Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
  • C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
  • C07D417/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
  • C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
  • C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
  • C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
  • C07D277/34—Oxygen atoms
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
  • C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
  • C07D417/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing aromatic rings
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
  • C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
  • C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
  • C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings

Definitions

• This invention relates to a novel process and in particular to a process for preparing certain substituted thiazolidinedione derivatives and to certain intermediates to the substituted thiazolidinedione derivatives
• a a represents a substituted or unsubstituted aromatic heterocyclyl group
• R a represents a hydrogen atom, an alkyl group, an acyl group, an aralkyl group, wherein the aryl moiety may be substituted or unsubstituted, or a substituted or unsubstituted aryl group;
• R D and R c each represent hydrogen or R D and R c together represent a bond;
• a D represents a benzene ring having in total up to five substituents; and
• n' represents an integer in the range of from 2 to 6.
• EP 0306228 also discloses a process for reducing the compounds of formula
• the present invention provides a process for preparing a compound of formula (I):
• T represents a substituted or unsubstituted aryl group and T ⁇ is O or S; which process comprises, reducing a compound of formula (II):
• T and T* are as defined in relation to formula (I), with a complex hydride reducing agent or a source of a complex hydride reducing agent; and thereafter, as required, preparing a pharmaceutically acceptable salt or a pharmaceutically acceptable solvate of the compound of formula (I) or a tautomeric form thereof.
• Suitable complex hydride reducing agents include borohydride reducing agents and aluminium hydride reducing agents.
• Suitable borohydride reducing agents include diborane and metal borohydrides.
• a suitable metal borohydride is an alkali metal borohydride, such as a lithium, sodium or potassium borohydride, especially lithium or potassium.
• Borohydrides include unsubstituted and substituted borohydrides.
• Suitable substituted borohydrides include borohydrides with up to three substituents on boron selected from such as alkyl and phenyl groups.
• Suitable alkyl groups are C ⁇ _6 alkyl groups, such as ethyl and, especially, butyl groups. Particular butyl groups are sec and tert butyl groups.
• Particular borohydride reducing agents are those which comprise the trihydroborane, triethylborane, tributylborane or triphenylborane moiety.
• Favoured borohydride reducing agents include lithium tri-sec-butyl borohydride, potassium tri-sec-butyl borohydride/lithium chloride, sodium tri-sec- butyl borohydride, potassium triphenylborohydride, lithium triethylborohydride, lithium borohydride and sodium borohydride.
• One preferred borohydride reducing agent is lithium borohydride.
• One preferred borohydride reducing agent is lithium tri-sec-butyl borohydride.
• a base such as pyridine a substituted pyridine, quinoline, a substituted quinoline, a secondary or tertiary amine, such as piperidine or triethylamine, or a phosphine such as triphenylphosphine.
• the said base is used as a solvent or co-solvent for the reaction.
• a preferred base is pyridine.
• a suitable aluminium hydride reducing agent is lithium aluminium hydride.
• reaction conditions for the reduction reaction are the appropriate conditions dictated by the nature of the complex hydride reducing agent chosen:
• suitable solvents include alkanols, such as methanol and ethanol, tetrahydrofuran and pyridine or mixtures thereof.
• reducing reagent is an alkali metal borohydride
• a preferred solvent is pyridine/tetrahydrofuran.
• a preferred solvent is tetrahydrofuran.
• the borohydride reduction is carried out at a temperature which provides a suitable rate of formation of the required product, usually at ambient or an elevated temperature, suitably at an elevated temperature, preferably above 50°C, for example 65°C and conveniently at the reflux temperature of the required solvent.
• the reactants are mixed at ambient temperature and the reaction mixture is heated at the reflux temperature of the solvent.
• suitable solvents include aprotic solvents such as tetrahydrofuran.
