CA1041908A - Amidinoureas - Google Patents
AmidinoureasInfo
- Publication number
- CA1041908A CA1041908A CA181,015A CA181015A CA1041908A CA 1041908 A CA1041908 A CA 1041908A CA 181015 A CA181015 A CA 181015A CA 1041908 A CA1041908 A CA 1041908A
- Authority
- CA
- Canada
- Prior art keywords
- urea
- composition
- amidino
- butyl
- dichlorophenylamidino
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/275—Nitriles; Isonitriles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/17—Amides, e.g. hydroxamic acids having the group >N—C(O)—N< or >N—C(S)—N<, e.g. urea, thiourea, carmustine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
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- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
A B S T R A C T
The invention relates to a novel composition com-prising a compound of the formula:
(I) wherein:
R2, R3, R4, R5 and R6 may be the same or different and are hydrogen (provided at least one of R2, R3, R4, R5 and R6 is other than hydrogen), halo, trifluoromethyl, nitro, loweralkoxy or loweralkyl;
and acid addition salts thereof in admixture with a pharmaceutically acceptable excipient.
The novel composition is useful as an anti-hypertensive agent and exert activities on the cardiovascular system.
The invention relates to a novel composition com-prising a compound of the formula:
(I) wherein:
R2, R3, R4, R5 and R6 may be the same or different and are hydrogen (provided at least one of R2, R3, R4, R5 and R6 is other than hydrogen), halo, trifluoromethyl, nitro, loweralkoxy or loweralkyl;
and acid addition salts thereof in admixture with a pharmaceutically acceptable excipient.
The novel composition is useful as an anti-hypertensive agent and exert activities on the cardiovascular system.
Description
10~ 0~, SUMMARY OF THE INVENTION
This invention describes a novel composition incorpo-rating substituted phenylamidinourea compounds. This invention further provides valuable pharmaceutical preparations which contain substituted phenylamidinourea compounds which possess an effective degree of antihypertensive properties and exert activities on the cardiovascular system. A method for the treatment of hypertensive disorders by the administration of a substituted phenylamidinourea compound is also described.
BACKGROUND OF THE INVENTION
The pharmaceutical compositions which have been used as antihypertensive agents have included such as the thiazides, reserpine, hydralazine, ~-methyl dopa, guanethidine and the like. These compounds, however, while being effective produce undesirable side effects such as electrolyte inbalance, ortho-static hypertension, and gastric secretory and spasmolytic properties.
I have unexpectedly found that amidinourea compounds exhibit valuable pharmacologic properties.
I have unexpectedly found that the amidinoureas of this invention are useful antihypertensive agents.
: I have further found that the amidinoureas compounds of this invention are novel and can easily be prepared.
I have also found that the compounds of this invention have a minimum of the side effects which accompany antihypertensive agents.
I have still further found a simple and effective ; method for the treatment of cardiovascular disorders such as hypertensive disorders.
~' .
-~4~0~
DESCRIPTION AND PREFERRED EMBODIMENT
This invention describes a class of novel composition which contains a substituted phenyl radical which is further attached to an amidinourea chain. This results in urea type compounds having a substituted phenylamidino group attached at one of the nitrogen atoms. This invention also describes the non-toxic pharmaceutically acceptable salts and the method of preparing these substituted phenylamidinourea compounds.
The invention compounds which are useful for the treatment of cardiovascular disorders and which are amidinourea compounds of formula I:
R 4~ N H - C - N H - e N H z where:
R2, R3, R4, R5 and R6 may be the same or different and are hydrogen (provided at least one of R2, R3, R4, R5 and R6 is other than hydrogen), halo, trifluoromethyl, nitro, loweralkoxy or loweralkyl; and the non-toxic acid addition salts thereof.
The preferred compounds which are useful in the treatment of cardiovascular disorders are exemplified by those compounds of formula II:
.. . ~ .
.. .
o~
xl r ~N H - C N H - C - NH 2 I I
where:
X', Y' and Z' may be the same or different and are hydrogen (provided at least one of X', Y' and Z' is other than hydrogen), halo, haloloweralkyl, nitro, cyano, loweralkylsulfonyl, loweralkoxy or loweralkyl. :
The more preferred compounds which are useful in the treatment of cardiovascular disorders are shown in formula II
~ where: ~ .
X', Y' and Z' are hydrogen (provided at least one of X', Y' and Z' is other than hydrogen), halo, haloloweralkyl or loweralkyl.
The most preferred compounds are described by formula II
where:
X' is hydrogen, chloro, bromo or :
- fluoro;
. .
. ; . .
~(~4~Q~
Y' is hydrogen, chloro, - methyl or trifluoromethyl Z' is chloro, bromo, fluoro, methyl or trifluoromethyl.
It is well known in the pharmacological arts that non-toxic acid addition salts of pharmacologically active amine compounds do not differ in activities from their free base.
; The salts merely provide a convenient solubility factor.
The amines of this invention may be readily converted to their non-toxic acid addition salts by customary methods in the art. The non-toxic salts of this invention are those salts the acid component of which is pharmacologically acceptable in the intended dosages; such salts would include those prepared from inorganic acids, organic acids, higher fatty acids, high molecular weight acids, etc., and include such as:
hydrochloric acid, succinic acid, hydrobromic acid, glycolic acid, sulfuric acid, lactic acid, nitric acid, salicylic acid, phosphoric acid, benzoic acid, methane sulfonic acid, nicotinic acid, benzene sulfonic acid, phthalic acid, acetic acid, stearic acid, propionic acid, oleic acid, malic acid, abietic acid, etc.
