MA28212A1 - 2-carbonylamino-6-piperidinaminopyridines substitues et 1-carbonylamino-3-piperidinaminobenzenes substitues utilises en tant qu'agonistes de 5-ht1f - Google Patents

2-carbonylamino-6-piperidinaminopyridines substitues et 1-carbonylamino-3-piperidinaminobenzenes substitues utilises en tant qu'agonistes de 5-ht1f

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Publication number
MA28212A1
MA28212A1 MA28928A MA28928A MA28212A1 MA 28212 A1 MA28212 A1 MA 28212A1 MA 28928 A MA28928 A MA 28928A MA 28928 A MA28928 A MA 28928A MA 28212 A1 MA28212 A1 MA 28212A1
Authority
MA
Morocco
Prior art keywords
substituted
hydrogen
alkyl
carbonylamino
piperidinaminopyridines
Prior art date
Application number
MA28928A
Other languages
English (en)
Inventor
Maria-Jesus Blanco-Pillado
Michael Philip Cohen
Sandra Ann Filla
Kevin John Hudziak
Daniel Timothy Kohlman
Dana Rae Benesh
Frantz Victor
Yao-Chang Xu
Bai-Ping Ying
Deanna Piatt Zacherl
Deyi Zhang
Brian Michael Mathes
Original Assignee
Lilly Co Eli
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Lilly Co Eli filed Critical Lilly Co Eli
Publication of MA28212A1 publication Critical patent/MA28212A1/fr

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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • A61K31/4468Non condensed piperidines, e.g. piperocaine having a nitrogen directly attached in position 4, e.g. clebopride, fentanyl
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • A61K31/4523Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
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    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/20Hypnotics; Sedatives
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    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
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    • C04B35/626Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B
    • C04B35/63Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B using additives specially adapted for forming the products, e.g.. binder binders
    • C04B35/632Organic additives
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    • 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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    • 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
    • C07D401/12Heterocyclic 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 chain containing hetero atoms as chain links
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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
    • C07D405/12Heterocyclic 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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  • Anesthesiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

La présente invention concerne des composés de formule ou un sel d'addition d'acide pharmaceutiquement acceptable de ceux-ci, où X représente -C(R3c)= ou ~N=; R1 représente alkyle en C2-C6, alkyle en C2-C6 substitué, cycloalkyle en C3-C7, cycloalkyle en C3-C7 substitué, phényle, phényle substitué, hétérocycle ou hétérocycle substitué; R2 représente hydrogène, n-alkyle en C1-C3, (cycloalkyle en C3-C6)-(alkyle en d- C3) ou un groupe de formule II à condition que lorsque R1 représente alkyle en C2-C6 ou alkyle en C2-C6 substitué, R2 représente hydrogène ou méthyle; R3a R3b et |orSqUe x représente -C(R3c)=, R3c, représentent, indépendamment l'un de l'autre hydrogène, fluoro ou méthyle, à condition que pas plus d'un radical parmi R3a, R3b et R3c puisse être différent d'hydrogène; R4 représente hydrogène ou alkyle en C1-C3; R5 représente hydrogène, alkyle en C1-C3 ou cycloalkylcarbonyle en C3-C6, à condition que lorsque R3a est différent d'hydrogène, R5 représente hydrogène; R6 représente hydrogène ou alkyle en C-i-Ce; et n représente un entier de 1 à 6 compris. Les composés de la présente invention sont utiles pour activer les récepteurs 5- HTIF, inhiber l'extravasation de protéines neuronales et pour le traitement ou la prévention de la migraine chez un mammifère.
MA28928A 2003-09-12 2006-04-10 2-carbonylamino-6-piperidinaminopyridines substitues et 1-carbonylamino-3-piperidinaminobenzenes substitues utilises en tant qu'agonistes de 5-ht1f MA28212A1 (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US50278003P 2003-09-12 2003-09-12

Publications (1)

Publication Number Publication Date
MA28212A1 true MA28212A1 (fr) 2006-10-02

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MA28928A MA28212A1 (fr) 2003-09-12 2006-04-10 2-carbonylamino-6-piperidinaminopyridines substitues et 1-carbonylamino-3-piperidinaminobenzenes substitues utilises en tant qu'agonistes de 5-ht1f

Country Status (30)

