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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1952223Generated: November 3, 2026

Benzene, 1-(chloromethyl)-2-fluoro- → HCID 59490939, compound

https://huagongshe.com/reaction/1952223

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzene, 1-(chloromethyl)-2-fluoro-HCID 9580—
ReactantCesium carbonateHCID 10796—
ReactantHCID 59490898HCID 59490898—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 59490939HCID 5949093996.9%

Reaction Steps

3-(2-Methoxy-pyridin-3-yl)-5-methyl-1H-pyrrolo[3,2-b]pyridine-2-carboxylic acid ethyl ester B3 (0.2 g, 0.64 mmol) was diluted with DMF (4 mL). To the resulting solution was added 2-fluorobenzyl chloride (0.14 g, 0.96 mmol) and cesium carbonate (0.312 g, 0.96 mmol) and the resulting suspension was allowed to stir at room temperature. After 24 hours the reaction mixture was then diluted with ethyl acetate (50 mL) and water (20 mL) and the layers were separated. The organic layer was sequentially washed with aqueous saturated sodium bicarbonate solution (10 mL), water (10 mL) and saturated brine (10 mL), dried (magnesium sulfate), filtered and concentrated in vacuo. The crude residue obtained was purified using flash chromatography to provide 1-(2-Fluoro-benzyl)-3-(2-methoxy-pyridin-3-yl)-5-methyl-1H-pyrrolo[3,2-b]pyridine-2-carboxylic acid ethyl ester B4 (0.26 g) MS: 420.20 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404845B2
Source datasetuspto-grants-2013_03
ORD IDord-16e340a66dd64e249f22dbea08998e10
Source noteuspto-grants-2013_03