PROGESS FOR PREPARATION OG 2-CARBALKOXY-AMINO BENZ IMIDAZOLE-5(6)-PHENYL ATHERS

    公开(公告)号:KR790000003B1

    公开(公告)日:1979-02-26

    申请号:KR740002736

    申请日:1974-06-13

    Applicant: HOECHST AG

    Abstract: Approx. 40 2-(Alkoxycarbonylamino) benzimidazole-5(6)-ylphenylethers(I ; R1 = C1-4 alkyl. R2,R3 = same or different H, OH, C1-4 alkoxy, halogen, trifluoromethyl, C1-4 alkyl, or C1-4 ! alkoxy contg. carboalkoxy. R4 = H or Cl atom.X = O or S), as anthelmintics, were prepd.via refluxing 3,4-diamino-diphenyl-ether with bis-methylthio-methylene-aminomethyl-formate in THF. These anthelmintics are specially effective for strongylides.

    PROCESS FOR PREPARING 2-CARBOALKOXY AMINO-5(6)-PHENYL SULFONYLOXY BENZIMIDAZOLES

    公开(公告)号:KR790001340B1

    公开(公告)日:1979-09-27

    申请号:KR750000704

    申请日:1975-04-04

    Applicant: HOECHST AG

    Abstract: Title compds (I; R1 = C1,-C4 alkyl, R2,R3 = H, OH, C1-C4 alkoxy, halogen, etc.) useful as anthelmintic, were prepd. by condensating O-phenylenediamine (II) (a) with alkyl-s-methylthiourea carboxylate(III) at pH 2-5, or (b) with NCNHCOOR1 at pH2-5, or treating II (c) with R1 CO2NCCl2 at-10-40≦̸C in the presence of base, (d) with bis-aryl (or alkyl)-thiomethylene-amino- formates (VI; R4 and/or R5 = C1-C4 alkyl, C3-C5 alkenyl, cycloalkyl, etc.).

    PROCESS FOR 2-CARBALKOXY-AMINO-BENZIMIDAZOLE-5(6)-PHENYL ETHER

    公开(公告)号:KR790000162B1

    公开(公告)日:1979-03-24

    申请号:KR740002797

    申请日:1974-06-17

    Applicant: HOECHST AG

    Abstract: Approx. 40 anthelmintics (I; R1 = alkyl, Ph, R2 and R3 = H, OH, alkoxy, halogen, trifluoromethyl, alkyl, R4 = H, Cl, X = O,S) were prepd. by refluxing 2-amino-benzimidazole with R1O-CO-OR5 (R1 and R3 = alkyl, Ph) in THF. Thus, 5-phenoxy-benzimidazole-2-methylcarbamate was prepd. by reaction of 41.5g 2-amino-5-phenoxy-benzimidazole with 16.5g CH3ONa and 22.5g CO(OCH3)2 in 300ml THF and neutralized with HCl.

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