DE19943815A1 - Use of thienopyrimidines - Google Patents

Abstract

The invention relates to the use of thienopyrimidines of formula (I) and to their physiologically safe salts and/or solvates, wherein R<1>, R<2> and X have the meanings cited in Claim No. 1. According to the invention, the thienopyrimidines are used in order to produce a medicament for treating angina, high blood pressure, pulmonary hypertension, congestive heart failure, atherosclerosis, conditions of reduced patency of the heart vessels, peripheral vascular diseases, stroke, bronchitis, allergic asthma, chronic asthma, allergic rhinitis, glaucoma, irritable bowel syndrome, tumors, renal insufficiency, cirrhosis of the liver, and for treating female impotence.

Description

The invention relates to the use of compounds of the formula I.

wherein
R ¹ , R ² each independently of one another H, A, OA, OH or Hal,
R ¹ and R ² together also alkylene with 3-5 C atoms, -O-CH ₂ -CH ₂ -, -CH ₂ -O-CH ₂ -, -O-CH ₂ -O- or -O-CH ₂ -CH ₂ -O-,
X is simply substituted by R ^7, R ⁴ , R ⁵ or R ⁶ ,
R ⁴ linear or branched alkylene with 1-10 C atoms, in which one or two CH ₂ groups can be replaced by -CH = CH groups,
R ⁵ cycloalkyl or cycloalkylalkylene with 5-12 C atoms,
R ⁶ phenyl or phenylmethyl,
R ⁷ COOH, COOA, CONH ₂ , CONHA, CON (A) ₂ or CN,
A alkyl with 1 to 6 carbon atoms and
Hal F, Cl, Br or I
mean,
as well as their physiologically acceptable salts and / or solvates for the manufacture of a medicament for the treatment of angina, high blood pressure, pulmonary hypertension, congestive heart failure, arteriosclerosis, conditions of reduced patency of the heart vessels, peripheral vascular diseases, stroke, bronchitis, allergic asthma, chronic Asthma, allergic rhinitis, glaucoma, irritable bowel syndrome, tumors, renal failure, cirrhosis of the liver and for the treatment of female impotence.

The use of other PDE-V inhibitors is described e.g. B. in the WO 94/28902.

Pyrimidine derivatives are, for example, from EP 201 188 or WO 93/06104 known.

The invention was based on the object, new compounds with valuable len properties to find, especially those that are used to manufacture of drugs can be used.

It has been found that the compounds of formula I and their salts good tolerance very valuable pharmacological properties Zen.

In particular, they show a specific inhibition of cGMP phospho diesterase (PDE V).

Quinazolines with cGMP phosphodiesterase inhibitory activity are e.g. B. in J. Med. Chem. 36, 3765 (1993) and ibid. 37, 2106 (1994).

The biological activity of the compounds of formula I can according to Metho which are determined as z. B. in WO 93/06104 or in WO 94/28902 are described.

The affinity of the compounds according to the invention for cGMP and cAMP phosphodiesterase is determined by determining their IC ₅₀ values (concentration of the inhibitor which is required in order to achieve a 50% inhibition of the enzyme activity).

Known methods can be used to carry out the determinations isolated enzymes can be used (e.g. W. J. Thompson et al., Biochem. 1971, 10, 311). A modified can be used to carry out the tests "batch" method by W. J. Thompson and M. M. Appleman (Biochem. 1979, 18, 5228) can be used.

The use of substituted pyrazolopyrimidinones for treatment of female impotence is e.g. B. described in WO 94/28902.

The compounds are effective as inhibitors of phenylephrine-induced contractions in corpus cavernosum preparations of rabbits. This biological effect can e.g. B. detected by the method by F. Holmquist et al. in J. Urol., 150, 1310-1315 (1993) be is written.

The inhibition of the contraction shows the effectiveness of the Invention moderate connections for the therapy and / or treatment of erectile dysfunction stanchions.

The invention relates to the use of the compounds of For mel I and their physiologically acceptable salts and / or solvates for the manufacture of a medicament for the treatment of angina, blood high pressure, pulmonary high pressure, congestive heart failure, Arteriosclerosis, conditions of reduced patency of the cardiovascular system ß, peripheral vascular diseases, stroke, bronchitis, allergy schem asthma, chronic asthma, allergic rhinitis, Glaucom, Irri table Bowel syndromes, tumors, renal failure, cirrhosis and for the treatment of female impotence.

The compounds of formula I can be used as active pharmaceutical ingredients in the Human and veterinary medicine are used. They can also be used as Intermediates for the production of other active pharmaceutical ingredients be set.

Above and below, the radicals R ¹ , R ² , R ³ , R ⁴ , R ⁵ , R ⁶ , R ⁷ , X and L have the meanings given in the formulas I, II and III, unless expressly stated otherwise .

A means alkyl with 1-6 C atoms.

In the above formulas, alkyl is preferably unbranched and has 1, 2, 3, 4, 5 or 6 carbon atoms and is preferably methyl, ethyl or Propyl, further preferably isopropyl, butyl, isobutyl, sec-butyl or tert.- Butyl, but also n-pentyl, neopentyl, isopentyl or hexyl.

X denotes an R ⁴ , R ⁵ or R ⁶ radical which is simply substituted by R ⁷ .

