72851-18-4Relevant articles and documents
Catalyst-Switchable Regiocontrol in the Direct Arylation of Remote C-H Groups in Pyrazolo[1,5-a]pyrimidines
Bedford, Robin B.,Durrant, Steven J.,Montgomery, Michelle
supporting information, p. 8787 - 8790 (2015/11/27)
The regiodivergent palladium-catalyzed C-H arylation of pyrazolo[1,5-a]pyrimidine has been achieved, wherein the switch in regioselectivity between positions C3 and C7 is under complete catalyst control. A phosphine-containing palladium catalyst promotes the direct arylation at the most acidic position (C7), whereas a phosphine-free catalyst targets the most electron-rich position (C3).
Pyrazolo[1,5-a]pyrimidines and imidazo-[1,5-a]pyrimidines
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, (2008/06/13)
This disclosure describes substituted pyrazolo[1,5-a]pyrimidines and imidazo[1,5-a]pyrimidines which possess anxiolytic activity.