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[ CAS No. 1616231-57-2 ] {[proInfo.proName]}

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Chemical Structure| 1616231-57-2
Chemical Structure| 1616231-57-2
Structure of 1616231-57-2 * Storage: {[proInfo.prStorage]}
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Product Details of [ 1616231-57-2 ]

CAS No. :1616231-57-2 MDL No. :
Formula : C27H18ClN3 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 419.90 Pubchem ID :-
Synonyms :

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Application In Synthesis of [ 1616231-57-2 ]

* 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 [ 1616231-57-2 ]

[ 1616231-57-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1700-02-3 ]
  • [ 1036378-83-2 ]
  • 2-([1,1′:3′,1″-terphenyl]-5′-yl)-4-chloro-6-phenyl-1,3,5-triazine [ No CAS ]
YieldReaction ConditionsOperation in experiment
70% With tetrakis(triphenylphosphine) palladium(0); potassium carbonate; In tetrahydrofuran; water; at 80℃; for 12h;Inert atmosphere; Synthesis Example 44: Synthesis of Intermediate I-44 Compound I-42 (50 g, 140 mmol) was dissolved in THF (1 L) under a nitrogen environment, Compound I-43 (31 g, 140 mmol) and tetrakis(triphenylphosphine)palladium (1.6 g, 1.4 mmol) were added thereto, and the mixture was stirred. Potassium carbonate saturated in water (48 g, 350 mmol) was added thereto, and the obtained mixture was heated and refluxed at 80 C. for 12 hours. When the reaction was complete, water was added to the reaction solution, and the mixture was extracted with dichloromethane (DCM) and then, filtered after removing moisture with anhydrous MgSO4 and concentrated under a reduced pressure. This obtained residue was separated and purified through flash column chromatography to obtain Compound I-44 (32 g and 70%). HRMS (70 eV, EI+): m/z calcd for C27H18ClN3: 419.1189. found: 419. Elemental Analysis: C, 77%; H, 4%
59% With tetrakis(triphenylphosphine) palladium(0); potassium carbonate; In tetrahydrofuran; water;Reflux; 2,4-dichloro-6-phenyl-1,3,5-Triazine 1eq (26.9g) and 1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-[1,1 ':3',1''-terphenyl]-5'-yl- 1.1eq(46.7g) was suspended in 350ml of THF and 170ml of distilled water, and then Pd(PPh3)4 0.05eq(6.8g) and potassium carbonate (K2CO3) 2eq (32.9g) was added and stirred under reflux. When the reaction was completed, the solvent was dried, dissolved in dichloromethane, dried over magnesium sulfate (MgSO4), filtered, and the filtrate was recrystallized from nucleic acid to obtain 29.7 g (Y=59%) of intermediate d-1.
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