R ^{4 represents} a linear or branched alkylene radical with 1-10 C atoms, the alkylene radical preferably z. B. methylene, ethylene, propylene, isopropylene, butylene, isobutylene, sec-butylene, pentylene, 1-, 2- or 3-methylbutylene, 1,1-, 1,2- or 2,2-dimethylpropylene, 1- Ethyl propylene, hexylene, 1-, 2-, 3- or 4-methylpentylene, 1,1-, 1,2-, 1,3-, 2,2-, 2,3- or 3,3-dimethylbutylene, 1- or 2-ethylbutylene, 1-ethyl-1-methylprop ylene, 1-ethyl-2-methylpropylene, 1,1,2- or 1,2,2-trimethylpropylene, linear or branched heptylene, octylene, nonylene or decylene. R ^{5 also} means z. B. but-2-en-ylene or hex-3-en-ylene. Ethylene, propylene or butylene is very particularly preferred.

R ⁵ means cycloalkylalkylene with 5-12 C atoms, preferably z. B. cyclopentylmethylene, cyclohexylmethylene, cyclohexylethylene, cyclohe xylpropylene or cyclohexylbutylene.

R ^{5 also} means cycloalkyl, preferably having 5-7 carbon atoms. Cycloal kyl means z. B. cyclopentyl, cyclohexyl or cycloheptyl.

Hal is preferably F, Cl or Br, but also I.

The radicals R ¹ and R ² can be the same or different and are preferably in the 3- or 4-position of the phenyl ring. They mean for example each independently of one another H, alkyl, F, Cl, Br or I or together alkylene, such as. As propylene, butylene or pentylene, furthermore ethyleneoxy, methylenedioxy or ethylenedioxy. They are preferably also each alkoxy, such as. B. for methoxy, ethoxy or propoxy, further for hydroxy.

The radical R ⁷ preferably means z. B. COOH, COOCH ₃ , COOC ₂ H ₅ , CONH ₂ , CON (CH ₃ ) ₂ , CONHCH ₃ or CN.

For the entire invention applies that all residues that occur multiple times kick, may be the same or different, d. H. independently of each other are.

Accordingly, the invention relates in particular to the use of those compounds of the formula I in which at least one of the said radicals has one of the preferred meanings indicated above. Some preferred groups of compounds can be expressed by the following sub-formulas Ia to Id, which correspond to the formula I and in which the radicals not specified have the meaning given for the formula I, but in which
in Ia
X denotes R ⁴ , phenyl or phenylmethyl which are substituted by COOH, COOA, CONH ₂ , CONA ₂ , CONHA or CN;
in Ib
R ¹ and R ² together alkylene with 3-5 C atoms, -O-CH ₂ -CH ₂ -, -O-CH ₂ -O- or -O-CH ₂ -CH ₂ -O,
X denotes R ⁴ , phenyl or phenylmethyl which are substituted by COOH, COOA, CONH ₂ , CONA ₂ , CONHA or CN;
in Ic
R ¹ , R ² each independently of one another H, A, OA or Hal,
R ¹ and R ² together alkylene with 3-5 C atoms, -O-CH ₂ -CH ₂ -,
-O-CH ₂ -O- or -O-CH ₂ -CH ₂ -O,
X is R ⁴ , phenyl or phenylmethyl substituted by COOH, COOA, CONH ₂ , CONA ₂ , CONHA or CN;
in Id
R ¹ , R ² each independently of one another H, A, OA or Hal,
R ¹ and R ² together also alkylene with 3-5 C atoms, -O-CH ₂ -CH ₂ -, -O-CH ₂ -O- or -O-CH ₂ -CH ₂ -O-,
X simply substituted by R ⁷ alkylene with 2-5 C atoms, cyclohexyl, phenyl or phenylmethyl,
R ⁷ COOH or COOA,
A alkyl with 1 to 6 carbon atoms,
Hal F, Cl, Br or I.

The compounds of formula I and also the starting materials for their manufacture position are otherwise produced by methods known per se, as described in literature (e.g. in standard works such as Houben-Weyl, Methods of organic chemistry, Georg-Thieme-Verlag, Stuttgart), be are written, namely under reaction conditions for the ge mentioned implementations are known and suitable. You can also do that use of known variants not mentioned here do.

In the compounds of the formulas II or III, R ¹ , R ² , R ³ , R ⁴ , X and n have the meanings given, in particular the meanings given before.

If L is a reactive esterified OH group, this is preferably alkylsulfonyloxy with 1-6 C atoms (preferably methyl sulfonyloxy) or arylsulfonyloxy with 6-10 C atoms (preferably phenyl- or p-tolylsulfonyloxy, and also 2-naphthalenesulfonyloxy).

The compounds of formula I can preferably be obtained in which one around compounds of formula II with compounds of formula III puts.

If desired, the starting materials can also be formed in situ, so that they are not isolated from the reaction mixture, but immediately further reacted to the compounds of formula I.

On the other hand, it is possible to carry out the reaction in stages.  

The starting compounds of the formula II and III are generally known. If they are not known, they can be made using methods known per se getting produced.

Compounds of formula II can, for. B. be obtained by reaction with POCl ₃ from the corresponding hydroxypyrimidines, which are built up from thio phenderivates and CN-substituted alkylene carboxylic acid esters (Eur. J. Med. Chem. 23, 453 (1988)).

