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. Author manuscript; available in PMC: 2013 Aug 22.
Published in final edited form as: J Comb Chem. 2008 Aug 1;10(5):658–663. doi: 10.1021/cc800055x

Table 2.

Library Data for Compounds 6{14–43}

graphic file with name nihms-489942-t0010.jpg

compound Ar yielda(%) purityb(%)
6{14} 5-indolyl 24 92
6{15} 6-methoxy-3-pyridinyl 29 95
6{16} 4-EtO2C-3-FC6H4 53 96
6{17} graphic file with name nihms-489942-t0011.jpg 5 87
6{18} 6-(N,N-dimethyl)-3-pyridinyl 22 94
6{19} 4-MeO-3-FC6H4 58 97
6{20} 3-MeO2-C-5-O2NC6H4 44 97
6{21} 5-indolyl 51 92
6{22} 6-methoxy-3-pyridinyl 26 95
6{23] 4-EtO2C-3-FC6H4 26 97
6{24} graphic file with name nihms-489942-t0012.jpg 0
6{25] 6-(N,N-dimethyl)-3-pyridinyl 7 100
6{26} 4-MeO-3-FC6H4 46 88
6{27} 3-MeO2C-5-O2NC6H4 0
6{28} 5-indolyl 79 97
6{29} 6-methoxy-3-pyridinyl 81 95
5{30} 4-EtO2C-3-FC6H4 73 99
6{31} graphic file with name nihms-489942-t0013.jpg 57 94
6{32} 6-(N,N-dimethyl)-3-pyridinyl 85 96
6{33} 4-MeO-3-FC6H4 73 99
6{34} 3,4,5-(MeO)3C6H4 73 99
6{35} 5-indolyl 75 96
6{36} 6-methoxy-3-pyridinyl 16 91
6{37} 4-EtO2C-3-FC6H4 64 98
6{38} graphic file with name nihms-489942-t0014.jpg 7 100
6{39} 6-(N,N-dimethyl)-3-pyridinyl 20 92
6{40} 4-MeO-3-FC6H4 60 99
6{41} 3-EtO2C-5-O2NC6H4 0
6{42} 3,4,5-(MeO)3C6H4 53 99
6{43} 3,4-(OCH2CH2O)C6H3 44 99
a

Isolated yield after preparative HPLC.

b

UV purities determined at 214 nm after preparative HPLC.