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Chemical Structure| 61196-37-0 Chemical Structure| 61196-37-0

Structure of 61196-37-0

Chemical Structure| 61196-37-0

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Product Details of [ 61196-37-0 ]

CAS No. :61196-37-0
Formula : C12H14N2O
M.W : 202.25
SMILES Code : O=C1CNCC2N1CCC3=C2C=CC=C3
MDL No. :MFCD09743876

Safety of [ 61196-37-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 61196-37-0 ]

* 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.

  • Upstream synthesis route of [ 61196-37-0 ]
  • Downstream synthetic route of [ 61196-37-0 ]

[ 61196-37-0 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 61196-37-0 ]
  • [ 5234-86-6 ]
YieldReaction ConditionsOperation in experiment
98%
Stage #1: With lithium aluminium tetrahydride In tetrahydrofuran for 6 h; Heating / reflux
Stage #2: With sodium hydroxide; water In tetrahydrofuran at 0℃;
Example 2; 2-(l,3,4,6,7,llbηexahydro-pyrazino[2,l-a]isoquinolin-2-yl)-3"methyl- 6-pyridin-4-yl-3H-pyrimidin-4-one (Compound No.Bl09); 1,3,4.6,7, llb-Hexahvdro-2H-pvrazino[2, l-alisoquinoline; 1,2,3,6,7, llb-Hexahydro-pyrazino[2,l-a]isoquinolin"4-one (3.03 g, 15.0 mmol) was added to a solution of lithium aluminum hydride (1.14 g, 30.0 mmol) in tetrahydrofuran (63 ml) and the mixture was refluxed for 6 hours. Water (1.2 ml), 15percent aqueous sodium hydroxide (1.2 ml) and water (3.2 ml) were added sequentially to the ice"cooled solution, and filtration of the precipitate and removal of the solvent under reduced pressure afforded 1,3, 4,6,7, llb-hexahydro-2H-pyrazino[2,l-a] isoquinoline (2.77 g, 98percent).
35% With lithium aluminium tetrahydride In tetrahydrofuran at 0℃; for 10 h; Inert atmosphere; Reflux Compound 1 (3.03 g, 15 mmol) was added to a solution of lithium aluminum hydride (1.14 g, 30 mmol) in tetrahydrofuran (63 mL) and the mixture was refluxed for 10 h After cooled to 0 °C, the reaction was quenched with aqueous sodium hydroxide (15percent, 1.2 mL), and the precipitate was filtrated. The organic phases were then processed in the usual way and chromatographed (10:1 CH2Cl2/MeOH) to afforded compound 16 (1 g, 35percent) as red oil.
References: [1] Patent: WO2007/119463, 2007, A1, . Location in patent: Page/Page column 180.
[2] Molecules, 2013, vol. 18, # 8, p. 9163 - 9178.
 

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