The hydroxypyrimidines are either represented by dehydration tion of corresponding tetrahydrobenzthienopyrimidine compounds or after the cyclization customary for the preparation of pyrimidine derivatives of 2-aminobenzthiophene-3-carboxylic acid derivatives with aldehydes or Nitriles (e.g. Houben Weyl E9b / 2).

In detail, the compounds of the formula II are reacted with the compounds of formula III in the presence or absence of a inert solvent at temperatures between about -20 and about 150 °, preferably between 20 and 100 °.

The addition of an acid-binding agent, for example an alkali or Alkaline earth metal hydroxides, carbonates or bicarbonates or another salt of a weak acid of the alkali or alkaline earth metals preferably of potassium, sodium or calcium, or the addition of a organic base such as triethylamine, dimethylamine, pyridine or quinoline or an excess of the amine component may be beneficial.

Suitable inert solvents are, for. B. hydrocarbons such as hexane, Petroleum ether, benzene, toluene or xylene; chlorinated hydrocarbons such as Trichlorethylene, 1,2-dichloroethane, carbon tetrachloride, chloroform or Dichloromethane; Alcohols such as methanol, ethanol, isopropanol, n-propanol, n-butanol or tert-butanol; Ethers such as diethyl ether, diisopropyl ether, Te trahydrofuran (THF) or dioxane; Glycol ethers such as ethylene glycol mono methyl or monoethyl ether (methyl glycol or ethyl glycol), ethylene glycol dimethyl ether (diglyme); Ketones such as acetone or butanone; Amides such as acetamide, dimethylacetamide, N-methylpyrrolidone or dimethyl form amide (DMF); Nitriles such as acetonitrile; Sulfoxides such as dimethyl sulfoxide (DMSO);  Nitro compounds such as nitromethane or nitrobenzene; Esters such as ethyl acetate or mixtures of the solvents mentioned.

It is also possible in a compound of the formula I to have a radical X in an egg to convert another X, e.g. B. by using an ester or a Cyan group hydrolyzed to a COOH group.

Ester groups can e.g. B. with NaOH or KOH in water, water-THF or saponified water-dioxane at temperatures between 0 and 100 ° the.

Carboxylic acids can e.g. B. with thionyl chloride in the corresponding car acid chlorides and these are converted into carboxamides. By dehydration in a known manner, you get from this car bonitrile.

An acid of formula I can with a base in the associated acid addition salt can be transferred, for example by reaction equi valent amounts of the acid and the base in an inert solvent such as ethanol and subsequent evaporation. For this implementation Men in particular bases, the physiologically acceptable salts deliver.

For example, the acid of formula I can be mixed with a base (e.g. sodium or potassium umhydroxid or carbonate) in the corresponding metal, in particular Alkali metal or alkaline earth metal, or in the corresponding ammonium salt are converted.

Organic bases are particularly suitable for this implementation Question that provide physiologically acceptable salts, such as. B. ethanol amine.

On the other hand, a base of formula I with an acid can be added to the acid addition salt are transferred, for example by conversion equivalent amounts of the base and the acid in an inert Lö solvent such as ethanol and subsequent evaporation. For this order Settling in particular acids that are physiologically unintended delivering saline salts. So you can use inorganic acids the, e.g. B. sulfuric acid, nitric acid, hydrohalic acids such as Hydrochloric acid or hydrobromic acid, phosphoric acids such as  Orthophosphoric acid, sulfamic acid, also organic acids, esp special aliphatic, alicyclic, araliphatic, aromatic or he terocyclic mono- or polybasic carboxylic, sulfonic or sulfuric acids, e.g. B. formic acid, acetic acid, propionic acid, pivalic acid, diethyl acetic acid acid, malonic acid, succinic acid, pimelic acid, fumaric acid, malein acid, lactic acid, tartaric acid, malic acid, citric acid, gluconic acid, Ascorbic acid, nicotinic acid, isonicotinic acid, methane or ethanesulfone acid, ethanedisulfonic acid, 2-hydroxyethanesulfonic acid, benzenesulfone acid, p-toluenesulfonic acid, naphthalene mono- and disulfonic acids, lauryl sulfuric acid. Salts with physiologically unacceptable acids, e.g. B. Picrates, can be used to isolate and / or purify the compounds of formula I can be used.

The invention furthermore relates to pharmaceutical preparations, containing at least one compound of formula I and / or one of them physiologically acceptable salts and / or solvates for treatment of angina, high blood pressure, pulmonary hypertension, congestive heart failure, atherosclerosis, conditions of decreased patency of the Cardiovascular, peripheral vascular diseases, stroke, bronchitis, allergic asthma, chronic asthma, allergic rhinitis, glaucoma com, Irritable Bowel Syndrome, tumors, renal failure, cirrhosis of the liver se and for the treatment of female impotence.

