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| | 1H-Pyrrolo[2,3-b]pyridine, 1-[(4-methylphenyl)sulfonyl]-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)- Basic information |
| Product Name: | 1H-Pyrrolo[2,3-b]pyridine, 1-[(4-methylphenyl)sulfonyl]-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)- | | Synonyms: | 1H-Pyrrolo[2,3-b]pyridine, 1-[(4-methylphenyl)sulfonyl]-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-;1-Tosyl-7-azaindole-3-boronic Acid Pinacol Ester;1-[(4-Methylbenzene)sulfonyl]-3-(tetraMethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrolo[2,3-b]pyridine;3-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-1-tosyl-1H-pyrrolo[2,3-b]pyridine;1-[(4-Methylbenzene)sulfonyl]-1H-pyrrolo[2,3-b]pyridine-3-boronic acid pinacol ester;1-[(4-Methylphenyl)sulfonyl]-7-Azaindole-3-boronic acid pinacol ester;1-Tosyl-7-azaindole-3-boronic Acid Pinacol Este;1-Tosyl-1H-pyrrolo[2,3-b]pyridine-3-boronic acid pinacol ester | | CAS: | 866545-91-7 | | MF: | C20H23BN2O4S | | MW: | 398.28 | | EINECS: | | | Product Categories: | | | Mol File: | 866545-91-7.mol | ![1H-Pyrrolo[2,3-b]pyridine, 1-[(4-methylphenyl)sulfonyl]-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)- Structure](CAS/GIF/866545-91-7.gif) |
| | 1H-Pyrrolo[2,3-b]pyridine, 1-[(4-methylphenyl)sulfonyl]-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)- Chemical Properties |
| Boiling point | 572.0±60.0 °C(Predicted) | | density | 1.24 | | storage temp. | Inert atmosphere,Store in freezer, under -20°C | | pka | 0.91±0.30(Predicted) | | Appearance | White to off-white Solid |
| | 1H-Pyrrolo[2,3-b]pyridine, 1-[(4-methylphenyl)sulfonyl]-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)- Usage And Synthesis |
| Synthesis | 3-Bromo-1-tosyl-1H-pyrrolo[2,3-b]pyridine (850 mg, 2.4 mmol) and pinacol ester of biphenylboronic acid (921 mg, 3.6 mmol) were added to [1,1'-bis(diphenylphosphino)ferrocene]palladium(II) dichloride (197 mg, 0.24 mmol) and potassium acetate (713 mg, 7.26 mmol) in 20 mL of 1,2-dimethoxyethane (DME). 0.24 mmol) and potassium acetate (713 mg, 7.26 mmol). The reaction mixture was stirred and refluxed at 90 °C for 18 hours. After completion of the reaction, the reaction solution was diluted with ethyl acetate, the organic phase was washed sequentially with water and saturated saline, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The crude product was purified by fast column chromatography (eluent: 20% ethyl acetate/80% hexane) to afford 1-tosyl-7-azaindole-3-boronic acid pinacol ester (900 mg, 99% yield) as a white solid. | | References | [1] Patent: WO2005/95400, 2005, A1. Location in patent: Page/Page column 326; 327
[2] Patent: KR2015/15252, 2015, A. Location in patent: Paragraph 0182;0183
[3] Journal of Medicinal Chemistry, 2015, vol. 58, # 18, p. 7195 - 7216 |
| | 1H-Pyrrolo[2,3-b]pyridine, 1-[(4-methylphenyl)sulfonyl]-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)- Preparation Products And Raw materials |
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