WO2003029217A2 - Pyridinic sulfonamide derivatives, method of production and use thereof - Google Patents

Pyridinic sulfonamide derivatives, method of production and use thereof Download PDF

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Publication number
WO2003029217A2
WO2003029217A2 PCT/EP2002/010532 EP0210532W WO03029217A2 WO 2003029217 A2 WO2003029217 A2 WO 2003029217A2 EP 0210532 W EP0210532 W EP 0210532W WO 03029217 A2 WO03029217 A2 WO 03029217A2
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group
pyridinic
alkyl
mixture
sulfonamide derivatives
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PCT/EP2002/010532
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English (en)
French (fr)
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WO2003029217A3 (en
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Jacques Delarge
Bernard Pirotte
Jean-Michel Dogne
Xavier De Leval
Fabien Julemont
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Universite De Liege
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Priority to EP02772326A priority Critical patent/EP1432684B1/en
Priority to DE60231729T priority patent/DE60231729D1/de
Priority to US10/488,553 priority patent/US7226936B2/en
Priority to JP2003532467A priority patent/JP4280631B2/ja
Priority to AU2002337116A priority patent/AU2002337116B2/en
Priority to CA2460144A priority patent/CA2460144C/en
Publication of WO2003029217A2 publication Critical patent/WO2003029217A2/en
Publication of WO2003029217A3 publication Critical patent/WO2003029217A3/en

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
    • C07D213/72—Nitrogen atoms
    • C07D213/76—Nitrogen atoms to which a second hetero atom is attached
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/89—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members with hetero atoms directly attached to the ring nitrogen atom

