2-(3-Nitro-6-methoxyphenyl)-5-phenylbenzoxazole → 2-(3-Amino-6-methoxyphenyl)-5-phenylbenzoxazole
反応式
[N+:1]([C:4]1[CH:5]=[C:6]([C:12]2[O:13][C:14]3[CH:20]=[CH:19][C:18]([C:21]4[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=4)=[CH:17][C:15]=3[N:16]=2)[C:7]([O:10][CH3:11])=[CH:8][CH:9]=1)([O-])=O>[Pd]>[NH2:1][C:4]1[CH:5]=[C:6]([C:12]2[O:13][C:14]3[CH:20]=[CH:19][C:18]([C:21]4[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=4)=[CH:17][C:15]=3[N:16]=2)[C:7]([O:10][CH3:11])=[CH:8][CH:9]=1参加物
3
実験手順
Prepared by the method of Example 15e), from palladium (10 mol %) on carbon and 2-(3-nitro-6-methoxyphenyl)-5-phenylbenzoxazole (450 mg, 1.3 mmol) the subtitle compound was obtained (420 mg, 99%). The product was used directly in the next step without purification.
出典と根拠
- ORDレコード
- ord-f9788927e70c458b94df1968c9ca1976
- 出典データセット
- uspto-grants-2006_11
- 特許番号
- US07138425B2
反応ノート
読み込み中…