HETEROCYCLIC COMPOUNDS Russian patent published in 2010 - IPC C07D471/04 C07D498/04 C07D491/04 C07D513/04 C07D495/04 C07D487/04 

Abstract RU 2390522 C2

FIELD: chemistry.

SUBSTANCE: invention relates to new compounds of formula I. In general formula I A is C or N; B, D and E independently represent CR4, NR5, N, O or S; and a ring containing groups A, B, D, E, selected from thienyl, furan, imidazole, oxazole, isothiazole, thiazole, pyrrol, pyrazole; provided that: b) when A is N, not any of B, D, E can be O or S; and c) when A is C, B is CR4 and one of D or E is N or NR5, when any of D or E cannot be NR5 or N; G is N or C; R1 represents one or more substitutes selected from H, Ra halogen, -OH and -ORa; R2 represents one or more substitutes selected from H, halogen and C1-6-alkyl, and also one of substitutes R2 can be -ORb' , -NRb' Rb', -SRb', -SORb', -SO2Rb', -SO2NRb' Rb'; R3 is H, or Cy, selected from phenyl optionally substituted with one or more substitutes selected from Rc , where Rc independently represents halogen, -ORg', where Rg' independently represents a Rg group, where Rg is C1-6-alkyl; each R4 independently represents H, Re, halogen, -CORe', -CO2Re', -CONRe'Re', -NRe'Re'; R5 independently represents H, Re, -CORe, -CONReRe, -SORe or -SO2Re; each Ra independently represents C1-6-alkyl or halogen- C1-6-alkyl; each R independently represents C1-6-alkyl optionally substituted with one or more substitutes selected from Rd and Rf; each Rb' independently represents H or Rb; each Rc independently represents halogen, -ORg', -CONRg'Rg', -NRg'Rg'; Rd is Cy optionally substituted with one or more Rf substitutes; each Rc independently represents C1-6-alkyl optionally substituted with one or more substitutes selected from Rc and Cy*, or Re is Cy, where any of the groups Cy or Cy* can optionally be substituted with one or more substitutes selected from Rc and Rg ; each Re' independently represents H or Re; each Rf independently represents a halogen, -ORh', -CO2Rh; each Rg independently represents Rd or C1-6-alkyl optionally substituted with one or more substitutes selected from Rd and Rf; each Rg' independently represents H or Rg; each Rh independently represents C1-6-alkyl, halogen-C1-6-alkyl or hydroxy- C1-6-alkyl; each Rh' independently represents H or Rh; and Cy or Cy* given in definitions above is a partially saturated, saturated or aromatic 3-7-member monocyclic carbocyclic ring which optionally contains 1-2 heteroatoms selected from N and O, and where the ring or rings can be bonded to the remaining part of the molecule through a carbon or nitrogen atom.

EFFECT: obtaining formula I compounds with p38-kinase inhibitory properties which can be used in making drugs for treating such diseases as tumour immune and autoimmune diseases etc.