Definitions

  • the present invention relates to new pyridinic sulfonamides, to their method of production, to pharmaceutical compositions comprising such derivatives and their use as active therapeutic substance in the treatment of diseases.
  • the new pyridinic sulfonamide derivatives are represented by a general formula (I):
  • X represents Oxygen, Sulphur or an element selected from the group consisting of ( -NR 3 , -CR3R4, -SO, -S0 2 , or -CO); wherein R 3 and R 4 which can be identical or different, denotes each independently one element selected from the group consisting of (hydrogen , a mono- or polyhalogenated C ⁇ - ⁇ 2 -alkyl, a mono- or polyhalogenated C 3 -8-cycloalkyl , a C ⁇ - 12 -alkyl or a C3-8-cycloalkyl) ;
  • Ri represents a mono- or polyhalogenated C ⁇ - 12 -alkyl, or a mono- or polyhalogenated C3-8-cycloalkyl group ;
  • R 2 represents a C 3 .8-cycloalkyl group or an aryl group substituted or not by one or several elements selected from the group consisting of (halogen, C ⁇ -12-alkyl, C3-8-cycloalkyl, R-i, hydroxy, Ci- ⁇ -alkoxy, C ⁇ - 6 -alkoxy-C ⁇ - 6 -alkyl, nitro, amino, cyano, cyanomethyl, perhalomethyl, C ⁇ .
  • R5 denotes one or several elements selected from the group consisting of (hydrogen, C ⁇ -6-alkyl, halogen, hydroxy or C-i- ⁇ -alkoxy).
  • C ⁇ - 6 -alkyl refers to a straight or branched, saturated hydrocarbon chain having 1 to 6 carbon atoms such as methyl, propyl, butyl, isopentyl, hexyl, 1-methylbutyl, 1 ,2- dimethylbutyl, 2-ethylbutyl, 2-methylpentyl, 3-methylpentyl and the like.
  • C ⁇ -i 2 -alkyl refers to a straight or branched, saturated hydrocarbon chain having 1 to 12 carbon atoms.
  • C 3 - 8 -cycloalkyl refers to a radical of a saturated cyclic hydrocarbon chain having 3 to 8 carbon atoms such as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, and the like.
  • C ⁇ - 6 -alkoxy refers to a straight or branched monovalent substituent comprising a C ⁇ -6-alkyl group linked through an ether oxygen having its free valence bond from the ether oxygen and having 1 to 6 carbon atoms such as methoxy, ethoxy, propoxy, isopropoxy, butoxy, pentoxy, tert-butoxy and the like.
  • C ⁇ . 6 -alkoxy-C ⁇ .6-alkyl refers to a group of 2-12 carbon atoms interrupted by an oxygen atom such as -CH2-O-CH3, -CH2CH2O- CH 3 , -CH 2 -0-CH 2 CH 3 , -CH 2 -0-CH(CH 3 ) 2 , -CH 2 CH 2 -O-CH(CH 3 )2 , - CH(CH 3 )CH 2 -O-CH 3 and the like.
  • halogen means fluorine, chlorine, bromine or iodine.
  • perhalomethyl means trifluoromethyl, trichloromethyl, tribromomethyl or triiodomethyl.
  • C- ⁇ -6-monoalkylamino refers to an amino group wherein one of the hydrogen atoms is substituted with a straight or branched, saturated hydrocarbon chain having 1 to 6 carbon atoms such as methylamino, ethylamino, propylamino, isopropylamino, butylamino, tert- butylamino, isopentylamino, hexylamino and the like.
  • Ci-6-dialkylamino refers to an amino group wherein the two hydrogen atoms independently are substituted with a straight or branched, saturated hydrocarbon chain having 1 to 6 carbon atoms such as dimethylamino, N-ethyl-N-methylamino, N-methyl-N-isopropylamino, N-butyl-N-methylamino, dihexylamino and the like.
  • C ⁇ -6-alkylthio refers to a straight or branched monovalent substituent comprising a C-i- ⁇ -alkyl group linked through a divalent sulfur atom having its free valence bond from the sulfur atom and having 1 to 6 carbon atoms such as methylthio, ethylthio, propylthio, isopropylthio, butylth io , pentylthi o , 3- methylpentylthio and the like.
  • a sulfinyl group such as methylsulfinyl, ethylsulfinyl, propylsulfinyl, isopropylsulfinyl, tert- butylsulfinyl, pentylsulfinyl, 2-ethylbutylsulfinyl and the like.
  • acyl refers to a monovalent substituent comprising a
  • C-i- ⁇ -alkyl group linked through a carbonyl group such as acetyl, propionyl, butyryl, isobutyryl, pivaloyl, valeryl and the like.
  • C ⁇ -6-alkylcarbonylamino refers to an amino group wherein one of the hydrogen atoms is substituted with an acyl group such as acetamido, propionamido, iospopropylcarbonylamino 2- ethylbutylcarbonylamino and the like.
  • aryl refers to phenyl, 1-naphthyl, or 2-naphthyl.
  • arylthio refers to an aryl group linked through a divalent sulfur atom having its free valence bond from the sulfur atom, the aryl group is substituted or not by one or several elements of R5 such as phenylthio, 1-naphthylthio, 2-methylphenylthio, 3- methoxyphenylthio and the like.
  • Carbonyl refers to a monovalent substituent comprising a C-i- ⁇ -alkoxy group linked through a carbonyl group such as methoxycarbonyl, isopropoxycarbonyl, butoxycarbonyl, tert- butoxycarbonyl, 2-methylpentoxycarbonyl and the like.
  • C ⁇ -6-monoalkylaminocarbony refers to a monovalent substituent comprising a C ⁇ -6-monoalkylamino group linked through a carbonyl group such as methylaminocarbonyl, isopropylaminocarbonyl, butylaminocarbonyl, 2-methylbutylaminocarbonyl and the like.
  • Ci-6-dialkylaminocarbonyl refers to a monovalent substituent comprising a C- ⁇ -6-dialkylamino group linked through a carbonyl group such as dimethylaminocarbonyl, diethylaminocarbonyl N- methyl-N-isopropylaminocarbonyl, N-methyl-N-butylaminocarbonyl, N- propyl-N-2-methylbutylaminocarbonyl and the like.
  • C ⁇ -6-monoalkylaminothiocarbonyl refers to a monovalent substituent comprising a C ⁇ -6-monoalkylamino group linked through a thiocarbonyl group such as methylaminothiocarbonyl, isopropylaminothiocarbonyl, butylaminothiocarbonyl, 3- methylpentylaminothiocarbonyl, 1 ,2-dimethylbutylaminothiocarbonyl and the like.
