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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347580Generated: October 26, 2026

Potassium Carbonate → 4-(3-Chloro-5-nitropyridin-2-yloxy)-1H-pyrrolo[2,3-b]pyridine

https://huagongshe.com/reaction/347580

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2,3-Dichloro-5-nitropyridineHCID 2763106—
Reactant1H-pyrrolo[2,3-b]pyridin-4-olHCID 178516467—
SolventAcetonitrileHCID 6342—
Product4-(3-Chloro-5-nitropyridin-2-yloxy)-1H-pyrrolo[2,3-b]pyridineHCID 2108166054.1%

Reaction Steps

To a solution of 1H-pyrrolo[2,3-b]pyridin-4-ol (210 mg, 1.56 mmol, see: Thibault, C. et al. Org. Lett. 2003, 5, 5023) in 3 mL of MeCN was added K2CO3 (240 mg, 1.74 mmol). The suspension was stirred for 10 min and treated with 2,3-dichloro-5-nitropyridine (270 mg, 1.40 mmol, see: Koch, V. and Schnatterer, S. Synthesis, 1990, 499). The reaction mixture was stirred for 12 h and quenched with 20 mL of H2O. The solution was extracted with EtOAc and the organic layer was washed with brine, and dried over MgSO4. After filtration and concentration in vacuo, the residue was purified by flash column chromatography (ISCO RediSep® silica gel cartridge) to give the title compound (220 mg, 54%). MS (ESI) m/z 291.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07173031B2
Source datasetuspto-grants-2007_02
ORD IDord-7921f5751a844f278738f8808c6927c4
Source noteuspto-grants-2007_02