EP1404681A1 - Procede de preparation de derives de tetrahydrothieno 3,2-c]pyridine - Google Patents
Procede de preparation de derives de tetrahydrothieno 3,2-c]pyridineInfo
- Publication number
- EP1404681A1 EP1404681A1 EP02745008A EP02745008A EP1404681A1 EP 1404681 A1 EP1404681 A1 EP 1404681A1 EP 02745008 A EP02745008 A EP 02745008A EP 02745008 A EP02745008 A EP 02745008A EP 1404681 A1 EP1404681 A1 EP 1404681A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- formula
- compound
- thienyl
- methyl
- chlorophenylglycinate
- 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- Withdrawn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
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
Definitions
- the present invention refers to a new process for the synthesis of tetrahydrothieno[3,2-c]pyridine derivatives, in particular 5-o-chlorobenzyl-4,5,6,7- tetrahydothieno[3,2-c]pyridine and racemic or enantiomerically enriched methyl ⁇ -(4,5,6,7-tetrahydro-5-thieno[3,2-c]pyridyl)-o-chlorophenylacetate, and intermediates thereof.
- Structure 1 known as Ticlopidine, is an antithrombotic drug with platelet aggregation inhibiting properties as disclosed in US 4,051,141 and US 4,127,580.
- the dextrorotatory enantiomer (Structure 2), bearing the International Non- Proprietary name (INN) Clopidogrel, has the absolute configuration S and is a commercially significant drug with excellent antithrombotic and platelet aggregation inhibiting activity as disclosed in US 4,847,265.
- the enantiomerically enriched compound can be prepared by means of enantioselective synthesis or starting from a racemic mixture of enantiomers in conjunction with a resolution process.
- a known process for the preparation of racemic Clopidogrel 2 is based on the nucleophilic displacement of racemic ⁇ -halophenylacetic acid derivatives 3 by 4,5,6,7-tetrahydrothieno[3,2c]pyridine 4 as described in US 4,529,596 and US 5,132,435 (Scheme 1).
- the enantiomerically enriched clopidogrel is obtained through the resolution of the racemic mixture of methyl ⁇ -(4,5,6,7-tetrahydro-5-thieno[3,2- c]pyridyl)-o-chlorophenylacetate 2 with R-camphorsulfonic acid as described in US 4,847,265 and US 5,132,435.
- Racemic clopidogrel can also be prepared starting with the Strecker synthesis of ⁇ -(2-thienyl)ethylamino-o-chlorophenylacetonitrile 6 as shown in Scheme 2. Hydrolysis of the nitrile followed by esterification leads to methyl ⁇ -(2- thienyl)ethylamino-o-chlorophenylacetate 8. This in turn generates the tetrahydrothieno[3,2-c]pyridine bicyclic system by reacting with a formylating agent (e.g. paraformaldehyde) under acidic conditions. The process is disclosed in WO 98/51682, WO 98/51689 and WO 98/51681. Scheme 2
- dextrorotatory clopidogrel can be obtained starting from enantiomerically enriched (R)-sulphonyloxyacetic ester derivatives 11 and 4,5,6,7-tetrahydrothieno[3,2c]pyridine 4 as disclosed in WO 99/18110.
- the same publication documents the reaction of the methyl (R)- ⁇ -tosyloxy-o- chlorophenylacetate 11 with 2-(2-thienyl)ethylamine 12 to result in methyl (S)- ⁇ - (2-(2-thienyl)ethylamino-o-chlorophenylacetate 8. This in turn generates enantiomerically enriched clopidogrel by reaction with a formylating reagent under acidic conditions. (Scheme 4). Scheme 4
- the present invention provides an improved process for the preparation of a racemic and enantiomerically enriched 4,5,6,7-tetrahydrothieno[3,2-c]pyridines of general formula I
- the compound of the general formula I is prepared (Scheme 6) by reducing the compound of formula II with suitable reducing agents, known to those skilled in the art, to a mixture of diastereoisomeric compounds of formula III which are reacted with formaldehyde or any chemical equivalent thereof to yield the compound of formula IV.
