Bochis R J, Dybas R A, Eskola P, Kulsa P, Linn B O, Lusi A, Meitzner E P, Milkowski J, Mrozik H, Olen L E, Peterson L H, Tolman R L, Wagner A F, Waksmunski F S, Egerton J R, Ostlind D A
J Med Chem. 1978 Feb;21(2):235-7. doi: 10.1021/jm00200a020.
A series of methyl imidazo-[11,2-a]pyridine-2-carbamates was synthesized for anthelmintic testing. The preparation of this class of compounds was simplified by utilization of a novel one-step condensation of the appropriately substituted 2-aminopyridine and methyl chloroacetylcarbamate. The most potent compound, methyl 6-(phenylsulfinyl)-imidazo[1,2-a]pyridine-2-carbamate, was orally effective against a broad range of helminths in sheep and cattle, at a dosage of 2.5 mg/kg. Limited trials in swine and dogs demonstrated anthelmintic activity at higher dosages. Limited observations in sheep and cattle indicated that, in both species, a single oral dose of 200 mg/kg was well tolerated.
合成了一系列甲基咪唑并-[1,2-a]吡啶-2-氨基甲酸酯用于驱虫测试。通过利用适当取代的2-氨基吡啶与甲基氯乙酰氨基甲酸酯的新型一步缩合反应,简化了这类化合物的制备。最有效的化合物,6-(苯基亚磺酰基)-咪唑并[1,2-a]吡啶-2-氨基甲酸甲酯,以2.5mg/kg的剂量对绵羊和牛体内的多种蠕虫具有口服活性。在猪和狗身上进行的有限试验表明,在较高剂量下具有驱虫活性。在绵羊和牛身上的有限观察表明,在这两个物种中,单次口服200mg/kg的剂量耐受性良好。