Acetic Acid → 6-(Phenyl)-1,2,4-triazolo[1,5-a]pyrimidine
反応式
[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]=1参加物
4
実験手順
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.
後処理
- 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.
出典と根拠
- ORDレコード
- ord-283ad2879ae04803951bae3c9283c4f9
- 出典データセット
- uspto-grants-1980_06
- 特許番号
- US04209621
反応ノート
読み込み中…