Methanol → 2-Methylpyrazolo[1,5-a]pyridine-3-carboxylic acid
反応式
CO.[CH3:3][C:4]1[C:12]([C:13]([O:15]CC)=[O:14])=[C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][N:6]2[N:5]=1>[OH-].[Na+]>[CH3:3][C:4]1[C:12]([C:13]([OH:15])=[O:14])=[C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][N:6]2[N:5]=1参加物
4
実験手順
A small amount of methanol was added to a solution of 0.356 g of ethyl 2-methyl-3-pyrazolo[1,5-a]-pyridinecarboxylate in 10 ml of 5N aq. NaOH solution, followed by stirring at room temperature for 24 hours. The reaction mixture was washed with benzene and then made acidic with concentrated hydrochloric acid. Crystals precipitated were collected by suction filtration. The crystals so obtained were dried and then recrystallized from benzene, whereby 0.16 g of the title compound was obtained (yield: 52.4%).
後処理
- washThe reaction mixture was washed with benzene
- customCrystals precipitated
- filtrationwere collected by suction filtration
- customThe crystals so obtained
- customwere dried
- customrecrystallized from benzene
出典と根拠
- ORDレコード
- ord-ffa7cb32f58540528db749a437ea17ad
- 出典データセット
- uspto-grants-1993_04
- 特許番号
- US05200415
反応ノート
読み込み中…