[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

BE672800A - - Google Patents

Info

Publication number
BE672800A
BE672800A BE672800DA BE672800A BE 672800 A BE672800 A BE 672800A BE 672800D A BE672800D A BE 672800DA BE 672800 A BE672800 A BE 672800A
Authority
BE
Belgium
Prior art keywords
methoxyoestradiol
ester
acid
adamantoate
preparation
Prior art date
Application number
Other languages
French (fr)
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed filed Critical
Publication of BE672800A publication Critical patent/BE672800A/fr

Links

Landscapes

  • Steroid Compounds (AREA)

Description

  

   <Desc/Clms Page number 1> 
 



  "Procédé de préparation d'un nouvel ester de 3-méthoxyoestradiol et produit obtenu". 



   La présente invention concerne un nouvel ester de 3-méthoxyoestradiol et un procédé de préparation de celui-ci. 



   Le composé visé pax l'invention est l'ester de l'acide 1-adamantoïque et du 3-méthoxyoestradiol. 

 <Desc/Clms Page number 2> 

 



   L'invention vise également un procédé de préparation d'unéster de 3-méthoxyoestradiol consistant à faire réagir le 
 EMI2.1 
 3-méthoxyoestradiol avec l'anhydride de l'acide 1-adamantolque, un anhydride mixte de l'acide 1-adaman.toqueet de l'acide trzfluoroacétique, ou un chlorure d'acide 1-adamantoique, en présence de pyridine comme catalyseur, pour former l'ester 1-adamantolque du 3-méthoxyoestradiol. 



   On utilise de préférence un solvent inerte comme milieu de dispersion. 
 EMI2.2 
 



  Le 5-méthoxyoestradiol¯17p-(l-adamantoate) , qui est le composé obtenu par le procédé objet de l'invention, est un produit solide cristallin blanc, soluble dans la plupart des solvants organiques. Ce nouveau composé est avantageux comme anti-androgène pour un certain nombre de mammifères, car il comoat es effets physiologiques des hormones mâles. Contraire- ment au 3-méthoxyoestradiol, qui est un inhibiteur général de la gonadotrophine, le   3-méthoxyoestradiol-17p-(l-adamantoate)   est un anti-androgène spécifique. 



   On donne l'exemple non limitatif suivant à titre . d'illustration de l'invention. 



    EXEMPLE.   
 EMI2.3 
 



  3-méthoxyoestradiol-120-(l-adamantoate) 
On dissout 800 mg de 3-méthoxyoestradiol dasn 50   cm   de benzène anhydre. On ajoute 662 mg de chlorure d'acide   adaman-   toïque dissous dans 5 cm de benzène, puis 0,04 cm de pyridine. 



  On chauffe le mélange réactionnel à la température de reflux pendant 2 heures environ et on le verse dans une solution aqueuse à 2% de bicarbonate de sodium maintenue à 0 C environ. 



  On extrait le mélange résultant avec de l'éther, on sépare l'extrait éthéré et on le sèche. En éliminant l'éther par 
 EMI2.4 
 évaporation'sous vide, on obtient le 3-méthoxyoestradiol-17P- 

 <Desc/Clms Page number 3> 

 (1-adamantoate) comme résidu. La recristallisation de celui-ci dans l'éther donne le 3-méthoxyoesradilol-178-(1-admanatoae), fondant à 210-212 C. 



  Analyse : Calculé : C= 80,31 ;H= 8,99. 



  Trouvé :C= 80,57 ; H= 9,07. 



   REVENDICATIONS. 



   1. Le   3-méthoxyoestradiol-17-(1-adamantoate).   



   2. Procédé de préparation d'un ester de 3-méthoxy- oestradiol, caractérisé en ce qu'on fait réagir le 3-méthoxy- oestradiol avec l'anhydride de l'acide 1-adamantoïque, un an- hydride mixte de l'acide 1-amonatoïque, et de l'acide trifluoro- acétique, ou le chlorure de l'adcie 1-amdahotïqaue en présence de pyridine comme catalyseur, pour former l'ester 1-adaman- rtoïqeu du 3-méthoxyoestradiol.



   <Desc / Clms Page number 1>
 



  "Process for the preparation of a novel 3-methoxyoestradiol ester and product obtained".



   The present invention relates to a novel 3-methoxyoestradiol ester and a process for the preparation thereof.



   The compound targeted by the invention is the ester of 1-adamantoic acid and 3-methoxyoestradiol.

 <Desc / Clms Page number 2>

 



   The invention also relates to a process for the preparation of an ester of 3-methoxyoestradiol consisting in reacting the
 EMI2.1
 3-methoxyoestradiol with 1-adamantoic acid anhydride, a mixed anhydride of 1-adaman.toque acid and trzfluoroacetic acid, or 1-adamantoic acid chloride, in the presence of pyridine as catalyst, to form the 1-adamantol ester of 3-methoxyoestradiol.



   Preferably, an inert solvent is used as the dispersing medium.
 EMI2.2
 



  5-Methoxyoestradiol¯17p- (1-adamantoate), which is the compound obtained by the process which is the subject of the invention, is a white crystalline solid product, soluble in most organic solvents. This new compound is advantageous as an antiandrogen for a number of mammals, since it coats the physiological effects of male hormones. Unlike 3-methoxyoestradiol, which is a general gonadotropin inhibitor, 3-methoxyoestradiol-17p- (1-adamantoate) is a specific antiandrogen.



