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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595851Generated: November 1, 2026

N-bromobutanimide → 3-bromo-4-fluoro-5-(1-methyl-1H-pyrazol-4-yl)pyridin-2-amine

https://huagongshe.com/reaction/595851

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant4-fluoro-5-(1-methyl-1H-pyrazol-4-yl)pyridin-2-amineHCID 118046326—
SolventAcetonitrileHCID 6342—
Product3-bromo-4-fluoro-5-(1-methyl-1H-pyrazol-4-yl)pyridin-2-amineHCID 11804520414.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4-fluoro-5-(1-methyl-1H-pyrazol-4-yl)pyridin-2-amine (150 mg, 0.780 mmol) in acetonitrile (7. 805 mL) was added NBS (142 mg, 0.796 mmol) in three portions at 0° C. The reaction mixture was stirred at 0° C. for 20 min. LCMS showed the reaction complete. After quenched with sat Na2SO3 and NaHCO3, stirred for 30 min. The reaction mixture was extracted with EtOAc 3 times. Filtered out solid. The solid was not the desired product. The EtOAc layers were washed by sat NaHCO3, water and brine. Dried and concentrated. The crude material was purified with flash chromatography eluting with 0-100% EtOAc (containing 10% MeOH/heptane to provide 30 mg of desired product. LCMS (m/z): 273.1 (MH+), 0.46 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242996B2
Source datasetuspto-grants-2016_01
ORD IDord-3b4eb4f2fd06407bb6a0fd71c7d1b625
Source noteuspto-grants-2016_01