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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1890534Generated: November 1, 2026

Water → Methyl 1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrolo[2,3-b]pyridine-2-carboxylate

https://huagongshe.com/reaction/1890534

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant2-Chloromethyl 2-(trimethylsilyl)ethyl etherHCID 2724271—
Reactantmethyl 1H-pyrrolo(2,3-b)pyridine-2-carboxylateHCID 17390026—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrolo[2,3-b]pyridine-2-carboxylateHCID 6730652481.6%

Reaction Steps

To a solution of methyl 1H-pyrrolo[2,3-b]pyridine-2-carboxylate (H-1) (528 mg, 3 mmol) in dried THF (5 mL) at 0° C. was added NaH (240 mg, 6 mmol). The reaction was stirred for 0.5 h under N2, and then SEMCl (526 mg, 3 mmol) was added dropwise. The mixture was stirred at room temperature for 2 h. H2O was added to quench the reaction. The resulting mixture was extracted with EtOAc. The organic layer was dried over Na2SO4, and concentrated to afford the title compound (750 mg), which was used for the next step without purification. MS (m/z): 307 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507487B2
Source datasetuspto-grants-2013_08
ORD IDord-4f35f9bc9a0c49818dfe75f5d2323954
Source noteuspto-grants-2013_08