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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 633514Generated: October 27, 2026

Cesium fluoride → 7-methoxy-3-(2-phenoxyphenyl)-1H-pyrrolo[2,3-c]pyridine

https://huagongshe.com/reaction/633514

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium fluorideHCID 25953—
Reactant(2-Phenoxyphenyl)boronic acidHCID 2773559—
Reactant3-Iodo-7-methoxy-1H-pyrrolo[2,3-c]pyridineHCID 53412719—
CatalystHCID 178418397HCID 178418397—
SolventMethanolHCID 887—
Product7-methoxy-3-(2-phenoxyphenyl)-1H-pyrrolo[2,3-c]pyridineHCID 9041667338.6%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 3-iodo-7-methoxy-1H-pyrrolo[2,3-c]pyridine (0.274 g, 1.0 mmol), 2-phenoxyphenylboronic acid (0.278 g, 1.3 mmol, 1.3 equivalents), Pd(PPh3)4 (0.058 g, 0.05 mmol), and cesium fluoride (0.456 g, 3 mmol) in dimethxoyethane (3 mL) and methanol (1.5 mL) was heated under microwave conditions (120° C., 30 minutes). The reaction mixture was partitioned between water and ethyl acetate. The aqueous layer was extracted three times with ethyl acetate. The combined organic layers were washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, filtered, and concentrated. The residue was purified by flash column chromatography (silica gel, 30% ethyl acetate/hexanes) to give the title compound (0.122 g, 38.6% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321764B2
Source datasetuspto-grants-2016_04
ORD IDord-c490091761d54383a603ffe9a2da55ae
Source noteuspto-grants-2016_04