Development of novel 2-substituted acylaminoethylsulfonamide derivatives as fungicides against Botrytis cinerea.

• Novel 2-substituted acylaminoethylsulfonamides with the taurine scaffold were synthesized as fungicides against Botrytis cinerea. • Compound V-A-12 showed the best activity in vitro with the EC 50 value of 0.66 mg·L−1. • A 3D-QSAR model was developed to identify some key structural features responsible for the potency. • The effeicacy of sulfonamides was verified in the activity evaluation against procymidone-resistant Botrytis cinerea strains. Botrytis cinerea is an economically important fungal pathogen with a host range of over 200 plant species. Unfortunately, gray mold disease caused by B. cinerea has not been effectively controlled because of its high risk for fungicide resistance development. As a part of our ongoing efforts to develop novel sulfonamides as agricultural fungicides against Botrytis cinerea , we introduced 2-aminoethanesulfonic acid (taurine) substructure, designed and synthesized a series of novel 2-substituted acylaminoethylsulfonamides. The newly synthesized sulfonamides were evaluated in vitro and in vivo for their fungicidal activity against Botrytis cinerea , of which the 2-ethoxyacetylamide derivative (V-A-12 , EC 50 = 0.66 mg·L−1) exhibited the highest potency in vitro and superior fungicidal activity compared with procymidone (EC 50 = 1.06 mg·L−1). In vivo bioassay indicated that compound V-A-12 could be effective for the control of tomato gray mold. Moreover, the structure-activity relationship of these sulfonamides was analyzed by establishing a three-dimensional quantitative structure-activity relationship (3D-QSAR) model, which can provide guidance for the development of sulfonamides as fungicides. Finally, the effeicacy of sulfonamide derivatives was again verified in the activity evaluation against resistant Botrytis cinerea strains. These results further enhance the development value of 2-substituted acylaminoethylsulfonamides to control the tomato gray mold. [ABSTRACT FROM AUTHOR]