IL90559A - History of active anti-pain phenothiazines - Google Patents
History of active anti-pain phenothiazinesInfo
- Publication number
- IL90559A IL90559A IL9055989A IL9055989A IL90559A IL 90559 A IL90559 A IL 90559A IL 9055989 A IL9055989 A IL 9055989A IL 9055989 A IL9055989 A IL 9055989A IL 90559 A IL90559 A IL 90559A
- Authority
- IL
- Israel
- Prior art keywords
- propyl
- kpa
- reduced pressure
- under reduced
- concentrated
- Prior art date
Links
- 230000000202 analgesic effect Effects 0.000 title claims abstract description 11
- 125000001484 phenothiazinyl group Chemical class C1(=CC=CC=2SC3=CC=CC=C3NC12)* 0.000 title abstract 2
- 239000000203 mixture Substances 0.000 claims abstract description 240
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 53
- 239000002253 acid Substances 0.000 claims abstract description 34
- 150000003839 salts Chemical class 0.000 claims abstract description 18
- 230000001882 diuretic effect Effects 0.000 claims abstract description 9
- 229940066767 systemic antihistamines phenothiazine derivative Drugs 0.000 claims abstract description 9
- 125000004433 nitrogen atom Chemical group N* 0.000 claims abstract description 8
- 125000000623 heterocyclic group Chemical group 0.000 claims abstract description 7
- 150000007513 acids Chemical class 0.000 claims abstract description 6
- 238000000034 method Methods 0.000 claims description 22
- 150000002990 phenothiazines Chemical class 0.000 claims description 22
- 150000001408 amides Chemical class 0.000 claims description 14
- 125000004432 carbon atom Chemical group C* 0.000 claims description 12
- 150000002825 nitriles Chemical class 0.000 claims description 10
- 125000004214 1-pyrrolidinyl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 claims description 9
- AEOCXXJPGCBFJA-UHFFFAOYSA-N ethionamide Chemical compound CCC1=CC(C(N)=S)=CC=N1 AEOCXXJPGCBFJA-UHFFFAOYSA-N 0.000 claims description 9
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 claims description 9
- 238000011282 treatment Methods 0.000 claims description 9
- 239000008194 pharmaceutical composition Substances 0.000 claims description 7
- 150000001412 amines Chemical class 0.000 claims description 6
- 239000002934 diuretic Substances 0.000 claims description 5
- KXMAIWXPZGQNCR-UHFFFAOYSA-N n-propyl-10-(1-pyrrolidin-1-ylpropan-2-yl)phenothiazine-2-carboxamide Chemical compound C12=CC(C(=O)NCCC)=CC=C2SC2=CC=CC=C2N1C(C)CN1CCCC1 KXMAIWXPZGQNCR-UHFFFAOYSA-N 0.000 claims description 5
- 150000003556 thioamides Chemical class 0.000 claims description 4
- 239000003814 drug Substances 0.000 claims description 3
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims description 3
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 claims description 3
- MTHMKPUPLVFWQT-UHFFFAOYSA-N n-(3-methylbutyl)-10-(1-piperidin-1-ylpropan-2-yl)phenothiazine-2-carboxamide Chemical compound C12=CC(C(=O)NCCC(C)C)=CC=C2SC2=CC=CC=C2N1C(C)CN1CCCCC1 MTHMKPUPLVFWQT-UHFFFAOYSA-N 0.000 claims description 2
- 239000004480 active ingredient Substances 0.000 claims 6
- 238000004519 manufacturing process Methods 0.000 claims 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 484
- 239000000243 solution Substances 0.000 description 275
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 225
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 177
