反応式
[C:1]([N:9]1[CH2:13][CH2:12][C:11]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)=[N:10]1)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[N:4][CH:3]=1.[ClH:20].C(O)C>C(O)C>[ClH:20].[C:1]([N:9]1[CH2:13][CH2:12][C:11]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)=[N:10]1)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[N:4][CH:3]=1参加物
4
実験手順
1-Nicotinoyl-3-phenyl-2-pyrazoline (0.1 g) synthesized in Example 3 was dissolved in ethanol (5 ml). Thereto was added 1 N hydrochloric acid-ethanol (0.9 ml) with ice-cooling. The resulting crystals were collected by filtration, washed with ether and dried to obtain 0.1 g of a title compound as yellow crystals.
後処理
- temperaturecooling
- filtrationThe resulting crystals were collected by filtration
- washwashed with ether
- customdried
出典と根拠
- ORDレコード
- ord-8764a4c9f00a4566963f254ddadb8093
- 出典データセット
- uspto-grants-2004_12
- 特許番号
- US06831083B2
関連ノート
読み込み中…