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Piperazine → 2-Fluoro-4-(piperazin-1-YL)benzonitrile

HRID 2354565
ノート
印刷プレビュー

反応式

HRID 2354565 の反応式
[NH:1]1[CH2:6][CH2:5][NH:4][CH2:3][CH2:2]1.C([O-])([O-])=O.[K+].[K+].[F:13][C:14]1[CH:21]=[C:20](F)[CH:19]=[CH:18][C:15]=1[C:16]#[N:17]>CC#N.CCOC(C)=O>[F:13][C:14]1[CH:21]=[C:20]([N:1]2[CH2:6][CH2:5][NH:4][CH2:3][CH2:2]2)[CH:19]=[CH:18][C:15]=1[C:16]#[N:17]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 4837PiperazineHCID 11430Potassium CarbonateHCID 775452,4-Difluorobenzonitrile

生成物 1

HCID 187600452-Fluoro-4-(piperazin-1-YL)benzonitrile

試薬・触媒・溶媒 2

HCID 6342Acetonitrile溶媒HCID 8857Ethyl Acetate溶媒

実験手順

Piperazine (20.0 g, 232.3 mmol) and K2CO3 (16.0 g, 118.5 mmol) are dissolved in CH3CN (85 ml). 2,4-Difluoro-benzonitrile (8.5 g, 61.1 mmol) is added and the mixture is stirred for 2 h at rt, then diluted with AcOEt and washed with water. The organic layer is separated, dried over Na2SO4 and evaporated. Excess piperazine is removed by MPLC (100 g silica gel, eluent CH2Cl2:MeOH 85:15). A second chromatographic purification (300 g silica gel, eluent toluene:EtOH:AcOH 4:4:1) yields the acetate salt of 2-fluoro-4-(piperazin-1-yl)-benzonitrile that is crystallized from AcOEt, filtered off and washed with ether. The free base is isolated by extraction with sat. aq. Na2CO3 solution/AcOEt.

後処理

  1. washwashed with water
  2. customThe organic layer is separated
  3. dry with materialdried over Na2SO4
  4. customevaporated
  5. customExcess piperazine is removed by MPLC (100 g silica gel, eluent CH2Cl2:MeOH 85:15)
  6. customA second chromatographic purification (300 g silica gel, eluent toluene:EtOH:AcOH 4:4:1)

出典と根拠

ORDレコード
ord-572eca8e33804dc6baa1dcb7fc7ae72d
出典データセット
uspto-grants-2010_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07754719B2

反応ノート

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