Acetic Acid → 6-(Phenyl)-1,2,4-triazolo[1,5-a]pyrimidine
Reaktionsgleichung
[C:1]1([C:7]([CH2:9]C=O)=N)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[NH2:12][C:13]1[N:17]=[CH:16][NH:15][N:14]=1.[C:18](O)(=O)C>>[C:1]1([C:7]2[CH:9]=[N:12][C:13]3[N:14]([N:15]=[CH:16][N:17]=3)[CH:18]=2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1Komponenten
4
Versuchsvorschrift
An equimolar mixture of (phenyl)formimidoylacetaldehyde and 3-amino-1,2,4-triazole in glacial acetic acid (5 ml. acetic acid to 0.01 mole of reagents) is refluxed for 2 hours and allowed to cool to room temperature. The solid which separates is collected, washed with glacial acetic acid and dried. The solid is recrystallized from glacial acetic acid to give the product, m.p. 164°-167° C.
Aufarbeitung
- temperatureis refluxed for 2 hours
- customThe solid which separates is collected
- washwashed with glacial acetic acid
- customdried
- customThe solid is recrystallized from glacial acetic acid
- customto give the product, m.p. 164°-167° C.
Quellen und Nachweise
- ORD-Eintrag
- ord-283ad2879ae04803951bae3c9283c4f9
- Quelldatensatz
- uspto-grants-1980_06
- Patentnummer
- US04209621
Notizen zur Reaktion
Wird geladen…