methylumbellifery (internal no. DEAV2002/0001 DE NP). The reaction takes place in a black microtiter plate at a temperature of 37 0 C. 120 pl of reaction buffer are prepared, with this buffer containing the following components: 100 ng of recombinant human protein tyrosine phosphatase PTP1b/ml; 50 mM 10 Hepes, pH 6.9; 150 mM NaCl; 1 mM EDTA; 2 mM DTT and inhibitors at suitable dilutions. The phosphatase reaction is started by adding 15 jd of DIFMUP solution, which contains the substrate at ten times the desired final concentration in the final volume and the fluorescence is measured, at time intervals of 30 seconds over 15 minutes, at 358-455 nm in a 15 fluorescence microtiter plate photometer. The measure of the enzyme activity is the increase in fluorescence, which can be represented graphically. The enzymatic activity is reduced in dependence on the inhibitor concentration employed; the inhibitor concentration at which half maximal enzyme activity is observed is designated the IC50. 20 Table 2: Biological activity Ex. IC50 PM 1 0.75 2 0.38 3 0.24 4 0.22 5 5.2 6 0.44 7 0.7 8 2.5 It can be seen from the table that the compounds of the formula I inhibit the 25 activity of phosphotyrosine 1 B. They are therefore well suited for lowering the blood sugar level and insulin level and for preventing and treating diabetes type 1 and type 2.

21 The preparation of some examples is described in detail below: the remaining compounds of the formula I were obtained in an analogous manner: 5 Experimental section: Chlorouracil (1) 0 N O N Cl 10 Phosphoryl chloride (55 ml) is carefully added to barbituric acid (10 g, 78.1 mmol) at 0*C. Water (1.7 ml) is then added dropwise such that the temperature does not exceed 5 0 C. The mixture is boiled under reflux for 5 h and, after it has cooled down, poured onto ice. The product is extracted 15 with ethyl acetate (3 x 100 ml) and dried (Na 2

SO

4 ). The mixture is filtered and the solvent is distilled off in vacuo. Yield: 10.7 g (93%) 20 NMR: H730335 MS: E32934 Ethylhydrazine (2) N,'N 25 A solution of ethyl bromide (38 ml) in ethanol (50 ml) is added dropwise, while stirring intensively, to hydrazine hydrate (250 ml) such that the temperature does not exceed 30 0 C. After the addition has come to an end, 30 the mixture is stirred for a further 2 h. Barium oxide is added to the mixture and the product is distilled through a Vigreux column. Yield: 37 ml.

22 6-(N-Ethylhydrazino)-3-methyl-1 H-pyrimidine-2,4-dione (3) 0 0 N N 5 Ethylhydrazine (2 ml) is added to compound 1 (1.5 g, 8 mmol) and the mixture is stirred at 600C. After 3.5 h, it was no longer possible to detect any starting material by thin layer chromatography. The mixture is concentrated in vacuo and the product is purified by preparative HPLC. 10 Yield: 582 mg Examples 1 and 2: 1-Ethyl-6-methyl-3-phenyl-1H-pyrimido[5,4-e]1,2,4]triazine-5,7-dione (4) 15 and 1-ethyl-6-methyl-4-oxy-3-phenyl-1H-pyrimido[5,4-e][1,2,4]triazine-5,7 dione (5). 0 0 0 N NNN N N N I< N 20 Benzaldehyde (55 ptl, 0.54 mmol) is added to a solution of compound 3 (115 mg, 0.54 mmol) in glacial acetic acid (2 ml) and the mixture is stirred at 100C for 20 min. An aqueous solution of sodium nitrite (40 mg of NaNO2 in 100 pl of water) is then added and the mixture is stirred at 100C for a further 30 min. The mixture is poured onto ice water and the product is 25 extracted with ethyl acetate (3 x 30 ml). The organic phases are dried (Na2SO4) and the solvent is distilled off in vacuo. The residue is purified by flash chromatography (7:3, toluene/ethyl acetate). 1-Ethyl-6-methyl-3 phenyl-1H-pyrimido[5,4-e][1,2,4]triazine-5,7-dione (44 mg, 28.8%) and 1- 23 ethyl-4-oxy-3-phenyl-6-propyl-1 H-pyrimido[5,4-e][1,2,4]triazine-5,7-dione (41 mg, 32%) are obtained. 1 -Ethyl-6-methyl-3-phenyl-1 H-pyrimido[5,4-e][1,2,4]triazine-5,7-dione 5 1 H-NMR: 8 = 7.75 (dd, 2 H, aryl), 7.6 (m, 3H, aryl), 4.4 (q, 2H, CH 2 ); 3.3 (3 H, NCH 3 ), 1.4 (t, 3H, CH 3 ) MS (M+1): 284.2 10 1 -Ethyl-6-methyl-4-oxy-3-phenyl-1 H-pyrimido[5,4-e][1,2,4]triazine-5,7-dione 'H-NMR: 6 = 8.2 (dd, 2H, aryl), 7.6 (m, 3H, aryl), 4.5 (q, 2H, CH 2 ); 3.3 (3 H,

