N-(amino)alkyl)-1-pyrrolidine, 1-piperidine and
1-homopiperidinecarboxamides (and thiocarboxamides) with sulfur linked
substitution in the 2, 3 or 4-positions
    21.
    发明授权
    N-(amino)alkyl)-1-pyrrolidine, 1-piperidine and 1-homopiperidinecarboxamides (and thiocarboxamides) with sulfur linked substitution in the 2, 3 or 4-positions 失效
    N-(氨基)烷基)-1-吡咯烷,1-哌啶和1-高哌啶甲酰胺(和硫代羧酰胺),其在2,3或4位具有硫连接取代

    公开(公告)号:US4642348A

    公开(公告)日:1987-02-10

    申请号:US750180

    申请日:1985-07-01

    摘要: Novel pyrrolidine, piperidine and homopiperidinecarboxamide and thiocarboxamide compounds having the formula: ##STR1## wherein X is --S--, --S(O)-- or --S(O).sub.2 --; A is a loweralkalene chain and A.sup.1 and A.sup.2 are alkalene chains when p and d are one; R, R.sup.1 and R.sup.2 are hydrogen, loweralkyl, phenyl cycloalkyl or phenylalkyl and R.sup.1 and R.sup.2 may form a heterocyclic residue with the adjacent nitrogen atom; Q is a selected aromatic radical, and the pharmaceutically acceptable acid addition salts useful as cardiac antiarrhythmia agents are disclosed.Novel chemical intermediates, unsubstituted on pyrrolidine, piperidine and homopiperidine nitrogen but with --(A.sup.2).sub.p --X--(A.sup.2).sub.d --Q side chain are also disclosed.

    摘要翻译: 具有下式的新型吡咯烷,哌啶和高哌啶甲酰胺和硫代甲酰胺化合物:其中X是-S - , - S(O) - 或-S(O)2 - ; A是下亚烯烃链,当p和d为1时,A 1和A 2为碱金属链; R,R 1和R 2是氢,低级烷基,苯基环烷基或苯基烷基,R 1和R 2可以与相邻的氮原子形成杂环残基; Q是选择的芳族基团,并且公开了可用作心脏抗心律失常药物的药学上可接受的酸加成盐。 还公开了在吡咯烷,哌啶和高哌啶氮上未取代的新型化学中间体,但具有 - (A2)p -X-(A2)d-Q侧链。