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[ CAS No. 571186-91-9 ] {[proInfo.proName]}

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Chemical Structure| 571186-91-9
Chemical Structure| 571186-91-9
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CAS No. :571186-91-9 MDL No. :
Formula : C29H31N7O2 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 509.60 Pubchem ID :-
Synonyms :

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Signal Word: Class:N/A
Precautionary Statements: UN#:N/A
Hazard Statements: Packing Group:N/A

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* 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 [ 571186-91-9 ]

[ 571186-91-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 152459-95-5 ]
  • [ 571186-91-9 ]
YieldReaction ConditionsOperation in experiment
With 3-chloro-benzenecarboperoxoic acid In dichloromethane at -20 - 20℃; for 72h; 4.1.9. 4-[(4-Methyl-4-oxido-1-piperazinyl)methyl]-N-[4-methyl-3-[[4-(3-pyridinyl)-2-pyrimidinyl]amino]-phenyl]benzamide (10) A stirred solution of 4-[[4-(methyl)-1-piperazinyl]methyl]-N-[4-methyl-3-[[4-(3-pyridinyl)-2-pyrimidinyl]amino]-phenyl]benzamide(1; 2 g, 4.05 mmol) in CH2Cl2 (70 mL) at 20 C was treatedwith MCPBA (2.06 g of 55%, 4.27 mmol) and stirred for 72 h atroom temperature. The mixture was evaporated to dryness underreduced pressure and the crude product was purified by columnchromatography (silica gel, water/CH3OH/CH2Cl2-5:30:70) andrecrystallised from EtOH to afford 10 as a yellow crystalline solid,mp 154-158 C; NMR (600 MHz; DMSO-d6) d 2.22 (s, 3H), 2.79-2.89 (m, 4H), 3.03 (s, 3H), 3.33-3.41 (m, 4H), 3.58-3.64 (m, 2H),7.20 (d, J = 8.5 Hz, 1H), 7.43 (d, J = 5.05 Hz, 1H), 7.44-7.47 (m,2H), 7.48 (dd, J = 8.1, 1.5 Hz, 1H), 7.52 (dd, J = 8.0, 4.7 Hz, 1H),7.91 (d, J = 7.9 Hz, 2H), 8.07 (s, 1H), 8.47 (d, J = 8.1 Hz, 1H), 8.51(d, J = 5.2 Hz, 1H), 8.68 (dd, J = 4.6, 1.1 Hz, 1H), 9.01 (s, 1H), 9.27(d, J = 1.6 Hz, 1H), 10.20 (s, 1H).
With 3-chloro-benzenecarboperoxoic acid
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Chemical Structure| 152459-95-5

A150400[ 152459-95-5 ]

N-(4-Methyl-3-((4-(pyridin-3-yl)pyrimidin-2-yl)amino)phenyl)-4-((4-methylpiperazin-1-yl)methyl)benzamide

Reason: Derivatives