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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1478139Generated: November 4, 2026

Triisopropylsilyl chloride → 5-Bromo-1-(triisopropylsilyl)-1H-pyrrolo[2,3-b]pyridine

https://huagongshe.com/reaction/1478139

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriisopropylsilyl chlorideHCID 139400—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant5-bromo-1H-pyrrolo[2,3-b]pyridineHCID 10307932—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product5-Bromo-1-(triisopropylsilyl)-1H-pyrrolo[2,3-b]pyridineHCID 24229223—

Reaction Steps

To a mixture of 5-bromo-1H-pyrrolo[2,3-b]pyridine (15.4 g) in tetrahydrofuran (250 mL) was added 1M lithium hexamethyldisilazide in tetrahydrofuran (86 mL), and after 10 minutes, triisopropylchlorosilane (18.2 mL) was added. The mixture was stirred at room temperature for 24 hours. The reaction was diluted with ether, and the resulting solution was washed twice with water. The extracts were dried (Na2SO4), filtered, and concentrated. The residue was purified by flash chromatography, eluting with 10% ethyl acetate in hexanes to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403822B2
Source datasetuspto-grants-2016_08
ORD IDord-164be4161f89441688d9199c0a6275bf
Source noteuspto-grants-2016_08