JP2004521150A5 - - Google Patents
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- Publication number
- JP2004521150A5 JP2004521150A5 JP2003510033A JP2003510033A JP2004521150A5 JP 2004521150 A5 JP2004521150 A5 JP 2004521150A5 JP 2003510033 A JP2003510033 A JP 2003510033A JP 2003510033 A JP2003510033 A JP 2003510033A JP 2004521150 A5 JP2004521150 A5 JP 2004521150A5
- Authority
- JP
- Japan
- Prior art keywords
- methyl
- dimethylamine
- ethoxy
- pyrazole
- thienylmethyl
- 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.)
- Pending
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- ROSDSFDQCJNGOL-UHFFFAOYSA-N dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 claims 12
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims 12
- KRKNYBCHXYNGOX-UHFFFAOYSA-K 2qpq Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 claims 6
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 6
- 150000001875 compounds Chemical class 0.000 claims 6
- -1 dimethylaminoethyl Chemical group 0.000 claims 6
- 241000124008 Mammalia Species 0.000 claims 4
- 206010046543 Urinary incontinence Diseases 0.000 claims 4
- 125000001424 substituent group Chemical group 0.000 claims 4
- 125000000217 alkyl group Chemical group 0.000 claims 3
- 239000003814 drug Substances 0.000 claims 3
- 238000004519 manufacturing process Methods 0.000 claims 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 3
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 2
- 239000000460 chlorine Substances 0.000 claims 2
- 229910052801 chlorine Inorganic materials 0.000 claims 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 2
- 229910052731 fluorine Inorganic materials 0.000 claims 2
- 239000011737 fluorine Substances 0.000 claims 2
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- 239000011780 sodium chloride Substances 0.000 claims 2
- KORIJXKQGMTQTO-UHFFFAOYSA-N 1H-pyrrol-2-ylmethanol Chemical class OCC1=CC=CN1 KORIJXKQGMTQTO-UHFFFAOYSA-N 0.000 claims 1
- 239000000654 additive Substances 0.000 claims 1
- 230000000996 additive Effects 0.000 claims 1
- 125000003282 alkyl amino group Chemical group 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims 1
- 125000001153 fluoro group Chemical group F* 0.000 claims 1
- 125000001072 heteroaryl group Chemical group 0.000 claims 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 125000004433 nitrogen atoms Chemical group N* 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
- 125000001544 thienyl group Chemical group 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
Claims (5)
- ヒトを含む哺乳動物の尿失禁治療用薬物の製造における一般式(I):
Arはフェニル基またはチエニル基を表し、これらは置換基を有しないか、またはフッ素、塩素、臭素、メチル、トリフルオロメチルおよびメトキシからなる群より選択される1、2または3個の同一または異なる置換基を任意に有する;
R1は水素原子またはC1ないしC4の低級アルキル基を表す;
R2はジ(C1〜C4)アルキルアミノ(C2〜C3)アルキルまたはアザへテロ環状(C2〜C3)アルキル基を表す;また、
Hetは5員の含窒素芳香族へテロ環を表し、該へテロ環は1ないし3個の窒素原子を含み、置換基を有しないか、またはフッ素、塩素、臭素およびメチルからなる群より選択される1または2個の同一または異なる置換基を任意に有する)
で示されるアリール(またはヘテロアリール)アゾリルカルビノール誘導体またはその生理学的に許容し得る塩の1種の使用。 - R1が水素原子から、またはメチル、エチル、プロピル、イソプロピル、ブチル、イソブチル、sec−ブチルおよびtert−ブチルからなる群より選択されるヒトを含む哺乳動物の尿失禁治療用薬物の製造における一般式(I)で示される化合物の請求項1記載の使用。
- R2がジメチルアミノエチル、ジメチルアミノプロピル、ジエチルアミノエチル、ピペリジニルエチル、モルホリニルプロピルおよびピロリジニルエチルからなる群より選択されるヒトを含む哺乳動物の尿失禁治療用薬物の製造における一般式(I)で示される化合物の請求項1記載の使用。
- 一般式(I)で示される化合物が、
(±)−5−{α−[2−(ジメチルアミン)エトキシ]ベンジル}−1−メチル−1H−ピラゾール;
(±)−5−{α−[2−(ジメチルアミン)エトキシ]ベンジル}−1−メチル−1H−ピラゾール・クエン酸塩;
(+)−5−{α−[2−(ジメチルアミン)エトキシ]ベンジル}−1−メチル−1H−ピラゾール;
(−)−5−{α−[2−(ジメチルアミン)エトキシ]ベンジル}−1−メチル−1H−ピラゾール;
(+)−5−{α−[2−(ジメチルアミン)エトキシ]ベンジル}−1−メチル−1H−ピラゾール・クエン酸塩:
(−)−5−{α−[2−(ジメチルアミン)エトキシ]ベンジル}−1−メチル−1H−ピラゾール・クエン酸塩;
(±)−5−{α−[2−(ジメチルアミン)エトキシ]−2−チエニルメチル}−1−メチル−1H−ピラゾール;