~U~l~O~
Representative compounds of this invention which are particularly useful are as follows:
o-chlorophenylamidinourea m-chlorophenylamidinourea p-chlorophenylamidinourea (2,3-dichlorophenylamidino)urea (2,4-dichlorophenylamidino)urea (2,5-dichlorophenylamidino)urea (3,4-dichlorophenylamidino)urea 10 (3,5-dichlorophenylamidino)urea p-bromophenylamidinourea (2-chloro-4-bromophenylamidino)urea p-fluorophenylamidinourea (2,4-difluorophenylamidino)urea (2,6-difluorophenylamidino)urea p-trifluoromethylphenylamidinourea (2-methyl-4-chlorophenylamidino)urea (2-methyl-4-bromophenylamidino)urea (2,6-dimethylphenylamidino)urea 20 (2-trifluoromethyl-4-methylphenylamidino)urea `
(4-iodo-2-methylphenylamidino)urea nitrate (2-trifluoromethyl-4-fluorophenylamidino)urea nitrate (2-ethyl-6-methylphenylamidino)urea nitrate (4-methoxy-2-methylphenylamidino)urea (4-chloro-2-methoxyphenylamidino)urea (2-methoxy-6-methylphenylamidino)urea (2,5-difluorophenylamidino)urea (3-chloro-4-fluorophenylamidino)urea (pentafluorophenylamidino)urea (2-chloro-6-fluorophenylamidino)urea (2,4,6-trimethylphenylamidino)urea ~. .
. ~ :-~ .
. . .
~o~i~o~
The compounds useful in the invention may be prepared by the following general synthesis:
Condensation of cyanamide and a substituted aniline results in the corresponding substituted phenylguanidine.
The reaction is preferably carried out on the aniline salt either in a polar medium or neat and using increased temperatures. The salt used may be any acid addition amine salt but preferably the salt of a mineral acid. The polar medium may be aqueous, partially aqueous or a non-aqueous solution. It is convenient to choose a solvent that will reflux at the desired reaction temperature. The more preferred solvents are water or alcohol but other solvents may be used such as DMS0, diethyleneglycol, ethyleneglycol, tetrahydro-furan, dimethylformamide, etc. The most preferred solvent is a mildly acidic solvent which is non-nucleophilic such as phenol, cresol, xylenol, etc. The reaction should also be carried out - at a temperature which is high enough so that condensation takes place readily, but not sufficient to decompose the guanidine formed. The reaction temperature can vary from room temperature to about 250C. although it is preferable to run the reaction at temperatures from about 50C. to 150C. The guanidine salt which is formed can be converted to the free base with a metal hydroxide or alkoxide solution. The iso-lation of the desired guanidine can be carried out by any method known in the art.
When the substituted phenylguanidine is reacted with t-butylisocyanate then the product formed is a l-substituted phenylamidino-3-t-butylurea. This reaction is preferably carried out in a non-polar medium using solvents such as benzene, toluene, xylene, etc. The reaction is also carried out as above at raised temperatures.
~`,i .
~(~4~90~
Treatment of the l-substituted phenylamidino-3-t-butylurea with acid results in the desired l-substituted phenylamidinourea. This reaction is carried out preferably as a 10% solution in a 1:1 mixture of conc. hydrochloric acid and glacial acetic acid at increased temperature. The resultant product is isolated as a salt by any method known in the art.
The followin~ reaction equations illustrate this synthesis:
~ R2 N
R4 ~ O ~ NH2 HX + C-NH2 1~
j~R2 R4 ~ O ~ NH-C-NH2 HX' ~ t-but NCO
\ / .' R4 ~ NH-C-NH-C-:H-I-CH3 H+ CH3 ~ 2 R4~NH-c-NH-c-NH2 ~04~
where:
! HX' is a mineral acid.
Appropriately desired end products having various X', Y'and Z'substituents may be prepared at various steps of synthesis using suitable reactions in order to convert one - group to another.
The starting anilines are either known, may be pre-pared by known techniques or reference to the preparation is shown. Thus, chlorination or bromination of an acetanilide or aniline may be carried out in acetic acid, or in the presence of a small amount of iodine dissolved in an inert solvent such as carbon tetrachloride. A solution of chlorine or bromine is then added while the temperature is held near 0C. Iodination may also be carried out by known methods using iodine mono-- chloride (ClI).
Alkylation may be carried out on an acetanilide using an alkyl halide and aluminum chloride under Friedel-Crafts conditions to obtain desired alkyl substitution.
Nitration may be carried out using fuming nitric acid at about 0C.
A nitro compound may be hydrogenated to the corre-sponding amine which may then be diazotized and heated in an alcohol medium to form the alkoxy compound.
An amino compound may also be diazotized to the diazonium fluoroborate which is then thermally decomposed to the fluoro compound. Diazotization followed by a Sandmeyer type reaction may yield the bromo, chloro or iodo compound.
Diazotization of an amino compound followed by addition of cuprous cyanide may result in the desired cyano compound.
When an amino compound is diazotized followed by . .
~o'~
reaction with potassium ethylxanthate and then hydrolyzed, the mercapto compound results. This in turn may be alkylated to the alkylthio group which is then oxidized to the corresponding alkylsulfonyl substituent.
A halo compound in which halo is chloro or bromo or iodo may be reacted with cuprous cyanide in guanidine at about 150C. to produce a cyano compound.
A chloro, bromo or iodo compound may also be reacted with trifluoromethyliodide and copper powder at about 150C. in dimethylformamide to obtain a trifluoromethyl compound ~etrahedron Letters:47, 4095 (1959 ~.
A halo compound may also be reacted with cuprous methanesulfinate in quinoline at about 150C. to obtain a methylsulfonyl compound.
Of course the above reactions may also be carried out on acetophenone in order to direct substitution. Formation of an oxime followed by Beckmann Rearrangement results in the acetamide which is then deacylated to the aniline.
Reactions may also be carried out on the substituted anilines which would result in di- and tri- substituted anilines.
Reactions may also be carried out at other stages of synthesis depending on the substituents present and the substi-tuents desired and various combinations of the foregoing reactions will be determined by one skilled in the art in order that the desired product results. Thus, a phenylguanidine may be halogenated or nitrated as above, etc.
The compounds of this invention exert activity on the cardiovascular system. They possess blood-pressure lowering effects and are useful as antihypertensive agents.
For these purposes, the amidinoureas of this g : ' . ~ . - . ' ' ' iO4~0~
invention can be normally administered orally or parenterally.