Country Link
US (3) US7291632B2 (fr)
EP (1) EP1663971B1 (fr)
JP (1) JP4700614B2 (fr)
KR (1) KR100777875B1 (fr)
CN (1) CN1849307B (fr)
AR (1) AR045619A1 (fr)
AT (1) ATE538093T1 (fr)
AU (1) AU2004280320B2 (fr)
BR (1) BRPI0414241A (fr)
CA (1) CA2537936C (fr)
CR (1) CR8275A (fr)
CY (1) CY1112475T1 (fr)
DK (1) DK1663971T3 (fr)
EA (1) EA011274B1 (fr)
EC (1) ECSP066415A (fr)
ES (1) ES2379665T3 (fr)
IL (1) IL173521A (fr)
MA (1) MA28212A1 (fr)
MX (1) MXPA06002767A (fr)
MY (1) MY144623A (fr)
NO (1) NO20061584L (fr)
NZ (1) NZ545049A (fr)
PE (1) PE20050350A1 (fr)
PL (1) PL1663971T3 (fr)
PT (1) PT1663971E (fr)
SI (1) SI1663971T1 (fr)
TW (1) TWI340740B (fr)
UA (1) UA82711C2 (fr)
WO (1) WO2005035499A1 (fr)
ZA (1) ZA200602072B (fr)

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TWI263497B (en) 2002-03-29 2006-10-11 Lilly Co Eli Pyridinoylpiperidines as 5-HT1F agonists
UA82711C2 (en) * 2003-09-12 2008-05-12 Эли Лилли Энд Компани Substituted 2-carbonylamino-6-piperidinaminopyridines and substituted 1-carbonylamino-3-piperidinaminobenzenes as 5-ht1f agonists
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NZ596161A (en) * 2009-04-02 2013-11-29 Colucid Pharmaceuticals Inc Composition of 2,4,6-trifluoro-n-[6-(1-methyl-piperidin-4-carbonyl)-pyridin-2-yl]-benzamide
EP2476677A1 (fr) * 2009-09-08 2012-07-18 Kyorin Pharmaceutical Co., Ltd. Procédé de production de dérivés de l'acide 4-(5-méthylpyridine-2-ylamino)pipéridine-1-carboxylique
CA2795062A1 (fr) 2010-04-02 2011-10-06 Colucid Pharmaceuticals, Inc. Compositions et methodes de synthese d'agonistes des recepteurs 5-ht1f derives de la pyridinoylpiperidine
EP3027590A1 (fr) * 2013-07-31 2016-06-08 Minoryx Therapeutics S.L. Di(hétéro)arylamides et sulfonamides, procédés permettant leur préparation et utilisations thérapeutiques de ceux-ci
CN109596521A (zh) * 2018-02-11 2019-04-09 中国科学院海洋研究所 磷钼蓝分光光度法中还原剂的保存方法
CN110437205B (zh) * 2018-08-24 2022-07-08 广东东阳光药业有限公司 吡啶烯基哌啶衍生物及其用途
AR119319A1 (es) 2019-07-09 2021-12-09 Lilly Co Eli Procesos e intermediario para la preparación a gran escala de hemisuccinato de 2,4,6-trifluoro-n-[6-(1-metil-piperidina-4-carbonil)-piridin-2-il]-benzamida y preparación de acetato de 2,4,6-trifluoro-n-[6-(1-metil-piperidina-4-carbonil)-piridin-2-il]-benzamida
CN111004214B (zh) * 2019-11-22 2021-06-08 广东东阳光药业有限公司 吡啶酰基哌啶衍生物及其用途
WO2021097781A1 (fr) * 2019-11-22 2021-05-27 广东东阳光药业有限公司 Dérivé de pyridine méthylène pipéridine et son utilisation
CN110845402B (zh) * 2019-11-22 2023-05-09 广东东阳光药业有限公司 吡啶亚甲基哌嗪衍生物及其用途
CN113045540B (zh) * 2019-12-27 2024-02-13 上海天慈国际药业有限公司 一种拉司米地坦的制备方法

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TWI263497B (en) * 2002-03-29 2006-10-11 Lilly Co Eli Pyridinoylpiperidines as 5-HT1F agonists
BRPI0409211A (pt) * 2003-04-18 2006-03-28 Lilly Co Eli composto, composição farmacêutica, métodos para ativar receptores 5-ht1f, para inibir extravasão de proteìna neuronial, e para o tratamento ou prevenção de enxaqueca em um mamìfero, e, uso de um composto
UA82711C2 (en) * 2003-09-12 2008-05-12 Эли Лилли Энд Компани Substituted 2-carbonylamino-6-piperidinaminopyridines and substituted 1-carbonylamino-3-piperidinaminobenzenes as 5-ht1f agonists

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AR045619A1 (es) 2005-11-02
ATE538093T1 (de) 2012-01-15
US20070270466A1 (en) 2007-11-22
TW200521113A (en) 2005-07-01
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