CA2492138C - N-phenyl-(2r,5s)dimethylpiperazine derivative - Google Patents
N-phenyl-(2r,5s)dimethylpiperazine derivative Download PDFInfo
- Publication number
- CA2492138C CA2492138C CA2492138A CA2492138A CA2492138C CA 2492138 C CA2492138 C CA 2492138C CA 2492138 A CA2492138 A CA 2492138A CA 2492138 A CA2492138 A CA 2492138A CA 2492138 C CA2492138 C CA 2492138C
- Authority
- CA
- Canada
- Prior art keywords
- phenyl
- alkyl
- optionally substituted
- dimethylpiperazine
- acid
- 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 - Fee Related
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- 150000001875 compounds Chemical class 0.000 claims abstract description 127
- 239000012971 dimethylpiperazine Substances 0.000 claims abstract description 17
- 206010060862 Prostate cancer Diseases 0.000 claims abstract description 12
- 208000000236 Prostatic Neoplasms Diseases 0.000 claims abstract description 12
- 229910052739 hydrogen Inorganic materials 0.000 claims description 65
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 47
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 42
- 150000003839 salts Chemical class 0.000 claims description 37
- -1 1-CN-cyclopropyl-1-yl Chemical group 0.000 claims description 32
- 238000004519 manufacturing process Methods 0.000 claims description 21
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 20
- JUJWROOIHBZHMG-UHFFFAOYSA-N pyridine Substances C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 18
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 15
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 13
- 229910052731 fluorine Inorganic materials 0.000 claims description 12
- 229910052794 bromium Inorganic materials 0.000 claims description 9
- 239000003795 chemical substances by application Substances 0.000 claims description 9
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical group O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 claims description 8
- 229910052801 chlorine Inorganic materials 0.000 claims description 7
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 7
- 239000003814 drug Substances 0.000 claims description 7
- 229910052736 halogen Inorganic materials 0.000 claims description 7
- 150000002367 halogens Chemical group 0.000 claims description 7
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 7
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 6
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims description 6
- 239000004480 active ingredient Substances 0.000 claims description 5
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 5
- 229960002317 succinimide Drugs 0.000 claims description 4
- PQKLYXQEYURPTM-UONOGXRCSA-N (2r,5s)-4-(4-cyano-3-methoxyphenyl)-2,5-dimethyl-n-[6-(trifluoromethyl)pyridin-3-yl]piperazine-1-carboxamide Chemical compound C1=C(C#N)C(OC)=CC(N2[C@H](CN([C@H](C)C2)C(=O)NC=2C=NC(=CC=2)C(F)(F)F)C)=C1 PQKLYXQEYURPTM-UONOGXRCSA-N 0.000 claims description 3
- WGSMVIHKBMAWRN-UHFFFAOYSA-N 2,3,3a,4-tetrahydro-1-benzofuran Chemical compound C1C=CC=C2OCCC21 WGSMVIHKBMAWRN-UHFFFAOYSA-N 0.000 claims description 3
- 239000005964 Acibenzolar-S-methyl Substances 0.000 claims description 3
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 3
- RFZAMFXGWQRWFN-QWHCGFSZSA-N (2r,5s)-4-(3-bromo-4-cyanophenyl)-2,5-dimethyl-n-[6-(trifluoromethyl)pyridin-3-yl]piperazine-1-carboxamide Chemical compound C([C@H](C)N(C[C@H]1C)C=2C=C(Br)C(C#N)=CC=2)N1C(=O)NC1=CC=C(C(F)(F)F)N=C1 RFZAMFXGWQRWFN-QWHCGFSZSA-N 0.000 claims description 2
- OPVZRAKKQZGKBN-UONOGXRCSA-N (2r,5s)-4-(3-chloro-4-cyanophenyl)-n-(2-cyclopropylpyrimidin-5-yl)-2,5-dimethylpiperazine-1-carboxamide Chemical compound C([C@H](C)N(C[C@H]1C)C=2C=C(Cl)C(C#N)=CC=2)N1C(=O)NC(C=N1)=CN=C1C1CC1 OPVZRAKKQZGKBN-UONOGXRCSA-N 0.000 claims description 2
