Methylhydrazine → HCID 19025418、化合物
反応式
[CH2:1]([N:3]([CH2:13][CH3:14])[C:4]1[CH:9]=[CH:8][C:7]([N:10]=[C:11]=[S:12])=[CH:6][N:5]=1)[CH3:2].[CH3:15][NH:16][NH2:17]>C(O)C>[CH2:13]([N:3]([CH2:1][CH3:2])[C:4]1[CH:9]=[CH:8][C:7]([NH:10][C:11](=[S:12])[N:16]([CH3:15])[NH2:17])=[CH:6][N:5]=1)[CH3:14]参加物
4
実験手順
Following procedures similar to those employed in Step A of Example 2, the reaction of 3.5 g (0.017 mole) of (2-diethylaminopyridin-5-yl) isothiocyanate with 0.86 (0.019 mole) of methylhydrazine in 150 ml of ethanol yielded 2.5 g of 4-(2-diethylaminopyridin-5-yl)-2-methyl-3-thiosemicarbazide as a solid, mp 147°-149° C. The nmr spectrum was consistent with the proposed structure.
出典と根拠
- ORDレコード
- ord-2829469738d54fe09d3de951c08cf83d
- 出典データセット
- uspto-grants-1992_04
- 特許番号
- US05108486
反応ノート
読み込み中…