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 144
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 135
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 133
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 124
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 115
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 115
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 108
- 239000012153 distilled water Substances 0.000 description 107
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 104
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 96
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 90
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 85
- 238000003756 stirring Methods 0.000 description 83
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 82
- 239000000047 product Substances 0.000 description 82
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 78
- 229920006395 saturated elastomer Polymers 0.000 description 78
- 239000012074 organic phase Substances 0.000 description 76
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 72
- 235000019341 magnesium sulphate Nutrition 0.000 description 72
- 238000004587 chromatography analysis Methods 0.000 description 71
- 239000007787 solid Substances 0.000 description 71
- 239000000741 silica gel Substances 0.000 description 67
- 229910002027 silica gel Inorganic materials 0.000 description 67
- 239000003921 oil Substances 0.000 description 63
- 235000019198 oils Nutrition 0.000 description 63
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 60
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 52
- 239000000706 filtrate Substances 0.000 description 52
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 51
- 235000011167 hydrochloric acid Nutrition 0.000 description 51
- 229960000443 hydrochloric acid Drugs 0.000 description 51
- 239000011780 sodium chloride Substances 0.000 description 51
- 235000019502 Orange oil Nutrition 0.000 description 47
- 239000010502 orange oil Substances 0.000 description 47
- 239000011541 reaction mixture Substances 0.000 description 46
- 239000000725 suspension Substances 0.000 description 46
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 45
- 235000011121 sodium hydroxide Nutrition 0.000 description 45
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 42
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 39
- 229960000583 acetic acid Drugs 0.000 description 37
- 125000003118 aryl group Chemical group 0.000 description 35
- -1 alkyl radical Chemical group 0.000 description 34
- 239000002244 precipitate Substances 0.000 description 34
- 239000013078 crystal Substances 0.000 description 33
- 238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 33
- 238000010992 reflux Methods 0.000 description 32
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 31
- 238000002329 infrared spectrum Methods 0.000 description 29
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 27
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 27
- BRMYZIKAHFEUFJ-UHFFFAOYSA-L mercury diacetate Chemical compound CC(=O)O[Hg]OC(C)=O BRMYZIKAHFEUFJ-UHFFFAOYSA-L 0.000 description 27
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 21
- 239000001530 fumaric acid Substances 0.000 description 21
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 20
