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. Author manuscript; available in PMC: 2012 Aug 24.
Published in final edited form as: Tetrahedron Lett. 2011 Aug 24;52(34):4375–4377. doi: 10.1016/j.tetlet.2011.05.114

Table 3.

Reaction of various indole based aldehydes with Rhodanine derivatives

graphic file with name nihms-305953-t0005.jpg


Entry
(%)
R1 R2 R3 R4 product Yielda,b
1 H H H H 7a 95
2 CH3 H H H 7b 96
3 CH3 CH3 H H 7c 90
4 CH3 H H OCH3 7d 93
5 OCH3 H H H 7e 95
6 OCH3 H H OCH3 7f 92
7 H H H OCH3 7g 94
8 CN H H OCH3 7h 90
9 CN H H H 7i 91
10 H H H Cl 7j 89
graphic file with name nihms-305953-t0006.jpg H H 7k 95
graphic file with name nihms-305953-t0007.jpg H OCH3 7l 93
graphic file with name nihms-305953-t0008.jpg H CN 7m 91
14 OH Br Br H 7n 90
15 OH Cl Cl H 7o 89
16 OH Br Br OCH3 7p 96
17 OH Cl Cl OCH3 7q 90
a

Isolated yield;

b

All the compounds were characterized by 1H NMR, 13C NMR, DEPT-135, IR and HRMS analysis.