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Chemical Structure| 601514-58-3 Chemical Structure| 601514-58-3

Structure of 601514-58-3

Chemical Structure| 601514-58-3

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Product Details of [ 601514-58-3 ]

CAS No. :601514-58-3
Formula : C15H16N2O
M.W : 240.30
SMILES Code : O=C1NC2=C(CN(CC3=CC=CC=C3)CC2)C=C1
MDL No. :MFCD11518944
InChI Key :BKSOOBNVMGYWAN-UHFFFAOYSA-N
Pubchem ID :22335145

Safety of [ 601514-58-3 ]

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

Application In Synthesis of [ 601514-58-3 ]

* 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 [ 601514-58-3 ]

[ 601514-58-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 601514-58-3 ]
  • [ 24424-99-5 ]
  • [ 1036381-91-5 ]
YieldReaction ConditionsOperation in experiment
With hydrogen; N-ethyl-N,N-diisopropylamine;palladium dihydroxide; In ethanol; under 4654.46 Torr; The Step 2 product (2 g, 8.32 mmol) was weighed into a Parr shaker bottle and dissolved in 20 mL of EtOH. Hunigs base (4.34 mL, 25 mmol), (Boc) 20 (2.36 g, 10.8 mmol) and catalyst (0.234 g, 1.7 mmol) were added. The bottle was placed on the Parr shaker and flushed 3* with H2. The reaction was placed under 90 psi H2 and left over the weekend. The reaction was filter through a glass frit packed with celite. The bottle was rinsed 3* with 5 mL MeOH and passed through the frit as well. The volatiles were evaporated and the residue dissolved in 10 mL of DCM. The solution was extracted with sat. bicarbonate. The organic layer was dried with sodium sulfate, filtered through a glass wool plug and the volatiles evaporated. This yielded a white solid, tert-butyl 3-bromo-2-oxo-1,2,7,8-tetrahydro-1,6-naphthyridine-6(5H)-carboxylate, (2.05 g). MS [M+H]+=251.13.
 

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[ 601514-58-3 ]

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