- 238000001914 filtration Methods 0.000 description 20
- 239000000155 melt Substances 0.000 description 20
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 18
- 239000003610 charcoal Substances 0.000 description 15
- 229940086542 triethylamine Drugs 0.000 description 15
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 14
- 239000008346 aqueous phase Substances 0.000 description 13
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 12
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 11
- 239000011521 glass Substances 0.000 description 11
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 10
- 238000009835 boiling Methods 0.000 description 10
- 238000002425 crystallisation Methods 0.000 description 10
- 230000008025 crystallization Effects 0.000 description 10
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 10
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 10
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 9
- BYORHHDOZQYRKQ-UHFFFAOYSA-N 10-[1-(ethylamino)propan-2-yl]phenothiazine-2-carbonitrile Chemical compound C1=C(C#N)C=C2N(C(C)CNCC)C3=CC=CC=C3SC2=C1 BYORHHDOZQYRKQ-UHFFFAOYSA-N 0.000 description 8
- LPPPABVBCXZTRD-UHFFFAOYSA-N 2-(2-cyanophenothiazin-10-yl)propyl methanesulfonate Chemical compound C1=C(C#N)C=C2N(C(COS(C)(=O)=O)C)C3=CC=CC=C3SC2=C1 LPPPABVBCXZTRD-UHFFFAOYSA-N 0.000 description 8
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 8
- 230000005587 bubbling Effects 0.000 description 8
- 239000003960 organic solvent Substances 0.000 description 8
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 8
- YAPQVCXMMMPTRU-UHFFFAOYSA-N 10-(1-pyrrolidin-1-ylpropan-2-yl)phenothiazine-2-carbothioamide Chemical compound C12=CC=CC=C2SC2=CC=C(C(N)=S)C=C2N1C(C)CN1CCCC1 YAPQVCXMMMPTRU-UHFFFAOYSA-N 0.000 description 7
- XZYJRLIBPLYWMK-UHFFFAOYSA-N 10-[1-(diethylamino)propan-2-yl]phenothiazine-2-carbonitrile Chemical compound C1=C(C#N)C=C2N(C(C)CN(CC)CC)C3=CC=CC=C3SC2=C1 XZYJRLIBPLYWMK-UHFFFAOYSA-N 0.000 description 7
- IIEWJVIFRVWJOD-UHFFFAOYSA-N ethyl cyclohexane Natural products CCC1CCCCC1 IIEWJVIFRVWJOD-UHFFFAOYSA-N 0.000 description 7
- 239000012362 glacial acetic acid Substances 0.000 description 7
- BMFVGAAISNGQNM-UHFFFAOYSA-N isopentylamine Chemical compound CC(C)CCN BMFVGAAISNGQNM-UHFFFAOYSA-N 0.000 description 7
- 229910000027 potassium carbonate Inorganic materials 0.000 description 7
- 238000006748 scratching Methods 0.000 description 7
- 230000002393 scratching effect Effects 0.000 description 7
- WYKWIDKHJCQELF-UHFFFAOYSA-N 10-(1-hydroxypropan-2-yl)phenothiazine-2-carbonitrile Chemical compound C1=C(C#N)C=C2N(C(CO)C)C3=CC=CC=C3SC2=C1 WYKWIDKHJCQELF-UHFFFAOYSA-N 0.000 description 6
- ATCUCVRYXYRJRY-UHFFFAOYSA-N 10-(1-pyrrolidin-1-ylpropan-2-yl)phenothiazine-2-carbonitrile Chemical compound C12=CC=CC=C2SC2=CC=C(C#N)C=C2N1C(C)CN1CCCC1 ATCUCVRYXYRJRY-UHFFFAOYSA-N 0.000 description 6
- KDSNLYIMUZNERS-UHFFFAOYSA-N 2-methylpropanamine Chemical compound CC(C)CN KDSNLYIMUZNERS-UHFFFAOYSA-N 0.000 description 6
- 101150041968 CDC13 gene Proteins 0.000 description 6
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 6
- 238000001816 cooling Methods 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 6
- 125000004493 2-methylbut-1-yl group Chemical group CC(C*)CC 0.000 description 5
