Pyrazolo [1,2-a][1,2,4] benzotriazines
    31.
    发明授权
    Pyrazolo [1,2-a][1,2,4] benzotriazines 失效
    吡唑并[1,2-a] [1,2,4]苯并三嗪

    公开(公告)号:US4260751A

    公开(公告)日:1981-04-07

    申请号:US144482

    申请日:1980-04-28

    Applicant: Uwe D. Treuner

    Inventor: Uwe D. Treuner

    CPC classification number: C07D487/04

    Abstract: Pyrazolo[1,2-a][1,2,4] benzotriazines having the formula ##STR1## wherein R.sub.1 is hydrogen, lower alkyl, nitro, amino, lower alkylamino, di(lower alkyl)amino, --SR.sub.4, --OR.sub.4 or halogen;R.sub.2 is hydrogen, lower alkyl or aralkyl;R.sub.3 is hydrogen, lower alkyl or a salt forming ion;R.sub.4 is hydrogen or lower alkyl; and Y is oxygen or sulfur.The compounds are useful as intermediates and as antiinflammatory agents.

    Abstract translation: 其中R 1为氢,低级烷基,硝基,氨基,低级烷基氨基,二(低级烷基)氨基,-SR 4,-OR 4或 - 或具有下式的吡唑并〔1,2-a〕〔1,2,4〕苯并三嗪 卤素; R2是氢,低级烷基或芳烷基; R3是氢,低级烷基或形成盐的离子; R4是氢或低级烷基; Y是氧或硫。 该化合物可用作中间体和抗炎剂。

    7.beta.-[[[2-Acylamino]-1,2-dioxoethyl]amino]acyl cephalosporins
    32.
    发明授权
    7.beta.-[[[2-Acylamino]-1,2-dioxoethyl]amino]acyl cephalosporins 失效
    7B - ((((2-氨基亚氨基)-1,2-二氧代乙基)氨基)乙酰氯化物

    公开(公告)号:US4169947A

    公开(公告)日:1979-10-02

    申请号:US910548

    申请日:1978-05-30

    CPC classification number: C07D307/68

    Abstract: 7.beta.-[[[2-Acylamino]-1,2-dioxoethyl]amino]acyl cephalosporins of the formula ##STR1## wherein R is hydrogen, lower alkyl, phenyl-lower alkyl, diphenyl-lower alkyl, tri(lower alkyl)silyl, trihaloethyl or a salt forming ion; R.sub.1 is hydrogen, lower alkyl, saturated or unsaturated cycloalkyl, phenyl, phenyl-lower alkyl, substituted phenyl or certain heterocyclic groups; R.sub.2 is hydrogen or methoxy; R.sub.3 is hydrogen, lower alkyl or phenyl-lower alkyl; R.sub.4 is lower alkyl, cycloalkyl, phenyl, substituted phenyl or certain heterocyclic groups; and X is hydrogen, lower alkanoyloxy, carbamoyloxy, lower alkoxy, lower alkylthio, ##STR2## or certain heterothio groups, are useful as antibacterial agents.

    6-[[[(2-Cyanomethyl)amino]-1,2-dioxoethyl]-amino]acyl penicillins
    33.
    发明授权
    6-[[[(2-Cyanomethyl)amino]-1,2-dioxoethyl]-amino]acyl penicillins 失效
    6- {8 {8(8-氰基甲基)氨基{9-1,2-二氧代乙基{9-氨基{9酰基青霉素

    公开(公告)号:US4168266A

    公开(公告)日:1979-09-18

    申请号:US910546

    申请日:1978-05-30

    CPC classification number: C07C255/00 C07D333/24 C07D499/00

    Abstract: 6-[[[(2-Cyanomethyl)amino]-1,2-dioxoethyl]amino]acyl pencillins which have the formula ##STR1## wherein R is hydrogen, lower alkyl, tri(lower alkyl)silyl, tri(lower alkyl)stannyl, trihaloethyl or a salt forming ion; R.sub.1 is hydrogen, lower alkyl, saturated or unsaturated cycloalkyl, phenyl, phenyl-lower alkyl, substituted phenyl or certain heterocyclic groups; R.sub.2 is hydrogen or methoxy; R.sub.3 is hydrogen, lower alkyl, phenyl-lower alkyl or cycloalkyl; and R.sub.4 and R.sub.5 each is hydrogen or lower alkyl, are useful as antibacterial agents.

