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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethylaminoethyl chloride | HCID 13364 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | N-(carboxymethyl)-N-(3,5-bis(decyloxy)-phenyl)glycine | HCID 192621 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-[3,5-bis(decyloxy)phenyl]-N-[2-[2-(diethylamino)ethoxy]-2-oxoethyl]glycine 2-(diethylamino)ethyl ester dihydrochloride | HCID 67788036 | 36.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05324747 |
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| Source dataset | uspto-grants-1994_06 |
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| ORD ID | ord-408791bd17b845508e01bbcc0501ffe4 |
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| Source note | uspto-grants-1994_06 |
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