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Chemical Structure| 1197160-55-6 Chemical Structure| 1197160-55-6

Structure of 1197160-55-6

Chemical Structure| 1197160-55-6

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Product Details of [ 1197160-55-6 ]

CAS No. :1197160-55-6
Formula : C26H29N7O5
M.W : 519.56
SMILES Code : O=C(OC)C1=CC=C(NC(NC2=CC=C(C3=NC(N4CCOCC4)=NC(N5CCOCC5)=N3)C=C2)=O)C=C1
MDL No. :MFCD16875677

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Application In Synthesis of [ 1197160-55-6 ]

* 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 [ 1197160-55-6 ]

[ 1197160-55-6 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 1197159-91-3 ]
  • [ 23138-53-6 ]
  • [ 1197160-55-6 ]
YieldReaction ConditionsOperation in experiment
90% In dichloromethane; at 20℃; for 5h;Product distribution / selectivity; The mixture of 4-(4,6-dimorpholin-4-yl-1,3,5-triazin-2-yl) aniline (4, 49 g, 0.14 mol) and methyl-4-isocyanato benzoate (5, 27.5 g, 0.15 mol) in dichloromethane (700 ml) was stirred at room temperature for 5 hours. To the reaction mixture was added ethyl ether (200 ml) and the solids were filtered. The cake was washed with 1 :1 dichloromethane/ether (200 ml) and ether. methyl 4-(3-(4-(4,6-dimorpholino-1,3,5- triazine-2-yl)ureido)benzoate was obtained as beige solids in 90 % yield (66 g, 0.12 mol); HPLC: 97 % product and 3 % of 4-(4,6-dimorpholin-4-yl-1,3,5-triazin-2-yl) aniline.
79% In dichloromethane; at 20℃; for 4h; 17A (2.17 g, 6.33 mmol) and methyl 4-isocyanatobenzoate (1.18 g, 6.65 mmol) were charged in a round bottom flask and dissolved in DCM (31.64 mL). The reaction stirred at room temperature for 4 hours. The product was precipitated with the addition of MTBE (50 mL), and the solid was isolated by vacuum filtration. The powder cake was washed with a 1 : 1 DCM/MTBE (50 mL) before it was dried under vacuum. 2.59 g of Compound 17B (79%) was obtained as an off-white solid (M+H = 520.3).
  • 2
  • [ 1197159-91-3 ]
  • [ 198476-21-0 ]
  • [ 1197160-55-6 ]
YieldReaction ConditionsOperation in experiment
75.6% With dmap; In dichloromethane; at 20℃; for 48h; Synthetic method: <strong>[1197159-91-3]4-(4,6-bismorpholine 1,3,5-triazin-2-yl)aniline</strong> (2.0 g, 5.84 mmol) was dissolved in CH2Cl2 (20 mL).DMAP (36 mg, 0.29 mmol) was added followed by methyl 4-isocyanobenzoate (1.30 g, 7.33 mmol).The solvent was evaporated under reduced pressure. EtOAc m.The solvent was evaporated under reduced pressure, and the residue was separated by column chromatography.Eluent: DCM / MeOH = 30/1 gave 2.29 g of the desired product.Yield: 75.6%.
 

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