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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2272691Erstellt: 26. Oktober 2026

Ammonium Chloride → N2-(3-Fluoro-4-methylphenyl)pyridine-2,3-diamine

https://huagongshe.com/reaction/2272691

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium ChlorideHCID 25517—
EduktN-(3-fluoro-4-methylphenyl)-3-nitro-2-pyridylamineHCID 40676958—
KatalysatorZincHCID 23994—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktN2-(3-Fluoro-4-methylphenyl)pyridine-2,3-diamineHCID 29067357110,9%

Reaktionsschritte

Zinc dust (14.3 g, 219 mmol) was added to a stirring mixture of N-(3-fluoro-4-methylphenyl)-3-nitropyridin-2-amine (C1) (6.78 g, 27.4 mmol) and ammonium chloride (11.7 g, 219 mmol) in tetrahydrofuran (55 mL) and water (55 mL), which caused the temperature of the mixture to rise to 45° C. The reaction mixture was stirred for 10 minutes, and then filtered through a pad of Celite, rinsing with ethyl acetate. The organic layer from the filtrate was further diluted with ethyl acetate, washed with aqueous ammonium chloride solution and with saturated aqueous sodium chloride solution, dried over magnesium sulfate, and filtered. The filtrate was concentrated in vacuo to afford the product as a black solid (6.6 g), the bulk of which was taken directly to the following step. LCMS m/z 218.1 [M+H]+. 1H NMR (400 MHz, CDCl3), characteristic product peaks: δ 7.84 (dd, J=4.9, 1.6 Hz, 1H), 7.01 (dd, J=7.6, 1.6 Hz, 1H), 6.82 (br dd, J=8, 2 Hz, 1H), 6.77 (dd, J=7.6, 4.9 Hz, 1H), 2.20 (d, J=2 Hz, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09120788B2
Quelldatensatzuspto-grants-2015_09
ORD IDord-45ced77ae4694299a580cf8281ae971c
Quellennotizuspto-grants-2015_09