HRP20140449T1 - Derivat 3,8-diaminotetrahidrokinolina - Google Patents

Derivat 3,8-diaminotetrahidrokinolina Download PDF

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HRP20140449T1
HRP20140449T1 HRP20140449AT HRP20140449T HRP20140449T1 HR P20140449 T1 HRP20140449 T1 HR P20140449T1 HR P20140449A T HRP20140449A T HR P20140449AT HR P20140449 T HRP20140449 T HR P20140449T HR P20140449 T1 HRP20140449 T1 HR P20140449T1
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group
compound
alkyl group
phenyl
membered
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HRP20140449AT
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Takeshi Watanabe
Masaru Terauchi
Masaaki Nagasawa
Kouichirou Tanaka
Masataka Washiduka
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Zeria Pharmaceutical Co., Ltd.
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    • C07D401/02Heterocyclic 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
    • C07D401/04Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
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    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/04Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/02Heterocyclic 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
    • C07D401/06Heterocyclic 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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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
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    • C07D401/14Heterocyclic 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 three or more hetero rings
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    • C07ORGANIC CHEMISTRY
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    • C07D405/00Heterocyclic 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
    • C07D405/02Heterocyclic 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
    • 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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    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
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    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
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    • C07K5/06017Dipeptides with the first amino acid being neutral and aliphatic
    • C07K5/0606Dipeptides with the first amino acid being neutral and aliphatic the side chain containing heteroatoms not provided for by C07K5/06086 - C07K5/06139, e.g. Ser, Met, Cys, Thr
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    • C07K5/06Dipeptides
    • C07K5/06139Dipeptides with the first amino acid being heterocyclic
    • C07K5/06156Dipeptides with the first amino acid being heterocyclic and Trp-amino acid; Derivatives thereof

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Claims (14)

