Synthetic Communications p. 427 - 432 (2000)
Update date:2022-08-17
Topics:
Sabol, Mark R.
Owen, John M.
Erickson, W. Randal
2,3-Dichloroquinoline was prepared in three steps in good overall yield from commercial 3-bromoquinoline via N-oxide formation and rearrangement to 3-bromocarbostyril, followed by a one-pot conversion to 3-bromo-2- chloroquinoline and halogen exchange to the title compound.
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