   The following non-limiting example is given as a title. illustration of the invention.



    EXAMPLE.
 EMI2.3
 



  3-methoxyoestradiol-120- (l-adamantoate)
800 mg of 3-methoxyoestradiol are dissolved in 50 cm of anhydrous benzene. 662 mg of adamantoid acid chloride dissolved in 5 cm of benzene are added, followed by 0.04 cm of pyridine.



  The reaction mixture is heated at reflux temperature for about 2 hours and poured into a 2% aqueous solution of sodium bicarbonate maintained at about 0 ° C.



  The resulting mixture is extracted with ether, the ethereal extract is separated and dried. By eliminating the ether by
 EMI2.4
 evaporation under vacuum, we obtain 3-methoxyoestradiol-17P-

 <Desc / Clms Page number 3>

 (1-adamantoate) as a residue. Recrystallization of this from ether gives 3-methoxyoesradilol-178- (1-admanatoae), melting at 210-212 C.



  Analysis: Calculated: C = 80.31; H = 8.99.



  Found: C = 80.57; H, 9.07.



   CLAIMS.



   1. 3-Methoxyoestradiol-17- (1-adamantoate).



   2. Process for the preparation of an ester of 3-methoxy-estradiol, characterized in that the 3-methoxy-estradiol is reacted with the anhydride of 1-adamantoic acid, a mixed anhydride of the. 1-amonatoic acid, and trifluoroacetic acid, or 1-amdahotic acid chloride in the presence of pyridine as a catalyst, to form the 1-adamantoid ester of 3-methoxyoestradiol.

 

Claims (1)

3. Procédé suivant la revendication 1, caractérisé en ce que la réaction est effectuée dans un solvant inerte. 3. Method according to claim 1, characterized in that the reaction is carried out in an inert solvent. 4. Procédé de préparation d'un ester de 3-méthoxy- oestradiol, tel que décrit ci-avant, en particulier en se ré- férant à l'exemple donné. 4. Process for the preparation of an ester of 3-methoxy-estradiol, as described above, in particular with reference to the example given. 5. Le produit obtenu par un procédé suivant l'une quelconque des revendications 2 à 4. 5. The product obtained by a process according to any one of claims 2 to 4. @ @
BE672800D 1964-12-02 1965-11-24 BE672800A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US41545164A 1964-12-02 1964-12-02

Publications (1)

Publication Number Publication Date
BE672800A true BE672800A (en) 1966-05-24

Family

ID=23645729

Family Applications (1)

Application Number Title Priority Date Filing Date
BE672800D BE672800A (en) 1964-12-02 1965-11-24

Country Status (1)

Country Link
BE (1) BE672800A (en)

Similar Documents

Publication Publication Date Title
CH375017A (en) Process for the preparation of novel imidazole derivatives
FR2619109A1 (en) SULFONAMIDOTHIENYLCARBOXYLIC ACIDS WITH THERAPEUTIC ACTION
FR2599739A1 (en) HYDROXAMIC BIPHENYL ACIDS WITH THERAPEUTIC ACTION
EP0117771B1 (en) Imino-2 pyrrolidines, process for their preparation and their therapeutical use
BE672800A (en)
BE779775A (en) DERIVATIVES OF UREA, METHOD FOR PREPARING THEM AND THEIR APPLICATIONS
EP0593497B1 (en) Process for the preparation of 2-alkyl-4-acyl-6-(tert)-butylphenol compounds
FR2590254A1 (en) PROCESS FOR OBTAINING ETHYL ESTER FROM APOVINCANIMIC ACID
CH392483A (en) Process for the preparation of new esters of 4-halo-3-sulfamoyl-benzoic acids
SU810693A1 (en) Method of preparing pentadecanolides
EP0057141B1 (en) Esters of halogene-biphenylcarboxylates, method of preparation and their application as medicines
EP0007839B1 (en) Process for the preparation of 3-substituted cyclo-propane-1-carboxylic acids and products obtained
CH426781A (en) Process for the conversion of 1,2,3,4-tetrahydro-anthracene compounds into 1,2,3,4,4a, 5,12,12a-octahydronaphtacene compounds
EP0119899B1 (en) Process for the preparation of 4-pentenoic acid derivatives
CH388975A (en) Process for the preparation of a reserpine derivative
CH268051A (en) Process for preparing 1-methyl-4-piperazine-N, N-diethyl-carboxamide.
BE661226A (en) ARYLACETHYDROXAMIC ACIDS, CORRESPONDING AMIDS AND METHODS OF PREPARATION.
BE837320A (en) 3-AMINO-1,2-PROPANODIOL ETHER DERIVATIVES
EP0022022A1 (en) Acylated derivatives of taurine and their salts, and process for their preparation
CH639085A5 (en) Process for the preparation of xanthone derivatives
CH220046A (en) Process for the preparation of a derivative of para-amino-benzene-sulfonamide.
CH284716A (en) Process for preparing an aromatic acylamidodiol, nitrated in the nucleus.
FR2534583A1 (en) Process for the production of hexahydro-5-hydroxy-4-hydroxymethyl-2H-cyclopenta[b]furan-2-one
BE904930A (en) 4- (N-METHYL-N-NICOTINOYL) -AMINO-2,3-DIMETHYL-1-PHENYL-3-PYRAZOLINE-5-ONE AND COMPOUND THUS OBTAINED.
CH288947A (en) Process for preparing an aromatic acylamidodiol.