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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1756094Generated: October 28, 2026

Bromomethyl 2-methoxyphenyl ketone → 3-Cyanomethyl-5-fluoro-2-methyl-7-(2-methoxyphenacyl)pyrrolo[2,3-b]pyridine hydrobromide

https://huagongshe.com/reaction/1756094

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromomethyl 2-methoxyphenyl ketoneHCID 123440—
ReactantHCID 19916787HCID 19916787—
SolventDiethyl EtherHCID 3283—
SolventAcetonitrileHCID 6342—
Product3-Cyanomethyl-5-fluoro-2-methyl-7-(2-methoxyphenacyl)pyrrolo[2,3-b]pyridine hydrobromideHCID 1991681681%

Reaction Steps

A mixture of 3-(cyanomethyl)-5-fluoro-2-methylpyrrolo[2,3-b]pyridine (20 mg, 0.11 mmol) and 2-methoxyphenacyl bromide (30 mg, 0.13 mmol) in acetonitrile (0.2 ml) was refluxed under argon for 6 h, during which time the initial solution was transformed into a suspension. Then the suspension was allowed to reach room temperature, diluted with diethyl ether (2 ml), filtered, and washed with diethylether to give 36 mg (81%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05439917
Source datasetuspto-grants-1995_08
ORD IDord-0e6c19c0e7d544b396278c3cd0d2f753
Source noteuspto-grants-1995_08