Lithium Hydroxide → Lithium 6-fluoropyrazolo[1,5-a]pyrimidine-3-carboxylate
反応式
[F:1][C:2]1[CH:3]=[N:4][C:5]2[N:6]([N:8]=[CH:9][C:10]=2[C:11]([O:13]CC)=[O:12])[CH:7]=1.[OH-].[Li+:17]>O.CO.C1COCC1>[F:1][C:2]1[CH:3]=[N:4][C:5]2[N:6]([N:8]=[CH:9][C:10]=2[C:11]([O-:13])=[O:12])[CH:7]=1.[Li+:17]参加物
6
実験手順
A suspension of ethyl 6-fluoropyrazolo[1,5-a]pyrimidine-3-carboxylate (512 mg, 2.45 mmol) and lithium hydroxide (61.5 mg, 2.57 mmol) in water (1 ml), MeOH (1 ml) and THF (1 ml) was irradiated to 100° C. for 10 min in the microwave. The reaction mixture was concentrated under vacuum, azeotroping with toluene (10 ml) to leave the title compound as a yellow powder (497 mg). This crude material was used directly in the subsequent reactions.
後処理
- customwas irradiated to 100° C. for 10 min in the microwave
- concentrationThe reaction mixture was concentrated under vacuum
- customazeotroping with toluene (10 ml)
出典と根拠
- ORDレコード
- ord-78e4efa998b94c459cd95d3d3dfe2962
- 出典データセット
- uspto-grants-2012_01
- 特許番号
- US08093249B2
反応ノート
読み込み中…