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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 596081Generated: November 2, 2026

N-bromobutanimide → Methyl 4-(2-amino-5-bromopyridin-3-yl)-2-methylbenzoate

https://huagongshe.com/reaction/596081

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantMethyl 4-(2-aminopyridin-3-yl)-2-methylbenzoateHCID 118046459—
SolventAcetonitrileHCID 6342—
ProductMethyl 4-(2-amino-5-bromopyridin-3-yl)-2-methylbenzoateHCID 118045889—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of methyl 4-(2-aminopyridin-3-yl)-2-methylbenzoate (4.2 g, 17.34 mmol) in acetonitrile (173 mL) was added NBS (3.15 g, 17.68 mmol) in two portions at 0° C. The reaction mixture was stirred at 0° C. for 20 min. LCMS showed the reaction completed. After quenched with sat. Na2SO3 and NaHCO3, the reaction mixture was stirred for 30 min. The reaction mixture was extracted with EtOAc 3 times, washed by sat NaHCO3, water and brine. The organics was dried over Na2SO4, filtered and concentrated. The crude material was triturated with ether and taken to the next step without further purification. LCMS (m/z): 323.1 (MH+), 0.68 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242996B2
Source datasetuspto-grants-2016_01
ORD IDord-4829d1540229494ab22631d82ec9770f
Source noteuspto-grants-2016_01