(±)−5−{α−[2−(ジメチルアミン)エトキシ]−2−チエニルメチル}−1−メチル−1H−ピラゾール・クエン酸塩;
(+)−5−{α−[2−(ジメチルアミン)エトキシ]−2−チエニルメチル}−1−メチル−1H−ピラゾール;
(−)−5−{α−[2−(ジメチルアミン)エトキシ]−2−チエニルメチル}−1−メチル−1H−ピラゾール;
(+)−5−{α−[2−(ジメチルアミン)エトキシ]−2−チエニルメチル}−1−メチル−1H−ピラゾール・クエン酸塩;および
(−)−5−{α−[2−(ジメチルアミン)エトキシ]−2−チエニルメチル}−1−メチル−1H−ピラゾール・クエン酸塩
からなる群より選択されるヒトを含む哺乳動物の尿失禁治療用薬物の製造における一般式(I)で示される化合物の請求項1記載の使用。 - ヒトを含む哺乳動物の尿失禁治療用医薬組成物であって、請求項1ないし4のいずれか1項に記載された一般式(I)で示される化合物の少なくとも1種またはその生理学的に許容し得る塩の1種、および医薬的に許容し得る添加剤を含有することを特徴とする組成物。
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
ES200101587A ES2180449B1 (es) | 2001-07-06 | 2001-07-06 | Derivados de aril (o heteroaril) azolilcarbinoles para el tratamiento de la incontinencia urinaria. |
PCT/ES2002/000326 WO2003004022A1 (es) | 2001-07-06 | 2002-07-01 | Derivados de aril(o heteroaril)azolilcarbinoles para el tratamiento de la incontinencia urinaria |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2004521150A JP2004521150A (ja) | 2004-07-15 |
JP2004521150A5 true JP2004521150A5 (ja) | 2005-10-06 |
Family
ID=8498326
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2003510033A Pending JP2004521150A (ja) | 2001-07-06 | 2002-07-01 | 尿失禁治療用アリール(またはヘテロアリール)アゾリルカルビノール誘導体 |
Country Status (23)
Country | Link |
---|---|
US (2) | US20030022925A1 (ja) |
EP (1) | EP1413305B1 (ja) |
JP (1) | JP2004521150A (ja) |
KR (1) | KR20040030788A (ja) |
CN (1) | CN1543344A (ja) |
AR (1) | AR034679A1 (ja) |
AT (1) | ATE327752T1 (ja) |
BR (1) | BR0211237A (ja) |
CA (1) | CA2452646A1 (ja) |
CY (1) | CY1105113T1 (ja) |
DE (1) | DE60211913T2 (ja) |
DK (1) | DK1413305T3 (ja) |
ES (2) | ES2180449B1 (ja) |
MA (1) | MA27056A1 (ja) |
MX (1) | MXPA04000065A (ja) |
NO (1) | NO20040031L (ja) |
NZ (1) | NZ530817A (ja) |
PL (1) | PL369062A1 (ja) |
PT (1) | PT1413305E (ja) |
RU (1) | RU2308268C2 (ja) |
UA (1) | UA79238C2 (ja) |
WO (1) | WO2003004022A1 (ja) |
ZA (1) | ZA200400780B (ja) |
Families Citing this family (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20040142929A1 (en) * | 2001-07-06 | 2004-07-22 | Ramon Merce-Vidal | Derivatives of aryl (or heteroaryl) azolylcarbinoles for the treatment of urinary incontinence |
DE10335566A1 (de) * | 2003-07-31 | 2005-02-24 | Grünenthal GmbH | Arzneimittel enthaltend Derivate von Aryl( oder Heteroaryl)azolylcarbinolen |
TW200533657A (en) * | 2004-02-17 | 2005-10-16 | Esteve Labor Dr | Substituted pyrazoline compounds, their preparation and use as medicaments |
EP1584335A3 (en) * | 2004-04-05 | 2006-02-22 | Laboratorios Del Dr. Esteve, S.A. | Active substance combination comprising a carbinol composition and an opioid |
ES2244326B1 (es) * | 2004-04-05 | 2007-02-16 | Laboratorios Del Dr. Esteve, S.A. | Combinacion de substancias activas. |
US20060040924A1 (en) * | 2004-06-22 | 2006-02-23 | Laboratorios Dr. Esteve S.A. | Derivatives of aryl (or heteroaryl) azolylcarbinols for the treatment of renal colic |
EP1784178A1 (en) * | 2004-07-30 | 2007-05-16 | Laboratorios Del Dr. Esteve, S.A. | Aryl (or heteroaryl) azolylcarbinols |
EP1757587A1 (en) * | 2005-07-15 | 2007-02-28 | Laboratorios Del Dr. Esteve, S.A. | Substituted pyrazoline compounds, their preparation and use as medicaments |
US7897589B2 (en) * | 2005-07-15 | 2011-03-01 | Laboratorios Del Dr. Esteve, S.A. | Substituted pyrazoline compounds, their preparation and use as medicaments |
EP1743892A1 (en) * | 2005-07-15 | 2007-01-17 | Laboratorios del Dr. Esteve S.A. | Substituted pyrazoline compounds, their preparation and use as medicaments |
EP1743890A1 (en) * | 2005-07-15 | 2007-01-17 | Laboratorios Del Dr. Esteve, S.A. | 4,5-Dihydro-1H-pyrazole derivatives, their preparation and use as medicaments |