NCH

3 ), 1.5 (t, 3H, CH 3 ) MS (M+1): 300. 15 Examples 3 and 4: 1-Ethyl-3,6-dimethyl-1H-pyrimido[5,4-e][1,2,4]triazine-5,7-dione (6) and 1 ethyl-3,6-dimethyl-4-oxy-1 H-pyrimido[5,4-e][1,2,4]triazine-5,7-dione (7). 20 0 0 0 0 N 0 ~ NN The compounds 6 and 7 are prepared, as described for 4 and 5, by reacting the hydrazine 3 (184 mg, 1 mmol) with acetaldehyde (57 pL, 25 1 mmol). 1 -Ethyl-3,6-dimethyl-1 H-pyrimido[5,4-e][1,2,4]triazine-5,7-dione (6) Yield: 62 mg (28%) 'H-NMR: 8 = 4.4 (q, 2H, NCH 2

CH

3 ); 3.5 (s, 3H, CH 3 ), 3.4 (s, 3H, NCH 3 ); 30 1.45 (t, 3H, NCH 2

CH

3 ). MS (221.22): 222. (M+H) 1 -Ethyl-3,6-dimethyl-4-oxy-1 H-pyrimido[5,4-e][1,2,4]triazine-5,7-dione (7).

24 Yield: 21 mg (9%) 'H-NMR: 8 = 4.57 (q, 2H, CH 2 ); 3.5 (s, 3H, CH 3 ), 1.5 (t, 3H, CH 3 ) MS (237.22): 238.3. (M+H). 5 Example 5: 1-Ethyl-6-methyl-3-(4-propylphenyl)-1 H-pyrimido[5,4-e][1,2,4]triazine-5,7 dione (8) 0 N ON N 10 Compound 8 was obtained, as described for compounds 4 and 5, by reacting the hydrazine 3 (100 mg, 0.54 mmol) with 4-propylbenzylaldehyde (80 mg, 0.54 mmol) and purified by flash chromatography. 15 Yield: 43 mg (24.5%) 'H-NMR: 8 = 8.15 (d, 2H, aryl), 7.4 (d, 2H, aryl), 4.5 (q, 2H, NCH 2 CH3); 3.35 (s, 3 H, NCH 3 ) 2.65 (t, 2H, benzyl, CH 2 ), 1.65 (m, 2H, CH 2

CH

2

CH

3 ), 20 1.45 (t, 3H, NCH 2

CH

3 ), 0.95 (t, 3H, CH 2

CH

2

CH

3 ). MS (325.37): 326.16 (M+H). Examples 6 and 7: 25 1-Ethyl-6-methyl-3-phenyl-1 H-pyrimido[5,4-e][1, 2 ,4]triazine-5,7-dione (9) and 1-ethyl-6-methyl-4-oxy-3-phenyl-1H-pyrimido[5,4-e][1,2,4]triazine-5,7 dione (10) 25 0 0 0 NNN 'N N -- N 0 N N O N The compounds 9 and 10 were obtained, as described for compound 4 and 5, by reacting the hydrazine 3 (100 mg, 0.54 mmol) with cinnamaldehyde 5 (71 mg, 0.54 mmol), and purified by flash chromatography. 1 -Ethyl-6-methyl-3-phenyl-1 H-pyrimido[5,4-e][1,2,4]triazine-5,7-dione (9) Yield: 52 mg (31%) 10 1H-NMR: 8 = 7.9 (m, 3H, 2 aryl-H, CH=CH), 7.4 (m, 3H, aryl H); 7.3 (d, 1H CH=CH), 4.4 (q, 2H, NCH 2 CH3); 3.3 (s, 3H, NCH 3 ); 1.4 (t, 3H, NCH 2

