Novel piperidyl-indoles of the formula ##STR1## wherein X is selected from the group consisting of fluorine, chlorine and bromine when Y and Z are hydrogen or together form a double bond and X is selected from the group consisting of hydrogen and alkoxy of 1 to 3 carbon atoms when Y and Z form a double bond and their non-toxic, pharmaceutically acceptable acid addition salts having antidepressant, antiemetic and antiparkinsonian activity and their preparations and novel intermediates therefore.
                            该专利描述了一种新型
哌啶基吲哚类化合物,其
化学式为##STR1##其中,当Y和Z为氢或结合形成双键时,X选自
氟、
氯和
溴的群体中;当Y和Z形成双键时,X选自1至3个碳原子的烷氧基和氢的群体中。该化合物及其无毒、药学上可接受的酸盐具有抗抑郁、抗恶心和抗帕
金森症活性,以及其制剂和新型中间体。