  • Ci-6-dialkylaminothiocarbonyl refers to a monovalent substituent comprising a C- ⁇ -6-dialkylamino group linked through a thiocarbonyl group such as dimethylaminothiocarbonyl, diethylaminothiocarbonyl N-methyl-N-isopropylaminothiocarbonyl, N- methyl-N-butylaminothiocarbonyl N-tert-butyl-N-hexylaminothiocarbonyl and the like.
  • C ⁇ -6-monoalkylaminocarbonylamino refers to an amino group wherein one of the hydrogen atoms is substituted with a C- ⁇ -6- monoalkylaminocarbonyl group such as methylaminocarbonylamino, ethylaminocarbonylamino, propylaminocarbonylamino, 3- methylbutylaminocarbonylamino, 1,2-dimethylbutylaminocarbonylamino and the like.
  • C i-e-dialkylaminocarbonylamino refers to an amino group wherein one of the hydrogen atoms is substituted with a C- ⁇ -6- dialkylaminocarbonyi group such as dimethylaminocarbonylamino, diethylaminocarbonylamino, N-methyl-N-ethylaminocarbonylamino, N- methyl-N-i s o p ro p l a m i n o ca r b o n y l a m i n o , N -propyl-N- pentylaminocarbonylamino and the like.
  • C ⁇ -6-monoalkylaminothiocarbonylamino refers to an amino group wherein one of the hydrogen atoms is substituted with a C ⁇ _ 6 -monoalkylaminothiocarbonyl group such as methylaminothiocarbonylamino, ethylaminothiocarbonylamino, propylaminothiocarbonylamino, 3-methylpentylaminothiocarbonylamino and the like.
  • C ⁇ -6-dialkylaminothiocarbonylamino refers to an amino group wherein one of the hydrogen atoms is substituted with a C-i- ⁇ - dialkylaminothiocarbonyl group such as dimethylaminothiocarbonylamino, diethylaminothiocarbonylamino, N-methyl-N- ethylaminothiocarbonylamino, N-methyl-N-propylaminothiocarbonylamino , N-isopropyl-N-hexylaminothiocarbonylamino, N-3-methylpentyl-N- pentylaminothiocarbonylamino and the like.
  • Ci- ⁇ -monoalkylaminosulfonyl refers to a monovalent substituent comprising a C ⁇ _ ⁇ -monoalkylamino group linked through a sulfonyl group such as methylaminosulfonyl, ethylaminosulfonyl, propylaminosulfonyl, hexylaminosulfonyl, tert-butylaminosulfonyl, 1,2- dimethylbutylaminosulfonyl and the like.
  • Ci- ⁇ -dialkylaminosulfonyl refers to a monovalent substituent comprising a C ⁇ _6-dialkylamino group linked through a sulfonyl group such as dimethylaminosulfonyl, diethylaminosulfonyl, N-methyl-N- ethylaminosulfonyl N-methyl-N-propylaminosulfonyl, N-hexyl-N-3- methylbutylaminosulfonyl and the like.
  • ureido as used herein means -NH-CO-NH 2
  • thioureido as used herein means -NH-CS-NH 2 .
  • arylalkyl refers to a straight or branched saturated carbon chain containing from 1 to 6 carbons substituted with an aromatic carbohydride. the aryl group is substituted or not by one or several elements of R5.
  • aryloxy refers to phenoxy, 1-naphthyloxy or 2- naphthyloxy, the aryl group is substituted or not by one or several elements of R5.
  • Rsaryl refers to aryl substituted or not by R_.
  • This invention also refers to all optical isomers of pyridinic sulfonamides derivatives covered by the formula (I), particularly the optically active isomers , and their mixtures including racemic mixtures thereof.
  • the invention refers as well to pure optical isomers than to racemic mixture.
  • the invention refers also to tautomeric forms of the pyridinic sulfonamide derivatives and to pharmacologically acceptable salts of the dervivatives covered by formula (I).
  • pharmacologically acceptable salts of the dervivatives one means pharmaceutically acceptable acid addition salts, pharmaceutically acceptable metal salts or optionally alkylated ammonium salts.
  • Preferred classes of pyridine sulfonamides derivatives according to the general formula are especially those in which Ri is trifluoromethyl.
  • the most preferred pyridine sulfonamide is N-(3-phenoxy-4- pyridinyl)trifluoromethanesulfonamide.
  • the invention also relates to a method of producing the above mentioned derivatives.
  • the method comprises the steps of
  • the pyridinic compound may be any pyridinic derivative unsubstituted in position 4 and susceptible to react with an oxydant such as H2O2 .
  • the pyridinic compound unsubstituted in the 4-position may be for example 3-bromopyridine or 3-methylpyridine as illustrated in figures 1 and 2.
  • nitration agent one means a mixture from 1 :1 to 1 :2 parts of concentrated nitric acid and concentrated sulphuric acid to be added between RT to 100°C and under continuous stirring to the pyridine N- oxide.
  • Figure 1 represents a schematic synthesis of compounds with an O, S, SO, SO 2 , NR 3 and CR3R4 linkage and Figure 2 represents a schematic synthesis of compounds with a CO and CH2 linkage.
  • the pyridine N-oxide of formula 1a may be prepared from 3- bromopyridine which can be oxidized using several oxidants such as H2O2.
  • the nitration at the 4-position of the pyridine N-oxide can be achieved by a mixture of nitric and sulphuric acids to form 1b.
  • the synthesis of 1c may be realized by reaction of 1 b with a cycloalkane derivative such as a cyclopentane, a cyclohexane, a cycloheptane derivative or a benzene derivative in presence of a suitable inorganic base such as K 2 CO 3 or NaOH in an inert solvent such as acetonitrile or dichloromethane.
  • the nitropyridine N-oxide 1c is converted into the aminopyridine 1d via a reduction reaction using a reductant such as iron in presence of acetic acid.
