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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1293741Generated: October 30, 2026

N-bromobutanimide → 2-Amino-5-bromo-3-fluoropyridine

https://huagongshe.com/reaction/1293741

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantSodium BicarbonateHCID 516892—
Reactant2-Amino-3-fluoropyridineHCID 2762809—
SolventAcetonitrileHCID 6342—
Product2-Amino-5-bromo-3-fluoropyridineHCID 5085113060.6%

Reaction Conditions

Temperature23 °C

Reaction Steps

To a solution of 3-fluoro-pyridin-2-ylamine (example C.29 step 2) (3 g, 26.8 mmol) in acetonitrile (50 mL) at 0° C. was added NBS (4.77 g, 26.8 mmol) and the mixture was stirred at 23° C. for 2 h. Poured on ice with sat. NaHCO3-sol., extracted thrice with AcOEt, dried over Na2SO4. Removal of the solvent in vacuum left a residue, which was purified by silica gel column chromatography with heptane/AcOEt 3:1 to give the title compound as a brown solid (3.1 g, 60%). MS (ISP) 191 [(M+H)+], 193 [(M+2+H)+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238808B2
Source datasetuspto-grants-2007_07
ORD IDord-0a7e208f934e4bf28e8c98bcccc2278a
Source noteuspto-grants-2007_07