6-Chloro-8-nitro-4H-benzo[1,4]oxazin-3-one → 8-Amino-2H-1,4-benzoxazin-3(4H)-one
反応式
Cl[C:2]1[CH:12]=[C:11]([N+:13]([O-])=O)[C:5]2[O:6][CH2:7][C:8](=[O:10])[NH:9][C:4]=2[CH:3]=1>CCO.[Pd]>[NH2:13][C:11]1[C:5]2[O:6][CH2:7][C:8](=[O:10])[NH:9][C:4]=2[CH:3]=[CH:2][CH:12]=1参加物
4
実験手順
Intermediate 57 (326 mg, 1.4 mmol) was dissolved in EtOH, then Pd/C (0.03 g) was added. The mixture was hydrogenated under H2 for 4 h at 50° C. The reaction mixture was filtered over Hyflo and the filtrate was concentrated in vacuo to give 8-amino-2H-benzo[b][1,4]oxazin-3(4H)-one (intermediate 58) (83%) as a brown solid, which was used in the next step without any further purification.
後処理
- filtrationThe reaction mixture was filtered over Hyflo
- concentrationthe filtrate was concentrated in vacuo
出典と根拠
- ORDレコード
- ord-56779accfbdc4bde94a89e23249d27ca
- 出典データセット
- uspto-grants-2015_10
- 特許番号
- US09156822B2
反応ノート
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