- the compound of formula IV is further rearranged in a suitable solution to produce the compound of formula V which upon reduction (by a suitable reducing agent) provides an enantiomerically enriched or racemic mixture of tetrahydrothieno[3,2-c]pyridine of formula I.
- X can be hydrogen, carboxyl, alkoxycarbonyl, aryloxycarbonyl, nitrile or carbamoyl of formula
- Ri and R 2 can be individually or simultaneously hydrogen, alkyl or part of a heterocyclic structure; Y can be hydroxyl, alkanoyloxy, aroyloxy, as well as carbonate derivatives of formula -OCOOR3 or carbamate derivatives of formula -
- R3 can be substituted or unsubstituted alkyl or aryl
- R4 and R5 can be individually or simultaneously substituted or unsubstituted alkyl, aryl or cycloalkyl
- Z can be hydrogen, halogen, alkyl, aryl, aryloxy or alkoxy group.
- the compound of formula II in its racemic or enantiomerically enriched form is obtained through the reaction of a racemic or enantiomerically enriched primary amine of general formula
- LG is a leaving group such as halogen, arysulphonyloxy, aryloxy, sulphonate, alkyloxy and its derivatives or activated aryl.
- Other obvious synthetic chemical equivalents of the phenylglycine counterpart, such as various salts as well as aliphatic or aromatic esters, amides, nitrile or free carboxyl group are also included in the present invention.
- the reaction may be carried out in an aromatic solvent (e.g. toluene and the like), polar aprotic solvents (e.g.
- polar protic solvents e.g. methanol, ethanol, propanol, butanol, n-butanol, isobutanol, n-propanol, isopropanol, and the like
- polar protic solvents e.g. methanol, ethanol, propanol, butanol, n-butanol, isobutanol, n-propanol, isopropanol, and the like
- the process according to one aspect of the present invention improves the previously reported synthesis of ticlopidine and extends the scope of the synthetic sequence to the structurally related clopidogrel.
- 2-bromoacetylthiophene 18 and methyl o- chlorophenylglycinate 19 can be prepared according to known literature procedures as reported in Bull. Chem. Soc. Jpn. 60, 1159 and J. Am. Chem. Soc. 1999, 121, 4284 respectively. Racemic or enantiomerically enriched methyl 2-o- chlorophenylglycine 19 reacts with 2-bromoacetylthiophene 18 in the presence of a base which acts as an acid scavenger.
- novel compounds of formulae 22, 21 and 20 which can be made as a racemic or diasteromeric mixture with set configuration at the carbon adjacent to the nitrogen, as well as its enantiomers either as free base or its salts with Bronstead and Lewis acids.
- Specific compounds arising from the preparation of formulae 22, 21 and 20 include:
- Methyl N-2-(2-thienyl)-2-oxoethyl)-o-chlorophenylglycinate (20) (5.4 g, 16.6 mmol) was dissolved in methanol and treated with sodium borohydride (0.69 g, 18.3 mmol). The reaction is allowed to stir at room temperature over the night and treated with 2N hydrochloric acid to acidic pH. Most of the methanol is evaporated under vacuum and then the remaining aqueous solution partitioned between methylene chloride and 5% sodium hydroxide.
- Methyl N-(2-(2-thienyl)-2-hydoxyethyl)-2-o-chlorophenylglycinate (21) (2.5 g, 7.6 mmol) was dissolved in ethanol and treated with 37% formaline (1.85 g, 22.8 mmol), then heated at 40°C over the night under nitrogen. The ethanol is evaporated under vacuum and the residual water was removed by azeotropic distillation with toluene to provide 2.3 g of desired product as a mixture of diastereoisomers.
- Methyl N-(2-(2-thienyl)-2-oxoethyl)-2S-o-chlorophenylglvcinate (20) Methyl(S)-o-chlorophenylglycinate (6.5g, 0.032 mol) was dissolved in toluene and treated with potassium carbonate (6.62 g, 0.048 mol) and 2- bromoacetylthiophene (7.2 g 0.035) mol. DMF was added to the reaction mixture and the content was stirred under nitrogen at room temperature. When the whole quantity of aminoester is consumed, the reaction mixture is partitioned between toluene and water and the aqueous layer back extracted several times with toluene. The combined organic phase is extracted with brine, then with 2 N HC1.