CH

3 ). MS (309.33): 310 (M+H) 15 Ethyl-6-methyl-4-oxy-3-phenyl-1 H-pyrimido[5,4-e][1,2,4]triazine-5,7-dione (10) Yield: 36 mg (20.5%) 20 'H-NMR: 5 = 7.75 (m, 3H, 2 aryl-H, CH=CH), 7.45 (m, 3H, 2 aryl H, CH=CH), 4.4 (q, 2H, NCH 2 CH3); 3.3 (s, 3H, NCH 3 ); 1.4 (t, 3H, NCH 2

CH

3 ). MS (TOF MS ES+; 325.33): 325. Example 8: 25 1 -Ethyl-6-methyl-3-(3-phenoxyphenyl)-1 H-pyrimido[5,4-e][1,2,4]triazine-5,7 dione (11) 26 0 N N 0 A N (ANN N ) The compound 11 was obtained, as described for compound 4, by reacting the hydrazine 3 (100 mg, 0.54 mmol) with 3-phenoxybenzaldehdye (94 pld, 5 0.54 mmol), and purified by flash chromatography (2:1 toluene-EtOAc). Yield: 88 mg (43%) 1 H-NMR: 8 = 8.05-7 (m, 9H, aryl-H); 4.5 (q, 2H, NCH 2 CH3); 3.3 (s, 3H, 10 NCH 3 ); 1.45 (t, 3H, NCH 2

CH

3 ). MS (TOF MS ES+; 375.39): 375. 1-Propylbarbituric acid (12) 0 N O N 0 15 Metallic sodium (2.6 g, 113 mmol) is added to ethanol (60 ml). The mixture is stirred until the sodium has completely finished reacting. Diethyl malonate (116 ml, 105 mmol) and n-propylurea (10 g, 98 mmol) are then added and the mixture is stirred under reflux for 5 h. After conc. HCI (5 ml) 20 and hot water (45 ml) have been added, the mixture is filtered and the filtrate is concentrated in vacuo. Ethanol is added to the residue and the mixture is stirred. The solid is filtered off with suction and dried. Yield: 10.68 g (64%). 25 NMR: 726434 (32165-91) 6-Chloro-3-propyl-1 H-pyrimidine-2,4-dione (13) 27 0 N 0 N Cl The compound 13 was obtained, as described for compound 1, by reacting the barbituric acid 12 (10 g, 58.8 mmol) with POC13 <55 ml). 5 Yield: 2.6 g (23.5%) 6-(N-ethylhydrazino)-3-propyl-1 H-pyrimidine-2,4-dione (14) NN 100 10 Compound 14 is obtained, as described in 3, by reacting compound 13 (1.5 g, 8 mmol) with ethylhydrazine (2 ml). 15 Yield: 528 mg (30.4%) Examples 9 and 10: I-Ethyl-6-propyl-3-phenyl-1 H-pyrimido[5,4-e][1,2,4]triazine-5,7-dione (15) 20 and 1-ethyl-6-propyl-4-oxy-3-phenyl-1H-pyrimido[5,4-e][1,2,4]triazine-5,7 dione (16) 0 0 0 NN N N N N 0 N N 0 N N 28 The compounds 15 and 16 are prepared, as described in 4 and 5, by reacting compound 14 (115 mg, 0.54 mmol) with benzaldehyde (55 Pd, 0.54 mmol). 5 1 -Ethyl-6-propyl-3-phenyl-1 H-pyrimido[5,4-e][1,2,4]triazine-5,7-dione (15) Yield: 44 mg (26%) 1 H-NMR: 5 = 8.2 (m, 2H, aryl-H), 7.6 (m, 3H, aryl-H); 4.5 (q, 2H, 10 NCH 2 CH3); 3.85 (q, 2H, NCH 2

