Organic compounds -- part of the class 532-570 series – Organic compounds – Heterocyclic carbon compounds containing a hetero ring...
Reexamination Certificate
2001-05-16
2002-04-09
Badio, Barbara P. (Department: 1616)
Organic compounds -- part of the class 532-570 series
Organic compounds
Heterocyclic carbon compounds containing a hetero ring...
C540S063000, C552S565000, C552S586000, C552S593000
Reexamination Certificate
active
06369218
ABSTRACT:
FIELD OF THE INVENTION
The present invention refers to a process for the conversion of 6&bgr;-fluoro derivatives into the corresponding 6&agr;-fluoro derivatives of pregnane compounds of formula (I) reported hereinafter, useful as intermediates for the preparation of anti-inflammatory pharmaceutical formulations.
PRIOR ART
6&agr;-fluoro substituted isomers of pregnane derivatives exert a pharmacological action, which makes them useful in the preparation of anti-inflammatory pharmaceutical formulations. Conversely, the corresponding 6&bgr;-fluoro derivatives do not exert any pharmacological action.
A number of procedures for the preparation of 6-fluoro pregnane derivatives have been developed so far. However, all of them yield mixtures of the two isomers with relatively high 6&bgr;/6&agr; ratios. It follows that, to obtain the pharmacologically active isomer only, isomer 6&bgr; must be converted into isomer 6&agr;.
By way of example, U.S. Pat. No. 2,961,441 discloses a process for the preparation of 6-fluoro substituted pregnane derivatives, which yields isomer 6&bgr;. This isomer is then converted into the corresponding isomer 6&agr; by treatment with an acid or a base, such as HCl or KOH, in an appropriate organic solvent, such as acetic acid, chloroform, methanol or ethanol.
U.S. Pat. No. 3,980,778 describes the preparation of a 6&agr;-fluoro substituted pregnane derivative by fluorination of a suitable substrate. Said reaction yields a 6&bgr;/6&agr; isomeric mixture in which isomer 6&bgr; predominates. According to said patent, the conversion of isomer 6&bgr; into the corresponding isomer 6&agr; may be carried out e.g. by treatment with HCl or with a dimethylformamide-HCl complex in an inert organic solvent, such as chloroform or chloroform-ethanol mixtures.
Still unresolved is the problem of converting 6&bgr;-fluorosteroids into the corresponding pharmacologically active 6&agr;-fluoro derivatives by means of processes not requiring drastic reaction conditions, though maintaining short reaction times. Said drastic conditions would make the process inapplicable to substrates with unstable functional groups, e.g. epoxides, esters or acetals.
SUMMARY OF THE INVENTION
It has surprisingly been found that it is possible to obtain a mixture of isomers with a 6&agr;/6&bgr; ratio above 95:5 also starting from pure isomer 6&bgr; or from mixtures in which isomer 6&bgr; predominates, simply by treating the starting mixture in an opportunely selected organic solvent with an organic base containing a diazoimino group.
It is, therefore, an object of the present invention to provide a process for the isomerisation of 6&bgr;-fluoro derivatives into the corresponding 6&agr;-fluoro derivatives of pregnane compounds of formula (I), comprising the reaction of 6&bgr;-fluorosteroids, or of 6&agr;/6&bgr; isomeric mixtures, with an organic base, to obtain a 6&agr;-enriched 6&agr;/6&bgr; mixture with a 6&agr;/6&bgr; ratio higher than 95:5
where R is H or an acyl group containing 1 to 5 carbon atoms in the alkyl chain; R′ is OH or an acyloxy group containing 1 to 5 carbon atoms in the alkyl chain; R″ is H or a methyl group; or R′ e R″, taken together, form a
group, in which A and B, identical or different from each other, are H or an alkyl group containing 1 to 4 carbon atoms; X is H, Y is OH or a carbonyl group; or X and Y, taken together, are an epoxy group,
and where a double bond may be present between positions 1 and 2. said isomerisation process being characterised by the fact that the organic base contains a diazoimino group and the reaction is carried out in an aprotic polar organic solvent.
DETAILED DESCRIPTION OF THE INVENTION
The present process allows the obtainment of 6-fluoro substituted pregnane derivatives of formula (I) in the form of 6&agr;-enriched isomeric mixtures with a 6&agr;/6&bgr; ratio higher than 95:5, through a simple basic isomerisation that yields the final product starting from pure isomer 6&bgr; or from mixtures with any 6&agr;/6&bgr; ratio. In the process according to the present invention preferred are the pregnane derivatives of formula (I) above reported wherein X and Y, taken together, are an epoxy group.
The 6&agr;/6&bgr; ratio of the final product was determined by NMR analysis and was found to be higher than 95:5.
Compared with the processes of the prior art, the reaction of the present invention is surprisingly advantageous because, under mild reaction conditions and within much shorter reaction times, it gives high-purity 6&agr;-fluorosteroids of formula (I) in high yields.
According to the present invention, the starting compound is caused to react with an organic base containing a diazoimino group, selected e.g. from the group consisting of 1,8-diazabicyclo[5.4.0]undec-7-ene(1,5-5)(DBU), 1,5-diazabicyclo[4.3.0]non-5-ene (DBN), and 1,1,3,3-tetramethylguanidine.
According to a preferred embodiment of the present process the organic base used is 1,8-diazabicyclo[5.4.0]undec-7-ene(1,5-5)(DBU).
Preferably the molar ratio between the organic base and the pregnane derivative of formula (I) ranges between 1:1 and 2:1, and more preferably is 1.3:1.
The solvent used in the present isomerisation process is any aprotic polar organic solvent; furthermore, to obtain the advantages described above, also solvents in the non-anhydrous form may be used.
According to a preferred embodiment of the present invention, the reaction solvent used is selected from the group consisting of dimethylformamide, tetrahydrofuran, acetone and acetonitrile.
The process of the invention may be carried out at room temperature, generally at a temperature ranging from 0 to 50° C.
According to the present invention, the reaction times range between 3 and 48 hrs. The following examples are conveyed by way of indication, not of limitation, of the present invention.
REFERENCES:
patent: 3681410 (1972-08-01), Crabbe et al.
patent: 4036831 (1977-07-01), Loken et al.
patent: 4340538 (1982-07-01), Shephard
Cainelli Gianfranco
Contento Michele
Da Col Marco
Sandri Sergio
Umani-Ronchi Achille
Badio Barbara P.
Farmabios S.r.L
Hedman & Costigan ,P.C.
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