Okuda Kensuke, Yoshida Masahiko, Hirota Takashi, Sasaki Kenji
Gifu Pharmaceutical University, Gifu 501-1196, Japan.
Chem Pharm Bull (Tokyo). 2010 Mar;58(3):363-8. doi: 10.1248/cpb.58.363.
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.
通过对特鲁斯-斯迈尔斯重排反应条件进行微小调整,实现了5-氨基-1,2-二氢呋喃并[2,3-c]异喹啉的改进合成。对所得到的5-氨基-1,2-二氢呋喃并[2,3-c]异喹啉进行酸处理,得到了意想不到的开环螺环化合物。还合成了此前未报道的母体化合物呋喃并[2,3-c]异喹啉。