These preparations can be used as medicinal products in human or veteri used in medicine. Organic or inorganic substances in question that are suitable for enteral (e.g. oral), parenteral or topical application and with the new compound not react, e.g. water, vegetable oils, benzylal alcohols, alkylene glycols, polyethylene glycols, glycerol triacetate, gelatin, Carbohydrates such as lactose or starch, magnesium stearate, talc, petroleum jelly. Tablets, pills, coated tablets, Capsules, powder, granules, syrups, juices or drops, for rectal application suppositories, for parenteral application solutions preferably oily or aqueous solutions, further suspensions, emulsions or implants, for topical application of ointments, creams or Powder. The new compounds can also be lyophilized and obtained  NEN lyophilisates e.g. B. used for the preparation of injectables become. The specified preparations can be sterilized and / or Auxiliaries such as lubricants, preservatives, stabilizers and / or Netzmit tel, emulsifiers, salts to influence the osmotic pressure, Buffer substances, color, taste and / or several other active ingredients contain substances, e.g. B. one or more vitamins.

The compounds of formula I and their physiologically acceptable Salts can be used in the fight against diseases in which an Er cGMP (cyclo-guanosine monophosphate) level increased to Ent leads to ignition inhibition or prevention and muscle relaxation, be used. Special uses can the fiction moderate connections in the treatment of angina, high blood pressure, pulmonary hypertension, congestive heart failure, arteriosclerosis, Be conditions of reduced patency of the cardiac vessels, peripheral vas specific diseases, stroke, bronchitis, allergic asthma, chro asthma, allergic rhinitis, glaucoma, irritable bowel syndrome, Tumors, renal failure, cirrhosis and for the treatment of female Impotence.

The substances are usually preferably in doses between about 1 and 500 mg, in particular between 5 and 100 mg per Dosage unit administered. The daily dosage is preferably between about 0.02 and 10 mg / kg body weight. The special dose for however, each patient depends on a variety of factors for example on the effectiveness of the special connection used, on age, body weight, general health, gender, of the food, the time and route of administration, the excretion application rate, drug combination and severity of each Disease to which the therapy applies. Oral application is preferred.

All temperatures above and below are given in ° C. In the following examples, "customary work-up" means: if necessary, water is added, if necessary, depending on the constitution of the end product, to a pH between 2 and 10, extracted with ethyl acetate or dichloromethane, separated, dried the organic phase over sodium sulfate, evaporates and purifies by chromatography on silica gel and / or by crystallization.
Mass spectrometry (MS):
EI (electron impact ionization) M ⁺
FAB (Fast Atom Bombardment) (M + H) ⁺

The invention relates in particular to the use of the Compounds of formula I listed below and their physiologically acceptable salts and / or solvates for their manufacture a drug for the treatment of angina, high blood pressure, pul high pressure, congestive heart failure, arteriosclerosis, bedin reduced cardiac patency, peripheral vascu diseases, stroke, bronchitis, allergic asthma, chronic schematic asthma, allergic rhinitis, glaucoma, irritable bowel syndrome, Tumors, renal failure, cirrhosis and for the treatment of female Impotence.

example 1

Methyl 3- (4-chloro-benzothieno [2,3-d] pyrimidin-2-yl) propionate [obtainable by cyclization of 2-amino-5,6,7,8-tetrahydrobenzothio phen-3-carboxylic acid methyl ester with 3-cyanopropionic acid methyl ester, De hydrogenation with sulfur and subsequent chlorination with phosphorus oxychloride / dimethylamine] and 3-chloro-4-methoxybenzylamine ("A") in N- Methylpyrrolidone are stirred at 110 ° for 5 hours. The solvent is removed and refurbished as usual. 3- [4- (3-Chloro-4- methoxy-benzylamino) benzothieno [2,3-d] pyrimidin-2-yl] propion Acid methyl ester as a colorless oil.

Analogously, by converting "A"
with 2- (4-chloro-benzothieno [2,3-d] pyrimidin-2-yl) acetic acid methyl ester
Methyl 2- [4- (3-chloro-4-methoxy-benzylamino) benzothieno [2,3-d] pyrimidin-2-yl] acetic acid.

An analogous reaction is obtained by reacting 3,4-methylenedioxybenzylamine
with methyl 3- (4-chloro-benzothieno [2,3-d] pyrimidin-2-yl) propionate
Methyl 3- [4- (3,4-methylenedioxybenzylamino) benzothieno [2,3-d] pyrimidin-2-yl] propionate.

Analogously, by converting "A"
with 4- (4-chloro-benzothieno [2,3-d] pyrimidin-2-yl) butyric acid methyl ester
Methyl 4- [4- (3-chloro-4-methoxy-benzylamino) benzothieno [2,3-d] pyrimidin-2-yl] butyrate.

An analogous reaction is obtained by reacting 3,4-methylenedioxybenzylamine
with 4- (4-chloro-benzothieno [2,3-d] pyrimidin-2-yl) butyric acid methyl ester
Methyl 4- [4- (3,4-methylenedioxybenzylamino) benzothieno [2,3-d] pyrimidin-2-yl] butyrate.

Analogously, by converting "A"
with 5- (4-chloro-benzothieno [2,3-d] pyrimidin-2-yl) valeric acid methyl ester
Methyl 5- [4- (3-chloro-4-methoxy-benzylamino) benzothieno [2,3-d] pyrimidin-2-yl] valerate.

