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Chemical Structure| 946517-74-4 Chemical Structure| 946517-74-4

Structure of 946517-74-4

Chemical Structure| 946517-74-4

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Product Details of [ 946517-74-4 ]

CAS No. :946517-74-4
Formula : C13H24N4O2
M.W : 268.36
SMILES Code : [N-]=[N+]=NCCCC1CCN(C(OC(C)(C)C)=O)CC1

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Application In Synthesis of [ 946517-74-4 ]

* 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 [ 946517-74-4 ]

[ 946517-74-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 946517-74-4 ]
  • [ 150349-65-8 ]
YieldReaction ConditionsOperation in experiment
95% With water; triphenylphosphine; In tetrahydrofuran; at 20℃; To a solution of 4-(3-azido-propyl)-piperidine-l-cafboxylic acid tert-butyl ester (1.738 g, 6.48 mmol) in dry tetrahydrofuran (50 mL) water (0.49 mL) and triphenyl phosphine (3.4 g, 12.96 mmol) were added. The reaction mixture was stirred at room temperature overnight, then concentrated. The residue was purified by column chromatography using Kieselgel 60 (0.015-0.040 mm) (Merck) as adsorbent, and methanol: ammonium hydroxide = 10:1 as eluent to yield 1.498 g (95 %) of the title compound. MS (EI) 243.2 (MH+).
95% With water; triphenylphosphine; In tetrahydrofuran; at 20℃; To a solution of 4-(3-azido-propyl)-piperidine-l-carboxylic acid tert-butyl ester (1.738 g, 6.48 mmol) in dry tetrahydrofuran (50 mL) water (0.49 mL) and triphenyl phosphine (3.4 g, 12.96 mmol) were added. The reaction mixture was stirred at room temperature overnight, then concentrated. The residue was purified by column chromatography using Kieselgel 60 (0.015-0.040 mm) (Merck) as adsorbent, and methanol: ammonium hydroxide = 10:1 as eluent to yield 1.498 g (95 %) of the title compound. MS (EI) 243.2 (MH+).
83% With triphenylphosphine; In tetrahydrofuran; water; acetonitrile; at 20℃; for 18h; (C). Preparation of 4-(3-aminopropyl)-piperidine-1-carboxylic acid tert-butyl ester; Triphenylphosphine (0.657 g, 2.50 mmol) is added to a stirred solution of 4-(3-azido-propyl)-piperidine-1-carboxylic acid tert-butyl ester (0.560 g, 2.09 mmol) in THF (2 mL)/CH3CN (5 mL)/H2O (1 mL) and the mixture is stirred at ambient temperature for 18 hours. After concentration and subsequent chromatography purification on silica gel, eluting with 2 M NH3/MeOH in dichloromethane 0-15%, the title compound is obtained as a clear oil (0.420 g, 83% yield).
 

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