21 cl, 10 dwg, 8 tbl, 57 ex

Similar patents RU2390522C2

Title Year Author Number
DERIVATIVES OF PYRAZOL PYRIDINE 2004
  • Al'Mansa Rosales Karmen
  • Virkhili Bernado Marina
RU2359971C2
(AZA)INDOLE-, BENZOTHIOPHENE- AND BENZOFURAN-3-SULPHONAMIDES 2017
  • Mueller Christa E.
  • Pegurier Cecile
  • Deligny Michael Louis Robert
  • El-Tayeb Ali
  • Hockemeyer Joerg
  • Ledecq Marie
  • Mercier Joel
  • Provins Laurent
  • Boshta Nader M.
  • Bhattarai Sanjay
  • Namasivayam Vigneshwaran
  • Funke Mario
  • Schwach Lukas
  • Gollos Sabrina
  • Von Laufenberg Daniel
  • Barre Anais
RU2767904C2
PYRIMIDINE AMIDE COMPOUNDS AS PGDS INHIBITORS 2006
  • Oldous S'Juzan S.
  • Tszjan' Dzhon Tszytsi
  • Lu Tszin'Tsi
  • Ma Ljan
  • Mu Lan'
  • Manson Khehrri Rendall
  • Sejbol Dzheffri Stefen
  • Tkhurajratnam Sukantkhini
  • Vandjuzen Kristofer Loren
RU2420519C2
PYRIMIDINE HYDRAZIDE COMPOUNDS AS PGDS INHIBITORS 2008
  • Oldous S'Juzan S.
  • Fenni Majkl V.
  • Tszjan' Dzhon Ts.
  • Dzhon Stehnli
  • Mu Lan'
  • Pedgrift Brajan
  • Prajbish Dzhejms R.
  • Rokmen Barbara
  • Sejbol Dzheffri S.
  • Stokloza Grzigorz T.
  • Tkhurajratnam Sukantkhini
  • Vandjuzen Kristofer L.
RU2464262C2
AZAINDOLYL PYRIDONE AND DIAZAINDOLYL PYRIDONE 2018
  • Lindstrem, Jokhan
  • Forsblom, Rikard
  • Ram, Fredrik
  • Viklund, Jenni
RU2788659C2
COMPOUND BASED ON DIHYDRONAPTHYRIDINONE, METHOD OF ITS OBTAINING, AND ITS USE IN MEDICINE 2021
  • Zhou, Fusheng
  • Xu, Xiaoming
  • Zhang, Leitao
  • Li, Xin
  • Tang, Lili
  • Lan, Jiong
RU2809869C1
2,6-SUBSTUTED-4-MONOSUBSTITUTED AMINO-PYRIMIDINES AS PROSTAGLANDIN D2 RECEPTOR ANTAGONISTS 2005
  • Lim Sungtaek
  • Kharris Kejt Dzhon
  • Stefani Dehvid
  • Gardner Charl'Z Dzh.
  • Tsao Bin
  • Boffi Rehj
  • Gillespi Timoti A.
  • Agiar Zhuasi K.
  • Khant Khejzel Dzh.
  • Desho Ehl'Za A.
RU2417990C2
NEW SUBSTITUTED BIARYL COMPOUNDS AS INDOLAMINE-2,3-DIOXYGENASE (IDO) INHIBITORS 2018
  • Khan, Yunsin
  • Achab, Abdelgkhani
  • Deng, Jongki
  • Fradera, Ksaver
  • Zhibo, Krejg
  • Khopkins, Brett, A.
  • Li, Dezhun
  • Lyu, Kun
  • Makgauan, Meredet, A.
  • Shammetta, Nuntsio
  • Sloman, Devid
  • Uajt, Ketrin
  • Chzhan, Khuntszyun
  • Chzhou, Khua
RU2786586C2
OXAZINMONOACYLGLYCERIN LIPASE (MAGL) INHIBITORS 2019
  • Bell, Charlz
  • Bents, Jerg
  • Gobbi, Luka
  • Greter, Uve
  • Grebke Tsbinden, Katrin
  • Khansen, Dennis Zhyul
  • Khornsperger, Benua
  • Kotser, Byulent
  • Kroll, Karsten
  • Kun, Bernd
  • O'Khara, Fionn
  • Rikhter, Khans
  • Ritter, Martin
  • Tsutiya, Satosi
  • Chen, Zhuj
RU2794334C2
2-ARYLIMIDAZO[1,2-b]PYRIDAZINE,2-PHENYLIMIDAZO[1,2-a]PYRIDINE AND 2-PHENYLIMIDAZO[1,2-a]PYRAZINE DERIVATIVES 2011
  • Etkinson Robert N.
  • Ommen Endi Dzh.
  • Vil Dzhejms M.
  • Khuan Kennet Kh.
  • Smit Emili D.
RU2598385C2

RU 2 390 522 C2

Authors

Al'Mansa Rosales Karmen

Virkhili Bernado Marina

Grima Poveda Pedro Manuehl'

Dates

2010-05-27Published

2005-08-02Filed