HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfate Ion → N-(2-((2-hydroxy-3-(4-(2-cyclobutylmethoxyethoxy)phenoxy)propyl)amino)ethyl)-4-morpholinecarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfate Ion | HCID 1117 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N-(2-Aminoethyl)-4-morpholinecarboxamide | HCID 11041198 | — |
| Reactant | 4-(2-Cyclobutylmethoxyethoxy)phenoxy-1,2-epoxypropane | HCID 86741207 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(2-((2-hydroxy-3-(4-(2-cyclobutylmethoxyethoxy)phenoxy)propyl)amino)ethyl)-4-morpholinecarboxamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04636501 |
| Source dataset | uspto-grants-1987_01 |
| ORD ID | ord-5c5a26d1ff074d4784a66c18afa989e5 |
| Source note | uspto-grants-1987_01 |