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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 427692Generated: October 25, 2026

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

https://huagongshe.com/reaction/427692

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant2-amino-N-(4-methoxyphenyl)benzamideHCID 478820—
Reactant4-(Pyridin-4-yl)benzoic acidHCID 1520811—
SolventPyridineHCID 1049—
SolventTolueneHCID 1140—
Product2-[[4-(4-Pyridyl)benzoyl]amino]-N-(4-methoxyphenyl)benzamide HydrochlorideHCID 1817443530.7%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313122B1
Source datasetuspto-grants-2001_11
ORD IDord-92487b1298a04a75a2327e0b76a8b884
Source noteuspto-grants-2001_11