Orally they may be administered as tablets, aqueous or oily suspensions, dispersible powders or granules, emulsions, hard or soft capsules, or syrups or elixirs.
Compositions intended for oral use may be prepared according to any method known in the art for the manufacture of pharmaceutical compositions and such compositions may contain one or more agents selected from the group consisting of sweetening agents, flavoring agents, coloring agents, pre-serving agents and the like, in order to provide a pharmaceuti-cally elegant and palatable preparation.
The dosage regimen in carrying out the methods of this invention is that which insures maximum therapeutic response until improvement is obtained and thereafter the minimum effective level which gives relief. Thus, in general, the dosages are those that are therapeutically effective in the alleviation of hypertensive disorders. In general, the daily dose can be between about 0.05 mg/kg/day and 70 mg/kgtday (preferably in the range of 1-25 mg/kg/day), bearing in mind, of course, that in selecting the appropriate dosage in any specific case, consideration must be given to the patient's weight, general health, age, and other factors which may influence response to the drug.
Various tests in animals have been carried out to show the ability of the compounds of this invention to exhibit reactions that can be correlated with activity in humans.
One such test is the ability of the compound to lower blood pressure in the spontaneous hypertensive rat (Ryo Tabei, et al., Clin. Pharm. & Therap. 11: 269-274, 1970).
Blood pressure measurements are recorded by both the tail cuff method and by direct cannulation of a common carotid artery.
.
104~L90~
Compounds that are effective antihypertensives in man have been shown to be active in lowering blood pressure in this animal model. In view of the results of this test, the amidinoureas of this invention can be considered to be active antihyper-tensive agents.
The following are detailed examples which show the preparation of the compounds of this invention. They are to be ; construed as illustrations of said compounds and not as limi-tations thereof.
This invention describes a novel composition incorpo-rating substituted phenylamidinourea compounds. This invention further provides valuable pharmaceutical preparations which contain substituted phenylamidinourea compounds which possess an effective degree of antihypertensive properties and exert activities on the cardiovascular system. A method for the treatment of hypertensive disorders by the administration of a substituted phenylamidinourea compound is also described.
BACKGROUND OF THE INVENTION
The pharmaceutical compositions which have been used as antihypertensive agents have included such as the thiazides, reserpine, hydralazine, ~-methyl dopa, guanethidine and the like. These compounds, however, while being effective produce undesirable side effects such as electrolyte inbalance, ortho-static hypertension, and gastric secretory and spasmolytic properties.
I have unexpectedly found that amidinourea compounds exhibit valuable pharmacologic properties.
I have unexpectedly found that the amidinoureas of this invention are useful antihypertensive agents.
: I have further found that the amidinoureas compounds of this invention are novel and can easily be prepared.
I have also found that the compounds of this invention have a minimum of the side effects which accompany antihypertensive agents.
I have still further found a simple and effective ; method for the treatment of cardiovascular disorders such as hypertensive disorders.
~' .
-~4~0~
DESCRIPTION AND PREFERRED EMBODIMENT
This invention describes a class of novel composition which contains a substituted phenyl radical which is further attached to an amidinourea chain. This results in urea type compounds having a substituted phenylamidino group attached at one of the nitrogen atoms. This invention also describes the non-toxic pharmaceutically acceptable salts and the method of preparing these substituted phenylamidinourea compounds.
The invention compounds which are useful for the treatment of cardiovascular disorders and which are amidinourea compounds of formula I:
R 4~ N H - C - N H - e N H z where:
R2, R3, R4, R5 and R6 may be the same or different and are hydrogen (provided at least one of R2, R3, R4, R5 and R6 is other than hydrogen), halo, trifluoromethyl, nitro, loweralkoxy or loweralkyl; and the non-toxic acid addition salts thereof.
The preferred compounds which are useful in the treatment of cardiovascular disorders are exemplified by those compounds of formula II:
.. . ~ .
.. .
o~
xl r ~N H - C N H - C - NH 2 I I
where:
X', Y' and Z' may be the same or different and are hydrogen (provided at least one of X', Y' and Z' is other than hydrogen), halo, haloloweralkyl, nitro, cyano, loweralkylsulfonyl, loweralkoxy or loweralkyl. :
The more preferred compounds which are useful in the treatment of cardiovascular disorders are shown in formula II
~ where: ~ .
X', Y' and Z' are hydrogen (provided at least one of X', Y' and Z' is other than hydrogen), halo, haloloweralkyl or loweralkyl.
The most preferred compounds are described by formula II
where:
X' is hydrogen, chloro, bromo or :
- fluoro;
. .
. ; . .
~(~4~Q~
Y' is hydrogen, chloro, - methyl or trifluoromethyl Z' is chloro, bromo, fluoro, methyl or trifluoromethyl.
It is well known in the pharmacological arts that non-toxic acid addition salts of pharmacologically active amine compounds do not differ in activities from their free base.
; The salts merely provide a convenient solubility factor.
The amines of this invention may be readily converted to their non-toxic acid addition salts by customary methods in the art. The non-toxic salts of this invention are those salts the acid component of which is pharmacologically acceptable in the intended dosages; such salts would include those prepared from inorganic acids, organic acids, higher fatty acids, high molecular weight acids, etc., and include such as:
hydrochloric acid, succinic acid, hydrobromic acid, glycolic acid, sulfuric acid, lactic acid, nitric acid, salicylic acid, phosphoric acid, benzoic acid, methane sulfonic acid, nicotinic acid, benzene sulfonic acid, phthalic acid, acetic acid, stearic acid, propionic acid, oleic acid, malic acid, abietic acid, etc.
