SUBSTITUTED DIHYDROQUINAZOLINES HAVING ANTIVIRAL PROPERTIES Russian patent published in 2009 - IPC C07D403/04 C07D405/14 A61K31/517 A61P31/12 

Abstract RU 2360912 C2

FIELD: chemistry, medicine.

SUBSTANCE: invention refers to the new substituted dihydroquinazolines of formula (I) and to their pharmaceutically acceptable salts having antiviral properties. In general formula (I) , Ar is phenyl group which can be mono-, di- or trisubstituted. The substituting group are independently selected from the group including C1-6 alkyl-, C1-6 alkoxy-, trifluoromethyl groups and halogen atoms or two substituting groups together with linked carbon atoms form 1,3-dioxolane; R1 is hydrogen atom, amine group, C1-6 alkyl group, C1-6 alkoxy group, C1-6 alkylthiol group, cyanic group, halogen atoms, nitro group or trifluoromethyl group; R2 is hydrogen atom, C1-6 alkyl group, C1-6 alkoxy group, C1-6 alkylthiol group, cyanic group, halogen atoms, nitro group or trifluoromethyl group; R3 is C1-6 alkyl group, C1-6 alkoxy group, C1-6 alkylthiol group, cyanic group, halogen atoms, nitro group or trifluoromethyl group; or one of the radicals R1, R2 and R3 is hydrogen atom and two others together with linked carbon atoms form cyclopentane or cyclohexane ring, R4 is hydrogen atom or C1-6 alkyl group, R5 is hydrogen atom or alkyl group, R6 is carboxyl, aminocarbonyl, alkoxycarbonyl groups, halogen atoms, cyanic or hydroxyl groups, R7 is hydrogen atom or halogen atoms and R8 is hydrogen atom or halogen atoms, its pharmaceutically acceptable salts.

EFFECT: claimed compounds can find application for treatment and prevention of diseases and as antiviral agents.

21 cl, 3 tbl, 201 ex

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RU 2 360 912 C2

Authors

Vunberg Tobias

Baumajster Judit

Betts Ul'Rikh

Jeske Mario

Lampe Tomas

Nikolich Suzanne

Reefshleger Jurgen

Shoeh-Loop Rudol'F

Zjusmajer Frank

Tsimmermann Khol'Ger

Grosser Rol'F

Khenninger Kerstin

Kh'Jullet Gaj

Kel'Denikh Jorg

Lang Diter

Nell Peter

Dates

2009-07-10Published

2004-04-17Filed