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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1756087Generated: October 28, 2026

Phenacyl bromide → 3-(Cyanomethyl)-5-fluoro-2-methyl-7-phenacylpyrrolo[2,3-b]pyridine hydrobromide

https://huagongshe.com/reaction/1756087

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenacyl bromideHCID 6259—
ReactantHCID 19916787HCID 19916787—
SolventAcetonitrileHCID 6342—
Product3-(Cyanomethyl)-5-fluoro-2-methyl-7-phenacylpyrrolo[2,3-b]pyridine hydrobromideHCID 1991682090%

Reaction Steps

A mixture of 3- (cyanomethyl)-5-fluoro-2-methylpyrrolo [2,3-b]pyridine (0.28 g, 1.5 mmol) and phenacyl bromide 0.32 g, 1.6 mmol) in acetonitrile (5 ml) was refluxed under argon for 3 h, during which time the initial solution was transformed into a suspension. Then the suspension was cooled in an ice bath, filtered and washed with diethyl ether (2×2 ml). The crystalline product was purified by recrystallization from hot acetonitrile to give 0.52 g (90% ) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05439917
Source datasetuspto-grants-1995_08
ORD IDord-5879f7c4c13e4d778b50aabf120b8135
Source noteuspto-grants-1995_08