Application of the Mild-Condition Phthalimidine Synthesis with Use of 1,2,3-1H-Benzotriazole and 2-Mercaptoethanol as Dual Synthetic Auxiliaries. Effective Synthesis of Phthalimidines Possessing a Variety of Substituents at 2-Position
摘要:
The mild-condition phthalimidine synthesis based on Mannich type 1:1 condensation reaction between o-phthalaldehyde with a variety of primary amines in the presence of excess 2-mercaptoethanol and 1,2,3-1H-benzotriazole as "dual synthetic auxiliaries" in MeCN for 13 h at room temperature afford 2-substituted phthalimidines (2,3-dihydroisoindol-1-one) in fair to good isolated yields.
Palladium-Catalyzed Cyclocarbonylation of 2-Halobenzaldehyde and Hydrazines: A Facile Synthesis of 2-Aminoisoindolin-1-ones
作者:Chao Han、Yang Shen、Ping Lu、Yanguang Wang
DOI:10.1002/cjoc.201200798
日期:2013.2
An efficient procedure for the synthesis of 2‐aminoisoindolin‐1‐ones via a palladium‐catalyzed three‐component reaction of 2‐halobenzaldehydes, hydrazines and carbon monoxide is reported. This cyclocarbonylation process can be performed smoothly under 1 atmospheric pressure of carbon monoxide to afford 2‐aminoisoindolin‐1‐ones in moderate to excellent yields.