An analogous reaction is obtained by reacting 3,4-methylenedioxybenzylamine
with 5- (4-chloro-benzothieno [2,3-d] pyrimidin-2-yl) valeric acid methyl ester
Methyl 5- [4- (3,4-methylenedioxybenzylamino) benzothieno [2,3-d] pyrimidin-2-yl] valerate.

Analogously, by converting "A"
with 7- (4-chloro-benzothieno- [2,3-d] pyrimidin-2-yl) -heptanoic acid methyl ester
7- [4- (3-Chloro-4-methoxybenzylamino) benzothieno [2,3-d] pyrimidin-2-yl] heptanoic acid methyl ester.

An analogous reaction is obtained by reacting 3,4-methylenedioxybenzylamine
with 7- (4-chloro-benzothieno- [2,3-d] pyrimidin-2-yl) -heptanoic acid methyl ester
7- [4- (3,4-Methylenedioxybenzylamino) benzothieno [2,3-d] pyrimidin-2-yl] heptanoic acid methyl ester.

Analogously, by converting "A"
with 2- [4- (4-chloro-benzothieno- [2,3-d] pyrimidin-2-yl) cyclohex-1-yl] methyl acetate
Methyl 2- {4- [4- (3-chloro-4-methoxy-benzylamino) benzothieno [2,3-d] pyrimidin-2-yl] cyclohexyl-1-yl} acetic acid.

An analogous reaction is obtained by reacting 3,4-methylenedioxybenzylamine
with 2- [4- (4-chloro-benzothieno- [2,3-d] pyrimidin-2-yl) cyclohex-1-yl] methyl acetate
Methyl 2- {4- [4- (3,4-methylenedioxybenzylamino) benzothieno [2,3-d] pyrimidin-2-yl] cyclohexyl-1-yl} acetic acid.

One obtains analogously by conversion of benzylamine
with methyl 3- (4-chloro-benzothieno [2,3-d] pyrimidin-2-yl) propionate
Methyl 3- (4-benzylamino-benzothieno [2,3-d] pyrimidin-2-yl) propionate;
with 4- (4-chloro-benzothieno [2,3-d] pyrimidin-2-yl) butyric acid methyl ester
4- (4-benzylamino-benzothieno [2,3-d] pyrimidin-2-yl) butyric acid methyl ester;
with 5- (4-chloro-benzothieno [2,3-d] pyrimidin-2-yl) valeric acid methyl ester
5- (4-Benzylamino-benzothieno [2,3-d] pyrimidin-2-yl) methyl valerate.

Analogously, by converting "A"
with 4- (4-chloro-benzothieno [2,3-d] pyrimidin-2-yl) cyclohexane carboxylic acid methyl ester
Methyl 4- [4- (3-chloro-4-methoxy-benzylamino) benzothieno [2,3-d] pyrimidin-2-yl] cyclohexane
and by reacting 3,4-methylenedioxybenzylamine
Methyl 4- [4- (3,4-methylenedioxybenzylamino) benzothieno [2,3-d] pyrimidin-2-yl] cyclohexane.

Example 2

3- [4- (3-chloro-4-methoxy-benzylamino) benzothieno- [2,3-d] pyrimidin-2-yl] - methyl propionate is dissolved in ethylene glycol monomethyl ether and after adding 32% NaOH, stirred at 110 ° for 5 hours. After To administration of 20% HCl is extracted with dichloromethane. By encore petroleum ether gives 3- [4- (3-chloro-4-methoxy-benzylamino) - benzothieno [2,3-d] pyrimidin-2-yl] propionic acid, mp 218 °.

The precipitated crystals are dissolved in isopropanol and with ethanol amine added. After crystallization, 3- [4- (3-chloro-4-methoxy benzylamino) benzothieno [2,3-d] pyrimidin-2-yl] propionic acid, ethanol min salt.

The connections are obtained analogously
4- [4- (3-chloro-4-methoxy-benzylamino) benzothieno [2,3-d] pyrimidin-2-yl] butyric acid, mp 225 °; Ethanolamine salt F. 150 °;
5- [4- (3-chloro-4-methoxy-benzylamino) benzothieno [2,3-d] pyrimidin-2-yl] valeric acid, mp 210 °; Ethanolamine salt F. 141 °;
4- [4- (3,4-methylenedioxybenzylamino) benzothieno [2,3-d] pyrimidin-2-y1] butyric acid, hydrochloride, mp 245 °.

The following carboxylic acids are obtained analogously from the esters listed in Example 1:
2- [4- (3-chloro-4-methoxy-benzylamino) benzothieno [2,3-d] pyrimidin-2-yl] acetic acid,
3- [4- (3,4-methylenedioxybenzylamino) benzothieno- (2,3-d] pyrimidin-2-yl] propionic acid,
5- [4- (3,4-methylenedioxybenzylamino) benzothieno [2,3-d] pyrimidin-2-yl] valeric acid,
7- [4- (3-chloro-4-methoxy-benzylamino) benzothieno [2,3-d] pyrimidin-2-yl] heptanoic acid,
7- [4- (3,4-methylenedioxybenzylamino) benzothieno [2,3-d] pyrimidin-2-yl] heptanoic acid,
2- {4- [4- (3-chloro-4-methoxy-benzylamino) benzothieno [2,3-d] pyrimidin-2-yl] cyclohexyl-1-yl} acetic acid,
2- {4- [4- (3,4-methylenedioxybenzylamino) benzothieno [2,3-d] pyrimidin-2-yl] cyclohexyl-1-yl) acetic acid,
3- (4-benzylamino-benzothieno- [2,3-d] pyrimidin-2-yl) propionic acid,
4- (4-benzylamino-benzothieno [2,3-d] pyrimidin-2-yl) butyric acid,
5- (4-benzylamino-benzothieno- [2,3-d] pyrimidin-2-yl) valeric acid,
4- [4- (3-chloro-4-methoxy-benzylamino) benzothieno [2,3-d] pyrimidin-2-yl] cyclohexane carboxylic acid, ethanolamine salt, mp 167 °;
4- [4- (3,4-methylenedioxybenzylamino) benzothieno [2,3-d] pyrimidin-2-yl] cyclohexane carboxylic acid, ethanolamine salt, mp 143 °.

