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Chemical Structure| 1190861-50-7 Chemical Structure| 1190861-50-7

Structure of 1190861-50-7

Chemical Structure| 1190861-50-7

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Product Details of [ 1190861-50-7 ]

CAS No. :1190861-50-7
Formula : C18H24BNO4
M.W : 329.20
SMILES Code : O=C1NC2=C(C=CC(B3OC(C)(C)C(C)(C)O3)=C2)C14CCOCC4

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Application In Synthesis of [ 1190861-50-7 ]

* 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 [ 1190861-50-7 ]

[ 1190861-50-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1190861-43-8 ]
  • [ 73183-34-3 ]
  • [ 1190861-50-7 ]
YieldReaction ConditionsOperation in experiment
100% With potassium acetate;dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; In dimethyl sulfoxide; at 90℃; for 16h;Inert atmosphere; An oven dried resealable Schlenk tube was charged with <strong>[1190861-43-8]6-bromo-2',3',5',6'-tetrahydrospiro[indoline-3,4'-pyran]-2-one</strong> (preparation 8, 0.10 g, 0.35 mmol), bis(pinacolato)diboron (0.18 g, 0.71 mmol), potassium acetate (0.07 g, 0.70 mmol) and dimethylsulphoxide (1 mL). The Schlenk tube was subjected to three cycles of evacuation-backfilling with argon, and 1,1'-bis(diphenylphosphino)ferrocene-palladium(II) dichloride dichloromethane complex (0.02 g, 0.02 mmol) was added. After three further cycles of evacuation-backfilling with argon, the Schlenk tube was capped and placed in an oil bath at 90 C. After 16h, the mixture was cooled and ethyl acetate was added. The organic layer was washed with water, dried (MgSO4) and evaporated. The mixture was filtered through a silica cartridge eluding with hexanes/ethyl acetate to give the title compound in quantitative yield as a pale-yellow oily residue, which was used without further purification. LRMS (m/z): 330 (M+1)+. 1H-NMR delta (CDCl3): 1.35 (m, 12H), 1.89-1.91 (m, 4H), 3.91-3.95 (m, 2H), 4.23-4.27 (m, 2H), 7.33 (s, 1 H), 7.40 (d, J = 7.5 Hz, 1 H), 7.56 (d, J = 7.5 Hz, 1H), 7.77 (brs, 1H).
100% With potassium acetate;dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; In dimethyl sulfoxide; at 90℃; for 16h;Inert atmosphere; An oven dried resealable Schlenk tube was charged with <strong>[1190861-43-8]6-bromo-2',3',5',6'-tetrahydrospiro[indoline-3,4'-pyran]-2-one</strong> (preparation 6, 0.10 g, 0.35 mmol), bis(pinacolato)diboron (0.18 g, 0.71 mmol), potassium acetate (0.07 g, 0.70 mmol) and dimethylsulphoxide (1 mL). The Schlenk tube was subjected to three cycles of evacuation-backfilling with argon, and 1,1'-bis(diphenylphosphino)ferrocene-palladium(II) dichloride dichloromethane complex (0.02 g, 0.02 mmol) was added. After three further cycles of evacuation-backfilling with argon, the Schlenk tube was capped and placed in an oil bath at 90 C. After 16h, the mixture was cooled and ethyl acetate was added. The organic layer was washed with water, dried (MgSO4) and evaporated. The mixture was filtered through a silica cartridge eluting with hexanes/ethyl acetate to give the title compound in quantitative yield as a pale-yellow oily residue, which was used without further purification. LRMS (m/z): 330 (M+1)+. 1H-NMR delta (CDCl3): 1.35 (m, 12H), 1.89-1.91 (m, 4H), 3.91-3.95 (m, 2H), 4.23-4.27 (m, 2H), 7.33 (s, 1H), 7.40 (d, J = 7.5 Hz, 1H), 7.56 (d, J = 7.5 Hz, 1H), 7.77 (br s, 1H).
 

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