CH634302A5 - Verfahren zur herstellung neuer mercaptomethylpyridin-derivate. - Google Patents
Verfahren zur herstellung neuer mercaptomethylpyridin-derivate. Download PDFInfo
- Publication number
- CH634302A5 CH634302A5 CH303278A CH303278A CH634302A5 CH 634302 A5 CH634302 A5 CH 634302A5 CH 303278 A CH303278 A CH 303278A CH 303278 A CH303278 A CH 303278A CH 634302 A5 CH634302 A5 CH 634302A5
- Authority
- CH
- Switzerland
- Prior art keywords
- derivatives
- mercaptomethylpyridin
- producing new
- compound
- acid
- Prior art date
Links
- SJIIDWBFRZACDQ-UHFFFAOYSA-N pyridin-2-ylmethanethiol Chemical class SCC1=CC=CC=N1 SJIIDWBFRZACDQ-UHFFFAOYSA-N 0.000 title description 4
- 238000004519 manufacturing process Methods 0.000 title 1
- 150000001875 compounds Chemical class 0.000 description 10
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 8
- 238000000034 method Methods 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- PZTHSDYEYQLIDM-UHFFFAOYSA-N 4-methoxy-2-methyl-5-methylsulfanylpyridin-3-ol Chemical compound COC1=C(O)C(C)=NC=C1SC PZTHSDYEYQLIDM-UHFFFAOYSA-N 0.000 description 5
- 239000002253 acid Substances 0.000 description 5
- 239000003814 drug Substances 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- NXLNNXIXOYSCMB-UHFFFAOYSA-N (4-nitrophenyl) carbonochloridate Chemical compound [O-][N+](=O)C1=CC=C(OC(Cl)=O)C=C1 NXLNNXIXOYSCMB-UHFFFAOYSA-N 0.000 description 4
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 230000037396 body weight Effects 0.000 description 3
- 229940079593 drug Drugs 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 206010039073 rheumatoid arthritis Diseases 0.000 description 3
- VVNCNSJFMMFHPL-VKHMYHEASA-N D-penicillamine Chemical compound CC(C)(S)[C@@H](N)C(O)=O VVNCNSJFMMFHPL-VKHMYHEASA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical group Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000002260 anti-inflammatory agent Substances 0.000 description 2
- 230000003356 anti-rheumatic effect Effects 0.000 description 2
- 201000010099 disease Diseases 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 239000012044 organic layer Substances 0.000 description 2
- 229960001639 penicillamine Drugs 0.000 description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- HVPZELCZNCVMBD-UHFFFAOYSA-N (4-nitrophenoxy)methanethioic s-acid Chemical compound [O-][N+](=O)C1=CC=C(OC(S)=O)C=C1 HVPZELCZNCVMBD-UHFFFAOYSA-N 0.000 description 1
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 1
- JXYDRIBYAKJTIW-UHFFFAOYSA-N 4-(hydroxymethyl)-2-methyl-5-(sulfanylmethyl)pyridin-3-ol Chemical compound CC1=NC=C(CS)C(CO)=C1O JXYDRIBYAKJTIW-UHFFFAOYSA-N 0.000 description 1
- BSYNRYMUTXBXSQ-UHFFFAOYSA-N Aspirin Chemical compound CC(=O)OC1=CC=CC=C1C(O)=O BSYNRYMUTXBXSQ-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 241000282472 Canis lupus familiaris Species 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 241000700198 Cavia Species 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 1
- 241000283086 Equidae Species 0.000 description 1
- 241000282326 Felis catus Species 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical group SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 1
- 241000699670 Mus sp. Species 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 241000283973 Oryctolagus cuniculus Species 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 241000700159 Rattus Species 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 229960001138 acetylsalicylic acid Drugs 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 239000000730 antalgic agent Substances 0.000 description 1
- 229940121363 anti-inflammatory agent Drugs 0.000 description 1
- 230000003110 anti-inflammatory effect Effects 0.000 description 1
- 239000002221 antipyretic Substances 0.000 description 1
- 229940125716 antipyretic agent Drugs 0.000 description 1
- 239000000010 aprotic solvent Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- JJBKVCQUFIBRFK-UHFFFAOYSA-N chloromethane;methanol Chemical compound OC.ClC JJBKVCQUFIBRFK-UHFFFAOYSA-N 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 230000037213 diet Effects 0.000 description 1
- 235000005911 diet Nutrition 0.000 description 1
- SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 description 1
- 239000003937 drug carrier Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000003480 eluent Substances 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000029142 excretion Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000001802 infusion Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 238000007918 intramuscular administration Methods 0.000 description 1
- 238000001990 intravenous administration Methods 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000002547 new drug Substances 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 150000003431 steroids Chemical class 0.000 description 1
- 239000007929 subcutaneous injection Substances 0.000 description 1
- 238000010254 subcutaneous injection Methods 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
Classifications
-
- 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
- C07D213/62—Oxygen or sulfur atoms
- C07D213/63—One oxygen atom
- C07D213/65—One oxygen atom attached in position 3 or 5
- C07D213/66—One oxygen atom attached in position 3 or 5 having in position 3 an oxygen atom and in each of the positions 4 and 5 a carbon atom bound to an oxygen, sulphur, or nitrogen atom, e.g. pyridoxal
-
- 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]
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
-
- 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
- C07D213/24—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 substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/26—Radicals substituted by halogen atoms or nitro radicals
-
- 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
- C07D213/24—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 substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/28—Radicals substituted by singly-bound oxygen or sulphur atoms
- C07D213/32—Sulfur atoms
-
- 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
- C07D213/62—Oxygen or sulfur atoms
- C07D213/63—One oxygen atom
-
- 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
- C07D213/62—Oxygen or sulfur atoms
- C07D213/70—Sulfur atoms
-
- 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
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
- C07D213/82—Amides; Imides in position 3
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D327/00—Heterocyclic compounds containing rings having oxygen and sulfur atoms as the only ring hetero atoms
- C07D327/02—Heterocyclic compounds containing rings having oxygen and sulfur atoms as the only ring hetero atoms one oxygen atom and one sulfur atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D497/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having oxygen and sulfur atoms as the only ring hetero atoms
- C07D497/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having oxygen and sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D497/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Rheumatology (AREA)
- Pharmacology & Pharmacy (AREA)
- Pain & Pain Management (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pyridine Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
634302
2
PATENTANSPRUCH Ein Verfahren zur Herstellung einer neuen Verbindung der Formel
CH-OH
OH
:H_— S— C— S—CH.
HO
2
CH
CH
bzw. ihrer pharmazeutisch annehmbaren Säureadditionssalze, dadurch gekennzeichnet, dass man 5-Mercaptopyridoxin mit p-Nitrophenylchlorformiat oder Phosgen umsetzt und eine erhaltene Verbindung gegebenenfalls in entsprechende Salze überführt.
Die vorliegende Erfindung bezieht sich auf ein Verfahren zur Herstellung von neuen Mercaptomethylpyridin-Derivaten, die als aktive Komponente in Arzneimitteln verwendet werden können, insbesondere zur Behandlung von rheumatoider Arthritis.
Vor allem bezieht sich die vorliegende Erfindung auf ein Verfahren zur Herstellung einer neuen Verbindung der folgenden Formel:
OH
HO
:H_— S - C— S— CH
2
CH
CH
und ihrer pharmazeutisch annehmbaren Säureadditionssalze.
Das erfindungsgemässe Verfahren zur Herstellung dieser Verbindung ist dadurch gekennzeichnet, dass man 5-Mercaptopyridoxin mit p-Nitrophenylchlorformiat oder Phosgen umsetzt und eine erhaltene Verbindung gegebenenfalls in die entsprechenden Säureadditionssalze überführt.