Example 3

A mixture of 1.5 g of 4- (4-chlorobenzothieno- [2,3-d] pyrimidin-2-yl) - phenylcarboxylic acid methyl ester ("B"), prepared by dehydrogenation of the corresponding 5,6,7,8-tetrahydrobenzthieno [2,3-d] pyrimidine compound with sulfur and subsequent chlorination with phosphorus oxychloride / Di methylamine, and 1.5 g of 3-chloro-4-methoxy-benzylamine in 20 ml of N-methyl pyrrolidone is heated to 110 ° for 4 hours. After cooling it will be like worked up as usual. 2.6 g of 4- [4- (3-chloro-4-methoxy-benzyl) are obtained amino) - [1] benzothieno- (2,3-d] pyrimidin-2-yl) benzoic acid methyl ester, F. 203-204 °.

Analogously to Example 2, 1.0 g is obtained from 1.2 g of the ester
4- [4- (3-chloro-4-methoxy-benzylamino) - [1] benzothieno [2,3-d] pyrimidin-2-yl] benzoic acid, ethanolamine salt, mp 189-190 °.

Analogously to Example 1, "B" and 3,4-methylenedioxybenzylamine are obtained
Methyl 4- [4- (3,4-methylenedioxy-benzylamino) - [1] benzothieno [2,3-d] pyrimidin-2-yl] -benzoate and therefrom by ester hydrolysis
4- [4- (3,4-Methylenedioxy-benzylamino) - [1] benzothieno [2,3-d] pyrimidin-2-yl] benzoic acid, sodium salt, mp <260 °.

The connection is obtained analogously
4- [4- (3-chloro-4-methoxy-benzylamino) - [1] benzothieno [2,3-d] pyrimidin-2-yl] phenylacetic acid, ethanolamine salt, mp 130 °; and
4- [4- (3,4-methylenedioxybenzylamino) - [1] benzothieno [2,3-d] pyrimidin-2-yl) phenylacetic acid, ethanolamine salt, mp 202 °.

Example 4

1 equivalent of 3- [4- (3-chloro-4-methoxy-benzylamino) benzothieno- [2,3-d] - pyrimidin-2-yl] propionic acid and 1.2 equivalents of thionyl chloride become 2 Stirred for hours in dichloromethane. The solvent is removed and 3- [4- (3-chloro-4-methoxy-benzylamino) -benzothieno- [2,3-d] - pyrimidin-2-yl] propionic acid chloride.  

It is transferred into aqueous ammonia, stirred for one hour and obtained usual work-up 3- [4- (3-chloro-4-methoxy-benzylamino) -benzothieno- [2,3-d] pyrimidin-2-yl] propionic acid amide.

Example 5

1 equivalent of DMF and 1 equivalent of oxalyl chloride are in Aceto at 0 ° nitrile dissolved. Thereafter, 1 equivalent of 3- [4- (3-chloro-4-methoxy benzylamino) -benzothieno- [2,3-d] pyrimidin-2-yl] propionic acid amide give. It is stirred for an hour. After the usual workup he if one keeps 3- [4- (3-chloro-4-methoxy-benzylamino) -benzothieno- [2,3-d] - pyrimidin-2-yl] propionitrile.

Example 6

Analogously to Examples 1, 2 and 3, the following carboxylic acids are obtained by reacting the corresponding chloropyrimidine derivatives with 3,4-ethylenedioxybenzylamine:
4- [4- (3,4-ethylenedioxybenzylamino) benzothieno [2,3-d] pyrimidin-2-yl] butyric acid,
3- [4- (3,4-ethylenedioxybenzylamino) benzothieno [2,3-d] pyrimidin-2-yl] propionic acid,
5- [4- (3,4-ethylenedioxybenzylamino) benzothieno [2,3-d] pyrimidin-2-yl] valeric acid,
7- [4- (3,4-ethylenedioxybenzylamino) benzothieno [2,3-d] pyrimidin-2-yl] heptanoic acid,
2- {4- [4- (3,4-ethylenedioxybenzylamino) benzothieno [2,3-d] pyrimidin-2-yl] cyclohexyl-1-yl} acetic acid,
4- [4- (3,4-ethylenedioxybenzylamino) benzothieno [2,3-d] pyrimidin-2-yl] cyclohexane carboxylic acid,
4- [4- (3,4-ethylenedioxybenzylamino) - [1] benzothieno- [2,3-d] pyrimidin-2-yl] benzoic acid, dec. 220-230 °;
4- [4- (3,4-ethylenedioxybenzylamino) - [1] benzothieno [2,3-d] pyrimidin-2-yl] benzoic acid, ethanolamine salt, mp 252 °;
4- [4- (3,4-ethylenedioxy-benzylamino) - [1] benzothieno- [2,3-d] pyrimidin-2-yl] phenylacetic acid.