- VJROPLWGFCORRM-UHFFFAOYSA-N 2-methylbutan-1-amine Chemical compound CCC(C)CN VJROPLWGFCORRM-UHFFFAOYSA-N 0.000 description 5
- ZSIQJIWKELUFRJ-UHFFFAOYSA-N azepane Chemical compound C1CCCNCC1 ZSIQJIWKELUFRJ-UHFFFAOYSA-N 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 5
- 150000002148 esters Chemical class 0.000 description 5
- 102000048260 kappa Opioid Receptors Human genes 0.000 description 5
- PVWOIHVRPOBWPI-UHFFFAOYSA-N n-propyl iodide Chemical compound CCCI PVWOIHVRPOBWPI-UHFFFAOYSA-N 0.000 description 5
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 5
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 5
- LPNYRYFBWFDTMA-UHFFFAOYSA-N potassium tert-butoxide Chemical compound [K+].CC(C)(C)[O-] LPNYRYFBWFDTMA-UHFFFAOYSA-N 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- 239000000377 silicon dioxide Substances 0.000 description 5
- 235000017557 sodium bicarbonate Nutrition 0.000 description 5
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 5
- 238000001228 spectrum Methods 0.000 description 5
- 108020001588 κ-opioid receptors Proteins 0.000 description 5
- XEVCYLKAXVWQJB-UHFFFAOYSA-N 10-[1-(diethylamino)propan-2-yl]-n-(3-methylbutyl)phenothiazine-2-carbothioamide Chemical compound C1=C(C(=S)NCCC(C)C)C=C2N(C(C)CN(CC)CC)C3=CC=CC=C3SC2=C1 XEVCYLKAXVWQJB-UHFFFAOYSA-N 0.000 description 4
- FCGDEHGBHMUDIB-UHFFFAOYSA-N 10-[1-[ethyl(methyl)amino]propan-2-yl]phenothiazine-2-carbothioamide Chemical compound C1=C(C(N)=S)C=C2N(C(C)CN(C)CC)C3=CC=CC=C3SC2=C1 FCGDEHGBHMUDIB-UHFFFAOYSA-N 0.000 description 4
- WJFKNYWRSNBZNX-UHFFFAOYSA-N 10H-phenothiazine Chemical compound C1=CC=C2NC3=CC=CC=C3SC2=C1 WJFKNYWRSNBZNX-UHFFFAOYSA-N 0.000 description 4
- 125000005917 3-methylpentyl group Chemical group 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 4
- 239000012267 brine Substances 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- IASVCSHUOARLNA-UHFFFAOYSA-N n-propyl-10-(1-pyrrolidin-1-ylpropan-2-yl)phenothiazine-2-carbothioamide Chemical compound C12=CC(C(=S)NCCC)=CC=C2SC2=CC=CC=C2N1C(C)CN1CCCC1 IASVCSHUOARLNA-UHFFFAOYSA-N 0.000 description 4
- 229950000688 phenothiazine Drugs 0.000 description 4
- 229910000029 sodium carbonate Inorganic materials 0.000 description 4
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 4
- 238000003786 synthesis reaction Methods 0.000 description 4
- QOQPYUSHDDPJQO-UHFFFAOYSA-N 10-(1-pyrrolidin-1-ylpropan-2-yl)phenothiazine-2-carboxylic acid;hydrochloride Chemical compound Cl.C12=CC=CC=C2SC2=CC=C(C(O)=O)C=C2N1C(C)CN1CCCC1 QOQPYUSHDDPJQO-UHFFFAOYSA-N 0.000 description 3
- OJMFSTAZIMHRCD-UHFFFAOYSA-N 10-[1-(azepan-1-yl)propan-2-yl]phenothiazine-2-carbonitrile Chemical compound C12=CC=CC=C2SC2=CC=C(C#N)C=C2N1C(C)CN1CCCCCC1 OJMFSTAZIMHRCD-UHFFFAOYSA-N 0.000 description 3
- AHNIZOFGMRUXHD-UHFFFAOYSA-N 10-[1-(diethylamino)propan-2-yl]phenothiazine-2-carbothioamide Chemical compound C1=C(C(N)=S)C=C2N(C(C)CN(CC)CC)C3=CC=CC=C3SC2=C1 AHNIZOFGMRUXHD-UHFFFAOYSA-N 0.000 description 3
- FXBNLZLPAIXLIP-UHFFFAOYSA-N 10-[1-(dimethylamino)propan-2-yl]-n-(3-methylbutyl)phenothiazine-2-carboxamide Chemical compound C1=CC=C2N(C(C)CN(C)C)C3=CC(C(=O)NCCC(C)C)=CC=C3SC2=C1 FXBNLZLPAIXLIP-UHFFFAOYSA-N 0.000 description 3
- XZSIGWOVDPSPMG-UHFFFAOYSA-N 10h-phenothiazine-2-carbonitrile Chemical compound C1=CC=C2NC3=CC(C#N)=CC=C3SC2=C1 XZSIGWOVDPSPMG-UHFFFAOYSA-N 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- 241000700199 Cavia porcellus Species 0.000 description 3
