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893441-86-6

893441-86-6 Structure

893441-86-6 Structure
IdentificationBack Directory
[Name]

1-Boc-indole-4-boronic Acid Pinacol Ester
[CAS]

893441-86-6
[Synonyms]

N-Boc-do-4-frequency ol borate
1-Boc-indole-4-boronic Acid Pinacol Ester
1-tert-Butoxycarbonyl-indole-4-boronic acid pinacol ester
tert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)indole-1-carboxylate
tert-Butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-1-carboxylate
1H-Indole-1-carboxylic acid, 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-, 1,1-dimethylethyl ester
[Molecular Formula]

C19H26BNO4
[MOL File]

893441-86-6.mol
[Molecular Weight]

343.23
Chemical PropertiesBack Directory
[Boiling point ]

454.6±37.0 °C(Predicted)
[density ]

1.08±0.1 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[Appearance]

White to off-white Solid
Spectrum DetailBack Directory
[Spectrum Detail]

1-Boc-indole-4-boronic Acid Pinacol Ester(893441-86-6)1HNMR
Hazard InformationBack Directory
[Synthesis]

4-BROMOINDOLE-1-CARBOXYLIC ACID TERT-BUTYL ESTER

676448-17-2

Bis(pinacolato)diboron

73183-34-3

1-Boc-indole-4-boronic Acid Pinacol Ester

893441-86-6

KOAc (9 g, 91 mmol) was added to a solution of tert-butyl 4-bromo-1H-indole-1-carboxylate (9 g, 30 mmol) and bis(pinacolato)diboron (8.45 g, 33 mmol) in DMSO (180 mL). The suspension was purged with nitrogen (3 times) before addition of Pd(dppf)Cl2 (744 mg, 912 μmol). The reaction mixture was stirred at 80 °C for 12 hours. Upon completion of the reaction, the suspension was poured into water (400 mL) and extracted with EtOAc (300 mL × 2). The combined organic layers were washed with brine (200 mL), dried over Na2SO4 and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography (PE:EtOAc = 40:1) to afford tert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-1-carboxylate (7.8 g, 22.7 mmol, 75.8% yield) as a white solid. nmr (cdcl3, 400 MHz) δ ppm. 1.38 (s, 12H), 1.68 (s, 9H), 7.09 (d, J = 3.6 Hz, 1H), 7.30 (t, J = 7.6 Hz, 1H), 7.61 (d, J = 3.2 Hz, 1H), 7.70 (d, J = 7.2 Hz, 1H), 8.24 (d, J = 8 Hz, 1H); ESIMS measured value c19h26bno4 [m+h]+ 344.1.

[References]

[1] Patent: WO2017/23993, 2017, A1. Location in patent: Paragraph 0687; 0688
[2] Patent: WO2017/23986, 2017, A1. Location in patent: Paragraph 0705; 0706
[3] Patent: WO2017/23973, 2017, A1. Location in patent: Paragraph 0704
[4] Patent: WO2017/24026, 2017, A1. Location in patent: Paragraph 0686; 0687
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