Pharmazeutisch annehmbare Säureadditionssalze umfassen diejenigen, die aus anorganischen sowie auch aus organischen Säuren hergestellt werden können, wobei diese Säuren im allgemeinen in der pharmazeutischen Praxis Anwendung finden. Es handelt sich insbesondere um Chlorwasserstoffsäure, Bromwasserstoffsäure, Schwefelsäure, Salpetersäure, Maleinsäure, Fumarsäure, Weinsäure oder Bernsteinsäure. Ebenfalls können Salze von Alkalimetallen der Mer-captangruppe sowie zweiwertige Metallkomplexe der Mer-captogruppe, wie z.B. mit Calcium oder mit Magnesium, eingesetzt werden.
Trotz der Tatsache, dass in den letzten zwei Jahrzehnten ausgedehnte Untersuchungen über gegen Entzündungen wirksame Mittel durchgeführt wurden, besteht immer noch eine dringende Notwendigkeit ein Mittel für eine wirksame Behandlung von rheumatoider Arthritis zu finden, das ebenfalls eine gute Verträglichkeit aufweist. Die üblichen, gegen Entzündungen wirksamen, analgetisch und antipyretisch wirkenden Mittel auf nicht-steroider Basis, wie z.B. Aspirin und auch viele andere experimentell neue Medikamente mit einer klinischen Bewertung, sind nur auf eine solche Weise wirksam, dass sie eine symptomatische Linderung des aktuten Krankheitsbildes bewirken, aber sie weisen nicht die Fähigkeit auf, den Verlauf der Krankheit zu ändern. Als Folge dieser Tatsache haben die antirheumatischen Wirksamkeiten der beiden alten Arzneimittel, nämlich Gold und D-Penicill-amin, trotz ihrer potentiellen Nebenwirkungen erneute Beachtung in den letzten Jahren gefunden. Die klinische Wirksamkeit der genannten beiden Medikamte wurde durch Ausführung gut kontrollierter, klinischer Studien in den verschiedensten Zentren abermals bestätigt. Verschiedene Rheumatologen. haben ihrer Meinung Ausdruck gegeben, dass eine Verbindung, die dem D-Penicillamin ähnlich sein würde, einen wertvollen Beitrag für die Medizin in diesem wichtigen Feld darstellen würde. Aus diesem Grund ist die Entdeckung sehr wichtig, dass viele der bekannten Mercaptomethylpyri-dine sowie auch die neuen Mercaptomethylpyridine der vorliegenden Erfindung in ausserordentlichem Massstab eine Aktivität gegen anti-rheumatoide Arthritis aufweisen.
Zur Feststellung dieser Eigenschaften wurden die erfin-dungsgemäss erhaltenen Verbindungen auf oralem oder topischem Wege, auf parenterale Weise, durch eine Inhalationsspray oder auch als rectal in Dosierungs-Einheitsformulie-rungen verabreicht, welche die üblichen, nicht toxischen, pharmazeutisch annehmbaren Trägermaterialien, Zusatzstoffe und andere Trägerstoffe enthielten. Der hier verwendete Ausdruck «parenteral» bezieht sich auf subcutane Injektionen, intravenöse, intramuskuläre oder intrasternale Injektionen, sowie auch auf intraarticulare oder Infusions-Verabreichungs-methoden. Zusätzlich zu der Behandlung warmblütiger Tiere, wie z.B. Mäuse, Ratten, Pferde, Hunde, Katzen, Meerschweinchen, Kaninchen u.s.w., ist die neue Verbindung ebenfalls bei der Behandlung von Menschen wirksam.
Dosierungsniveaus in einer Grössenordnung von 1 mg bis 140 mg pro Kilogramm Körpergewicht pro Tag sind bei der Behandlung der weiter oben beschriebenen Zustände nützlich. Im allgemeinen wird eine wirksame Dose in einem Bereich von 5 bis 50 mg pro Kilogramm Körpergewicht pro Tag betragen.
Es wird jedoch selbstverständlich sein, dass das spezifische Dosierungsniveau für einen beliebigen Patienten von einer Vielfalt von Faktoren abhängig sein wird, einschliesslich der Aktivität der speziell verwendeten Verbindung, abhängig von dem Alter, dem Körpergewicht, dem allgemeinen Gesundheitszustand, dem Geschlecht, der Diät, der Zeit der Verabreichung, dem Weg der Verabreichung, dem Ausscheidungsweg, der Kombination verschiedener Medikamente und dem Schwerheitsgrad der besonderen Krankheit, die behandelt werden soll.