~U~l~O~
Representative compounds of this invention which are particularly useful are as follows:
o-chlorophenylamidinourea m-chlorophenylamidinourea p-chlorophenylamidinourea (2,3-dichlorophenylamidino)urea (2,4-dichlorophenylamidino)urea (2,5-dichlorophenylamidino)urea (3,4-dichlorophenylamidino)urea 10 (3,5-dichlorophenylamidino)urea p-bromophenylamidinourea (2-chloro-4-bromophenylamidino)urea p-fluorophenylamidinourea (2,4-difluorophenylamidino)urea (2,6-difluorophenylamidino)urea p-trifluoromethylphenylamidinourea (2-methyl-4-chlorophenylamidino)urea (2-methyl-4-bromophenylamidino)urea (2,6-dimethylphenylamidino)urea 20 (2-trifluoromethyl-4-methylphenylamidino)urea `
(4-iodo-2-methylphenylamidino)urea nitrate (2-trifluoromethyl-4-fluorophenylamidino)urea nitrate (2-ethyl-6-methylphenylamidino)urea nitrate (4-methoxy-2-methylphenylamidino)urea (4-chloro-2-methoxyphenylamidino)urea (2-methoxy-6-methylphenylamidino)urea (2,5-difluorophenylamidino)urea (3-chloro-4-fluorophenylamidino)urea (pentafluorophenylamidino)urea (2-chloro-6-fluorophenylamidino)urea (2,4,6-trimethylphenylamidino)urea ~. .
. ~ :-~ .
. . .
~o~i~o~
The compounds useful in the invention may be prepared by the following general synthesis:
Condensation of cyanamide and a substituted aniline results in the corresponding substituted phenylguanidine.
The reaction is preferably carried out on the aniline salt either in a polar medium or neat and using increased temperatures. The salt used may be any acid addition amine salt but preferably the salt of a mineral acid. The polar medium may be aqueous, partially aqueous or a non-aqueous solution. It is convenient to choose a solvent that will reflux at the desired reaction temperature. The more preferred solvents are water or alcohol but other solvents may be used such as DMS0, diethyleneglycol, ethyleneglycol, tetrahydro-furan, dimethylformamide, etc. The most preferred solvent is a mildly acidic solvent which is non-nucleophilic such as phenol, cresol, xylenol, etc. The reaction should also be carried out - at a temperature which is high enough so that condensation takes place readily, but not sufficient to decompose the guanidine formed. The reaction temperature can vary from room temperature to about 250C. although it is preferable to run the reaction at temperatures from about 50C. to 150C. The guanidine salt which is formed can be converted to the free base with a metal hydroxide or alkoxide solution. The iso-lation of the desired guanidine can be carried out by any method known in the art.
When the substituted phenylguanidine is reacted with t-butylisocyanate then the product formed is a l-substituted phenylamidino-3-t-butylurea. This reaction is preferably carried out in a non-polar medium using solvents such as benzene, toluene, xylene, etc. The reaction is also carried out as above at raised temperatures.
~`,i .
~(~4~90~
Treatment of the l-substituted phenylamidino-3-t-butylurea with acid results in the desired l-substituted phenylamidinourea. This reaction is carried out preferably as a 10% solution in a 1:1 mixture of conc. hydrochloric acid and glacial acetic acid at increased temperature. The resultant product is isolated as a salt by any method known in the art.
The followin~ reaction equations illustrate this synthesis:
~ R2 N
R4 ~ O ~ NH2 HX + C-NH2 1~
j~R2 R4 ~ O ~ NH-C-NH2 HX' ~ t-but NCO
\ / .' R4 ~ NH-C-NH-C-:H-I-CH3 H+ CH3 ~ 2 R4~NH-c-NH-c-NH2 ~04~
where:
! HX' is a mineral acid.
Appropriately desired end products having various X', Y'and Z'substituents may be prepared at various steps of synthesis using suitable reactions in order to convert one - group to another.
The starting anilines are either known, may be pre-pared by known techniques or reference to the preparation is shown. Thus, chlorination or bromination of an acetanilide or aniline may be carried out in acetic acid, or in the presence of a small amount of iodine dissolved in an inert solvent such as carbon tetrachloride. A solution of chlorine or bromine is then added while the temperature is held near 0C. Iodination may also be carried out by known methods using iodine mono-- chloride (ClI).
Alkylation may be carried out on an acetanilide using an alkyl halide and aluminum chloride under Friedel-Crafts conditions to obtain desired alkyl substitution.
Nitration may be carried out using fuming nitric acid at about 0C.
A nitro compound may be hydrogenated to the corre-sponding amine which may then be diazotized and heated in an alcohol medium to form the alkoxy compound.
An amino compound may also be diazotized to the diazonium fluoroborate which is then thermally decomposed to the fluoro compound. Diazotization followed by a Sandmeyer type reaction may yield the bromo, chloro or iodo compound.
Diazotization of an amino compound followed by addition of cuprous cyanide may result in the desired cyano compound.
When an amino compound is diazotized followed by . .
~o'~
reaction with potassium ethylxanthate and then hydrolyzed, the mercapto compound results. This in turn may be alkylated to the alkylthio group which is then oxidized to the corresponding alkylsulfonyl substituent.
A halo compound in which halo is chloro or bromo or iodo may be reacted with cuprous cyanide in guanidine at about 150C. to produce a cyano compound.
A chloro, bromo or iodo compound may also be reacted with trifluoromethyliodide and copper powder at about 150C. in dimethylformamide to obtain a trifluoromethyl compound ~etrahedron Letters:47, 4095 (1959 ~.
A halo compound may also be reacted with cuprous methanesulfinate in quinoline at about 150C. to obtain a methylsulfonyl compound.
Of course the above reactions may also be carried out on acetophenone in order to direct substitution. Formation of an oxime followed by Beckmann Rearrangement results in the acetamide which is then deacylated to the aniline.
Reactions may also be carried out on the substituted anilines which would result in di- and tri- substituted anilines.
Reactions may also be carried out at other stages of synthesis depending on the substituents present and the substi-tuents desired and various combinations of the foregoing reactions will be determined by one skilled in the art in order that the desired product results. Thus, a phenylguanidine may be halogenated or nitrated as above, etc.
The compounds of this invention exert activity on the cardiovascular system. They possess blood-pressure lowering effects and are useful as antihypertensive agents.
For these purposes, the amidinoureas of this g : ' . ~ . - . ' ' ' iO4~0~
invention can be normally administered orally or parenterally.
