USRE28532E - 5-Fluoro-3-pyridinemethanol, esters thereof and therapeutically acceptable salts thereof - Google Patents
5-Fluoro-3-pyridinemethanol, esters thereof and therapeutically acceptable salts thereof Download PDFInfo
- Publication number
- USRE28532E USRE28532E US35127173A USRE28532E US RE28532 E USRE28532 E US RE28532E US 35127173 A US35127173 A US 35127173A US RE28532 E USRE28532 E US RE28532E
- Authority
- US
- United States
- Prior art keywords
- acid
- percent
- fluoro
- solution
- mixture
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
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- 150000003839 salts Chemical class 0.000 title claims description 24
- GGGJYJXAFSEWNM-UHFFFAOYSA-N (5-fluoropyridin-3-yl)methanol Chemical compound OCC1=CN=CC(F)=C1 GGGJYJXAFSEWNM-UHFFFAOYSA-N 0.000 title claims description 19
- 150000002148 esters Chemical class 0.000 title description 7
- 150000001875 compounds Chemical class 0.000 claims abstract description 76
- 229910052736 halogen Inorganic materials 0.000 abstract description 21
- 210000002966 serum Anatomy 0.000 abstract description 10
- 150000002632 lipids Chemical class 0.000 abstract description 4
- 125000005843 halogen group Chemical group 0.000 abstract description 2
- 230000005764 inhibitory process Effects 0.000 abstract description 2
- 125000000962 organic group Chemical group 0.000 abstract description 2
- 150000003222 pyridines Chemical class 0.000 abstract description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 129
- 239000000243 solution Substances 0.000 description 78
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 75
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 62
- 239000000203 mixture Substances 0.000 description 58
- 239000000047 product Substances 0.000 description 48
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 41
- 229910052739 hydrogen Inorganic materials 0.000 description 41
- 239000002904 solvent Substances 0.000 description 40
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 39
- 239000001257 hydrogen Substances 0.000 description 37
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 37
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 30
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 30
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 27
- 239000002253 acid Substances 0.000 description 27
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 26
- 238000004458 analytical method Methods 0.000 description 26
- -1 hydrochloric Chemical class 0.000 description 25
- 238000006243 chemical reaction Methods 0.000 description 23
- 239000000460 chlorine Substances 0.000 description 23
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 22
- 238000002360 preparation method Methods 0.000 description 21
- 150000002367 halogens Chemical group 0.000 description 20
- 229920006395 saturated elastomer Polymers 0.000 description 18
- 239000011541 reaction mixture Substances 0.000 description 17
- 239000000706 filtrate Substances 0.000 description 16
- 239000003921 oil Substances 0.000 description 16
- 235000019198 oils Nutrition 0.000 description 16
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 15
- 238000007792 addition Methods 0.000 description 14
- 238000001704 evaporation Methods 0.000 description 14
- 230000008020 evaporation Effects 0.000 description 14
- 239000007788 liquid Substances 0.000 description 14
- 235000017557 sodium bicarbonate Nutrition 0.000 description 14
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 14
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 13
- 235000011167 hydrochloric acid Nutrition 0.000 description 13
- 229960000443 hydrochloric acid Drugs 0.000 description 13
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 12
- 229960004132 diethyl ether Drugs 0.000 description 12
- 150000002431 hydrogen Chemical group 0.000 description 12
- 238000001953 recrystallisation Methods 0.000 description 12
- 239000007787 solid Substances 0.000 description 12
- 239000003826 tablet Substances 0.000 description 12
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 11
- 238000001816 cooling Methods 0.000 description 11
- PVNIIMVLHYAWGP-UHFFFAOYSA-N Niacin Chemical compound OC(=O)C1=CC=CN=C1 PVNIIMVLHYAWGP-UHFFFAOYSA-N 0.000 description 10
- 239000002244 precipitate Substances 0.000 description 10
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 9
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 9
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 9
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 9
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 239000007864 aqueous solution Substances 0.000 description 9
- 239000005457 ice water Substances 0.000 description 9
- 229910052751 metal Inorganic materials 0.000 description 9
- 239000002184 metal Substances 0.000 description 9
- 238000000034 method Methods 0.000 description 9
- 229910052938 sodium sulfate Inorganic materials 0.000 description 9
- 235000011152 sodium sulphate Nutrition 0.000 description 9
- BXZSBDDOYIWMGC-UHFFFAOYSA-N 5-fluoropyridine-3-carboxylic acid Chemical compound OC(=O)C1=CN=CC(F)=C1 BXZSBDDOYIWMGC-UHFFFAOYSA-N 0.000 description 8
- 239000013543 active substance Substances 0.000 description 8
- 238000004821 distillation Methods 0.000 description 8
- 229910052753 mercury Inorganic materials 0.000 description 8
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 8
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 8
- 238000003756 stirring Methods 0.000 description 8
- 241000282472 Canis lupus familiaris Species 0.000 description 7
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 7
- 150000005690 diesters Chemical class 0.000 description 7
- 238000005984 hydrogenation reaction Methods 0.000 description 7
- 239000012280 lithium aluminium hydride Substances 0.000 description 7
- 239000003208 petroleum Substances 0.000 description 7
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 7
- 239000007858 starting material Substances 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 6
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
- 238000005481 NMR spectroscopy Methods 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 125000000217 alkyl group Chemical group 0.000 description 6
- 239000002775 capsule Substances 0.000 description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 6
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 6
- 239000003054 catalyst Substances 0.000 description 6
- 229910052801 chlorine Chemical group 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 239000007903 gelatin capsule Substances 0.000 description 6
- KJIFKLIQANRMOU-UHFFFAOYSA-N oxidanium;4-methylbenzenesulfonate Chemical compound O.CC1=CC=C(S(O)(=O)=O)C=C1 KJIFKLIQANRMOU-UHFFFAOYSA-N 0.000 description 6
- 238000010992 reflux Methods 0.000 description 6
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 6
- 238000005406 washing Methods 0.000 description 6
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 5
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 5
- 239000002585 base Substances 0.000 description 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 5
- 229910052731 fluorine Inorganic materials 0.000 description 5
- 239000011737 fluorine Substances 0.000 description 5
- 235000021588 free fatty acids Nutrition 0.000 description 5
- 238000002329 infrared spectrum Methods 0.000 description 5
- 239000011664 nicotinic acid Substances 0.000 description 5
- 235000001968 nicotinic acid Nutrition 0.000 description 5
- 239000012258 stirred mixture Substances 0.000 description 5
- 239000000725 suspension Substances 0.000 description 5
- 239000006188 syrup Substances 0.000 description 5
- 235000020357 syrup Nutrition 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 5
- 125000004417 unsaturated alkyl group Chemical group 0.000 description 5
- WGNUNYPERJMVRM-UHFFFAOYSA-N 3-pyridylacetic acid Chemical compound OC(=O)CC1=CC=CN=C1 WGNUNYPERJMVRM-UHFFFAOYSA-N 0.000 description 4
- LQJWCPZRNHAVJD-UHFFFAOYSA-N 5-fluoropyridine-3-carbonitrile Chemical compound FC1=CN=CC(C#N)=C1 LQJWCPZRNHAVJD-UHFFFAOYSA-N 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 4
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 4
- 108010010803 Gelatin Proteins 0.000 description 4
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 4
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 4
- 238000010533 azeotropic distillation Methods 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 4
- 125000001309 chloro group Chemical group Cl* 0.000 description 4
- ORTQZVOHEJQUHG-UHFFFAOYSA-L copper(II) chloride Chemical compound Cl[Cu]Cl ORTQZVOHEJQUHG-UHFFFAOYSA-L 0.000 description 4
- GAOUAPNRNSFZGW-UHFFFAOYSA-N ethyl 5-fluoropyridine-3-carboxylate Chemical compound CCOC(=O)C1=CN=CC(F)=C1 GAOUAPNRNSFZGW-UHFFFAOYSA-N 0.000 description 4
- 239000000284 extract Substances 0.000 description 4
- 125000001153 fluoro group Chemical group F* 0.000 description 4
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 4
- 239000008273 gelatin Substances 0.000 description 4
- 229920000159 gelatin Polymers 0.000 description 4
- 235000019322 gelatine Nutrition 0.000 description 4
- 235000011852 gelatine desserts Nutrition 0.000 description 4
- 239000008187 granular material Substances 0.000 description 4
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 4
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
- 238000002347 injection Methods 0.000 description 4
- 239000007924 injection Substances 0.000 description 4
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 229960003512 nicotinic acid Drugs 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 229910000027 potassium carbonate Inorganic materials 0.000 description 4
- 235000011181 potassium carbonates Nutrition 0.000 description 4
- 229920001592 potato starch Polymers 0.000 description 4
- 235000010288 sodium nitrite Nutrition 0.000 description 4
- 231100000419 toxicity Toxicity 0.000 description 4
- 230000001988 toxicity Effects 0.000 description 4
- SFLSHLFXELFNJZ-QMMMGPOBSA-N (-)-norepinephrine Chemical compound NC[C@H](O)C1=CC=C(O)C(O)=C1 SFLSHLFXELFNJZ-QMMMGPOBSA-N 0.000 description 3
- FMCCVRHTUFNEPV-UHFFFAOYSA-N 3-(chloromethyl)-5-fluoropyridine Chemical compound FC1=CN=CC(CCl)=C1 FMCCVRHTUFNEPV-UHFFFAOYSA-N 0.000 description 3
- MVQVNTPHUGQQHK-UHFFFAOYSA-N 3-pyridinemethanol Chemical compound OCC1=CC=CN=C1 MVQVNTPHUGQQHK-UHFFFAOYSA-N 0.000 description 3
- QCQCHGYLTSGIGX-GHXANHINSA-N 4-[[(3ar,5ar,5br,7ar,9s,11ar,11br,13as)-5a,5b,8,8,11a-pentamethyl-3a-[(5-methylpyridine-3-carbonyl)amino]-2-oxo-1-propan-2-yl-4,5,6,7,7a,9,10,11,11b,12,13,13a-dodecahydro-3h-cyclopenta[a]chrysen-9-yl]oxy]-2,2-dimethyl-4-oxobutanoic acid Chemical compound N([C@@]12CC[C@@]3(C)[C@]4(C)CC[C@H]5C(C)(C)[C@@H](OC(=O)CC(C)(C)C(O)=O)CC[C@]5(C)[C@H]4CC[C@@H]3C1=C(C(C2)=O)C(C)C)C(=O)C1=CN=CC(C)=C1 QCQCHGYLTSGIGX-GHXANHINSA-N 0.000 description 3
- DINIMVOXGAFQJL-UHFFFAOYSA-N 5-fluoropyridine-3-carbonyl chloride Chemical compound FC1=CN=CC(C(Cl)=O)=C1 DINIMVOXGAFQJL-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 3
- 241000699670 Mus sp. Species 0.000 description 3
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 3
- 229920002472 Starch Polymers 0.000 description 3
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 125000000278 alkyl amino alkyl group Chemical group 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 125000004103 aminoalkyl group Chemical group 0.000 description 3
- 235000011114 ammonium hydroxide Nutrition 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 230000037396 body weight Effects 0.000 description 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 3
- 239000003638 chemical reducing agent Substances 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 238000009833 condensation Methods 0.000 description 3
- 230000005494 condensation Effects 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 239000012458 free base Substances 0.000 description 3
- 150000004820 halides Chemical class 0.000 description 3
- 229960000367 inositol Drugs 0.000 description 3
- CDAISMWEOUEBRE-GPIVLXJGSA-N inositol Chemical compound O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@H](O)[C@@H]1O CDAISMWEOUEBRE-GPIVLXJGSA-N 0.000 description 3
- 238000007912 intraperitoneal administration Methods 0.000 description 3
- 239000008101 lactose Substances 0.000 description 3
- 239000000155 melt Substances 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 229910052987 metal hydride Inorganic materials 0.000 description 3
- 150000004681 metal hydrides Chemical class 0.000 description 3
- 229960002748 norepinephrine Drugs 0.000 description 3
- SFLSHLFXELFNJZ-UHFFFAOYSA-N norepinephrine Natural products NCC(O)C1=CC=C(O)C(O)=C1 SFLSHLFXELFNJZ-UHFFFAOYSA-N 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 125000000369 oxido group Chemical group [*]=O 0.000 description 3
- 239000000825 pharmaceutical preparation Substances 0.000 description 3
- 239000011591 potassium Substances 0.000 description 3
- 229960003975 potassium Drugs 0.000 description 3
- CDAISMWEOUEBRE-UHFFFAOYSA-N scyllo-inosotol Natural products OC1C(O)C(O)C(O)C(O)C1O CDAISMWEOUEBRE-UHFFFAOYSA-N 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 239000012279 sodium borohydride Substances 0.000 description 3
- 229910000033 sodium borohydride Inorganic materials 0.000 description 3
- 239000011780 sodium chloride Substances 0.000 description 3
- 235000019698 starch Nutrition 0.000 description 3
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 3
- 229940088594 vitamin Drugs 0.000 description 3
- 235000013343 vitamin Nutrition 0.000 description 3
- 239000011782 vitamin Substances 0.000 description 3
- 229930003231 vitamin Natural products 0.000 description 3
- RYICOVXDBBDCNT-UHFFFAOYSA-N (5-fluoropyridin-3-yl)methanamine Chemical compound NCC1=CN=CC(F)=C1 RYICOVXDBBDCNT-UHFFFAOYSA-N 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- PFOZTYJEKXOWQS-UHFFFAOYSA-N 3-(chloromethyl)-5-fluoropyridine;hydrochloride Chemical compound Cl.FC1=CN=CC(CCl)=C1 PFOZTYJEKXOWQS-UHFFFAOYSA-N 0.000 description 2
- HXIYCKAAQPHZBM-UHFFFAOYSA-N 3-methyl-1,2-oxazole-5-carboxylic acid Chemical compound CC=1C=C(C(O)=O)ON=1 HXIYCKAAQPHZBM-UHFFFAOYSA-N 0.000 description 2
- XYLPLVUYPAPCML-UHFFFAOYSA-N 5-chloropyridine-3-carboxylic acid Chemical compound OC(=O)C1=CN=CC(Cl)=C1 XYLPLVUYPAPCML-UHFFFAOYSA-N 0.000 description 2
- 244000215068 Acacia senegal Species 0.000 description 2
- 229920000945 Amylopectin Polymers 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 2
- 229910021591 Copper(I) chloride Inorganic materials 0.000 description 2
- 229920002261 Corn starch Polymers 0.000 description 2
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 2
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 2
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 2
- 101100391174 Dictyostelium discoideum forC gene Proteins 0.000 description 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-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
- 229920000084 Gum arabic Polymers 0.000 description 2
- 229930195725 Mannitol Natural products 0.000 description 2
- 235000019483 Peanut oil Nutrition 0.000 description 2
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- 239000004615 ingredient Substances 0.000 description 1
- 208000014674 injury Diseases 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- BYXYCUABYHCYLY-UHFFFAOYSA-N isoindole-1,3-dione;potassium Chemical compound [K].C1=CC=C2C(=O)NC(=O)C2=C1 BYXYCUABYHCYLY-UHFFFAOYSA-N 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 230000037356 lipid metabolism Effects 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 210000003141 lower extremity Anatomy 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000011702 manganese sulphate Substances 0.000 description 1
- 235000007079 manganese sulphate Nutrition 0.000 description 1
- SQQMAOCOWKFBNP-UHFFFAOYSA-L manganese(II) sulfate Chemical compound [Mn+2].[O-]S([O-])(=O)=O SQQMAOCOWKFBNP-UHFFFAOYSA-L 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- VRWLBMGRSLQKSU-UHFFFAOYSA-N methanol;pyridine Chemical class OC.C1=CC=NC=C1 VRWLBMGRSLQKSU-UHFFFAOYSA-N 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000002808 molecular sieve Substances 0.000 description 1
- PBMIETCUUSQZCG-UHFFFAOYSA-N n'-cyclohexylmethanediimine Chemical compound N=C=NC1CCCCC1 PBMIETCUUSQZCG-UHFFFAOYSA-N 0.000 description 1
- NCYVXEGFNDZQCU-UHFFFAOYSA-N nikethamide Chemical compound CCN(CC)C(=O)C1=CC=CN=C1 NCYVXEGFNDZQCU-UHFFFAOYSA-N 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 101150061302 och1 gene Proteins 0.000 description 1
- 229940006093 opthalmologic coloring agent diagnostic Drugs 0.000 description 1
