Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595989Generated: October 30, 2026

N-bromobutanimide → Methyl 4-(3-amino-6-bromopyrazin-2-yl)-2-fluorobenzoate

https://huagongshe.com/reaction/595989

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantSodium BicarbonateHCID 516892—
ReactantMethyl 4-(3-aminopyrazin-2-yl)-2-fluorobenzoateHCID 118045820—
SolventAcetonitrileHCID 6342—
ProductMethyl 4-(3-amino-6-bromopyrazin-2-yl)-2-fluorobenzoateHCID 11804617296%

Reaction Steps

To a suspension of methyl 4-(3-aminopyrazin-2-yl)-2-fluorobenzoate (31.5 g, 127 mmol) in acetonitrile (430 mL) at 0° C. was added NBS (23.9 g, 134 mmol). The reaction mixture was stirred in ice bath for 1 h, sat. sodium bicarbonate was added, stirred 30 min and product was extracted with ethylacetate. The organic extracts were combined, washed with brine, dried over sodium sulfate, filtered and evaporated. The crude product was recrystallized in EtOAc and heptane to give methyl 4-(3-amino-6-bromopyrazin-2-yl)-2-fluorobenzoate as brown color solid in 96% yield. LCMS (m/z): 326.0/328.0 (MH+), 0.87 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242996B2
Source datasetuspto-grants-2016_01
ORD IDord-6cc97469cd2f4be0bc9977d100da46bb
Source noteuspto-grants-2016_01