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858116-66-2

858116-66-2 Structure

858116-66-2 Structure
IdentificationBack Directory
[Name]

5-BROMO-1-TRIISOPROPYLSILANYL-1H-PYRROLO[2,3-B]PYRIDINE
[CAS]

858116-66-2
[Synonyms]

5-BroMo-1-triisopropylsil...
N-triisopropylsilyl-5-bromo-7-azaindole
5-Bromo-1-triisopropylsilanyl-7-azaindole
n-Triisopropylsilyl-5-bromo-7-azaindole 98%
5-Bromo-1-(triisopropylsilyl)pyrrolo[2,3-b]pyridine
5-BROMO-1-TRIISOPROPYLSILANYL-1H-PYRROLO[2,3-B]PYRIDINE
(5-Bromopyrrolo[2,3-b]pyridin-1-yl)-triisopropyl-silane
5-broMo-1-(triisopropylsilyl)-1H-pyrrolo[2,3-b]pyridine
5-BROMO-1-TRIISOPROPYLSILANYL-1H-PYRROLO[2,3-B]PYRIDINE-2
(5-bromo-1-pyrrolo[2,3-b]pyridinyl)-tri(propan-2-yl)silane
5-bromo-1-[tris(propan-2-yl)silyl]-1H-pyrrolo[2,3-b]pyridine
1H-Pyrrolo[2,3-b]pyridine, 5-bromo-1-[tris(1-methylethyl)silyl]-
[Molecular Formula]

C16H25BrN2Si
[MDL Number]

MFCD08688597
[MOL File]

858116-66-2.mol
[Molecular Weight]

353.37
Chemical PropertiesBack Directory
[Boiling point ]

333.7±35.0 °C(Predicted)
[density ]

1.19±0.1 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,2-8°C
[form ]

solid
[pka]

2.87±0.30(Predicted)
[Appearance]

off-white solid
[InChI]

1S/C16H25BrN2Si/c1-11(2)20(12(3)4,13(5)6)19-8-7-14-9-15(17)10-18-16(14)19/h7-13H,1-6H3
[InChIKey]

UJUSITKTVXDVLQ-UHFFFAOYSA-N
[SMILES]

CC(C)[Si](C(C)C)(C(C)C)n1ccc2cc(Br)cnc12
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictograms
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[Hazard Codes ]

Xi,Xn
[Risk Statements ]

22
[HazardClass ]

IRRITANT
[HS Code ]

2933998090
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Spectrum DetailBack Directory
[Spectrum Detail]

5-BROMO-1-TRIISOPROPYLSILANYL-1H-PYRROLO[2,3-B]PYRIDINE(858116-66-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

Triisopropylsilyl chloride

13154-24-0

5-BROMO-1-TRIISOPROPYLSILANYL-1H-PYRROLO[2,3-B]PYRIDINE

858116-66-2

General procedure for the synthesis of 1-triisopropylsilyl-5-bromo-7-azaindole from triisopropylchlorosilane: Sodium hydride (0.63 g, 25.15 mmol) was added batchwise to a stirred solution of tetrahydrofuran (THF, 50 mL) of 5-bromo-7-azaindole (3.3 g, 16.75 mmol) at room temperature with continuous stirring for 15 min. Subsequently, triisopropylchlorosilane (5.3 mL, 25.15 mmol) was added and the reaction mixture was heated to 80 °C and maintained for 3 hours. After completion of the reaction, the solvent was removed by evaporation and the residue was dissolved in water (50 mL). The aqueous layer was extracted with ethyl acetate (EtOAc, 3 x 50 mL) and the organic phase was dried with anhydrous sodium sulfate (Na2SO4) and concentrated under reduced pressure. The crude product was purified by Biotage HPFC system (eluent: 10% ethyl acetate/hexane) to afford the target compound 5-bromo-1-(triisopropylsilyl)-1H-pyrrolo[2,3-b]pyridine as a white solid (5.2 g, 88% yield). Mass spectrometry analysis showed the molecular ion peak m/z 355 (M + 1).

[References]

[1] Patent: WO2005/103050, 2005, A2. Location in patent: Page/Page column 180
[2] Patent: WO2006/128692, 2006, A2. Location in patent: Page/Page column 158
[3] Patent: US2007/49615, 2007, A1. Location in patent: Page/Page column 62-63
[4] Patent: US2007/49615, 2007, A1. Location in patent: Page/Page column 68
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