- 239000010502 orange oil Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229940094443 oxytocics prostaglandins Drugs 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 210000005259 peripheral blood Anatomy 0.000 description 1
- 239000011886 peripheral blood Substances 0.000 description 1
- 230000036581 peripheral resistance Effects 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 229950010765 pivalate Drugs 0.000 description 1
- IUGYQRQAERSCNH-UHFFFAOYSA-N pivalic acid Chemical compound CC(C)(C)C(O)=O IUGYQRQAERSCNH-UHFFFAOYSA-N 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000000244 polyoxyethylene sorbitan monooleate Substances 0.000 description 1
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 1
- 229920000053 polysorbate 80 Polymers 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- 229910000105 potassium hydride Inorganic materials 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 229940086066 potassium hydrogencarbonate Drugs 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- WYDUSKDSKCASEF-UHFFFAOYSA-N procyclidine Chemical compound C1CCCCC1C(C=1C=CC=CC=1)(O)CCN1CCCC1 WYDUSKDSKCASEF-UHFFFAOYSA-N 0.000 description 1
- SSOLNOMRVKKSON-UHFFFAOYSA-N proguanil Chemical compound CC(C)\N=C(/N)N=C(N)NC1=CC=C(Cl)C=C1 SSOLNOMRVKKSON-UHFFFAOYSA-N 0.000 description 1
- VPKZYIQISRGLMK-UHFFFAOYSA-N prop-2-enoic acid;pyridine Chemical compound OC(=O)C=C.C1=CC=NC=C1 VPKZYIQISRGLMK-UHFFFAOYSA-N 0.000 description 1
- 229960004063 propylene glycol Drugs 0.000 description 1
- 235000013772 propylene glycol Nutrition 0.000 description 1
- KFUSANSHCADHNJ-UHFFFAOYSA-N pyridine-3-carbohydrazide Chemical compound NNC(=O)C1=CC=CN=C1 KFUSANSHCADHNJ-UHFFFAOYSA-N 0.000 description 1
- OYSBZLVHMPNJMR-UHFFFAOYSA-N pyridine-3-carboxylic acid Chemical compound OC(=O)C1=CC=CN=C1.OC(=O)C1=CC=CN=C1 OYSBZLVHMPNJMR-UHFFFAOYSA-N 0.000 description 1
- 230000008707 rearrangement Effects 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 239000010948 rhodium Substances 0.000 description 1
- 235000019204 saccharin Nutrition 0.000 description 1
- CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 1
- 229940081974 saccharin Drugs 0.000 description 1
- 239000000901 saccharin and its Na,K and Ca salt Substances 0.000 description 1
- 239000012047 saturated solution Substances 0.000 description 1
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
- 239000012312 sodium hydride Substances 0.000 description 1
- 229910000104 sodium hydride Inorganic materials 0.000 description 1
- 229910052979 sodium sulfide Inorganic materials 0.000 description 1
- GRVFOGOEDUUMBP-UHFFFAOYSA-N sodium sulfide (anhydrous) Chemical compound [Na+].[Na+].[S-2] GRVFOGOEDUUMBP-UHFFFAOYSA-N 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000001256 steam distillation Methods 0.000 description 1
- 231100000240 steatosis hepatitis Toxicity 0.000 description 1
- 238000000859 sublimation Methods 0.000 description 1
- 230000008022 sublimation Effects 0.000 description 1
- 239000001117 sulphuric acid Substances 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- DLYUQMMRRRQYAE-UHFFFAOYSA-N tetraphosphorus decaoxide Chemical compound O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 150000007970 thio esters Chemical group 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 230000008733 trauma Effects 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- ILWRPSCZWQJDMK-UHFFFAOYSA-N triethylazanium;chloride Chemical compound Cl.CCN(CC)CC ILWRPSCZWQJDMK-UHFFFAOYSA-N 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- 230000002792 vascular Effects 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 229940117958 vinyl acetate Drugs 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- 230000003442 weekly effect Effects 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 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
- C07D213/24—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
- C07D213/30—Oxygen atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/455—Nicotinic acids, e.g. niacin; Derivatives thereof, e.g. esters, amides
-
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- 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
- C07D213/36—Radicals substituted by singly-bound nitrogen atoms
- C07D213/38—Radicals substituted by singly-bound nitrogen atoms having only hydrogen or hydrocarbon radicals attached to the substituent nitrogen atom
-
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- 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
- C07D213/36—Radicals substituted by singly-bound nitrogen atoms
- C07D213/40—Acylated substituent nitrogen atom
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- 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
- C07D213/54—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/55—Acids; Esters
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- 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
- C07D213/61—Halogen atoms or nitro radicals
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- C—CHEMISTRY; METALLURGY
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- 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
- C07D213/73—Unsubstituted amino or imino radicals
-
- C—CHEMISTRY; METALLURGY
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- 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
- C07D213/79—Acids; Esters
- C07D213/80—Acids; Esters in position 3
-
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- 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
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- C—CHEMISTRY; METALLURGY
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
Definitions
- ABSTRACT 3.5-substituted pyridines, which in one of the positions 3 and 5 may be substituted by halogen or NH and in the other position are substituted by an organic group.
- the compounds are useful for the inhibition of serum lipid mobilization.
- a is B can also be a member of the group consisting of and B not being hydrogen when A is and R is H; B not being hydrogen when A is o it and R' is a member of the group consisting ofhydrogen.
- halogen and NH in which formulas n is an integer from to 3 inclusive. R being hydrogen when n is l; p is an integer from i to 4 inclusive, R being hydrogen when p is 2; m is an integer from 0 to 4 inclusive, m being 0 when B is a member of the class consisting of the radicals l )(4), and is linked to A via a member of the group consisting of oxygen and nitrogen atoms; R is a member of the group consisting of hydrogen,
- halogen and NH R is a member of the group consisting of hydrogen, halogen, NH straight. branched, saturated and unsaturated alkyl groups; D is selected from the class consisting of straight. branched saturated and unsaturated alkylene groups containing at most 6 carbon atoms; the group of atoms AB can also be a member of the class consisting of ig/[ and U wherein R and R are selected from the class consisting of straight. branched, saturated. and unsaturated alkyl groups, hydroxylalkyl and carboxyalkyl groups.
- therapeutically acceptable salt is recognized in the art to designate an acid addition salt, which is physiologically innocuous when administered in a dosage and at an interval (e.g. frequency of administration) that is effective for the indicated therapeutic use of the parent compound.
- Typical therapeutically acceptable acid addition salts include but are not limited to the salts of mineral acids, such as hydrochloric,
- n is one of the integers 0, 2 and 3, and R is hydrogen, halogen or NH;,, R being halogen when n is 0, may be prepared according to the following reaction schemes:
- the pyridine acrylic acid may be prepared by condensation of 5-substituted 3-pyridinecarboxaldehyde with malonic acid, or (by the similar Perkin and Claisen condensations) with acetic anhydride and ethyl acetate.
- the reduction of the S-substituted, 3- pyridineacrylic acid may be carried out by catalytical hydrogenation or by the use of various reducing agents, such as a mixture of red phosphorus and hydroiodic acid.
- the preferred method is condensation of malonic acid with 5-substituted 3-pyridinecarboxaldehyde and reduction of the acrylic acid;
- Compounds of Formula 6, wherein R is fluoro or chloro and n is (J, may also be prepared by reacting a compound of the formula with sodium nitrite and (l) cupric chloride in'hydrochloric acid solution,
- reaction of the aminonicotinic acid is carried out in a cooled water solution also containing tetrahydrofuran.
- R" is hydrogen, halogen, NH- or an alkyl group which may be straight, branched, saturated or unsaturated, are prepared by reacting a compound of the formula with a compound of the formula wherein R, n and B have the meaning specified above, Y is halogen or a hydroxy group and X is carboxyl, a metal carboxylate group or an activated carboxyl group, in which case the compound of Formula II is an acid chloride, an alkyl ester, an acid anhydride or a mixed anhydride with alkoxy formic acids, carboxylic acids, sulphonic or inorganic acids or derivatives obtained by a reaction between a carboxylic acid and a carbodiimide or similarly functioning compounds such as N,N-carbonyldiimidazole or N-ethyl-S- phenylisoxazolium-3-sulphonate, X being a metal carboxylate group when Y is halogen, whereafter the com pound of Formula I thus
- the reaction may be performed in the presence of aqueous or anhydrous organic solvents such as chloroform, diethyl ether, tetrahydrofuran, benzene and toluene, or without solvents.
- aqueous or anhydrous organic solvents such as chloroform, diethyl ether, tetrahydrofuran, benzene and toluene, or without solvents.
- an acid catalyst such as sulphuric acid, hydrogen chloride, p-toluene sulphonic acid, benzene sulphonic acid or salts with high to intermediate acid strength, even including ion exchangers saturated with hydrogen ions.
- the water formed during the reaction may be removed from the reaction mixture by azeotropic distillation or taken up by drying agents such as anhydrous cupric or manganese sulphate and molecular sieves.
- the hydrogen halide liberated may be neutralized and the reaction catalyzed by a base such as pyridine and triethylamine.
- a dehydrating reagent such as sulfuric acid or alumina at higher temperatures may be used.
- Y is a halogen atom
- X is a metal oxido group
- the reaction is preferably carried out in a solvent such as ether, tetrahydrofurane and benzene or the alcohol corresponding to the metal alcoholate.
- the metal alcoholate in the alcohol solvent could be obtained by dissolving a suitable amount of metal, such as sodium, in the excess of alcohol.
- the compound of Formula IX thus obtained is transformed, if necessary, into a therapeutically acceptable salt by reaction with the appropriate acid.
- Ethers of the formula wherein p and R have the meaning specified above, R being hydrogen when p is 2, and A is an alkyl group or pyranyl, may be prepared by adding in known manner an alcohol of the formula RILH/XYKJ 11,-) For:
- p is an integer from l to 4 inclusive; particularly p may be I; and R is hydrogen, halogen or NH R being hydrogen when p is 2, particularly R may be a fluorine, chlorine or bromine atom; a compound of the general formula or a salt thereof, wherein R and p have the meaning specified above, particularly, R may be a fluorine,
- X is a formyl, carboxyl, chlorocarbonyl, alkoxycarbonyl, thiolester or a cyano group
- X is a formyl, carboxyl, chlorocarbonyl, alkoxycarbonyl, thiolester or a cyano group
- methods known to be applicable to the reduction of the unsubstituted analogues, for example catalytical hydrogenation and reduction by means of a complex metal hydride, to the formation of a compound of the general formula and, where a therapeutically acceptable salt is required, reacting the compound of Formula XI with the appropriate acid.
- a compound of the Formula XII is reduced by means of complex metal hydrides, such as sodium or potassium borohydride and lithium aluminum hydride.
- complex metal hydrides such as sodium or potassium borohydride and lithium aluminum hydride.
- the reaction may be performed in such solvents as methanol, ethanol, water or mixtures thereof.
- lithium aluminum hydride is used as the reducing agent, the reaction is preferably performed in inert solvents such as diethyl ether and tetrahydrofuran.
- Compounds of Formula XI may also be prepared by treating an amine of the formula with a nitrite such as sodium nitrite in a water solution under such conditions that the intermediate diazonium compound decomposes and reacts with water to form an alcohol.
- a nitrite such as sodium nitrite
- R is hydrogen, halogen or NH D is a straight, branched, saturated or unsaturated alkylene group containing at most 6 carbon atoms
- B is a member of the class consisting of hydrogen, straight, branched, saturated and unsaturated alkyl groups; the group-D-B containing at most 12 carbon atoms when B is alkyl; eycloalkyl, phenylalkyl, alkyloxyalkyl, aryloxyalkyl, aminoalkyl, lower alkylaminoalkyl, dialkylaminoalkyl,
- R and R are hydrogen or alkyl groups which may be straight, branched, saturated or unsaturated, may be prepared by reduction of a compound of the formula wherein p and R have the meaning specified above and X is CHO or CN.
- the reduction is carried out by catalytical hydrogenation in the presence of an amine of the formula when X is CHO; R and R are hydrogen when X is CN.
- the reduction may be carried out by means of catalytical hydrogenation or by using a complex metal hydride such as lithium aluminum hydride, when X is not CHO.
- Compounds of Formula XIV wherein R and R are hydrogen may also be prepared by reduction of the compound When a cyano or azido group is reduced, the reduction may be carried out by hydrogenation in the presence of catalysts such as rhodium, palladium, platina or Raney-nickel, preferably in the presence of hydrochloric acid or ammonia in suitable solvents such as dry or aqueous methanol and ethanol.
- catalysts such as rhodium, palladium, platina or Raney-nickel
- suitable solvents such as dry or aqueous methanol and ethanol.
- X is -CONR R
- the reduction is preferably carried out by means of lithium aluminum hydride in inert solvents such as diethyl ether or tetahydrofuran.
- Compounds of Formula XIV wherein R and R are hydrogen may also be prepared by reduction of the corresponding oxime or hydrazone.
- the oxime may be reduced by zinc and acetic acid. The reduction may also be carried out by means of catalytical hydrogenation.
- Primary amines may also be prepared by reacting the corresponding amide with NaOX, wherein X is a chlorine or bromine atom (Hofmann rearrangement); by reacting the corresponding carboxylic acid with HN;, according to Schmidt; and by rearrangement of a compound of the formula with an amine of the formula wherein p, R, R and R have the meaning specified above.
- the compounds of Formula XIV are transformed into therapeutically acceptable salts by reaction with the appropriate acid.
- Another method to prepare compounds of Formula XV is to react a compound of the formula with a compound of the formula wherein R, R and R have the meaning specified above and X is a member of the class consisting of activated carboxyl groups such as an acid halide, an alkyl ester, an acid anhydride, a mixed anhydride with formic esters or carboxylic acids, sulphonic or inorganic acids or derivatives obtained by a reaction between a carboxylic acid and a carbodiimide or similarly functioning compounds such as N,N-carbonyl-diimidazole or N-ethyl-5-phenylisoxazolium-3'-sulphonate.
- activated carboxyl groups such as an acid halide, an alkyl ester, an acid anhydride, a mixed anhydride with formic esters or carboxylic acids, sulphonic or inorganic acids or derivatives obtained by a reaction between a carboxylic acid and a carbodiimide or similarly functioning
- EXAMPLE 1 Preparation of 5-fluoronicotinic acid A mixture of S-aminonicotinic acid (108 g.) in 700 ml. of fluoboric acid (48-50% w./w.), 530 ml. of tetrahydrofuran and 350 ml. of water was cooled in an icesalt bath and with stirring sodium nitrite (71 g.) in a sat urated water solution was added at such a rate that the temperature was lower than 3 C. 350 ml. of tetrahydrofuran was added and the mixture stirred for one hour at -5 C.l0 C.
- EXAMPLE 3 Preparation of tablets containing S-fluoronicotinic acid 100 g. of -fluoronicotinic acid were mixed with 50 g. of lactose and 45 g. of potato starch and moistened with a starch paste prepared from 5 g. of potato starch and distilled water, whercafter the mixture was granulated through a sieve. The granulate was dried and sieved whereafter 2 g. of magnesium stearate were mixed in. Finally the mixture was pressed into tablets. each weighing 202 mg.
