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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1110303Generated: November 3, 2026

Diethylaminoethyl chloride → N-[3,5-bis(decyloxy)phenyl]-N-[2-[2-(diethylamino)ethoxy]-2-oxoethyl]glycine 2-(diethylamino)ethyl ester dihydrochloride

https://huagongshe.com/reaction/1110303

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethylaminoethyl chlorideHCID 13364—
ReactantDiisopropylethylamineHCID 81531—
ReactantN-(carboxymethyl)-N-(3,5-bis(decyloxy)-phenyl)glycineHCID 192621—
SolventDimethylformamideHCID 6228—
ProductN-[3,5-bis(decyloxy)phenyl]-N-[2-[2-(diethylamino)ethoxy]-2-oxoethyl]glycine 2-(diethylamino)ethyl ester dihydrochlorideHCID 6778803636.8%

Reaction Steps

A mixture of 0.50 g (0.96 mmol) of N-(carboxymethyl)-N-[3,5-bis(decyloxy)phenyl]glycine, 1.3 g (9.6 mmol) of 2-diethylaminoethyl chloride and 1.34 ml (7.7 mmol) of N,N-diisopropyl ethylamine in 15 ml of DMF was stirred at room temperature for 48 hours. The reaction mixture was concentrated on the oil pump and the residue was treated with NaHCO3 solution. The product was extracted with ethyl acetate and the dried extract was concentrated at reduced pressure to an oil which was purified by chromatography on 25 g of 230-400 mesh silica gel using methylene chloride(90):methanol(10);concentrated ammonium hydroxide(0.1). The resultant pure free base (0.51 g) was converted to the dihydrochloride salt by treatment of a methylene chloride solution was 0.95 ml of 3N HCl in ethanol. After concentration, the product was dissolved in ether and stored at -18° until crystals formed. Filtration gave 0.28 g, mp 132°-135° of N-[3,5-bis-(decyloxy)phenyl]-N-[ 2-[2-(diethylamino)ethoxy]-2-oxoethyl]glycine 2-(diethylamino)ethyl ester dihydrochloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05324747
Source datasetuspto-grants-1994_06
ORD IDord-408791bd17b845508e01bbcc0501ffe4
Source noteuspto-grants-1994_06