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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 15977Generated: October 26, 2026

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

https://huagongshe.com/reaction/15977

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 numberUS07732616B2
Source datasetuspto-grants-2010_06
ORD IDord-0456192a69e843a3a707b1c622c11a17
Source noteuspto-grants-2010_06