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Chemical Structure| 247058-06-6 Chemical Structure| 247058-06-6

Structure of 247058-06-6

Chemical Structure| 247058-06-6

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Product Details of [ 247058-06-6 ]

CAS No. :247058-06-6
Formula : C17H13N3O2
M.W : 291.30
SMILES Code : O=C(C1=CC(C2=NC=CC=C2)=NC(C3=NC=CC=C3)=C1)OC
MDL No. :MFCD11042546

Safety of [ 247058-06-6 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P302+P352-P305+P351+P338

Application In Synthesis of [ 247058-06-6 ]

* 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 [ 247058-06-6 ]

[ 247058-06-6 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 67-56-1 ]
  • [ 148332-36-9 ]
  • [ 247058-06-6 ]
YieldReaction ConditionsOperation in experiment
89% With thionyl chloride; at 60℃; for 16h; Compound 8 (5.05 g, 18.2 mmol) was dispersed in 200 ml of dry methanol and cooled to 0°C. Thionyl chloride (7.93 ml, 13.0 g, 109 mmol) was added dropwise. After complete addition the mixture was heated for 60°C and stirred for 16 h. The solvent was removed under reduced pressure and 80 mlof saturated aqueous NaHCO3 solution was added. The mixture wasextracted with DCM (3x50 ml). The combined organic phases weredried over Na2SO4 and the solvent was removed underreduced pressure. The product was obtained as a white solid. Yield: 4.74 g(89percent) mp:208-209°C.1H-NMR(500 MHz, DMSO-d6): delta 8.86 (s, 2H), 8.76 (ddd, J = 4.7 Hz, 1.7 Hz, 0.9 Hz, 2H), 6.64 (dt, J = 7.9 Hz, 0.9 Hz, 2H), 8.04 (td, J = 7.8 Hz, 1.8 Hz, 2H), 7.54 (ddd, J = 7.5 Hz, 4.7 Hz, 1.1 Hz, 2H), 3.98 (s, 3H) 13C-NMR (126 MHz, DMSO-d6): delta165.0, 156.1, 154.0, 149.5, 139.3, 137.6, 124.9, 120.9, 119.3, 52.9HRMS (ESI, m/z): calcd for C17H14N3O2 [M+H]+: 292.1081; Found: 292.1079.
General procedure: Typically, 2-(4-carboxyphenyl)-4,6-dipyrid-2-yltriazine (1.0 g,2.81 mmol) was heated to reflux in thionyl chloride (30 mL) for0.5 h, after which no solid suspension remained. The excess thionylchloride was removed by distillation and the residue was driedunder vacuum, dry methanol (60 mL) was added and the reactionmixture was heated to reflux until no solid suspension remained(2 h). The solution was cooled to room temperature and addedto H2O (300 mL) forming a voluminous precipitate of the methylester ligand which was isolated by filtration and dried in vacuowithout further purification. Typically, the ligand (0.25 g,0.68 mmol) was heated to reflux in DMF with RuCl3 (0.07 g,0.34 mmol) and AgNO3 (0.173 g, 1.02 mmol) after which the solutionwas filtered to remove AgCl(s). The filtrate was then decantedinto a solution of NH4PF6 (aq) (300 mL), and the resultant heavyprecipitate was isolated by filtration and washed with water, thendissolved in a minimal amount of acetonitrile for chromatographicpurification using silica and a 7:2 CH3CN/KNO3 (aq, sat) mixture aseluent. The collected fractions are combined, and to this addedNH4PF6 and enough DCM to effect a phase separation. After washingthe organic phase, the aqueous phase was discarded and theprocess repeated, with a final washing with water alone. Theorganic phase was dried and the residue taken up in a minimalamount of acetonitrile, then poured into H2O (300 mL) to give aheavy precipitate which was filtered and dried in vacuo. Yield:0.263 g (69percent), Rf = 0.55 (silica, 7:2 CH3CN/KNO3 (sat, aq) as eluent).1H NMR (400 MHz, CD3CN) d ppm 9.19 (d, J = 8.4 Hz, 4H), 9.14 (d,J = 7.7 Hz, 4H), 8.44 (d, J = 8.4 Hz, 4H), 8.16 (m, 4H), 7.73 (d,J = 5.3 Hz, 4H), 7.41 (m, 4H), 4.02 (s, 3H). ESI-MS: [M]2+ Cald. forC42H30N10O4Ru: 420.07475. Found: 420.07499.
  • 2
  • [ 148332-36-9 ]
  • [ 74-88-4 ]
  • [ 247058-06-6 ]
YieldReaction ConditionsOperation in experiment
With potassium carbonate; In N,N-dimethyl-formamide; at 20℃; for 16h;Inert atmosphere; (Step 1)To a solution of 2,2?:6?,2?-terpyridine-4?-carboxylic acid (200 mg, 0.72 mmol) in DMF (3.6 mE) were added potassium carbonate (20 mg, 1.4 mmol) and methyl iodide (0.07mE, 1.1 mmol), and the reaction mixture was stirred at room temperature for 16 hr. To the reaction mixture was added brine, and the aqueous layer was extracted with ethyl acetate (3x5.0 mE), and the extract was washed with brine, anddried over magnesium sulfate. The mixture was filtered, and concentrated under reduced pressure to give a crude product.The obtained crude product was used for the next reaction without purification. To a solution of the crude product (0.72 mmol) in tetrahydrofuran (7.2 mE) was added lithium alu15 minum hydride (28 mg, 0.7 mmol) at 00 C. After stirring for3 hr, sodium sulfate 10 hydrate was added to the reactionmixture, and the mixture was stirred at room temperature for1 hr. The reaction mixture was filtered through a celite pad,and the filtrate was concentrated under reduced pressure. The residue was dissolved in pyridine (3.6 mE), and acetic anhydride (0.14 mE, 1.4 mmol) was added to the solution. Afier stirring for 16 hr, toluene was added to the mixture, and concentrated under reduced pressure. The residue waspurified by CHROMATOREX Diol silica gel column chromatography (eluent: n-hexane:ethyl acetate=1:0-1 :1) to give 2,2?:6?,2?-terpyridine-4?-ylmethyl acetate (88 mg, yield 40%3 steps) as a white solid.
 

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