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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 922513Generated: October 29, 2026

Benzaldehyde → N-{4-[trans-2-(benzylamino)cyclopropyl]phenyl}-3-[(phenylcarbonyl)amino]benzamide

https://huagongshe.com/reaction/922513

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium borohydrideHCID 4311764—
ReactantN-[4-(trans-2-aminocyclopropyl)phenyl]-3-[(phenylcarbonyl)amino]benzamide hydrochlorideHCID 86729850—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductN-{4-[trans-2-(benzylamino)cyclopropyl]phenyl}-3-[(phenylcarbonyl)amino]benzamideHCID 86729854—

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of N-[4-(trans-2-aminocyclopropyl)phenyl]-3-[(phenylcarbonyl)amino]benzamide hydrochloride (85.5 mg) in methanol (2 mL) were added benzaldehyde (21 μL) and sodium hydrogen carbonate (26.4 mg). The mixture was stirred at 70° C. for 1 hr, and ice-cooled to 0° C. and sodium borohydride (11.9 mg) was added. The mixture was stirred for 1 hr and water was added. The mixture was extracted with ethyl acetate, and the extract was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) and crystallized (hexane/ethyl acetate) to give the title compound (6.2 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278931B2
Source datasetuspto-grants-2016_03
ORD IDord-977d15938a364d448cac8e21a333ea1b
Source noteuspto-grants-2016_03