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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 724203Generated: October 30, 2026

Cyclopropylamine → 6-Bromo-N-cyclopropyl-2-naphthalenecarboxamide

https://huagongshe.com/reaction/724203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopropylamineHCID 69828—
ReactantDiisopropylethylamineHCID 81531—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactant6-Bromo-2-naphthalenecarboxylic acidHCID 4549852—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product6-Bromo-N-cyclopropyl-2-naphthalenecarboxamideHCID 2187961870%

Reaction Steps

6-Bromo-2-naphthoic acid (1.01 g), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (0.92 g) and 1-hydroxy-1H-benzotriazole monohydrate (0.735 g; HOBt) were dissolved in dimethylformamide (16 ml) under an argon atmosphere. N-Ethyldiisopropylamine (0.62 g) was added with stirring under ice-cooling. Cyclopropylamine (0.37 g) was added and the mixture was stood with stirring at room temperature for 18 h. The reaction mixture was poured into ethyl acetate (0.15 L) and the mixture was washed successively with water and saturated brine. The mixture was dried over anhydrous sodium sulfate and the solvent was concentrated. The precipitated crystals were collected by filtration and dried to give the title compound (0.817 g) as colorless needle crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07141598B2
Source datasetuspto-grants-2006_11
ORD IDord-51a367fb97a947cc92917363d1a065c2
Source noteuspto-grants-2006_11