The following compounds are obtained analogously by reaction with 3,4-dichlorobenzylamine:
4- [4- (3,4-dichlorobenzylamino) benzothieno [2,3-d] pyrimidin-2-yl] butyric acid,
3- [4- (3,4-dichlorobenzylamino) benzothieno [2,3-d] pyrimidin-2-yl] propionic acid,
5- [4- (3,4-dichlorobenzylamino) benzothieno [2,3-d] pyrimidin-2-yl] valeric acid, ethanolamine salt, mp 160 °;
7- [4- (3,4-dichlorobenzylamino) benzothieno [2,3-d] pyrimidin-2-yl] heptanoic acid,
2- {4- [4- (3,4-dichlorobenzylamino) benzothieno [2,3-d] pyrimidin-2-yl] cyclohexyl-1-yl} acetic acid,
4- [4- (3,4-dichlorobenzylamino) benzothieno [2,3-d] pyrimidin-2-yl] cyclohexane carboxylic acid,
4- (4- (3,4-dichlorobenzylamino) - [1] benzothieno- [2,3-d] pyrimidin-2-yl] benzoic acid,
4- [4- (3,4-dichlorobenzylamino) - [1] benzothieno- [2,3-d] pyrimidin-2-yl] phenylacetic acid.

The following compounds are obtained analogously by reaction with 3-chloro-4-ethoxybenzylamine:
4- [4- (3-chloro-4-ethoxybenzylamino) benzothieno [2,3-d] pyrimidin-2-yl] butyric acid,
3- (4- (3-chloro-4-ethoxybenzylamino) benzothieno [2,3-d] pyrimidin-2-yl] propionic acid,
5- [4- (3-chloro-4-ethoxybenzylamino) benzothieno [2,3-d] pyrimidin-2-yl] valeric acid,
7- [4- (3-chloro-4-ethoxybenzylamino) benzothieno [2,3-d] pyrimidin-2-yl] heptanoic acid,
2- {4- [4- (3-chloro-4-ethoxybenzylamino) benzothieno [2,3-d] pyrimidin-2-yl] cyclohexyl-1-yl} acetic acid,
4- [4- (3-chloro-4-ethoxybenzylamino) benzothieno [2,3-d] pyrimidin-2-yl] cyclohexane carboxylic acid,
4- [4- (3-chloro-4-ethoxybenzylamino) - [1] benzothieno- [2,3-d] pyrimidin-2-yl] benzoic acid, mp 185-187 °;
4- [4- (3-chloro-4-ethoxybenzylamino) - [1] benzothieno [2,3-d] pyrimidin-2-yl] phenylacetic acid.

The following compounds are obtained analogously by reaction with 3-chloro-4-isopropoxybenzylamine:
4- [4- (3-chloro-4-isopropoxybenzylamino) benzothieno [2,3-d] pyrimidin-2-yl] butyric acid,
3- [4- (3-chloro-4-isopropoxybenzylamino) benzothieno [2,3-d] pyrimidin-2-yl] propionic acid,
5- [4- (3-chloro-4-isopropoxybenzylamino) benzothieno [2,3-d] pyrimidin-2-yl] valeric acid, ethanolamine salt, mp 130 °;
7- [4- (3-chloro-4-isopropoxybenzylamino) benzothieno [2,3-d] pyrimidin-2-yl] heptanoic acid,
2- {4- [4- (3-chloro-4-isopropoxybenzylamino) benzothieno [2,3-d] pyrimidin-2-yl] cyclohexyl-1-yl} acetic acid,
4- [4- (3-chloro-4-isopropoxybenzylamino) benzothieno [2,3-d] pyrimidin-2-yl] cyclohexane carboxylic acid,
4- [4- (3-chloro-4-isopropoxybenzylamino) - [1] benzothieno [2,3-d] pyrimidin-2-yl] benzoic acid, mp 240-241 °;
4- [4- (3-chloro-4-isopropoxybenzylamino) - [1] benzothieno [2,3-d] pyrimidin-2-yl] phenylacetic acid.

The following examples relate to pharmaceutical preparations:

Example A Injection glasses

A solution of 100 g of an active ingredient of the formula I and 5 g of disodium Hydrogen phosphate is dissolved in 3 liters of double distilled water with 2N salt acid adjusted to pH 6.5, sterile filtered, filled into injection glasses, lyophilized under sterile conditions and sealed sterile. Every In jection glass contains 5 mg of active ingredient.

Example B Suppositories

A mixture of 20 g of an active ingredient of the formula I is melted with 100 g soy lecithin and 1400 g cocoa butter, pour into molds and leave cold. Each suppository contains 20 mg of active ingredient.

