反応式
F[C:2]1[C:3]([CH:8]=O)=[N:4][CH:5]=[CH:6][CH:7]=1.[NH2:10][NH2:11]>O>[NH:10]1[C:2]2[C:3](=[N:4][CH:5]=[CH:6][CH:7]=2)[CH:8]=[N:11]1参加物
4
実験手順
A mixture of 3-fluoro-2-pyridinecarboxaldehyde (4 g, 32 mmol) and hydrazine (20.5 g) was kept at 115° C. for 7 hr, then cooled to rt. The reaction mixture was diluted with water and extracted with EtOAc. The organic phases were combined, washed with brine, and dried. Concentration followed by flash chromatography afforded 1H-pyrazolo[4,3-b]pyridine (2.3 g, 60.4%).
後処理
- extractionextracted with EtOAc
- washwashed with brine
- customdried
- concentrationConcentration
出典と根拠
- ORDレコード
- ord-2a2bc17e86064d979af9365c6fef2b04
- 出典データセット
- uspto-grants-2012_06
- 特許番号
- US08198456B2
関連ノート
読み込み中…