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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2047387Generated: November 1, 2026

O-Phenylenediamine → N-(2-amino-phenyl)-5-bromo-2-fluoro-benzamide

https://huagongshe.com/reaction/2047387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-PhenylenediamineHCID 7243—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant5-Bromo-2-fluorobenzoic acidHCID 2736315—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDimethylformamideHCID 6228—
ProductN-(2-amino-phenyl)-5-bromo-2-fluoro-benzamideHCID 2469331381%

Reaction Steps

5-Bromo-2-fluoro-benzoic acid (4.96 g, 22.6 mmol), benzene-1,2-diamine (4.90 g, 45.3 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC) (5.21 g, 27.2 mmol), 1-hydroxybenzotriazole hydrate (1-HOBt) (3.67 g, 27.2 mmol) and dimethyl-pyridin-4-yl-amine (DMAP) (0.03 g, 0.2 mmol) were placed into a 100 mL round bottom flask. Dry DMF (60 mL) was added and the reaction was stirred at room temperature overnight. Solvent was removed under reduced pressure, then the crude diluted with DCM (15 mL) and 0.4 M Na2CO3 solution (15 mL) A white precipitate formed and it was filtered off and washed again with DCM (10 mL) and dried to afford 4.96 g of the title compound. Solutions were collected, the organic phase was separated from the aqueous one and concentrated under reduced pressure: other precipitate formed and it was filtered off, washed with DCM (3 mL) to afford other 0.68 g of desired compound. Total yield 81%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592463B2
Source datasetuspto-grants-2013_11
ORD IDord-74c9009bcd7344189865a893ce70d4a4
Source noteuspto-grants-2013_11