- EXAMPLE 4 Pyrazole- 3-methyl 5 -fluoronicotinate To a stirred and refluxed mixture of 3- pyrazolmethanol (2.95 g. 5-fluoronicotinic acid chloride hydrochloride (4/3 equivalents) and 8 ml. of 30% wjw. hydrochlorine-diethylether in 100 ml. of anhydrous tetrahydrofuran, 30 ml. of triethylaminc was added during 1.75 hours. The stirred mixture was further refluxed during 4.5 hours and then the precipitated hydrochloride was filtered off and washed with 300 ml. of diethyl ether.
- EXAMPLE 8 5 fluoronicotinic acid methyl ester S-fluoronicotinic acid (6.00 g.) was disolved in a mixture of 10 ml. of concentrated sulfuric acid and ml. of anhydrous methanol and the solution obtained was refluxed for 5 hours. Excess methanol was evaporated in vacuo and the residue poured on about 150 ml. of icewater. The mixture was made alkaline with solid sodium hydrogen carbonate and extracted with 4 portions of 50 ml. of ether. The ether solution was dried over anhydrous sodium sulphate. filtered and evaporated. The crystalline colourless residue weighed 5.75 g. and melted at 49.5-50.5 C. Recrystallization from petroleum ether gave 4.85 g. of colourless crystals melting at 50.0-50.5 C.
- S-fluoronicotinic acid allylester A solution of S-fluoronicotinic acidchloride in pyridine-chloroform was prepared in the following way. 5- fluoronicotinic acid (33.0 g.) was refluxed with thionyl chloride ml.) for 4 hours. The excess of thionyl chloride was evaporated under reduced pressure and then anhydrous chloroform (1 10 ml.) followed by anhydrous pyridine (45 ml.) was added. The mixture was heated at 90 C. for a few minutes and then cooled in an ice-bath. To this solution (42 m1.
- EXAMPLE 1 2 5-fluoro-3-pyridinemethyl nicotinate Nicotinic acid (3.7 g.) was refluxed 1 hour with thionyl chloride (11.9 g.). Evaporation of excess thionyl chloride gave 4.95 g. of crude nicotinic acid chloride hydrochloride, which was covered with 10 ml. of anhydrous benzene. To this mixture a solution of 5-fluoro-3- pyridinemethanol in a mixture of 12 ml. of triethylaminc and 40 ml. of benzene was added with stirring. The resulting mixture was refluxed for 5 hours.
- EXAMPLE 14 5-chloro-3-pyridinemethyl 3-pyridineacetate
- 3-py'ridineacetic acid 5.50 g.
- 5-chloro-3-pyridinemethanol 6.05 g.
- a solution of N,N-cyclohexylcarbodiimide in 50 ml. of anhydrous diethylether was added at C. during 10 minutes.
- the mixture was stirred at room temperature during 2.5 hours and then urea formed was filtered off.
- the filtrate was evaporated to give 14.2 g. of product. which was transformed to its hydrochloride and crystallized from ethanol-ether.
- the pure hydrochloride had M.P. 165-167 C.
- esters were also prepared:
- fluoro-3--pyridinemethanol (6.35 g.) was p-toluenesulfonic acid monohydrate (14.3 g.) was refluxed 47 hours in 100 ml. of toluene.
- the water in the reaction mixture was continuously removed by azeotropic distillation.
- the residue after evaporation of the solvent was treated with an excess of saturated aqueous solution of sodium hydrogencarbonate.
- the precipitate was filtered off and recrystallized from diisopropyl ether to give 4.75 g. weakly yellow product.
- M.P. 7981 C. which could be raised to 80.081.5 C. by repeated recrystallization from diisopropylether.
- D CH CH S-fluoronicotinic acid was refluxed for 3.5 hours with 60 ml. of thionyl chloride. Excess thionylchoride was distilled offin vacuo and the residue heated with a mixture of pyridine (25 ml.) and benzene (50 ml.) at 60-70 C. during one hour. The solution was cooled in an ice-bath and ethylene glycol 1.50 g.) was added with stirring. The mixture was allowed to stand for 24 hours at room temperature and was then poured out on 200 ml. of ice-water.
- EXAMPLE 26 S-fluoro-3-pyridinemethanol To a stirred solution of ethyl S-fluoronicotinate (54. l g.) in 270 ml. of methanol, potassium borohydride (53.9 g.) was added with cooling over a period of one hour. The mixture was stirred 30 minutes at room temperature and then refluxed for 6 hours. The solution was stirred over night at room temperature and then most of the solvent was evaporated. The residue was dissolved in 300 ml. of water and after one hour extracted with five ml. portions of ether. The ether solution was dried over anhydrous sodium sulfate, filtered and the solvent evaporated to give 38 g. of a yellow oil.
- EXAMPLE 28 5 -chloro-B-pyridinemethanol
- sodium borohydride 31 g.
- 5-fluoro-3-cyanopyridine (1.50 g.) was dissolved in a mixture of 2.5 ml. of concentrated hydrochloric acid and 25 ml. of water and hydrogenated at atmospheric pressure and room temperature over Pd/C (0.40 g. After 8 hours 535 ml. of hydrogen had been consumed. The hydrogenation was interrupted for 3 days and then further hydrogenated during one hour over an additional amount of 10% Pd/C (0.30 g.). A total amount of 600 ml. of hydrogen was consumed. The catalyst was filtered off and washed with water. The com bined filtrate and washings were concentrated to a volume of 25 ml. made alkaline by addition of solid sodium hydrogen carbonate and extracted five times with 40 ml. of butyl acetate.
- EXAMPLE 32 S-fluoro-B-pyridinemethanol
- S-benzyl 5-fluoro-3- pyridinecarbothioate M.P. 4244 C. was prepared by the reaction of S-fluoronicotinoyl chloride with benzylmercaptan.
- EXAMPLE 33 5-fluoro-3-methoxymethylpyridine
- the starting material 5-fluoro-3- chloromethylpyridine hydrochloride was prepared by reacting 5-fluoro3-pyridinemethanol with thionylchloride.
- 5-fluoro-3-chloromethylpyridine hydrochloride 15.0 g. was converted to its base form by treatment with aqueous sodium hydrogen carbonate and the base collected by extraction with benzene.
- the residue after evaporation of the solvent was dissolved in 40 ml. of methanol. This solution was added drop by drop to a stirred solution made by the addition of sodium (4.0 g.) to 100 ml. of methanol.
- the reaction mixture was refluxed one hour and the solvent evaporated in vacuo.
- the residue was extracted with ether and the ether solution extracted twice with water.
- the water solution was extracted twice with ether and this ether solution combined with the original ether solution.
- EXAMPLE 36 -fluoro-3-methylpyridine 5-fluoro-3-pyridinemethanol hydrochloride (5.05 g.) was dissolved in a mixture of 50 ml. ethanol and 2 ml. of concentrated aqueous hydrochloride acid and hydrogenated over 0.5 g. of lO% Pd/C at room temperature and atmospheric pressure. A total amount of 740 ml. of hydrogen was absorbed. The catalyst was filtered off, and the solvent of the filtrate evaporated. The residue was dissolved in water made alkaline with solid sodium hydroxide and the product isolated by steam distillation. 3 g. colourless product was separated and dried over sodium carbonate. The structure of the compound was confirmed by NMR spectroscopy.
- EXA M PLE 38 5-fluoro-3-aminomethylpyridine
- 5-fluoro-3-pyridinemethylazide (3.2 g.) was hydrogenated over lO% Pd/C (0.32 g.) at room temperature and a pressure of 3.5 atm. in a mixture of 25 ml. 2 M hydrochloric acid and l00 ml. of 50% aqueous methanol.
- the catalyst was filtered off and the solvent evaporated to give a yellow semi-solid material. This material crystallized from aqueous ethanol to give [.2 g. colourless dihydrochloride, M.P. 223225 C.
- EXAMPLE 39 5-fluoro-3aminomethylpyridine
- the starting material 5-fluoro-3-pyridinemethyl phthalimide (MP. l3l.5-l32.5 C.) was prepared by reaction of 5-fluoro-3-chloromethylpyridine (preparation, see Example 33) with potassium phtalimide.
- EXAMPLE 40 C -C00 CHICHJN S-fluoronicotinic acid 12.7 g. was refluxed for 4.5 hours with 100 ml. of thionyl chloride and then the excess of thionyl chloride was evaporated at reduced pressure.
- the -fluoronicotinic acid chloride so ob tained was stirred with ice-cooling in 200 ml. of dry benzene and to this mixture a solution of N,N- dimethylaminoethanol (8.05 g.) in a mixture of ml. triethylamine and 50 ml. ofdry benzene was added during one hour.
- the reaction mixture was stirred at 80 C. for two hours and then the precipitate was filtered off.
- EXAMPLE 42 l-nicotinoyl-3 ,S-dimethylpyrazole Nicotinic acid hydrazide (3.4 g.), acetylacetone (2.5 g. 2 M hydrochloric acid (0.19 ml.) and 2-propanaol (25 ml.) was refluxed for one hour and the solution allowed to stand over night. Evaporation of the solvent gave 4.9 g. yellow oil which soon became crystalline. The product was triturated with 25 ml. of water to give 4.2 g. colourless material, M.P.4344 C.
- EXAMPLE 43 Mesoinositol hcxa- 5-fluoronicotinate To a stirred mixture of S-fluoronicotinic acid (8.5 g.), meso-inositol (0.9 g.) and dry pyridine (20 m1.) ptoluenesulfonyl chloride (7.0 g.) was added in small portions while the reaction mixture was cooled in cold water. When a too thick precipitate had formed a further [0 ml. portion ofdry pyridine was added. The mixture was stirred one hour at room temperature and one hour at about 110 C. and was then cooled in room temperature. The precipitate was filtered off and dried to give 3.0 g. colourless product, M.P. 220230 C.
- a further 2.4 g. colourless product, M.P. 2 l 7227 C. was obtained by precipitating from the filtrate by addition to ice-water. Through recrystallization from pyridineethanol the melting point of the product could be raised to 22823 1 C.
- EXAMPLE 45 Pharmacological tests Compounds according to the invention were tested with regard to lowering the concentration of free fatty acids in the serum of dogs according to the method described in Carlsson, L. A. and Liljedahl, S. 0., Lipid metabolism and trauma. ll. Studies on the effect of nicotinic acid on norepinephrine induced fatty liver. Acta Med. Scand. 173 (1963), 787-791 and Bergstrom, S., Carlsson, L. A. and 0rd, L. Effect of prostaglandins on catecholamine induced changes in the free fatty acids of plasma and in blood pressure in the dog. Prostaglandin and related factors 22," Acta Physiol. Scand.
- Triethanolamine trl-6-fluoronlcotlnate -chloronicotinic acid and 5-fluoronicotinic acid have a low toxicity.
- the toxicity of 5- fiuoronicotinic acid upon i.p. administration in mice given as the LD,-,.,-value was found to be 2.0 g./kg. bodyweight.
- the corresponding toxicity of nicotinic acid was found to be 0.5 g./kg. bodyweight.
- the resorption of S-chloroand 5-fluoronicotinic acid in serum of dogs was studied. 200 mg. of the test compound were orally administered to the dog in the form of a tablet also containing 200 mg. of physiologically inert material. The amount of the test compound in the blood serum was analyzed at different times according to Hughes, D. E. and Williamson, D. H., Biochem. J. 55 (1953), 851. A comparison with nicotinic acid was made in each case. The maximum resorption and the duration (given as the time after administration when the serum concentration had decreased to 25% of the maximum concentration) is given in Table IV.
- the blood of the femoral artery was bypassed in a loop of polyethylene tubing inserted into the artery.
- the blood flow through the loop was adjusted by a digital pump. .lust distal of the pump arterial pressure was measured. The pressure recorded is then dependent on the pump flow and the resistance distally of the pump. if the flow is kept constant the pressure changes will thus reflect changes in the peripheral resistance.
- the compounds of the invention will normally be administered orally or by injection in the form of pharmaceutical preparations comprising the active ingredient either as a free base or as a therapeutically acceptable acid addition salt, eg the hydrochloride, hydrosulphate, or the like, in association with a pharmaceutically acceptable carrier.
- a pharmaceutically acceptable carrier e.g. the hydrochloride, hydrosulphate, or the like.
- the carrier may be a solid, semisolid or liquid diluent or an ingestible capsule.
- the selected compound may be mixed with a solid pulverulent carrier, e.g. lactose. saccharose, sorbitol. mannitol; starches such as potato starch, corn starch or amylopectin; cellulose derivatives. or gelatin, and a lubricant such as magnesium stearate. calcium stearate. a polyethylene glycol wax and the like.
- a solid pulverulent carrier e.g. lactose. saccharose, sorbitol. mannitol
- starches such as potato starch, corn starch or amylopectin
- cellulose derivatives. or gelatin e.g. lactose. saccharose, sorbitol. mannitol
- a lubricant such as magnesium stearate. calcium stearate. a polyethylene glycol wax and the like.
- the cores, prepared as described above. may be coated with a concentrated sugar solution which may, for example, contain gum arab
- sustained release tablets By using several layers of the active drug. separated by slowly dissolving coated sustained release tablets are obtained. Another way of preparing sustained release tablets is to divide the dose of the active drug into granules with coats of different thickness and compress the granules into tablets together with the carrier substance.
- the active substance can also be incorporated in slowly dissolving tablets made for instance of fat and wax substances or evenly distributed in a tablet of an insoluble substance such as a physiologically inert plastic substance.
- Effervescent powders are prepared by mixing the active ingredient with non-toxic carbonates or hydrogen carbonates, such as calcium carbonate, potassium carbonate and potassium hydrogen carbonate, solid, nontoxic acids such as tartaric acid and citric acid, and for example aroma.
- non-toxic carbonates or hydrogen carbonates such as calcium carbonate, potassium carbonate and potassium hydrogen carbonate
- nontoxic acids such as tartaric acid and citric acid, and for example aroma.
- the active substance may be admixed with a vegetable oil.
- Hard gelatin capsules may contain granulates of the active substance in combination with solid, pulverulent carriers such as lactose. saccharose, sorbitol, mannitol, a starch (e.g. potato starch, corn starch or amylopectin) a cellulose derivative or gelatin.
- Liquid preparations for oral application may be in the form of syrups or suspensions, for example solutions containing from 0.2% to by weight of the active substance. the balance being sugar and a mixture of ethanol, water, glycerol. and propylene-glycol.
- Such liquid preparations may contain colouring agents. flavouring agents, saccharin and carboxymethyl-cellulose as a thickening agent.
- Solutions for parenteral application by injection can comprise aqueous solutions of a water-soluble pharmaceutically acceptable salt of the active substance, preferably in a concentration of 0.5% to 10% by weight. These solutions may also contain stabilizing agents and- /or buffering agents, and may conveniently be provided in various dosage unit ampoules.
- EXAMPLE 46 Preparation of soft gelatin capsules containing 5- fluoronicotinic acid ethylester 500 g. of S-fluoronicotinic acid ethylester were mixed with 500 g. of corn oil whereafter the mixture was filled in soft gelatin capsules, each capsule containing 100 mg. of mixture (i.e. 50 mg. of active substance).
- EXAMPLE 47 Preparation of soft gelatin capsules containing 5- fluoronicotinic acid methylester 500 g. of S-fluoronicotinic acid methylester were mixed with 750 g. of peanut oil whereafter the mixture was filled in soft gelatin capsules. each capsule containing l25 mg. of mixture (i.e. 50 mg. of active substance).