Bei einer bevorzugten Ausführungsform des erfindungs-gemässen Verfahrens wird 2-Methyl-3-hydroxy-4-hydroxy-methyl-5-mercaptomethylpyridin mit p-Nitrophenylchlorformiat in einem aprotischen Lösungsmittel, wie z.B. Tetra-hydrofuran, Äther, Glyme, Diglyme oder anderen, bei einer Temperatur von 0 bis 10°C 1 bis 3 Stunden lang umgesetzt, gefolgt von einer Erwärmung bei 20 bis 50°C.
Beispiel
Bis-[2-methyl-3-hydroxy-4-hydroxymethylpyridyl-5--methylthio ]-carbonat
Eine Lösung von 0,1 Mol 5-Mercaptopyridoxin in 100 ml trockenem Tetrahydrofuran wird bei einer Temperatur von 0 bis 5°C gerührt, während welcher Zeit man 0,1 Mol P-Nitrophenylchlorformiat in 10 ml trockenem Tetrahydrofuran im Laufe einer Stunde hinzufügt. Nach einer weiteren Stunde wird die Lösung bei einer Temperatur von 10°C auf 10 ml eingedampft. Falls nötig, kann man das sich als Zwischenprodukt gebildete p-Nitrophenylmonothiocarbonat von 5-Mercaptopyridoxin durch Filtration während dieser Stufe isolieren.
Es besteht aber auch die Möglichkeit, weitere 0,1 Mol von 5-Mercaptopyridoxin vor dem Verdampfen hinzuzufügen u. die Tetrahydrofuran-Lösung auf eine Temperatur von 40°C zu erwärmen. Verdampfung, gefolgt von einer Extraktion des s
io
15
20
25
30
35
40
45
50
55
60
65
3
Dithiocarbonates im Äthylacetat (3 x 100 ml) aus einer gesättigten wässrigen Bicarbonatlösung wird durch das Trocknen der organischen Schicht über Magnesiumsulfat gefolgt. Die organische Schicht wird filtriert und zur Trockne eingedampft. Man chromatographiert das rohe Produkt an einer 5
634302
Silikagelkolonne mit den Massen 2 in. x 2 ft., unter Verwendung von Lösungen von Methylchlorid-Methanol als Eluiermittel, wobei man die folgende Verbindung erhält: Bis--[2-methyl-3-hydroxy-4-hydroxymethylpyridyl-5-methylthio]--carbonat.
v
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US36877473A | 1973-06-15 | 1973-06-15 | |
| US05/470,231 US3971797A (en) | 1973-06-15 | 1974-05-16 | S,S'-bis(pyridylmethyl)-carbonodithioates |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH634302A5 true CH634302A5 (de) | 1983-01-31 |
Family
ID=27004328
Family Applications (4)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH812274A CH613951A5 (de) | 1973-06-15 | 1974-06-13 | |
| CH821974A CH610305A5 (de) | 1973-06-15 | 1974-06-14 | |
| CH303278A CH634302A5 (de) | 1973-06-15 | 1978-03-20 | Verfahren zur herstellung neuer mercaptomethylpyridin-derivate. |
| CH972578A CH618428A5 (de) | 1973-06-15 | 1978-09-18 |
Family Applications Before (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH812274A CH613951A5 (de) | 1973-06-15 | 1974-06-13 | |
| CH821974A CH610305A5 (de) | 1973-06-15 | 1974-06-14 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH972578A CH618428A5 (de) | 1973-06-15 | 1978-09-18 |
Country Status (21)
| Country | Link |
|---|---|
| US (1) | US3971797A (de) |
| JP (3) | JPS5032180A (de) |
| AR (1) | AR203749A1 (de) |
| BG (1) | BG24408A3 (de) |
| CA (1) | CA1037956A (de) |
| CH (4) | CH613951A5 (de) |
| DD (1) | DD113001A5 (de) |
