US20020198391A1

US20020198391A1 - Method for the preparation of citalopram

Info

Publication number: US20020198391A1
Application number: US10/186,337
Authority: US
Inventors: Hans Petersen; Michael Rock
Original assignee: H Lundbeck AS
Current assignee: H Lundbeck AS
Priority date: 1999-12-30
Filing date: 2002-06-27
Publication date: 2002-12-26
Also published as: HUP0203840A2; NO20023150L; US7271273B2; TR200201688T2; AU1858400A; CN1211377C; CA2395733A1; JP2003519218A; EA200200728A1; MXPA02006504A; UA73336C2; EA004055B1; DE69912652D1; NO328359B1; PL355531A1; PT1246813E; DE69912652T2; ES2207312T3; IS6433A; HRP20020633A2

Abstract

The invention provides a new and improved method for the preparation of 5-cyano-phtalid, which is a key intermediate in the preparation of the antidepressant compound citalopram.

Description

This application is a continuation of International application no. PCT/DK99/00740, filed Dec. 30, 1999. The disclosure of the prior application is hereby incorporated by reference.[0001]

The present invention relates to a method for the preparation of key intermediates in the process for the preparation of the well known antidepressant drug citalopram, 1-[3-(dimethylamino)propyl]-1-(4-fluorophenyl)-1,3-dihydro-5-isobenzofurancarbonitrile.

BACKGROUND OF THE INVENTION

Citalopram is a well known antidepressant drug that has now been on the market for some years and has the following structure:

It is a selective, centrally acting serotonin (5-hydroxytryptamine; 5-HT) reuptake inhibitor, accordingly having antidepressant activities. The antidepressant activity of the compound has been reported in several publications, eg. J. Hyttel, Prog Neuro-Psychopharmacol. & Biol. Psychiat., 1982, 6, 277-295 and A. Gravem, Acta Psychiatr. Scand., 1987, 75, 478-486. The compound has further been disclosed to show effects in the treatment of dementia and cerebrovascular disorders, EP-A 474580.

Citalopram can be prepared by several disclosed methods. A method and an intermediate for the preparation of citalopram were described in U.S. Pat. No 4,650,884. Commercially useful processes are disclosed in International patent application Nos. WO 98019511, WO 98019512 and WO 98019513.

With respect to the above methods for the preparation of citalopram, the process comprising exchange of the 5-bromo group with cyano proved not to be very convenient in commercial scale, since the yield was rather low, the product was impure and, in particular, since it was difficult to separate the resulting citalopram from the corresponding 5-bromo compound.

It has now been found that in a new process for the preparation of citalopram, this key intermediate may be obtained in a high yield as a very pure product by a new catalytic process in which a halogen or a group of the general formula CF ₃—(CF₂)_n—SO₂— wherein n is any suitable whole number between 0 and 4, situated in the 5-position of a 3-H-isobenzofuran-1-one, is exchanged with a cyanide group. By obtaining the correct cyanide substitution at an early stage of the citalopram synthesis, the extensive work up of the old cyanide exchange processes of the previous described processes is avoided. The intermediates of the presently described process are easily purified and obtained in very high yields. The key intermediate is then subjected to two successive Grignard reactions, i.e. with 4-fluorophenyl magnesium halogenide and N.N-dimethylaminopropyl magnesium halogenide, respectively, whereby citalopram is obtained.

The preparation of the key intermediate of the invention is described earlier in J.Chem. Soc., 1931, 867 and by Tiroflet, J. in Bull. Soc. Sci. Betagne, 26, 35, 1951. The process for preparation of the compound is a three step synthesis starting from 5-nitro-phtalimide with low yields, especially in the last step of the synthesis.

SUMMARY OF THE INVENTION

Accordingly, the present invention relates to a novel method for the preparation of an intermediate in the preparation of citalopram comprising reacting a compound of Formula IV

wherein R′ is Cl, Br, I or a group of the formula CF ₃—(CF₂)_n—SO₂—, wherein n is 0-4, with a cyanide source in the presence or absence of a catalyst, whereby 5-cyano-isobenzofuran-1-one is obtained. This intermediate product can be further reacted to citalopram as described above.

The reaction of IV to 5-cyanophtalide may be carried out in more convenient solvents, at a low temperature and at a minimal excess of CN ⁻. The process has environmental advantages in that it only uses small amounts of heavy metals.

The cyano sources may conveniently be selected from a group consisting of cyanide sources such as (R″ ₄N)CN wherein each R″ represents C_1-8-alkyl optionally two R″ together with the nitrogen form a ring structure; NaCN, KCN, Zn(CN)₂or Cu(CN).