- EXAMPLE 48 Preparation of tablets containing S-fluoronicotinic acid ethylester
- EXAMPLE 49 Preparation of an emulsion containing 5-fluoronicotinic acid ethylester 100 g of 5-fluoronicotinic acid ethylester were dissolved in 2500 g. of peanut oil. From the solution thus obtained. 99 g. of gum arabic. aroma and colour (q.s.) and 2500 g. of water and emulsion was prepared.
- EXAMPLE 5 1 Preparation of a solution containing 5fluoronicotinic acid ethylester l00 g of 5-fluoronic0tinic acid ethylester were dissolved in 2.000 g of polyoxyethylene sorbitan monooleate, whereafter aroma and colour (q.s.) and water to 5.000 ml. were mixed in. A clear drop solution was thus obtained.
- Vitamin B rng Vitamin B rng.
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Abstract
The invention relates to 3.5-substituted pyridines, which in one of the positions 3 and 5 may be substituted by halogen or -NH2, and in the other position are substituted by an organic group. The compounds are useful for the inhibition of serum lipid mobilization.
Description
United States Patent 1 1 Carlsson et al.
{73] Assignee: Aktiebolaget Astra. Sodertalje.
Sweden [22] Filed: Apr. 16, I973 [2H App]. No.: 35l,27l
Related U.S. Patent Documents Reissue of:
[64] Patent No:
Issued: Appl. No.: Filed:
3,637,714 Jan. 25, 1972 689,75]
Nov. 15, i967 [30] Foreign Application Priority Data Nov. 16. 1966 Sweden ..l5717/66 Mar. 23. 1967 United Kingdom ..l3687/67 Apr. 26. 1967 United Kingdom v.l9l74/67 [52] U.S. Cl...260/294.8 R; 260/295 5; 260/295 R;
[ll] E Re. 28,532
[ 1 Reissued Aug. 26, 1975 [5]] Int. Cl C07d 31/36 [58] Field of Search. 260/295.5 R, 297 R, 294.8 R, 260/295 5 [56] References Cited UNlTED STATES PATENTS l/l971 Yoshimura et al. 260/2955 OTHER PUBLICATIONS Beaty et ill. Chem. Abstracts, Vol. 46. l8), 8654ab, Sept. 25. 1952.
Beaty et al., J. Chem. Soc, London. p. 35l2. I951, QBl C. 6.
Primary Examiner-Alan L. Rotman Allurney. Agent, or Firm-Brumbaugh. Graves. Donohue & Raymond (57] ABSTRACT The invention relates to 3.5-substituted pyridines, which in one of the positions 3 and 5 may be substituted by halogen or NH and in the other position are substituted by an organic group. The compounds are useful for the inhibition of serum lipid mobilization.
2 Claims, No Drawings 1 5-FLUORO-3-PYRIDINEMETHANOL. ESTERS THEREOF AND THERAPEUTICALLY ACCEPTABLE SALTS THEREOF Matter enclosed in heavy brackets I: appears in the original patent but forms no part of this reissue specification; matter printed in italics indicates the additions made by reissue.
in the form of free fatty acids from stored triglycerides g in adipose tissue It has now been found that compounds of the general formula R A-B and therapeutically acceptable salts thereof have vasodilating properties and are of particular value of lowering of excessive serum lipid concentration, in which formula R is hydrogen, halogen or NH- A is a radical selected from the class consisting of B and E are members of the class consisting of hydro gen. straight, branched, saturated and unsaturated alkyl groups containing at most 12 carbon atoms; the group of atoms DB containing at most 12 carbon atoms when B is alkyl; cycloalkyl, phenylalkyl, alkyloxyalkyl, aryloxyalkyl, aminoalkyl. lower alkylaminoalkyl. dialkylaminoalkyl,
when A is (CH ),,OB
can also be pyranyl and. when A is B can also be a member of the group consisting of and B not being hydrogen when A is and R is H; B not being hydrogen when A is o it and R' is a member of the group consisting ofhydrogen. halogen and NH in which formulas n is an integer from to 3 inclusive. R being hydrogen when n is l; p is an integer from i to 4 inclusive, R being hydrogen when p is 2; m is an integer from 0 to 4 inclusive, m being 0 when B is a member of the class consisting of the radicals l )(4), and is linked to A via a member of the group consisting of oxygen and nitrogen atoms; R is a member of the group consisting of hydrogen,
halogen and NH R is a member of the group consisting of hydrogen, halogen, NH straight. branched, saturated and unsaturated alkyl groups; D is selected from the class consisting of straight. branched saturated and unsaturated alkylene groups containing at most 6 carbon atoms; the group of atoms AB can also be a member of the class consisting of ig/[ and U wherein R and R are selected from the class consisting of straight. branched, saturated. and unsaturated alkyl groups, hydroxylalkyl and carboxyalkyl groups.
The expression therapeutically acceptable salt" is recognized in the art to designate an acid addition salt, which is physiologically innocuous when administered in a dosage and at an interval (e.g. frequency of administration) that is effective for the indicated therapeutic use of the parent compound. Typical therapeutically acceptable acid addition salts include but are not limited to the salts of mineral acids, such as hydrochloric,
wherein n is one of the integers 0, 2 and 3, and R is hydrogen, halogen or NH;,, R being halogen when n is 0, may be prepared according to the following reaction schemes:
(1 Arndt-Eistert method Rl- 4311,0001! R CIhN- l m cmoooum m0 R (C MJ OH I TN The homologues are prepared analogously.
(2) Preparation by the general method (3) Preparation by carbonation of Grignard reagents (X is halogen) (4) Preparation by oxidation of the corresponding alcohol or aldehyde A specific method for the preparation of R- CI-I- CH:COH
is reduction of the corresponding 3'acrylic acid,
-ru=cu--coon The pyridine acrylic acid may be prepared by condensation of 5-substituted 3-pyridinecarboxaldehyde with malonic acid, or (by the similar Perkin and Claisen condensations) with acetic anhydride and ethyl acetate. The reduction of the S-substituted, 3- pyridineacrylic acid may be carried out by catalytical hydrogenation or by the use of various reducing agents, such as a mixture of red phosphorus and hydroiodic acid. The preferred method is condensation of malonic acid with 5-substituted 3-pyridinecarboxaldehyde and reduction of the acrylic acid;
Compounds of Formula 6, wherein R is fluoro or chloro and n is (J, may also be prepared by reacting a compound of the formula with sodium nitrite and (l) cupric chloride in'hydrochloric acid solution,
preferably in the presence of small amounts of cuprous chloride or (2) fluoboric acid in an aqueous solution and heating the fluoborate salt thus formed to the formation of a compound of the formula 8 -COOH wherein R is a fluorine or chlorine atom.
Preferably the reaction of the aminonicotinic acid is carried out in a cooled water solution also containing tetrahydrofuran.
(b) Compounds of the formula 0 n l (cmrii-o-B B not being ethyl when n is l) and R is H; wherein q is an integer from 0 to 4 inclusive, wherein m is an integer from 1 to 4 inclusive, R is hydrogen. halogen or -NH. and R" is hydrogen, halogen, NH- or an alkyl group which may be straight, branched, saturated or unsaturated, are prepared by reacting a compound of the formula with a compound of the formula wherein R, n and B have the meaning specified above, Y is halogen or a hydroxy group and X is carboxyl, a metal carboxylate group or an activated carboxyl group, in which case the compound of Formula II is an acid chloride, an alkyl ester, an acid anhydride or a mixed anhydride with alkoxy formic acids, carboxylic acids, sulphonic or inorganic acids or derivatives obtained by a reaction between a carboxylic acid and a carbodiimide or similarly functioning compounds such as N,N-carbonyldiimidazole or N-ethyl-S- phenylisoxazolium-3-sulphonate, X being a metal carboxylate group when Y is halogen, whereafter the com pound of Formula I thus obtained if necessary is transformed into a therapeutically acceptable salt by reaction with the appropriate acid.
The reaction may be performed in the presence of aqueous or anhydrous organic solvents such as chloroform, diethyl ether, tetrahydrofuran, benzene and toluene, or without solvents. Particularly when X represents a carboxyl group and Y is a hydroxy group there may be used an acid catalyst such as sulphuric acid, hydrogen chloride, p-toluene sulphonic acid, benzene sulphonic acid or salts with high to intermediate acid strength, even including ion exchangers saturated with hydrogen ions. In this case, in order to get a more favourable equilibrium, the water formed during the reaction may be removed from the reaction mixture by azeotropic distillation or taken up by drying agents such as anhydrous cupric or manganese sulphate and molecular sieves. When the compound of Formula II is an acid halide, the hydrogen halide liberated may be neutralized and the reaction catalyzed by a base such as pyridine and triethylamine.
(c) Compounds of the formula R I -(CHz),OiJ-B N IV are prepared by reacting a compound of the formula R fir- N v with a compound of the formula N vm wherein n, p, R, D and B have the meaning specified above; B excluding hydrogen, R being hydrogen when n is l or when p is 2, are prepared by reacting respectively with compounds of the formulas respectively or by reacting compounds of the formula respectively with compounds of the formula respectively wherein X and Y have the meaning specified in (b). The reaction conditions are the same as in (b). If B is an aminoalkyl or an alkylaminoalkyl group the yield may be increased by protection of the amino group In case the compounds of Formulas VII and VIII are they can be prepared by reacting compounds of the formulas respectively 1H (Cll ,Y
with compounds of the formulas YDY respectively X-DX wherein X and Y have the meaning specified above. The reaction conditions are the same as in (b),
(e) Compounds of the formula are prepared by reacting a compound of the formula with a compound of the formula wherein p is an integer from I to 4 inclusive, R and B have the meaning specified above; B excluding hydrogen, R being hydrogen when p is 2; particularly R may be a hydrogen, fluor e or chlorine atom; X and Y are selected from the group consisting of hydroxyl, metal oxido groups and halogen; X being different from Y when X and Y are selected from the group consisting of halogen and metal oxido groups.
When both X and Y are hydroxyl groups a dehydrating reagent such as sulfuric acid or alumina at higher temperatures may be used. Where Y is a halogen atom and X is a metal oxido group the reaction is preferably carried out in a solvent such as ether, tetrahydrofurane and benzene or the alcohol corresponding to the metal alcoholate. In the latter case the metal alcoholate in the alcohol solvent could be obtained by dissolving a suitable amount of metal, such as sodium, in the excess of alcohol.
The compound of Formula IX thus obtained is transformed, if necessary, into a therapeutically acceptable salt by reaction with the appropriate acid.
Ethers of the formula wherein p and R have the meaning specified above, R being hydrogen when p is 2, and A is an alkyl group or pyranyl, may be prepared by adding in known manner an alcohol of the formula RILH/XYKJ 11,-) For:
wherein p is an integer from l to 4 inclusive; particularly p may be I; and R is hydrogen, halogen or NH R being hydrogen when p is 2, particularly R may be a fluorine, chlorine or bromine atom; a compound of the general formula or a salt thereof, wherein R and p have the meaning specified above, particularly, R may be a fluorine,
chlorine or bromine atom, and X is a formyl, carboxyl, chlorocarbonyl, alkoxycarbonyl, thiolester or a cyano group is reduced by methods, known to be applicable to the reduction of the unsubstituted analogues, for example catalytical hydrogenation and reduction by means of a complex metal hydride, to the formation of a compound of the general formula and, where a therapeutically acceptable salt is required, reacting the compound of Formula XI with the appropriate acid.
According to a preferred embodiment, a compound of the Formula XII, wherein p=l,R is fluorine, chlorine or bromine, particularly R is fluorine, and X is an alkoxy carbonyl group of at most 5 carbon atoms, is reduced by means of complex metal hydrides, such as sodium or potassium borohydride and lithium aluminum hydride. In cases when potassium or sodium borohydride is used as the reducing agent, the reaction may be performed in such solvents as methanol, ethanol, water or mixtures thereof. When lithium aluminum hydride is used as the reducing agent, the reaction is preferably performed in inert solvents such as diethyl ether and tetrahydrofuran.
Compounds of Formula XI may also be prepared by treating an amine of the formula with a nitrite such as sodium nitrite in a water solution under such conditions that the intermediate diazonium compound decomposes and reacts with water to form an alcohol.
(g) Compounds of the formula wherein R is hydrogen, halogen or NH D is a straight, branched, saturated or unsaturated alkylene group containing at most 6 carbon atoms, and B is a member of the class consisting of hydrogen, straight, branched, saturated and unsaturated alkyl groups; the group-D-B containing at most 12 carbon atoms when B is alkyl; eycloalkyl, phenylalkyl, alkyloxyalkyl, aryloxyalkyl, aminoalkyl, lower alkylaminoalkyl, dialkylaminoalkyl,
in I W4) ML'N wherein R is hydrogen or halogen, are prepared by condensation of two pyridinealdehydes, analogous to the benzoin condensation, and complete reduction of the product.
Compounds of the formula wherein R is hydrogen, halogen or NH and G is an alkyl group, may be prepared by reduction of the corresponding halide, or reduction of the alcohol in cases where G is a hydroxymethyl group.
(h) Compounds of the formula XIY wherein R is halogen or NH and p is an integer from 1 to 4 inclusive,
R and R are hydrogen or alkyl groups which may be straight, branched, saturated or unsaturated, may be prepared by reduction of a compound of the formula wherein p and R have the meaning specified above and X is CHO or CN. The reduction is carried out by catalytical hydrogenation in the presence of an amine of the formula when X is CHO; R and R are hydrogen when X is CN. The reduction may be carried out by means of catalytical hydrogenation or by using a complex metal hydride such as lithium aluminum hydride, when X is not CHO.
Compounds of Formula XIV wherein R and R are hydrogen may also be prepared by reduction of the compound When a cyano or azido group is reduced, the reduction may be carried out by hydrogenation in the presence of catalysts such as rhodium, palladium, platina or Raney-nickel, preferably in the presence of hydrochloric acid or ammonia in suitable solvents such as dry or aqueous methanol and ethanol.
When X is -CONR R the reduction is preferably carried out by means of lithium aluminum hydride in inert solvents such as diethyl ether or tetahydrofuran.
Compounds of Formula XIV wherein R and R are hydrogen may also be prepared by reduction of the corresponding oxime or hydrazone. The oxime may be reduced by zinc and acetic acid. The reduction may also be carried out by means of catalytical hydrogenation. Primary amines may also be prepared by reacting the corresponding amide with NaOX, wherein X is a chlorine or bromine atom (Hofmann rearrangement); by reacting the corresponding carboxylic acid with HN;, according to Schmidt; and by rearrangement of a compound of the formula with an amine of the formula wherein p, R, R and R have the meaning specified above.
If necessary, the compounds of Formula XIV are transformed into therapeutically acceptable salts by reaction with the appropriate acid.
(i) Compounds of the formula wherein R is hydrogen, halogen or NH R and R" are straight, branched saturated or unsaturated alkyl groups, hydroxyalkyl or carboxylakyl, are prepared by reacting a compound of formula with a compound of the formula 0 II II wherein R, R and R have the meaning specified above. The reaction is preferably carried out in the presence of solvents such as ethanol or isopropanol, and as a catalyst an acid such as hydrochloric acid may be used.
Another method to prepare compounds of Formula XV is to react a compound of the formula with a compound of the formula wherein R, R and R have the meaning specified above and X is a member of the class consisting of activated carboxyl groups such as an acid halide, an alkyl ester, an acid anhydride, a mixed anhydride with formic esters or carboxylic acids, sulphonic or inorganic acids or derivatives obtained by a reaction between a carboxylic acid and a carbodiimide or similarly functioning compounds such as N,N-carbonyl-diimidazole or N-ethyl-5-phenylisoxazolium-3'-sulphonate.
(j) Compounds of the general formula wherein n, R and B have the meanings specified in (b), B including ethyl; m being an integer from 0 to 4 inclusive, and p is an integer from 1 to 4 inclusive, R being hydrogen when p is 2, are prepared by reacting a compound of the formula with a compound of the formula are prepared in a similar way by reacting a compound of the formula CIIdr-X with a compound of the formula H N-B wherein n, R, B and X have the meaning specified in (j) m excluding 0.