- the aqueous phase was treated with sodium bicarbonate solution to basic pH and extracted with toluene. After the concentration of the toluene solution one obtains
- Methyl N-(2-(2-thienyl)-2-oxoethyl)-2S-o-chlorophenylglycinate (20) (6.2 g, 19 mmol) was dissolved in methanol and treated in portions with sodium borohydride (0.79 g, 21 mmol) to keep the temperature below 10°C. The reaction is allowed to stir at room temperature for two hours and treated with 2N hydrochloric acid to acidic pH. Most of the methanol is evaporated under vacuum and then the remaining aqueous solution partitioned between methylene chloride and aqueous sodium bicarbonate.
- Methyl N-(2-(2-thienyl)-2-hydoxyethyl)-2S-o-chlorophenylglycinate (21 ) was dissolved in ethanol and treated with 37% formaline (4.08 g, 50.4 mmol), then heated at 40°C under nitrogen. After four hours, the ethanol is evaporated under vacuum and the residual water was removed by azeotropic distillation with toluene to provide 5.6 g of desired product as a mixture of diastereoisomers.
Abstract
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA 2352520 CA2352520C (fr) | 2001-07-06 | 2001-07-06 | Synthese de derives de tetrahydrothieno-[3,2-c]-pyridine |
CA2352520 | 2001-07-06 | ||
PCT/CA2002/001017 WO2003004502A1 (fr) | 2001-07-06 | 2002-07-05 | Procede de preparation de derives de tetrahydrothieno[3,2-c]pyridine |
Publications (1)
Publication Number | Publication Date |
---|---|
EP1404681A1 true EP1404681A1 (fr) | 2004-04-07 |
Family
ID=4169420
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP02745008A Withdrawn EP1404681A1 (fr) | 2001-07-06 | 2002-07-05 | Procede de preparation de derives de tetrahydrothieno 3,2-c]pyridine |
Country Status (3)
Country | Link |
---|---|
EP (1) | EP1404681A1 (fr) |
CA (1) | CA2352520C (fr) |
WO (1) | WO2003004502A1 (fr) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100678287B1 (ko) | 2005-06-23 | 2007-02-02 | 한미약품 주식회사 | 클로피도그렐의 제조방법 및 이에 사용되는 중간체 |
US20070191609A1 (en) * | 2006-02-13 | 2007-08-16 | Lee Pharma Limited | Process for preparation of clopidogrel bisulphate form-1 |
PL380849A1 (pl) * | 2006-10-17 | 2008-04-28 | Adamed Spółka Z Ograniczoną Odpowiedzialnością | Krystaliczna postać racemicznego -(2-chlorofenylo)-6,7-dihydrotieno[3,2-c]pirydylo-5(4H)-octanu metylu, sposób jej wytwarzania i zastosowanie |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2424278A1 (fr) * | 1978-04-24 | 1979-11-23 | Parcor | Procede de preparation de thieno(2,3-c) et thieno(3,2-c)pyridines |
FR2530247B1 (fr) * | 1982-07-13 | 1986-05-16 | Sanofi Sa | Nouveaux derives de la thieno (3, 2-c) pyridine, leur procede de preparation et leur application therapeutique |
-
2001
- 2001-07-06 CA CA 2352520 patent/CA2352520C/fr not_active Expired - Fee Related
-
2002
- 2002-07-05 WO PCT/CA2002/001017 patent/WO2003004502A1/fr not_active Application Discontinuation
- 2002-07-05 EP EP02745008A patent/EP1404681A1/fr not_active Withdrawn
Non-Patent Citations (1)
Title |
---|
See references of WO03004502A1 * |
Also Published As
Publication number | Publication date |
---|---|
CA2352520A1 (fr) | 2003-01-06 |
WO2003004502A1 (fr) | 2003-01-16 |
CA2352520C (fr) | 2007-10-02 |
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Inventor name: MCCONACHIE, LAURA KAYE Inventor name: NAGIREDDY, JAIPAL, REDDY Inventor name: COMANITA, BOGDAN, M. Inventor name: WEERATUNGA, GAMINI Inventor name: HORNE, STEPHEN, E. |
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