  • a reductant such as iron in presence of acetic acid.
  • water may be added to the mixture and the temperature may be ranging from room temperature to the reflux of the solvent.
  • the synthesis of the sulfonamide 1e is completed by reaction of the amino-substituted pyridine derivative 1d and the appropriate sulfonyl derivative such as sulfonyl chloride, sulfonyl fluoride or sulfonic anhydride in presence of a suitable inorganic base such as K2CO3 or NaOH in an inert anhydrous solvent such as acetonitrile, dioxane or dichloromethane.
  • the oxidation of 1e use an oxidant such as H2O2 to form 1f.
  • the synthesis of the sulfoxide and the sulfone family 1i and 1j is realized throughout oxidation of the thio derivative 1c by an oxidant such as meta-chloroperbenzoic acid to form 1g.
  • This oxidation is followed by a reduction (1h) and the formation of the sulfonamide (1i) and finally by an oxidation (1j) of the pyridine comparable to the methods used for the preparation of 1d, 1e and 1f.
  • Figure 2 :
  • the synthesis of the ceto derivatives is achieved by the pathway of scheme 2.
  • This scheme begins by an oxidation of 3-methylpyridine by hydrogen peroxide in presence of acetic acid (2a). Nitration by nitric acid and sulphuric acid at the 4-position of the N-oxide lead to the formation of 2b. The methyl group of 2b is oxidized by KMn ⁇ to produce the carboxylic acid 2c.
  • the synthesis of the cyano derivative 2d is achieved in three steps. The first one is a conversion of carboxylic acid into carboxylic halide by SOC . The second is the formation of carboxamide and the last step is a deshydration of the amide to form the nitrile 2d.
  • the ceto linkage is prepared by reaction between 2d and an organosmagnesium compound such as an alkyl magnesium bromide or an aryl magnesium bromide.
  • the ceto group is then protected as an acetal by reaction of 2e and ethyleneglycol in an acidic medium. After that, the nitro group and the N-oxide of 2f is reduced by iron in presence of acetic acid to produce 2g.
  • This compound reacts with the appropriate sulfonyl chloride such as an alkyl or an aryl sulfonyl chloride to form the sulfonamide 2h.
  • the acetal may be hydrolysed to generate the ceto compound 2i.
  • the last step is an oxidation of the pyridine 2i by H 2 O 2 to form 2j.
  • Conversion of the ceto compounds into the corresponding methylene derivatives is achieved by a Wolff-Kishner reaction as described in Organic Reactions, Vol IV, p 378, 1948.
  • Example 1 preparation of N-(3-phenoxy-4-pyridinyl)trifluoromethane- sulfonamide (compound I).
  • Step 1 To 1.58 g of 3-bromopyridine (10 mmol) dissolved in 6 mL of glacial acetic acid, 4 mL of 30% hydrogen peroxide are added. The solution is heated with reflux for 48 hours. The solvent is evaporated under depression. The residue is purified by column chromatography using ethyl acetate as eluent.
  • Step 2 To 1.74 g of 3-bromopyridine N-oxide dissolved in 4 mL of concentrated sulphuric acid , a mixture of 4 mL of concentrated sulphuric acid and 6.7 mL of concentrated nitric acid is added under continuous stirring. The solution is heated at 90 °C for 90 minutes. Then the solution is poured into ice and supplemented with a 50% aqueous solution of NaOH until complete precipitation of the final compound. The yellow solid is filtered off and washed with water to give 1.51g of 3- bromo-4-nitropyridine N-oxide.
  • Step 3 4.8 mL of 10 % aqueous solution of NaOH are added to 1.12 g of phenol. After stirring for 5 minutes, water is evaporated under reduced pressure. A white solid is obtained and taken up by 10 mL of acetonitrile and the resulting suspension is supplemented with 2.19 g of 3-bromo-4- nitropyridine N-oxide. The obtained mixture is heated under reflux during 5 minutes. The mixture is further poured into ice and extracted with ethyl acetate. Organic layers are collected and dried over anhydrous magnesium sulphate. After evaporation of the solvent , a solid residue is purified by column chromatography using ethyl acetate as eluent to give 1.27 g of a yellow solid.
  • Step 4 2.32 g of 4-nitro-3-phenoxypyridine N-oxide dissolved in 55 mL of acetic acid and 14 mL of water are heated under reflux. Then 3.48 g of iron powder are added and the reflux is maintained for 12 hours. The solution is filtered and evaporated under reduced pressure. An oily residue is taken up with water and pH adjusted to 10 by addition of a 10 % aqueous solution of NaOH . The suspension is filtered and the filtrate is extracted by ethyl acetate. Organic layers are collected and dried over anhydrous magnesium sulfate. After evaporation, 4-amino-3- phenoxypyridine is obtained as a yellow oil. Yield: 80-90 %.
  • Step 5 To 1.81 g of 4-amino-3-phenoxypyridine dissolved in 112 mL of dry acetonitrile are added 8.29 g anhydrous potassium carbonate. The suspension is stirred for 5 minutes and 2.02 mL of trifluoromethanesulfonyl chloride are added. The mixture is stirred for 12 h, then filtered and the solvent evaporated under reduced pressure. The residue is taken up with 10 % aqueous solution of NaOH and the pH of the solution is adjusted to 5 with 1 N HCI to separate 2.53 g of a final compound as a white solid.
  • Step 1 and step 2 similar to example 1