(k) Compounds of the formula and wherein n and R have the meaning specified in (b); R being hydrogen when n is l, are prepared by reacting compounds of the formula respectively Re. 28, l
(CH-HEY Y-(cH2u-N tcHgi -Y 5 with a compound of the formula R -icn, .-x
wherein n and R have the meaning specified in (b), R being hydrogen when n is l, are prepared by reacting 4 wherein X and Y have the meaning specified 11'] (b). The reaction conditions are the same as in (b).
(m) Compounds of the formula wherein R and n have the meaning specified in (b), are prepared by reacting meso-inositol or a stereoisomer thereof with in which Formula X has the meaning specified in (j).
The following examples illustrate the invention:
EXAMPLE 1 Preparation of 5-fluoronicotinic acid A mixture of S-aminonicotinic acid (108 g.) in 700 ml. of fluoboric acid (48-50% w./w.), 530 ml. of tetrahydrofuran and 350 ml. of water was cooled in an icesalt bath and with stirring sodium nitrite (71 g.) in a sat urated water solution was added at such a rate that the temperature was lower than 3 C. 350 ml. of tetrahydrofuran was added and the mixture stirred for one hour at -5 C.l0 C. The precipitate formed was filtered off and thoroughly washed with cold ethanol, cold ether and petroleum ether until it was nearly colourless. This fluoborate salt was transferred to a large flask fitted with a stirrer and two reflux condensers and with about 500 ml. of dry ligroin (B.P. about C.) and the flask was gently heated with an open flame at one point. An exothermic reaction started which soon spread to the whole mass of the salt. The decomposition was completed by refluxing for 30 minutes. The ligroin phase was recanted and the yellow product washed with ether. The product was dissolved in dilute aqueous sodium bicarbonate and reprecipitated with dilute aqueous hydrochloric acid. The precipitate was washed with water and dried to give 67 g. of weekly yellow product. This product may be purified by recrystallization. treatment with active carbon and a final sublimation to give a colourless product. M.P. 194 C. its identity was also established by Ill-spectroscopy.
EXAMPLE 2 Preparation of S-chloronicotinic acid S-aminonicotinic acid (93 g.) was dissolved in a hot solution of 370 ml. of concentrated hydrochloric acid in 100 ml. of water. The solution was cooled to +5 C. and the resulting suspension stirred while a solution of sodium nitrite (52 g.) in 70 ml. of water was added over a period of one hour and at a temperature not exceeding +8 C. The mixture was stirred 15 minutes and then 450 ml. of a 10% (w./w.) aqueous solution of hydro chloric acid was added. The cold mixture was added during 30 minutes to a stirred solution of cupric chloride g.) and cuprous chloride (0.69 g.) in 1850 ml. of l0% (w./w.) aqueous hydrochloric acid kept at 60 C. The mixture was stirred for 10 minutes and then cooled to 10 C. At this temperature sodium sulfide (with 9 molecules of crystal water, 231 g.) was added. The precipitate was filtered off and the filtrate treated with concentrated aqueous ammonium hydroxide (to pH 2.5-3) in order to precipitate the product. The crude product was filtered off and immediately dissolved in 3 l. of water. The solution was treated with active carbon, filtered and the product allowed to crystallize. It was obtained 60 g. product with M.P. -6 C. A further recrystallization raised the melting point to 167-168 C.
EXAMPLE 3 Preparation of tablets containing S-fluoronicotinic acid 100 g. of -fluoronicotinic acid were mixed with 50 g. of lactose and 45 g. of potato starch and moistened with a starch paste prepared from 5 g. of potato starch and distilled water, whercafter the mixture was granulated through a sieve. The granulate was dried and sieved whereafter 2 g. of magnesium stearate were mixed in. Finally the mixture was pressed into tablets. each weighing 202 mg.
EXAMPLE 4 Pyrazole- 3-methyl 5 -fluoronicotinate To a stirred and refluxed mixture of 3- pyrazolmethanol (2.95 g. 5-fluoronicotinic acid chloride hydrochloride (4/3 equivalents) and 8 ml. of 30% wjw. hydrochlorine-diethylether in 100 ml. of anhydrous tetrahydrofuran, 30 ml. of triethylaminc was added during 1.75 hours. The stirred mixture was further refluxed during 4.5 hours and then the precipitated hydrochloride was filtered off and washed with 300 ml. of diethyl ether. The filtrate was washed with 3 portions of an aqueous saturated solution of sodium bicarbonate followed by one portion of water and dried over anhydrous sodium sulphate. Filtering and evaporation of the solvent gave 68 g. of oil. which crystallized upon cooling. After repeated recrystallization from isopropyl ether the product melted at 88.09l.5 C. The structure was confirmed by IR- and NMR- spectroscopy.
In an analogous way the following ester was also prev pared 5-methylpyrazole-3'methyl S-fluoronicotinate, yield 70% MP. 77 C. The structure was confirmed by lR and NMR-spectroscopy.
EXAMPLE 5 5-fluoronicotinic acid ethylester S-fluoronicotinic acid (43.6 g.) was refluxed for 4 hours with 550 ml. of thionyl chloride. Excess thionyl chloride was evaporated. To the acid chloride hydrochloride thus obtained 420 ml. of absolute ethanol were slowly added at room temperature. The mixture, which soon became homogenous, was refluxed for 2.5 hours. Excess ethano was evaporated and the solid residue was treated with excess of saturated sodium hydrogen carbonate solution to liberate the basic form of the product. The mixture obtained was extracted three times with ether and the ether solution dried over sodium sulphate. Evaporation of solvent and distillation of the residue in vacuo gave 40.9 g. of nearly colourless liquid. B.P. 9294 C. at 13 mm. Hg, n,, =1.4820.
Analysis.Equivalent weight Found: 172. Calculated for C H FNO 169.
EXAMPLE 6 5-fluoronicotinic acid n-hexyl ester S-fluoronicotinic acid (4.0 g.) was dissolved by heating in a mixture of 6.0 ml. of sulfuric acid (95% w./w.) and 75 ml. of redistilled l-hexanol and the solution was alllowed to stand at 120 C. for 3.5 hours. The main part of the excess of l-hexanol was driven off in vacuo at 80 C. and the residue was poured on about 200 ml. of icewater. The mixture was made slightly alkaline with concentrated ammonia solution and extracted with 4 portions of ether. The ether solution was dried over anhydrous sodium sulphate. The residue after evaporation was distilled at 13 mm. Hg and gave 2.9 g. of colourless liquid, B.P. 146-147 C.. n,, l.473().
Analysis.-Found (percent): C, 63.98; H, 7.22; F, 8.62; N. 6.18. Calculated for C H,. FNO- ,(percent):C, 63.98;H. 7.16;F. 8.43;N, 6.22.
EXAMPLE 7 5-ch1oronicotinic acid ethyl ester 5-chloronicotinic acid (121.5 g.) was refluxed for 4 hours with 1.400 ml. of thionyl chloride. A homogenous solution was obtained after 2.5 hours. Excess thionyl chloride was evaporated and to the acid chloride hydrochloride thus obtained 1.100 ml. of absolute eth' anol were slowly added at room temperature. The mixture was refluxed for 3 hours and excess ethanol was then driven off in vacuo. The solid residue was treated with excess sodium hydrogen carbonate solution to liberate the basic form of the product. The mixture obtained was extracted with ether and the ether solution dried over anhydrous sodium sulphate. Evaporation of the solvent and distillation of the residue in vacuo gave 126.1 g. of nearly colourless liquid. B.P. 121-123 C. at 14 mm. Hg. n,, =1.5l75.
Analysis.Found (percent); Cl. 18.9. Calculated for C H ClNO- (percent): CI, 19.1.
EXAMPLE 8 5 fluoronicotinic acid methyl ester S-fluoronicotinic acid (6.00 g.) was disolved in a mixture of 10 ml. of concentrated sulfuric acid and ml. of anhydrous methanol and the solution obtained was refluxed for 5 hours. Excess methanol was evaporated in vacuo and the residue poured on about 150 ml. of icewater. The mixture was made alkaline with solid sodium hydrogen carbonate and extracted with 4 portions of 50 ml. of ether. The ether solution was dried over anhydrous sodium sulphate. filtered and evaporated. The crystalline colourless residue weighed 5.75 g. and melted at 49.5-50.5 C. Recrystallization from petroleum ether gave 4.85 g. of colourless crystals melting at 50.0-50.5 C.
Equivalent weight-Found: 158.7. Calculated for C H FNO 155.1.
EXAMPLE 9 S-fluoronicotinic acid allylester A solution of S-fluoronicotinic acidchloride in pyridine-chloroform was prepared in the following way. 5- fluoronicotinic acid (33.0 g.) was refluxed with thionyl chloride ml.) for 4 hours. The excess of thionyl chloride was evaporated under reduced pressure and then anhydrous chloroform (1 10 ml.) followed by anhydrous pyridine (45 ml.) was added. The mixture was heated at 90 C. for a few minutes and then cooled in an ice-bath. To this solution (42 m1. out of a total volume of 184 m1.) a solution of freshly distilled allyl alcohol (2.9 g.) in anhydrous chloroform (20 ml.) was added with stirring during 15 minutes. The reaction mixture was allowed to stand 20 hours at room temperature and was then added to a small amount of water. The chloroform layer was separated, washed twice with a saturated sodium bicarbonate solution and once with water. and then dried over anhydrous sodium sulfate. Evaporation of the chloroform gave 7.5 g. yellow oil, which was purified by distillation in vacuo to give 5.6 g. colourless liquid. B.P. 99l01 C./l2 mm., n,, =l.4953.
Analysis.-Found (percent): C, 59.47; H, 4,52; F, 10.7 1; N, 7.92. Calculated for C,,H,,FNO (percent): C, 59.67; H, 4.45; F, 10.49; N, 7.73.
By the same procedure and using the same solution of 5-fluoronicotinic acidchloride, the following esters were prepared: 5-fluoronicotinic acid butylester, yield 60%, B.P. 113-1 14 C712 mm., n,, "=1.4764.
Equivalent weightFound: 200. Calculated: 197.
S-fluoronicotinic acid iso-propylester, yield 60%, B.P. 90-9l C./12 mm., n,,=l,4734.
Analysis.Found: C, 58.78; H, 5.33; F, 10.24; N, 7.81. Calculated for C H FNO (percent): C, 59.01; H, 5.50; F, 10.37: N. 7.65.
5-fluoronicotinic acid l-undecylester, yield 60%, BR l53155 C./0.1 mm. Hg. n,, =l.471l.
Analysis-Found: C, 69.20; H, 8.41; F, 6.30; N, 4.93. Calculated for C H- FNO (percent): C, 69.15; H, 8.87; F, 6.43; N, 4.74.
By the same procedure but using a benzene solution of S-fluoronicotinic acidchloride, the following ester was also prepared:
5-fluoronicotinic acid cyclohexylester, yield 60%, B.P. 104-106 C./1.0l.3 mm., n,, ==l.50l7.
Analysis.Found (percent): C, 64.70; H, 6.47; F, 8.57; N, 6.19. Calculated forC l-l FNO (percent): C, 64.56; H, 6.32; F, 8.51; N, 6.28.
EXAMPLE l S-fluoro-3-pyridinemethy1 5-11 uoronicotinate S-fluoronicotinic acid (5.94 g.) was refluxed 4.5 hours with 24 ml. of thionyl chloride. Excess thionyl chloride was evaporated and the residue heated for minutes at 80 C. with a mixture of chloroform (20 ml.) and pyridine (8 ml. The solution was cooled in an icebath and a solution of 5-fluoro-3-pyridinemethanol (5.10 g.) in ml. of chloroform was added with stirring during 30 minutes. The reaction mixture was stirred at room temperature for 2 hours and was then allowed to stand overnight. The mixture was poured out on ice-water and the chloroform phase separated and washed twice with a saturated aqueous solution of sodium hydrogen carbonate. The chloroform solution was dried over anhydrous sodium sulfate, filtered and the solvent evaporated to give 9.0 g. of nearly colour less product. M.P. 105.5l06.0 C.
Analysis.Found (percent): C, 57.84; H, 3.35; F, 15.41; N, 11.11. Calculated for C, H,,F N O (percent): C, 57,60; H, 3.22; F, 15.19; N, 11.20.
The following compounds were prepared in an analogous way:
5-chloro-3-pyridinemethyl nicotinate 3-pyridinemethyl S-fluoronicotinate Yield 75%. M.P. 56.6-57.0 C. 62.063.0 C. (needles).
Analysis-Found (percent): C, 62.21; H, 4.02; F, 8.35; N. 12.03. Calculated for CUHHNQO (percent): C. 62.07; H, 3.91; F, 8.18; N, 12.07.
(prisms) and EXAMPLE 1 1 5-fluoro-3-pyridinemethyl S-fluoronicotinate To a stirred suspension of S-fluoronicotinic acid (7.05 g.) and 5-fluoro-3-pyridinemethanol (6.35 g.) in ml. of anhydrous dioxane, a solution of N,N-dicyclohexylcarbodiimide (10.3 g.) in 50 ml. of anhydrous dioxane was added during one hour with ice-cooling. The reaction mixture was stirred at roomtemperature during 16 hours and was then poured on a small amount of cold ethyl acetate. The urea precipitated was filtered off and the filtrate evaporated. The yellow semi-solid residue was dissolved in a small amount of chloroform, put on a short column of aluminum oxide and eluted with 200 ml. of chloroform. The residue after evaporation of the chloroform solution was recrystallized from petroleum ether with a little ethanol added. The product, 4.2 g., M.P. l05106 C., was identical with the one prepared according to Example 10.
3-pyridinemethyl 5-chloronicotinate was prepared in an analogous way. Yield 35%. MP. 9l C.
Analysis-Found (percent): C, 58.1; H, 3.39; N, ll.7; O, 12.8; C1, 14.4. Calculated for C H N O CI (percent): C, 57.95; H, 3.65; N, 11.26; 0, 12.86; Cl, 14.25.
EXAMPLE 1 2 5-fluoro-3-pyridinemethyl nicotinate Nicotinic acid (3.7 g.) was refluxed 1 hour with thionyl chloride (11.9 g.). Evaporation of excess thionyl chloride gave 4.95 g. of crude nicotinic acid chloride hydrochloride, which was covered with 10 ml. of anhydrous benzene. To this mixture a solution of 5-fluoro-3- pyridinemethanol in a mixture of 12 ml. of triethylaminc and 40 ml. of benzene was added with stirring. The resulting mixture was refluxed for 5 hours. After cooling the triethylamine hydrochloride was filtered off and washed with benzene. The combined washings and the filtrate were evaporated in vacuo to give a semi-solid residue. The crude product was recrystallized from pe troleum ether to give 3.5 g. of crystals with M.P. 6567.5 C. Repeated recrystallizations from petroleum ether gave a completely colourless product with M.P. 68.5-69.5 C.
Analysis.Calculated for C H FN O (percent): C, 62.07; H, 3.91; F, 8.18; N, 12.07; 0, 13.78. Found (percent): C, 62.03; H, 3.87; F, 8.05; N, 12.14.
EXAMPLE 1 3 3-pyridineethyl 3-pyridineacetate A mixture of 3-pyridineacetic acid 10.4 g.), 3- pyridinemethanol (9.3 g.) and concentrated sulfuric acid 10 ml.) in 200 ml. of benzene was refluxed during 6 hours. The reaction water formed was continually taken away by azeotropic distillation. The benzene phase was decanted and the oily residue dissolved in 50 ml. of cold water and the solution made alkaline with aqueous sodium carbonate. The alkaline mixture was extracted several times with diethyl ether, the extract dried over anhydrous potassium carbonate, filtered and the solvent evaporated to give 9.1 g. product. Distillation in vacuo gives 7.3 g. product, B.P. 162162.5 C./0.3 mm. Hg; n l .5540; hydrochloride M.P.
