摘要 |
There is provided a process for the preparation of substituted amino alcohols HO-(CH<SUB>2</SUB>)<SUB>n</SUB>-NR<SUP>1</SUP>R<SUP>2 </SUP>from haloalcohols HO-(CH<SUB>2</SUB>)<SUB>n</SUB>-X, where X is Cl, Br or I, by reaction with an amine HNR<SUP>1</SUP>R<SUP>2</SUP>, in water as solvent at a temperature range of about 20° C. to about 90° C. optionally in the presence of a catalytic amount of an iodide source metal iodides. The haloalcohols are useful in the preparation of 6-[(substituted)phenyl]-triazolopyrimidine compounds which are useful in the treatment of cancer.
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