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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Bromo-2-fluoroaniline | HCID 123050 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | Methyl 2-chloro-1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylate | HCID 57442171 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 2-(4-bromo-2-fluorophenylamino)-1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylate | HCID 66673525 | 65.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07732616B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-0456192a69e843a3a707b1c622c11a17 |
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| Source note | uspto-grants-2010_06 |
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