21 Analysis (hydrochloride).--Found (percent): C, 52.8; H, 5.26; N. 8.76; 0.9.96; C1. 22.65. Calculated for C H N O- Cl (percent): C. 53.34; H. 5.12; N. 8.89; O, 10.15; Cl, 22.49.
In an analogous way the following compounds were prepared:
3-pyridinemethy1 3-pyridineacetate Reflux period 5 hours. Yield 40%. M.P. 53-54 C.
Analysis.Found (percent): C, 68.1; H, 5.29; N. 12.3; 0, 14.2. Calculated for C,,,H, N O. (percent): C, 68.41; H, 5.30; N. 12.27; 0. 14.02.
5-fluoro-3-pyridinemethyl S-pyridinehutyrate Reflux periods 70 hours with p-toluenesulfonic acid instead of sulfuric acid. Yield 60%. n,, "*=1.535.
Analysis-Found (percent): C, 65.55; H, 5.49; F, 6.80; N. 10.40. Calculated for C, H ,,FN O (percent): C, 65.68; H, 5.51; F. 6.93; N, 10.21.
5-fluoro-3-pyridinemethyl S-pyridineacetate Reflux period 20 hours with p-toluenesulfonic acid instead of sulfuric acid. Yield 60%. M.P. 58.0-60.0 C.
Analysis-Found (percent): C, 63.33; H. 4.77; F, 7.55; N, l 1.53. Calculated for C H FN- O- (percent): C, 63.41; H, 4.50; F, 7.72; N, 11.38.
EXAMPLE 14 5-chloro-3-pyridinemethyl 3-pyridineacetate To a stirred mixture of 3-py'ridineacetic acid (5.50 g.) and 5-chloro-3-pyridinemethanol (6.05 g.) in 190 ml. of anhydrous diethyl ether a solution of N,N-cyclohexylcarbodiimide in 50 ml. of anhydrous diethylether was added at C. during 10 minutes. The mixture was stirred at room temperature during 2.5 hours and then urea formed was filtered off. The filtrate was evaporated to give 14.2 g. of product. which was transformed to its hydrochloride and crystallized from ethanol-ether. The pure hydrochloride had M.P. 165-167 C.
Analysis.-Found (percent): C, 45.8; H, 4.23; N, 8.28; O, 9.58; Cl, 32.3. Calculated for C l-l N O Cl (percent): C, 46.52; H, 3.90; N, 8.35; O, 9.53; Cl, 31.69.
EXAMPLE 15 F' CHaCHzCOOH 22 Analysis-Found (percent): C. 57.42; H. 5.11; N, 8.10. Calculated for C,,H,.FNO (percent): C. 56.80; H. 4.76; N, 8.28.
EXAMPLE 16 Diazomethane (0.05-0.06 mole) in 200 ml. of ether was slowly added at room temperature to a suspension of 5-fluoro-3-pyridine-propionic acid (5.1 g.) in 200 ml. of dry ether. After standing over night, the ether solution was filtered and the solvent evaporated to give 5 g. oil. The oil was distilled at 0.6 mm. Hg and 4.3 g. product with 8.1. -78 C. and n,, =l .4862 was obtained.
Analysis-Found (percent): C, 58.83; H, 5.61; N, 7.83. Calculated for C,,H,.,FN 2 (percent): C, 59.00; H, 5.50; N, 7.65.
EXAMPLE 17 Pyridine-3-methyl 5-methylpyrazole-3-carboxylate S-methylpyrazole-3-carboxylic acid (5.05 g.) and 3- pyradinemethanol (4.36 g.) was refluxed together with p-toluenesulfonic acid monohydrate (19 g.) in ml. of benzene. A water-separator was used in order to withdraw the water in the reaction mixture. After 27 hours the benzene phase of the reaction mixture was decanted and the residue treated with the excess aqueous sodium bicarbonate. The aqueous mixture was extracted with the decanted benzene phase and three portions of chloroform. The combined extracts were dried over anhydrous sodium sulfate, filtered and the solvent evaporated to give 4.9 g. of a yellow oil which spontaneously crystallized upon cooling. After recrystallization from benzene the product melted at 123.5-124.5 C.
Analysis.-Found (percent): C, 60.5; H, 5.12; N, 19,4; 0. 14.9. Calculated for C H N O (percent): C, 60.82; H, 5.11; N, 19.43; 0. 14.73.
In an analogous way using toluene as solvent, the following esters were also prepared:
5-fluoropyridine-3-methyl 5-methylpyrazole-3- carboxylate, yield 75%, M.P. 141.5l43 C.
Analysis-Found (percent): C. 55.96; H, 4.36; F, 7.96; N, 17.75. Calculated for C,,H,.,FN,0, (percent): C, 56.17; H, 4.29; F. 8.08; N, 17.86.
5-fluoropyridine-3-methyl pyrazole-3-carboxylate yield 75%, M.P. 162 C. Equivalent weightFound: 219. Calculated: 221.
EXAMPLE l8 5-fluoro-3-pyridinemethyl acetate To 50 ml. of stirred acetic anhydride. 5-fluoro-3- pyridinemethanol 10.2 g.) was added slowly at room temperature. The reaction solution was allowed to stand for 3 days and then excess acetic anhydride was driven off in vacuo. The residue was distilled in vacuo to give 9.3 g. of colourless product, B.P. l02l05C./10 mm. Hg, n,, =1.4850.
Analysis-Found (percent): C. 57.02; H. 4.87; F, 1 1.07; N, 8.45. Calculated for C,..H.,FNO (percent): C, 56.80; H, 4.76; F, 11.23; N, 8.28.
EXAMPLE 19 -fluoro-3-pyridinemethyl capyrylate To a stirred solution of S-fluoro-3-pyridinemethanol (3.8 g.) and 13 ml. of triethylamine in 100 ml. of anhydrous benzene, a solution of capyrylic acid chloride (4.9 g.) in 25 ml. of benzene was slowly added at room temperature. The mixture was stirred for 30 minutes at room temperature and then refluxed during 2 hours. After cooling the precipitate of amine hydrochloride was filtered off and washed with benzene. The combined washings and filtrate were evaporated in vacuo to give 8.3 g. of liquid residue. This was distilled in vacuo to give 51 g. of nearly colourless liquid. B.P. l45-l50 C7005 mm. Hg; n,, =l.4730.
Analysis-Found (percent): C, 66.25; H. 7.86; F. 7.33; N. 5.60. Calculated for C H- ,.,FNO (percent): C. 66.38; H. 7.96; F. 7.50; N. 5.53.
EXAMPLE 20 5'fluoro-3-pyridinemethy1 pivalate To a well stirred and ice-cooled solution of 5-fluoro- 3-pyridinemethanol (6.35 g.) and ml. of triethylamine in 100 ml. of dry benzene, a solution of pivaloyl chloride (6.0 g.) in 10 ml. of dry benzene was added during one hour. The reaction mixture was stirred 4.5 hours at room temperature and then filtered. The filtrate was washed twice with 50 ml. of a saturated aqueous solution of sodium hydrogen carbonate and then dried over anhydrous sodium sulfate. Filtering and evaporation of the solvent gave 8.7 g. of yellow-red oil. which was distilled in vacuo to give 5.45 of colourless product, B.P. 119l2l.5 C713 mm. Hg; n,, =l.47O.
Analysis.Found (percent): C. 62.50; H. 6.53; F. 8.91; N. 6.80. Calculated for C H FNO (percent): C, 62.54; H. 6.68; F, 8.99; N. 6.63.
5-fluoro-3-pyridinemethyl vinylacetate was prepared in an analogous way. Yield 55%; RP. 899l C./0.8 mm. Hg; n,, =1.497.
Analysis.Found (percent): C. 61.05; H, 5.55; F. 9.63; N. 7.15. Calculated forC H FNO (percent): C. 61.53; H. 5.16; F. 9.73; N. 7.18.
EXAMPLE 2 l 5-chloro-3-pyridinemethyl propionate EXAMPLE 22 5-fluoro-3-pyridinemethyl 3-methyl-5-isoxazolecarboxylate 3methyl5-isoxazolecarboxylic acid (6.35 g.), 5-
fluoro-3--pyridinemethanol (6.35 g.) was p-toluenesulfonic acid monohydrate (14.3 g.) was refluxed 47 hours in 100 ml. of toluene. The water in the reaction mixture was continuously removed by azeotropic distillation. The residue after evaporation of the solvent was treated with an excess of saturated aqueous solution of sodium hydrogencarbonate. The precipitate was filtered off and recrystallized from diisopropyl ether to give 4.75 g. weakly yellow product. M.P. 7981 C., which could be raised to 80.081.5 C. by repeated recrystallization from diisopropylether.
Analysis.Found (percent): C, 55.35; H. 3.80; F, 8.31; N. 1 1.90. Calculated for C H FN O (percent): C. 55.93; H, 3.84; F. 8.04; N, ll.86.
In the same way S-fluoro-3-pyridinemethyl S-methyl- 3-isoxazolecarboxylic acid was prepared; M.P. 69.0-7 l .5 C.
Analysis.Found (percent): C, 56.03; H, 3.97; F. 7.79; N, l 1.54. Calculated for C H,,FN O (percent): C, 55.93; H, 3.84; F. 8.04; N, 11.86.
EXAMPLE 23 Diester of 5-fluoro nicotinic acid and ethylene glycol R=R=F. D= CH CH S-fluoronicotinic acid was refluxed for 3.5 hours with 60 ml. of thionyl chloride. Excess thionylchoride was distilled offin vacuo and the residue heated with a mixture of pyridine (25 ml.) and benzene (50 ml.) at 60-70 C. during one hour. The solution was cooled in an ice-bath and ethylene glycol 1.50 g.) was added with stirring. The mixture was allowed to stand for 24 hours at room temperature and was then poured out on 200 ml. of ice-water. The aqueous mixture was made alcoline with sodium hydrogen carbonate and extracted with four portions of diethyl ether. The extract was dried over anhydrous sodium sulphate, filtered and the solvent evaporated to give a crystalline residue. which was triturated with a little cold petroleum ether. Yield 6.21 g., M.P. 84-90 C. Recrystallization from diisopropyl ether gave 535 g. of colourless product with M.P. 91.0-91.5 C.
Analysis.Found (percentz) C, 54.88; H, 3.39; F, 12.53; N, 9.05. Calculated for C H F NJJ, (percent): C. 54.55; H. 3.27; F. 12.33; N. 0.09.
In an analogous way the following compounds were prepared:
Diester of S-fluoronicotinic acid and hexane-1.2-diol R=R =F; D=(CH Yield MP. 56.056.5 C. Analysis.-Found (percent): C, 59.75; H. 5.16; F, l 1.07; N, 8.17. Calculated for C H F N- o (percent): C. 59.34; H, 4.98; F, 10.43; N, 7.69.
Diester of S-fluoronicotinic acid and propane-1.2-diol Analysis.-Found (percent): C, 55.66; H. 4.17; F, l 1.24; N, 8.24. Calculated for C H F N O (percent): C. 55.91: H, 3.75; F. 11.79; N. 8.69.
Diester of 5-fluoronicotinic acid and trans-2-butene-l .4
Yield 75%; M.P. 115.5-1 l6.0 C.
Analysis-Found (percent): C, 57.67; H, 3.70; F, l 1.24; N, 8.24. Calculated for C,,,-H,- ,l-" l\l O (percent): C. 57.49.
EXAMPLE 24 Diestcr of succinic acid and 5-fluoro3-pyridine methanol Succinic acid (2.36 g. 5-fluoro-3-pyridine methanol 45. 1 g.) and p-toluene sulfonic acid monohydrate 10.0 g.) were refluxed 23 hours in 50 ml. of benzene. The water in the reaction mixture was continuously removed by azeotropic distillation. The mixture was poured out on ice-water and made alkaline with sodium hydrogen carbonate. The precipitate formed was filtered off, washed with water and dried. It weighed 2.9 g., M.P. 80.08l.0 C., after recrystallization from ether-ethanol, M.P. 80.0815 C.
Analysis-Found (percent): C, 57.30; H, 4.22; F, 1 1.33; N, 8.57. Calculated for C H F N O (percent): C, 57.14; H, 4.20; F, ll.30; N, 8.33.
In an analogous way the following compounds were also prepared:
Diester of Adipic acid and 5-fluoro-3-pyridine methanol R =R F, D=(CH Yield 65%, M.P. 57.0-57.5 C. Analysis.Found (percent): C, 59.59; H, 4.96; F, 10.59; N, 7.70. Calculated for C H F NJL (percent): C, 59.34; H, 4.98; F, 10.43; N, 7.69.
Diester of suberic acid and 5-fluoro-3-pyridine methanol R=R '-F, D=(CH Yield 45%; M.P. 63.0-64.0 C. Analysis-Found (percent): C, 61.40; H, 5.60; F, 9.53; N, 7.09. Calculated for C ,,H F N O (percent): C, 61.22; H, 5.65; F, 9.68; N, 7.14.
Diester of fumaric acid and 5-fluoro-3-pyridine methanol Yield M.P. l20.5l22 C.
Equivalent weight (titration as base)Found: 167. Calculated for C -H F N O 167.2.
The identity and purity of the product was also established by NMR spectroscopy.
EXAMPLE 26 S-fluoro-3-pyridinemethanol To a stirred solution of ethyl S-fluoronicotinate (54. l g.) in 270 ml. of methanol, potassium borohydride (53.9 g.) was added with cooling over a period of one hour. The mixture was stirred 30 minutes at room temperature and then refluxed for 6 hours. The solution was stirred over night at room temperature and then most of the solvent was evaporated. The residue was dissolved in 300 ml. of water and after one hour extracted with five ml. portions of ether. The ether solution was dried over anhydrous sodium sulfate, filtered and the solvent evaporated to give 38 g. of a yellow oil. The oil was distilled in vacuo to give 29.6 g. colourless product, B.P. 8385 C./0.050.01 mm. Hg. The hydrochloric melts (after repeated recrystalli zations from ethanol) at 162 C.
Analysis-Found (percent): C, 44.19; H, 4.59; N, 8.70; F. l 1.42; CI. 21.52. Calculated for C H NOFCI (percent): C, 44.05; H, 4.32; N, 8.56; F, 11.61; Cl, 21.68.
EXAM PLE 27 S-fluoro- 3-pyridineme thanol To a stirred ice-cooled solution of lithium aluminum hydride (14.4 g.) in 530 ml. of anhydrous ether a precooled solution of ethyl S-fluoronicotinate (64.3 g.) in 370 ml. of anhydrous ether was added during 1.5 hours at a reaction temperature not exceeding 6 C. The mixture was stirred with cooling 30 minutes and then 72 ml. of a sodium sulfate solution in water (5 ml./g.) was slowly added with stirring and cooling. The mixture was filtered and the solid material washed with ether. The combined ether solutions were dried. filtered and the solvent evaporated to give 36.6 g. red oil. This was converted to the hydrochloride, which after repeated recrystallizations from ethanol melts at 162 C. The product was shown to be identical with the one prepared according to Example 26.
EXAMPLE 28 5 -chloro-B-pyridinemethanol To a stirred ice-cooled solution of ethyl S- chloronicotinate (50 g.) in ml. of methanol, sodium borohydride (31 g.) was slowly added. The reaction mixture was stirred one hour at room temperature and then refluxed for 7 hours. After this time 500 ml. of ice-water was added and the mixture was acidified to pH=1-0.l with hydrochloric acid and stirred for 15 minutes. The mixture was then made slightly alkaline (pH=8-9) with 30% sodium hydroxide solution and extracted with 4 portions of 100- l 50 ml. of ethyl acetate. The combined ethyl acetate extract was washed once with water and once with a sodium chloride solution, dried, and the solvent evaporated to give 32 g. oil. The product was purified with vacuum distillation to give 20 g. colourless liquid, B.P. l00106l().1 mm. Hg.
