申请人:——
公开号:US20030207884A1
公开(公告)日:2003-11-06
The use of compounds of formula (1) is described, in which compounds R
1
, R
2
and R
3
are each independently of the others hydrogen; C
1
-C
20
alkyl; C
3
-C
7
cycloalkyl; C
2
-C
20
alkenyl; C
4
-C
7
cycloalkenyl; C
2
-C
20
alkynyl, C
4
-C
7
cycloalkynyl; or unsubstituted or C
1
-C
5
alkyl-, C
3
-C
7
cylcoalkyl-, C
1
-C
5
alkoxyl-, C
3
-C
7
cycloakoxy-, halo-, oxo-, carboxy-, carboxy-C
1
-C
7
alkyl ester-, carboxy-C
3
-C
7
cylcloalkyl ester-, cyano-, trifluoromethyl-, pentafluoroethyl-, amino-, N,N-mono- or di-C
1
-C
20
alkylamino- or nitro-substituted phenyl-C
1
-C
5
alkyl, naphthyl-C
1
-C
5
alkyl, phenylcarbonyl-C
1
-C
5
alkyl, naphthylcarbonyl-C
1
-C
5
alkyl, pyrrolylalkyl, furanylalkyl, thiophenylalkyl, pyrazolylalkyl, imidazolylalkyl, oxazolylalkyl, thiazolylalkyl, isoxazolylalkyl, isothiazolylalkyl, 1,2,3-triazolylalkyl, 1,2,4-triazolylalkyl, 1,2,3-oxadiazolylalkyl, 1,3,4-oxadiazolylalkyl, 1,2,3-thiadiazolylalkyl, 1,3,4-thiadiazolylalkyl, indolylalkyl, pyridylalkyl, pyridazinylalkyl, pyrimidinylalkyl, pyridazinylalkyl, quinolinylalkyl, isoquinolinylalkyl, pyrrolyl, furanyl, thiophenyl, pyrazolyl, imidazolyl, oxazolyl, thiazolyl, isoxazolyl, isothiazolyl, 1,2,3-triazolyl, 1,2,4-triazolyl, 1,2,3-oxadiazolyl, 1,3,4-oxadiazolyl, 1,2,3-thiadiazolyl, 1,3,4-thiadiazolyl, indolyl, pyridyl, pyridazinyl, pyrimidinyl, pyridazinyl, quinolinyl or isoquinolinyl; R
4
, R
5
, R
6
and R
7
are each independently of the others hydrogen; C
1
-C
20
alkyl; C
3
-C
7
cycloalky; C
2
-C
20
alkenyl; C
4
-C
7
cycloalkenyl; C
2
-C
20
alkynyl; or C
4
-C
7
cycloalkynyl; and m and n are each independently of the other 0 or 1, for antimicrobial treatment of surfaces. The compounds exhibit a pronounced activity against pathogenic gram-positive and gram-negative bacteria, and also against yeasts and moulds. They are accordingly suitable for the antimicrobial treatment, especially preservation and disinfection, of surfaces.
描述了化合物的使用,其中化合物R1、R2和R3分别独立地是氢;C1-C20烷基;C3-C7环烷基;C2-C20烯基;C4-C7环烯基;C2-C20炔基,C4-C7环炔基;或未取代或C1-C5烷基,C3-C7环烷基,C1-C5烷氧基,C3-C7环烷氧基,卤素,酮基,羧基,羧基-C1-C7烷酯基,羧基-C3-C7环烷基酯基,氰基,三氟甲基,五氟乙基,氨基,N,N-单或二-C1-C20烷基氨基或硝基取代的苯基-C1-C5烷基,萘基-C1-C5烷基,苯基羰基-C1-C5烷基,萘基羰基-C1-C5烷基,吡咯基烷基,呋喃基烷基,噻吩基烷基,吡唑基烷基,咪唑基烷基,噁唑基烷基,噻唑基烷基,异噁唑基烷基,异噻唑基烷基,1,2,3-三唑基烷基,1,2,4-三唑基烷基,1,2,3-噁二唑基烷基,1,3,4-噁二唑基烷基,1,2,3-噻二唑基烷基,1,3,4-噻二唑基烷基,吲哚基烷基,吡啶基烷基,吡啶并咪唑基烷基,嘧啶基烷基,吡啶并嘧啶基烷基,喹啉基烷基,异喹啉基烷基,吡咯基,呋喃基,噻吩基,吡唑基,咪唑基,噁唑基,噻唑基,异噁唑基,异噻唑基,1,2,3-三唑基,1,2,4-三唑基,1,2,3-噁二唑基,1,3,4-噁二唑基,1,2,3-噻二唑基,1,3,4-噻二唑基,吲哚基,吡啶基,吡啶并咪唑基,嘧啶基,吡啶并嘧啶基,喹啉基,异喹啉基;R4、R5、R6和R7分别独立地是氢;C1-C20烷基;C3-C7环烷基;C2-C20烯基;C4-C7环烯基;C2-C20炔基;或C4-C7环炔基;m和n分别独立地是0或1,用于对抗菌处理表面。这些化合物对致病的革兰氏阳性和阴性细菌,以及酵母和霉菌表现出显著的活性。因此,它们适用于对表面进行抗菌处理,特别是保护和消毒。