    Abstract translation: 具有式“IMAGE”的6 - [[(2-氰基甲基)氨基] -1,2-二氧代乙基]氨基]酰基青霉素,其中R是氢,低级烷基,三(低级烷基)甲硅烷基,三(低级烷基) 甲锡烷基,三卤代乙基或成盐离子; R 1是氢,低级烷基,饱和或不饱和环烷基,苯基,苯基 - 低级烷基,取代的苯基或某些杂环基; R2是氢或甲氧基; R3是氢,低级烷基,苯基 - 低级烷基或环烷基; 并且R 4和R 5各自为氢或低级烷基,可用作抗菌剂。

    Carboxyalkylureido cephalosporins
    35.
    发明授权
    Carboxyalkylureido cephalosporins 失效
    羧甲基脲基头孢菌素

    公开(公告)号:US4097670A

    公开(公告)日:1978-06-27

    申请号:US673222

    申请日:1976-04-05

    CPC classification number: C07C265/00 C07D333/24

    Abstract: Carboxyalkylureido cephalosporins of the formula ##STR1## wherein R is hydrogen, lower alkyl, phenyl-lower alkyl, diphenyl-lower alkyl, tri(lower alkyl)silyl, trihaloethyl, a salt forming ion, or the group ##STR2## R.sub.1 is hydrogen or methoxy; A is straight or branched chain alkylene of 1 to 6 carbons; R.sub.2 is hydrogen, lower alkyl, phenyl, phenyl-lower alkyl, diphenyl-lower alkyl, alkali metal ion or alkaline earth metal ion; R.sub.3 is hydrogen or lower alkyl; R.sub.4 is hydrogen, lower alkyl, cycloalkyl, cycloalkenyl, cycloalkadienyl, phenyl, phenyl-lower alkyl, substituted phenyl, substituted phenyl-lower alkyl, or certain heterocyclic groups; R.sub.5 is hydrogen or lower alkyl; R.sub.6 is lower alkyl; and X is hydrogen, lower alkanoyloxy, ##STR3## or certain heterothio groups; are disclosed. These compounds are useful as antibacterial agents.

    Abstract translation: 其中R为氢,低级烷基,苯基 - 低级烷基,二苯基 - 低级烷基,三(低级烷基)甲硅烷基,三卤代乙基,成盐离子或基团R 1的羧基烷基脲基头孢菌素为其中R为氢, 甲氧基 A是1至6个碳的直链或支链亚烷基; R2是氢,低级烷基,苯基,苯基 - 低级烷基,二苯基 - 低级烷基,碱金属离子或碱土金属离子; R3是氢或低级烷基; R4是氢,低级烷基,环烷基,环烯基,环链二烯基,苯基,苯基 - 低级烷基,取代的苯基,取代的苯基 - 低级烷基或某些杂环基; R5是氢或低级烷基; R6是低级烷基; X是氢,低级烷酰氧基,或者某些杂硫基; 被披露。 这些化合物可用作抗菌剂。

    (Carbamoyl)pyridino derivatives of ureidocephalosporins
    38.
    发明授权
    (Carbamoyl)pyridino derivatives of ureidocephalosporins 失效
    (氨基甲酰基)吡啶衍生物脲基头孢菌素

    公开(公告)号:US4024135A

    公开(公告)日:1977-05-17

    申请号:US664335

    申请日:1976-03-05

    CPC classification number: C07D333/24

    Abstract: Ureido cephalosporin derivatives of the formula ##STR1## wherein R.sub.1 is hydrogen or methoxy; R.sub.2 is hydrogen or lower alkyl; R.sub.3 is hydrogen, lower alkyl, cycloalkyl, cycloalkenyl, cycloalkadienyl, phenyl, phenyl-lower alkyl, substituted phenyl, substituted phenyl-lower alkyl; or certain heterocyclic groups; are disclosed. These compounds are useful as antibacterial agents.

