Ethyl Acetate → 1-Acetyl-4-[3-(piperidin-1-yl)phenylamino]-piperidine dihydrochloride

HRID 1079399ノート

反応式

HRID 1079399 の反応式
[ClH:1].Cl.[NH2:3][C:4]1[CH:5]=[C:6]([N:10]2[CH2:15][CH2:14][CH2:13][CH2:12][CH2:11]2)[CH:7]=[CH:8][CH:9]=1.[C:16]([N:19]1[CH2:24][CH2:23][C:22](=O)[CH2:21][CH2:20]1)(=[O:18])[CH3:17].C([BH3-])#N.[Na+].C(OCC)(=O)C>CO.O>[ClH:1].[ClH:1].[C:16]([N:19]1[CH2:24][CH2:23][CH:22]([NH:3][C:4]2[CH:9]=[CH:8][CH:7]=[C:6]([N:10]3[CH2:15][CH2:14][CH2:13][CH2:12][CH2:11]3)[CH:5]=2)[CH2:21][CH2:20]1)(=[O:18])[CH3:17]

参加物

7

反応物 4

HCID 8857Ethyl AcetateHCID 122563N-Acetyl-4-piperidoneHCID 5003444Sodium cyanoborohydrideHCID 233669441-(3-Aminophenyl)piperidine dihydrochloride

生成物 1

HCID 233669001-Acetyl-4-[3-(piperidin-1-yl)phenylamino]-piperidine dihydrochloride収率 132.1%

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 962Water溶媒

実験手順

To a solution of N-(3-aminophenyl)piperidine dihydrochloride (3.73 g) and 1-acetyl-4-piperidone (2.1 g) in methanol (30 ml) was added sodium cyano borohydride (1.9 g), followed by stirring at room temperature for 5 hours. To the mixture were added ethyl acetate ester (20 ml) and water (30 ml), the organic layer was dried over anhydrous sodium sulfate and then the solvent was distilled off. The residual oily compound was separated and purified by silica gel column chromatography (developing solvent: ethyl acetate ester). The oily compound was dissolved in dioxane (10 ml) and to the mixture was added 6N solution of hydrogen chloride in dioxane (2 ml). Then, the solvent was removed to obtain a colorless amorphous solid (3.7 g).

後処理

  1. dry with materialthe organic layer was dried over anhydrous sodium sulfate
  2. distillationthe solvent was distilled off
  3. customThe residual oily compound was separated
  4. custompurified by silica gel column chromatography (developing solvent: ethyl acetate ester)
  5. dissolutionThe oily compound was dissolved in dioxane (10 ml) and to the mixture
  6. additionwas added 6N solution of hydrogen chloride in dioxane (2 ml)
  7. customThen, the solvent was removed

出典と根拠

ORDレコード
ord-3f0c13b8f65045b798b39ce173b37ba1
出典データセット
uspto-grants-1996_12
特許番号
US05580883

反応ノート

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