Acetic Acid → 4-Amino-6-fluoroisoindolin-1-one
反応式
C[O:2][C:3](=O)[C:4]1[CH:9]=[C:8]([F:10])[CH:7]=[C:6]([N+:11]([O-])=O)[C:5]=1[CH2:14][N:15]=[N+]=[N-].C(O)(=O)C>C(O)C.[Pd]>[NH2:11][C:6]1[CH:7]=[C:8]([F:10])[CH:9]=[C:4]2[C:5]=1[CH2:14][NH:15][C:3]2=[O:2]参加物
5
実験手順
1.86 g (7.32 mmol) of 2-(azidomethyl)-5-fluoro-3-nitrobenzoic acid methyl ester is added in 46 ml of ethanol and 3.4 ml of glacial acetic acid and mixed with 256.6 mg of Pd/C. After stirring overnight at room temperature under hydrogen atmosphere, the catalyst is suctioned off via a glass-fiber filter, and the filtrate is evaporated to the dry state. The residue, 1.18 mg (97.5%) of the desired compound, is further incorporated in crude form.
後処理
- filtrationfilter
- customthe filtrate is evaporated to the dry state
出典と根拠
- ORDレコード
- ord-3e55a77e528e4606a259b4b1e3967f63
- 出典データセット
- uspto-grants-2009_12
- 特許番号
- US07638515B2
反応ノート
読み込み中…