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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948622Generated: October 30, 2026

Sodium Carbonate → 2-(Triethylsilyl)-1H-pyrrolo[2,3-b]pyridine-3-ethanol

https://huagongshe.com/reaction/1948622

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantLithium ChlorideHCID 433294—
Reactant4-(Triethylsilyl)-3-butyn-1-olHCID 2760694—
Reactant2-Amino-3-iodopyridineHCID 2763151—
CatalystHCID 178418807HCID 178418807—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventDiethylether ethylacetateHCID 21584169—
Product2-(Triethylsilyl)-1H-pyrrolo[2,3-b]pyridine-3-ethanolHCID 1535100280%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 3-iodopyridin-2-amine (0.46 g, 2.09 mmole), 4-(triethylsilyl)but-3-in-1-ol (0.58 g, 3.14 mmole), 1,1′-bis(diphenylphosphino)ferrocene-palladium(II)dichloride dichloromethane (0.083 g, 0.105 mmole), lithium chloride (0.086 g, 2.09 mmole) and sodium carbonate (0.44 g, 4.18 mmole) in DMF (21 ml) was stirred under nitrogen for 15 hours at 100° C. The reaction mixture was cooled to RT, EtOAc/ether (1:1) was added and the mixture was poured into H2O. The two-phase suspension was filtered through filter earth. After separating the phases the aqueous phase was extracted with EtOAc (2×). The organic phases were combined and washed with H2O and with saturated NaCl solution and dried over MgSO4. After filtering off the drying agent the solvents were removed on a rotary evaporator. Column chromatography of the residue (n-hexane/EtOAc=2:1, then n-hexane/EtOAc=1:1) yielded 2-(2-(triethylsilyl)-1H-pyrrolo[2,3-b]pyridin-3-yl)ethanol (0.46 g, 80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399503B2
Source datasetuspto-grants-2013_03
ORD IDord-43627da9ba3f47e29089f3068481d981
Source noteuspto-grants-2013_03