- XJDABILWSKTHIE-UONOGXRCSA-N (2r,5s)-4-(3-chloro-4-cyanophenyl)-n-(6-cyanopyridin-3-yl)-2,5-dimethylpiperazine-1-carboxamide Chemical compound C([C@H](C)N(C[C@H]1C)C=2C=C(Cl)C(C#N)=CC=2)N1C(=O)NC1=CC=C(C#N)N=C1 XJDABILWSKTHIE-UONOGXRCSA-N 0.000 claims description 2
- WDJWDRYTWXGAEU-UONOGXRCSA-N (2r,5s)-4-[4-cyano-3-(trifluoromethyl)phenyl]-n-(2-cyclopropylpyrimidin-5-yl)-2,5-dimethylpiperazine-1-carboxamide Chemical compound C([C@H](C)N(C[C@H]1C)C=2C=C(C(C#N)=CC=2)C(F)(F)F)N1C(=O)NC(C=N1)=CN=C1C1CC1 WDJWDRYTWXGAEU-UONOGXRCSA-N 0.000 claims description 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 2
- 239000008194 pharmaceutical composition Substances 0.000 claims description 2
- VVUVJGRVEYHIHC-UHFFFAOYSA-N 2-(4-Morpholinyl)benzothiazole Chemical group C1COCCN1C1=NC2=CC=CC=C2S1 VVUVJGRVEYHIHC-UHFFFAOYSA-N 0.000 claims 1
- HKSKLECHCQBNJQ-UHFFFAOYSA-N 4-quinolin-2-ylmorpholine Chemical compound C1COCCN1C1=CC=C(C=CC=C2)C2=N1 HKSKLECHCQBNJQ-UHFFFAOYSA-N 0.000 claims 1
- 230000000694 effects Effects 0.000 abstract description 38
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- 206010004446 Benign prostatic hyperplasia Diseases 0.000 abstract description 5
- 208000004403 Prostatic Hyperplasia Diseases 0.000 abstract description 5
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 66
- 238000006243 chemical reaction Methods 0.000 description 51
- 239000000243 solution Substances 0.000 description 49
- 239000002904 solvent Substances 0.000 description 33
- 238000001704 evaporation Methods 0.000 description 32
- 230000008020 evaporation Effects 0.000 description 32
- 125000000217 alkyl group Chemical group 0.000 description 30
- 238000003756 stirring Methods 0.000 description 27
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 24
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 24
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- 238000005160 1H NMR spectroscopy Methods 0.000 description 22
- IAZDPXIOMUYVGZ-WFGJKAKNSA-N Dimethyl sulfoxide Chemical compound [2H]C([2H])([2H])S(=O)C([2H])([2H])[2H] IAZDPXIOMUYVGZ-WFGJKAKNSA-N 0.000 description 22
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 20
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- 238000000034 method Methods 0.000 description 17
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 16
- 239000005089 Luciferase Substances 0.000 description 16
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 15
- 108060001084 Luciferase Proteins 0.000 description 15
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 15
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 15
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 15
- 239000007864 aqueous solution Substances 0.000 description 15
- 150000002513 isocyanates Chemical class 0.000 description 15
- 239000012044 organic layer Substances 0.000 description 15
- 239000002253 acid Substances 0.000 description 14
- 238000001816 cooling Methods 0.000 description 14
- 101150041968 CDC13 gene Proteins 0.000 description 13
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 13
- UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Substances C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 13
- 210000004027 cell Anatomy 0.000 description 13
- OAYLNYINCPYISS-UHFFFAOYSA-N ethyl acetate;hexane Chemical compound CCCCCC.CCOC(C)=O OAYLNYINCPYISS-UHFFFAOYSA-N 0.000 description 13
- 238000010438 heat treatment Methods 0.000 description 13
- 238000010898 silica gel chromatography Methods 0.000 description 13
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 12
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 12
