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RU2002114345A - Новые 4-(пиперазинил(8-хинолинил)метил)бензамиды - Google Patents

Новые 4-(пиперазинил(8-хинолинил)метил)бензамиды

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Publication number
RU2002114345A
RU2002114345A RU2002114345/04A RU2002114345A RU2002114345A RU 2002114345 A RU2002114345 A RU 2002114345A RU 2002114345/04 A RU2002114345/04 A RU 2002114345/04A RU 2002114345 A RU2002114345 A RU 2002114345A RU 2002114345 A RU2002114345 A RU 2002114345A
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compound
methyl
quinolinyl
piperazinyl
diethyl
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RU2002114345/04A
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RU2260006C2 (ru
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Уиль м БРАУН (CA)
Уильям БРАУН
Кристофер УОЛПОЛ (CA)
Кристофер Уолпол
Никлас ПЛОБЕК (CA)
Никлас ПЛОБЕК
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Астразенека Аб (Se)
Астразенека Аб
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    • A61P25/00Drugs for disorders of the nervous system
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    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D211/56Nitrogen atoms
    • C07D211/58Nitrogen atoms attached in position 4
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    • C07DHETEROCYCLIC COMPOUNDS
    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/12Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
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    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
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    • C07D405/06Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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    • C07D405/12Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/06Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/12Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links

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  • Chemical & Material Sciences (AREA)
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  • Biomedical Technology (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Rheumatology (AREA)
  • Pain & Pain Management (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Use Of Switch Circuits For Exchanges And Methods Of Control Of Multiplex Exchanges (AREA)
  • Quinoline Compounds (AREA)
  • Pyridine Compounds (AREA)

Claims (20)

1. Соединение формулы
Figure 00000001
где R1 выбран из (1) фенила;
(2)пиридинила
Figure 00000002
(3) тиофенила
Figure 00000003
(4) фуранила
Figure 00000004
(5) имидазолила
Figure 00000005
и
(6) триазолила
Figure 00000006
где каждое фенильное кольцо и гетероароматическое кольцо может быть возможно и независимо дополнительно замещено 1, 2 или 3 заместителями, выбранными из прямого и разветвленного С16алкила, NO2, CF3, С16алкокси, хлоро, фторо, бромо и йодо;
а также его фармацевтически приемлемые соли и его изомеры.
2. Соединение по п.1, где возможный(ые) заместитель(ли) на ароматическом или гетероароматическом кольце(ах) выбран(ы) любой из NO2, изобутила, CF3, метокси, метила или хлоро.
3. Соединение по п.1 или 2, выбранное из любого из
4-[(4-бензил-1-пиперазинил)(8-хинолинил)метил]-N,N-диэтилбензамида дигидрохлорида (соединение 2);
N,N-диэтил-4-[[4-(4-метилбензил)-1-пиперазинил](8-хинолинил)метил]бензамида (соединение 5);
4-[{4-[4-(трет-бутил)бензил]-1-пиперазинил}(8-хинолинил)метил]-N,N-диэтилбензамида дигидрохлорида (соединение 8);
N,N-диэтил-4-[[4-(4-нитробензил)-1-пиперазинил](8-хинолинил)метил]бензамида дигидрохлорида (соединение 9);
4-[{4-[2,4-бис(трифторметил)бензил]-1-пиперазинил}(8-хинолинил)метил]-N,N-диэтилбензамида дигидрохлорида (соединение 10);
N,N-диэтил-4-[[4-(4-метоксибензил)-1-пиперазинил](8-хинолинил)метил]бензамида дигидрохлорида (соединение 11);
4-[[4-(2,4-дихлорбензил)-1-пиперазинил](8-хинолинил)метил]-N,N-диэтилбензамида дигидрохлорида (соединение 12);
N,N-диэтил-4-[[4-(2-пиридинилметил)-1-пиперазинил](8-хинолинил)метил]бензамида дигидрохлорида (соединение 13);
N,N-диэтил-4-[[4-(3-тиенилметил)-1-пиперазинил](8-хинолинил)метил]бензамида (соединение 14);
N,N-диэтил-4-[[4-(2-фуранилметил)-1-пиперазинил](8-хинолинил)метил]бензамида (соединение 15);
N,N-диэтил-4-[[4-(3-фуранилметил)-1-пиперазинил](8-хинолинил)метил]бензамида (соединение 16);
N,N-диэтил-4-[[4-(2-тиофенилметил)-1-пиперазинил](8-хинолинил)метил]бензамида дигидрохлорида (соединение 17);
N,N-диэтил-4-[[4-(2-имидазолилметил)-1 -пиперазинил](8-хинолинил)метил]бензамида дигидрохлорида (соединение 18);
N,N-диэтил-4-[[4-(4-имидазолилметил)-1-пиперазинил](8-хинолинил)метил]бензамида дигидрохлорида (соединение 19) и
N,N-диэтил-4-[[4-(3-триазолилметил)-1-пиперазинил](8-хинолинил)метил]бензамида дигидрохлорида (соединение 20).
4. Соединение по любому из пп.1-3, которое находится в виде (+)-энантиомера.
5. Соединение по любому из пп.1-3, которое находится в виде (-)-энантиомера.
6. Соединение по любому из пп.1-5 в форме его солей гидрохлорида, сульфата, тартрата или цитрата.
7. Соединение по п.4, выбранное из любого из
(+)4-[(4-бензил-1-пиперазинил)(8-хинолинил)метил]-N,N-диэтилбензамида и
(+)4-[[4-(4-метилбензил-1-пиперазинил](8-хинолинил)метил]-N,N-диэтилбензамида.
8. Соединение по п.5, выбранное из любого из
(-)4-[(4-бензил-1-пиперазинил)(8-хинолинил)метил]-N,N-диэтилбензамида и
(-)4-[[4-(4-метилбензил-1-пиперазинил](8-хинолинил)метил]-N,N-диэтилбензамида.
9. Соединение по любому из пп.1-8 для применения в терапии.
10. Соединение по п.9, где терапия представляет собой устранение боли.
11. Соединение по п.9, где терапия направлена на желудочно-кишечные расстройства.
12. Соединение по п.9, где терапия направлена на повреждения спинного мозга.
13. Соединение по п.9, где терапия направлена на расстройства симпатической нервной системы.
14. Применение соединения формулы I по п.1 для производства лекарства для применения при лечении боли.
15. Применение соединения формулы I по п.1 для производства лекарства для применения при лечении желудочно-кишечных расстройств.
16. Применение соединения формулы I по п.1 для производства лекарства для применения при лечении повреждений спинного мозга.
17. Фармацевтическая композиция, содержащая соединение формулы I по п.1 в качестве активного ингредиента вместе с фармакологически и фармацевтически приемлемым носителем.
18. Способ лечения боли, при котором субъекту, нуждающемуся в устранении боли, вводят эффективное количество соединения формулы I по п.1.
19. Способ лечения желудочно-кишечных расстройств, при котором субъекту, страдающему указанным желудочно-кишечным расстройством, вводят эффективное количество соединения формулы I по п.1.
20. Способ лечения повреждений спинного мозга, при котором субъекту, страдающему указанным повреждением спинного мозга, вводят эффективное количество соединения формулы I по п.1.
RU2002114345/04A 1999-12-20 2000-12-15 4-(пиперазинил(8-хинолинил)метил)бензамиды, фармацевтическая композиция и способ лечения боли RU2260006C2 (ru)

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