US20070021485A1 (en) * | 2005-07-22 | 2007-01-25 | Gomis Antonio F | Aryl (or heteroaryl) azolylcarbinols |
WO2007017127A2 (en) * | 2005-07-29 | 2007-02-15 | Laboratorios Del Dr. Esteve, S.A | Controlled realease dosage form of pirazole compounds to treat urinary incontinence |
US8722079B2 (en) | 2008-04-18 | 2014-05-13 | Warsaw Orthopedic, Inc. | Methods for treating conditions such as dystonia and post-stroke spasticity with clonidine |
EP2151234A1 (en) * | 2008-07-28 | 2010-02-10 | Laboratorios Del. Dr. Esteve, S.A. | Pharmaceutical formulation comprising a CB1-receptor compound in a solid solution and/or solid dispersion |
WO2010123999A2 (en) * | 2009-04-21 | 2010-10-28 | Auspex Pharmaceuticals, Inc. | 1-methylpyrazole modulators of substance p, calcitonin gene-related peptide, adrenergic receptor, and/or 5-ht receptor |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE891865A (fr) * | 1981-01-30 | 1982-07-22 | Sandoz Sa | Nouveaux medicaments a base de derives condenses de l'imidazole pour le traitement des troubles urinaires |
ES2150353B1 (es) * | 1998-04-15 | 2001-07-01 | Esteve Labor Dr | Tienilazolilalcoxietanaminas, su preparacion y su aplicacion como medicamentos. |
ES2137136B1 (es) * | 1998-05-18 | 2000-07-01 | Esteve Labor Dr | Empleo de derivados de aril (o heteroaril) azolilcarbinoles en la elaboracion de un medicamento para el tratamiento de la inflamacion neurogenica. |
ES2150378B1 (es) * | 1998-08-07 | 2001-07-01 | Esteve Labor Dr | Empleo de derivados de aril(o heteroaril)azolilcarbinoles en la elaboracion de un medicamento para el tratamiento de los trastornos mediados por un exceso de substancia p. |
-
2001
- 2001-07-06 ES ES200101587A patent/ES2180449B1/es not_active Expired - Fee Related
-
2002
- 2002-01-07 UA UA2004020880A patent/UA79238C2/uk unknown
- 2002-07-01 WO PCT/ES2002/000326 patent/WO2003004022A1/es active IP Right Grant
- 2002-07-01 AR ARP020102482A patent/AR034679A1/es not_active Application Discontinuation
- 2002-07-01 NZ NZ530817A patent/NZ530817A/en unknown
- 2002-07-01 ES ES02745440T patent/ES2263792T3/es not_active Expired - Lifetime
- 2002-07-01 DE DE60211913T patent/DE60211913T2/de not_active Expired - Fee Related
- 2002-07-01 MX MXPA04000065A patent/MXPA04000065A/es unknown
- 2002-07-01 PT PT02745440T patent/PT1413305E/pt unknown
- 2002-07-01 CN CNA028161009A patent/CN1543344A/zh active Pending
- 2002-07-01 AT AT02745440T patent/ATE327752T1/de not_active IP Right Cessation
- 2002-07-01 RU RU2004103475/15A patent/RU2308268C2/ru not_active IP Right Cessation
- 2002-07-01 PL PL02369062A patent/PL369062A1/xx not_active Application Discontinuation
- 2002-07-01 DK DK02745440T patent/DK1413305T3/da active
- 2002-07-01 KR KR10-2004-7000056A patent/KR20040030788A/ko not_active Application Discontinuation
- 2002-07-01 BR BR0211237-0A patent/BR0211237A/pt not_active IP Right Cessation
- 2002-07-01 JP JP2003510033A patent/JP2004521150A/ja active Pending
- 2002-07-01 CA CA002452646A patent/CA2452646A1/en not_active Abandoned
- 2002-07-01 EP EP02745440A patent/EP1413305B1/en not_active Expired - Lifetime
- 2002-07-03 US US10/189,915 patent/US20030022925A1/en not_active Abandoned
-
2004
- 2004-01-05 NO NO20040031A patent/NO20040031L/no not_active Application Discontinuation
- 2004-01-30 ZA ZA200400780A patent/ZA200400780B/en unknown
- 2004-02-04 MA MA27514A patent/MA27056A1/fr unknown
-
2005
- 2005-01-28 US US11/045,708 patent/US20050131049A1/en not_active Abandoned
-
2006
- 2006-07-28 CY CY20061101049T patent/CY1105113T1/el unknown
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