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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 44239Erstellt: 23. Oktober 2026

Pyridine → N-(4-chloropyridin-3-yl)-2-nitrobenzamide

https://huagongshe.com/de/reaction/44239

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
Edukt2-Nitrobenzoyl chlorideHCID 11875—
Edukt3-Amino-4-chloropyridineHCID 581932—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktN-(4-chloropyridin-3-yl)-2-nitrobenzamideHCID 67434091—

Reaktionsschritte

A solution of 3-amino-4-chloropyridine (5 g, 39 mmol), 2-nitrobenzoyl chloride (5.1 mL, 39 mmol) and pyridine (11 mL) in tetrahydrofuran (50 mL) was stirred for 20 hours. The reaction mixture was partitioned between water (200 mL) and dichloromethane (600 mL). The phases were separated and the organic phase was washed with water (150 mL) then brine (150 mL). The organic phase was dried over sodium sulfate, filtered and concentrated in vacuo. The crude product was purified by flash chromatography (SiO2, 10% ethyl acetate in dichloromethane). The N-(4-chloropyridin-3-yl)-2-nitrobenzamide was obtained as a brown solid (2.0 g). LCMS [M+H]: 279.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08541407B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-fa642dc6671442b284ddd57048d9fa5b
Quellennotizuspto-grants-2013_09