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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 42033Erstellt: 23. Oktober 2026

1,3-Difluorobenzene → 6-(2,6-Difluorophenyl)pyridin-3-amine

https://huagongshe.com/de/reaction/42033

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,3-DifluorobenzeneHCID 9741—
Edukt6-Bromopyridin-3-amineHCID 642811—
EduktButyllithiumHCID 178418339—
KatalysatorZincchlorideHCID 3007855—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt6-(2,6-Difluorophenyl)pyridin-3-amineHCID 5841587530,2%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

In a three neck round bottle flask, to a mixture of 1,3-difluorobenzene (23.24 mmol, 2.29 ml) in THF (30 ml) at −78° C. under argon atmosphere, a solution of n-BuLi (10.2 ml) in THF (2.5M) was added. The mixture was stirred at −78° C. for 30 minutes and then it was heated to −50° C. A solution of ZnCl2 (51 ml) in THF (0.5M) was added drop wise and the mixture was stirred at this temperature for 20 minutes. A solution of 6-bromopyridin-3-amine (11.56 mmol, 2.0 g) in THF (20 ml) and Pd(PPh3)4 (1.16 mmol, 1.3 g) were added respectively and the crude mixture was heated at 40° C. overnight. The solvent was evaporated and the crude mixture was purified by reverse phase chromatography eluting with a water-MeOH/AcN system affording 0.72 g (yield 30%) of the expected product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08536165B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-887e871e69e540029f5e78fea7682c0c
Quellennotizuspto-grants-2013_09