The hydrochloride melts at l38l42 C. Calculated (percent): Cl (as HCl), [9.7. Titration gave 19.5%. The compound was also characterized by its IR spectrum.
EXAMPLE 29 5-bromo-3-pyridinemethanol To a stirred solution of lithium aluminum hydride (9.0 g.) in 200 ml. of anhydrous ether, ethyl 5- bromonicotinate (54.7 g.) dissolved in 230 ml. of anhydrous ether was added during 85 minutes at a temperature of-l0 C. To the yellow reaction mixture 45 ml. of a saturated aqueous sodium sulfate solution was then added and the precipitated salts was immediately filtered off and washed with ether. The combined washings and filtrate was dried over anhydrous sodium sulfate, filtered and the solvent evaporated until a small amount of a red solution was obtained. This solution was treated with hydrogen chloride in ether and the hydrochloride formed was immediately recrystallized from ethanol. The product, thus isolated as the hydrochloride weighed l3.0 g. M.P. l37 C.. also characterized by its IR spectrum.
Analysis.Found (percent); Cl, 15.9. Calculated for C H NOBrCl (percent); Cl, 15.8.
EXAMPLE 3O 5-fluoro-3-pyridinemethanol The starting material 5-fluoro-3-cyanopyridine, M.P. 5354.5 C., was prepared by dehydration of the known S-iluoronicotinamide with phosphorus pentaoxide.
5-fluoro-3-cyanopyridine (1.50 g.) was dissolved in a mixture of 2.5 ml. of concentrated hydrochloric acid and 25 ml. of water and hydrogenated at atmospheric pressure and room temperature over Pd/C (0.40 g. After 8 hours 535 ml. of hydrogen had been consumed. The hydrogenation was interrupted for 3 days and then further hydrogenated during one hour over an additional amount of 10% Pd/C (0.30 g.). A total amount of 600 ml. of hydrogen was consumed. The catalyst was filtered off and washed with water. The com bined filtrate and washings were concentrated to a volume of 25 ml. made alkaline by addition of solid sodium hydrogen carbonate and extracted five times with 40 ml. of butyl acetate. The extract was dried over anhydrous sodium sulfate. filtered and the solvent evaporated to give an oily residue, which was transformed to a hydrochloride salt. This product, which was colourless, weighed L42 g. and had an IR spectrum which was identical with the one obtained from the product according to Example 26.
EXAMPLE 3 l 5-fluoro-3-pyridinemethanol 5-fluoronicotinic acid (3.00 g.) was refluxed 4 hours with 30 ml. of thionyl chloride and the excess of thionyl chloride evaporated in vacuo. The 5-fluoronicotinic acid chloride thus obtained was dissolved in 30 ml. of diglyme and treated while stirring with sodium borohydride (2.40 g.). first minutes at 35 C. and then 30 minutes at 80 C. The mixture was poured out on ice and carefully acidified with diluted aqueous hydrochloric acid. The aqueous solution was washed with two portions of ether and its volume reduced in vacuo to about 50 ml. It was then made alkaline with aqueous ammonium and extracted with five portions of chloroform. The chloroform solution was dried over anhydrous sodium sulfate, filtered and the solvent evaporated to give an oily product, which was transformed to a hydrochloride salt. The dry salt weighed 1.35 g. and had an IR spectrum which was identical with the one obtained from the product prepared according to Example 26.
EXAMPLE 32 S-fluoro-B-pyridinemethanol The starting material S-benzyl 5-fluoro-3- pyridinecarbothioate M.P. 4244 C., was prepared by the reaction of S-fluoronicotinoyl chloride with benzylmercaptan.
S-benzyl S-fluoro-B-pyridinecarbothioate 1.00 g.) was stirred 3 hours at room temperature with freshly prepared Raney-nickel (W4, 10 g.) in ml. of ethanol. The metal was filtered off and thoroughly washed with ethanol. To the combined filtrate and washings were added a small excess of hydrogen chloride in ether. Evaporation of the solvent in vacuo gave the hydrochloride salt, which was washed with ether and airdried. The colourless product weighed 043 g. and had an IR spectrum which was identical with the one obtained from the product according to Example 26.
EXAMPLE 33 5-fluoro-3-methoxymethylpyridine The starting material 5-fluoro-3- chloromethylpyridine hydrochloride was prepared by reacting 5-fluoro3-pyridinemethanol with thionylchloride.
5-fluoro-3-chloromethylpyridine hydrochloride 15.0 g.) was converted to its base form by treatment with aqueous sodium hydrogen carbonate and the base collected by extraction with benzene. The residue after evaporation of the solvent was dissolved in 40 ml. of methanol. This solution was added drop by drop to a stirred solution made by the addition of sodium (4.0 g.) to 100 ml. of methanol. The reaction mixture was refluxed one hour and the solvent evaporated in vacuo. The residue was extracted with ether and the ether solution extracted twice with water. The water solution was extracted twice with ether and this ether solution combined with the original ether solution. The final ether solution was dried over potassium carbonate, filtered and the solvent evaporated to give 8.5 g. oil. Distillation at reduced pressure gave 6.6 g. colourless liquid, B.P. 70-72 C./l2.5 mm. Hg, n =l.4793.
Analysis.-Found (percent); C, 60.25; H, 5.84; F, 13.09; N, 9.74. Calculated for C H FNO (percent): C, 59.56; H,5.7l; F, 13.46; N. 9.93.
EXAMPLE 34 FOCIIIOCH- O 5-fluoro-3-pyridinemethyl benzyl ether The starting material 5-fluoro-3- chloromethylpyridine was prepared by reacting 5- fluoro-3-pyridinemethanol with thionyl chloride and subsequent isolation of the base. Yield 94%.
Sodiumhydride (2.70 g., 50% dispersion in oil) was added in portions during one hour at room temperature, ml. offreshly distilled benzyl alcohol. The mixture was continuously stirred and kept under nitrogen. The formation of foams was largely prevented by a small addition of diethyl ether (10 ml.). To the stirred mixture kept under nitrogen, a solution of 5-fiuoro-3- chloromethylpyridine (8.39 g.) in 25 ml. of freshly distilled benzylalcohol was added during 10 minutes at room temperature. The stirred mixture, with 20 ml. of diethylether added, was refluxed for 18 hours and was then cooled to room temperature. The precipitate of sodium chloride was filtered off and the filtrate. after evaporation of the solvents, distilled in vacuo. It was obtained 8.40 g., B.P. l22-l28C./0. l5 mm. Hg. This product was dissolved in cold 5 M hydrochloric acid. The acidic solution was extracted with three portions of petroleum ether and then made alkaline by addition of an excess of aqueous ammonia. The alkaline solution was extracted with four portions of diethylether. The ether solution was dried over anhydrous magnesium sulfate, filtered and the solvent evaporated to give 7.76 g. yellow oil. Distillation in vacuo gave 6.8l g. colourless liquid, B.P. l25l27 C./O.l5 mm. Hg, n,, "=l.S45 l.
Analysis-Found (percent): C, 71.5l; H, 5.78; F, 9.06; N, 6.4l. Calculated for C,;,H, FNO (percent): C, 7l.87; H, 5.57; F, 8.75; N, 6.45.
EXAMPLE 35 CHaCIhCllgOH To a suspension of lithium aluminum hydride L? g.) in I50 ml. ether, methyl 5-fluoro-3-pyridinepropionate (4.0 g.) in 50 ml. of ether was added with stirring and ice-cooling during 30 minutes. The mixture was stirred at room temperature for 30 minutes and then gently refluxed for one hour. After cooling, the excess hydride was destroyed by the addition of l ml. of saturated aqueous sodium sulfate. The precipitated salts was filtered off, washed twice with ether, and the combined washings and filtrate dried over anhydrous sodium sulfate. Filtering and evaporation of the solvent gave 3.8 g. oil, which was distilled twice to give 1.6 g. colourless product, B.P. 86-88 C./0.02 mm. Hg, n,, =1.5076.
Analysis.Found (percent): C, 61.71; H, 6.48; N, 9.20. Calculated for C H FNO (percent): C, 6] .92; H, 6.50; N, 9.03.
EXAMPLE 36 -fluoro-3-methylpyridine 5-fluoro-3-pyridinemethanol hydrochloride (5.05 g.) was dissolved in a mixture of 50 ml. ethanol and 2 ml. of concentrated aqueous hydrochloride acid and hydrogenated over 0.5 g. of lO% Pd/C at room temperature and atmospheric pressure. A total amount of 740 ml. of hydrogen was absorbed. The catalyst was filtered off, and the solvent of the filtrate evaporated. The residue was dissolved in water made alkaline with solid sodium hydroxide and the product isolated by steam distillation. 3 g. colourless product was separated and dried over sodium carbonate. The structure of the compound was confirmed by NMR spectroscopy.
EXAMPLE 37 CHIN:
S-fluoro-S-aminomethylpyridine The starting material 5-fluoro-3-cyanopyridine was prepared by dehydration of 5-fluoronicotinamide.
5-fluoro-3-cyanopyridine (8.0 g.) was hydrogenated at 45 p.s.i. and room temperature over rhodium on alumina (5%) in I60 ml. ofa solution of lO% ammonia in ethanol. When the hydrogen absorption had ceased, the catalyst was filtered off and the solvent of the filtrate evaporated to give 7.3 yellow oil. Distillation twice at reduced pressure gave 2.35 g., B.P. 9394 C./l4 mm. Hg, n,, "*=l.520.
Analysis-Found (percent): C. 56.2l; H, 5.68; F, l5.3 l; N, 22.53. Calculated for C H FN, (percent): C, 57.13; H, 5.60; F, 15.06; N, 22.2l.
EXA M PLE 38 5-fluoro-3-aminomethylpyridine The starting material 5-fluoro-B-pyridinemethylazide (B.P. 9899 C./l5 mm. Hg, n,, =l .523) was prepared by reacting 5-fluoro-3-chloromethylpyridine (prepared by the treatment of 5-fluoro-3-pyridinemethanol with thionyl chloride) with sodium azide.
5-fluoro-3-pyridinemethylazide (3.2 g.) was hydrogenated over lO% Pd/C (0.32 g.) at room temperature and a pressure of 3.5 atm. in a mixture of 25 ml. 2 M hydrochloric acid and l00 ml. of 50% aqueous methanol. When the hydrogen absorption had ceased (4 hours) the catalyst was filtered off and the solvent evaporated to give a yellow semi-solid material. This material crystallized from aqueous ethanol to give [.2 g. colourless dihydrochloride, M.P. 223225 C.
Analysis-Found (percent): Cl, 35.6. Calculated for C H FN '2HCl (percent): Cl, 35.6.
EXAMPLE 39 5-fluoro-3aminomethylpyridine The starting material 5-fluoro-3-pyridinemethyl phthalimide (MP. l3l.5-l32.5 C.) was prepared by reaction of 5-fluoro-3-chloromethylpyridine (preparation, see Example 33) with potassium phtalimide.
5-fluoro-3-pyridinemethyl phthalimide (3.4 g.) and hydrazine hydrate (0.66 g.) was refluxed for 2 hours in 20 ml. ethanol. The reaction mixture was allowed to cool and then treated with concentrated aqueous hydrochloride acid to a pH of about l After warming the mixture l hour at the steambath, it was filtered and the solvent evaporated to give a solid residue. This material was triturated with ethanol to give 1.9 g. crystalline dihydrochloride, which was identical with the product prepared in Example 38.
EXAMPLE 40 C; -C00 CHICHJN S-fluoronicotinic acid 12.7 g.) was refluxed for 4.5 hours with 100 ml. of thionyl chloride and then the excess of thionyl chloride was evaporated at reduced pressure. The -fluoronicotinic acid chloride so ob tained was stirred with ice-cooling in 200 ml. of dry benzene and to this mixture a solution of N,N- dimethylaminoethanol (8.05 g.) in a mixture of ml. triethylamine and 50 ml. ofdry benzene was added during one hour. The reaction mixture was stirred at 80 C. for two hours and then the precipitate was filtered off. The solvent of the filtrate was evaporated to give a brown semi-solid material, which was treated with an excess of aqueous sodium hydrogen carbonate. The mixture was extracted with four portions 100 ml.) of ether. The ether solution was dried over anhydrous sodium sulfate, filtered, and the solvent evaporated to give 13.1 g. brown liquid. This was distilled at 0.03 mm. Hg to give 10.2 g. nearly colourless liquid, B.P. 8587 C., n 1.4894;
Equivalent weightFound: 216. Calculated: 212. The product identity was established by NMR measurements EXAMPLE 41 5-fluoro-3-( N,N-diethylaminomethy1)-pyridine To lithium aulminumhydride (1.38 g.) in 150 ml. of
dry ether a solution of 5-fluoro-N,N' diethylnicotinamide (14.7 g.) in [50 ml. of dry ether was added at such a rate that a steady reflux was maintained. The reaction mixture was refluxed further for one hour and was then cooled in ice-water. The excess of hydride was destroyed by addition of 9.4 ml. ofa saturated aqueous solution of sodoum sulfate. The precipitated inorganic salts were filtered off and soaked with boiling ether. The combined ether solutions were dried over anhydrous potassium carbonate, filtered and the solvent evaporated to give 10.8 g. orange oil. A pure product was obtained by distillation at reduced pressure: obtained 2.2 g., B.P. 98l0l C./l3 mm. Hg, n,, =1.4820.
Analysis.Found (percent): C, 65.88; H, 8.33; F, [0.76; N, 15.43. Calculated for C H FN (percent): C, 65.90; H, 8.30; F, 10.43; N, 15.37.
EXAMPLE 42 l-nicotinoyl-3 ,S-dimethylpyrazole Nicotinic acid hydrazide (3.4 g.), acetylacetone (2.5 g. 2 M hydrochloric acid (0.19 ml.) and 2-propanaol (25 ml.) was refluxed for one hour and the solution allowed to stand over night. Evaporation of the solvent gave 4.9 g. yellow oil which soon became crystalline. The product was triturated with 25 ml. of water to give 4.2 g. colourless material, M.P.4344 C.
Analysis.Found (percent): C, 64.95; H, 5.58; N, 21.44; 0, 8.34. Calculated fo C H N O (percent): C, 65.66; H. 5.51; N. 20.88, O, 7.95.
EXAMPLE 43 Mesoinositol hcxa- 5-fluoronicotinate To a stirred mixture of S-fluoronicotinic acid (8.5 g.), meso-inositol (0.9 g.) and dry pyridine (20 m1.) ptoluenesulfonyl chloride (7.0 g.) was added in small portions while the reaction mixture was cooled in cold water. When a too thick precipitate had formed a further [0 ml. portion ofdry pyridine was added. The mixture was stirred one hour at room temperature and one hour at about 110 C. and was then cooled in room temperature. The precipitate was filtered off and dried to give 3.0 g. colourless product, M.P. 220230 C. A further 2.4 g. colourless product, M.P. 2 l 7227 C. was obtained by precipitating from the filtrate by addition to ice-water. Through recrystallization from pyridineethanol the melting point of the product could be raised to 22823 1 C.
Analysis.Found (percent: N, 9.00. Calculated for C H- F N O (percent): N, 9.15.
