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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 900661Generated: October 25, 2026

4-methoxy-N-ethylamphetamine → 1-(2-{Ethyl-[2-(4-methoxyphenyl)-1-methylethyl]amino}ethyl)-azepan-2-one

https://huagongshe.com/reaction/900661

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-methoxy-N-ethylamphetamineHCID 85725—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant(2-Oxo-azepan-1-yl)acetaldehydeHCID 62024269—
Solvent1,2-DichloroethaneHCID 11—
Product1-(2-{Ethyl-[2-(4-methoxyphenyl)-1-methylethyl]amino}ethyl)-azepan-2-oneHCID 1211269791.9%

Reaction Steps

A mixture of [2-(4-methoxyphenyl)-1-methylethyl]ethylamine (0.53 g, 2.75 mmole), (2-oxo-azepan-1-yl)acetaldehyde (0.5 g, 3.2 mmole), and sodium triacetoxyborohydride (0.88 g, 4.1 mmole) in 1,2-dichloroethane (15 mL) was stirred at room temperature for 60 hours. The mixture was concentrated, and the residue was partitioned between diethyl ether (50 mL) and saturated aqueous sodium bicarbonate (25 mL). The organic solution was extracted with 5% hydrochloric acid (20 mL), and the aqueous acidic phase was washed with diethyl ether and the pH was adjusted to 12 with 25% sodium hydroxide. The mixture was extracted with dichoromethane, and the organic phase was dried (sodium sulfate) and concentrated to give 1-(2-{ethyl-[2-(4-methoxyphenyl)-1-methylethyl]amino}ethyl)-azepan-2-one 11 (0.84 g) as a viscous oil, which was converted to the dibenzoyl-L-tartrate salt, Anal.: Calcd. for C38H46N2O10: C, 66.07; H, 6.71; N, 4.06%. Found C, 64.69; H, 6.45; N, 3.90%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07361648B2
Source datasetuspto-grants-2008_04
ORD IDord-cae9b61043d44f25884e80fd788b63fe
Source noteuspto-grants-2008_04