发明名称 METHOD OF OBTAINING NOVEL DERIVATIVES OF 3-/2-HYDROXY-4-/SUBSTITUTED/PHENYL/CYCLOALKANONES
摘要 <p>Compounds are disclosed having the formula <CHEM> R1 is hydrogen, benzyl or an ester moiety; Y is -CH(R2 sec )CH(R2)- or -CH(R3)CH2-; R2 sec is hydrogen or methyl; R2 is OH or X-substituted (C1-6)alkyl; R3 is OH, cyano or X-substituted (C1-3)alkyl; X is -OR6, -SR6, -S(O)R6, -S(O)2R6, -NR6R7, -COOR7, -CONR7R8 or oxo; with the proviso that when X is -NR6R7, -COOR7 or -CONR7R8, said group is located on the terminal carbon atom of R2 or R3; R6 is hydrogen, (C1-6)alkyl or acetyl, with the provisos that, when R6 in -NR6R7 is acetyl, R7 is hydrogen, and R6 in S(O)R6 and S(O)2R6 cannot be acetyl; each of R7 and R8 is hydrogen or (C1-6)alkyl; s is an integer of 1 or 2; and Z-W is alkyl or oxaalkyl having 5 to 13 carbon atoms, or phenyl- or pyridyl-alkyl or -oxaalkyl having 3 to 8 carbon atoms in the alkyl or oxaalkyl group. Pharmaceutical compositions of such compounds, other than those in which <CHEM> is mandeloyl or R1 is benzyl, are useful as analgesic or CNS agents and as anti-emetic agents.</p>
申请公布号 PL137360(B1) 申请公布日期 1986.05.31
申请号 PL19810238378 申请日期 1981.09.14
申请人 发明人
分类号 A61K31/085;A61K31/05;A61K31/11;A61K31/13;A61K31/135;A61K31/16;A61K31/165;A61K31/19;A61K31/215;A61K31/275;A61K31/335;A61K31/66;A61P1/08;A61P25/04;A61P29/00;C07C27/00;C07C33/38;C07C35/21;C07C39/17;C07C39/23;C07C39/42;C07C43/20;C07C43/21;C07C45/00;C07C45/44;C07C45/51;C07C45/59;C07C45/60;C07C45/64;C07C45/67;C07C45/69;C07C47/27;C07C47/277;C07C47/46;C07C47/47;C07C49/245;C07C49/255;C07C49/747;C07C49/753;C07C49/757;C07C59/54;C07C59/72;C07C67/00;C07C69/732;C07C69/734;C07C213/00;C07C215/64;C07C217/74;C07C219/26;C07C223/04;C07C231/00;C07C233/18;C07C235/34;C07C235/40;C07C253/00;C07C255/45;C07C255/46;C07D209/48;C07D213/30;C07D303/32;(IPC1-7):C07C49/487;C07C49/517 主分类号 A61K31/085
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