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 12
- 125000004093 cyano group Chemical group *C#N 0.000 description 12
- 238000000605 extraction Methods 0.000 description 12
- 239000012948 isocyanate Substances 0.000 description 12
- 239000000460 chlorine Substances 0.000 description 11
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 10
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- 238000004992 fast atom bombardment mass spectroscopy Methods 0.000 description 10
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- 229950006489 mibolerone Drugs 0.000 description 9
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 9
- 241000713333 Mouse mammary tumor virus Species 0.000 description 8
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 8
- 230000004913 activation Effects 0.000 description 8
- 150000001412 amines Chemical class 0.000 description 8
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- 239000000203 mixture Substances 0.000 description 8
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- RXYPXQSKLGGKOL-UHFFFAOYSA-N 1,4-dimethylpiperazine Chemical class CN1CCN(C)CC1 RXYPXQSKLGGKOL-UHFFFAOYSA-N 0.000 description 7
- 101000775732 Homo sapiens Androgen receptor Proteins 0.000 description 7
- 101000928259 Homo sapiens NADPH:adrenodoxin oxidoreductase, mitochondrial Proteins 0.000 description 7
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- 150000001540 azides Chemical class 0.000 description 7
- 150000002148 esters Chemical class 0.000 description 7
- 102000046818 human AR Human genes 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
- CYSGHNMQYZDMIA-UHFFFAOYSA-N 1,3-Dimethyl-2-imidazolidinon Chemical compound CN1CCN(C)C1=O CYSGHNMQYZDMIA-UHFFFAOYSA-N 0.000 description 6
- VHYFNPMBLIVWCW-UHFFFAOYSA-N 4-Dimethylaminopyridine Chemical compound CN(C)C1=CC=NC=C1 VHYFNPMBLIVWCW-UHFFFAOYSA-N 0.000 description 6
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- SJRJJKPEHAURKC-UHFFFAOYSA-N N-Methylmorpholine Chemical compound CN1CCOCC1 SJRJJKPEHAURKC-UHFFFAOYSA-N 0.000 description 6
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- 230000003213 activating effect Effects 0.000 description 6
- 230000037396 body weight Effects 0.000 description 6
- 239000013078 crystal Substances 0.000 description 6
- MKRTXPORKIRPDG-UHFFFAOYSA-N diphenylphosphoryl azide Chemical compound C=1C=CC=CC=1P(=O)(N=[N+]=[N-])C1=CC=CC=C1 MKRTXPORKIRPDG-UHFFFAOYSA-N 0.000 description 6
- ZCSHNCUQKCANBX-UHFFFAOYSA-N lithium diisopropylamide Chemical compound [Li+].CC(C)[N-]C(C)C ZCSHNCUQKCANBX-UHFFFAOYSA-N 0.000 description 6
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- SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 description 1
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- 125000001584 benzyloxycarbonyl group Chemical group C(=O)(OCC1=CC=CC=C1)* 0.000 description 1
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- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
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- 230000000144 pharmacologic effect Effects 0.000 description 1
- AHWALFGBDFAJAI-UHFFFAOYSA-N phenyl carbonochloridate Chemical compound ClC(=O)OC1=CC=CC=C1 AHWALFGBDFAJAI-UHFFFAOYSA-N 0.000 description 1
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- XQZYPMVTSDWCCE-UHFFFAOYSA-N phthalonitrile Chemical compound N#CC1=CC=CC=C1C#N XQZYPMVTSDWCCE-UHFFFAOYSA-N 0.000 description 1
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- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
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- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
