Aluminum(III) Chloride → 3-(2-Amino-6-phenoxy-3,4-dihydro-quinolin-3-yl)-N-cyclohexyl-N-methyl-propionamide

HRID 502889ノート

反応式

HRID 502889 の反応式
[CH:1]1([N:7]([CH3:30])[C:8](=[O:29])[CH2:9][CH2:10][CH:11]([C:27]#[N:28])[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[NH2:26])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[Cl-].[Al+3].[Cl-].[Cl-]>C1(C)C=CC=CC=1>[NH2:28][C:27]1[CH:11]([CH2:10][CH2:9][C:8]([N:7]([CH:1]2[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]2)[CH3:30])=[O:29])[CH2:12][C:13]2[C:14](=[CH:15][CH:16]=[C:17]([O:19][C:20]3[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=3)[CH:18]=2)[N:26]=1

参加物

4

反応物 2

HCID 6451240Aluminum(III) ChlorideHCID 672689265-(2-Amino-5-phenoxy-phenyl)-4-cyano-pentanoic acid cyclohexyl-methyl-amide

生成物 1

HCID 594281643-(2-Amino-6-phenoxy-3,4-dihydro-quinolin-3-yl)-N-cyclohexyl-N-methyl-propionamide

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

5-(2-amino-5-phenoxy-phenyl)-4-cyano-pentanoic acid cyclohexyl-methyl-amide (0.20 g, 0.46 mmol) was dissolved in toluene (5 mL), followed by addition of aluminum chloride (0.184 g, 1.38 mmol). The reaction mixture was heated to reflux for 10 minutes and then allowed to cool to room temperature. The crude reaction mixture was poured into a separatory funnel and partitioned between ethyl acetate and 10% Na2CO3 solution. The organic layer was washed 2 more times with 10% Na2CO3 solution and one time with saturated brine solution. The organic layer was dried with anhydrous sodium sulfate and the solvent was removed under reduced pressure to yield a residue which was purified by flash chromatography using chloroform:methanol:triethylamine as the mobile phase to yield the title compound as a residue.

後処理

  1. temperatureThe reaction mixture was heated
  2. temperatureto reflux for 10 minutes
  3. customThe crude reaction mixture
  4. additionwas poured into a separatory funnel
  5. custompartitioned between ethyl acetate and 10% Na2CO3 solution
  6. washThe organic layer was washed 2 more times with 10% Na2CO3 solution and one time with saturated brine solution
  7. dry with materialThe organic layer was dried with anhydrous sodium sulfate
  8. customthe solvent was removed under reduced pressure
  9. customto yield a residue which
  10. customwas purified by flash chromatography

出典と根拠

ORDレコード
ord-119b3f1a4c44492c90ac9ce9a2edf19c
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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