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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1964992Generated: October 29, 2026

1,4-Dioxane → 2-(6-bromo-1H-pyrrolo[2,3-b]pyridin-1-yl)(phenyl)methanone

https://huagongshe.com/reaction/1964992

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
Reactant1-Benzoyl-6-bromo-7-azaindoleHCID 15013893—
SolventPotassium HydroxideHCID 14797—
Product2-(6-bromo-1H-pyrrolo[2,3-b]pyridin-1-yl)(phenyl)methanoneHCID 86623135—

Reaction Steps

(6-bromo-1H-pyrrolo[2,3-b]pyridin-1-yl)(phenyl)methanone, 586 was dissolved in 20 mL of dioxane and 20 mL of 2M KOH (aq). This was stirred at ambient temperature until analysis indicated all of the starting material had been consumed (2 to 4 hours). The reaction was diluted with 50 mL of ethyl acetate and washed with 2×25 mL of NaHCO3 (aq. satd.) and 25 mL of brine. The organic layer was dried with sodium sulfate, evaporated and purified by column chromatography. Combined steps 2 and 3 gave approximately 65% overall yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415469B2
Source datasetuspto-grants-2013_04
ORD IDord-7a4c0160a7fe4f3a97372dbf5eb815a2
Source noteuspto-grants-2013_04