(6aR,7S,9aS,11S,13aS)-11-amino-5-benzyloxy-2,3,6,6a,7,8,9,9a,10,11,12,13-dodecahydro-6a,7,10,10-tetramethyl-3-oxo-1H-benzo[8,8a][1]benzopyrano[2,3-e]isoindole → (6aR,7S,9aS,11S,13aS)-11-amino-2,3,6,6a,7,8,9,9a,10,11,12,13-dodecahydro-5-hydroxy-6a,7,10,10-tetramethyl-3-oxo-1H-benzo[8,8a][1]benzopyrano[2,3-e]isoindole
反応式
[NH2:1][C@@H:2]1[C:31]([CH3:33])([CH3:32])[C@H:30]2[C@@:5]3([O:26][C:9]4[C:10]5[CH2:11][NH:12][C:13](=[O:25])[C:14]=5[CH:15]=[C:16]([O:17]CC5C=CC=CC=5)[C:8]=4[CH2:7][C@:6]3([CH3:35])[C@@H:27]([CH3:34])[CH2:28][CH2:29]2)[CH2:4][CH2:3]1>CO.[C].[Pd]>[NH2:1][C@@H:2]1[C:31]([CH3:33])([CH3:32])[C@H:30]2[C@@:5]3([O:26][C:9]4[C:10]5[CH2:11][NH:12][C:13](=[O:25])[C:14]=5[CH:15]=[C:16]([OH:17])[C:8]=4[CH2:7][C@:6]3([CH3:35])[C@@H:27]([CH3:34])[CH2:28][CH2:29]2)[CH2:4][CH2:3]1参加物
4
反応物 1
生成物 1
試薬・触媒・溶媒 2
実験手順
To Compound (46a) (30 mg, 0.063 mmol) dissolved in 4.0 ml of methanol was added 6 mg of 10% palladium-carbon, and the mixture stirred under hydrogen atmosphere for 1 hour at room temperature. After the palladium-carbon was removed by filtration, the filtrate was concentrated under reduced pressure. The residue was crystallized from diethyl ether, and recrystallized from diethyl ether-methanol to give 16 mg (48%) of Compound (47a).
後処理
- customAfter the palladium-carbon was removed by filtration
- concentrationthe filtrate was concentrated under reduced pressure
- customThe residue was crystallized from diethyl ether
- customrecrystallized from diethyl ether-methanol
出典と根拠
- ORDレコード
- ord-4d9b3d0489af427ab925535da3167757
- 出典データセット
- uspto-grants-1999_03
- 特許番号
- US05876984
反応ノート
読み込み中…