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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 422826Generated: October 31, 2026

4-Bromo-2-fluoroaniline → Methyl 2-(4-bromo-2-fluorophenylamino)-1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylate

https://huagongshe.com/reaction/422826

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-2-fluoroanilineHCID 123050—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantMethyl 2-chloro-1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylateHCID 57442171—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 2-(4-bromo-2-fluorophenylamino)-1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylateHCID 6667352565.3%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 4-bromo-2-fluoroaniline (0.192 g, 1.01 mmol) in THF (5 mL) at −78° C. under N2 was added lithium bis(trimethylsilyl)amide (1.50 mL, 1.50 mmol, 1 M solution in hexanes) dropwise. The reaction mixture was stirred for one hour at −78° C. Methyl 2-chloro-1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylate (0.202 g, 1.00 mmol) was then added dropwise as a solution in THF (5 mL) and the reaction mixture was stirred for one hour at −78° C. The reaction mixture was quenched by the addition of H2O and the pH was adjusted to pH 7 with saturated NH4Cl and then diluted with EtOAc. The organic layer was separated and washed with saturated NaCl, dried (Na2SO4), and concentrated under reduced pressure. Purification by flash column chromatography (methylene chloride/EtOAc, 15:1) gave 0.232 g (65%) pure desired product as a white crystalline solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101639B2
Source datasetuspto-grants-2012_01
ORD IDord-b536d9e841c844eeb0b79a30e5a3ed72
Source noteuspto-grants-2012_01