• the aluminium hydride reduction is carried out at a temperature which provides a suitable rate of formation of the required product, usually at low to ambient temperature, for example a temperature in the range of from -10 to 10°C, suitably in the range of from -5 to 0°C.
• the present invention provides a process for preparing a compound of the above defined formula (III), which process comprises, reducing a compound of the above defined formula (II) with a metal hydride reducing agent, preferably a borohydride reducing agent, preferably wherein the reaction is carried at low temperature, suitably below ambient temperature, for example between 0° and 5°C; and thereafter, as required, preparing a salt or a solvate of the compound of formula (III).
• a metal hydride reducing agent preferably a borohydride reducing agent
• a preferred reducing agent for preparing a compound of formula (III) is lithium or potassium (also known as “L-selectride” or “K- selectride”), preferably lithium tri-seobutylborohydride.
• the present invention further provides a compound of the above defined formula (III) or a tautomeric form thereof, or salt thereof, or a solvate thereof, which compound is useful as an intermediate.
• the present invention further comprises a process for converting the above defined compound of formula (III) into the above defined compound of formula (I), which process comprises heating the compound of formula (III), suitably in a solvent, and thereafter as required preparing a pharmaceutically acceptable salt or a pharmaceutically acceptable solvate of the compound of formula (I).
• Suitable solvents for the said conversion of the compound of formula (III) into compound (I) include those mentioned above for the preparation of the compound of formula (III).
• the reduction of the compound of formula (II) to provide a compound of formula (I), especially when employing borohydride reducing agents, is preferably carried out at a temperature high enough to ensure conversion of the intermediate of formula (III) into the compound of formula (I), suitably the temperature is above 50°C , for example 65°C and conveniently the reflux temperature of the reaction solvent.
• a temperature high enough to ensure conversion of the intermediate of formula (III) into the compound of formula (I) suitably the temperature is above 50°C , for example 65°C and conveniently the reflux temperature of the reaction solvent.
• Suitable general reaction conditions for the borohydride and aluminium hydride reductions are also as described in "Reductions by the Alumino- and Borohydrides in Organic Synthesis" by J. Seyden-Penne (VCH Publishers, Inc. / Lavoisier - Tec & Doc, published 1991) and the references disclosed therein.
• the compounds of formula (I) are isolated from the reaction and subsequently purified by use of conventional isolation and purification methods such as chromatography and crystallization/recrystalliazation.
• the complex hydride reducing agents of the process are usually commercially available or they can be prepared using conventional procedures, for example the borohydride and aluminium hydride reagents can be prepared using methods such as those described in "Reductions by the Alumino- and Borohydrides in Organic Synthesis” (ibid) and particularly in the references cited therein.
• lithium tri-sec-butyl borohydride is conveniently prepared from tri-sec- butyl borane and lithium aluminium hydride.
• lithium borohydride is conveniently prepared from sodium borohydride and a lithium salt according to known procedures such as those disclosed in Inorg. Chem. 1981, 20, 4454; J. Am. Chem. Soc. 1953, 75, 209; Nature 1954, 173, 125 and J. Am. Chem. Soc. 1955, 77, 6209.
• T represents a moiety selected from the list consisting of (la), (lb), (Ic), (Id), (Ie), (If), (Ig), (Ih), (Ii), (Ij), (Ik), (II), (Im), (In), (Io), (Ip) and (Iq):
• a , A ⁇ , Rl and n are as defined in relation to formula (I) of EP 0306228;
• R 2 , L 1 , L 2 and L 3 are as defined in relation to formula (I) of EP 0008203;
• R*, R 2 , R 3 , R4 ; R5 ? ⁇ nd n are as defined in relation to formula (I) of EP 0139421;
• R 1 , R 2 and R 3 are as defined in relation to formula (I) of EP 0032128;
• R is as defined in relation to formula (I) of EP 0489663;
• R , R 2 , R3 and n are as defined in relation to formula (I) of EP 0155845;
• V, W, X, Y, Z, Z 1 and n are as defined in EP 0332332;
• T represents a moiety of the above defined formula (la), (Ic), (le), (If),(Ii),(Ik)or(Io).
• T represents a moiety selected from the list consisting of (a), (b),
• T represents a moiety of the above defined formula (la).
• T* represents S.
• J represents O.
• the invention provides a process for preparing a compound of formula (I) as defined in EP 0306228: Accordingly, the invention provides a process for preparing a compound of formula (IA):
• A represents a substituted or unsubstituted aromatic heterocyclyl group