CH

2

CH

3 ); 1.6 (dq, 2H, NCH 2

CH

2

CH

3 ); 1, 5 (t, 3H, NCH 2

CH

3 ); 0.9 (t, 3 H, NCH 2

CH

2

CH

3 ). 1-Ethyl-6-propyl-4-oxy-3-phenyl-1H-pyrimido[5,4-e][1,2,4]triazine-5,7-dione (16) 15 Yield: 41 mg (23.2%) 'H-NMR: 8 = 8.0 (m, 2H, aryl-H), 7.6 (m, 3H, aryl-H); 4.4 (q, 2H,

NCH

2 CH3); 3.85 (q, 2H, NCH 2

CH

2

CH

3 ); 1.58 (dq, 2H, NCH 2

CH

2

CH

3 ); 1, 4 20 (t, 3H, NCH 2

CH

3 ); 0.9 (t, 3H, NCH 2

CH

2

CH

3 ). --Ethyl-6-propyl-3-[3,4-dimethoxyphenyl]-1 H-pyrimido[5,4-e][1,2,4]triazine 5,7-dione (17) 0 0,1 N O N N 25 Compound 17 is prepared, as described in 4, by reacting the hydrazine 13 (115 mg, 0.54 mmol) with 3,4-dimethoxybenzaldehyde (90 mg, 0.54 mmol). 30 Yield: 31 mg (15.4%).

29 'H-NMR: 8 = 7.85 (dd, 1H, aryl-H); 7.7 (d, 1H, aryl-H); 7, (dd, 1H, aryl-H); 4.5 (q, 2H, NCH 2 CH3); 3.85 (m, 8H, 2xOCH 3 , NCH 2

CH

2

CH

3 ); 1.6 (dt,.2H,

NCH

2

CH

2

CH

3 ); 1, 45 (t, 3H, NCH 2

CH

3 ); 0.9 (t, 3H, NCH 2

CH

2

CH

3 ). 5 1 -Ethyl-6-propyl-3-[3-phenoxyphenoxy]-1 H-pyrimido[5,4-e][1,2,4]triazine 5,7-dione (18) 0 N N~ 0 NN 10 Compound 18 is prepared, as described for 4, by reacting the hydrazine 3 (115 mg, 0.54 mmol) with 3-phenoxybenzaldehyde (93 p.l, 0.54 mmol). Yield: 78 mg (35.8%) 'H-NMR: 8 = 7.95 (dd, 1H, aryl-H); 7.8 (d, 1H, aryl-H); 7.63 (dd, 1H, aryl-H); 15 7.43 (m, 2H, aryl-H); 7.2 (m, 2H, aryl-H); 7.1 (m, 2H, aryl-H); 4.45 (q, 2H,

NCH

2

CH

3 ); 3.85 (dt, 2H, NCH 2

CH

2

CH

3 ); 1.6 (m, 2H, NCH 2

CH

2

CH

3 ); 1.45 (t, 3H, NCH 2

CH

3 ); 0.9 (t, 3H, NCH 2

CH

2

CH

3 ). 6-(N-Butylhydrazino)-3-methyl-1H-pyrimidine-2,4-dione (19) 20 0 NN O N N Compound 19 is prepared, as described in 3, by reacting chlorouracil 1 (1 g, 6.2 mmol) with butylhydrazine (5.3 g, 60 mmol). 25 Yield: 1.1 g (83%) 1-Butyl-6-methyl-3-[3-phenoxyphenyl]-1H-pyrimido[5,4-e][1,2,4]triazine-5,7 dione (20) 30 0 0 I ~N O N N Compound 20 is prepared, as described for 4, by reacting the hydrazine 19 5 (176 mg, 0.54 mmol) with 3-phenoxybenzaldehyde (94 pl, 0.54 mmol). Yield: 75 mg (34.5%) 1 H-NMR: 8 = 8.05 (m, 1H, aryl-H); 7.8 (d, 1H, aryl-H); 7.75 (dd, 1H, aryl-H); 7.43 (m, 2H, aryl-H); 7.15 (m, 2H, aryl-H); 7.1 (m, 2H, aryl-H); 3.9 (q, 2H, 10 NCH 2