The reaction of the present invention is performed in the presence or absence of a catalyst. The catalysts are i.e. Ni (0), Pd(0) or Pd(II) catalysts as described by Sakakibara et. al. in Bull. Chem. Soc. Jpn., 61, 1985-1990, (1988). Preferred catalysts are Ni(PPh₃)₃or Pd(PPh₃)₄, or Pd(PPh)₂Cl₂.

In a particularly preferred embodiment, a Nickel(0) complex is prepared in situ before the cyanide exchange reaction by reduction of a Nickel(II) precursor such as NiCl ₂or NiBr₂by a metal, such as zinc, magnesium or mangan in the presence of excess of complex ligands, preferably triphenylphosphin.

The Pd or Ni-catalyst is conveniently used in an amount of 0.5-10, preferably 2-6, most preferably about 4-5 mol %.

Cu ⁺ and Zn²⁺ may be added to the reaction mixture in substoichiometric amounts and may function as recycleable cyanide sources, which receives the cyanide from other cyanide sources such as NaCN or KCN. Substoichiometric amounts of Cu⁺ and Zn²⁺, respectively, means 1-20%, preferably 5-10%.

The reactions may be performed in any convenient solvent as described in Sakakibara et. al. in Bull. Chem. Soc. Jpn., 61, 1985-1990, (1988). Preferred solvents are acetonitrile, ethylacetate, THF, DMF or NMP;

In one aspect of the invention, a compound of Formula IV wherein R is Cl is reacted with NaCN in the presence of a Ni(PPh ₃)₃which is preferably prepared in situ as described above.

In another aspect of the invention, a compound of formula IV, wherein R is Br or I, is reacted with KCN, NaCN, CuCN or Zn(CN) ₂in the presence of Pd(PPh₃)₄. In a particular aspect of the invention, substoichiometric amounts of Cu(CN) and Zn(CN)₂are added as recycleable cyanide sources.

In another aspect of same invention, the Cu(CN) is the cyanide source and without catalyst. In a preferred embodiment of this invention, the reaction is performed at elevated temperature.

In a particular aspect of this invention, the reaction is performed as a neat reaction i.e. without added solvent.

In another aspect of the invention, the reaction is performed in an ionic liquid of the general formula R ₄N⁺, X⁻, wherein R are alkyl-groups or two of the R groups together form an ring and X⁻ is the counterion. In one embodiment of the invention, R₄N⁺X⁻ represents

In another particular aspect of this invention, the reaction is conducted with apolar solvents such as benzene, xylene or mesitylene and under the influence of microwaves by using i.e. Synthewave 1000™ by Prolabo. In a particular aspect of this invention, the reaction is performed without added solvent.

The temperature ranges are dependent upon the reaction type. If no catalyst is present preferred temperatures are in the range of 100-200° C. However, when the reaction is conducted under the influence of microwaves the temperature in the reaction mixture may raise to above 300° C. More preferred temperature ranges are between 120-170° C. The most preferred range is 130-150° C.

If catalyst is present, the preferred temperature range is between 0 and 100° C. More preferred are temperature ranges of 40-90° C. Most preferred temperature ranges are between 60-90° C.

Other reaction conditions, solvents, etc. are conventional conditions for such reactions and may easily be determined by a person skilled in the art.

EXAMPLES

The invention is further illustrated by the following examples. [0027]

Experimental

Example 1

[0028]
A mixture of Zn(CN)[0029] ₂(2.4 g, 0.02 mol) and 5-bromo-3H-isobenzofuran-1-one (4.2 g, 0.02 mol) in DMF (80 mL) were stirred at room temperature under an atmosphere of argon for 30 minutes. Then dissolved oxygen was removed by bubbling argon through the reaction mixture for 10 minutes before the addition of tetrakis(triphenylphosphine)palladium (0) (1.2 g, 0.00096 mol,). Then the reaction was heated at 75° C. for 3 hrs, and then the solvent was removed under reduce pressure and the residue poured into water (150 mL). Filtration and followed by drying in vacuo give the crude 5-cyano-3H-isobenzofuran-1-one (2.8 g) (HPLC 95%). An analytical sample was obtained by recrystalisation from acetic acid.

Example 2

A mixture of Zn(CN)[0030] ₂(0.3 g, 0.00256 mol), NaCN (1 g, 0,02 mol) and 5-bromo-3H-isobenzofuran-1-one (4.2 g, 0.02 mol) in DMF (80 mL) were stirred at room temperature under an atmosphere of argon for 30 minutes. Then dissolved oxygen was removed by bubbling argon through the reaction mixture for 10 minutes before the addition of tetrakis(triphenylphosphine)palladium (0) (1.2 g, 0.00096 mol). Then the reaction was heated at 75° C. for 3 hrs, and then the solvent was removed under reduce pressure and the residue poured into water (150 mL). Filtration and followed by drying in vacuo give the crude 5-cyano-3H-isobenzofuran-1-one (2.7 g) (HPLC 94%). An analytical sample was obtained by recrystalisation from acetic acid.