• R represents a hydrogen atom, an alkyl group, an acyl group, an aralkyl group, wherein the aryl moiety may be substituted or unsubstituted, or a substituted or unsubstituted aryl group;
• a 2 represents a benzene ring having in total up to five substituents; and n represents an integer in the range of from 2 to 6; which process
• the suitable, apt, favoured and preferred values of the variables A , A 2 , Rl and n in formulae (IA), (IIB) and (IIIA) are as defined in relation to formula (I) of EP 0306228.
• a most preferred value of A I in formulae (I A), (IIB) and (IIIA) is a 2-pyridyl group.
• a most preferred value of A 2 in formulae (I A), (IIB) and (IIIA) is a moiety of formula:
• a most preferred value of R in formulae (I A), (IIB) and (IIIA) is a methyl group.
• a most preferred value of n in formulae (IA), (IIB) and (IIIA) is 2.
• T represents a moiety of the above defined formula (a), (c) or (d).
• a preferred value of T is a moiety of the above defined formula (a).
• a most preferred value of formula (I A) is 5- ⁇ 4-[2-(N-methyl-N-(2- pyridyl)amino)ethoxy]benzyl ⁇ -2,4-thiazolidinedione, or a tautomeric form thereof or a salt thereof, or a solvate thereof.
• a most preferred value of formula (IIB) is 5- ⁇ 4-[2-(N-me yl-N-(2-pyridyl)amino)ethoxy]benzylidene ⁇ -2,4-thiazolidinedione or a tautomeric form thereof or a salt thereof, or a solvate thereof.
• the reaction comprises a compound of formula (IIB) as substrate it is preferred if the reaction is carried out at an elevated temperature, preferably above 50° C, for example at 65°C.
• a preferred example of a compound of formula (IIIB) is 5- ⁇ 4-[2-(N-methyl-N- (2-pyridyl)amino)ethoxy]benzyl ⁇ -5- ⁇ l-[2,4-dioxothiazolidin-5-yI]-l-[4-(2-(N-methyl- N-(2-pyridyl)amino)ethoxy)phenyl]methyl ⁇ -2,4-thiazolidinedione.
• Suitable salts are pharmaceutically acceptable salts.
• Suitable solvates are pharmaceutically acceptable solvates.
• suitable pharmaceutically acceptable salts include metal salts, such as for example aluminium, alkali metal salts such as sodium or potassium, alkaline earth metal salts such as calcium or magnesium and ammonium or substituted ammonium salts, for example those with lower alkylamines such as triethylamine, hydroxy alkylamines such as 2-hydroxyethylamine, bis-(2-hydroxyethyl)-amine or tri-(2-hydroxyethyl)-amine, cycloalkylamines such as bicyclohexylamine, or with procaine, dibenzylpiperidine, N-benzyl-b- phenethylamine, dehydroabietylamine, N,N'-bisdehydroabietylamine, glucamine, N- methylglucamine or bases of the pyridine type such as pyridine, collidine or quinoline.
• metal salts such as for example aluminium, alkali metal salts such as sodium or potassium, alkaline earth metal salts
• salts provided by pharmaceutically acceptable acids including mineral acids for example for compounds of formula (I) wherein T represents a moiety of formula (la) suitable salts are those disclosed in WO 94/05659 including salts provided by mineral acids, such as hydrobromic, hydrochloric and sulphuric acids, and organic acids, such as methanesulphonic, tartaric and maleic acids, especially tartaric and maleic acid.
• the compounds of formula (II) may be prepared according to known methods, for example by use of the appropriate method disclosed in the abovementioned European and International patent applications or United States patents. The contents of the abovementioned European and International patent applications and United States patents are incorporated herein by reference.
• Example 1 Preparation of 5- ⁇ 4-[2-(N-methyl-N-(2-pyridyl)amino)ethoxy]benzyl ⁇ - 2,4-thiazolidinedione (I A) via reduction of 5- ⁇ 4-[2-(N-methyl-N-(2- pyridy l)amino)ethoxy ] benzylidene ⁇ 2 ,4-thiazolidinedione (IIB) .
• Example 2 Preparation of 5- ⁇ 4-[2-(N-methyl-N-(2-pyridyl)amino)ethoxy]benzyl ⁇ - 2,4-thiazolidinedione (IA) via reduction of 5- ⁇ 4-[2-(N-methyl-N-(2- pyridyl)amino)ethoxy]benzylidene ⁇ 2,4-thiazolidinedione (IIB), using lithium aluminium hydride.
• Example 3 Preparation of 5- ⁇ 4-[2-(N-methyl-N-(2-pyridyl)amino)ethoxy]benzyl ⁇ -5- ⁇ l-[2,4-dioxothiazolidin-5-yl]-l-[4-(2-(N-methyl-N-(2- pyridyl)amino)ethoxy)phenyl]methyl ⁇ -2,4-thiazolidinedione (IIIA) from 5- ⁇ 4-[2-(N- methyl-N-(2-pyridyl)amino)ethoxy]benzylidene ⁇ 2,4-thiazolidinedione (IIB).
• the resulting mixture was heated under reflux for 4 h (reaction monitored by HPLC) and then cooled to ambient temperature and added dropwise to an efficiently stirred solution of cone, hydrochloric acid (13.5 ml) in water (88.7 ml) between 10°C and 20°C.
• the resulting orange suspension was heated to reflux temperature and held for 30 minutes and then cooled to ambient temperature.
• the resulting suspension was stirred for 30 minutes and the product was collected by filtration and washed with water (20 ml x 3).

