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Chemical Structure| 10511-51-0 Chemical Structure| 10511-51-0

Structure of 10511-51-0

Chemical Structure| 10511-51-0

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Product Details of [ 10511-51-0 ]

CAS No. :10511-51-0
Formula : C16H13NO
M.W : 235.28
SMILES Code : O=CC1=CN(CC2=CC=CC=C2)C3=C1C=CC=C3
MDL No. :MFCD00022894

Safety of [ 10511-51-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H317-H319
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of [ 10511-51-0 ]

* 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 [ 10511-51-0 ]

[ 10511-51-0 ] Synthesis Path-Downstream   1~2

  • 2
  • [ 10511-51-0 ]
  • [ 6882-68-4 ]
  • 14-[N-benzyl-1H-indol-3-ylmethylene]sophoridine [ No CAS ]
YieldReaction ConditionsOperation in experiment
51% General procedure: A 100mL round-bottomed flask was charged with <strong>[6882-68-4]sophoridine</strong> (1.24g, 5mmol), NaH (2.4g, 100mmol) and anhydrous tetrahydrofuran (50mL). The solution was stirred at room temperature for 1h followed by addition of N-substituted indole-carboxyaldehyde (5mmol) and then refluxed for 48h. The reaction mixture was cooled and then poured into water slowly (100mL). It was then extracted with dichloromethane (3×40mL). The combined phases were dried with anhydrous Na2SO4 and concentrated to obtain crude product. The residue was purified by silica gel flash column chromatography (methanol/dichloromethane, 2%) to afford 5a-5y in 24%-53% yields.
51% With sodium hydride; In tetrahydrofuran; at 85℃; for 48h; 2.4 g (100 mmol) of sodium hydride and 50 mL of anhydrous tetrahydrofuran were added to a 100 mL round bottom flask.Stir well, add 1.24 g (5 mmol) of <strong>[6882-68-4]sophoridine</strong>, slowly warm to 85 C, add 1.41 g (6 mmol) of N-benzyl-3-indolaldehyde, and react for 48 h to the end point (TLC detection).After cooling to room temperature, excess sodium hydride was neutralized by dropwise addition of 3N hydrochloric acid.Dichloromethane extraction (40 mL×3), the organic phase was combined, dried over anhydrous Na2SO4.(V Dichloromethane: V methanol = 50:1) was purified to give 1.185 g of a white solid powder as a base compound LMY-22: 14-[N-benzylindolin-3-ylmethylene]<strong>[6882-68-4]sophoridine</strong> The yield is 51%;
 

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