Journal
ORGANIC LETTERS
Volume 24, Issue 46, Pages 8498-8502Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.2c03361
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The synthesis of bromo-substituted indeno[1,2-b]-pyridin-2-ones and 3-iodo-5-benzyl-substituted 2-pyridones, starting from easily available 6-benzyl-3,6-dihydropyridin-2(1H)-ones, triggered by NBS and NIS, respectively, was reported. A novel aza-semipinacol-type rearrangement was observed with a transfer of a benzyl group from the C6 to C5 lactam position in both syntheses. The identification of intermediate compounds supported the proposed reaction mechanisms, and functionalized indeno[1,2-b]pyridin-2-ones and 5-benzyl-2-pyridones were obtained during the scope check of the method's application.
The synthesis of bromo-substituted indeno[1,2-b]-pyridin-2-ones and 3-iodo-5-benzyl-substituted 2-pyridones, starting from easily available 6-benzyl-3,6-dihydropyridin-2(1H)-ones, trig-gered by NBS and NIS, respectively, is described. In both syntheses, a transfer of a benzyl group from the C6 to C5 lactam position occurred, indicating a novel aza-semipinacol-type rearrangement. Identification of intermediate compounds in both transformations supported the proposed reaction mechanisms. In the process of checking the scope of the method's application, functionalized indeno[1,2-b]pyridin-2-ones and 5-benzyl-2-pyridones were obtained.
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