Substituted pyrazolo{8 3,4-e{9 {8 1,4{9 thiazepines and isoxazolo{8 5,4-e{9 {8 1,4{9 thiazepines
    7.
    发明授权
    Substituted pyrazolo{8 3,4-e{9 {8 1,4{9 thiazepines and isoxazolo{8 5,4-e{9 {8 1,4{9 thiazepines 失效
    取代的吡唑并[8,3-e {9 {8 1,4 {9]硫杂杂环和异恶唑并[8,5,4-e {9 {

    公开(公告)号:US3891630A

    公开(公告)日:1975-06-24

    申请号:US44808674

    申请日:1974-03-04

    Applicant: ABBOTT LAB

    Inventor: SWETT LEO RALPH

    CPC classification number: C07D471/04 C07D513/04

    Abstract: 1-H Pyrazolo(3,4-e)(1,4)thiazepin-7(8H)-ones which may be substituted in the 1, 3, 4, 6 and 8-position, and the corresponding isoxazolo(5,4-e)(1,4)thiazepin-7(8H)-ones which may be substituted in the 3, 4, 6 and/or 8-position are prepared by converting 5-aminopyrazole which may be substituted in the 1and/or 3-positions or a 5-aminoisoxazole which may be substituted in the 3-position into 4-arylidene or alkylidine-5-imino derivatives and subsequent condensation with thioglycolic acid or a substituted thioglycolic acid. The new compounds are useful anti-inflammatories.

    Abstract translation: 可以在1,3,4,6和8位取代的1-H吡唑并[3,4-e] [1,4]硫氮杂-7(8H) - 酮和相应的异恶唑并[5,4 可以在3,4,6和/或8位上被取代的-e] [1,4]硫氮杂-7(8H) - 酮,其可通过将5-氨基吡唑转化成1-和/ 或3-位或5-氨基异恶唑,其可以在3-位被取代成4-亚芳基或亚烷基-5-亚氨基衍生物,随后与巯基乙酸或取代的巯基乙酸缩合。 新化合物是有用的抗炎药。

    Pyrazolothiazepines and isoxazolothiazepines
    8.
    发明授权
    Pyrazolothiazepines and isoxazolothiazepines 失效
    吡咯并嘧啶和异佛尔泽菌素

    公开(公告)号:US3669983A

    公开(公告)日:1972-06-13

    申请号:US3669983D

    申请日:1970-08-20

    Applicant: ABBOTT LAB

    CPC classification number: C07D231/38

    Abstract: 7,8-Dihydro-4-oxopyrazolo(3,4-d) (1,3)thiazepines which may be substituted in the 1-, 3-, 5-, 7- and/or 8- position and the corresponding isoxazolo(5,4-d) (1,3)thiazepines which may be substituted in the 3-, 5-, 7- and/or 8- position are prepared by converting a 5-aminopyrazole which may be substituted in the 1and/or 3-positions or a 5-aminoisoxazole which may be substituted in the 3-position into a Schiff base and subsequent condensation of the Schiff base with thioglycolic acid or a substituted thioglycolic acid. The new compounds are useful antiinflammatories.

    Abstract translation: 可以在1-,3-,5-,7-和/或8-位置被取代的7,8-二氢-4-氧代吡唑并[3,4-d] [1,3]噻吩并与相应的异恶唑并[ 可以在3-,5-,7-和/或8-位置被取代的5,4-d] [1,3]硫杂吗啉是通过将可被取代的5-氨基吡唑转化成1-和/ 或3-位或5-氨基异恶唑,其可以在3-位被取代成席夫碱,随后将席夫碱与巯基乙酸或取代的巯基乙酸缩合。 新化合物是有用的抗炎药。

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