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- W2023523145 abstract "by using thecommercially available 2-amino-6-methylpyrimidin-4(3H)-one (5) as a starting material, and this procedure (Scheme 1)was expected to be very efficient in synthesizing our targetmolecule 3. The treatment of 6 with 2.2 equivalent of N,N-dimethyl-formamide dimethyl acetal at room temperature providedthe corresponding 2-(dimethylamino)methyleneimino deri-vative 8, which was converted to 3-benzyl-2-[(dimethyl-amino)methyleneimino]-5-nitro-6-methylpyrimidin-4-one(9) by treating with benzyl chloride in the presence ofDBU." @default.
- W2023523145 created "2016-06-24" @default.
- W2023523145 date "2003-09-20" @default.
- W2023523145 modified "2023-10-14" @default.
- W2023523145 title "An Alternative Synthesis of 5-Aminopyrazolo[4,3-d]pyrimidin-7(6H)-one" @default.
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- W2023523145 doi "https://doi.org/10.5012/bkcs.2003.24.9.1365" @default.
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