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  • 1 - Piperidinyl) Methyl-2 - (4-Substituted Styryl) - 5-Chloro-Benzimidazole Derivatives: Synthesis and Analgesic Activity

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    1. The authors synthesized derivatives of 1-(1-piperidinyl)methyl-2-(4-substituted styryl)-5-chlorobenzimidazole and tested their analgesic activity. 2. 2-Methyl-5-chlorobenzimidazole was used as a starting material to synthesize 2-(p-substituted styryl)-5-chlorobenzimidazoles, which were then reacted with formaldehyde and piperidine to obtain the final compounds. 3. Compounds 3c and 3g showed higher analgesic activity than aspirin in modified Koster tests, while 3a, 3b, and 3e showed lower activity and 3

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    1-(1-Piperidinyl)Methyl-2-(4-Substituted Styryl)-5-Chlorobenzimidazole Derivatives - Synthesis and Analgesic Activity - J Pharm Pharmacol Sep 1998, 50(S9), 231

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    1. The authors synthesized derivatives of 1-(1-piperidinyl)methyl-2-(4-substituted styryl)-5-chlorobenzimidazole and tested their analgesic activity. 2. 2-Methyl-5-chlorobenzimidazole was used as a starting material to synthesize 2-(p-substituted styryl)-5-chlorobenzimidazoles, which were then reacted with formaldehyde and piperidine to obtain the final compounds. 3. Compounds 3c and 3g showed higher analgesic activity than aspirin in modified Koster tests, while 3a, 3b, and 3e showed lower activity and 3

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    182 vizualizări1 pagină

    1 - Piperidinyl) Methyl-2 - (4-Substituted Styryl) - 5-Chloro-Benzimidazole Derivatives: Synthesis and Analgesic Activity

    Încărcat de

    muopioidreceptor
    1. The authors synthesized derivatives of 1-(1-piperidinyl)methyl-2-(4-substituted styryl)-5-chlorobenzimidazole and tested their analgesic activity. 2. 2-Methyl-5-chlorobenzimidazole was used as a starting material to synthesize 2-(p-substituted styryl)-5-chlorobenzimidazoles, which were then reacted with formaldehyde and piperidine to obtain the final compounds. 3. Compounds 3c and 3g showed higher analgesic activity than aspirin in modified Koster tests, while 3a, 3b, and 3e showed lower activity and 3

    Drepturi de autor:

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    din 1

    J. Pharm. Pharmacol.

    1998, 50 (Supplement): 231

    1998 J. Pharm. Pharmacol.

    1-( 1-Piperidinyl)methyl-2-(4-substituted styryl)-5-chlorobenzimidazole derivatives: synthesis and analgesic activity


    A. U L V I TOSUN, B I L G E CAKIR AND M . FETHI $AHIN

    Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Gazi University, Ankara, Turkey

    Benzimidazoles bearing 0- or p-substituted phenyl moiety at position 2 have a wide spectrum of biological activity such as anthelmintic, antifungal, antituberculous and anti-inflammatory activity (Dandegaonker & Daulatabad 1967, Vishnevskii 1988, Fuveau 1972). It is well known that alkylaminoalkyl groups at position 1 of 2benzylbentimidazoles confer analgesic activity to these derivatives (Hunger et al 1960). Therefore, we have synthesized 1-(I -piperidinyl) methyl-2-(4-substituted styryl)-5-chlorobenziniidazole derivatives and investigated analgesic activity. 2-Metliyl-5-chlorobenzimidazole ( I ) has been prepared as a starting material by refluxing 4chloro-o-phenylenediaminewith glacial acetic acid in hydrochloric acid for 6 hours according to the Phillips method (Isikdag et a1 1989). 2-(p-Substituted st)~y1)-5-~lilorobenzimidazoles (?a-g) have been obtained by refluxing 2-methyl-5chlorobeiizimidazole with p-subst ituted at-) laldehydes in acetic anhydride for 30 hours (Sullivan 1970, Uzunoglu et al 1997). l-substituted-2-(p-substituted styryl)-5Seven ch lorobenzimidazole derivatives (3a-g) have been

    Synthesis of the final compounds has been carried out for the first time in this study. Compounds 3a, 3b and 3e exhibit lower analgesic activity than that of aspirin (40.8 % activity), compounds 3d and 3f are nearly as potent as the standard, compounds 3c (78.1 % activity) and 3g (77.5 YO activity) showed higher analgesic activity than that of aspirin [modified KOSTER test (Gyires & Toma)]. The results of analgesic activity studies will be presented in detail.

    References Dandegaonker,S.H., Daulatabad,C.D. ( 1967) Bromchlor benzimidazole. Monatsh. Chem. 98:1873-7 Fuveau.S.A. (March 03 1972) (Fluorophenyl)benzimidazoles with anti-inflammatory and analgesic activities. Fr.Demande Appl. 2,092.618 (CI. A 61k, C 07d). Chem. Abaracts 77: 1 18208s.( 1 972) Gjires. K..T o m a Z. (1984)The use of writhing test in mice for screening different types of analgesics. Arch. Int. Phamiacodyn. 267: I3 1-40. Hunger.A.. Kebr1e.J.. Rossi,A., Hoffmann,K. (1960) Benzimidazole-derivate, synthese von I-aminoalkyl-2benzyl-benzimidazolen. Helv. Chim. Ada 43:800-5 Isilidag.1.. Ucucu.U., Demirayak,S., Cakir,B. (1989) Benziniidazole derivatives: Synthesis, antibacterial activity and QSAR's of some 2-alky1-5-chlorobenzimidazoles. Guede- J. Fac. Pharm. Gazi 6:31-6 Sul1ivan.W.R. (1970)New benzimidazoles. J. Med. Chem. 13:

    784-6
    Uzunoglu.S., Cakir,B., Tosun,A., SahinJ4.F. (1 997) Synthesis and antimicrobial activities of 2-(p-substituted styryI)-5(6)chlorobenzimidazoles. 1. Fac. Pharm. Hacetlepe 17:47-54 \'ishnevskii,B.I. (1987)Potentiating specific activity of isoniazid and streptomycin by benzimidazole derivatives. Probl. Tuberk. 2:58.Chem. Abstracts 108:48752x,(1988).

    synthesized by the reaction of 2-(p-substituted styryl)-5-chlorobenzimidazoles with formaldehyde and piperidine in methanol.

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