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1-Benzyl-2-piperidone → 5-Phenyl-3-[1-(phenylmethyl)-1,2,3,6-tetrahydro-4-pyridinyl]-1H-indole-7-carboxamide

HRID 2267482
ノート
印刷プレビュー

反応式

HRID 2267482 の反応式
[C:1]1([C:7]2[CH:8]=[C:9]3[C:13](=[C:14]([C:16]([NH2:18])=[O:17])[CH:15]=2)[NH:12][CH:11]=[CH:10]3)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH2:19]([N:26]1[CH2:31][CH2:30][CH2:29][CH2:28][C:27]1=O)[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1.C[O-].[Na+]>CO>[C:1]1([C:7]2[CH:8]=[C:9]3[C:13](=[C:14]([C:16]([NH2:18])=[O:17])[CH:15]=2)[NH:12][CH:11]=[C:10]3[C:29]2[CH2:30][CH2:31][N:26]([CH2:19][C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=3)[CH2:27][CH:28]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 51700761-Benzyl-2-piperidoneHCID 10942334Sodium MethoxideHCID 112070915-phenyl-1H-indole-7-carboxamide

生成物 1

HCID 114525415-Phenyl-3-[1-(phenylmethyl)-1,2,3,6-tetrahydro-4-pyridinyl]-1H-indole-7-carboxamide収率 54.4%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
80 °C

実験手順

To the solution of 5-phenyl-1H-indole-7-carboxamide (3.11 g, 12 mmol) in methanol (100 mL) was added benzyl piperidone (7.4 g, 36 mmol), followed by 156 mL of NaOMe (0.5 M in MeOH). The reaction mixture was then heated at 80° C. overnight. The solution was cooled to ambient temperature and the solvent removed under reduced pressure, and the resulting residue redisolved in a bilayer of ethyl acetate and 5% sodium hydroxide solution. The organic phase washed with brine, dried over potassium carbonate, and the solvent removed under reduced pressure. The residue was purified by silica gel chromatography (CH2Cl2:MeOH:NH4OH=96:3:1) to provide the desired product (2.66 g, 51%).

後処理

  1. temperatureThe solution was cooled to ambient temperature
  2. customthe solvent removed under reduced pressure
  3. washThe organic phase washed with brine
  4. dry with materialdried over potassium carbonate
  5. customthe solvent removed under reduced pressure
  6. customThe residue was purified by silica gel chromatography (CH2Cl2:MeOH:NH4OH=96:3:1)

出典と根拠

ORDレコード
ord-a8ad7f01f3d84c81837c1564f27f1d03
出典データセット
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07858796B2

反応ノート

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