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Chemical Structure| 479226-58-9 Chemical Structure| 479226-58-9

Structure of 479226-58-9

Chemical Structure| 479226-58-9

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Product Details of [ 479226-58-9 ]

CAS No. :479226-58-9
Formula : C13H19ClN4O2
M.W : 298.77
SMILES Code : O=C(N1CCN(C2=NC=C(Cl)N=C2)CC1)OC(C)(C)C
MDL No. :MFCD14581981

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Application In Synthesis of [ 479226-58-9 ]

* 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 [ 479226-58-9 ]

[ 479226-58-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 19745-07-4 ]
  • [ 57260-71-6 ]
  • [ 479226-58-9 ]
YieldReaction ConditionsOperation in experiment
93% With potassium carbonate; In dimethyl sulfoxide; at 75℃; A solution of <strong>[19745-07-4]2,5-dichloropyrazine</strong> (1.03 g, 6.91 mmol) in DMSO (10 mL) was treated sequentially with K2C03(s) (2.867 g, 20.74 mmol) and tert-butyl piperazine-1-carboxylate (1.288 g, 6.9 14 mmol), then stirred overnight at 75 °C. After cooling to ambient temperature, the mixture was partitioned between EtOAc (10 mL) and water (20 mL). After phase separation, the organic extracts were concentrated in vacuo to provide the title compound (1.928 g, 93percent yield). MS (apci) m/z = 199.1 (M-Boc). ?HNIVIR(CDC13) 8.07 (m, 1H), 7.86 (m, 1H), 3.56 (s, 8H), 1.48 (s, 9H).
With potassium carbonate; In 1-methyl-pyrrolidin-2-one; at 100℃; for 1h; To an NMP (7.5 ml) solution of 1.51 g of <strong>[19745-07-4]2,5-dichloropyrazine</strong> were added 2.00 g of 1-(t-butoxycarbonyl)piperazine and 2.00 g of potassium carbonate, followed by 1 hour of stirring under heating at 100°C. The mixture was cooled to room temperature, and water was added thereto, followed by extraction with ethyl acetate. The organic layer was washed with water and brine and then dried over anhydrous magnesium sulfate, and thereafter, the solvent was evaporated. The residue was purified by silica gel column chromatography (chloroform-methanol) to obtain 2.73 g of 2-chloro-5-(4-t-butoxycarbonylpiperazin-1-yl)pyrazine. Using this compound, 2-chloro-5-{4-[6-(3,4-dimethoxyphenyl)pyridine-2-carbonyl]piperazin-1-yl}pyrazine was obtained in a similar manner to Example 14 as colorless crystals.
 

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