Example C solution

A solution is prepared from 1 g of an active ingredient of the formula I, 9.38 g of NaH ₂ PO ₄ .2 H ₂ O, 28.48 g of Na ₂ HPO ₄ .12 H ₂ O and 0.1 g of benzalkonium chloride in 940 ml double distilled water. It is adjusted to pH 6.8, made up to 1 l and sterilized by irradiation. This solution can be used in the form of eye drops.

Example D ointment

500 mg of an active ingredient of the formula I are mixed with 99.5 g of petroleum jelly under aseptic conditions.

Example E Tablets

A mixture of 1 kg of active ingredient of formula I, 4 kg lactose, 1.2 kg kar Potato starch, 0.2 kg talc and 0.1 kg magnesium stearate are common Formed into tablets in such a way that each tablet contains 10 mg of active ingredient contains.  

Example F Dragees

Analogously to Example E, tablets are pressed, which are then made in the usual manner Wise with a coating of sucrose, potato starch, talc, tragacanth and dye are coated.

Example 6 Capsules

2 kg of active ingredient of formula I are in the usual way in hard gelatin capsules filled so that each capsule contains 20 mg of the active ingredient.

Example H Ampoules

A solution of 1 kg of active ingredient of formula I in 60 l of double distilled Water is sterile filtered, filled into ampoules, under sterile conditions lyophilized and sealed sterile. Each ampoule contains 10 mg of active ingredient material.

example 1 Inhalation spray

14 g of active ingredient of the formula I are dissolved in 10 l of isotonic NaCl solution and fills the solution into commercially available spray vessels with a pump mechanism. The solution can be sprayed into the mouth or nose. A spray (about 0.1 ml) corresponds to a dose of approximately 0.14 mg.

Claims (2)

1. Use of compounds of formula I.
wherein
R ¹ , R ² each independently of one another H, A, OA, OH or Hal,
R ¹ and R ² together also alkylene with 3-5 C atoms, -O-CH ₂ -CH ₂ -, -CH ₂ -O-CH ₂ -, -O-CH ₂ -O- or -O-CH ₂ -CH ₂ -O-,
X is simply substituted by R ^7, R ⁴ , R ⁵ or R ⁶ ,
R ⁴ linear or branched alkylene with 1-10 C atoms, in which one or two CH ₂ groups can be replaced by -CH = CH groups,
R ⁵ cycloalkyl or cycloalkylalkylene with 5-12 C atoms,
R ⁶ phenyl or phenylmethyl,
R ⁷ COOH, COOA, CONH ₂ , CONHA, CON (A) ₂ or CN,
A alkyl with 1 to 6 carbon atoms and
Hal F, Cl, Br or I
mean,
as well as their physiologically acceptable salts and / or solvates for the manufacture of a medicament for the treatment of angina, high blood pressure, pulmonary high pressure, congestive heart failure, arteriosclerosis, conditions of reduced patency of the cardiovascular system, peripheral vascular diseases, stroke, bronchitis, allergic asthma, chronic asthma, allergic rhinitis, glaucoma, irritable bowel syndrome, tumors, renal failure, cirrhosis of the liver and for the treatment of female impotence. 2. Use of compounds of formula I according to claim 1

• a) 3- [4- (3-chloro-4-methoxy-benzylamino) benzo [4,5] thieno [2,3-d] pyrimidin-2-yl] propionic acid;
• b) 4- [4- (3,4-methylenedioxybenzylamino) benzo [4,5] thieno [2,3-d] pyrimidin-2-yl] butyric acid;
• c) 7- [4- (3,4-methylenedioxybenzylamino) benzo [4,5] thieno [2,3-d] pyrimidin-2-yl] heptanoic acid;
• d) 7- [4- (3-chloro-4-methoxybenzylamino) benzo [4,5] thieno [2,3-d] pyrimidin-2-yl] heptanoic acid;
• e) 5- [4- (3-chloro-4-methoxybenzylamino) benzo [4,5] thieno [2,3-d] pyrimidin-2-yl] valeric acid;
• f) 2- {4- [4- (3-Chloro-4-methoxybenzylamino) benzo [4,5] thieno [2,3-d] pyrimidin-2-yl] cyclohexyl-1-yl }-acetic acid;
• g) 4- [4- (3,4-methylenedioxybenzylamino) benzo [4,5] thieno [2,3-d] pyrimidin-2-yl] cyclohexane carboxylic acid;
• h) 4- [4- (3,4-methylenedioxybenzylamino) benzo [4,5] thieno [2,3-d] pyrimidin-2-yl] benzoic acid;
• i) 4- [4- (3,4-methylenedioxybenzylamino) benzo [4,5] thieno [2,3-d] pyrimidin-2-yl] phenylacetic acid;
• j) 2- {4- [4- (3-Chloro-4-methoxy-benzylamino) -benzo [4,5] thieno [2,3-d] pyrimidin-2-yl] cyclohexyl-1-yl } -cyclohexane carboxylic acid;

as well as their physiologically acceptable salts and / or solvates for the manufacture of a medicament for the treatment of angina, high blood pressure, pulmonary high pressure, congestive heart failure, arteriosclerosis, conditions of reduced patency of the heart vessels, peripheral vascular diseases, stroke, bronchitis, allergic asthma, chronic asthma, allergic rhinitis, glaucoma, irritable bowel syndrome, tumors, renal failure, cirrhosis of the liver and for the treatment of female impotence.