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Chemical Structure| 936368-55-7 Chemical Structure| 936368-55-7

Structure of 936368-55-7

Chemical Structure| 936368-55-7

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Product Details of [ 936368-55-7 ]

CAS No. :936368-55-7
Formula : C15H22N4O4
M.W : 322.36
SMILES Code : O=[N+](C1=C(C)N=C(N2CCN(C(OC(C)(C)C)=O)CC2)C=C1)[O-]

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Application In Synthesis of [ 936368-55-7 ]

* 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 [ 936368-55-7 ]

[ 936368-55-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 22280-60-0 ]
  • [ 57260-71-6 ]
  • [ 936368-55-7 ]
YieldReaction ConditionsOperation in experiment
99% With triethylamine; In butan-1-ol; at 20 - 65℃; Mechanically stir mixture of <strong>[22280-60-0]6-chloro-2-methyl-3-nitro-pyridine</strong> (Asymchem, 25.00 g, 144.9 mmol), tert-butyl 1-piperazinecarboxylate (29.68 g, 159.4 mmol), and triethylamine (23.2 niL, 167 mmol) in K-BuOH (250 mL) at 50 C under nitrogen for 4 hours, at 65 C for 2 hours, then at room temperature overnight. Add additional tert-butyl 1-piperazinecarboxylate (1.5 g), and heat the reaction at 65 C for 4 hours. Cool the resulting slurry to 30 C then add hexanes (75 mL). Cool the slurry to room temperature over 1 hour, then add water (150 mL). Allow the slurry to stand for 45 min then filter. Wash the cake with water (4 x 100 mL) then hexanes (100 mL) and air-dry overnight to yield 4-(6-methyl-5-nitro-pyridin-2-yl)- rhoiperazine-1-carboxylic acid tert-butyl ester as bright yellow crystals (46.30 g, 99% yield, MS(ES): m/z = 267 [MH-H-C4H8]).
With N-ethyl-N,N-diisopropylamine; In acetonitrile; at 50℃; for 4h; Step 1HLJNIG base (62.82 mL, 0.435 mol) is added to the solution of 6-chloro-3-nitro-2- methylpyridine SM-3 (50 g, 290 mmol) and N-Boc-piperazine SM-5b (53.95 g, 290 mmol) in dry AcCN (200 mL) and stirred for 4 h at 50 C. After the reaction is finished the reaction mixture is diluted with AcCN and water and stirred for 30 min. The precipitated product is collected by filtration, washed with water and the solid is dried in vacuo.
With N-ethyl-N,N-diisopropylamine; In acetonitrile; at 50℃; for 4h; HUeNIG base (62.82 mL, 0.435 mol) is added to the solution of <strong>[22280-60-0]6-chloro-3-nitro-2-methylpyridine</strong> SM-3 (50 g, 290 mmol) and N-Boc-piperazine SM-5b (53.95 g, 290 mmol) in dry AcCN (200 mL) and stirred for 4 h at 50 C. After the reaction is finished the reaction mixture is diluted with AcCN and water and stirred for 30 min. The precipitated product is collected by filtration, washed with water and the solid is dried in vacuo.
With N-ethyl-N,N-diisopropylamine; for 4h; DIPEA (62.82 mL, 0.435 mol) is added to the solution of 6-chloro-3-nitro-2- methylpyridine (1) (50 g, 290 mmol) and N-Boc-piperazine (2) (53.95 g, 290 mmol) in dry MeCN (200 mL) and stirred for 4 h at 50 C. After the reaction is finished the reaction mixture is diluted with MeCN and water and stirred for 30 min. The precipitated product is collected by filtration, washed with water and the solid is dried in vacuo.

 

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