A versatile route to 3-(pyrimidin-4-yl)-imidazo[1,2-a]pyridines and 3-(pyrimidin-4-yl)-pyrazolo[1,5-a]pyridines
✍ Scribed by Richard Ducray; Pascal Boutron; Myriam Didelot; Hervé Germain; Franck Lach; Maryannick Lamorlette; Antoine Legriffon; Mickael Maudet; Morgan Ménard; Georges Pasquet; Fabrice Renaud; Iain Simpson; Gail L. Young
- Book ID
- 104098061
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- French
- Weight
- 509 KB
- Volume
- 51
- Category
- Article
- ISSN
- 0040-4039
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📜 SIMILAR VOLUMES
Eingegangen am 16. Juli 1986 New 3-(pyridin-6-yl) pyraolo [ 1,5-u]pyrimidines were synthesized from (pyridin-6-y1)malonodinitrile 58, ethyl (pyridin-6-y1)cyanoacetate 5b and (pyridin-6-y1)benzoylacetonitrile 5c. Compounds 58-c were obtained from the 4,4,4-trichlorobut-2-enenitriles 2 and 1-pheny1et
## Abstract While 3(5)‐aminopyrazole reacts with enaminonitrile to yield pyrazolo[1,5‐__a__]pyrimidines, 3‐amino‐5‐pyrazolone reacts with the same reagents to yields pyrazolo[3,4‐__b__]pyridines.