EXAMPLE 44 Triethanolamine tri-S-fluoronicotinate S-fluoronicotinic acid (8.5 g.) was refluxed with 100 m1. of thionyl chloride for 4.5 hours and then the excess of the reagent was evaporated in vacuo. The 5- fluoronicotinic acid chloride thus obtained was stirred with a mixture of 30 ml. of dry benzene and 30 m1. of dry pyridine and to this mixture triethanolamine (3.1 g.) was added slowly at room temperature. After the addition the reaction mixture was refluxed during two hours and was allowed to stand at room temperature over night. The mixture was poured out on ice-water and made alkaline by the addition of an excess of aqueous sodium hydrogen carbonate and extracted with three portions ml.) of benzene. The combined benzene solutions were washed with two portions ml.) of a saturated aqueous solution of sodium chloride and dried over anhydrous sodium sulfate. The solvent was evaporated and the residue triturated with petroleum ether and recrystallized from 2-propanol. Yield of recrystallized product 1.7 g., M.P. 6l63.5 C. The identity of the product was established by NMR analysis.
EXAMPLE 45 Pharmacological tests Compounds according to the invention were tested with regard to lowering the concentration of free fatty acids in the serum of dogs according to the method described in Carlsson, L. A. and Liljedahl, S. 0., Lipid metabolism and trauma. ll. Studies on the effect of nicotinic acid on norepinephrine induced fatty liver. Acta Med. Scand. 173 (1963), 787-791 and Bergstrom, S., Carlsson, L. A. and 0rd, L. Effect of prostaglandins on catecholamine induced changes in the free fatty acids of plasma and in blood pressure in the dog. Prostaglandin and related factors 22," Acta Physiol. Scand. 60 (1964), -]80. In this method the com- 33 34 pound is tested on a model for the stress situation. in which noradrenaline stimulated lipid mobilization is F (H known to occur. F LL Anaesthetized dogs were given continuous intrave- F Hot-t Cl CH CH nous infusions of noradrenaline at a constant rate (0.5 5 p.g./kg. bodyweight and minute). The test substance was injected intravenously 60 min. after the start of in fusion. The arterial level of free fatty acids as a function g l of time was followed. Nicotinic acid was used as refer F enro- CHI ence. The qualitative effect is given in Table I. H) l The qualitative effect was judged from the total depression of free fatty acid serum concentration and the duration of the depression. 0 0
TABLE l H R Ji 0- m-o-d R Qualita- J I Compound live effect N N Nicotinie acid (reference) 4-H S-chloronieotinie acid Qualitaifluoronicotinie acid +l+-+ 2U Compound the effect 5-fluoronicotinic acid methylester R:\ R S-fluoronicotinic acid ethylestcr +-H+ S-fluoronicotinic acid n-hutylcster 4-H" S-fluoronicotinic acid n-hexylester F CH2(H1 S-fluoronicotinic acid p-undecylester l-i-tg t fi H! S-fluoronicotinic acid i-propylester kt-H F F ::H S-fluoronicotinic acid allycster +4 5-fluoronieotinie acid cyelohcxylester -Hl S-Chloronicotinic acid cthylcster F F HEHL' H H CH- ll 0 0 R (CII'lJm C 0- (Cibh- R I a cm-e-e-R -a-o-cn, 1 R N N I l f/ m n t R R' R 0 1 F H +H+ F r CH .CH (l I H F -+i++ F F CH. U I F F F F (CH- )5 u Cl H F F CH%H (lrans4) t) l H C] H++ 1 I H H ++i+ 1 l H F +4-H l 1 H Cl ++i+- R CH|0 II I 2 H H +-Hl- F 3 l H 1-" cmcmcooca,
I F +H+ Cl N Br -w 0 I F- mammomon BL- (CH O), -[OCH1)D N N l N, -l b-fluoro-a-mathoxymethylpyrldlno F-- 0H| m n R' R2 L J N 0 I H CH1; O I F CH3 l e F CH CHI F} -CH2NH'| t? /Clll i l- F C-ClhCll.N
C If C F Clix-N I i t n |-CH| 113C -LN/ Mam-lnosltolhnxa-fi-fluoronlcntlnatn.. Triethanolamine trl-6-fluoronlcotlnate -chloronicotinic acid and 5-fluoronicotinic acid have a low toxicity. For instance the toxicity of 5- fiuoronicotinic acid upon i.p. administration in mice given as the LD,-,.,-value was found to be 2.0 g./kg. bodyweight. The corresponding toxicity of nicotinic acid was found to be 0.5 g./kg. bodyweight.
The resorption of S-chloroand 5-fluoronicotinic acid in serum of dogs was studied. 200 mg. of the test compound were orally administered to the dog in the form of a tablet also containing 200 mg. of physiologically inert material. The amount of the test compound in the blood serum was analyzed at different times according to Hughes, D. E. and Williamson, D. H., Biochem. J. 55 (1953), 851. A comparison with nicotinic acid was made in each case. The maximum resorption and the duration (given as the time after administration when the serum concentration had decreased to 25% of the maximum concentration) is given in Table IV.
The resorption of pyridine methanols in serum of dogs was also studied. 100-200 mg. of the substance to be tested was orally administered to the dog in the form of a tablet or a capsule. The amount of the test compound was analyzed as the corresponding nicotinic acid derivative (the metabolism to these acids is very rapid) at different times according to Hughes, D. E. and Williamson, D. H., Biochem. J. 55 (1953), 851. A comparison with the unsubstituted analogue was made. The maximum resorption and the duration (given as the time after administration when the serum concentration had decreased to 25% of the maximum concentration) of compounds of Formula I, wherein R has specifled significance is given in Table II.
These compounds have a low toxicity as may be seen from Table Ill below, wherein the toxicity in mice upon intraperitoneal administration of a compound of the Formula I wherein R has the specified significance is given.
TABLE III Toxicity (i.p.] [.D, gJkg mice F 2 CI 0.5 Br 0.5
The compound 5-fluoro-3-pyridinemethanol was also tested with respect to its vasodilating properties. Changes in the peripheral blood flow of one hind leg of cat was recorded as follows:
The blood of the femoral artery was bypassed in a loop of polyethylene tubing inserted into the artery. The blood flow through the loop was adjusted by a digital pump. .lust distal of the pump arterial pressure was measured. The pressure recorded is then dependent on the pump flow and the resistance distally of the pump. if the flow is kept constant the pressure changes will thus reflect changes in the peripheral resistance.
lntraarterial injections of 5-fluoro-3- pyridinemethanol (0.1% solution in isotonic sodium chloride solution, l mg. substance/min.) gave 23% decrease in the vascular resistance.
In clinical practice the compounds of the invention will normally be administered orally or by injection in the form of pharmaceutical preparations comprising the active ingredient either as a free base or as a therapeutically acceptable acid addition salt, eg the hydrochloride, hydrosulphate, or the like, in association with a pharmaceutically acceptable carrier. Accordingly, terms relating to the novel compounds of this invention whether generically or specifically are intended to include both the free base and the acid addition salts of the free base, unless the content in which such terms are used, e.g. in the specific examples, would be inconsistent with the broad meaning. The carrier may be a solid, semisolid or liquid diluent or an ingestible capsule. These pharmaceutical preparations constitute a further aspect of this invention. Usually the active substance will constitute between 0.l and by weight of the preparation, more especially between 0.5 and 20% by weight for preparations intended for injection and between 2 and 50% by weight for preparations suitable for oral administration.
To produce pharmaceutical preparations containing a compound of the invention in the form of dosage units for oral application, the selected compound may be mixed with a solid pulverulent carrier, e.g. lactose. saccharose, sorbitol. mannitol; starches such as potato starch, corn starch or amylopectin; cellulose derivatives. or gelatin, and a lubricant such as magnesium stearate. calcium stearate. a polyethylene glycol wax and the like. and then compressed to form tablets. [f coated tablets are required. the cores, prepared as described above. may be coated with a concentrated sugar solution which may, for example, contain gum arabic, gelatin, talcum. titanium dioxide. or the like. Alternatively, the tablet can be coated with a lacquer dissolved in a readily volatile organic solvent or mixture of organic solvent. Dyestuffs may be added to these coatings in order to readily distinguish between tablets containing different active components or different amounts of the active. compound.
By using several layers of the active drug. separated by slowly dissolving coated sustained release tablets are obtained. Another way of preparing sustained release tablets is to divide the dose of the active drug into granules with coats of different thickness and compress the granules into tablets together with the carrier substance. The active substance can also be incorporated in slowly dissolving tablets made for instance of fat and wax substances or evenly distributed in a tablet of an insoluble substance such as a physiologically inert plastic substance.
Effervescent powders are prepared by mixing the active ingredient with non-toxic carbonates or hydrogen carbonates, such as calcium carbonate, potassium carbonate and potassium hydrogen carbonate, solid, nontoxic acids such as tartaric acid and citric acid, and for example aroma.
For the preparation of soft gelatin capsules (pearl shaped closed capsules) consisting of gelatin and for example glycerol or similar closed capsules, the active substance may be admixed with a vegetable oil. Hard gelatin capsules may contain granulates of the active substance in combination with solid, pulverulent carriers such as lactose. saccharose, sorbitol, mannitol, a starch (e.g. potato starch, corn starch or amylopectin) a cellulose derivative or gelatin.
Liquid preparations for oral application may be in the form of syrups or suspensions, for example solutions containing from 0.2% to by weight of the active substance. the balance being sugar and a mixture of ethanol, water, glycerol. and propylene-glycol. Optionally such liquid preparations may contain colouring agents. flavouring agents, saccharin and carboxymethyl-cellulose as a thickening agent.
Solutions for parenteral application by injection can comprise aqueous solutions of a water-soluble pharmaceutically acceptable salt of the active substance, preferably in a concentration of 0.5% to 10% by weight. These solutions may also contain stabilizing agents and- /or buffering agents, and may conveniently be provided in various dosage unit ampoules.
EXAMPLE 46 Preparation of soft gelatin capsules containing 5- fluoronicotinic acid ethylester 500 g. of S-fluoronicotinic acid ethylester were mixed with 500 g. of corn oil whereafter the mixture was filled in soft gelatin capsules, each capsule containing 100 mg. of mixture (i.e. 50 mg. of active substance).
EXAMPLE 47 Preparation of soft gelatin capsules containing 5- fluoronicotinic acid methylester 500 g. of S-fluoronicotinic acid methylester were mixed with 750 g. of peanut oil whereafter the mixture was filled in soft gelatin capsules. each capsule containing l25 mg. of mixture (i.e. 50 mg. of active substance).
EXAMPLE 48 Preparation of tablets containing S-fluoronicotinic acid ethylester EXAMPLE 49 Preparation of an emulsion containing 5-fluoronicotinic acid ethylester 100 g of 5-fluoronicotinic acid ethylester were dissolved in 2500 g. of peanut oil. From the solution thus obtained. 99 g. of gum arabic. aroma and colour (q.s.) and 2500 g. of water and emulsion was prepared.
EXAMPLE 50 Preparation of a syrup containing S-fluoronicotinic acid isopropylester I00 g of 5fluoronicotinic acid allylester were dissolved in 300 g. of 95% ethanol where 300 g. of glycerol, aroma and color (q.s.) and water 1.000 ml. were mixed in. A syrup was thus obtained.
EXAMPLE 5 1 Preparation of a solution containing 5fluoronicotinic acid ethylester l00 g of 5-fluoronic0tinic acid ethylester were dissolved in 2.000 g of polyoxyethylene sorbitan monooleate, whereafter aroma and colour (q.s.) and water to 5.000 ml. were mixed in. A clear drop solution was thus obtained.
EXAMPLE 52 Preparation of a syrup containing vitamins and S-fluoronicotinic acid The syrup was prepared from the following ingredients:
S-fluoronicotinic acid7.0 g.
Polyoxyethylenesorbitol monooleate0.4 g.
Vitamin A12.000 1E Vitamin C-2 g.
Vitamin B 50 mg.
Vitamin B rng.
Claims (2)
1. A COMPOUND OF THE STRUCTURAL FORMULA
2. 5-fluoro-3-pyridinemethanol, and its therapeutically acceptable salts.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SE15717/66A SE327987B (en) | 1966-11-16 | 1966-11-16 | |
GB03687/67A GB1213162A (en) | 1966-11-16 | 1967-03-23 | Serum lipid lowering pyridine derivatives and their preparation |
GB19174/67A GB1157186A (en) | 1966-11-16 | 1967-04-26 | Serum Lipid Lowering Pyridine Derivatives |
US689751A US3637714A (en) | 1966-11-16 | 1967-11-15 | 5 - fluoro-3-pyridinemethanol esters thereof and therapeutically acceptable salts thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
USRE28532E true USRE28532E (en) | 1975-08-26 |
Family
ID=27448204
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US00173678A Expired - Lifetime US3737542A (en) | 1966-11-16 | 1971-08-20 | Lowering excessive serum lipid concentrations and preparations containing fluoro-pyridine derivatives |
US00173679A Expired - Lifetime US3781280A (en) | 1966-11-16 | 1971-08-20 | Fluoro-pyridine derivatives and therapeutically acceptable salts thereof |
US35127173 Expired USRE28532E (en) | 1966-11-16 | 1973-04-16 | 5-Fluoro-3-pyridinemethanol, esters thereof and therapeutically acceptable salts thereof |
Family Applications Before (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US00173678A Expired - Lifetime US3737542A (en) | 1966-11-16 | 1971-08-20 | Lowering excessive serum lipid concentrations and preparations containing fluoro-pyridine derivatives |
US00173679A Expired - Lifetime US3781280A (en) | 1966-11-16 | 1971-08-20 | Fluoro-pyridine derivatives and therapeutically acceptable salts thereof |
Country Status (1)
Country | Link |
---|---|
US (3) | US3737542A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5436344A (en) * | 1990-11-29 | 1995-07-25 | Pfizer Inc. | 3-bromo-5-chloro-pyridines used as intermediates in the synthesis of azatetralones |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4198416A (en) * | 1976-09-30 | 1980-04-15 | Meiji Seika Kaisha, Ltd. | 5-Alkoxy-picolinic esters and anti-hypertensive composition containing 5-alkoxy-picolinic esters |
AU4232985A (en) * | 1984-04-13 | 1985-11-01 | Fmc Corporation | Fluoropyridinylmethyl cyclopropanecarboxylate insecticides and intermediates |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3557131A (en) * | 1965-06-15 | 1971-01-19 | Dainippon Pharmaceutical Co | Nicotinate derivatives of vitamin b6 |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1213162A (en) * | 1966-11-16 | 1970-11-18 | Astra Ab | Serum lipid lowering pyridine derivatives and their preparation |
US3466294A (en) * | 1967-11-30 | 1969-09-09 | Nepera Chem Co Inc | Tertiary acetylenic esters of pyridine carboxylic acids |
-
1971
- 1971-08-20 US US00173678A patent/US3737542A/en not_active Expired - Lifetime
- 1971-08-20 US US00173679A patent/US3781280A/en not_active Expired - Lifetime
-
1973
- 1973-04-16 US US35127173 patent/USRE28532E/en not_active Expired
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3557131A (en) * | 1965-06-15 | 1971-01-19 | Dainippon Pharmaceutical Co | Nicotinate derivatives of vitamin b6 |
Non-Patent Citations (2)
Title |
---|
Beaty et al., Chem. Abstracts, Vol. 46, (18), 8654a-b, Sept. 25, 1952. * |
Beaty et al., J. Chem. Soc., London, p. 3512, 1951, QB1 C. 6. * |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5436344A (en) * | 1990-11-29 | 1995-07-25 | Pfizer Inc. | 3-bromo-5-chloro-pyridines used as intermediates in the synthesis of azatetralones |
US5608071A (en) * | 1990-11-29 | 1997-03-04 | Pfizer Inc. | Synthesis of 3-bromo-5-chloro-2-alkyl-pyridine derivatives |
US5677458A (en) * | 1990-11-29 | 1997-10-14 | Pfizer Inc. | Method of preparing azatetralones |
Also Published As
Publication number | Publication date |
---|---|
US3781280A (en) | 1973-12-25 |
US3737542A (en) | 1973-06-05 |
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