- 244000166102 Eucalyptus leucoxylon Species 0.000 description 3
- 235000004694 Eucalyptus leucoxylon Nutrition 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 3
- QARBMVPHQWIHKH-UHFFFAOYSA-N methanesulfonyl chloride Chemical compound CS(Cl)(=O)=O QARBMVPHQWIHKH-UHFFFAOYSA-N 0.000 description 3
- BQJCRHHNABKAKU-KBQPJGBKSA-N morphine Chemical compound O([C@H]1[C@H](C=C[C@H]23)O)C4=C5[C@@]12CCN(C)[C@@H]3CC5=CC=C4O BQJCRHHNABKAKU-KBQPJGBKSA-N 0.000 description 3
- UQOUMLXRSACUFD-UHFFFAOYSA-N n-(2-methylbutyl)-10-(1-pyrrolidin-1-ylpropan-2-yl)phenothiazine-2-carbothioamide Chemical compound C12=CC(C(=S)NCC(C)CC)=CC=C2SC2=CC=CC=C2N1C(C)CN1CCCC1 UQOUMLXRSACUFD-UHFFFAOYSA-N 0.000 description 3
- HFVMCRNNWMTEKF-UHFFFAOYSA-N n-(2-methylpropyl)-10-(1-pyrrolidin-1-ylpropan-2-yl)phenothiazine-2-carbothioamide;hydrochloride Chemical compound Cl.C12=CC(C(=S)NCC(C)C)=CC=C2SC2=CC=CC=C2N1C(C)CN1CCCC1 HFVMCRNNWMTEKF-UHFFFAOYSA-N 0.000 description 3
- WADFRUXRLYENMW-UHFFFAOYSA-N n-(3-methylpentyl)-10-(1-pyrrolidin-1-ylpropan-2-yl)phenothiazine-2-carbothioamide;hydrochloride Chemical compound Cl.C12=CC(C(=S)NCCC(C)CC)=CC=C2SC2=CC=CC=C2N1C(C)CN1CCCC1 WADFRUXRLYENMW-UHFFFAOYSA-N 0.000 description 3
- OICIEUFHJBQUQC-UHFFFAOYSA-N n-butyl-10-(1-pyrrolidin-1-ylpropan-2-yl)phenothiazine-2-carbothioamide Chemical compound C12=CC(C(=S)NCCCC)=CC=C2SC2=CC=CC=C2N1C(C)CN1CCCC1 OICIEUFHJBQUQC-UHFFFAOYSA-N 0.000 description 3
- 230000007935 neutral effect Effects 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 235000011837 pasties Nutrition 0.000 description 3
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 3
- VYMPLPIFKRHAAC-UHFFFAOYSA-N 1,2-ethanedithiol Chemical compound SCCS VYMPLPIFKRHAAC-UHFFFAOYSA-N 0.000 description 2
- RQEUFEKYXDPUSK-UHFFFAOYSA-N 1-phenylethylamine Chemical compound CC(N)C1=CC=CC=C1 RQEUFEKYXDPUSK-UHFFFAOYSA-N 0.000 description 2
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- QFUXBUQNDBZTCZ-UHFFFAOYSA-N n-pentyl-10-(1-pyrrolidin-1-ylpropan-2-yl)phenothiazine-2-carbothioamide Chemical compound C12=CC(C(=S)NCCCCC)=CC=C2SC2=CC=CC=C2N1C(C)CN1CCCC1 QFUXBUQNDBZTCZ-UHFFFAOYSA-N 0.000 description 1
- VIAQPZQMBWKWBJ-UHFFFAOYSA-N n-pentyl-10-(1-pyrrolidin-1-ylpropan-2-yl)phenothiazine-2-carboxamide;hydrochloride Chemical compound Cl.C12=CC(C(=O)NCCCCC)=CC=C2SC2=CC=CC=C2N1C(C)CN1CCCC1 VIAQPZQMBWKWBJ-UHFFFAOYSA-N 0.000 description 1
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- CBMSDILKECEMOT-UHFFFAOYSA-N potassium;2-methylpropan-1-olate Chemical compound [K+].CC(C)C[O-] CBMSDILKECEMOT-UHFFFAOYSA-N 0.000 description 1
- 230000037452 priming Effects 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- RBWSWDPRDBEWCR-RKJRWTFHSA-N sodium;(2r)-2-[(2r)-3,4-dihydroxy-5-oxo-2h-furan-2-yl]-2-hydroxyethanolate Chemical compound [Na+].[O-]C[C@@H](O)[C@H]1OC(=O)C(O)=C1O RBWSWDPRDBEWCR-RKJRWTFHSA-N 0.000 description 1
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- 238000002560 therapeutic procedure Methods 0.000 description 1
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- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical class CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D279/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom and one sulfur atom as the only ring hetero atoms
