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Chemical Structure| 187589-36-2 Chemical Structure| 187589-36-2

Structure of 187589-36-2

Chemical Structure| 187589-36-2

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Product Details of [ 187589-36-2 ]

CAS No. :187589-36-2
Formula : C5H9N3
M.W : 111.15
SMILES Code : N#CC1CNCCN1
English Name :Piperazine-2-carbonitrile
MDL No. :MFCD09878601

Safety of [ 187589-36-2 ]

Application In Synthesis of [ 187589-36-2 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 187589-36-2 ]

[ 187589-36-2 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 187589-35-1 ]
  • [ 187589-36-2 ]
YieldReaction ConditionsOperation in experiment
With sodium hydrogencarbonate In water
  • 2
  • [ 187589-36-2 ]
  • [ 859518-35-7 ]
YieldReaction ConditionsOperation in experiment
With triethylamine 1.B piperazine-2-carbonitrile Step B tert-Butyl 3-cyanopiperazine-1-carboxylate To a solution of compound piperazine-2-carbonitrile, prepared as described in the previous step, (90.6 g, 0.492 mol) was added triethylamine (206 mL, 1.476 mol) and Boc2O (117 g, 0.542 mol). The reaction mixture was stirred at room temperature overnight, and then concentrated. The residue was purified by silica gel chromatography to provide the title compound. 1H NMR: (CDCl3, 400 MHz): δ (ppm) 4.06-3.91 (m, 3H), 3.28-2.83 (m, 4H), 1.47 (s, 9H).
  • 3
  • [ 187589-36-2 ]
  • [ 24424-99-5 ]
  • [ 859518-35-7 ]
YieldReaction ConditionsOperation in experiment
With triethylamine at 20℃; 1.B tert-Butyl 3-cyanopiperazine-1-carboxylate To a solution of compound piperazine-2-carbonitrile, prepared as described in the previous step, (90.6 g, 0.492 mol) was added triethylamine (206 mL, 1.476 mol) and Boc2O (117 g, 0.542 mol). The reaction mixture was stirred at room temperature overnight, and then concentrated. The residue was purified by silica gel chromatography to provide the title compound. 1H NMR: (CDCl3, 400 MHz): δ (ppm) 4.06-3.91 (m, 3H), 3.28-2.83 (m, 4H), 1.47 (s, 9H).
With triethylamine at 20℃; 1.B Step B
tert-Butyl 3-cyanopiperazine-1-carboxylate To a solution of compound piperazine-2-carbonitrile, prepared as described in the previous step, (90.6 g, 0.492 mol) was added triethylamine (206 mL, 1.476 mol) and Boc2O (117 g, 0.542 mol). The reaction mixture was stirred at room temperature overnight, and then concentrated. The residue was purified by silica gel chromatography to provide the title compound. 1H NMR: (CDCl3, 400 MHz): δ (ppm) 4.06-3.91 (m, 3H), 3.28-2.83 (m, 4H), 1.47 (s, 9H).
  • 4
  • [ 859518-35-7 ]
  • [ 187589-36-2 ]
YieldReaction ConditionsOperation in experiment
With trifluoroacetic acid In dichloromethane at 20℃; for 1h; 39 Piperazine-2-carbonitrile Example 39 Piperazine-2-carbonitrile To a mixture of tert-butyl 3-cyanopiperazine-1-carboxylate (200 mg, 0.95 mmol) in dichloromethane (10 mL), CF3COOH (2 mL) was added and the resulting was stirred at RT for 1 h. The mixture was concentrated in vacuo to afford the crude product.
With trifluoroacetic acid In dichloromethane at 20℃; for 1h; 51 Piperazine-2-carbonitrile To a mixture of tert-butyl 3 -cyanopiperazine- 1 -carboxylate (200 mg, 0.95 mmol) in dichioromethane (10 mL), CF3COOH (2 mL) was added and theresulting was stirred at RT for 1 h. The mixture was concentrated in vacuo to afford the crude product.
 

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