Nitroimidazolyl pyrimidines
    1.
    发明授权
    Nitroimidazolyl pyrimidines 失效
    硝基咪唑基嘧啶

    公开(公告)号:US3966732A

    公开(公告)日:1976-06-29

    申请号:US568117

    申请日:1975-04-14

    CPC分类号: C07D409/14 C07D403/04

    摘要: Nitroimidazolyl pyrimidines of the formula ##SPC1##And physiologically acceptable acid addition salts thereon wherein X is alkyl of 1-4 carbon atoms, R.sub.1 and R.sub.2 each are a hydrogen atom, alkyl of 1-4 carbon atoms, phenyl triflouromethyl or a monocyclic heterocyclic ring and R.sub.3 is a hydrogen atoms, alkyl of 1-4 carbon atoms, hydroxyalkoxy of 2-4 carbon atoms or an ester thereof of an alkanocarboxylic acid of 1-4 carbon atoms, oxoalkyl of 8-6 carbon atoms, or, when R.sub.1 or R.sub.2 is phenyl, alkylene having 1-2 carbon atoms in the chain joined to the 2-position of the phenyl ring possess trichomonicidal activity.

    摘要翻译: 式的硝基咪唑基嘧啶及其生理学上可接受的酸的添加剂其中X是1-4个碳原子的烷基,R1和R2各自是氢原子,1-4个碳原子的烷基,苯基三氟乙基或单环杂环,R3是 1-4个碳原子的烷基,2-4个碳原子的羟基烷氧基或其1-4个碳原子的链烷酸的酯,8-6个碳原子的氧代烷基,或当R1或R2是苯基时 在与苯环的2-位连接的链中具有1-2个碳原子的亚烷基具有杀虫活性。

    Amino-, mercapto- and -oxy-substituted-phenyl and -phenalkyl imidazoles
    5.
    发明授权
    Amino-, mercapto- and -oxy-substituted-phenyl and -phenalkyl imidazoles 失效
    氨基,巯基和 - 氧基取代的苯基和 - 苯基烷基咪唑

    公开(公告)号:US4006243A

    公开(公告)日:1977-02-01

    申请号:US567361

    申请日:1975-04-11

    摘要: Compounds of the formula ##STR1## wherein Z is a direct bond or alkylene of 1 - 3 carbon atoms which is unsubstituted or substituted on the carbon atom alpha to the phenyl group by alkyl or unsubstituted or substituted phenyl, R.sub.2 and R.sub.3 singly are H, alkyl, alkoxy, alkylmercapto, halo, nitro or, collectively, C.sub.4 H.sub.4, and R.sub.4 is alkenyl, alkinyl, unsubstituted or substituted phenyl or phenylalkyl, or, when Z is substituted methylene, also alkyl, are useful in combating Germatophyte infections, especially Trichophyton rubrum and mentagrophytes, and yeast infections, especially Candida albicans, as well as bacterial and fungal infections.

    摘要翻译: 其中Z是直链键或1-3个碳原子的亚烷基,未被取代或被烷基或未取代或取代的苯基的苯基的α-碳原子取代,R2和R3单独为H, 烷基,烷氧基,烷基巯基,卤素,硝基,或者共同的C4H4和R4是烯基,炔基,未取代的或取代的苯基或苯基烷基,或当Z是取代亚甲基也是烷基时,可用于防治生殖癣菌感染,特别是红色毛癣菌 和营养元素,酵母感染,特别是白色念珠菌,以及细菌和真菌感染。

    4-Nitroperhydropyrido[1,2-a][1,4]diazepines
    7.
    发明授权
    4-Nitroperhydropyrido[1,2-a][1,4]diazepines 失效
    4-硝基哌啶氢化{8,1-a {9 {8 1,4 {9二氮杂

    公开(公告)号:US3965103A

    公开(公告)日:1976-06-22

    申请号:US507684

    申请日:1974-09-20

    IPC分类号: C07D471/04 C07D471/02

    CPC分类号: C07D471/04

    摘要: Compounds of the formula v,2/12Wherein R.sub.1 is H, lower-alkyl, hydroxyalkyl, phenyl, aralkyl, or --(CH.sub.2) .sub.n --X wherein n is 0-4 and X is --COO-lower-alkyl, C.tbd.N or --COOH and R.sub.2 is H, lower-alkyl or aralkyl, produced by condensing a diamine of the formula ##SPC1##With a nitro compound of the formula R.sub.1 --CH.sub.2 --NO.sub.2 in the presence of formalin or paraformaldehyde, or with the R.sub.1 -- C(CH.sub.2 OH).sub.2 NO.sub.2 reaction product of the above nitro compound and formalin or paraformaldehyde, or with formalin or paraformaldehyde followed by reaction with the above nitro compound, and their acid addition salts, possess antimicrobial activity against both gram-positive and gram-negative bacteria and also against dermatophytes, yeasts and other fungi.

    摘要翻译: 式v,2/12的化合物,其中R 1是H,低级烷基,羟基烷基,苯基,芳烷基或 - (CH 2)n X,其中n是0-4,X是-COO-低级烷基,C 3或N或 -COOH和R 2是H,低级烷基或芳烷基,其通过在甲醛或多聚甲醛的存在下将式II的二胺与式R 1 -CH 2 -NO 2的硝基化合物或与R 1 -C(CH 2 OH) 上述硝基化合物和福尔马林或多聚甲醛的2NO2反应产物,或与福尔马林或多聚甲醛反应,随后与上述硝基化合物及其酸加成盐反应,具有抗革兰氏阳性和革兰氏阴性菌以及皮肤真菌的抗微生物活性 ,酵母和其他真菌。