Landscapes

• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
• Plural Heterocyclic Compounds (AREA)
• Nitrogen Condensed Heterocyclic Rings (AREA)

Priority Applications (1)

Applications Claiming Priority (7)

Related Child Applications (1)

Publications (1)

Family

ID=27268725

Family Applications (2)

Family Applications Before (1)

Country Status (29)

Families Citing this family (11)

Family Cites Families (8)

• 1998
  • 1998-02-11 UY UY24886A patent/UY24886A1/es not_active Application Discontinuation
  • 1998-02-13 SK SK63-2007A patent/SK287512B6/sk not_active IP Right Cessation
  • 1998-02-13 CZ CZ0292499A patent/CZ296272B6/cs not_active IP Right Cessation
  • 1998-02-13 NZ NZ337179A patent/NZ337179A/en not_active IP Right Cessation
  • 1998-02-13 AU AU66223/98A patent/AU6622398A/en not_active Abandoned
  • 1998-02-13 SK SK1120-99A patent/SK285979B6/sk not_active IP Right Cessation
  • 1998-02-13 TR TR1999/02019T patent/TR199902019T2/xx unknown
  • 1998-02-13 HU HU0001459A patent/HUP0001459A3/hu unknown
  • 1998-02-13 AP APAP/P/1999/001626A patent/AP1359A/en active
  • 1998-02-13 ID IDW990876A patent/ID22222A/id unknown
  • 1998-02-13 PL PL98335163A patent/PL195482B1/pl not_active IP Right Cessation
  • 1998-02-13 KR KR1019997007427A patent/KR20000071138A/ko not_active Application Discontinuation
  • 1998-02-13 JP JP53622998A patent/JP2001514619A/ja not_active Withdrawn
  • 1998-02-13 EP EP06002536A patent/EP1770092A1/en not_active Withdrawn
  • 1998-02-13 IL IL13139298A patent/IL131392A/xx unknown
  • 1998-02-13 EP EP98908093A patent/EP0970063A1/en not_active Withdrawn
  • 1998-02-13 CA CA002281695A patent/CA2281695C/en not_active Expired - Fee Related
  • 1998-02-13 CN CN98804121A patent/CN1252065A/zh active Pending
  • 1998-02-13 BR BR9807395-8A patent/BR9807395A/pt not_active Application Discontinuation
  • 1998-02-13 EA EA199900754A patent/EA199900754A1/ru unknown
  • 1998-02-13 WO PCT/EP1998/000818 patent/WO1998037073A1/en not_active Application Discontinuation
  • 1998-02-14 MY MYPI98000629A patent/MY129475A/en unknown
  • 1998-02-16 PE PE1998000107A patent/PE71899A1/es not_active Application Discontinuation
  • 1998-02-16 MA MA24966A patent/MA24475A1/fr unknown
  • 1998-02-16 AR ARP980100684A patent/AR011447A1/es active IP Right Grant
  • 1998-02-17 DZ DZ980040A patent/DZ2430A1/xx active
  • 1998-02-18 IN IN417DE1998 patent/IN188379B/en unknown
  • 1998-03-11 TW TW087103522A patent/TWI222446B/zh active
• 1999
  • 1999-08-17 NO NO19993949A patent/NO313290B1/no not_active IP Right Cessation
  • 1999-08-18 OA OA9900183A patent/OA11148A/en unknown
  • 1999-09-15 BG BG103735A patent/BG64311B1/bg unknown
• 2002
  • 2002-08-19 NO NO20023937A patent/NO20023937D0/no not_active Application Discontinuation
• 2008
  • 2008-11-20 JP JP2008296785A patent/JP2009149616A/ja active Pending

Non-Patent Citations (1)

Also Published As

Similar Documents

Legal Events