Example 3

A mixture of 5-bromo-3H-isobenzofuran-1-one (4.2 g, 0.02 mol) and Cu(CN)[0031] ₂(2.3 g, 0.02 mol) in NMP (60 mL) were stirred at 140° C. for 3hrs. Then solvent was removed by distilation under reduced pressure and the residue was refluxed in water (150 mL) for 10 minutes and allowed to cool to room temperature. Filtration and followed by drying in vacuo give the crude 5-cyano-3H-isobenzofuran-1-one (2.1 g) (HPLC 97%). An analytical sample was obtained by recrystalisation from acetic acid.

Example 4

A mixture of Zn(CN)[0032] ₂(2.4 g, 0.02 mol) and 5-iodo-3H-isobenzofuran-1-one (5.24 g, 0.02 mol) in DMF (80 mL) were stirred at room temperature under an atmosphere of argon for 30 minutes. Then dissolved oxygen was removed by bubbling argon through the reaction mixture for 10 minutes before the addition of tetrakis(triphenylphosphine)palladium (0) (1.2 g, 0.00096 mol). Then the reaction was heated at 75° C. for 3 hrs, and then the solvent was removed under reduce pressure and the residue poured into water (150 mL). Filtration and followed by drying in vacuo give the crude 5-cyano-3H-isobenzofuran-1-one (2.4 g) (HPLC 93%). An analytical sample was obtained by recrystalisation from acetic acid.

Example 5

Under a nitrogen atmosphere, a mixture of NiCl[0033] ₂(0.2 g, 0.0015 mol) and triphenylphosphine (1.6 g, 0.0061 mol) in acetonitrile (80 ml)was heated at reflux for 45 minutes. After cooling to room temperature, zinic powder was added (0.39 g, 0.006 mol) at stirred for 15 minutes before a solution of 5-chloro-3H-isobenzofuran-1-one (3.4 g, 0.02 mol) in THF (40 mL) was added. After stirring for a further 10 minutes, NaCN (1.1 g, 0.021 mol) was added and the reaction heated at 70° C. for 3 hrs, cooled, diluted with acetonitrile (50 mL), and then filtered through celite. The filtrate was concentrated under reduced pressure and the residue was refluxed in water (150 mL) for 10 minutes and allowed to cool to room temperature. Filtration and followed by drying in vacuo give the crude 5-cyano-3H-isobenzofuran-1-one (2.5 g). An analytical sample was obtained by recrystalisation from acetic acid.

Claims

1. A method for the preparation of a compound of the formula

comprising reacting an isobenzofuran-1-one of the formula

wherein R′ is a halogen or CF₃—(CF₂)_n—SO₂—, wherein n is 0-7, with a cyanide source optionally in the presence of a catalyst.

2. The process of claim 1 wherein R′ is Cl, Br or I.

3. The process of claim 1 wherein R′ is CF₃—(CF₂)_n—SO₂—, wherein n is 0, 1,2,3 or 4.

4. The process of claim 1, wherein the cyanide source is selected from (R″₄N)CN wherein each R″ is C_1-8-alkyl, optionally two R″ together with the nitrogen form a ring structure; KCN, NaCN, Zn(CN)₂or CuCN or combinations thereof.

5. The process of claim 1, wherein Zn²⁺ or Cu⁺ are added in substoichiometric amounts in combination with another cyanide source.

6. The process of claim 1, wherein the catalyst is selected from Ni(PPh₃)₃, Pd(PPh₃)₄, Pd(dba)₃or Pd(PPh)₂Cl₂.

7. The process of claim 1, wherein a 5-chloro-isobenzofuran-1-one is subjected to NaCN in the presence of Ni-catalyst.

8. The process of claim 7 wherein the Ni-catalyst is Ni(PPh₃)₃prepared in situ by subjecting NiCl₂to a reducing agent, in the presence of PPh₃.

9. The process of claim 8 wherein the reducing agent is Zn.

10. The process of claim 1, wherein a 5-bromo- or 5-iodo-isobenzofuran-1-one is subjected to KCN, NaCN, Zn(CN)₂, or CuCN or combinations thereof in the presence of Pd(PPh₃)₄.

11. The process according to claim 1, 2 and 4 wherein a 5-bromo- or 5-iodo-isobenzofuran-1-one is subjected to KCN, NaCN, Zn(CN)₂, or CuCN or combinations thereof and the process is performed without catalysts.

12. The process of claim 10 wherein the reaction is performed in an ionic liquid of the general formula R₄N⁺X⁻ wherein each R represents C_1-8-alkyl optionally two R″ together with the nitrogen form a ring.

13. The process of claim 10 wherein the reaction is performed under the influence of microwaves in an apolar solvent.

14. The process according to claim 10 or claim 12 wherein the reaction is performed as a neat reaction.