Ammonium Chloride → 5-(2-Amino-5-phenoxy-phenyl)-4-cyano-pentanoic acid cyclohexyl-methyl-amide
反応式
[CH:1]1([N:7]([CH3:32])[C:8](=[O:31])[CH2:9][CH2:10][CH:11]([C:29]#[N:30])[CH2:12][C:13]2[CH:18]=[C:17]([O:19][C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=3)[CH:16]=[CH:15][C:14]=2[N+:26]([O-])=O)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[Cl-].[NH4+]>[Zn].CO>[CH:1]1([N:7]([CH3:32])[C:8](=[O:31])[CH2:9][CH2:10][CH:11]([C:29]#[N:30])[CH2:12][C:13]2[CH:18]=[C:17]([O:19][C:20]3[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=3)[CH:16]=[CH:15][C:14]=2[NH2:26])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1参加物
5
実験手順
4-cyano-5-(2-nitro-5-phenoxy-phenyl)-pentanoic acid cyclohexyl-methyl-amide (0.200 g, 0.46 mmol), ammonium chloride (0.31 g, 5.75 mmol) and methanol (3.0 mL) were added to a round bottom flask followed by addition of powdered zinc (0.4 g). The vessel was equipped with a condenser and the reaction was headed to reflux for 2 h followed by filtration through a pad of Celite®. The solvent was removed and the resulting residue was dissolved in ethyl acetate, then washed 3 times with 10% aqueous sodium carbonate solution. The organic layer was dried with sodium sulfate, filtered and the solvent was removed under reduced pressure. The resulting residue was used in subsequent steps without further purification.
後処理
- customThe vessel was equipped with a condenser
- temperatureto reflux for 2 h
- filtrationfollowed by filtration through a pad of Celite®
- customThe solvent was removed
- dissolutionthe resulting residue was dissolved in ethyl acetate
- washwashed 3 times with 10% aqueous sodium carbonate solution
- dry with materialThe organic layer was dried with sodium sulfate
- filtrationfiltered
- customthe solvent was removed under reduced pressure
- customThe resulting residue was used in subsequent steps without further purification
出典と根拠
- ORDレコード
- ord-2beef67311c742df8b3b5600af04c18d
- 出典データセット
- uspto-grants-2011_01
- 特許番号
- US07868022B2
反応ノート
読み込み中…