    Abstract translation: 其中R1是氢或甲氧基的式(Ⅰ)所示的脲基头孢菌素衍生物; R2是氢或低级烷基; R3是氢,低级烷基,环烷基,环烯基,环链二烯基,苯基,苯基 - 低级烷基,取代的苯基,取代的苯基 - 低级烷基; 或某些杂环基团; 被披露。 这些化合物可用作抗菌剂。

    3-Heterothio derivatives of (.alpha.-thiocarbonylamino) cephalosporins
    39.
    发明授权
    3-Heterothio derivatives of (.alpha.-thiocarbonylamino) cephalosporins 失效
    ({ - 硫代羰基氨基)头孢菌素的3-异硫脲衍生物

    公开(公告)号:US3996219A

    公开(公告)日:1976-12-07

    申请号:US581446

    申请日:1975-05-28

    CPC classification number: C07D333/24

    Abstract: 3-Heterothio(.alpha.-thiocarbonylamino)cephalosporin derivatives of the general formula ##STR1## wherein R is hydrogen, lower alkyl, phenyl-lower alkyl, tri(lower alkyl)silyl, trihaloethyl, a salt forming ion or the group ##STR2## R.sub.1 is hydrogen, lower alkyl, cyclo-lower alkyl, unsaturated cyclo-lower alkyl, phenyl, substituted phenyl or thienyl; R.sub.2 and R.sub.5 each is hydrogen or lower alkyl; R.sub.3 is a five or six membered nitrogen, sulfur and/or oxygen containing ring system; and R.sub.4 is lower alkyl, phenyl or phenyl-lower alkyl; are useful as antibacterial agents.

    Abstract translation: 其中R为氢,低级烷基,苯基 - 低级烷基,三(低级烷基)甲硅烷基,三卤代乙基,形成成盐离子或基团的3-异硫代(α-硫代羰基氨基)头孢菌素衍生物 是氢,低级烷基,环低级烷基,不饱和环 - 低级烷基,苯基,取代的苯基或噻吩基; R2和R5各自为氢或低级烷基; R3是五或六元氮,硫和/或含氧环系; 和R4是低级烷基,苯基或苯基 - 低级烷基; 作为抗菌剂是有用的。

    4-Amino derivatives of pyrozolo[1,5-a]quinoxaline-3-carboxylic acid and
esters
    40.
    发明授权
    4-Amino derivatives of pyrozolo[1,5-a]quinoxaline-3-carboxylic acid and esters 失效
    吡咯并[8,1,5-a {9喹喔啉-3-羧酸和酯的4-氨基衍生物

    公开(公告)号:US3994893A

    公开(公告)日:1976-11-30

    申请号:US628277

    申请日:1975-11-03

    Applicant: Uwe D. Treuner

    Inventor: Uwe D. Treuner

    CPC classification number: C07D487/04 C07D231/14

    Abstract: New 4-amino derivatives of pyrazolo[1,5-a]quinoxaline-3-carboxylic acid, esters and their salts have the formula ##SPC1##R.sub.1 is hydrogen, lower alkyl or a salt forming ion;R.sub.2 and R.sub.3 each is hydrogen, lower alkyl, cyclolower alkyl, phenyl, substituted phenyl, phenyl-lower alkylene, di-lower alkylamino-lower alkylene or R.sub.2 and R.sub.3 together with the nitrogen form an unsubstituted or substituted 5- or 6-membered nitrogen heterocyclic in which an additional nitrogen or oxygen may be present.R.sub.4 is hydrogen, lower alkyl or halogen.The new compounds are useful as anti-inflammatory agents.

    Abstract translation: 吡唑并[1,5-a]喹喔啉-3-羧酸的新4-氨基衍生物,酯及其盐具有式+ q,10 R1是氢,低级烷基或形成盐的离子; R 2和R 3各自为氢,低级烷基,环己烷基,苯基,取代的苯基,苯基 - 低级亚烷基,二低级烷基氨基 - 低级亚烷基或R 2和R 3与氮一起形成未取代或取代的5-或6-元氮 可以存在另外的氮或氧的杂环。

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