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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 395841Erstellt: 24. Oktober 2026

Thionyl Chloride → 2-[[4-(4-Pyridyl)benzoyl]amino]-N-(4-methoxyphenyl)benzamide Hydrochloride

https://huagongshe.com/de/reaction/395841

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktThionyl ChlorideHCID 24386—
Edukt2-amino-N-(4-methoxyphenyl)benzamideHCID 478820—
Edukt4-(Pyridin-4-yl)benzoic acidHCID 1520811—
LösungsmittelPyridineHCID 1049—
LösungsmittelTolueneHCID 1140—
Produkt2-[[4-(4-Pyridyl)benzoyl]amino]-N-(4-methoxyphenyl)benzamide HydrochlorideHCID 1817443530,7%

Reaktionsschritte

To a stirring suspension of 4-(4-pyridyl)benzoic acid (0.2 g, 1 mmol) in toluene (35 mL) was added thionyl chloride (0.55 mL, 7.5 mmol) and the mixture was heated to reflux. After 1 h the solution was cooled and added to a solution of 2-amino-N-(4-methoxyphenyl)benzamide (0.176 g, 0.73 mmol) in pyridine (2 mL) and toluene (5 mL). After stirring for 48 h, the solvent was removed in vacuo and the residue was partitioned between ethyl acetate and water. The organic phase was separated and washed with sat. NaHCO3, brine and dried (MgSO4), filtered and concentrated to give 103 mg of brown solid which was chromatographed by RPHPLC Method B. Upon standing, a sample of the title compound (14 mg, 4%) crystalized from one of the product containing fractions.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06605626B2
Quelldatensatzuspto-grants-2003_08
ORD IDord-f64df43c3e664dbc9dab3e6aa122d8da
Quellennotizuspto-grants-2003_08