  • Step 3 4 mL of a 10 % aqueous solution of NaOH are added to 1.4 g of 4-chlorophenol. After stirring for 5 minutes, water is evaporated under reduced pressure. A white solid is obtained and taken up by 10 mL of acetonitrile and the resulting suspension is supplemented with 2 g of 3- bromo-4-nitropyridine N-oxide to obtain a mixture which is then heated under reflux for 5 minutes. The mixture is further filtered and the filtrate is concentrated under reduced pressure. A solid is obtained and is dissolved in a minimum of methanol and 4-nitro-3-(4-chlorophenoxy)- pyridine N-oxide is precipitated by addition of water. The precipitate is collected by filtration to give 1.15 g of a yellow solid.
  • Step 4 0.37 g of 4-nitro-3-(4-chlorophenoxy)-pyridine N-oxide dissolved in 9 mL of acetic acid and 2 mL of water are heated under reflux. To such warm solution are added 0.5 g of iron powder and the reflux is maintained for 1 hour. A suspension is obtained and filtered and the filtrate is evaporated under reduced pressure. An oily residue is obtained and taken up with water and pH adjusted to 10 by addition of a 10 % aqueous solution of NaOH. The resulting suspension is filtered and the filtrate is extracted by ethyl acetate. Organic layers are collected and dried over anhydrous magnesium sulfate. After evaporation, 4-amino-3- (4-chlorophenoxy)pyridine is obtained as a yellow oil. Yield: 80-90 %.
  • Step 5 To 0.56 g of 4-amino-3-(4-chlorophenoxy)pyridine dissolved in 20 mL of dry acetonitrile is added 1 g of anhydrous potassium carbonate. The suspension is stirred for 5 minutes and 0.794 mL of trifluoromethanesulfonyl chloride are added. The mixture is stirred for 15 minutes, then filtered and the filtrate concentrated under reduced pressure. The residue is taken up with a 10 % aqueous solution of NaOH and the pH of the solution is adjusted to 7 with 1N HCI to separate 0.61 g of the final compound as a white solid which is filtered, washed with water and dried.
  • Step 1 and step 2 similar to example 1
  • Step 4 0.95 g of 4-nitro-3-(3,5-dichlorophenoxy)pyridine N-oxide dissolved in 18 mL of acetic acid and 5 mL of water are heated under reflux. To the warm solution are added 1.12 g of iron powder and the reflux is maintained for 12 hours. The solution is filtered and the filtrate is evaporated under reduced pressure. An oily residue is obtained and taken up with water and the pH adjusted to 10 by addition of a 10 % aqueous solution of NaOH. The suspension is filtered and the filtrate is extracted by ethyl acetate. Organic layers are collected and dried over anhydrous magnesium sulfate. After evaporation, 4-amino-3-(3,5- dichlorophenoxy)pyridine is obtained as a yellow oil.
  • Step 5 To 0.45 g of 4-amino-3-(3,5-dichlorophenoxy)pyridine dissolved in 20 mL of dry acetonitrile are added 0.73 g anhydrous potassium carbonate. The suspension is stirred for 5 minutes and 0.551 mL of trifluoromethanesulfonyl chloride are added. The mixture is stirred for 30 minutes, then filtered and the filtrate concentrated under reduced pressure. A residue is obtained and taken up with a 10 % aqueous solution of NaOH and the pH of the solution is adjusted to 7 with 1 N HCI to separate 0.33 g of the final compound as a white solid which is filtered, washed with water and dried.
  • Step 3 5.5 mL of a 10 % aqueous solution of NaOH are added to 1.88 g of 4-bromophenol. After stirring for 5 minutes, water is evaporated under reduced pressure. A white solid is obtained and taken up by 10 mL of acetonitrile and the suspension is supplemented with 2 g of 3-bromo-4- nitropyridine N-oxide and then heated under reflux 5 minutes. The mixture is filtered and the filtrate is evaporated under reduced pressure. A solid is obtained and is dissolved in a minimum of methanol and 4-nitro- 3-(4-bromophenoxy)-pyridine N-oxide is precipitated by addition of water. The precipitated is collected by filtration, washed with water and dried, to give 0.96 g of a yellow solid.
  • Step 4 3 g of 4-nitro-3-(4-bromophenoxy)-pyridine N-oxide dissolved in 72 mL of acetic acid and 18 mL of water are heated under reflux. To the warm solution are added 4.2 g of iron powder and the reflux is maintained for 12 hours. The solution is filtered and the filtrate is evaporated under reduced pressure. Oily residue is obtained and is taken up with water and the pH adjusted to 10 by addition of a 10 % aqueous solution of NaOH. The suspension is filtered and the filtrate is extracted by ethyl acetate. Organic layers are collected and dried over anhydrous magnesium sulfate. After evaporation, 4-amino-3-(4- bromophenoxy)-pyridine is obtained as a yellow oil.
  • Step 5 To 0.2 g of 4-amino-3-(4-bromophenoxy)-pyridine dissolved in 20 mL of dry acetonitrile are added 2.25 g anhydrous potassium carbonate. The suspension is stirred for 5 minutes and 0.235 mL of trifluoromethanesulfonyl chloride are added. The mixture is stirred for 1 hour, then filtered and the filtrate concentrated under reduced pressure. A residue is taken up with a 10 % aqueous solution of NaOH and the pH of the solution is adjusted to 7 with 1 N HCI to separate 0.21 g of the final compound as a white solid.
  • Step 1 and step 2 similar to example 1