- C07D279/10—1,4-Thiazines; Hydrogenated 1,4-thiazines
- C07D279/14—1,4-Thiazines; Hydrogenated 1,4-thiazines condensed with carbocyclic rings or ring systems
- C07D279/18—[b, e]-condensed with two six-membered rings
- C07D279/22—[b, e]-condensed with two six-membered rings with carbon atoms directly attached to the ring nitrogen atom
- C07D279/24—[b, e]-condensed with two six-membered rings with carbon atoms directly attached to the ring nitrogen atom with hydrocarbon radicals, substituted by amino radicals, attached to the ring nitrogen atom
- C07D279/28—[b, e]-condensed with two six-membered rings with carbon atoms directly attached to the ring nitrogen atom with hydrocarbon radicals, substituted by amino radicals, attached to the ring nitrogen atom with other substituents attached to the ring system
-
- 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
- A61K31/54—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/10—Antioedematous agents; Diuretics
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Neurology (AREA)
- Diabetes (AREA)
- Pain & Pain Management (AREA)
- Biomedical Technology (AREA)
- Hematology (AREA)
- Neurosurgery (AREA)
- Epidemiology (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Indole Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR8807770A FR2632520B1 (fr) | 1988-06-10 | 1988-06-10 | Derives de la phenothiazine analgesiques |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| IL90559A0 IL90559A0 (en) | 1990-01-18 |
| IL90559A true IL90559A (en) | 1994-08-26 |
Family
ID=9367166
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL9055989A IL90559A (en) | 1988-06-10 | 1989-06-07 | History of active anti-pain phenothiazines |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US5049669A (de) |
| EP (1) | EP0346238B1 (de) |
| JP (1) | JP2504830B2 (de) |
| KR (1) | KR0125575B1 (de) |
| AT (1) | ATE90346T1 (de) |
| AU (1) | AU621120B2 (de) |
| CA (1) | CA1325631C (de) |
| DE (1) | DE68906965T2 (de) |
| DK (1) | DK283089A (de) |
| ES (1) | ES2058569T3 (de) |
| FR (1) | FR2632520B1 (de) |
| HU (1) | HU205752B (de) |
| IE (1) | IE63300B1 (de) |
| IL (1) | IL90559A (de) |
| MX (1) | MX9203585A (de) |
| PT (1) | PT90813B (de) |
| ZA (1) | ZA894397B (de) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2632522B1 (fr) * | 1988-06-10 | 1990-09-14 | Rhone Poulenc Sante | Nouveaux derives de la phenothiazine, leur preparation et les compositions qui les contiennent |
| FR2632521B1 (fr) * | 1988-06-10 | 1990-09-14 | Rhone Poulenc Sante | Nouveaux derives de la phenothiazine, leur preparation et les compositions pharmaceutiques qui les contiennent |
| FR2652084B1 (fr) * | 1989-09-21 | 1991-10-31 | Rhone Poulenc Sante | Nouveaux derives de la phenothiazine, leur preparation et les compositions pharmaceutiques qui les contiennent. |
| FR2689013B1 (fr) * | 1992-03-30 | 1995-05-05 | Rhone Poulenc Rorer Sa | Nouvelle application thérapeutique des dérivés de la phénothiazine. |
| FR2720940A1 (fr) * | 1994-06-13 | 1995-12-15 | Rhone Poulenc Rorer Sa | Application du (+)-N-propyl [(pyrrolidinyl-1)-1 propyl-2]-10 phénothiazinecarboxamide comme antidépresseur. |
| PT946157E (pt) * | 1996-12-16 | 2002-07-31 | Alcon Lab Inc | Utilizacao topica de agonistas kapa-opioides para o tratamento da dor ocular |
