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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 980162Generated: November 2, 2026

Sulfate Ion → N-(2-((2-hydroxy-3-(4-(2-cyclobutylmethoxyethoxy)phenoxy)propyl)amino)ethyl)-4-morpholinecarboxamide

https://huagongshe.com/reaction/980162

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfate IonHCID 1117—
ReactantSodium HydroxideHCID 14798—
ReactantN-(2-Aminoethyl)-4-morpholinecarboxamideHCID 11041198—
Reactant4-(2-Cyclobutylmethoxyethoxy)phenoxy-1,2-epoxypropaneHCID 86741207—
SolventEthanolHCID 702—
ProductN-(2-((2-hydroxy-3-(4-(2-cyclobutylmethoxyethoxy)phenoxy)propyl)amino)ethyl)-4-morpholinecarboxamideHCID 20222111—

Reaction Steps

12.0 g of the neutral sulphate of N-2-aminoethyl-4-morpholinecarboxamide and 2.16 g NaOH was refluxed in 100 ml of ethanol for 1 h. Thereafter 10 g of 3-(4-(2-cyclobutylmethoxyethoxy)phenoxy-1,2-epoxypropane in 50 ml of ethanol was added and the mixture refluxed for 20 h, filtered, and evaporated. The residue was dissolved in 175 ml of ethyl acetate and washed twice with water. Thereafter the title compound crystallized from the ethyl acetate phase. The crystals were filtered off and washed with ether. Yield 7.1 g. Melting point 91°-93° C. (base). The structure was determined using NMR-analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04636501
Source datasetuspto-grants-1987_01
ORD IDord-5c5a26d1ff074d4784a66c18afa989e5
Source noteuspto-grants-1987_01