EP0245276A1 - 1$g(a).7$g(a)-DITHIOSUBSTITUIERTE SPIROLACTONE, VERFAHREN ZU IHRER HERSTELLUNG UND IHRE VERWENDUNG ALS ARZNEIMITTEL - Google Patents
1$g(a).7$g(a)-DITHIOSUBSTITUIERTE SPIROLACTONE, VERFAHREN ZU IHRER HERSTELLUNG UND IHRE VERWENDUNG ALS ARZNEIMITTELInfo
- Publication number
- EP0245276A1 EP0245276A1 EP86901339A EP86901339A EP0245276A1 EP 0245276 A1 EP0245276 A1 EP 0245276A1 EP 86901339 A EP86901339 A EP 86901339A EP 86901339 A EP86901339 A EP 86901339A EP 0245276 A1 EP0245276 A1 EP 0245276A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- methylene
- carbolactone
- oxo
- pregn
- dithio
- 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.)
- Withdrawn
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J53/00—Steroids in which the cyclopenta(a)hydrophenanthrene skeleton has been modified by condensation with a carbocyclic rings or by formation of an additional ring by means of a direct link between two ring carbon atoms, including carboxyclic rings fused to the cyclopenta(a)hydrophenanthrene skeleton are included in this class
- C07J53/002—Carbocyclic rings fused
- C07J53/004—3 membered carbocyclic rings
- C07J53/008—3 membered carbocyclic rings in position 15/16
Definitions
- the invention relates to new 1 ⁇ .7 ⁇ -disubstituted spirolactones, processes for their preparation and pharmaceutical preparations containing them according to the claims.
- R 1 in formula I as an alkyl radical having 1 to 3 carbon atoms represents, for example, a methyl, ethyl, propyl or isopropyl group.
- 1 to 3 carbon atoms represents, for example, the formyl
- the new compounds of general formula I have the property of canceling or reversing the effect of aldosterone or deoxycorticosterone on the sodium and potassium salt excretion.
- the compounds according to the invention are therefore suitable for the treatment of certain forms of hypertension, of edema, for example in the case of heart failure, in liver cirrhosis and nephrotic syndrome, primary and secondary aldosteronism and other endocrinological disorders caused by aldosterone. They can also be used as diuretics.
- the active compounds according to the invention Compared to the commercially available spironolactone and its metabolites, which contain a mercapto or methylthio group instead of the acetylthio group in the 7 ⁇ position (Steroids 20 (1972) 41), the active compounds according to the invention have the advantage of higher activity and a prolonged duration of action, the effect also occurring is delayed.
- This activity profile indicates that the compounds according to the invention are biologically active compounds which are metabolic only in the organism be activated to so-called pro-drugs.
- such compounds have the advantage that the content of active substance in the blood plasma is less exposed to fluctuations.
- the compounds according to the invention are further characterized in that they are endocrinologically ineffective. You bind e.g. practically not at all on the androgen receptor.
- the compounds according to the invention which contain a thio group in both the 1 ⁇ and 7 ⁇ positions, have been shown to be superior to the known spironolactone in their antialdosterone activity in the test model by Hollmann (Naunyn-Schmiedebergs Arch. Exp. Path. Pharmak. 247 (1964) 419) and are distinguished from spironolactone by a later onset of action.
- the new active ingredients can be used in the same way as for spironolactone.
- the dosage of the active ingredients is below that of spironolactone. Due to the longer lasting effect, however, the new active ingredients usually only need to be applied once a day.
- the active ingredients can be processed into pharmaceutical preparations, preferably for enteral application, according to methods of galenics known per se.
- enteral application can be considered in particular tablets, coated tablets or capsules which contain about 25 to 200 mg of active ingredient per dose unit in an inert carrier material.
- the ⁇ 1.4.6 -unsaturated 3-ketopregnatriene of the formula II is expediently dissolved in a suitable protic solvent or in a mixture thereof, the desired thioalkanoic acid is added and warms the reaction mixture to temperatures above room temperature up to the boiling point of the solvent.
- suitable solvents or mixtures thereof are methanol, acetone and tetrahydrofuran.
- solubilizers such as diisopropyl ether, benzene and heptane do not disturb the course of the reaction.
- the starting material of the formula II is reacted with the corresponding alkyl mercaptan in a suitable solvent.
- suitable solvents are in particular organic bases such as pyridine, piperidine, collidine and lutidine.
- the reaction mixture can be warmed to temperatures above room temperature if extremely long reaction times are undesirable.
- alkali metal alcoholate e.g. Potassium methylate
- Any subsequent esterification of the mercapto group is carried out according to the steroid chemistry methods for the esterification of sterols.
- the esterification is preferably carried out with an activated derivative of a lower aliphatic carboxylic acid in the presence of pyridine and / or 4-dimethylaminopyridine.
- Suitable derivatives are, in particular, the anhydrides and halides of lower carboxylic acids, in particular acetic and propionic acids.
- reaction products according to the invention are separated off by methods known per se, such as precipitation, filtration or extraction, and are purified, for example, by chromatography and / or recrystallization.
- UV: ⁇ 236 16,000 (in methanol).
- Example 3a an ice-cooled solution of 6.0 g of 15 ⁇ .16ß-methylene-1 ⁇ .7 ⁇ -dimethylthio-3-oxo-17 ⁇ -pregn-4-en-21.17-carbolactone in 187 ml of ethanol is mixed with 2.27 g of potassium ethylate added and stirred for 45 minutes while cooling and passing argon. For working up, it is poured into ice water. The precipitate is filtered off, washed with water and dried.
- UV: ⁇ 236 11 600 (in methanol).
