Home Cart Sign in  
Chemical Structure| 1426154-41-7 Chemical Structure| 1426154-41-7

Structure of 1426154-41-7

Chemical Structure| 1426154-41-7

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • {[ item.pr_size ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of [ 1426154-41-7 ]

CAS No. :1426154-41-7
Formula : C15H20BNO2
M.W : 257.14
SMILES Code : CC1(C)OB(C2=C(C)C=CC3=C2C=CN3)OC1(C)C
MDL No. :MFCD28403648

Safety of [ 1426154-41-7 ]

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

Application In Synthesis of [ 1426154-41-7 ]

* 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 [ 1426154-41-7 ]

[ 1426154-41-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 73183-34-3 ]
  • [ 610794-15-5 ]
  • [ 1426154-41-7 ]
YieldReaction ConditionsOperation in experiment
43% With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; potassium acetate; at 90℃; for 2.5h;Inert atmosphere; A solution of <strong>[610794-15-5]4-bromo-5-methylindole</strong> (805 mg, 3.64 mmol, 1.0 eq) in degassed1,4-dioxane (10 mL) was degassed with argon for a further 5 mm before the addition of bis(pinacolato)diboron (1 .20 g, 4.73 mmol, 1 .3 eq). Whilst degassing,potassium acetate (1.07 g, 10.9 mmol, 3.0 eq) and PdCI2(dppf)CH2CI2 (149 mg,0.182 mmol, 5 mol%) were added. The vessel was then sealed and stirred at90C for 2.5 h. Upon cooling, the reaction mixture was diluted with H20 (10 mL),poured into 50% brine (50 mL) and extracted with EtOAc (3 x 50 mL). Thecombined organic extracts were dried over MgSO4, filtered and concentrated invacuo. Purification twice by silica gel column chromatography with hexane/EtOAc (1 :0-14:1) then hexane/CH2CI2 (1:0-1:1) yielded Intermediate 38 as a white solid (400 mg, 43%).1H NMR (300MHz, ODd3) oH. 8.05 (br 5, 1H), 7.34 (d, J=8.3 Hz, 1H), 7.20 (t,J=2.7 Hz, 1H), 7.03 (d, J=8.3 Hz, 1H), 6.98 (td, J=2.0, 1.0 Hz, 1H), 2.64 (5, 3H),1.42 (5, 12H).MS (ESj 258.2 (100%, [M+H]j, 280.1 (40%, [M+Na]j.
33% With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium acetate; In dimethyl sulfoxide; at 180℃; for 0.666667h;Microwave irradiation; 4-Bromo-5-methylindole (0.7 g, 3.35 mmol), bis(pinacolato)diboron (1.7 g, 6.7 mmol), KOAc (1 g, 10 mmol) and Pd(dppf)CI2 (73 mg, 3 mol%) were suspended in dry DMSO (20 mL) in two 40 mL glass tubes which were tightly sealed with an aluminium/Teflon crimp. The samples were irradiated at 250 W, 180 C for 40 min in a CEM-Discover mono-mode microwave reactor. After completion of the reactions, the vessels were cooled down to 60C, combined and the crude mixture was filtered through a thin plug of celite. The celite plug was washed with EtOAc (50 mL), the organic fractions were combined and the solvent was removed under reduced pressure. The crude product was purified by silica gel column chromatography and then prep-HPLC to give 5 (280mg, 33 %). 1H NMR CDCI3400 MuEtazeta delta 1.41 (s, 12H), 2.63 (s, 3H), 6.96-6.97 (m, 1 H), 7.01-7.03 (m, 1 H), 7.18-7.20(m, 1 H), 7.32-7.34 (m, 1 H), 8.13 (s, 1 H)
33% With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium acetate; In dimethyl sulfoxide; at 180℃; for 0.666667h;Sealed tube; Microwave irradiation; 4-Bromo-5-methylindole (0.7 g, 3.35 mmol), bis(pinacolato)diboron (1.7 g, 6.7 mmol), KOAc (1 g, 10 mmol) and Pd(dppf)Cl2 (73 mg, 3 mol %) were suspended in dry DMSO (20 mL) in two 40 mL glass tubes which were tightly sealed with an aluminium/Teflon crimp. The samples were irradiated at 250 W, 180 C. for 40 min in a CEM-Discover mono-mode microwave reactor. After completion of the reactions, the vessels were cooled down to 60 C., combined and the crude mixture was filtered through a thin plug of celite. The celite plug was washed with EtOAc (50 mL), the organic fractions were combined and the solvent was removed under reduced pressure. The crude product was purified by silica gel column chromatography and then prep-HPLC to give 5 (280 mg, 33%). 1H NMR CDCl3400 MHz delta 1.41 (s, 12H), 2.63 (s, 3H), 6.96-6.97 (m, 1H), 7.01-7.03 (m, 1H), 7.18-7.20 (m, 1H), 7.32-7.34 (m, 1H), 8.13 (s, 1H)
 

Historical Records

Categories