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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 576280Generated: October 25, 2026

N-Ethyl-1-naphthalenamine → Ethyl 7-bromo-3-(3-(ethyl(naphthalen-1-yl)amino)propyl)-1h-indole-2-carboxylate

https://huagongshe.com/reaction/576280

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Ethyl-1-naphthalenamineHCID 67043—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactantethyl 7-bromo-3-(3-oxopropyl)-1H-indole-2-carboxylateHCID 86628021—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductEthyl 7-bromo-3-(3-(ethyl(naphthalen-1-yl)amino)propyl)-1h-indole-2-carboxylateHCID 68938635—

Reaction Steps

To a solution of EXAMPLE 531A (130 mg) and N-ethylnaphthalen-1-amine (82 mg) in dichloromethane (3 mL) was added sodium triacetoxyborohydride (2.35 g). The mixture was stirred at room temperature overnight. After this time the mixture was diluted with ethyl acetate (1500 mL) and washed with 1N NaOH, water, brine, and dried over Na2SO4. After filtration and concentration of the filtrate, the residue was purified by flash chromatography using silica gel and eluenting with 5% ethyl acetate in hexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09035047B2
Source datasetuspto-grants-2015_05
ORD IDord-6cd87c6596114d6ba0b4f35bd098973b
Source noteuspto-grants-2015_05