Heterocyclic carboxamide-containing thiourea inhibitors of...

C - Chemistry – Metallurgy – 07 – D

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C07D 307/00 (2006.01) C07D 233/90 (2006.01) C07D 263/34 (2006.01) C07D 277/56 (2006.01) C07D 285/06 (2006.01) C07D 307/68 (2006.01)

Patent

CA 2351690

Compounds of formula (I) wherein R1-R5 are independently selected from hydrogen, or substituents R9-R12 are independently hydrogen, or substituents provided that at least one of R9-12 is not hydrogen; G is a monocyclic heteroaryl: X is a bond, -NH, alkyl of 1 to 6 carbon atoms, alkenyl of 1 to 6 carbon atoms, alkoxy of 1 to 6 carbon atoms, or thioalkyl of 1 to 6 carbon atoms, alkylamino of 1 to 6 carbon atoms, or (CH)J; J is alkyl of 1 to 6 carbon atoms, cycloalkyl of 3 to 7 carbon atoms, phenyl or benzyl, useful in the treatment of diseases associated with herpes viruses including human cytomegalovirus, herpes simplex viruses, Epstein-Barr virus, varicella-zoster virus, human herpesviruses-6 and -7, and Kaposi herpesvirus.

L'invention concerne des composés de formule I, dans laquelle: R1-R5 sont choisis indépendamment entre hydrogène et des substituants de celui-ci; R9-R12 représentent indépendamment hydrogène ou des substituants de celui-ci, à condition qu'au moins un parmi R9-R12 ne désigne pas hydrogène; G symbolise un hétéroaryle monocyclique; X représente une liaison,NH, alkyle avec 1 à 6 atomes de carbone, alkényle avec 1 à 6 atomes de carbone, alkoxy avec 1 à 6 atomes de carbone, thioalkyle avec 1 à 6 atomes de carbone, alkylamino avec 1 à 6 atomes de carbone, ou (CH)J; J désigne alkyle avec 1 à 6 atomes de carbone, cycloalkyle avec 3 à 7 atomes de carbone, phényle, ou benzyle. Ces composés sont utiles pour traiter les maladies liés aux virus de l'herpès, notamment les maladies des inclusions cytomégaliques humaines, l'herpès simplex virus, le virus d'Epstein-Barr, le virus varicelle-zona, les virus de l'herpès humain types 6 et 7, et le virus de l'herpès de Kaposi.

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