| DE (2) | DE2428294A1 (de) |
| DK (1) | DK148595C (de) |
| ES (1) | ES427277A1 (de) |
| FI (1) | FI58775C (de) |
| FR (2) | FR2233057B1 (de) |
| GB (2) | GB1466295A (de) |
| IE (1) | IE39467B1 (de) |
| IL (1) | IL44998A (de) |
| LU (1) | LU70342A1 (de) |
| NL (2) | NL7407618A (de) |
| NO (1) | NO144149C (de) |
| PH (1) | PH10366A (de) |
| RO (2) | RO71434A (de) |
| SE (1) | SE411346B (de) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4061759A (en) * | 1975-05-19 | 1977-12-06 | Merck & Co., Inc. | Ethenyl and ethynyl mercaptoalkyl pyridines |
| CH655110A5 (de) * | 1982-09-03 | 1986-03-27 | Otsuka Pharma Co Ltd | Carbostyrilderivate, verfahren zu deren herstellung und arzneimittel, welche diese enthalten. |
| EP0640072B1 (de) * | 1992-05-15 | 2000-08-23 | Btg International Limited | Pyridinderivate als Hydroxylase- und Lyase-Inhibitoren |
| GB2266887B (en) * | 1992-05-15 | 1996-04-17 | British Tech Group | Substituted pyridines,their preparation and pharmaceutical use |
| GB201718148D0 (en) * | 2017-11-02 | 2017-12-20 | Ipotts Ltd | Hair cutting comb |
| GB2603007B (en) * | 2021-01-26 | 2023-01-11 | Pickuls Gizmo Ltd | A hair cutting guide |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3515726A (en) * | 1968-10-16 | 1970-06-02 | Olin Mathieson | 2,2'-bis(pyridyl-n-oxide) dithiolcarbonates and trithiocarbonates |
-
1974
- 1974-05-16 US US05/470,231 patent/US3971797A/en not_active Expired - Lifetime
- 1974-06-03 FI FI1685/74A patent/FI58775C/fi active
- 1974-06-04 SE SE7407296A patent/SE411346B/xx not_active IP Right Cessation
- 1974-06-06 NL NL7407618A patent/NL7407618A/xx not_active Application Discontinuation
- 1974-06-06 DK DK303274A patent/DK148595C/da not_active IP Right Cessation
- 1974-06-06 NL NLAANVRAGE7407616,A patent/NL185841C/xx not_active IP Right Cessation
- 1974-06-06 NO NO742042A patent/NO144149C/no unknown
- 1974-06-10 CA CA202,346A patent/CA1037956A/en not_active Expired
- 1974-06-10 IL IL44998A patent/IL44998A/en unknown
- 1974-06-10 PH PH15930A patent/PH10366A/en unknown
- 1974-06-11 IE IE1219/74A patent/IE39467B1/xx unknown
- 1974-06-12 GB GB2617874A patent/GB1466295A/en not_active Expired
- 1974-06-12 DE DE19742428294 patent/DE2428294A1/de not_active Ceased
- 1974-06-12 GB GB2617674A patent/GB1466386A/en not_active Expired
- 1974-06-12 DE DE2428409A patent/DE2428409C3/de not_active Expired
- 1974-06-13 CH CH812274A patent/CH613951A5/xx not_active IP Right Cessation
- 1974-06-13 FR FR7420549A patent/FR2233057B1/fr not_active Expired
- 1974-06-13 FR FR7420548A patent/FR2233056B1/fr not_active Expired
- 1974-06-14 BG BG026975A patent/BG24408A3/xx unknown
- 1974-06-14 DD DD179177A patent/DD113001A5/xx unknown
- 1974-06-14 CH CH821974A patent/CH610305A5/xx not_active IP Right Cessation
- 1974-06-14 ES ES427277A patent/ES427277A1/es not_active Expired
- 1974-06-14 AR AR254190A patent/AR203749A1/es active
- 1974-06-14 RO RO7479181A patent/RO71434A/ro unknown
- 1974-06-14 RO RO7490744A patent/RO70852A/ro unknown
- 1974-06-15 JP JP49067657A patent/JPS5032180A/ja active Pending
