Basic information Safety Supplier Related

1-BOC-5-chloroindole-3-boronic acid, pinacol ester

Basic information Safety Supplier Related

1-BOC-5-chloroindole-3-boronic acid, pinacol ester Basic information

Product Name:
1-BOC-5-chloroindole-3-boronic acid, pinacol ester
Synonyms:
  • 1-BOC-5-chloroindole-3-boronic acid, pinacol ester
  • tert-Butyl 5-chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-1-carboxylate
  • 1H-Indole-1-carboxylicacid,5-chloro-3-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-,1,1-diMethylethylester
  • tert-butyl 5-chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)indole-1-carboxylate
CAS:
1218790-30-7
MF:
C19H25BClNO4
MW:
377.67
Mol File:
1218790-30-7.mol
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1-BOC-5-chloroindole-3-boronic acid, pinacol ester Chemical Properties

Boiling point:
479.5±48.0 °C(Predicted)
Density 
1.16±0.1 g/cm3(Predicted)
storage temp. 
Sealed in dry,Store in freezer, under -20°C
Appearance
White to off-white Solid
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Safety Information

HS Code 
2933998090
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1-BOC-5-chloroindole-3-boronic acid, pinacol ester Usage And Synthesis

Synthesis

1048039-49-1

25015-63-8

1218790-30-7

GENERAL STEPS: Pd(dppf)Cl2 (29 mg, 0.04 mmol, 3 mol%) and tert-butyl 5-chloro-3-iodo-1H-indole-1-carboxylate (500 mg, 1.32 mmol) were added to a dry screw-capped reaction flask equipped with a septum under argon protection. Subsequently, anhydrous toluene (6.5 mL) was added and the mixture was degassed with argon for 5 minutes. Under argon atmosphere, dry triethylamine (0.7 mL) and 4,4,5,5-tetramethyl-1,3,2-dioxaborolane (0.3 mL, 2 mmol) were added sequentially. The reaction mixture was placed in an oil bath preheated to 80 °C and stirred for 3 h. The reaction progress was monitored by TLC. After completion of the reaction, the mixture was cooled to room temperature and filtered through diatomaceous earth. The filtrate was concentrated under reduced pressure and the residue was purified by fast column chromatography (eluent: hexane/ethyl acetate = 10/1) to afford the target product 1-Boc-5-chloroindole-3-boronic acid pinacol ester (418 mg, 84% yield). The product characterization data were consistent with those reported in the literature.1H NMR (500 MHz, CDCl3) δ 8.08 (d, J=8.8 Hz, 1H), 8.00 (s, 1H), 7.95 (d, J=2.1 Hz, 1H), 7.26 (dd, J=8.8,2.1 Hz, 1H), 1.65 (s, 9H), 1.38 (s, 12H).

References

[1] Bioorganic and Medicinal Chemistry, 2017, vol. 25, # 5, p. 1622 - 1629
[2] European Journal of Organic Chemistry, 2011, # 24, p. 4532 - 4535
[3] European Journal of Organic Chemistry, 2013, # 21, p. 4564 - 4569

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