1-Methyl-3-propyl-1H-pyrazole-5-carboxylic acid (3) was exclusively brominated at the 4-position by bromine in the dark. Brominated product 8 was then converted into 1-methyl-3-propyl-1H-pyrazole-5-carboxamide 9 by successive treatment with thionyl chloride and ammonium hydroxide. Carboxamide 9 was
A Modified, Economical and Efficient Synthesis of Variably Substituted Pyrazolo[4,3-d]pyrimidin-7-ones.
✍ Scribed by Khalid Mohammed Khan; Ghulam Murtaza Maharvi; Muhammad Igbal Choudhary; Atta-ur-Rahman Atta-ur-Rahman; Shahnaz Perveen
- Publisher
- John Wiley and Sons
- Year
- 2006
- Weight
- 24 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0931-7597
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📜 SIMILAR VOLUMES
## Abstract A general synthetic approach to pyrazolo[4,3‐__d__]pyrimidines is reported. Aldehydes, arylideneanilines, carboxylic acids and orthoesters are used as one‐carbon units for bridging the two amino functions of 4‐amino‐1‐alkyl‐3‐propylpyrazole‐5‐carboxamides.
## Abstract Pyrazolo‐[3,4‐__d__]pyrimidine‐4,6‐diones **5** and pyrazolo[4,3‐__d__]pyrimidine‐5,7‐diones **7** were synthesized by Curtius rearrangement of pyrazolic mono‐esters **2** and **3** followed by hetero‐cyclization __via__ the ureas derivatives **4** and **6** under alkaline conditions.