Orally they may be administered as tablets, aqueous or oily suspensions, dispersible powders or granules, emulsions, hard or soft capsules, or syrups or elixirs.
Compositions intended for oral use may be prepared according to any method known in the art for the manufacture of pharmaceutical compositions and such compositions may contain one or more agents selected from the group consisting of sweetening agents, flavoring agents, coloring agents, pre-serving agents and the like, in order to provide a pharmaceuti-cally elegant and palatable preparation.
The dosage regimen in carrying out the methods of this invention is that which insures maximum therapeutic response until improvement is obtained and thereafter the minimum effective level which gives relief. Thus, in general, the dosages are those that are therapeutically effective in the alleviation of hypertensive disorders. In general, the daily dose can be between about 0.05 mg/kg/day and 70 mg/kgtday (preferably in the range of 1-25 mg/kg/day), bearing in mind, of course, that in selecting the appropriate dosage in any specific case, consideration must be given to the patient's weight, general health, age, and other factors which may influence response to the drug.
Various tests in animals have been carried out to show the ability of the compounds of this invention to exhibit reactions that can be correlated with activity in humans.
One such test is the ability of the compound to lower blood pressure in the spontaneous hypertensive rat (Ryo Tabei, et al., Clin. Pharm. & Therap. 11: 269-274, 1970).
Blood pressure measurements are recorded by both the tail cuff method and by direct cannulation of a common carotid artery.
.
104~L90~
Compounds that are effective antihypertensives in man have been shown to be active in lowering blood pressure in this animal model. In view of the results of this test, the amidinoureas of this invention can be considered to be active antihyper-tensive agents.
The following are detailed examples which show the preparation of the compounds of this invention. They are to be ; construed as illustrations of said compounds and not as limi-tations thereof.
2,6-Dichlorophenylguanidine To 51 9. (0.315 mole) of 2,6-dichloroaniline is added 0.4 moles of etherial HCl and 200 ml of m-cresol. The mixture is then stirred and heated on a steam bath to drive off the ether and excess hydrogen chloride. To the resultant mixture is then added 13.3 g. (0.315 mole) of cyanamide then heated for 2 hours on a steam bath. The reaction mixture is then cooled, added to 150 ml of conc. sodium hydroxide solution, cooled and extracted with 2 liters of ether. The ether layer is washed with 2 x 1 liter of water, dried over sodium sulfate, charcoal-ed and evaporated. The residue is triturated with hexane and the precipitate is filtered off and washed with ether and dried to obtain 2,6-dichlorophenylguanidine.
The free base is prepared by dissolving 2,6-dichloro-phenylguanidine hydrochloride in 10% sodium hydroxide solution and extracting with ether. The ether is dried and evaporated to dryness to obtain 2,6-dichlorophenylguanidine.
When the above procedures are followed using the amines of Table I, below, then the corresponding product of Table II, below, is prepared.
TABLE I ~O~L9U~ TABLE II
o-chloroaniline o-chlorophenylguanidine m-chloroaniline m-chlorophenylguanidine p-chloroaniline p-chlorophenylguanidine 2,3-dichloroaniline 2,3-dichlorophenylguanidine 2,4-dichloroaniline 2,4-dichlorophenylguanidine
The free base is prepared by dissolving 2,6-dichloro-phenylguanidine hydrochloride in 10% sodium hydroxide solution and extracting with ether. The ether is dried and evaporated to dryness to obtain 2,6-dichlorophenylguanidine.
When the above procedures are followed using the amines of Table I, below, then the corresponding product of Table II, below, is prepared.
TABLE I ~O~L9U~ TABLE II
o-chloroaniline o-chlorophenylguanidine m-chloroaniline m-chlorophenylguanidine p-chloroaniline p-chlorophenylguanidine 2,3-dichloroaniline 2,3-dichlorophenylguanidine 2,4-dichloroaniline 2,4-dichlorophenylguanidine
3,4-dichloroaniline 3,4-dichlorophenylguanidine 3,5-dichloroaniline 3,5-dichlorophenylguanidine p-bromoaniline p-bromophenylguanidine 10 2-chloro-4-bromoaniline 2-chloro-4-bromophenylguanidine p-fluoroaniline p-fluorophenylguanidine 2,4-difluoroaniline 2,4-difluorophenylguanidine 2,5-difluoroaniline 2,5-difluorophenylguanidine 2,6-difluoroaniline 2,6-difluorophenylguanidine `
p-nitroaniline p-nitrophenylguanidine 2-methyl-4-chloroaniline 2-methyl-4-chlorophenylguanidine 2-methyl-4-bromoaniline 2-methyl-4-bromophenylguanidine 2-methyl-4-iodoaniline 2-methyl-4-iodophenylguanidine 2-bromo-4-methylaniline 2-bromo-4-methylphenylguanidine 20 2-methyl-6-chloroaniline 2-methyl-6-chlorophenylguanidine 2,6-dimethylaniline 2,6-dimethylphenylguanidine 2-trifluoromethyl-4-fluoro- 2-trifluoromethyl-4-fluorophenyl-aniline guanidine 2-methoxy-4-chloroaniline 2-methoxy-4-chlorophenylguanidine 2,4-dimethoxyaniline 2,4-dimethoxyphenylguanidine 2-methoxy-6-methylaniline 2-methoxy-6-methylphenylguanidine 2-ethyl-6-methylaniline 2-ethyl-4-nitrophenylguanidine 2-ethyl-4-bromoaniline 2-ethyl-4-bromophenylguanidine 3-chloro-4-fluoroaniline 2,4-dichloro-6-fluorophenyl-guanidine 2-chloro-6-fluoroaniline 2-chloro-4-bromo-6-fluorophenyl-guanidine 2,3,4,5,6-pentafluoroaniline 2,3,4,5,6-pentafluorophenyl-guanidine 2,4,6-trimethylaniline 2,4,6-trimethylphenylguanidine - .
~34 1L~
1-(2,6-Dichlorophenylamidino)-3-(t-butyl)urea To a mixture of 10 9. (0.05 mole) of 2,6-dichloro-; phenylguanidine and 10 ml xylene is added 5 9. of t-butyliso-cyanate (O.OS mole) and the mixture is refluxed for 2 hours.
