Abstract
An improved synthesis of 5-amino-1,2-dihydrofuro[2,3-c]isoquinoline has been achieved using a slight modification of reaction conditions for the Truce-Smiles rearrangement. Acid treatment of the obtained 5-amino-1,2- dihydrofuro[2,3-c]isoquinolines gave unexpected ring-opened spiro ring compounds. The previously unreported parent compound, furo[2,3-c]isoquinoline, was also synthesized. © 2010 Pharmaceutical Society of Japan.
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Okuda, K., Yoshida, M., Hirota, T., & Sasaki, K. (2010). Polycyclic N-heterocyclic compounds. Part 631 improved synthesis of 5-amino-1,2-dihydrofuro[2,3-c]isoquinolines via truce-smiles rearrangement and subsequent formation to furo[2,3-c]isoquinoline. Chemical and Pharmaceutical Bulletin, 58(3), 363–368. https://doi.org/10.1248/cpb.58.363
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