PROCESS FOR PREPARING IMIDAZOLIDINE DERIVATIVES

    公开(公告)号:KR820002388B1

    公开(公告)日:1982-12-29

    申请号:KR820004632

    申请日:1982-10-14

    Abstract: The imidazolidines I(R=Cl, CF3; R1=H,F, Cl; R2=H, Cl; Z=O, NH) were prepd. for use as schistosomicides and antiandrogenic substances (test data tabulated). Thus, 3,4-(F3C)CLC6H3NCO reacted with Me2CH(NH2)CN at 100≦̸C to give I(R = CF5, R1 = Cl, R2 = H, Z = NH), which was hydrolyzed to give I(Z = O)

    PROCESS FOR PREPARING IMIDAZOLIDINE DERIVATIVES

    公开(公告)号:KR820002387B1

    公开(公告)日:1982-12-29

    申请号:KR820004633

    申请日:1982-10-14

    Abstract: Title compds. (I; R=II, III, IV, V, VI), useful as an schistosomicide and antiandrogenic substance were prepd. by hydrolyzing Ia. Thus, 61 mg 1-(3-trifluoromethy1-4-chloro-pheny1)-5-imino-4, 4-dimethy1-2-imidazolidinone was dissolved in 4 ml 0.1N HCl, added 2ml H2O and filtrated after 20 hr to give 3-(3-trifluoromethy1-4-chloropheny1)-5,5-dimethylhydantoin(m.p. 156-157.5oC).

    PROCESS FOR PREPARING IMIDAZOLIDINE DERIVATIVES

    公开(公告)号:KR820002386B1

    公开(公告)日:1982-12-29

    申请号:KR780003228

    申请日:1978-10-27

    Abstract: The imidazolidines I(R=Cl, CF3; R1=H,F, Cl; R2=H, Cl; Z=O, NH) were prepd. for use as schistosomicides and antiandrogenic substances. Thus, 3, 4-(F3C)ClC6H3NCO reacted with Me2CHCH(NH2)CN at 100≦̸ to give I(R=CF5, R1=Cl, R2=H, z= NH), which washydrolyzed to I(Z=O).

    9.
    发明专利
    未知

    公开(公告)号:BR8103216A

    公开(公告)日:1982-02-16

    申请号:BR8103216

    申请日:1981-05-22

    Abstract: 2-Nitroimidazoles having filaricidal activity of the formula I wherein A is one of the groups -C(R3)=C(R1)(R2),-CHBr-CH2Br or -CH2-CCl=CH2; n is 1, 2, 3 or 4; R1 and R2 are hydrogen or C1-3-alkyl and R3 is hydrogen, C1-3-alkyl, chlorine or bromine, and processes for their preparation are described. The compounds of formula I and compounds of formula VII wherein R4 is -CH2-CH2OH, -CH2-CHOH-CH2OCH3, -CH2-CHOH-CH2OH or are useful in the treatment of filariasis is also described.

Patent Agency Ranking