The reaction product is cooled, triturated with heptane and filtered. Recrystallization from 1:1 isopropyl/water results in 1-(2,6-dichlorophenylamidino)-3-(t-butyl)urea.
When the above procedure is followed using the guanidines of Table II, Example 1, then the products prepared are shown in Table III below.
TABLE III
l-(o-chlorophenylamidino)-3-(t-butyl)urea l-(m-chlorophenylamidino)-3-(t-butyl)urea l-(p-chlorophenylamidino)-3-(t-butyl)urea 1-(2,3-dichlorophenylamidino)-3-(t-butyl)urea 1-(2,4-dichlorophenylamidino)-3-(t-butyl)urea 1-(3,4-dichlorophenylamidino)-3-(t-butyl)urea 1-(3,5-dichlorophenylamidino)-3-(t-butyl)urea 1-(p-bromophenylamidino)-3-(t-butyl)urea 1-(2-chloro-4-bromophenylamidino)-3-(t-butyl)urea l-(p-fluorophenylamidino)-3-(t-butyl)urea 1-(2,4-dimethoxyphenylamidino)-3-(t-butyl)urea 1-(2-methoxy-6-methylphenylamidino)-3-(t-butyl)urea 1-(2,4-difluorophenylamidino)-3-(t-butyl)urea 1-(2,5-difluorophenylamidino)-3-(t-butyl)urea 1-(2,6-difluorophenylamidino)-3-(t-butyl)urea l-(p-nitrophenylamidino)-3-(t-butyl)urea 1-(2-methyl-4-chlorophenylamidino)-3-(t-butyl)urea 1-(2-methyl-4-bromophenylamidino)-3-(t-butyl)urea '- . '' :
lU~G~
1-(2-methyl-4-iodophenylamidino)-3-(t-butyl)urea 1-(2-bromo-4-methylphenylamidino)-3-(t-butyl)urea 1-(2-methyl-6-chlorophenylamidino)-3-(t-butyl)urea 1-(2,6-dimethylphenylamidino)-3-(t-butyl)urea 1-(2-trifluoromethyl-4-fluorophenylamidino)-3-(t-butyl)urea 1-(2-methoxy-4-chlorophenylamidino)-3-(t-butyl)urea 1-(2-ethyl-6-methylphenylamidino)-3-(t-butyl)urea 1-(3-chloro-4-fluorophenylamidino)-3-(t-butyl)urea 1-(2-chloro-6-fluorophenylamidino)-3-(t-butyl)urea 1-(2,3,4,5,6-pentafluorophenylamidino)-3-(t-butyl(urea 1-(2,4,6-trimethylphenylamidino)-3-(t-butyl)urea.
(2,6-Dichlbrophenylamidino)urea hydrochloride A mixture of 32.1 9. (0.106 moles) of 1-(2,6-dichlorophenylamidino)-3-(t-butyl)urea and 200 ml of conc.
hydrochloric acid is refluxed for 1/2 hour. The reaction mixture is cooled, filtered and washed with 10 ml of 1:1 HCl/H20 and dried. The product is then recrystallized from ethanol-ether to obtain (2,6-dichlorophenylamidino)urea hydro-- chloride, m.p. 212-213C.
In a similar manner other desired salts may be prepared using the appropriate acid.
':
The free base is prepared according to Example 1.
EXAMPLES 4 to 36 By proceeding with the compounds of Tables I, II and I I I and following the procedures of Examples 1, 2 and 3, the following compounds corresponding to the following formula:
- - . . . -.
1()'~1~0~
i~ N H O
R4~ NH-C-NH-~-NH2 are obtained and identified in Table IV.
~ . .
.
TABLE IY
Ex R2 R3R4 R5 R6 Mel ti ng Poi nt i n C .
_ BASEHydroch 1 ori de N i trate
p-nitroaniline p-nitrophenylguanidine 2-methyl-4-chloroaniline 2-methyl-4-chlorophenylguanidine 2-methyl-4-bromoaniline 2-methyl-4-bromophenylguanidine 2-methyl-4-iodoaniline 2-methyl-4-iodophenylguanidine 2-bromo-4-methylaniline 2-bromo-4-methylphenylguanidine 20 2-methyl-6-chloroaniline 2-methyl-6-chlorophenylguanidine 2,6-dimethylaniline 2,6-dimethylphenylguanidine 2-trifluoromethyl-4-fluoro- 2-trifluoromethyl-4-fluorophenyl-aniline guanidine 2-methoxy-4-chloroaniline 2-methoxy-4-chlorophenylguanidine 2,4-dimethoxyaniline 2,4-dimethoxyphenylguanidine 2-methoxy-6-methylaniline 2-methoxy-6-methylphenylguanidine 2-ethyl-6-methylaniline 2-ethyl-4-nitrophenylguanidine 2-ethyl-4-bromoaniline 2-ethyl-4-bromophenylguanidine 3-chloro-4-fluoroaniline 2,4-dichloro-6-fluorophenyl-guanidine 2-chloro-6-fluoroaniline 2-chloro-4-bromo-6-fluorophenyl-guanidine 2,3,4,5,6-pentafluoroaniline 2,3,4,5,6-pentafluorophenyl-guanidine 2,4,6-trimethylaniline 2,4,6-trimethylphenylguanidine - .
~34 1L~
1-(2,6-Dichlorophenylamidino)-3-(t-butyl)urea To a mixture of 10 9. (0.05 mole) of 2,6-dichloro-; phenylguanidine and 10 ml xylene is added 5 9. of t-butyliso-cyanate (O.OS mole) and the mixture is refluxed for 2 hours.
The reaction product is cooled, triturated with heptane and filtered. Recrystallization from 1:1 isopropyl/water results in 1-(2,6-dichlorophenylamidino)-3-(t-butyl)urea.
When the above procedure is followed using the guanidines of Table II, Example 1, then the products prepared are shown in Table III below.