  • Step 3 4 mL of a 10 % aqueous solution of NaOH are added to 1.4 g of 3-chlorophenol. After stirring for 5 minutes, water is evaporated under reduced pressure. A white solid is obtained and taken up by 40 mL of acetonitrile and the suspension is supplemented with 2 g of 3-bromo-3- nitropyridine N-oxide and then heated under reflux for 5 minutes. The mixture is filtered and the filtrate is concentrated under reduced pressure. A solid is obtained and is dissolved in a minimum of cold methanol and 4-nitro-3-(3-chlorophenoxy)-pyridine N-oxide is collected by filtration to give 1.06 g of a yellow solid.
  • Step 4 1 g of 4-nitro-3-(3-chlorophenoxy)-pyridine N-oxide dissolved in 20 mL of acetic acid and 6 mL of water are heated under reflux. To the warm solution are added 2.98 g of iron powder and then heated under reflux for 3 hours. The suspension is filtered and the filtrate is concentrated under reduced pressure. Oily residue is obtained and taken up with water and the pH adjusted to 10 by addition of a 10 % aqueous solution of NaOH. The suspension is filtered and the filtrate is extracted by ethyl acetate. Organic layers are collected and dried over anhydrous magnesium sulfate. After evaporation, 4-amino-3-(3- chlorophenoxy)pyridine is obtained as a yellow oil.
  • Step 5 To 0.2 g of 4-amino-3-(3-chlorophenoxy)pyridine dissolved in 15 mL of dry dichloromethane are added 0.5 mL of triethylamine. The solution is stirred for 5 minutes and 0.19 mL of trifluoromethanesulfonyl chloride are added. The mixture is stirred for 12 h, then filtered and the filtrate concentrated under reduced pressure. The residue is taken up with a 10 % aqueous solution of NaOH and the pH of the solution is adjusted to 7 with 1 N HCI to separate 0.2 g of the final compound as a white solid which is filtered, washed with water and dried.
  • Step 1 and step 2 similar to example 1
  • Step 3 2 mL of thiophenol is dissolved in 80 mL of toluene. 2.5g of K2CO3 is added and the suspension is heated until reflux occur. Then, 4 g of 3-bromo-4-nitropyridine N-oxide is added and the reflux is maintained for 2 hours. The mixture is filtered and the filtrate is concentrated under reduced pressure. A residue is taken up by a minimum of cold ethanol and 4-nitro-3-thiophenoxypyridine N-oxide is collected by filtration to give 2.52 g of a yellow solid.
  • Step 4 0.5 g of 4-nitro-3-thiophenoxypyridine N-oxide dissolved in 20 mL of glacial acetic acid are heated under reflux. To the warm solution are added 0.37 g of iron powder and the reflux is maintained for 2 hours. The solution is filtered and the filtrate concentrated under reduced pressure. Oily residue is obtained and taken up with water and the pH adjusted to 10 by addition of a 10 % aqueous solution of NaOH solution. The suspension is filtered and the filtrate is extracted by ethyl acetate. Organic layers are collected and dried over anhydrous magnesium sulfate. After evaporation, 4-amino-3-thiophenoxypyridine is obtained as a yellow oil.
  • Step 5 To 0.45 g of 4-amino-3-thiophenoxypyridine dissolved in 20 mL of dry acetonitrile are added 1.84 g anhydrous potassium carbonate. The suspension is stirred for 5 minutes and 0.47 mL of trifluoromethanesulfonyl chloride are added. The mixture is stirred for 4 h, then filtered and acetonitrile is evaporated under reduced pressure. The residue is taken up with a 10 % aqueous solution of NaOH and the pH of the solution is adjusted to 5 with 1 N HCI to separate 0.36 g of the final compound as a white solid which is filtered, washed with water and dried.
  • the invention also refers to the use of the pyridinic sulfonamides derivatives covered by formula (1)and their salts for drug manufacture for treatment and/or prevention of diseases such as inflammation, arthrosis, cancer, angiogenesis and asthma and for other pathologies in which they can play a role of COX-2 selective inhibitor.
  • Prostaglandins are key mediators involved in the inflammation processes. According to Bergstr ⁇ m, S.; Ryhage, R.; Samuelsson, B.; Sj ⁇ vall, J. in J. Biol. Chem., 1963, 238, 3555-3563. prostaglandins are synthesized by cyclooxygenases (COXs) from arachidonic acid.
  • COXs cyclooxygenases
  • COX-1 is a constitutive enzyme responsible for physiological production of PG. This enzyme is involved in several homeostatic processes and is thus considered as a "house keeping" enzyme.
  • COX-2 is an inducible enzyme which is mainly produced during inflammation processes.
  • COX-2 is expressed during different pathologies such as arthrosis, angiogenesis and asthma.
  • NSAID common non-steroidal anti- inflammatory drugs
  • the present invention deals with the use of new COX-2 selective inhibitors represented by the pyridinic sulfonamide derivatives described above.
  • new COX-2 selective inhibitors advantageously does not exhibit such side effects.
  • the pyridinic sulfonamide derivatives described above have been evaluated as COX inhibitors on one in vitro test and on one in vivo test. For the in vitro assay the methodology is described by X. de Leval,
  • the activity of the derivatives has also been evaluated by using a rat paw oedema pharmacological model.
  • the invention also refers to a Pharmaceutical composition
  • a Pharmaceutical composition comprising a pyridinic sulfonamide derivative or a pharmaceutical acceptable salt thereof with a pharmaceutical acceptable acid or base, or any optical isomer or mixture of optical isomers, including a racemic mixture or any tautomeric form together with one or more acceptable carriers or diluents.
  • the pharmaceutical composition may be in a form of an oral dosage unit or parenteral dosage unit.

