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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227021Generated: October 28, 2026

3-Bromobenzyl bromide → HCID 57754513, compound

https://huagongshe.com/reaction/227021

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromobenzyl bromideHCID 69979—
ReactantHCID 57754654HCID 57754654—
SolventDimethylformamideHCID 6228—
ProductHCID 57754513HCID 5775451335.1%

Reaction Steps

Experimental conditions analogous to those described for Example 1 step 3 were used with 68 mg (0.257 mmol) of 3-(5-Methyl-pyridine-2-carbonyl)-1H-quinolin-4-one, 77.2 mg (0.309 mmol) of 3-bromobenzyl bromide, 12.4 mg (0.309 mmol, 60% dispersion in oil), and 1 mL of DMF. The crude product was purified by reverse phase HPLC with a C18 column, gradient of 20-70% acetonitrile—0.1% TFA to yield 39.1 mg of 1-(3-Bromo-benzyl)-3-(5-methyl-pyridine-2-carbonyl)-1H-quinolin-4-one as a white solid. LC-MSD, m/z for C23H17BrN2O2 [M+H]: 433.05 LC retention time on HPLC, C18 column gradient 20-95% acetonitrile with 0.1% TFA in 4 minutes: 2.5 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557213B2
Source datasetuspto-grants-2009_07
ORD IDord-b8e82067d8a1429283954c883c19dc7b
Source noteuspto-grants-2009_07