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Chemical Structure| 23099-21-0 Chemical Structure| 23099-21-0

Structure of 23099-21-0

Chemical Structure| 23099-21-0

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Product Details of [ 23099-21-0 ]

CAS No. :23099-21-0
Formula : C6H14N2
M.W : 114.19
SMILES Code : NCC1CNCCC1
MDL No. :MFCD03427344

Safety of [ 23099-21-0 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H227-H314
Precautionary Statements:P210-P260-P264-P280-P301+P330+P331+P310-P303+P361+P353+P310+P363-P304+P340+P310-P305+P351+P338+P310-P403+P235-P405-P501
Class:8
UN#:2735
Packing Group:

Application In Synthesis of [ 23099-21-0 ]

* 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 [ 23099-21-0 ]

[ 23099-21-0 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 23099-21-0 ]
  • [ 93107-30-3 ]
  • 7-(3-Aminomethyl-piperidin-1-yl)-1-cyclopropyl-6-fluoro-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid [ No CAS ]
  • 2
  • [ 4138-26-5 ]
  • [ 23099-21-0 ]
YieldReaction ConditionsOperation in experiment
55% Piperidine-3-carboxylic acid amide 1a (25 g, 0.195 mol) was added portionwise to a stirred solution of lithium aluminum hydride (14.8 g, 0.39 mol, 2.0 equiv) in dry THF (0.6 L). When the initial effervescence had subsided, the reaction was heated at reflux under N2 at rt for 24 h. The reaction was quenched by dropwise addition of saturated sodium sulfate solution with stirring until no further effervescence was observed. The suspension was filtered through a celite plug, washed with THF (400 mL), and the filtrate concentrated under reduced pressure. The crude residue was distilled to yield pure product 1b as a colorless oil (12.4 g, 55percent).
In tetrahydrofuran; methanol; EXAMPLE XIV 3-Aminomethylpiperidine 7 g of <strong>[4138-26-5]piperidine-3-carboxamide</strong> in 30 ml of tetrahydrofuran are added dropwise in portions to 8 g of lithium aluminium hydride in 250 ml of tetrahydrofuran while stirring at room temperature. The mixture is then heated to boiling for 10 hours. It is cooled to 0° C., and 10percent strength potassium hydroxide solution is cautiously added dropwise until a white precipitate has formed. After decantation, the precipitate is washed four times by addition of 50 ml of tetrahydrofuran and decantation each time. The organic phases are combined, the solvent is distilled off in a rotary evaporator, and the residue is puritied by column chromatography on alumina with a methylene chloride/methanol (16:1) mixture. Yield: 4.8 g (77percent of theory) as colourless oil. The following compound is obtained in analogy to Example XIV:
  • 3
  • [ 23099-21-0 ]
  • [ 1022980-69-3 ]
  • [ 1217709-55-1 ]
 

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