HCID 67021327、化合物 → 2-benzyl-7-isopropyl-3-phenyl-2H-indazole
反応式
[CH2:1]([N:8]1[C:16]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)=[C:15]2[C:10]([C:11]([C:23]([CH3:25])=[CH2:24])=[CH:12][CH:13]=[CH:14]2)=[N:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>C(O)C.O=[Pt]=O>[CH2:1]([N:8]1[C:16]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)=[C:15]2[C:10]([C:11]([CH:23]([CH3:25])[CH3:24])=[CH:12][CH:13]=[CH:14]2)=[N:9]1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1参加物
4
実験手順
Thirty milligrams (30 mg; 0.092 mmol) of 2-benzyl-7-isopropenyl-3-phenyl-2H-indazole (Example 521) were dissolved in 2 ml of dry ethanol followed by the addition of 30 mg of PtO2. The reaction mixture was stirred under H2 atmosphere at room temperature for 2 hours, then filtered and the EtOH evaporated. Flash column chromatography (SiO2, dichloromethane/heptane, 1:1, as an eluant) afforded 2-benzyl-7-isopropyl-3-phenyl-2H-indazole in 80% yleld.
後処理
- filtrationfiltered
- customthe EtOH evaporated
出典と根拠
- ORDレコード
- ord-c273b8eb44dd43bba06e8d9d0ba91261
- 出典データセット
- uspto-grants-2009_09
- 特許番号
- US07592363B2
反応ノート
読み込み中…