Organic compounds -- part of the class 532-570 series – Organic compounds – Unsubstituted hydrocarbyl chain between the ring and the -c-...
Reexamination Certificate
2000-01-19
2001-02-20
Shah, Mukund J. (Department: 1624)
Organic compounds -- part of the class 532-570 series
Organic compounds
Unsubstituted hydrocarbyl chain between the ring and the -c-...
C540S476000
Reexamination Certificate
active
06191272
ABSTRACT:
BACKGROUND OF THE INVENTION
1. Field of the Invention
The invention relates to a process for the preparation of endo-nortropine using 8-benzyl-nortropan-3-one perchlorate as the intermediate, as well as the latter salt.
2. Description of the Related Art
The prior art discloses numerous processes for the preparation of endo-nortropine and the latter substance itself. Endo-nortropine is the key product for the production of important azoniaspironortropanol esters, which are used as pharmaceuticals, particularly spasmolytics (cf. particularly German patent 1 194 422), whereas 8-benzyl-nortropan-3-one perchlorate is not known.
Hitherto only the picrate, hydrochloride and hydrobromide of 8-benzyl-nortropan-3-one are known, but for which no further use possibilities exist. 8-benzyl-nortropan-3-one is also mentioned in EP-A1-42 705 as an intermediate in the production of azabicycloalkane derivatives, whose pharmacological activity is described.
In principle, there are three known process procedures for the preparation of endo-nortropine, namely the saponification of tropane alkaloids, such as nor-1-hyoscyamine, convolvine and convolamine. However, the saponification of three alkaloids is not profitable, because the starting products are rare and expensive. Thus, as is known tropine is oxidatively demethylated in order to prepare endo-nortropine. In addition, photochemical methods for the demethylation and demethylation with ethyl chloroformates are known, cf. e.g. DE-A1-35 46 218. However, it is a disadvantage of said dealkylation process that expensive and in part environmentally prejudicial chemicals have to be used as starting products, which in turn can only be produced with difficulty. The known processes mainly also operate with overpressure and are usually not stereoselective.
SUMMARY OF THE INVENTION
Therefore the problem of the present invention is to provide an alternative process for the preparation of endo-nortropine, which can be simply and rapidly economically performed and which is also environmentally friendly. A further aim is to be able to obviate the need for overpressure process stages, whilst still operating as stereoselectively as possible. This is intended to permit an economic preparation of trospium chloride.
Surprisingly this problem is solved by the aforementioned process, which is based on a two-stage treatment of 8-benzyl-nortropan-3-one perchlorate with catalytically activated hydrogen, the starting product being initially prehydrogenated in aqueous suspension at atmospheric pressure and ambient temperature with a palladium catalyst, at the end of the reaction the catalyst is recovered by filtration, the filtrate is passed over an anion exchanger and the now alkaline reacting solution is rendered turbulent with hydrogen activated by Raney nickel at atmospheric pressure and ambient temperature and at 1000 to 1500 revolutions per minute.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
Of particular significance for the present invention is the fact that as a novel substance 8-benzyl-nortropan-3-one perchlorate is initially prepared as an intermediate by the per se known Robinson-Schöpf method and subsequent addition of perchlorate acid and precipitation of the corresponding perchlorate salt.
The perchlorate is then treated in aqueous suspension and at ambient temperature of preferably 20° C. under normal pressure with catalytically activated hydrogen. A ready-to-use 10 palladium catalyst on activated carbon is used as the catalyst.
In the said process the benzyl group is split off and the substrate reacted to 3-nortropanone, which then dissolves as a perchlorate acid salt.
Following the filtering off of the catalyst the aqueous solution is passed over a strong basic anion exchanger of the styrene-divinyl benzene type having the counterion OH
−
.
The now basic, aqueous 3-nortropanone solution, on adding Raney nickel catalyst, is now hydrogenated with hydrogen to endo-nortropine.
The aqueous solution is then freed from the catalyst by filtration and carefully concentrated in vacuo. What is left is a crude endo-nortropine which, if necessary, is recrystallized from acetone.
Compared with the prior art, the advantages of the process according to the invention can be described as follows:
The process for the preparation of endo-nortropine obviates the need for the complicated dealkylation process, no matter what method is used and where in part expensive and in part environmentally prejudicial chemicals are used.
Working takes place throughout in aqueous solutions and the auxiliary products such as catalysts and ion exchangers can easily be separated and regenerated.
In the catalytic transfer of hydrogen hydrogenation takes place at ambient temperature and without pressure in both stages. This is particularly surprising, because all known processes operate with an overpressure.
None of the known processes is based on 8-benzyl-nortropan-3-one perchlorate for the purpose of producing 3-nortropanone.
As a result of the salt formation to the perchlorate, the tropane substances are extremely stable during processing.
Hereinafter preferred examples for the preparation of 8-benzyl-nortropan-3-one perchlorate and the endo-nortropine are described relative to the following formula flow diagrams of the inventive process.
REFERENCES:
patent: 1194422 (1965-06-01), None
patent: 3546218 (1987-07-01), None
patent: 0042705 (1981-12-01), None
K.Nador et al, “N-AlkyInortrop. & their HO”Arzneimittle-Forsch. 12, 305-9(1962)/CAOLD;CA58:3384d, Jan. 1962.
K. Nader et al. Chemical Abstracts, vol. 58, No. 4, 1963.
Sachse Rolf
Schaupp Albert
Dr. Robert Pfleger Chemische Fabrik, GmbH
Patel Sudhaker B.
Roberts & Mercanti LLP
Shah Mukund J.
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