TABLE III
l-(o-chlorophenylamidino)-3-(t-butyl)urea l-(m-chlorophenylamidino)-3-(t-butyl)urea l-(p-chlorophenylamidino)-3-(t-butyl)urea 1-(2,3-dichlorophenylamidino)-3-(t-butyl)urea 1-(2,4-dichlorophenylamidino)-3-(t-butyl)urea 1-(3,4-dichlorophenylamidino)-3-(t-butyl)urea 1-(3,5-dichlorophenylamidino)-3-(t-butyl)urea 1-(p-bromophenylamidino)-3-(t-butyl)urea 1-(2-chloro-4-bromophenylamidino)-3-(t-butyl)urea l-(p-fluorophenylamidino)-3-(t-butyl)urea 1-(2,4-dimethoxyphenylamidino)-3-(t-butyl)urea 1-(2-methoxy-6-methylphenylamidino)-3-(t-butyl)urea 1-(2,4-difluorophenylamidino)-3-(t-butyl)urea 1-(2,5-difluorophenylamidino)-3-(t-butyl)urea 1-(2,6-difluorophenylamidino)-3-(t-butyl)urea l-(p-nitrophenylamidino)-3-(t-butyl)urea 1-(2-methyl-4-chlorophenylamidino)-3-(t-butyl)urea 1-(2-methyl-4-bromophenylamidino)-3-(t-butyl)urea '- . '' :
lU~G~
1-(2-methyl-4-iodophenylamidino)-3-(t-butyl)urea 1-(2-bromo-4-methylphenylamidino)-3-(t-butyl)urea 1-(2-methyl-6-chlorophenylamidino)-3-(t-butyl)urea 1-(2,6-dimethylphenylamidino)-3-(t-butyl)urea 1-(2-trifluoromethyl-4-fluorophenylamidino)-3-(t-butyl)urea 1-(2-methoxy-4-chlorophenylamidino)-3-(t-butyl)urea 1-(2-ethyl-6-methylphenylamidino)-3-(t-butyl)urea 1-(3-chloro-4-fluorophenylamidino)-3-(t-butyl)urea 1-(2-chloro-6-fluorophenylamidino)-3-(t-butyl)urea 1-(2,3,4,5,6-pentafluorophenylamidino)-3-(t-butyl(urea 1-(2,4,6-trimethylphenylamidino)-3-(t-butyl)urea.
(2,6-Dichlbrophenylamidino)urea hydrochloride A mixture of 32.1 9. (0.106 moles) of 1-(2,6-dichlorophenylamidino)-3-(t-butyl)urea and 200 ml of conc.
hydrochloric acid is refluxed for 1/2 hour. The reaction mixture is cooled, filtered and washed with 10 ml of 1:1 HCl/H20 and dried. The product is then recrystallized from ethanol-ether to obtain (2,6-dichlorophenylamidino)urea hydro-- chloride, m.p. 212-213C.
In a similar manner other desired salts may be prepared using the appropriate acid.
':
The free base is prepared according to Example 1.
EXAMPLES 4 to 36 By proceeding with the compounds of Tables I, II and I I I and following the procedures of Examples 1, 2 and 3, the following compounds corresponding to the following formula:
- - . . . -.
1()'~1~0~
i~ N H O
R4~ NH-C-NH-~-NH2 are obtained and identified in Table IV.
~ . .
.
TABLE IY
Ex R2 R3R4 R5 R6 Mel ti ng Poi nt i n C .
_ BASEHydroch 1 ori de N i trate
4 Cl ~59-160 Cl 171-173 6 Cl 182-183 7 Cl Cl 194-195 8 Cl Cl 184-185 9 Cl Cl 187 Cl Cl 197-198 11 Cl Cl 198-199 12 Br 177-179 13 Cl Br 188.5-189 .
16 F F 212 ..
19 CH3 Cl 190-190.5 CH3 Br 178-180 21 Br CH3 205-206 22 CH3 Cl 205-206 C2H5 Br152-153 26 CH3 I 189.5-190.5 CH30 Cl 197 .. . .
: ~ - . . . .
.. .
10`~1~0~
TABLE IY (Cont'd) Ex. R2R3 R4 R5 R6 -~ ~ lelting Point ir C. -_ __ BASE Hydroch 1 ori de Ni trate 33 Cl F 208 ' . I
16 F F 212 ..
19 CH3 Cl 190-190.5 CH3 Br 178-180 21 Br CH3 205-206 22 CH3 Cl 205-206 C2H5 Br152-153 26 CH3 I 189.5-190.5 CH30 Cl 197 .. . .
: ~ - . . . .
.. .
10`~1~0~
TABLE IY (Cont'd) Ex. R2R3 R4 R5 R6 -~ ~ lelting Point ir C. -_ __ BASE Hydroch 1 ori de Ni trate 33 Cl F 208 ' . I
Claims (13)
1. A composition useful for reducing blood-pressure and hypertension which comprises an amidinourea of the formula:
wherein:
R2, R3, R4, R5 and R6 may be the same or different and are hydrogen, trifluoromethyl, nitro, loweralkoxy or loweralkyl;
and non-toxic acid addition salts thereof, provided at least one of R2, R3, R4, R5 and R6 is other than hydrogen, in admixture with a pharmaceutically acceptable carrier.
wherein:
R2, R3, R4, R5 and R6 may be the same or different and are hydrogen, trifluoromethyl, nitro, loweralkoxy or loweralkyl;
and non-toxic acid addition salts thereof, provided at least one of R2, R3, R4, R5 and R6 is other than hydrogen, in admixture with a pharmaceutically acceptable carrier.