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Steroid Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Description
Claims
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19853506100 DE3506100A1 (de) | 1985-02-18 | 1985-02-18 | 1(alpha).7(alpha)-dithiosubstituierte spirolactone, verfahren zu ihrer herstellung und ihre verwendung als arzneimittel |
DE3506100 | 1985-02-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
EP0245276A1 true EP0245276A1 (de) | 1987-11-19 |
Family
ID=6263198
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP86901339A Withdrawn EP0245276A1 (de) | 1985-02-18 | 1986-02-13 | 1$g(a).7$g(a)-DITHIOSUBSTITUIERTE SPIROLACTONE, VERFAHREN ZU IHRER HERSTELLUNG UND IHRE VERWENDUNG ALS ARZNEIMITTEL |
Country Status (5)
Country | Link |
---|---|
US (1) | US4789668A (de) |
EP (1) | EP0245276A1 (de) |
JP (1) | JPS62501844A (de) |
DE (1) | DE3506100A1 (de) |
WO (1) | WO1986004900A1 (de) |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2224222A1 (en) * | 1995-06-07 | 1996-12-19 | G.D. Searle & Co. | Spironolactone and angiotensin ii antagonist combination therapy for treatment of congestive heart failure |
US6410524B1 (en) | 1998-11-06 | 2002-06-25 | G. D. Searle & Co. | Combination therapy of angiotensin converting enzyme inhibitor and aldosterone antagonist for reducing morbidity and mortality from cardiovascular disease |
US6716829B2 (en) | 2000-07-27 | 2004-04-06 | Pharmacia Corporation | Aldosterone antagonist and cyclooxygenase-2 inhibitor combination therapy to prevent or treat inflammation-related cardiovascular disorders |
AU2001285318A1 (en) * | 2000-08-28 | 2002-03-13 | Pharmacia Corporation | Use of an aldosterone receptor antagonist to improve cognitive function |
AU2003222010A1 (en) * | 2002-03-18 | 2003-10-08 | Pharmacia Corporation | Combination of an aldosterone receptor antagonist and a bile acid sequestering agent |
JP6148175B2 (ja) | 2010-05-10 | 2017-06-14 | アンスティチュ ナショナル ドゥ ラ サンテ エ ドゥ ラ ルシェルシュ メディカル | 網膜中および/または網膜下における液体貯留の処置のための方法および組成物 |
JP6180930B2 (ja) | 2010-06-16 | 2017-08-16 | アンスティチュ ナショナル ドゥ ラ サンテ エ ドゥ ラ ルシェルシュ メディカル | 創傷治癒過程における再上皮化を刺激するための方法及び組成物 |
WO2017055248A1 (en) | 2015-09-28 | 2017-04-06 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods and pharmaceutical compositions for the treatment of heart failure |
WO2017064121A1 (en) | 2015-10-13 | 2017-04-20 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods and pharmaceutical compositions for the treatment of choroidal neovascularisation |
WO2018019843A1 (en) | 2016-07-26 | 2018-02-01 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Antagonist of mineralocorticoid receptor for the treatment of osteoarthritis |
WO2023031277A1 (en) | 2021-08-31 | 2023-03-09 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods for the treatment of ocular rosacea |
CN116925170A (zh) * | 2023-07-20 | 2023-10-24 | 浙江朗华制药有限公司 | 一种螺内酯双硫代杂质化合物及其制备方法和应用 |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3013012A (en) * | 1960-12-22 | 1961-12-12 | Searle & Co | Alkanoylthio-17alpha-carboxyethyl-17beta-hydroxyandrosten-3-one lactones |
DE3227598A1 (de) * | 1982-07-22 | 1984-01-26 | Schering AG, 1000 Berlin und 4709 Bergkamen | 7(alpha)-acylthio-15.16-methylen-3-oxo-17(alpha)-pregna-1.4-dien-21,17-carbolactone, verfahren zu ihrer herstellung und verwendung als arzneimittel |
DE3240510A1 (de) * | 1982-10-29 | 1984-05-03 | Schering AG, 1000 Berlin und 4709 Bergkamen | Neue 7(alpha)-acylthio-1(alpha),2(alpha)-methylen-3-oxo-17(alpha)-pregn-4-en-21,17-carbolactone, deren herstellung und diese enthaltende arzneimittel |
-
1985
- 1985-02-18 DE DE19853506100 patent/DE3506100A1/de not_active Withdrawn
-
1986
- 1986-02-13 EP EP86901339A patent/EP0245276A1/de not_active Withdrawn
- 1986-02-13 JP JP61501205A patent/JPS62501844A/ja active Pending
- 1986-02-13 WO PCT/DE1986/000055 patent/WO1986004900A1/de not_active Application Discontinuation
- 1986-02-13 US US06/929,292 patent/US4789668A/en not_active Expired - Fee Related
Non-Patent Citations (1)
Title |
---|
See references of WO8604900A1 * |
Also Published As
Publication number | Publication date |
---|---|
JPS62501844A (ja) | 1987-07-23 |
US4789668A (en) | 1988-12-06 |
DE3506100A1 (de) | 1986-08-21 |
WO1986004900A1 (en) | 1986-08-28 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
17P | Request for examination filed |
Effective date: 19870812 |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AT BE CH DE FR GB IT LI LU NL SE |
|
17Q | First examination report despatched |
Effective date: 19880810 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN |
|
18D | Application deemed to be withdrawn |
Effective date: 19890221 |
|
RIN1 | Information on inventor provided before grant (corrected) |
Inventor name: WIECHERT, RUDOLF Inventor name: NICKISCH, KLAUS Inventor name: BITTLER, DIETER Inventor name: LAURENT, HENRY Inventor name: LOSERT, WOLFGANG |