Imidazole-2-carbamates
    1.
    发明授权
    Imidazole-2-carbamates 失效
    咪唑-2-碳酸酯

    公开(公告)号:US4110463A

    公开(公告)日:1978-08-29

    申请号:US803016

    申请日:1977-06-03

    CPC分类号: C07C255/00 C07D233/48

    摘要: Compounds represented by the formula ##STR1## wherein R is hydrogen or alkyl of 1-4 carbons, R.sup.1 is alkyl of 1-6 carbons and the naphthyl group is attached to the imidazole ring at the 1 or 2 positions of the naphthyl ring and the pharmaceutically acceptable salts thereof are useful as centrally acting skeletal muscle relaxants.

    摘要翻译: 由式CHEM表示的咪唑-2-氨基甲酸酯,其中R是氢或1-4个碳的烷基,R 1是1-6个碳的烷基,萘基在咪唑环上连接1或2个 萘环的位置及其药学上可接受的盐。 这些化合物可用作中枢作用的骨骼肌松弛剂。 该化合物通过闭合式(CHEM)化合物来制备

    1-Lower alkyl-4,5-dihydro-5-phenyl-2-lower alkoxy
carbonylaminoimidazoles and substituted phenyl derivatives thereof
    2.
    发明授权
    1-Lower alkyl-4,5-dihydro-5-phenyl-2-lower alkoxy carbonylaminoimidazoles and substituted phenyl derivatives thereof 失效
    1-低级烷基-4,5-二氢-5-苯基-2-低级烷氧羰基氨基咪唑及其取代的苯基衍生物

    公开(公告)号:US4088771A

    公开(公告)日:1978-05-09

    申请号:US708651

    申请日:1976-07-26

    CPC分类号: C07D233/46 C07D233/48

    摘要: 1-Lower alkyl-4,5-dihydro-5-phenyl-2-lower alkoxycarbonylaminoimidazoles, and substituted phenyl derivatives thereof, and pharmaceutically acceptable salts thereof, and methods of preparing such compounds. In one method, the compounds can be prepared by treating the corresponding .beta.-lower alkylamino-.beta.-(phenyl or substituted phenyl)-ethylamine with the desired 1,3-bis (alkoxycarbonyl)-S-methylisothiourea or 1-alkoxycarbonyl-S-methylisothiourea. The compounds can also be prepared by treating the corresponding 1-lower alkyl-2-amino-4,5-dihydro-5-(phenyl or substituted phenyl)-imidazole with the desired dialkylcarbonate. The subject compounds are useful as psychotherapeutic agents in treating or palliating abnormal conditions, in mammals, which involve the central nervous system.

    摘要翻译: 1-低级烷基-4,5-二氢-5-苯基-2-低级烷氧基羰基氨基咪唑及其取代的苯基衍生物及其药学上可接受的盐,以及制备这些化合物的方法。 在一种方法中,化合物可以通过用所需的1,3-双(烷氧基羰基)-S-甲基异硫脲或1-烷氧基羰基-S-苯基酯处理相应的β-低级烷基氨基-β-(苯基或取代的苯基) 甲基异硫脲 化合物也可以通过用所需的二烷基碳酸酯处理相应的1-低级烷基-2-氨基-4,5-二氢-5-(苯基或取代的苯基) - 咪唑来制备。 本发明化合物在涉及中枢神经系统的哺乳动物中用作治疗或缓解异常状况的心理治疗剂。

    4-Phenyl-and 5-phenyl-1,4,5,6-tetrahydro-pyrimidine derivatives
    7.
    发明授权
    4-Phenyl-and 5-phenyl-1,4,5,6-tetrahydro-pyrimidine derivatives 失效
    4-苯基 - 和5-苯基-1,4,5,6-四氢 - 嘧啶衍生物

    公开(公告)号:US4322421A

    公开(公告)日:1982-03-30

    申请号:US211610

    申请日:1980-12-01

    摘要: Certain 1,4,5,6-tetrahydropyrimidine compounds which are substituted with an amino, amido or carbamate at the 2-position, with an optionally substituted phenyl at the 5-position or at the 4-position when there is no alkyl at the 1-position and optionally a lower alkyl at the 1-position when the phenyl is at the 5-position are useful as CNS agents and as antihypertensives.

    摘要翻译: 在2位被氨基,酰氨基或氨基甲酸酯取代的某些1,4,5,6-四氢嘧啶化合物与5位或4位上没有烷基的任选取代的苯基 当苯基在5位时,1-位和任选的1-位的低级烷基可用作CNS剂和作为抗高血压药。

    4-Phenyl-and 5-phenyl-1,4,5,6-tetrahydropyrimidine derivatives
    8.
    发明授权
    4-Phenyl-and 5-phenyl-1,4,5,6-tetrahydropyrimidine derivatives 失效
    4-苯基和5-苯基-1,4,5,6-四氢嘧啶衍生物

    公开(公告)号:US4261995A

    公开(公告)日:1981-04-14

    申请号:US71442

    申请日:1979-08-31

    CPC分类号: C07D239/14 C07D239/16

    摘要: Certain 1,4,5,6-tetrahydropyrimidine compounds which are substituted with an amino, amido or carbamate at the 2-position, with an optionally substituted phenyl at the 5-position or at the 4-position when there is no alkyl at the 1-position and optionally a lower alkyl at the 1-position when the phenyl is at the 5-position are useful as CNS agents and as antihypertensives.

    摘要翻译: 在2位被氨基,酰氨基或氨基甲酸酯取代的某些1,4,5,6-四氢嘧啶化合物与5位或4位上没有烷基的任选取代的苯基 当苯基在5位时,1-位和任选的1-位的低级烷基可用作CNS剂和作为抗高血压药。