Synthesis of New 8‐Azapurines The ethyl 5‐amino‐1__H__‐1,2,3‐triazole‐4‐carboxylates 1 react with orthoformate and hydrazine or substituted phenethylamine to yield the 8‐azapurines 3, 5, and 8, respectively.
Synthese neuartiger triazoloanellierter 8-Azapurine
✍ Scribed by Ried, Walter ;Laoutidis, Joannis
- Publisher
- John Wiley and Sons
- Year
- 1988
- Tongue
- English
- Weight
- 270 KB
- Volume
- 1988
- Category
- Article
- ISSN
- 0947-3440
No coin nor oath required. For personal study only.
✦ Synopsis
Treatnicnt of the S-amino4-cyano-l.2.3-triazoles I a-I with I tricthyl orthoformatc and orthoacctatc 2 gives the cthoxymctiiylcncamino-~,2,3-tna~oics 3a -f which react with hydrazinc hydrate at rocmi tcniperaturc to yield thc l-amino-6-imino-8-a7apurincs 411-f. Thc pyriniidincs 6a-I arc obtaincd from J a -f by reaction with tricthyl orthoacetate and orthoformate 5.
8-Azapurine sind aufgrund ihrer Ahnlichkeit mit den Purinen von groljem pharmakologischem Interesse2
). Im Rahmen unserer Arbciten konnten wir neue Vertreter dieser Substanzklasse herstellen und als Bausteine in der Heterocyclen-Synthese einsetzen. Die Aminonitrile la-f3' reagieren mit den Orthoestern 2 zu den Imidsaureestern 3a-f4).
📜 SIMILAR VOLUMES
Synthesis of New Heteroannulated 8‐Azapurines The 1,2,3‐Triazoles 1 react with biselectrophiles 2, 3, 4, 7, and 9 to the pyrimido‐annulated 8‐Azapurines 5a–d, 6a, b, 8a–c, and 10a–d.