1. Derivat 3,8-diaminotetrahidrokinolina, naznačen time, da je to spoj predstavljen formulom (1 a): [image] (pri čemu X predstavlja CH2, C=O, CH-OR, CH-SR, ili CH-NRR'; m je broj 1 ili 2; Ar predstavlja fenilnu skupinu, naftilnu skupinu, 5-članu ili 6-članu aromatsku heterocikličku skupinu koji ima jedan ili dva elementa odabrana između S, N, i O, ili kondenziranu aromatsku heterocikličku skupinu formiranu između benzenskog prstena i 5-članog ili 6-članog heterocikličkog prstena koji ima jedan ili dva elementa odabrana između S, N, i O ( pri čemu fenil, naftil, ili aromatske heterocikličke skupine mogu biti supstituirane s 1 do 3 atoma halogena, C1 do C6 alkil skupinom, ili C1 do C6 alkoksi skupinom); R1 i R2, koji mogu biti identični ili međusobno različiti, svaki predstavlja atom vodika ili metilnu skupinu; R3 predstavlja C1 do C6 alkil skupinu (alkilna skupina može po izboru biti supstituirana s metiltio, ili benziloksi skupinom), fenilnom skupinom, alkilnom skupinom fenil-C1-4, ili indolil-C1-4 alkil skupinom (fenilna skupina ili indolilna skupina po izboru su supstituirane s C1 do C6 alkil skupinom, atomom halogena, ili C1 do C6 alkoksi skupinom); n je broj 0 ili 1; R4 i R5, koji mogu biti identični ili međusobno različiti, svaki predstavlja atom vodika, ili linearni C1 do C6, razgranatu ili cikličku alkil skupinu (alkilna skupina je po izboru supstituirana atomom halogena, hidroksilnom skupinom, C1 do C6 alkoksi skupinom, fenilnom skupinom, benziloksi skupinom ili hidroksifenil skupinom), ili R4 ili R5 i R6 ili R7 mogu biti povezani sa susjednim atomom dušika te tvore pirolidinski prsten ili piperidinski prsten (pirolidinski prsten ili piperidinski prsten po izboru su supstituirani s hidroksilnom skupinom); R6 i R7, koji mogu biti identični ili međusobno različiti, svaki predstavlja atom vodika ili C1 do C6 alkilnu skupinu; i R i R', koji mogu biti identični ili međusobno različiti, svaki predstavlja atom vodika ili linearnu C1 do C6, razgranatu ili cikličku alkil skupinu), ili njegova sol.
2. Spoj ili sol prema zahtjevu 1, naznačen time, da je m 1.
3. Spoj ili sol prema zahtjevu 1 ili 2, naznačen time, da je Ar fenilna skupina, naftil skupina, piridil skupina, kinolilna skupina, izokinolilna skupina, tienilna skupina, furilna skupina, pirolil skupina, benzotienil skupina, benzofurilna skupina, indolil skupinu, tiazolil skupina, pirimidinil skupina, kinazolinil skupina, imidazolil skupina, benzimidazolilna skupina ili benzotiazolilna skupina (pri čemu ti prstenovi mogu biti supstituirani sa 1 do 3 atoma halogena, C1 do C6 alkilnom skupinom, ili C1 do C6 alkoksi skupinom).
4. Spoj ili sol prema zahtjevu 1 ili 2, naznačen time, da je Ar fenilna skupina, piridilna skupina, tienilna skupina, ili furil skupina.
5. Spoj ili sol prema bilo kojem od zahtjeva 1 do 4, naznačen time, da je R3 C1 do C6 alkilna skupina, benzilna skupina, ili indolilmetilna skupina (indolilna skupina po izboru je supstituirana na dušikovom atomu s C1 do C6 alkilnom skupinom).
6. Spoj ili sol prema bilo kojem od zahtjeva 1 do 5, naznačen time, da je n 0.
7. Spoj ili sol prema bilo kojem od zahtjeva 1 do 6, naznačen time, da je svaki od R4 i R5, koji su jednaki ili različiti jedan od drugog, atom vodika, ili linearna C1 do C4, razgranata ili ciklična alkil skupina.
8. Spoj ili sol prema bilo kojem od zahtjeva 1 do 7, naznačen time, da je svaki od R6 i R7 atom vodika.
9. Spoj ili sol prema bilo kojem od zahtjeva 1 do 8, naznačen time, da je R3 C4 alkilna skupina.
10. Spoj ili sol prema bilo kojem od zahtjeva 1 do 9, naznačen time, da je svaki od R4 i R5, koji su jednaki ili različiti jedan od drugoga, vodikov atom, metilna skupina, ili etilna skupina, ili su R4 i R5 vezani zajedno da formiraju ciklobutil skupinu.
11. Lijek, naznačen time, da sadrži spoj ili sol kao što je navedeno u bilo kojem od zahtjeva 1 do 10.
12. Farmaceutski pripravak, naznačen time, da sadrži spoj ili sol kao što je navedeno u bilo kojem od zahtjeva 1 do 10, i farmaceutski prihvatljiv nosač.
13. Upotreba spoja ili soli kao što je navedeno u bilo kojem od zahtjeva 1 do 10, naznačena time, da se rabi za proizvodnju terapijskog sredstva za razorne sistemske bolesti.
14. Spoj naznačen time, da je to spoj predstavljen formulom (F1): [image] (pri čemu X predstavlja CH2 ili C=O, m je broj 1 ili 2, i Ar predstavlja fenilnu skupinu, naftilnu skupinu, 5-članu ili 6-člana aromatsku heterocikličnu skupinu koji ima jedan ili dva elementa odabrana između S, N, i O, ili kondenziranu aromatsku heterocikličku skupinu formiranu između benzenskog prstena i 5- članog ili 6-članog heterocikličkog prstena koji ima jedan ili dva elementa odabrana između S, N, i O (pri čemu fenil, naftil, ili aromatske heterocikličke skupine mogu biti supstituirane s 1 do 3 atoma halogena, C1 do C6 alkilnom skupinom, ili C1 do C6 alkoksi skupinom), ili njegova sol.
HRP20140449AT 2008-02-08 2014-05-20 Derivat 3,8-diaminotetrahidrokinolina HRP20140449T1 (hr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP2008029781 2008-02-08
JP2008277044 2008-10-28
PCT/JP2009/000487 WO2009098901A1 (ja) 2008-02-08 2009-02-06 3,8-ジアミノテトラヒドロキノリン誘導体

