magnified imageA series of 3‐substituted phenoxy‐6‐((substituted)1H‐pyrazol‐1‐yl) pyridazines were synthesized from the condensation of various phenols and 3‐chloro‐6‐(1H‐pyrazol‐1‐yl) pyridazine 2 or 3‐chloro‐6‐(5′‐methyl‐4‐ethoxycarbonyl‐1H‐pyrazol‐1‐yl) pyridazine 6 in N,N‐dimethylformamide (DMF) at 120°C with K2CO3 as an acid receptor. The intermediates 2 or 6 were obtained from the cyclization of 3‐chloro‐6‐hydrazinyl pyridazine 1 with 3‐dimethylamino‐acrylaldehyde or ethyl 2‐((dimethylamino) methylene)‐3‐oxobutanoate in n‐butanol under reflux, respectively, and side products 3 or 7 were also generated. All of the title compounds were confirmed by 1H NMR, infrared spectometry (IR) and elemental analyses. Preliminary bioassay indicated that some of the title compounds showed high inhibitory activity against Brassica campestris L. (B. campestris) and moderate inhibitory activity against Echinochloa crusgalli. For example, the inhibition percentages of compound 4b and 4c against B. campestris were both 94% at 10 μg/mL. J. Heterocyclic Chem., (2009).