HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfate Ion → N-(2-((2-hydroxy-3-(4-(2-methoxyethoxy)phenoxy)propyl)amino)ethyl)-4-morpholinecarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfate Ion | HCID 1117 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-MorpholinecarboxaMide, N-(2-aMinoethyl)- | HCID 11041198 | — |
| Reactant | 1-(2,3-Epoxypropoxy)-4-(2-methoxyethoxy)benzene | HCID 12621549 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | N-(2-((2-hydroxy-3-(4-(2-methoxyethoxy)phenoxy)propyl)amino)ethyl)-4-morpholinecarboxamide | HCID 20222106 | — |
Reaction Steps
4 g of 3-(4-(2-methoxyethoxy)phenoxy)-1,2-epoxypropane, 5.8 g of the sulphate of N-2-aminoethyl-4-morpholinecarboxamide, and 5.8 g of K2CO3 were refluxed in 2-propanol for 2 days. The mixture was filtered and concentrated in vacuo. The residue was dissolved in methylene chloride and washed with H2O. The organic phase was dried over Na2SO4, filtered and evaporated. The product was recrystallized from ethyl acetate. Yield 2.3 g. Melting point 69° C. (base). The structure was determined using NMR and equivalent weight.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04636501 |
| Source dataset | uspto-grants-1987_01 |
| ORD ID | ord-ef615be404514c78b21cfad46faf6846 |
| Source note | uspto-grants-1987_01 |