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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 12142Erstellt: 23. Oktober 2026

Toluene → 2-Amino-5-chloro-N-(5-chloropyridin-2-yl)benzamide

https://huagongshe.com/de/reaction/12142

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTolueneHCID 1140—
Edukt2-Amino-5-chloropyridineHCID 66174—
Edukt5-Chloroisatoic anhydrideHCID 78480—
EduktPotassium bis(trimethylsilyl)amideHCID 3251421—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-Amino-5-chloro-N-(5-chloropyridin-2-yl)benzamideHCID 2190641899%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

To a solution of 2-amino-5-chloropyridine (787 mg, 6.1 mmol) in tetrahydrofuran (5 ml) was added 0.5M potassium bis(trimethylsilyl)amide in toluene (20 ml, 10.1 mmol) dropwise at −78° C. After stirred for additional 0.5 hr at −78° C., the mixture was added 5-chloroisatoic anhydride (1 g, 5.1 mmol) at −78° C. The mixture was warmed up to r.t gradually and stirred overnight. After concentrated, the crude was washed with saturated ammonium chloride solution and extracted by ethyl acetate. The organic layer was dried over magnesium sulfate and concentrated to give (2-amino-5-chlorophenyl)-N-(5-chloro(2-pyridyl))carboxamide as yellow solid (1.39 g, 99%). MS found for C12H9Cl2N3O M+=282, (M+2)+=284.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07727982B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-77362edf322045e8a72f238e86be1f41
Quellennotizuspto-grants-2010_06