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- 150000003335 secondary amines Chemical class 0.000 description 1
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- 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
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- 125000004434 sulfur atom Chemical group 0.000 description 1
- 239000000829 suppository Substances 0.000 description 1
- 239000003765 sweetening agent Substances 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- PGZCVLUQTJRRAA-DTWKUNHWSA-N tert-butyl (2r,5s)-2,5-dimethylpiperazine-1-carboxylate Chemical compound C[C@H]1CN(C(=O)OC(C)(C)C)[C@H](C)CN1 PGZCVLUQTJRRAA-DTWKUNHWSA-N 0.000 description 1
- OCSBBAFGXAGDNH-UONOGXRCSA-N tert-butyl (2r,5s)-4-(3,4-dicyanophenyl)-2,5-dimethylpiperazine-1-carboxylate Chemical compound C[C@H]1CN(C(=O)OC(C)(C)C)[C@H](C)CN1C1=CC=C(C#N)C(C#N)=C1 OCSBBAFGXAGDNH-UONOGXRCSA-N 0.000 description 1
- OHLKGLYZLUEAAT-QWHCGFSZSA-N tert-butyl (2r,5s)-4-(3-chloro-4-cyanophenyl)-2,5-dimethylpiperazine-1-carboxylate Chemical compound C[C@H]1CN(C(=O)OC(C)(C)C)[C@H](C)CN1C1=CC=C(C#N)C(Cl)=C1 OHLKGLYZLUEAAT-QWHCGFSZSA-N 0.000 description 1
- OUEKPCYETGVRLP-NWDGAFQWSA-N tert-butyl (2r,5s)-4-(4-cyano-3,5-difluorophenyl)-2,5-dimethylpiperazine-1-carboxylate Chemical compound C[C@H]1CN(C(=O)OC(C)(C)C)[C@H](C)CN1C1=CC(F)=C(C#N)C(F)=C1 OUEKPCYETGVRLP-NWDGAFQWSA-N 0.000 description 1
- DNXWMJORMDCJQB-UONOGXRCSA-N tert-butyl (2r,5s)-4-(4-cyano-3-methoxyphenyl)-2,5-dimethylpiperazine-1-carboxylate Chemical compound C1=C(C#N)C(OC)=CC(N2[C@H](CN([C@H](C)C2)C(=O)OC(C)(C)C)C)=C1 DNXWMJORMDCJQB-UONOGXRCSA-N 0.000 description 1
- HXUQETXTBKMLAE-QWHCGFSZSA-N tert-butyl (2r,5s)-4-[4-cyano-3-(trifluoromethyl)phenyl]-2,5-dimethylpiperazine-1-carboxylate Chemical compound C[C@H]1CN(C(=O)OC(C)(C)C)[C@H](C)CN1C1=CC=C(C#N)C(C(F)(F)F)=C1 HXUQETXTBKMLAE-QWHCGFSZSA-N 0.000 description 1
- GQQWHFJQDVWDGD-JKSUJKDBSA-N tert-butyl (2r,5s)-4-[4-cyano-3-[(2-methylpropan-2-yl)oxy]phenyl]-2,5-dimethylpiperazine-1-carboxylate Chemical compound C[C@H]1CN(C(=O)OC(C)(C)C)[C@H](C)CN1C1=CC=C(C#N)C(OC(C)(C)C)=C1 GQQWHFJQDVWDGD-JKSUJKDBSA-N 0.000 description 1
- PORXJOIBOYMOMQ-UHFFFAOYSA-N tert-butyl n-(6-cyanopyridin-3-yl)carbamate Chemical group CC(C)(C)OC(=O)NC1=CC=C(C#N)N=C1 PORXJOIBOYMOMQ-UHFFFAOYSA-N 0.000 description 1
- 125000005931 tert-butyloxycarbonyl group Chemical group [H]C([H])([H])C(OC(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 238000001890 transfection Methods 0.000 description 1
- 229940126307 triamcinolone acetate Drugs 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 125000005951 trifluoromethanesulfonyloxy group Chemical group 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- GTLDTDOJJJZVBW-UHFFFAOYSA-N zinc cyanide Chemical compound [Zn+2].N#[C-].N#[C-] GTLDTDOJJJZVBW-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/72—Nitrogen atoms
- C07D213/75—Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/08—Drugs for disorders of the urinary system of the prostate
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/08—Antiseborrheics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/14—Drugs for dermatological disorders for baldness or alopecia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/24—Drugs for disorders of the endocrine system of the sex hormones
- A61P5/28—Antiandrogens
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/84—Nitriles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/42—One nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
- C07D295/20—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carbonic acid, or sulfur or nitrogen analogues thereof
- C07D295/215—Radicals derived from nitrogen analogues of carbonic acid
