Ammonium Chloride → 5-(2-Amino-5-phenoxy-phenyl)-4-cyano-pentanoic acid cyclohexyl-methyl-amide

HRID 502888ノート

反応式

HRID 502888 の反応式
[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% 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

  1. customThe vessel was equipped with a condenser
  2. temperatureto reflux for 2 h
  3. filtrationfollowed by filtration through a pad of Celite®
  4. customThe solvent was removed
  5. dissolutionthe resulting residue was dissolved in ethyl acetate
  6. washwashed 3 times with 10% sodium carbonate solution
  7. dry with materialThe organic layer was dried with sodium sulfate
  8. filtrationfiltered
  9. customthe solvent was removed under reduced pressure
  10. customThe resulting residue was used in subsequent steps without further purification

出典と根拠

ORDレコード
ord-512793aa975a44168f3ad9e4ca2fc29b
出典データセット
uspto-grants-2010_08
特許番号
US07776882B2

反応ノート

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