HRP20070421T3 - Ariloksialkilkarbamatni derivati, njihova priprema i terapeutska primjena - Google Patents

Ariloksialkilkarbamatni derivati, njihova priprema i terapeutska primjena

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Publication number
HRP20070421T3
HRP20070421T3 HR20070421T HRP20070421T HRP20070421T3 HR P20070421 T3 HRP20070421 T3 HR P20070421T3 HR 20070421 T HR20070421 T HR 20070421T HR P20070421 T HRP20070421 T HR P20070421T HR P20070421 T3 HRP20070421 T3 HR P20070421T3
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Croatia
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group
cycloalkyl
phenyl
alkyl
alkylene
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HR20070421T
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English (en)
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Abouabdellah Ahmed
Almario Garcia Antonio
Froissant Jacques
Hoornaert Christian
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Sanofi-Aventis
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Publication of HRP20070421T3 publication Critical patent/HRP20070421T3/hr

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    • C07D207/04Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom 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
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    • 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
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Abstract

Spoj formule (I) naznačen time da: m predstavlja 0, 1, 2 ili 3; n predstavlja 0, 1, 2 ili 3; X predstavlja atom kisika ili sumpora ili grupu SO ili SO2;R1 i R2 predstavljaju, neovisno jedan od drugog, atom vodika ili C1-3-alkilnu grupu, ili R1 i R2 zajedno tvore -(CH2)p- grupu, gdje p predstavlja cijeli broj između 1 i 5, tako da n + p iznosi cijeli broj od 2 do 5; R3 predstavlja atom vodika ili fluora ili hidroksi- ili metilnu grupu; R4 predstavlja grupu opće formule CHR5CONHR6 u kojojR5 predstavlja atom vodika ili C1-6-alkilnu grupu, a R6 predstavlja atom vodika ili C1-6-alkilnu, C3-7-cikloalkilnu, C3-7-cikloalkil-C1-6-alkilensku grupu; Y predstavljaY1 grupu, izabranu naročito između fenila, piridinila, piridazinila, pirimidinila, pirazinila, triazinila, tiazolila, naftila, kinolinila, izokinolinila, ftalazinila, kinazolinila, kinoksalinila, naftiridinila, kinolinila, benzofuranila, dihidrobenzofuranila, benzotienila, dihidrobenzotienila, indolila, izoindolila, indolinila, benzimidazoilila, benzoksazolila, benzizoksazolila, benzotiazolila, benzizotiazolila, benzotriazolila, benzoksadiazolila, benzotiadiazolila; pri čemu je Y1 grupa eventualno supstituirana jednim ili više Y2 supstituenata, identičnih ili različitih jedan od drugog, ili grupom Y3; Y2 predstavlja halogeni atom, grupu cijano, nitro, C1-8-alkil, C1-8-alkoksi, C1-8-tioalkil, C1-8-fluoroalkil, C1-8-fluoroalkoksi, C1-8-fluorotioalkil, C3-7-cikloalkil, C3-7-cikloalkiloksi, C3-7-cikloalkil-C1-8-alkilen; C3-7-cikloalkil-C1-8-alkiloksi, hidroksi, NR7R8, NHCOR7, NHSO2R7, COR7, CO2R7, CONR7R8, SO2R7, SO2NR7R8, -O-(C1-3-alkilen)-O-, feniloksi, feniltio, fenil-C1-C8-alkilen, fenil-C1-C8-alkiloksi ili fenil-C1-C8-alkiltio; Y3 predstavlja grupu izabranu naročito između fenila, piridinila, pirimidinila, pirazinila ilipiridazinila; grupa (grupe) Y3 može biti supstituirana jednom ili više Y2 grupa, identičnih ili međusobno različitih; R7 i R8 predstavljaju, neovisnojedan od drugog, atom vodika ili C1-6-alkilnu grupu, ili, zajedno s atomom dušika na koji su vezani, tvore azetidinski, pirolidinski, piperidinski, morfolinski, tiomorfolinski, azepinski ili piperazinski prsten, po želji supstituiran C1-3-alkilnom ili benzilnom grupom; u obliku baze, kisele adicijske soli, hidrata ili solvata. Patent sadrži još 12patentnih zahtjeva.
HR20070421T 2004-01-16 2007-09-13 Ariloksialkilkarbamatni derivati, njihova priprema i terapeutska primjena HRP20070421T3 (hr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR0400389A FR2865205B1 (fr) 2004-01-16 2004-01-16 Derives de type aryloxyalkylcarbamates, leur preparation et leur application en therapeutique
PCT/FR2005/000028 WO2005077898A1 (fr) 2004-01-16 2005-01-07 Derives de type aryloxyalkylcarbamates, leur preparation et leur application en therapeutique

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HRP20070421T3 true HRP20070421T3 (hr) 2007-10-31

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US (3) US7439257B2 (hr)
EP (1) EP1708994B1 (hr)
JP (1) JP4705590B2 (hr)
KR (1) KR101171462B1 (hr)
CN (1) CN100537534C (hr)
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ES (1) ES2289701T3 (hr)
FR (1) FR2865205B1 (hr)
HK (1) HK1101283A1 (hr)
HR (1) HRP20070421T3 (hr)
IL (1) IL176769A (hr)
MA (1) MA28343A1 (hr)
ME (1) MEP26408A (hr)
NO (1) NO20063681L (hr)
NZ (1) NZ548530A (hr)
PL (1) PL1708994T3 (hr)
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TW (1) TWI402067B (hr)
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ZA (1) ZA200605698B (hr)

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FR2865205B1 (fr) * 2004-01-16 2006-02-24 Sanofi Synthelabo Derives de type aryloxyalkylcarbamates, leur preparation et leur application en therapeutique
FR2866884B1 (fr) * 2004-02-26 2007-08-31 Sanofi Synthelabo Derives d'aryl-et d'heteroaryl-piperidinecarboxylates, leur preparation et leur application en therapeutique
FR2866888B1 (fr) * 2004-02-26 2006-05-05 Sanofi Synthelabo Derives de alkylpiperazine- et alkylhomopiperazine- carboxylates, leur preparation et leur application en therapeutique
US7269708B2 (en) * 2004-04-20 2007-09-11 Rambus Inc. Memory controller for non-homogenous memory system
CA2598294C (en) 2005-02-17 2011-10-18 Astellas Pharma Inc. Pyridyl non-aromatic nitrogen-containing heterocyclic-1-carboxylate derivative
US7918848B2 (en) 2005-03-25 2011-04-05 Maquet Cardiovascular, Llc Tissue welding and cutting apparatus and method
US8197472B2 (en) 2005-03-25 2012-06-12 Maquet Cardiovascular, Llc Tissue welding and cutting apparatus and method
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CA2552565A1 (fr) 2005-08-25
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ZA200605698B (en) 2007-11-28
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ATE369336T1 (de) 2007-08-15
AR047384A1 (es) 2006-01-18
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