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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 38254Generated: October 30, 2026

Benzyl Bromide → HCID 42645471, compound

https://huagongshe.com/reaction/38254

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
ReactantN-(3-chloro-4-(piperazin-1-yl)phenyl)picolinamideHCID 67441344—
SolventAcetonitrileHCID 6342—
ProductHCID 42645471HCID 42645471192.2%

Reaction Steps

According to Scheme 5 Step 5 Method B: A suspension of (bromomethyl)benzene (0.61 mmol, 74 μL), N-(3-chloro-4-(piperazin-1-yl)phenyl)picolinamide (0.51 mmol, 161 mg) and of K2CO3 (0.51 mmol, 70 mg) in ACN (3 mL) was stirred at 80° C. for 30 minutes. After evaporation of the solvent, water and AcOEt were added. The aqueous phase was extracted with AcOEt. The organic phase was washed with brine, was dried over Na2SO4, was filtered and was concentrated under reduced pressure. The crude product was purified by flash chromatography over silica gel using DCM/AcOEt (80:20) as eluent and finally crystallized in pentane to obtain N-(4-(4-benzylpiperazin-1-yl)-3-chlorophenyl)picolinamide (0.98 mmol, 40 mg, 20%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524726B2
Source datasetuspto-grants-2013_09
ORD IDord-ffabc75a608944ac845f7dfd6409fe52
Source noteuspto-grants-2013_09