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  • Chemical & Material Sciences (AREA)
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  • General Chemical & Material Sciences (AREA)
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  • Rheumatology (AREA)
  • Pyridine Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Liquid Crystal Substances (AREA)
PCT/EP2002/010532 2001-09-27 2002-09-19 Pyridinic sulfonamide derivatives, method of production and use thereof WO2003029217A2 (en)

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EP02772326A EP1432684B1 (en) 2001-09-27 2002-09-19 Pyridinic sulfonamide derivatives, method of production and use thereof
DE60231729T DE60231729D1 (de) 2001-09-27 2002-09-19 Hren und verwendung
US10/488,553 US7226936B2 (en) 2001-09-27 2002-09-19 Pyridinic sulfonamide derivatives method of production and use thereof
JP2003532467A JP4280631B2 (ja) 2001-09-27 2002-09-19 ピリジンスルホンアミド誘導体、その生産方法、およびその使用
AU2002337116A AU2002337116B2 (en) 2001-09-27 2002-09-19 Pyridinic sulfonamide derivatives, method of production and use thereof
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Cited By (3)

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WO2005016984A1 (de) * 2003-08-07 2005-02-24 Bayer Materialscience Ag Neue katalysatoren für die selektive isocyanatdimerisierung
WO2008049605A1 (en) * 2006-10-26 2008-05-02 F. Hoffmann-La Roche Ag Heterocyclyl pyridyl sulfonamide derivatives, their manufacture and use as pharmaceutical agents
WO2008138594A1 (en) * 2007-05-16 2008-11-20 F. Hoffmann-La Roche Ag Aryl pyridyl sulfonamide derivatives, their manufacture and use as pharmaceutical agents

