Acetic Acid → HCID 12468024、化合物
反応式
[Cl:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[C:7]1=[N:11][C:12]([CH3:14])=[N:13][N:6]1[C:5]2([C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)N.C(O)(=[O:24])C>CO>[Cl:1][C:2]1[CH:10]=[CH:9][C:8]([C:7]2[N:11]=[C:12]([CH3:14])[NH:13][N:6]=2)=[C:4]([CH:3]=1)[C:5]([C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)=[O:24]参加物
4
実験手順
Ten milligrams of 7-chloro-2-methyl-5-phenyl-5H-[1,2,4]triazolo-[5,1-a]-isoindol-5-amine (as prepared in Example 1) are refluxed for 10 minutes in 2 ml of 50% aqueous methanol containing a drop of acetic acid. The methanol is removed under vacuum and the aqueous residue made basic with 10% NaOH. The aqueous solution is washed with chloroform, neutralized with 10% HCl and extracted with chloroform. The chloroform solution is evaporated to dryness and the residue is recrystallized from a water-ethanol mixture, m.p. 149° to 150°.
後処理
- customThe methanol is removed under vacuum
- washThe aqueous solution is washed with chloroform
- extractionextracted with chloroform
- customThe chloroform solution is evaporated to dryness
- customthe residue is recrystallized from a water-ethanol mixture, m.p. 149° to 150°
出典と根拠
- ORDレコード
- ord-0ef3825a6c99435f97e2425fff98bfb6
- 出典データセット
- uspto-grants-1978_11
- 特許番号
- US04127587
反応ノート
読み込み中…