CH

2

CH

2

CH

3 ); 3.1 (s, 3H, NCH 3 ); 1.6-1.3 (m, 4H, NCH 2

CH

2

CH

2

CH

3 ); 0.9 (q, 2 H, NCH 2

CH

2

CH

2

CH

3 ); 1 -Butyl-6-methyl-3-[3,4-dimethoxyphenyl]-1 H-pyrimido[5,4-e][1,2,4]triazine 5,7-dione (21) 15 N 0 0 N N O N Compound 21 is prepared, as described in 4, by reacting the hydrazine 20 (176 mg, 0.54 mmol) with 3,4-dimethoxybenzaldehyde (88 mg, 0.54 mmol). 20 Yield: 24 mg (12%) 'H-NMR: 8 = 7.95 (s, 1H, aryl-H); 7.6 (d, 1H, aryl-H); 7.45 (dd, 1H, aryl-H); 3.9-3.8 (m, 8H, 2xOCH 3 , NCH 2

CH

2

CH

2

CH

3 ); 3.1 (s, 3H, NCH 3 ); 1.6-1.2 (m, 4H, NCH 2

CH

2

CH

2

CH

3 ); 0.9 (q, 2H, NCH 2

CH

2

CH

2

CH

3 ); 25 1-Butyl-6-methyl-3-phenyl-1H-pyrimido[5,4-e][1,2,4]triazine-5,7-dione (22) 31 0 O N NN 0ON N Compound 22 is prepared, as described in 4, by reacting the hydrazine 20 (176 mg, 0.54 mmol) with benzaldehyde (55 i, 0.54 mmol). 5 Yield: 13 mg (7.8 %)

Claims

1. A compound of the formula 1, 0 R1 N R3 O N N R4 1 5 in which R1, R3 and R4 are, independently of each other, H, F, Cl, Br, OH, CF 3 , 10 NO 2 , CN, OCF 3 , (C1-C)-alkyl, (C 2 -C 6 )-alkenyl, (C 2 -C 6 )-alkynyl, 0-(C1-C 1 o)-alkyl, 0-(C 1 -C 1 o)-alkenyl, 0-(C2-Clo)-alkynyl, S-(C 1 -C 6 ) alkyl, S-(C 2 -C 6 )-alkenyl, S-(C 2 -C 6 )-alkynyl, (C3-C 7 )-cycloalkyl, (C 3 C7)-cycloalkyl-(C1-C 4 )-alkyl, where alkyl, alkenyl, alkynyl and cycloalkyl can be substituted more than once by F, Cl, Br, SO 15 phenyl, S0 2 -phenyl or phenyl, where the phenyl ring can be substituted by F, Cl, Br or R13, or by OR13, COOR13, CON(R14)(R15), N(R14)(R15) or CO-heteroalkyl, O-SO-(C 1 -C 6 ) alkyl, O-SO2-(C1-C 6 )-alkyl, O-SO 2 -(C 6 -C 1 o)-aryl, 0-(C 6 -C 1 o)-aryl, where aryl can be substituted up to two times by F, Cl, CN, OR13, 20 R13, CF 3 or OCF 3 , SO-(C1-C)-alkyl, S02-(Cl-C6)-alkyl, S02 (C 6 -C 1 o)-aryl, where the phenyl ring can be substituted up to two times by F, Cl, Br, CN, OR13, R13, CF 3 , OCF 3 , COOR13 or CON(R14)(R15), S0 2 -N(R14)(R15), COOR13, CO-heteroalkyl, N(R14)(R15) or heteroalkyl; 25 R13, R14 and R15, are, independently of each other, H, (C1-C)-alkyl or phenyl; and the physiologically tolerated salts thereof. 30

2. A compound of the formula I as claimed in claim 1, wherein 33 R1 is H or (C-C 6 )-alkyl; R3 and R4 are, independently of each other, H, F, Cl, Br, OH, CF