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- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Dermatology (AREA)
- Diabetes (AREA)
- Endocrinology (AREA)
- Urology & Nephrology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2002-203690 | 2002-07-12 | ||
| JP2002203690 | 2002-07-12 | ||
| PCT/JP2003/008860 WO2004007471A1 (ja) | 2002-07-12 | 2003-07-11 | Ｎ−フェニル−（２ｒ，５ｓ）ジメチルピペラジン誘導体 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2492138A1 CA2492138A1 (en) | 2004-01-22 |
| CA2492138C true CA2492138C (en) | 2011-01-11 |
Family
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA2492138A Expired - Fee Related CA2492138C (en) | 2002-07-12 | 2003-07-11 | N-phenyl-(2r,5s)dimethylpiperazine derivative |
Country Status (11)
| Country | Link |
|---|---|
| US (2) | US7297698B2 (enExample) |
| EP (1) | EP1557411B1 (enExample) |
| JP (1) | JP4449746B2 (enExample) |
| AU (1) | AU2003248052A1 (enExample) |
| CA (1) | CA2492138C (enExample) |
| CY (1) | CY1113335T1 (enExample) |
| DK (1) | DK1557411T3 (enExample) |
| ES (1) | ES2393333T3 (enExample) |
| PT (1) | PT1557411E (enExample) |
| SI (1) | SI1557411T1 (enExample) |
| WO (1) | WO2004007471A1 (enExample) |
Families Citing this family (25)
| Publication number | Priority date | Publication date | Assignee | Title |
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| US7879328B2 (en) * | 2000-06-16 | 2011-02-01 | Human Genome Sciences, Inc. | Antibodies that immunospecifically bind to B lymphocyte stimulator |
| ATE450533T1 (de) * | 2003-02-14 | 2009-12-15 | Glaxo Group Ltd | Carboxamidderivate |
| CA2535416A1 (en) * | 2003-08-15 | 2005-02-24 | Banyu Pharmaceutical Co., Ltd. | Imidazopyridine derivatives |
| WO2005108399A1 (ja) * | 2004-05-10 | 2005-11-17 | Banyu Pharmaceutical Co., Ltd. | イミダゾピリジン化合物 |
| TW200628446A (en) * | 2004-12-14 | 2006-08-16 | Takeda Pharmaceuticals Co | Substituted pyrrole derivative |
| MX2009000508A (es) * | 2006-07-14 | 2009-01-27 | Pfizer Prod Inc | Sal tartrato de (7s)-7-[(5-fluoro-2-metil-bencil)oxi]-2-[(2r)-2-me tilpiperazin-1-il]-6,7-dihidro-5h-ciclopenta[b]piridina. |
| BRPI0907844B8 (pt) * | 2008-02-22 | 2021-05-25 | Radius Health Inc | compostos e método para modular um receptor de andrógeno, processos de preparação e composição farmacêutica dos mesmos e seus usos |
| US8268872B2 (en) | 2008-02-22 | 2012-09-18 | Radius Health, Inc. | Selective androgen receptor modulators |
| CN102548991B (zh) | 2009-09-24 | 2015-03-25 | 霍夫曼-拉罗奇有限公司 | 作为磷酸二酯酶10a抑制剂的咪唑并吡啶或咪唑并嘧啶衍生物 |
| JP5964756B2 (ja) | 2010-02-04 | 2016-08-03 | ラジウス ヘルス，インコーポレイテッド | 選択的アンドロゲン受容体モジュレーター |
| EP2539706B1 (en) * | 2010-02-24 | 2015-03-04 | Research Triangle Institute | Arylpiperazine opioid receptor antagonists |
| DK2568806T3 (en) | 2010-05-12 | 2016-08-15 | Radius Health Inc | therapy Programs |
| US8642632B2 (en) | 2010-07-02 | 2014-02-04 | Radius Health, Inc. | Selective androgen receptor modulators |
| EP2621901B1 (en) | 2010-09-28 | 2015-07-29 | Radius Health, Inc | Selective androgen receptor modulators |
| TW201305130A (zh) * | 2010-10-22 | 2013-02-01 | Astellas Pharma Inc | 突變雄激素受體拮抗藥 |
| WO2013058361A1 (ja) | 2011-10-21 | 2013-04-25 | アステラス製薬株式会社 | アンドロゲン受容体拮抗化合物の結晶 |
| US8765767B2 (en) * | 2012-03-16 | 2014-07-01 | Bristol-Myers Squibb Company | Positive allosteric modulators of mGluR2 |
| PL3231800T3 (pl) * | 2014-12-08 | 2020-04-30 | Lsk Nrdo Co., Ltd. | Nowa pochodna 4-(arylo) -n-(2-alkoksytieno[3,2-b]pirazyn-3-ylo)-piperazyno-1-karboksyamidu oraz jej działanie antyproliferacyjne |
| WO2016196955A1 (en) | 2015-06-04 | 2016-12-08 | Drexel University | Inhibitors of RAD52 Recombination Protein and Methods Using Same |
