Sulfuric Acid → 1-[(3,4-Dihydro-2-naphthalenyl)methyl]-4-anilino isonipecotamide
反応式
[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH2:4][CH2:3][C:2]=1[CH2:11][N:12]1[CH2:19][CH2:18][C:15]([NH:20][C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)([C:16]#[N:17])[CH2:14][CH2:13]1.S(=O)(=O)(O)[OH:28].[OH-].[NH4+]>>[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH2:4][CH2:3][C:2]=1[CH2:11][N:12]1[CH2:19][CH2:18][C:15]([NH:20][C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)([C:16]([NH2:17])=[O:28])[CH2:14][CH2:13]1参加物
4
反応条件
- 温度
- 70 °C
実験手順
A mixture of 1-[(3,4-dihydro-2-naphthalenyl)methyl]-4-anilino isonipecotonitrile (5.0 g) and 90% sulfuric acid (60.0 g) is heated for 10 minutes at 70° C. The mixture is then stirred at room temperature for an additional hour. The reaction mixture is poured into ice-water, basified with ammonium hydroxide, and extracted with chloroform. Concentration of the dried chloroform solution followed by trituration with benzene yields the title compound.
後処理
- extractionextracted with chloroform
出典と根拠
- ORDレコード
- ord-5252351b68534317b9ddf53e3f6ec849
- 出典データセット
- uspto-grants-1977_09
- 特許番号
- US04051248
反応ノート
読み込み中…