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JP (1) JP5493870B2 (hr)
KR (1) KR101553725B1 (hr)
CN (1) CN101939313B (hr)
AU (1) AU2009212645B2 (hr)
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CA (1) CA2714480C (hr)
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HR (1) HRP20140449T1 (hr)
MX (1) MX2010008740A (hr)
PL (1) PL2241564T3 (hr)
PT (1) PT2241564E (hr)
RU (1) RU2482117C2 (hr)
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CN103328449A (zh) * 2011-01-26 2013-09-25 霍夫曼-拉罗奇有限公司 新的四氢喹啉衍生物
TWI662967B (zh) 2013-03-25 2019-06-21 日商志瑞亞新藥工業股份有限公司 食後期之胃運動亢進劑
CN104193722A (zh) * 2014-08-27 2014-12-10 湖南华腾制药有限公司 一种n-叔丁氧羰基-3-甲胺噻吩的制备方法

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US5206235A (en) * 1991-03-20 1993-04-27 Merck & Co., Inc. Benzo-fused lactams that promote the release of growth hormone
JP3817746B2 (ja) 1994-06-20 2006-09-06 株式会社竹屋 パチンコ島台
CA2301566A1 (en) 1997-08-22 1999-03-04 Kaken Pharmaceutical Co., Ltd. N-acylated lipophilic amino acid derivatives
US6211174B1 (en) * 1997-10-31 2001-04-03 Merck & Co., Inc. Naphtho-fused lactams promote release of growth hormone
UA73530C2 (uk) 1999-11-10 2005-08-15 Ново Нордіск А/С Сполука з властивостями вивільнювати гормон росту
RU2277092C2 (ru) * 2000-09-15 2006-05-27 Анормед, Инк. Гетероциклические соединения, их применение и фармацевтическая композиция для лечения состояний, опосредованных схсr4 и ccr5
WO2005007628A1 (en) * 2003-07-11 2005-01-27 Bristol-Myers Squibb Company Tetrahydroquinoline derivatives as cannabinoid receptor modulators
WO2008116107A2 (en) 2007-03-21 2008-09-25 Takeda San Diego, Inc. Piperazine derivatives as glucokinase activators

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TWI422585B (zh) 2014-01-11
CA2714480A1 (en) 2009-08-13
JP5493870B2 (ja) 2014-05-14
US8299255B2 (en) 2012-10-30
WO2009098901A1 (ja) 2009-08-13
JPWO2009098901A1 (ja) 2011-05-26
MX2010008740A (es) 2010-08-30
CA2714480C (en) 2017-03-28
CN101939313B (zh) 2013-05-22
DK2241564T3 (da) 2014-05-19
RU2482117C2 (ru) 2013-05-20
ZA201005346B (en) 2011-11-30
RU2010137336A (ru) 2012-03-20
US8501772B2 (en) 2013-08-06
TW200940530A (en) 2009-10-01
BRPI0907749A2 (pt) 2015-07-21
PL2241564T3 (pl) 2014-09-30
KR20100116175A (ko) 2010-10-29
KR101553725B1 (ko) 2015-09-16
CY1115138T1 (el) 2016-12-14
AU2009212645B2 (en) 2012-07-19
US20130012537A1 (en) 2013-01-10
EP2241564A4 (en) 2011-07-20
SI2241564T1 (sl) 2014-06-30
US20100317693A1 (en) 2010-12-16
ES2464342T3 (es) 2014-06-02
CN101939313A (zh) 2011-01-05
EP2241564B1 (en) 2014-04-30
EP2241564A1 (en) 2010-10-20
PT2241564E (pt) 2014-06-12
AU2009212645A1 (en) 2009-08-13

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