posted on 2004-07-09, 00:00authored byDong Joon Lee, Kyongtae Kim
Treatment of 3-{3-alkyl (and aryl)amino-5-arylthieno-2-yl}-2-diazo-3-oxopropanoates 8 with TMSOTf
(3 equiv) in the presence of Et3N (6 equiv) in CH2Cl2 for 1 h
at room temperature afforded 4-alkyl (and aryl)-2-aryl-6-diazo-4H-thieno[3,2-b]pyridine-5,7-diones 14 in excellent
yields. On heating of 14 in the presence of a catalytic amount
of Rh2(CF3CF2CF2CO2)4 in PhH for 4−10 h at reflux,
corresponding ring contraction products, 4-alkyl (and aryl)-5,6-dihydro-4H-thieno[3,2-b]pyrrol-5-ones 16, were produced
in good to excellent yields.