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Chemical Structure| 101336-63-4 Chemical Structure| 101336-63-4

Structure of 101336-63-4

Chemical Structure| 101336-63-4

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Product Details of [ 101336-63-4 ]

CAS No. :101336-63-4
Formula : C10H11ClN4O2
M.W : 254.67
SMILES Code : O=[N+](/C=C1NCCN/1CC2=CN=C(Cl)C=C2)[O-]
MDL No. :MFCD05670547

Safety of [ 101336-63-4 ]

Application In Synthesis of [ 101336-63-4 ]

* 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 [ 101336-63-4 ]

[ 101336-63-4 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 6971-45-5 ]
  • [ 101336-63-4 ]
  • [ 111-30-8 ]
  • [ 1534384-25-2 ]
  • 2
  • [ 1794-45-2 ]
  • [ 101336-63-4 ]
  • (5R,7S)-7-(2-chlorophenyl)-1-((6-chloropyridin-3-yl)methyl)-5-methoxy-8-nitro-1,2,3,5,6,7-hexahydroimidazo[1,2-a]pyridine [ No CAS ]
  • (5S,7R)-7-(2-chlorophenyl)-1-((6-chloropyridin-3-yl)methyl)-5-methoxy-8-nitro-1,2,3,5,6,7-hexahydroimidazo[1,2-a]pyridine [ No CAS ]
  • (5R,7R)-7-(2-chlorophenyl)-1-((6-chloropyridin-3-yl)methyl)-5-methoxy-8-nitro-1,2,3,5,6,7-hexahydroimidazo[1,2-a]pyridine [ No CAS ]
  • (5S,7S)-7-(2-chlorophenyl)-1-((6-chloropyridin-3-yl)methyl)-5-methoxy-8-nitro-1,2,3,5,6,7-hexahydroimidazo[1,2-a]pyridine [ No CAS ]
  • 3
  • [ 1794-45-2 ]
  • [ 101336-63-4 ]
  • C19H18Cl2N4O3 [ No CAS ]
YieldReaction ConditionsOperation in experiment
With (2S)-2-{diphenyl[(trimethylsilyl)oxy]methyl}pyrrolidine; acetic acid; In dichloromethane; at -20℃; General procedure: To a solution of the catalyst 4c (10mol%, 0.01mmol, 6.5mg) in CH2Cl2 (1.0mL) was added nitro-methylene imidazole 1 (0.1mmol), and the mixture was cooled to -20C, and then the alpha,beta-unsaturated aldehyde 2 (0.15mmol) and acetic acid (0.1mmol, 11.4mg) were added. The resulting mixture was vigorously stirred at -20C. When the reaction was finished (determined by TLC analysis), the crude mixture was warmed to the room temperature. Saturated NaHCO3 aqueous solution (10mL) was added to quench the reaction. And the resulting mixture was extracted with CH2Cl2 (15mL×3) and the combined organic layer was washed by brine (10mL). The combined organic extracts were dried over Na2SO4, and filtered and concentrated in vacuo. The crude product was purified by column chromatography to afford the products 3. (0012) For entries 8-16, the alcohol product was diluted in the methanol (2.0mL), p-TsOH (0.01mmol, 1.7mg) was added and reflux until the reaction completed. Saturated NaHCO3 aqueous solution (10mL) was added to quench the reaction. And the resulting mixture was extracted with CH2Cl2 (15mL×3) and the combined organic layer was washed by brine (10mL). The combined organic extracts were dried over Na2SO4, and filtered and concentrated in vacuo. The crude product was purified by column chromatography to afford the methyl ethers product.
 

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