| Identification | Back Directory | [Name]
5-BROMO-2,3-DIHYDRO-1H-PYRROLO[2,3-B]PYRIDINE | [CAS]
115170-40-6 | [Synonyms]
5-broMo-2
5-Bromo-7-azaindoline
3-dihydro-1H-pyrrolo[2
5-BROMO-2,3-DIHYDRO-7-AZAINDOLE
5-Bromo-2,3-dihydro-7-azaindole 95%
5-broMo-1H,2H,3H-pyrrolo[2,3-b]pyridine
BROMO-2,3-DIHYDRO-1H-PYRROLO[2,3-B]PYRIDINE
5-BROMO-2,3-DIHYDRO-1H-PYRROLO[2,3-B]PYRIDINE
1H-Pyrrolo[2,3-b]pyridine, 5-bromo-2,3-dihydro-
5-BROMO-2,3-DIHYDRO-1H-PYRROLO[2,3-B]PYRIDINE ISO 9001：2015 REACH | [EINECS(EC#)]
634-550-3 | [Molecular Formula]
C7H7BrN2 | [MDL Number]
MFCD06659750 | [MOL File]
115170-40-6.mol | [Molecular Weight]
199.05 |
| Chemical Properties | Back Directory | [Melting point ]
186-191 (Decomposition) | [Boiling point ]
315.8±42.0 °C(Predicted) | [density ]
1.606 | [Fp ]
136℃ | [storage temp. ]
Keep in dark place,Sealed in dry,Room Temperature | [form ]
solid | [pka]
9.31±0.20(Predicted) | [color ]
Brown |
| Hazard Information | Back Directory | [Uses]
5-Bromo-2,3-dihydro-1H-pyrrolo[2,3-b]pyridine is a useful intermediate for organic synthesis. | [Synthesis]
a) 16.8 g (0.14 mol) of 2,3-dihydro-1H-pyrrolo[2,3-b]pyridine, 24.13 g (0.143 mol) of 48% hydrobromic acid and 260 g of methylene chloride were added to a reaction flask and stirred thoroughly to obtain reaction mixture C; b) The temperature of reaction mixture C was controlled at 25~30°C, and 20.20 g of 20% hydrogen peroxide solution was added slowly dropwise. hydrogen peroxide solution to obtain mixture D; c) Neutralize mixture D using 60 g of saturated aqueous sodium bisulfite solution until the red color of the reaction solution completely disappeared, and carry out partitioning to obtain the organic phase E and the aqueous phase F; d) Wash the organic phase E with 200 g of water; e) Recover the dichloromethane solvent from the organic phase E obtained in step d) to obtain 26.6 g of 5-bromo-2,3-dihydro-1H-pyrrolo[ 2,3-b]pyridine in 95.6% yield and the product was ≥99% pure by liquid chromatography. | [References]
[1] Patent: CN107987076, 2018, A. Location in patent: Paragraph 0048-0053; 0064-0069; 0074; 0080-0085
[2] Patent: CN105461718, 2016, A. Location in patent: Paragraph 0016
[3] Patent: WO2004/78757, 2004, A2. Location in patent: Page 48; 50-51
[4] Patent: WO2015/157504, 2015, A1. Location in patent: Page/Page column 37
[5] Patent: EP1782811, 2007, A1. Location in patent: Page/Page column 63 |
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