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Chemical Structure| 955978-85-5 Chemical Structure| 955978-85-5

Structure of 955978-85-5

Chemical Structure| 955978-85-5

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Product Details of [ 955978-85-5 ]

CAS No. :955978-85-5
Formula : C14H17BFNO2
M.W : 261.10
SMILES Code : CC1(C)C(C)(C)OB(C2=CC(F)=CC3=C2C=CN3)O1
MDL No. :MFCD16987817

Safety of [ 955978-85-5 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 955978-85-5 ]

* 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 [ 955978-85-5 ]

[ 955978-85-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 885520-70-7 ]
  • [ 73183-34-3 ]
  • [ 955978-85-5 ]
YieldReaction ConditionsOperation in experiment
61% With potassium acetate;(1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In dimethyl sulfoxide; at 80℃; for 18h; To a solution of 4-bromo-6-fluoro-lH-indole (6.0 g, 25.53 mmol) and bis(pinacolato)diboron (9.7 g, 38.19 mmol) in anhydrous DMSO (120 mL) were added KOAc (7.5 g, 76.41 mmol) and [l,r-bis(diphenylphosphine)ferrocene]-dichloropalladium (1.0 g, 1.22 mmol). The mixture was heated at 80 °C for 18 h. The reaction mixture was cooled to RT and partioned between EtOAc and H2O. The organic layer was isolated, washed successively with H2O and brine, dried (Na2SO4) and concentrated in vacuo. The resulting residue was purified by column chromatography (silica gel, pentane:EtOAc 75:25) to provide the title compound as a white solid (4.6 g, 61 percent). <n="41"/>^NMR deltaH (300 MHz, CDCl3) 1.39 (s, 12H), 7.02 (m, IH), 7.14-7.19 (m, IH), 7.20-7.26 (m, IH), 7.38 (dd, J = 2.4, 9.9, IH) and 8.16 (s, IH).
61% With potassium acetate;(1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In dimethyl sulfoxide; at 80℃; for 18h; To a solution of 4-bromo-6-fluoro-lH-indole (6.0 g, 25.53 mmol) and bis(pinacolato)diboron (9.7 g, 38.19 mmol) in anhydrous DMSO (120 mL) were added KOAc (7.5 g, 76.41 mmol) and [l,r-bis(diphenylphosphine)ferrocene]-dichloropalladium (1.0 g, 1.22 mmol). The mixture was heated at 80 °C for 18 h. The reaction mixture was cooled to RT and partioned between EtOAc and H2O. The organic layer was washed successively with H2O and brine, dried (Na2SO4) and concentrated in vacuo. The resulting residue was purified by column chromatography (silica gel, pentane:EtOAc 75:25) to provide the title compound as a white solid (4.6 g, 61 percent).NMR deltaH (300 MHz, CDCl3) 1.39 (s, 12H), 7.02 (m, IH), 7.14-7.19 (m, IH), 7.20-7.26 (m, IH), 7.38 (dd, J = 2.4, 9.9, IH) and 8.16 (s, IH).
With potassium acetate;(1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In dimethyl sulfoxide; at 100℃; for 16h; To a stirring mixture of 4-bromo-6-fluoro-lH-indole (6.76 g, 31.5 mmol), bis(pinacolato)diboron (12.8 g, 94.7 mmol) and potassium acetate (9.3 g, 94.7 mmol) in methyl sulfoxide (100 mL) was added l,r-bis(diphenylphosphine)ferrocene- dichloropalladium (1.29 g, 5 mol percent). The reaction mixture was flushed out with nitrogen and heated to 100 0C for 16 hours. The mixture was partitioned between ethyl acetate and water and the organic layer washed with brine, dried over MgSO4 and evaporated down. The crude product was purified by column chromatography followed by triturating to yield the title compound (7.87 g). deltaH(400MHz, CDCl3) 1.41 (s, 12H)5 7.04 (m, IH), 7.16 (dd, IH), 7.26 (t, IH)5 7.40 (dd, IH)5 8.14 (br S5 IH).
With potassium acetate;(1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In dimethyl sulfoxide; at 100℃; for 16h; Reference Example 56-FIuoro-4-(4,4,5,5-tetramethyl-[l,3,2]dioxaborolan-2-yl)-lH-indoleTo a stirring mixture of 4-bromo-6-fluoro-lH-indole (6.76 g, 31.5 mmol), bis(pinacolato)diboron (12.8 g, 94.7 mmol) and potassium acetate (9.3 g, 94.7 mmol) in methyl sulfoxide (100 mL) was added l,l'-bis(diphenylphosphine)ferrocene- dichloropalladium (1.29 g, 5 mol percent). The reaction mixture was flushed out with nitrogen and heated to 100 0C for 16 hours. The mixture was partitioned between ethyl acetate and water and the organic layer washed with brine, dried over MgSO4 and evaporated down. The crude <n="58"/>product was purified by column chromatography followed by triturating to yield the title compound (7.87 g). deltaH(400MHz, CDCl3) 1.41 (s, 12H), 7.04 (m, IH), 7.16 (dd, IH), 7.26 (t, IH), 7.40 (dd, IH), 8.14 (br s, IH).

 

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