Organic compounds -- part of the class 532-570 series – Organic compounds – Carboxylic acids and salts thereof
Reexamination Certificate
2002-02-25
2003-06-10
Barts, Samuel (Department: 1621)
Organic compounds -- part of the class 532-570 series
Organic compounds
Carboxylic acids and salts thereof
C562S554000
Reexamination Certificate
active
06576790
ABSTRACT:
The present invention generally relates to the pharmaceutical chemistry field.
More particularly, the invention relates to process for the preparation of 1-(aminomethyl)-1-cyclohexaneacetic acid, also known under the name gabapentin, having the following chemical structure:
Gabapentin is an active ingredient used in the treatment of various cerebral diseases, such as epilepsy, hypokinesia, cranial traumas and the like and is the object of U.S. Pat. No. 4,024,175 and U.S. Pat. No. 4,087,544.
A number of processes for preparation of gabapentin are reported in literature; U.S. Pat. No. 4,024,175, for example, discloses some preparation methods starting from cyclohexyl-1,1-diacetic acid.
All the prior art processes yield, however, gabapentin hydrochloride, which has then to be transformed into the free amino acid by treatment with a basic ion exchanger followed by crystallization from an ethanol/ether mixture.
U.S. Pat. No. 4,894,476 discloses a process for the transformation of gabapentin hydrochloride into the free amino acid, which comprises passing an hydrochloride aqueous solution on a ion exchange resin column with use of large water volumes.
Due to the high water solubility of unsalified gabapentin, large water volumes have to be evaporated off in order to recover said compound, operating at low temperatures to prevent the formation of lactams. This makes said process hardly convenient from the industrial point of view.
Alternative methods have been suggested to overcome said drawbacks, which methods avoid the formation of the hydrochloride or any other salt. Examples of said methods can be found in U.S. Pat. No. 5,132,451, U.S. Pat. No. 5,095,148 e U.S. Pat. No. 5,068,413 and they comprise the formation of a cyanic derivative, which is then hydrogenated under drastic conditions to give the free amino acid.
These methods, however, involve the use of hydrocyanic acid derivatives, which makes them industrially impractical.
In a recent patent application, WO-A-98/28255, a novel process for the preparation of the gabapentin starting from the corresponding hydrochloride is described, which allows to solve the problems of the prior art processes, in particular U.S. Pat. No. 4,894,476, connected with the need for evaporating large water volumes at low temperatures to recover free gabapentin.
Said process comprises the following steps:
liberation of gabapentin hydrochloride from inorganic salts from the synthesis, by solubilization of gabapentin hydrochloride in organic solvents in which the inorganic salts are insoluble, followed by filtration and evaporation of the solvent;
displacement of HCl with amines, such as tributylamine, triethylamine and the like, in a solvent in which the hydrochlorides of said amines are soluble but free gabapentin is not soluble, which therefore precipitates in the crystalline form III;
conversion of gabapentin form III into gabapentin form II.
The present invention aims at providing a process for the preparation of free gabapentin starting from gabapentin hydrochloride, which would overcome the drawbacks mentioned above connected with the process of U.S. Pat. No. 4,894,476, according to alternative procedures to those suggested in WO-A-98/28255.
Said problem is solved, according to the invention, by a process which comprises the steps of:
preparing a gabapentin hydrochloride aqueous solution;
adjusting the pH of said solution to or about to gabapentin isoelectric point by addition of a basic compound comprising a monovalent anion;
diafiltering said solution through a membrane highly selective for organic compounds with molecular weight higher than 150 and poorly selective for inorganic monovalent ions, to separate said solution into an aqueous permeate containing chloride ions and a retentate containing unsalified gabapentin substantially free from chloride ions;
concentrating said retentate by increasing the pressure exerted on said membrane to obtain a concentration of unsalified gabapentin in the retentate not lower than 5%;
evaporating the retentate under reduced pressure and at T°<35°;
precipitating gabapentin by addition of an alcohol.
The process according to the invention conveniently comprises a further crystallization step of the precipitated unsalified gabapentin with methanol.
The above basic compound is preferably selected from the group consisting of alkali metal and ammonium hydroxides.
The pH of the starting aqueous solution is preferably adjusted to 7.14.
During the diafiltration step, the pressure exerted on the membrane is 10-16 bars, preferably 14-15 bars.
During the concentration step, the concentration of unsalified gabapentin in the retentate is preferably brought to an about 8-10% w/v value. During said concentration step, pressure increases gradually to reach a value of about 18-22 bars.
During the diafiltration and of concentration steps, temperature is preferably kept below 25° C.
The diafiltration step is preferably carried out with the aid of nanofiltration multilayer composite membranes, such as those sold by PERMEARE S.r.l. (Italy), in particular the membrane named ACN2540HS. Such are membranes have a rejection rate of inorganic salts lower than or equal to 50% and a rejection rate of organic molecules higher than or equal to 96%. Suitable composite membranes have a thin polyamide material coating as the active layer. Other suitable membranes for the process of the invention are those made of polysulfonic resins, nylon, cellulose acetate, polypropylene and polyvinylydene fluoride (PVDF).
The process according to the invention solves the problems mentioned above with reference to the prior art processes based on the use of ion exchange resins, by means of a simple technique which requires no drastic operative conditions, such as high temperatures, which would cause the undesired formation of the gabapentin lactam.
REFERENCES:
patent: 4024175 (1977-05-01), Satzinger et al.
patent: 4960931 (1990-10-01), Butler et al.
patent: 5491259 (1996-02-01), Grierson et al.
patent: 0 340 677 (1989-11-01), None
patent: WO 98/28255 (1998-07-01), None
Caraccia Nicola
Giordani Cristiana
Tenconi Franco
Bioindustria Laboratorio Italiano Medicinali S.p.A.
Zucker Paul A.
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