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PL2114970T3 (pl) 2007-02-02 2011-11-30 Pfizer Prod Inc Związki trójcykliczne i ich zastosowanie jako modulatorów receptora glukokortykoidowego
PL2177512T3 (pl) * 2007-08-01 2012-09-28 Taisho Pharmaceutical Co Ltd Inhibitor wiązania S1P1

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JP2930731B2 (ja) * 1994-12-20 1999-08-03 エフ・ホフマン−ラ ロシュ アーゲー アリール−及びヘテロアリール−スルホンアミド誘導体、その製造法及びエンドセリンアンタゴニストとしてのその用途

Non-Patent Citations (2)

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Title
CIGNARELLA G. ET AL: "Synthesis and pharmacological evaluation of nimesulide analogues" EUROP.JOURN. OF MED.CHEM., vol. 31, 8 January 1996 (1996-01-08), pages 359-364, XP002228167 Paris *
F. JULEMONT ET AL: "Spectral and Crystallographic Study of Pyridinic Analogues of Nimesulide: Determination of the Active Form of Methanesulfonamides as COX-2 Selective Inhibitors" J.MED.CHEM., vol. 45, 10 March 2002 (2002-03-10), pages 5182-5185, XP002228168 *

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005016984A1 (de) * 2003-08-07 2005-02-24 Bayer Materialscience Ag Neue katalysatoren für die selektive isocyanatdimerisierung
US7317112B2 (en) 2003-08-07 2008-01-08 Bayer Materialscience Ag Catalysts for selective isocyanate dimerization
WO2008049605A1 (en) * 2006-10-26 2008-05-02 F. Hoffmann-La Roche Ag Heterocyclyl pyridyl sulfonamide derivatives, their manufacture and use as pharmaceutical agents
US7939532B2 (en) 2006-10-26 2011-05-10 Hoffmann-La Roche Inc. Heterocyclyl pyridyl sulfonamide derivatives, their manufacture and use as pharmaceutical agents
WO2008138594A1 (en) * 2007-05-16 2008-11-20 F. Hoffmann-La Roche Ag Aryl pyridyl sulfonamide derivatives, their manufacture and use as pharmaceutical agents
US7879884B2 (en) 2007-05-16 2011-02-01 Hoffmann-La Roche Inc. Aryl pyridyl sulfonamide derivatives, their manufacture and use as pharmaceutical agents

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RU2004112562A (ru) 2005-10-10
ATE426593T1 (de) 2009-04-15
WO2003029217A3 (en) 2003-08-28
DE60231729D1 (de) 2009-05-07
US20070173534A1 (en) 2007-07-26
EP1432684A2 (en) 2004-06-30
AU2002337116B2 (en) 2008-01-31
JP2005504125A (ja) 2005-02-10
ES2324705T3 (es) 2009-08-13
US7226936B2 (en) 2007-06-05
RU2309148C2 (ru) 2007-10-27
CA2460144C (en) 2010-11-02

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