| US6174878B1 (en) | 1999-08-31 | 2001-01-16 | Alcon Laboratories, Inc. | Topical use of kappa opioid agonists to treat otic pain |
| JP4371142B2 (ja) * | 2004-12-28 | 2009-11-25 | 株式会社村田製作所 | イオン発生ユニットおよびイオン発生装置 |
| KR101646962B1 (ko) | 2014-09-29 | 2016-08-10 | 한국과학기술연구원 | CaM 저해활성을 가지는 페노싸이아진 유도체 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2956996A (en) * | 1960-10-18 | Alkylated phenotfflazenecarboxamede | ||
| NL222355A (de) * | 1957-11-05 | |||
| US3112310A (en) * | 1962-01-15 | 1963-11-26 | Searle & Co | 10-alkylaminoalkylphenothiazine-2-carboxamides |
| FR180F (fr) * | 1964-11-30 | Bruneau & Cie Lab | Médicament a base de dérivés d'acide phénothiazine carboxylique-3. | |
| FR2632522B1 (fr) * | 1988-06-10 | 1990-09-14 | Rhone Poulenc Sante | Nouveaux derives de la phenothiazine, leur preparation et les compositions qui les contiennent |
| FR2632521B1 (fr) * | 1988-06-10 | 1990-09-14 | Rhone Poulenc Sante | Nouveaux derives de la phenothiazine, leur preparation et les compositions pharmaceutiques qui les contiennent |
-
1988
- 1988-06-10 FR FR8807770A patent/FR2632520B1/fr not_active Expired - Lifetime
-
1989
- 1989-06-07 IL IL9055989A patent/IL90559A/en not_active IP Right Cessation
- 1989-06-09 DE DE89401601T patent/DE68906965T2/de not_active Expired - Fee Related
- 1989-06-09 AT AT89401601T patent/ATE90346T1/de not_active IP Right Cessation
- 1989-06-09 DK DK283089A patent/DK283089A/da not_active Application Discontinuation
- 1989-06-09 ZA ZA894397A patent/ZA894397B/xx unknown
- 1989-06-09 HU HU893033A patent/HU205752B/hu not_active IP Right Cessation
- 1989-06-09 PT PT90813A patent/PT90813B/pt not_active IP Right Cessation
- 1989-06-09 EP EP89401601A patent/EP0346238B1/de not_active Expired - Lifetime
- 1989-06-09 AU AU36240/89A patent/AU621120B2/en not_active Ceased
- 1989-06-09 ES ES89401601T patent/ES2058569T3/es not_active Expired - Lifetime
- 1989-06-09 CA CA000602376A patent/CA1325631C/fr not_active Expired - Fee Related
- 1989-06-10 KR KR1019890008027A patent/KR0125575B1/ko not_active Expired - Fee Related
- 1989-06-12 US US07/364,155 patent/US5049669A/en not_active Expired - Lifetime
- 1989-06-12 JP JP1149261A patent/JP2504830B2/ja not_active Expired - Lifetime
- 1989-06-12 IE IE186589A patent/IE63300B1/en unknown
-
1992
- 1992-06-26 MX MX9203585A patent/MX9203585A/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| KR910000680A (ko) | 1991-01-30 |
| FR2632520A1 (fr) | 1989-12-15 |
| PT90813A (pt) | 1989-12-29 |
| DE68906965T2 (de) | 1993-12-09 |
| IL90559A0 (en) | 1990-01-18 |
| EP0346238A1 (de) | 1989-12-13 |
| IE891865L (en) | 1989-12-10 |
| EP0346238B1 (de) | 1993-06-09 |
| IE63300B1 (en) | 1995-04-05 |
| KR0125575B1 (ko) | 1998-07-01 |
| JPH037269A (ja) | 1991-01-14 |
| MX9203585A (es) | 1992-09-01 |
| ZA894397B (en) | 1990-02-28 |
| PT90813B (pt) | 1994-10-31 |
| HU205752B (en) | 1992-06-29 |
| FR2632520B1 (fr) | 1990-09-14 |
| AU3624089A (en) | 1989-12-21 |
| DE68906965D1 (de) | 1993-07-15 |
| US5049669A (en) | 1991-09-17 |
| DK283089A (da) | 1989-12-11 |
| AU621120B2 (en) | 1992-03-05 |
| CA1325631C (fr) | 1993-12-28 |
| HUT50464A (en) | 1990-02-28 |
| JP2504830B2 (ja) | 1996-06-05 |
| ATE90346T1 (de) | 1993-06-15 |
| ES2058569T3 (es) | 1994-11-01 |
| DK283089D0 (da) | 1989-06-09 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| KB | Patent renewed | ||
| RH1 | Patent not in force |