2. The composition of Claim 1, wherein the amidino-urea is the (2,3-dichlorophenylamidino)urea.
3. The composition of Claim 1, wherein the amidino-urea is the (2,4-dichlorophenylamidino)urea.
4. The composition of Claim 1, wherein the amidino-urea is the (3,5-dichlorophenylamidino)urea.
5. The composition of Claim 1, wherein the amidino-urea is the (3-chloro-4-fluorophenylamidino)urea.
6. The composition of Claim 1, wherein the amidino-urea is the (3,4-dichlorophenylamidino)urea.
7. The composition of Claim 1, wherein the amidino-urea is the (2-chloro-4-bromophenylamidino)urea.
8. The composition of Claim 1, wherein the amidino-urea is the (2-bromo-4-methylphenylamidino)urea.
9. The composition of Claim 1, wherein the amidino-urea is the (2-methyl-4-bromophenylamidino)urea.
10. The composition of Claim 1, wherein the amidino-urea is the (2-ethyl-4-bromophenylamidino)urea.
11. The composition of Claim 1, wherein the amidino-urea is the (2,6-dimethylphenylamidino)urea.
12. The composition of Claim 1, wherein the amidino-urea is the (2,6-dichlorophenylamidino)urea.
13. The composition of Claim 1, wherein the amidino-urea is the (p-fluorophenylamidino)urea.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US29147472A | 1972-09-22 | 1972-09-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
CA1041908A true CA1041908A (en) | 1978-11-07 |
Family
ID=23120445
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA181,015A Expired CA1041908A (en) | 1972-09-22 | 1973-09-13 | Amidinoureas |
Country Status (14)
Country | Link |
---|---|
JP (1) | JPS593471B2 (en) |
AR (1) | AR200024A1 (en) |
BE (1) | BE805138A (en) |
CA (1) | CA1041908A (en) |
CH (2) | CH614430A5 (en) |
DE (1) | DE2345951C2 (en) |
ES (1) | ES418987A1 (en) |
FR (1) | FR2200002B1 (en) |
GB (5) | GB1451477A (en) |
IL (1) | IL43280A (en) |
NL (1) | NL7313040A (en) |
PH (1) | PH12016A (en) |
SE (2) | SE416952B (en) |
ZA (1) | ZA737475B (en) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4025652A (en) * | 1975-03-31 | 1977-05-24 | William H. Rorer, Inc. | Amidinoureas |
US4488993A (en) * | 1972-09-22 | 1984-12-18 | William H. Rorer, Inc. | Amidinoureas |
US4220658A (en) * | 1972-09-22 | 1980-09-02 | William H. Rorer, Inc. | Treatment of hypertension with amidinoureas |
US4326074A (en) | 1972-09-22 | 1982-04-20 | William H. Rorer, Inc. | Amidinoureas |
US4713382A (en) * | 1985-05-30 | 1987-12-15 | Syntex (U.S.A.) Inc. | N-phenyl-4-phenyl-1-piperazinecarboxamidines and related compounds as antiarrhythmic agents |
ATE157351T1 (en) * | 1993-02-20 | 1997-09-15 | Hoechst Ag | SUBSTITUTED BENZOYLGUANIDINES, METHOD FOR THE PRODUCTION THEREOF, THEIR USE AS A MEDICATION, AS INHIBITORS OF CELLULAR NA+/H+ EXCHANGE OR AS A DIAGNOSTIC, AND MEDICINE CONTAINING THEM |
-
1973
- 1973-09-10 PH PH15001A patent/PH12016A/en unknown
- 1973-09-12 DE DE2345951A patent/DE2345951C2/en not_active Expired
- 1973-09-13 CA CA181,015A patent/CA1041908A/en not_active Expired
- 1973-09-17 CH CH1605977A patent/CH614430A5/en not_active IP Right Cessation
- 1973-09-17 CH CH1330773A patent/CH605703A5/xx not_active IP Right Cessation
- 1973-09-20 AR AR250179A patent/AR200024A1/en active
- 1973-09-21 ZA ZA737475A patent/ZA737475B/en unknown
- 1973-09-21 ES ES418987A patent/ES418987A1/en not_active Expired
- 1973-09-21 JP JP48107418A patent/JPS593471B2/en not_active Expired
- 1973-09-21 BE BE135886A patent/BE805138A/en not_active IP Right Cessation
- 1973-09-21 SE SE7312880A patent/SE416952B/en unknown
- 1973-09-21 FR FR7333963A patent/FR2200002B1/fr not_active Expired
- 1973-09-21 NL NL7313040A patent/NL7313040A/xx not_active Application Discontinuation
- 1973-09-21 IL IL43280A patent/IL43280A/en unknown
- 1973-09-24 GB GB4465473A patent/GB1451477A/en not_active Expired
- 1973-09-24 GB GB2491476A patent/GB1451479A/en not_active Expired
- 1973-09-24 GB GB2499276A patent/GB1451480A/en not_active Expired
- 1973-09-24 GB GB3221175A patent/GB1451478A/en not_active Expired
-
1975
- 1975-05-30 GB GB23574/75A patent/GB1514198A/en not_active Expired
-
1976
- 1976-11-02 SE SE7612176A patent/SE416953B/en not_active IP Right Cessation
Also Published As
Publication number | Publication date |
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DE2345951A1 (en) | 1974-04-04 |
BE805138A (en) | 1974-01-16 |
SE7612176L (en) | 1976-11-02 |
ES418987A1 (en) | 1976-07-01 |
PH12016A (en) | 1978-10-06 |
GB1514198A (en) | 1978-06-14 |
GB1451479A (en) | 1976-10-06 |
IL43280A (en) | 1977-06-30 |
FR2200002A1 (en) | 1974-04-19 |
SE416952B (en) | 1981-02-16 |
IL43280A0 (en) | 1973-11-28 |
GB1451478A (en) | 1976-10-06 |
JPS593471B2 (en) | 1984-01-24 |
CH605703A5 (en) | 1978-10-13 |
DE2345951C2 (en) | 1986-10-23 |
GB1451477A (en) | 1976-10-06 |
JPS4985046A (en) | 1974-08-15 |
ZA737475B (en) | 1974-10-30 |
GB1451480A (en) | 1976-10-06 |
AU6047973A (en) | 1975-03-20 |
SE416953B (en) | 1981-02-16 |
NL7313040A (en) | 1974-03-26 |
FR2200002B1 (en) | 1977-07-15 |
CH614430A5 (en) | 1979-11-30 |
AR200024A1 (en) | 1974-10-15 |
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