- 1974-06-15 JP JP49067658A patent/JPS5032181A/ja active Pending
- 1974-06-17 LU LU70342A patent/LU70342A1/xx unknown
-
1978
- 1978-01-13 JP JP209778A patent/JPS5387363A/ja active Granted
- 1978-03-20 CH CH303278A patent/CH634302A5/de not_active IP Right Cessation
- 1978-09-18 CH CH972578A patent/CH618428A5/de not_active IP Right Cessation
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE2711451C2 (de) | ||
| DE2721171C3 (de) | Vincamin-5-pyridoxalphosphat, seine Herstellung und enthaltende Zubereitungen | |
| CH649545A5 (de) | Arzneimittel gegen theileriosen. | |
| DE3537656C2 (de) | ||
| DE1770171C3 (de) | 2,2-Dimethyl-7-alkyl-4-(4-pyridyl)-2H-chromen-5-ole, Verfahren zu ihrer Herstellung und diese Verbindungen enthaltende Arzneipräparate | |
| DE3000743A1 (de) | Arzneipraeparat auf der basis eines salzes der acetylsalicylsaeure und einer basischen aminosaeure und verfahren zu seiner herstellung | |
| CH634302A5 (de) | Verfahren zur herstellung neuer mercaptomethylpyridin-derivate. | |
| DE2729414A1 (de) | Thiazolidincarbonsaeurederivate, verfahren zu ihrer herstellung und sie enthaltende arzneimittel | |
| DE2625053C3 (de) | Arzneimittel zur Kontrolle von Leberkrankheiten | |
| DE3016549C2 (de) | 2-Isopropylamino-5-halogenopyrimidine, Verfahren zu deren Herstellung und diese enthaltende therapeutische Zusammensetzungen | |
| DE2630015C3 (de) | 4,5,6,7-Tetrahydro-3(4-methoxyphenyl)-indazol und diese Verbindung enthaltende Arzneimittel | |
| DE2104851A1 (de) | ||
| DE1695298B2 (de) | S-AcetamMo-e-methyl-e-n-propyl-striazolo eckige Klammer auf 4,3-a eckige Klammer zu pyrazin und Verfahren zu seiner Herstellung und Arzneimittel | |
| DE2521905C2 (de) | Arzneimittel zur cerebralen Durchblutungsförderung | |
| DE2158801C3 (de) | ||
| DE2716374C2 (de) | N-2-(p-Chlorphenoxy)-isobutyryl-N'-morpholinmethylharnstoff, dessen Salze, Verfahren zu deren Herstellung und pharmazeutische Zubereitung | |
| DE2102246C3 (de) | ||
| CH654302A5 (de) | Acylaminophenolderivate, ihre herstellung und arzneimittel, welche sie enthalten. | |
| DE2361488C3 (de) | Verwendung von Tri-n-propylessigsäurederivaten | |
| DE3237438C2 (de) | 2-Thiazolamin-Derivate und dieselben enthaltende pharmazeutische Zusammensetzungen | |
| DE2544100A1 (de) | Arzneimittel mit einem gehalt an 2-naphthyl-buttersaeurederivaten | |
| DE1695907C3 (de) | Verwendung von 3,5-Dimethyl-l,2oxazinon-(6) | |
| DE2227487C3 (de) | Derivate von 3-Äthoxycarbonyl-S-hydroxy-2-methyl-4-piperazinomethyl-indol, Verfahren zu ihrer Herstellung und Arzneimittel | |
| DE2542154A1 (de) | 6-aryloxy-2-oxo-1-aza-oxa (oder -thia) -spiro eckige klammer auf 4,5 eckige klammer zu -decane, verfahren zu ihrer herstellung und sie enthaltende arzneimittel | |
| DE2416302B2 (de) | Dimeres sowie trimeres silybin und deren n-methylglucaminsalz und verfahren zu deren herstellung sowie diese verbindungen enthaltende arzneimittel |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PL | Patent ceased | ||
| PL | Patent ceased |