| CN105130847A (zh) * | 2015-09-10 | 2015-12-09 | 成都大学 | 一种制备高纯邻甲基苯腈及其衍生物的方法 |
| SG11201811225RA (en) | 2016-06-22 | 2019-01-30 | Radius Health Inc | Ar+ breast cancer treatment methods |
| SG11202009388XA (en) | 2018-03-26 | 2020-10-29 | Basf Se | Novel hyperbranched polyesters and their use as wax inhibitor, as pour point depressant, as lubricant or in lubricating oils |
| EP4034114A4 (en) * | 2019-09-23 | 2023-07-26 | Accutar Biotechnology Inc. | NEW UREAES HAVING ANDROGEN RECEPTOR DEGRADING ACTIVITY AND THEIR USES |
| AU2022333206A1 (en) | 2021-08-27 | 2024-04-11 | Basf Se | Aqueous dispersions of paraffin inhibitors |
| AU2022336800A1 (en) | 2021-08-30 | 2024-04-11 | Basf Se | Hyperbranched polyesters modified with branched fatty acids and their use as paraffin inhibitors |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3875229A (en) | 1972-11-24 | 1975-04-01 | Schering Corp | Substituted carboxanilides |
| EP0100172B1 (en) | 1982-07-23 | 1987-08-12 | Imperial Chemical Industries Plc | Amide derivatives |
| US4694004A (en) * | 1984-07-09 | 1987-09-15 | Fujisawa Pharmaceutical Co., Ltd. | Semicarbazide derivatives, processes for preparation thereof and pharmaceutical composition comprising the same |
| CA2181358A1 (en) | 1994-01-21 | 1995-07-27 | Nancy M. Gray | Methods and compositions for treating androgen-dependent diseases using optically pure r-(-)-casodex |
| BR9914018A (pt) * | 1998-09-22 | 2001-07-03 | Yamanouchi Pharmaceuticals Co | Derivado de cianofenila |
| JP2001328938A (ja) * | 2000-03-17 | 2001-11-27 | Yamanouchi Pharmaceut Co Ltd | シアノフェニル誘導体を有効成分とする医薬 |
| US20030236287A1 (en) * | 2002-05-03 | 2003-12-25 | Piotrowski David W. | Positive allosteric modulators of the nicotinic acetylcholine receptor |
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2003
- 2003-07-11 DK DK03764179.2T patent/DK1557411T3/da active
- 2003-07-11 AU AU2003248052A patent/AU2003248052A1/en not_active Abandoned
- 2003-07-11 EP EP03764179A patent/EP1557411B1/en not_active Expired - Lifetime
- 2003-07-11 ES ES03764179T patent/ES2393333T3/es not_active Expired - Lifetime
- 2003-07-11 US US10/521,119 patent/US7297698B2/en not_active Expired - Lifetime
- 2003-07-11 WO PCT/JP2003/008860 patent/WO2004007471A1/ja not_active Ceased
- 2003-07-11 PT PT03764179T patent/PT1557411E/pt unknown
- 2003-07-11 JP JP2004521198A patent/JP4449746B2/ja not_active Expired - Fee Related
- 2003-07-11 SI SI200332218T patent/SI1557411T1/sl unknown
- 2003-07-11 CA CA2492138A patent/CA2492138C/en not_active Expired - Fee Related
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2007
- 2007-09-26 US US11/861,327 patent/US7666873B2/en not_active Expired - Fee Related
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2012
- 2012-11-19 CY CY20121101108T patent/CY1113335T1/el unknown
Also Published As
| Publication number | Publication date |
|---|---|
| JP4449746B2 (ja) | 2010-04-14 |
| US20050261303A1 (en) | 2005-11-24 |
| US7666873B2 (en) | 2010-02-23 |
| WO2004007471A1 (ja) | 2004-01-22 |
| ES2393333T3 (es) | 2012-12-20 |
| JPWO2004007471A1 (ja) | 2005-11-17 |
| AU2003248052A1 (en) | 2004-02-02 |
| US7297698B2 (en) | 2007-11-20 |
| EP1557411A1 (en) | 2005-07-27 |
| EP1557411B1 (en) | 2012-10-17 |
| CA2492138A1 (en) | 2004-01-22 |
| CY1113335T1 (el) | 2016-06-22 |
| EP1557411A4 (en) | 2011-02-23 |
| SI1557411T1 (enExample) | 2013-01-31 |
| DK1557411T3 (da) | 2012-11-05 |
| US20080214543A1 (en) | 2008-09-04 |
| PT1557411E (pt) | 2012-11-22 |
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Legal Events
| Date | Code | Title | Description |
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| EEER | Examination request | ||
| MKLA | Lapsed |
Effective date: 20150713 |