3 , NO 2 , CN, OCF 3 , (CrC 6 )-alkyl, (C2-C6)-alkenyl, (C2-C 6 )-alkynyl, 5 0-(C-C 1 o)-alkyl, 0-(C-C1o)-alkenyl, 0-(C2-C1o)-alkynyl, S-(CrC 6 )-alkyl, S-(C 2 -C 6 )-alkenyl, S-(C2-C 6 )-alkynyl, (C3-C7)-cycloalkyl, (C3-C7)-cycloalkyl-(Cr-C 4 )-alkyl, where alkyl, alkenyl, alkynyl and cycloalkyl can be substituted more than once by F, Cl, Br, SO-phenyl, S02-phenyl or phenyl, where the 10 phenyl ring can be substituted by F, Cl, Br or R13, or by OR13, COOR13, CON(R14)(R15), N(R14)(R15) or CO-heteroalkyl, O-SO-(Cr C6)-alkyl, O-SO2-(C-C 6 )-alkyl, O-SO 2 -(C 6 -C1o)-aryl, 0-(C6-Clo)-aryl, where aryl can be substituted up to two times by F, Cl, CN, OR13, R13, CF 3 or OCF 3 , SO-(C-C 6 )-alkyl, 15 S02-(C-C 6 )-alkyl, S02-(C 6 -Clo)-aryl, where the phenyl ring can be substituted up to two times by F, Cl, Br, CN, OR13, R13, CF 3 , OCF 3 , COOR13 or CON(R14)(R15), S0 2 -N(R14)(R15), COOR13, CO-heteroalkyl, N(R14)(R15) or heteroalkyl; 20 R13, R14 and R15 are, independently of each other, H, (C-C 6 )-alkyl or phenyl; and the physiologically tolerated salts thereof. 25 3. A compound of the formula I as claimed in claim 1 or 2, wherein R1 is (Cr1C6)-alkyl; R3 is (C-C6)-alkyl-phenyl or (C2-C6)-alkenyl-phenyl, where the phenyl 30 ring can be substituted by F, Cl, Br, OR13 or R13; R4 is (Cr1C6)-alkyl or (C-C6)-alkylene-D; R13 is (C-C 6 )-alkyl or phenyl; 35 and the physiologically tolerated salts thereof.

4. A pharmaceutical comprising one or more of the compounds as claimed in one or more of claims 1 to 3. 34

5. A pharmaceutical comprising one or more of the compounds as claimed in one or more of claims 1 to 3 and at least one additional active compound. 5

6. A pharmaceutical as claimed in claim 5, which comprises, as additional active compound, one or more antidiabetics, hypoglycaemic active compounds, HMGCoA reductase inhibitors, cholesterol absorption inhibitors, PPAR gamma agonists, PPAR alpha agonists, PPAR alpha/gamma agonists, fibrates, MTP inhibitors, bile acid absorption 10 inhibitors, CETP inhibitors, polymeric bile acid absorbers, LDL receptor inducers, ACAT inhibitors, antioxidants, lipoprotein lipase inhibitors, ATP citrate lyase inhibitors, squalene synthetase inhibitors, lipoprotein(a) antagonists, lipase inhibitors, insulins, sulfonylureas, biguanides, meglitinides, thiazolidinediones, a-glucosidase inhibitors, active 15 compounds acting on the ATP-dependent potassium channel in beta cells, CART agonists, NPY agonists, MC4 agonists, orexin agonists, H3 agonists, TNF agonists, CRF agonists, CRF BP antagonists, urocortin agonists, p3 agonists, MSH (melanocyte-stimulating hormone) agonists, CCK agonists, serotonin reuptake inhibitors, mixed serotoninergic and noradrenergic 20 compounds, 5HT agonists, bombesin agonists, galanin antagonists, growth hormones, growth hormone-releasing compounds, TRH agonists, uncoupling protein 2 or 3 modulators, leptin agonists, DA agonists (Bromocriptine, Doprexin), lipase/amylase inhibitors, PPAR modulators, RXR modulators or TR-p agonists or amphetamines. 25

7. The use of the compounds as claimed in one or more of claims 1 to 3 for producing a medicament for lowering blood sugar.

8. The use of the compounds as claimed in one or more of claims 1 to 30 3 for producing a medicament for treating type 2 diabetes.

9. The use of the compounds as claimed in one or more of claims 1 to 3 for producing a medicament for treating disturbances of lipid and carbohydrate metabolism. 35

10. The use of the compounds as claimed in one or more of claims 1 to 3 for producing a medicament for treating arteriosclerotic symptoms. 35

11. The use of the compounds as claimed in one or more of claims 1 to 3 for producing a medicament for treating insulin resistance.

12. A process for producing a pharmaceutical comprising one or more of 5 the compounds as claimed in one or more of claims 1 to 3, which comprises mixing the active compound with a pharmaceutically suitable excipient and bringing this mixture into a form which is suitable for administration.