Ethanol → 1-(5-amino-2-(1-(tert-butyldimethylsilyloxy)-2-methylpropan-2-yloxy)phenyl)-4-methyl-1H-tetrazol-5(4H)-one
反応式
[Si:1]([O:8][CH2:9][C:10]([CH3:29])([O:12][C:13]1[CH:18]=[CH:17][C:16]([N+:19]([O-])=O)=[CH:15][C:14]=1[N:22]1[C:26](=[O:27])[N:25]([CH3:28])[N:24]=[N:23]1)[CH3:11])([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2].CCO.CC1C=C2N=C3C(=NC(NC3=O)=O)N(C[C@H](O)[C@H](O)[C@H](O)CO)C2=CC=1C>O.[Pd]>[NH2:19][C:16]1[CH:17]=[CH:18][C:13]([O:12][C:10]([CH3:29])([CH3:11])[CH2:9][O:8][Si:1]([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2])=[C:14]([N:22]2[C:26](=[O:27])[N:25]([CH3:28])[N:24]=[N:23]2)[CH:15]=1参加物
反応物 3
生成物 1
試薬・触媒・溶媒 2
実験手順
A round-bottom flask was charged with 1-(2-(1-(tert-butyldimethylsilyloxy)-2-methylpropan-2-yloxy)-5-nitrophenyl)-4-methyl-1H-tetrazol-5(4H)-one (2.54 g, 6.00 mmol), EtOH (60 mL), and 10% Pd/C (50% in water, Degussa type E101; 510 mg, 20 wt % by weight of the starting nitro compound). The flask was sealed with a rubber septum, degassed, and back-filled with H2 (3×) from a balloon filled with H2. The reaction was stirred for 4 h using a H2 filled balloon. The reaction mixture was filtered through a pad of celite, and the pad of celite was rinsed with EtOAc/MeOH. The filtrate was evaporated to dryness to provide 1-(5-amino-2-(1-(tert-butyldimethylsilyloxy)-2-methylpropan-2-yloxy)phenyl)-4-methyl-1H-tetrazol-5(4H)-one (2.26 g, 96%) as a light brown solid that was used without further purification.
後処理
- customThe flask was sealed with a rubber septum
- customdegassed
- additionback-filled with H2 (3×) from a balloon
- additionfilled with H2
- filtrationThe reaction mixture was filtered through a pad of celite
- washthe pad of celite was rinsed with EtOAc/MeOH
- customThe filtrate was evaporated to dryness
出典と根拠
- ORDレコード
- ord-661c7a0c2a6047f3992dce9122bbea37
- 出典データセット
- uspto-grants-2016_04
- 特許番号
- US09321763B2
反応ノート
読み込み中…