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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 550056Generated: October 31, 2026

Pyridine → 3-{[4-(benzyloxy)benzoyl]amino}-N-cyclopropyl-4-methylbenzamide

https://huagongshe.com/reaction/550056

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantOxalyl chlorideHCID 65578—
Reactant4-(Benzyloxy)benzoic acidHCID 73880—
Reactant3-amino-N-cyclopropyl-4-methylbenzamideHCID 11983854—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product3-{[4-(benzyloxy)benzoyl]amino}-N-cyclopropyl-4-methylbenzamideHCID 1138402387%

Reaction Steps

To a solution of 4-benzyloxybenzoic acid (11.0 g, 48 mmol) in DCM (100 mL) at 0° C. was added oxalyl chloride (8.4 mL, 96 mmol) followed by DMF (two drops). The resulting mixture was stirred at room temperature for 2 hours. The mixture was evaporated giving a white solid which was dissolved in DCM (50 mL). The resulting solution was added portionwise to a stirred solution of 3-amino-N-cyclopropyl-4-methylbenzamide (7.61 g, 40 mmol) and pyridine (7.76 mL, 96 mmol) in DCM (100 mL) at 0° C. The resulting mixture was stirred at room temperature for 2 hours. The solid was collected by filtration and washed three times with DCM to give the title compound as a white solid (13.9 g, 87%); NMR Spectrum: (DMSOd6) 0.60 (m, 4H), 2.25 (s, 3H), 2.84 (m, 1H), 5.20 (s, 2H), 7.14 (d, 2H), 7.39 (m, 6H), 7.63 (d, 1H), 7.79 (s, 1H), 7.97 (d, 2H), 8.37 (s, 1H), 9.82 (s, 1H); Mass Spectrum: M+H+ 399.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943776B2
Source datasetuspto-grants-2011_05
ORD IDord-cdbc16b3f60a44d2bcc035d8b629ed64
Source noteuspto-grants-2011_05