
Heterocyclic Communications p. 7 - 16 (2001)
Update date:2022-07-30
Topics:
Jennings, Sharon A.
Toth, James L.
Roller, Shane G.
Brooks, Natalie
O'Hare, Caroline
Kiakos, Konstantinos
Hartley, John A.
Burke, Philip J.
Lee, Moses
An efficient method for the preparation of racemic seco-cyclopropaneindoline, or seco-CI, analogs of the anticancer agent CC1065 is described. The syntheses of seco-CI compounds containing either 5,6,7-trimethoxyindole-2-carbonyl, 4, or 5-(benzofuran-2-carboxamido)indole-2-carbonyl, 10, or 2-(4-N,N-diethyl)aminophenyl)benzimidazole-6-carbonyl, 11, or 4-(4-butanamido-1-methylpyrrole-2-carboxamido)-1-methylpyrrole-2-carbonyl, 12, subunit are detailed. At μM concentrations, compounds 4, 10-12 inhibited the growth of human leukemic K562 cells in culture.
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