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Chemical Structure| 886588-63-2 Chemical Structure| 886588-63-2

Structure of 886588-63-2

Chemical Structure| 886588-63-2

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Product Details of [ 886588-63-2 ]

CAS No. :886588-63-2
Formula : C33H30N8O4
M.W : 602.64
SMILES Code : O=C(N1CC2=NC(C)=C3C=CC=CC3=N2)N(C)C4=C(N(CC#CC)C(N5C[C@H](N(C(C6=C7C=CC=C6)=O)C7=O)CCC5)=N4)C1=O

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Application In Synthesis of [ 886588-63-2 ]

* 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 [ 886588-63-2 ]

[ 886588-63-2 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 666816-98-4 ]
  • [ 853029-57-9 ]
  • [ 886588-63-2 ]
  • 2
  • [ 853029-57-9 ]
  • 3-(R)-piperidinyl phthalimide hydrochloride [ No CAS ]
  • [ 886588-63-2 ]
YieldReaction ConditionsOperation in experiment
88.7% 1-[(4-methyl-quinazolin-2-yl)methyl]-3-methyl-7-(2-butyn-1-yl)-8-bromoxanthine (Compound VIII, 1.86 g, 0.0041 mol), potassium carbonate (base, 2.27 g, 0.016 mol), (R)-3-phthalimidopiperidine hydrochloride (Compound IV, 1.2 g, 0.0045 mol) and isopropyl acetate (50 mL) were added to a reaction flask and stirred for 0.5 hours, followed by addition of trimethylbenzylammonium chloride (PTC, 0.23 g, 0.001 mol). The mixture in the reaction flask was heated to reflux for 16 hours, cooled to room temperature, added with 50 mL of water, stirred and filtered. The filter cake was dissolved in 100 mL of dichloromethane, and washed with 5% diluted HCl, water and saturated sodium chloride solution, respectively. The above dichloromethane solution was concentrated to give the xanthine precursor, i.e. 1-[(4-methyl-quinazolin-2-yl)methyl]-3-methyl-7-(2-butyn-1-yl)-8-(3-(R)-phthalimido-piperidin-1-yl)xanthine. (0128) Yield: 2.19 g (88.7% of theoretical value) (0129) MS: [M+H]+=603.1
  • 3
  • [ 853029-57-9 ]
  • [ 886588-62-1 ]
  • [ 886588-63-2 ]
 

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