关键词: 异吲哚啉-1-酮, 三组分反应, 氟化, 内酰胺化, 合成

A one-pot, metal-free three-component reaction has been developed for the synthesis of fluorinated isoindolin-1-one derivatives at room temperatures. This method employs readily available 2-formylbenzoic acids, primary amines, and fluorinated dialkyl malonates. The reaction takes place smoothly in a mild system of ethanol at room temperature, avoiding metal contamination of the products. The transformation proceeds via a sequential condensation/Michael addition/in situ lactamization process, efficiently constructing the isoindolin-1-one core while precisely introducing a fluorine atom in one step to enhance the drug-likeness of the target products. Furthermore, a malonate ester functionality is introduced, providing convenience for further structural diversification of the molecules. The reaction exhibits good functional group compatibility with a variety of aromatic and aliphatic amines, and electron-rich aromatic amines as well as benzylamine derivatives afford the corresponding 3-(fluoromalonate)-substituted isoindolin-1-ones in moderate to excellent yields (up to 90%). This metal-free, mild-condition multicomponent strategy provides a direct and versatile new approach for constructing structurally diverse fluorinated bioactive compound libraries based on the privileged isoindolin-1-one scaffold.

Key words: isoindolin-1-one, three-component reaction, fluorination, lactamization, synthesis