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

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Company Name: Guangzhou Yuheng Pharmaceutical Technology Co., Ltd
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Products Intro: Product Name:tert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-1-carboxylate
CAS:893441-86-6
Purity:0.97 Package:1KG;25KG
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Products Intro: Product Name:TERT-BUTYL 4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-1H-INDOLE-1-CARBOXYLATE
CAS:893441-86-6
Purity:95% Package:100g; 1kg Remarks:LN01377071
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Products Intro: Product Name:1-Boc-indole-4-boronic Acid Pinacol Ester
CAS:893441-86-6
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Products Intro: Product Name:1-Boc-indole-4-boronic Acid Pinacol Ester
CAS:893441-86-6
Purity:97% Package:100G;500G;
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Products Intro: Product Name:1-Boc-indole-4-boronic Acid Pinacol Ester
CAS:893441-86-6
Purity:0.97 Package:mgs,gs,kgs Remarks:A861235
1-Boc-indole-4-boronic Acid Pinacol Ester Basic information
Product Name:1-Boc-indole-4-boronic Acid Pinacol Ester
Synonyms:1-Boc-indole-4-boronic Acid Pinacol Ester;tert-Butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-1-carboxylate;1-tert-Butoxycarbonyl-indole-4-boronic acid pinacol ester;1H-Indole-1-carboxylic acid, 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-, 1,1-dimethylethyl ester;N-Boc-do-4-frequency ol borate;tert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)indole-1-carboxylate
CAS:893441-86-6
MF:C19H26BNO4
MW:343.23
EINECS:
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Mol File:893441-86-6.mol
1-Boc-indole-4-boronic Acid Pinacol Ester Structure
1-Boc-indole-4-boronic Acid Pinacol Ester Chemical Properties
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
AppearanceWhite to off-white Solid
Safety Information
MSDS Information
1-Boc-indole-4-boronic Acid Pinacol Ester Usage And Synthesis
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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