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Water → HCID 59900540、化合物

HRID 2228769
ノート
印刷プレビュー

反応式

HRID 2228769 の反応式
[H-].[Al+3].[Li+].[H-].[H-].[H-].[CH2:7]([N:14]1[CH2:19][CH2:18][C@@H:17]([CH3:20])[CH2:16][C@@H:15]1[C:21]([NH2:23])=O)[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1.O.[OH-].[Na+]>O1CCCC1>[NH3:14].[CH2:7]([N:14]1[CH2:19][CH2:18][C@@H:17]([CH3:20])[CH2:16][C@@H:15]1[CH2:21][NH2:23])[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 962Water2 回HCID 14798Sodium HydroxideHCID 21226445Aluminium lithium hydrideHCID 53986202HCID 53986202、化合物

生成物 2

HCID 222AmmoniaHCID 59900540HCID 59900540、化合物収率 39.7%

試薬・触媒・溶媒 1

HCID 8028
Tetrahydrofuran
溶媒

実験手順

Lithium aluminium hydride (9.2 ml, 1 M in tetrahydrofuran, 9.2 mmol) was added to a solution of (2R,4R)-1-benzyl-4-methyl-2-piperidinecarboxamide (preparation 86) (3.5 g, 15.0 mmol) in tetrahydrofuran (60 ml), and the reaction heated under reflux ovemight. The reaction was cooled in an ice-bath, water (0.4 ml), 15% NaOH solution (0.4 ml), and water (1.2 ml) were added consecutively, and the resulting precipitate filtered off. The filtrate was concentrated under reduced pressure, re-dissolved in dichloromethane and washed with brine, dried over Na2SO4 and evaporated under reduced pressure. The crude product was purified by column chromatography on silica gel using an elution gradient of dichloromethane:methanol:0.88 ammonia (100:0:0 to 85:15:1) to give the title compound as a yellow oil, (650 mg, 20%).

後処理

  1. temperaturethe reaction heated
  2. temperatureunder reflux ovemight
  3. temperatureThe reaction was cooled in an ice-bath
  4. filtrationthe resulting precipitate filtered off
  5. concentrationThe filtrate was concentrated under reduced pressure
  6. dissolutionre-dissolved in dichloromethane
  7. washwashed with brine
  8. dry with materialdried over Na2SO4
  9. customevaporated under reduced pressure
  10. customThe crude product was purified by column chromatography on silica gel using an elution gradient of dichloromethane

出典と根拠

ORDレコード
ord-073a98b8362a4a3c973e629cf3e443f7
出典データセット
uspto-grants-2002_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06417203B1

反応ノート

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